The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index; 33 of the 42 sources its claims cite were checked for support.
Insulator dysfunction and oncogene activation in IDH mutant gliomas
Open accessAbstract
Gain-of-function IDH mutations are initiating events that define major clinical and prognostic classes of gliomas. Mutant IDH protein produces a new onco-metabolite, 2-hydroxyglutarate, which interferes with iron-dependent hydroxylases, including the TET family of 5'-methylcytosine hydroxylases. TET enzymes catalyse a key step in the removal of DNA methylation. IDH mutant gliomas thus manifest a CpG island methylator phenotype (G-CIMP), although the functional importance of this altered epigenetic state remains unclear. Here we show that human IDH mutant gliomas exhibit hypermethylation at cohesin and CCCTC-binding factor (CTCF)-binding sites, compromising binding of this methylation-sensitive insulator protein. Reduced CTCF binding is associated with loss of insulation between topological domains and aberrant gene activation. We specifically demonstrate that loss of CTCF at a domain boundary permits a constitutive enhancer to interact aberrantly with the receptor tyrosine kinase gene PDGFRA, a prominent glioma oncogene. Treatment of IDH mutant gliomaspheres with a demethylating agent partially restores insulator function and downregulates PDGFRA. Conversely, CRISPR-mediated disruption of the CTCF motif in IDH wild-type gliomaspheres upregulates PDGFRA and increases proliferation. Our study suggests that IDH mutations promote gliomagenesis by disrupting chromosomal topology and allowing aberrant regulatory interactions that induce oncogene expression.
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33 of 42 cited sources checked · 18 supported · 0 flagged · accuracy not yet measured
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Mutant IDH protein produces a novel onco-metabolite, 2-hydroxyglutarate (2-HG), that interferes with iron-dependent hydroxylases, including the TET family of 5′-methylcytosine hydroxylases3–7.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [3] Dang, L. et al. Cancer-associated IDH1 mutations produce 2-hydroxyglutarate. Nature 462, 739–744 (2009) source
The Discussion states that mutant IDH1 catalyzes the conversion of α-ketoglutarate to 2HG and describes 2HG production as a result of IDH1 mutations. This supports the production claim attributed to this source; the supplied passages do not give page numbers. (LLM, conf=0.94)
- Supportedcites [4] Figueroa, M. E. et al. Leukemic IDH1 and IDH2 mutations result in a hypermethylation phenotype, disrupt TET2 function, and impair hematopoietic differentiation. Cancer Cell 18, 553–567 (2010) source
The Introduction states that common IDH1/2 mutations acquire an enzymatic activity that produces 2HG. The Results section reports markedly elevated 2HG levels in cells expressing mutant IDH1 or IDH2 compared with the corresponding wild-type enzymes. Page numbers were not supplied. (LLM, conf=0.94)
- Supportedcites [5] Xu, W. et al. Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases. Cancer Cell 19, 17–30 (2011) source
The Introduction states that mutant IDH1 and IDH2 gain the ability to produce D-2-HG. The Results also report increased D-2-HG after expression of mutant IDH1 in human glioma cells. (LLM, conf=0.94)
- Supportedcites [6] Lu, C. et al. IDH mutation impairs histone demethylation and results in a block to cell differentiation. Nature 483, 474–478 (2012) source
The paper reports that cells expressing mutant IDH2 produced 2HG, whereas cells expressing wild-type IDH2 or a control vector did not (passage [3], labeled Abstract, Fig. 2a). This directly supports the attributed claim. (LLM, conf=0.95)
- Not checked — no full text of the sourcecites [7] Cairns, R. A. & Mak, T. W. Oncogenic isocitrate dehydrogenase mutations: mechanisms, models, and clinical opportunities. Cancer Dis. 3, 730–741 (2013) source
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“IDH mutant gliomas thus manifest a CpG island methylator phenotype (G-CIMP)10,11, though the functional significance of this altered epigenetic state remains unclear.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [10] Noushmehr, H. et al. Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. Cancer Cell 17, 510–522 (2010) sourceExperimental — accuracy not yet measured
The Results sections report a strong association between IDH1 mutation and G-CIMP in gliomas. But in an independent set, only 35 of 48 IDH1-mutant tumors (72.9%) were G-CIMP-positive, and the paper observed no IDH2 mutations in its TCGA set. The claim is therefore broader than the paper’s finding: not all IDH1-mutant gliomas showed the phenotype, and it does not establish the association for IDH mutations generally. (LLM, conf=0.84)
- Supportedcites [11] Turcan, S. et al. IDH1 mutation is sufficient to establish the glioma hypermethylator phenotype. Nature 483, 479–483 (2012) source
The Abstract states that IDH mutation establishes glioma CIMP (G-CIMP). The tumour-sequencing passage reports that 49 of 50 G-CIMP-positive tumours had an IDH1 or IDH2 mutation, while none of the G-CIMP-negative tumours did. The citation supports the G-CIMP clause; the sentence’s separate comment about functional significance is not attributed to it. (LLM, conf=0.94)
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Consistent with prior studies16, we found that genes in the same domain correlate across samples, but that genes separated by a boundary show lower correlation (Fig. 1e).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [16] Nora, E. P. et al. Spatial partitioning of the regulatory landscape of the X-inactivation centre. Nature 485, 381–385 (2012) sourceExperimental — accuracy not yet measured
The transcriptome-analysis passage (labeled Abstract, Fig. 4b) reports that genes within the same TAD had more correlated expression profiles than genes in different domains. But it measured 17 time points during female mouse embryonic stem-cell differentiation, not correlations across normal brain samples. (LLM, conf=0.88)
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Mutant IDH protein produces a novel onco-metabolite, 2-hydroxyglutarate (2-HG), that interferes with iron-dependent hydroxylases, including the TET family of 5′-methylcytosine hydroxylases3–7.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [3] Dang, L. et al. Cancer-associated IDH1 mutations produce 2-hydroxyglutarate. Nature 462, 739–744 (2009) sourceExperimental — accuracy not yet measured
The section “Mutant IDH1 directly converts αKG to 2HG” confirms that mutant IDH1 produces 2HG. The Discussion suggests that 2HG may inhibit αKG-dependent prolyl hydroxylases, but presents this as a possibility, not an established effect. Our copy does not identify TET 5-methylcytosine hydroxylases as targets. (LLM, conf=0.88)
- Partly supportedcites [4] Figueroa, M. E. et al. Leukemic IDH1 and IDH2 mutations result in a hypermethylation phenotype, disrupt TET2 function, and impair hematopoietic differentiation. Cancer Cell 18, 553–567 (2010) sourceExperimental — accuracy not yet measured
The Results section (page unavailable) identifies TET enzymes as iron-dependent 5-methylcytosine hydroxylases and shows that mutant IDH inhibits TET2-mediated hydroxylation. The paper proposes 2-HG as the mechanism, but does not establish interference with the TET family as a whole or with other iron-dependent hydroxylases; the Discussion treats effects on other enzyme families as a possibility for future study. (LLM, conf=0.83)
- Supportedcites [5] Xu, W. et al. Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases. Cancer Cell 19, 17–30 (2011) source
The Results section, “2-HG Inhibits the Activity of TET 5-Methylcytosine Hydroxylases” (page not provided), reports that 2-HG inhibits TET1 and TET2 in assays of 5-methylcytosine hydroxylation. The Enzymatic Assays section includes an iron salt in the TET reaction mixture, consistent with the description of these hydroxylases as iron-dependent. (LLM, conf=0.92)
- Partly supportedcites [6] Lu, C. et al. IDH mutation impairs histone demethylation and results in a block to cell differentiation. Nature 483, 474–478 (2012) sourceExperimental — accuracy not yet measured
The paper’s Abstract (page unavailable) states that mutant IDH produces 2HG, reports mutant IDH-induced inhibition of the α-ketoglutarate-dependent enzyme TET2, and shows that 2HG inhibits a histone demethylase. It does not explicitly establish inhibition of the TET family as a whole or describe these enzymes as iron-dependent hydroxylases. (LLM, conf=0.82)
- Not checked — no full text of the sourcecites [7] Cairns, R. A. & Mak, T. W. Oncogenic isocitrate dehydrogenase mutations: mechanisms, models, and clinical opportunities. Cancer Dis. 3, 730–741 (2013) source
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Every source the paper cites for this claim was checked and supports it.
In the paper
“Our ChIP-seq data confirm that this boundary contains a strong CTCF binding site over a canonical CTCF motif with a CpG dinucleotide in a position previously linked to methylation-sensitivity25 (Fig. 3b).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [25] Wang, H. et al. Widespread plasticity in CTCF occupancy linked to DNA methylation. Genome Res. 22, 1680–1688 (2012) source
The Results section (‘Variable CTCF occupancy linked to CpG methylation’) reports that CpGs at particular positions in the CTCF recognition sequence are associated with methylation-sensitive occupancy, and that methylation at position 1 has been shown to inhibit CTCF binding in vitro. The citation supports the prior link to methylation sensitivity; the citing authors attribute the strong binding at their particular boundary to their own ChIP-seq data. (LLM, conf=0.92)
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Nonetheless, IDH mutant gliomas strongly express PDGFRA (Fig. 2b), and share the proneural transcriptional program characteristic of PDGFRA-amplified tumors23,24.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [23] Brennan, C. W. et al. The somatic genomic landscape of glioblastoma. Cell 155, 462–477 (2013) sourceExperimental — accuracy not yet measured
In Results, under “Molecular subclasses defined by global mRNA expression and DNA Methylation” (page unavailable), the paper describes G-CIMP and non-G-CIMP proneural glioblastomas as transcriptomically similar and associates PDGFRA amplification with the non-G-CIMP proneural subgroup. It reports that all IDH1-mutant cases had the G-CIMP pattern. These findings support the shared proneural program in the glioblastomas studied, but do not establish it for IDH-mutant gliomas more broadly. (LLM, conf=0.82)
- Partly supportedcites [24] Verhaak, R. G. et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 . Cancer Cell 17, 98–110 (2010) sourceExperimental — accuracy not yet measured
In Results > Functional Annotation of Subtypes (page unavailable), the paper reports that 11 of 12 IDH1 mutations occurred in the Proneural class, which was also enriched for PDGFRA amplification and had a proneural expression signature. This supports the shared-program claim for the glioblastomas studied, but not its extension to IDH-mutant gliomas generally. (LLM, conf=0.85)
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The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Consistent with prior studies16, we found that genes in the same domain correlate across samples, but that genes separated by a boundary show lower correlation (Fig. 1e).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [16] Nora, E. P. et al. Spatial partitioning of the regulatory landscape of the X-inactivation centre. Nature 485, 381–385 (2012) sourceExperimental — accuracy not yet measured
The passage on gene expression dynamics during early differentiation reports that genes within the same TAD had more correlated expression profiles than genes in different domains. It measured female mouse embryonic stem cells over a differentiation time course, not normal brain samples, so it does not support that setting. (LLM, conf=0.88)
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A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Here we show that IDH mutant gliomas exhibit hyper-methylation at CTCF binding sites, compromising binding of this methylation-sensitive insulator protein.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Treatment of IDH mutant gliomaspheres with demethylating agent partially restores insulator function and down-regulates PDGFRA.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“We found that these loci have higher GC content, and exhibit significantly higher levels of DNA methylation in IDH mutant gliomas, relative to IDH wildtype (Fig. 1c–d).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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- It may state two separate claims as one. 19
- Probably not a substantial claim. 27
- The quote only partly states this claim. 1
Every source the paper cites for this claim was checked and supports it.
In the paper
“Genomic alterations that remove CTCF-associated boundaries allow aberrant enhancer-gene interactions and alter gene expression17.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [17] Lupiáñez, D. G. et al. Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions. Cell 161, 1012–1025 (2015) source
The Discussion section “Boundary structures are important for TAD integrity” identifies CTCF-binding clusters at the tested boundaries and reports that preserving those boundaries prevented ectopic interactions and gene misexpression. “A framework for interpreting human structural variation” states that deletions removing a boundary permit enhancer contact with genes outside the TAD, causing misexpression. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“TET enzymes catalyze a key step in the removal of DNA methylation8,9.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [8] Pastor, W. A., Aravind, L. & Rao, A. TETonic shift: biological roles of TET proteins in DNA demethylation and transcription. Nature Rev. Mol. Cell Biol. 14, 341–356 (2013) source
The passage headed “TET-mediated DNA demethylation: mechanisms” describes TET oxidation of 5-methylcytosine as a step in pathways that ultimately replace it with cytosine. The “Active DNA demethylation through DNA repair” passage likewise explains how TET oxidation products are removed and replaced with cytosine. Page numbers were not supplied. (LLM, conf=0.93)
- Supportedcites [9] Kohli, R. M. & Zhang, Y. TET enzymes, TDG and the dynamics of DNA demethylation. Nature 502, 472–479 (2013) source
The Abstract states that TET enzymes oxidize 5-methylcytosine, advancing the understanding of DNA demethylation. The passage headed “BOX 1. Roles of 5hmC in DNA demethylation” describes TET-mediated oxidation as a step in pathways that return methylated cytosine to unmodified cytosine. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Recent studies have solidified the role of the CTCF insulator protein in creating chromatin loops and boundaries that partition such domains15.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [15] Rao, S. S. et al. A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping. Cell 159, 1665–1680 (2014) source
The Results section reports that most loop anchors bind CTCF and that many loops demarcate domains. The Discussion says loops often demarcate domains and discusses the mechanism by which CTCF and cohesin form loops, supporting the citing sentence’s broad paraphrase. (LLM, conf=0.87)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Gain-of-function IDH mutations are initiating events that define major clinical and prognostic classes of gliomas1,2.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [1] Parsons, D. W. et al. An integrated genomic analysis of human glioblastoma multiforme. Science 321, 1807–1812 (2008) sourceExperimental — accuracy not yet measured
The ‘High-frequency alterations of IDH1 in GBM’ section links IDH1 mutations to secondary GBM and substantially longer survival, supporting their clinical and prognostic relevance. The Discussion calls an activating effect a speculation and says further analysis is needed to determine the effect on enzyme activity. The paper does not establish that these mutations increase enzyme activity or are initiating events, and its findings concern GBM rather than gliomas broadly. (LLM, conf=0.90)
- Partly supportedcites [2] The Cancer Genome Atlas Research Network. Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas. N. Engl. J. Med. 372, 2481–2498 (2015) sourceExperimental — accuracy not yet measured
The Results (Mutational Landscape of Lower-Grade Gliomas; page not provided) suggest that IDH mutation is an initial event in molecular progression. The Results (Clinical Characteristics and Outcomes; page not provided) and Discussion show that IDH status, together with 1p/19q status, distinguishes groups with different clinical outcomes. Our copy does not characterize the IDH mutations as gain-of-function or establish increased enzyme activity, and it presents the proposed sequence as a suggestion rather than a proven initiating event. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“To control for copy number changes, we first called copy number profiles from input sequencing data using CNVnator37. We then removed all regions where at least one sample had a strong deletion (<0.25), and normalized by copy number.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Immunoprecipitation
What the sources say
- Supportedcites [37] Abyzov, A., Urban, A. E., Snyder, M. & Gerstein, M. CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res. 21, 974–984 (2011) source
The Discussion describes CNVnator as a method for discovering copy-number variation from sequencing read depth. The citation is attached to the use of CNVnator to call copy-number profiles; the deletion threshold and subsequent normalization are the citing authors’ own steps, not claims attributed to this source. (LLM, conf=0.93)
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- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“FIP1L1 encodes an RNA processing protein that is constitutively expressed in neural tissues, and particularly active in oligodendrocyte precursors, a putative glioma cell-of-origin22 (Extended Data Fig. 2a).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [22] Sturm, D. et al. Paediatric and adult glioblastoma: multiform (epi)genomic culprits emerge. Nature Rev. Cancer 14, 92–107 (2014) source
Citation 22 is attached to the description of oligodendrocyte precursors as a putative glioma cell of origin. In the Introduction, under “The cells of origin of glioblastoma” (page unavailable), the review says OPCs can be considered cells of origin for Nf1- and Trp53-mutant glioblastoma. (LLM, conf=0.91)
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- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Although PDGFRA is a frequent target of genomic amplification and gain-of-function mutations in glioblastoma (15%), such alterations are rare in IDH mutant tumors23,24.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [23] Brennan, C. W. et al. The somatic genomic landscape of glioblastoma. Cell 155, 462–477 (2013) sourceExperimental — accuracy not yet measured
The Results section on molecular subclasses associates PDGFRA amplification with the non-G-CIMP+ proneural subgroup and describes concurrent amplification in a group predominantly lacking IDH1 mutations. The Results section on somatic alterations also finds IDH1 mutations more prevalent in GBM without RTK alterations. These findings support the direction of the amplification claim in GBM, but the cited passages do not establish that PDGFRA gain-of-function mutations are rare in IDH-mutant tumors. (LLM, conf=0.84)
- Partly supportedcites [24] Verhaak, R. G. et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 . Cancer Cell 17, 98–110 (2010) sourceExperimental — accuracy not yet measured
The Results (Functional Annotation of Subtypes; page not available) say that most IDH1-mutant samples did not have a PDGFRA abnormality, supporting limited overlap in the glioblastomas studied. They do not establish that these alterations are rare across IDH-mutant tumors generally, or identify the observed PDGFRA mutations as gain-of-function. (LLM, conf=0.84)
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- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Genes in top scoring domains include PDGFRA (p<10−21), an established glioma oncogene22, and other candidate regulators of gliomagenesis (Table S1).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [22] Sturm, D. et al. Paediatric and adult glioblastoma: multiform (epi)genomic culprits emerge. Nature Rev. Cancer 14, 92–107 (2014) source
The Structural variations in glioblastoma section reports recurrent PDGFRA amplification in adult and paediatric glioblastoma and describes it as a suggested key oncogenic event in diffuse intrinsic pontine glioma. This supports the citing sentence’s characterization of PDGFRA as an established glioma oncogene. (LLM, conf=0.91)
Load-bearingStrength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Insulator dysfunction may also be accompanied by promoter silencing events28,29, and by alterations to other pathways affected by 2-HG7,30.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [28] Baylin, S. B. & Jones, P. A. A decade of exploring the cancer epigenome – biological and translational implications. Nature Rev. Cancer 11, 726–734 (2011) source
The citation to this paper is attached to “promoter silencing events,” not to the separate clause about other pathways affected by 2-HG. The “Promoter CpG island DNA hypermethylation” section reports that abnormal promoter methylation in cancer stabilizes transcriptional repression and causes loss of gene function. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [29] Costello, J. F., Berger, M. S., Huang, H. S. & Cavenee, W. K. Silencing of p16/CDKN2 expression in human gliomas by methylation and chromatin condensation. Cancer Res. 56, 2405–2410 (1996)
- Not checked — no full text of the sourcecites [7] Cairns, R. A. & Mak, T. W. Oncogenic isocitrate dehydrogenase mutations: mechanisms, models, and clinical opportunities. Cancer Dis. 3, 730–741 (2013) source
- Supportedcites [30] Koivunen, P. et al. Transformation by the (R)-enantiomer of 2-hydroxyglutarate linked to EGLN activation. Nature 483, 484–488 (2012) source
This source is cited for the second clause, concerning other pathways affected by 2-HG, not for promoter silencing. In the supplied passages labeled Abstract, the paper identifies additional 2-HG targets, including TET2 and histone demethylases, and proposes that alterations in other 2-HG-affected enzymes may contribute to epigenetic changes. No page number is supplied. (LLM, conf=0.90)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“L1CAM (p<10−8), a regulator of the glioma stem cells and tumor growth39”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Genomic Scan for Deregulated Boundaries
What the sources say
- Supportedcites [39] Bao, S. et al. Targeting cancer stem cells through L1CAM suppresses glioma growth. Cancer Res. 68, 6043–6048 (2008) source
The Abstract reports that L1CAM knockdown inhibited growth in CD133+ glioma stem cells and suppressed tumor growth in glioma xenografts. The Results and Discussion section also describes L1CAM's role in maintaining CD133+ glioblastoma cell growth. The p-value appears to belong to the citing paper's analysis, not the claim attributed to this source. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Conversely, disruption of chromosomal topology and oncogene insulation may be more generally relevant to methylator phenotypes observed in colorectal and renal cell carcinomas, leukemia and other malignancies28.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Partly supportedcites [28] Baylin, S. B. & Jones, P. A. A decade of exploring the cancer epigenome – biological and translational implications. Nature Rev. Cancer 11, 726–734 (2011) sourceExperimental — accuracy not yet measured
In “Promoter CpG island DNA hypermethylation” (page unavailable), the paper describes methylation of an H19 insulator, loss of CTCF binding, and IGF2 activation in pre-neoplastic kidneys, with a link to colon cancer progression. In “Genetics meets epigenetics” (page unavailable), it discusses methylator phenotypes in gliomas and increased DNA hypermethylation in leukaemia. It does not link disrupted chromosomal topology or oncogene insulation to methylator phenotypes across the named cancers, and its kidney example concerns Wilms’ tumour rather than renal cell carcinoma. (LLM, conf=0.84)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Although PDGFRA is a frequent target of genomic amplification and gain-of-function mutations in glioblastoma (15%), such alterations are rare in IDH mutant tumors23,24.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Supportedcites [23] Brennan, C. W. et al. The somatic genomic landscape of glioblastoma. Cell 155, 462–477 (2013) source
The Results section (‘The landscape of somatic alterations in glioblastoma’) reports PDGFRA alterations in 13.1% of glioblastomas and specifies focal amplification and/or mutation. That supports the paraphrase’s approximate 15% figure. (LLM, conf=0.92)
- Partly supportedcites [24] Verhaak, R. G. et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 . Cancer Cell 17, 98–110 (2010) sourceExperimental — accuracy not yet measured
The Results (Functional Annotation of Subtypes; page unavailable) report PDGFRA amplification across glioblastoma subtypes and PDGFRA mutations in some Proneural tumors. They do not give an approximately 15% frequency or establish that the mutations are gain-of-function; the authors say the point mutations may disrupt ligand interaction. (LLM, conf=0.86)
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- Supported
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In the paper
“BT142 G-CIMP status was confirmed by evaluating LINE methylation with the “Global DNA Methylation Assay – LINE-1″ kit (Active Motif), as described36, and by methylation-sensitive restriction digests.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Primary glioma specimens and gliomasphere models
What the sources say
- Partly supportedcites [36] Lai, R. K. et al. Genome-wide methylation analyses in glioblastoma multiforme. PLoS ONE 9, e89376 (2014) sourceExperimental — accuracy not yet measured
The “Levels of 5m-dC, 5hm-dC and LINE1 Methylation” section describes evaluating LINE-1 methylation, but by pyrosequencing, not with the named Active Motif kit. The cited paper does not report confirming BT142 G-CIMP status or using methylation-sensitive restriction digests for that purpose. No page number is available in our copy. (LLM, conf=0.82)
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- Partly supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In support of an enhancer identity, the element is enriched for H3 lysine 4 mono-methylation (H3K4me1), but lacks H3K4me3, and contains conserved motifs bound by the glioma master transcription factors, OLIG2 and SOX2.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“This analysis highlighted 203 domain boundaries (Fig. 2a; Table S1; see Methods).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe quote only partly states this claim.
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In the paper
“This is associated with reduced CTCF binding and a global deregulation of boundary elements that partition topological domains.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“Consistently, 3C reveals a strong interaction between FIP1L1 enhancer and PDGFRA promoter that is specific to the mutant line (Fig. 3i), and PDGFRA is highly expressed.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The human genome is organized into topological domains that represent discrete structural and regulatory units12.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Not checked — no full text of the sourcecites [12] Bickmore, W. A. & van Steensel, B. Genome architecture: domain organization of interphase chromosomes. Cell 152, 1270–1284 (2013) source
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In the paper
“Reduced CTCF binding is associated with loss of insulation between topological domains and aberrant gene activation.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“These results directly implicate DNA hyper-methylation in compromising CTCF binding, boundary function and oncogene insulation in IDH mutant tumors.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“Cultures were confirmed to be mycoplasma-free via PCR methods.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Primary glioma specimens and gliomasphere models
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In the paper
“CHD4 (p<10−32), a driver of glioblastoma tumor initiation38”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Genomic Scan for Deregulated Boundaries
What the sources say
- Not checked — no full text of the sourcecites [38] Chudnovsky, Y. et al. ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor-initiating cell state. Cell Rep. 6, 313–324 (2014) source
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In the paper
“Notably, CTCF knock-down has been shown to increase cross-boundary interactions and decrease intra-domain interactions21.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
What the sources say
- Not checked — no full text of the sourcecites [21] Zuin, J. et al. Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells. Proc. Natl Acad. Sci. USA 111, 996–1001 (2014) source
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In the paper
“To ensure robustness to noise from lowly expressed genes, we first filtered out 6,476 genes expressed < 1 TPM in more than half of the samples (keeping 14,055 genes).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Genomic Scan for Deregulated Boundaries
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In the paper
“Data was normalized across days using an ATP standard curve.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Cell Growth Assay
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In the paper
“We conservatively estimate that CTCF motif disruption causes a ~3-fold increase in PDGFRA expression, given that DNA level analysis indicates that <50% of insulator CRISPR cells were successfully edited.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“Sonication of tumor specimens and gliomaspheres was calibrated such that DNA was sheared to between 400bp and 2000bp.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Immunoprecipitation
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In the paper
“Single live cells were selected for analysis via side and forward scatter, and viable cells were selected by lack of an unstained channel (APC) autofluorescence.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > PDGFRA Flow Cytometry
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In conclusion, we present a novel epigenetic mechanism by which gain-of-function IDH mutations induce PDGFRA expression and thereby promote fitness in a subset of gliomas.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
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In the paper
“To account for batch effects and difference in ChIP efficiency, we quantile normalized each dataset.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Immunoprecipitation
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In the paper
“To ensure robustness to cell type-specific boundaries, we repeated the analysis with GM12878, K562 and NHEK defined boundaries.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Genomic Scan for Deregulated Boundaries
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In the paper
“In order to avoid possible saturation, reads were downsampled to 5% reads collapsed as PCR duplicates, or 5 million fragments.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Immunoprecipitation
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In the paper
“To ensure robustness, we also repeated the analysis using boundaries defined from HiC data for K562 and NHEK.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Cross-Boundary and Intra-Domain Gene Pair Correlation Analysis
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In the paper
“PCR signal from tumor and gliomasphere 3C was normalized to digestion efficiency and BAC primer signal.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Conformation Capture (3C)
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In the paper
“We confirmed IDH1 mutant status of GSC119 by RNA-seq (82 out of 148 reads overlapping the relevant position in the transcript correspond the mutant allele).”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Primary glioma specimens and gliomasphere models
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What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Normalization was also verified by β-actin, F: 5′-AGA AAA TCT GGC ACC ACA CC -3′, R: 5′-AGA GGC GTA CAG GGA TAG CA -3′.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > PDGFRA Quantitative PCR
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In the paper
“For sequence analysis, identical reads were collapsed to a single paired-end read in order to avoid PCR duplicates.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Chromatin Immunoprecipitation
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
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In the paper
“All samples were acquired with Institutional Review Board approval, and were deidentified prior to receipt.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > Primary glioma specimens and gliomasphere models
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“For correlation analysis, patients with copy number variation in either gene were excluded from the analysis to control for effects of co-amplification.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Methods and Materials > TCGA Correlation and Outcome Analysis
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The observation that genetic disruption of this CTCF boundary element induces PDGFRA expression and enhances proliferation provides strong support for our model that epigenetic disruption of this element offers similar growth advantage to IDH mutant gliomas.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although disruption of this single boundary confers a growth advantage, it is unlikely to be the only mediator of IDH mutations in gliomas.”
§ Insulator dysfunction and oncogene activation in IDH mutant gliomas > Abstract
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
The functional importance of the altered epigenetic state in IDH mutant gliomas is not yet known.
“though the functional significance of this altered epigenetic state remains unclear”
The authors state this as an assumption.
The CRISPR-induced deletion within the CTCF motif disrupts CTCF binding.
“contain a deletion within the CTCF motif expected to disrupt binding”
The paper relies on this without support.
The contact domains and boundaries defined in the cell lines used (IMR90, GM12878, K562, NHEK) are representative of those in glioma tumors.
“Contact domains of IMR90, GM12878, K562 and NHEK cells were obtained from published HiC data15.”
The paper relies on this without support.
CTCF binding sites in IDH wild-type tumors mark domain boundaries.
“Gene pairs were considered to span a boundary if they were assigned to different domains in both GM12878 and IMR90, and separated by a CTCF binding site in IDH wild type tumors.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“These include mutations in DNA methylases and demethylases, histones 144 and histone modifiers, and genes involved in chromatin remodelling and chromosome architecture, but also metabolic genes such as IDH1 and IDH2 that affect histone and DNA methylation 57 and might perturb 3D genome architecture 145 (Fig. 4b).”
From Advances in epigenetics link genetics to the environment and disease (2019) · cites this paper as [145]
In the citing paper
“Inhibition of TET2 promotes leukemic transformation and is also suspected of playing a role in IDH mutant gliomas (Flavahan et al., 2016; Losman and Kaelin, 2013).”
From Transaminase Inhibition by 2-Hydroxyglutarate Impairs Glutamate Biosynthesis and Redox Homeostasis in Glioma (2018) · cites this paper as Flavahan et al., 2016
In the citing paper
“Mutations in IDH1 and IDH2 are mutually exclusive in AML, and IDH1/2 mutations induce cytosine hypermethylation and inhibit TET2-mediated 5-hydroxymethylation 95,96 .”
From The roles of DNA, RNA and histone methylation in ageing and cancer (2019) · cites this paper as [96]
In the citing paper
“In one well characterized example, aberrant gain of 5mC at the binding site of insulator protein CCCTC-binding factor (CTCF) is observed in the Igf2/H19 locus in Beckwith-Wiedemann (fetal overgrowth) syndrome, and in the PDGFRA locus of IDH mutant gliomas (8, 9).”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [9]
In the citing paper
“In both cases, hypermethylation of the binding site prevents CTCF binding and results in the disruption of chromatin topological domains leading to ectopic enhancer-promoter interactions.”
From Dynamic DNA methylation: In the right place at the right time (2018) · cites this paper as [9]
In the citing paper
“IDH mutant gliomas have been shown to exhibit hypermethylation at CTCF binding sites, which leads to a reduction in CTCF binding”
From Transcription factors as readers and effectors of DNA methylation (2016) · cites this paper as [117]
In the citing paper
“loss of CTCF in topologically associated domains removed the domain boundary and caused aberrant gene activation117.”
From Transcription factors as readers and effectors of DNA methylation (2016) · cites this paper as [117]
In the citing paper
“Therefore, the dysregulation of chromatin looping may be causally related to carcinogenesis (Extended Data Fig. 7a) 31,32.”
From The structural basis for cohesin–CTCF-anchored loops (2020) · cites this paper as [32]
In the citing paper
“For example, modest increases in the expression of receptor tyrosine kinase genes can have meaningful effects on cell proliferation (Flavahan et al., 2016).”
From Cohesin Loss Eliminates All Loop Domains (2017) · cites this paper as Flavahan et al., 2016
In the citing paper
“Moreover, amplifications and rare mutations of the platelet-derived growth factor receptor alpha gene (PDGFRA) often co-occur with H3.3K27M and TP53 mutations, indicating a potential role of this receptor in tumorigenesis”
From H3.3K27M Cooperates with Trp53 Loss and PDGFRA Gain in Mouse Embryonic Neural Progenitor Cells to Induce Invasive High-Grade Gliomas (2017) · cites this paper as Flavahan et al., 2016
In the citing paper
“While genetic perturbation of CTCF binding has been shown to result in misregulation of gene expression in various cell lines and cancer9–11,28”
From Tissue-specific CTCF-cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo (2017) · cites this paper as [9]
In the citing paper
“Boundary disruption has recently been linked to cancer and diseases of limb development (Flavahan et al., 2016; Hnisz et al., 2016; Lupianez et al., 2015)”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Flavahan et al., 2016
In the citing paper
“Recent high-resolution Chromosome-Conformation-Capture sequencing studies have revealed that TAD boundaries are perturbed in rare human limb malformation diseases (Lupianez et al., 2015) and certain types of cancers (Flavahan et al., 2016; Hnisz et al., 2016), leading to enhancer miswiring and pathogenic disruption of gene expression.”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Flavahan et al., 2016
In the citing paper
“Domain insulation has been shown to be important for gene expression and physiology (Flavahan et al., 2016, Lupiáñez et al., 2015).”
From Multiscale 3D Genome Rewiring during Mouse Neural Development (2017) · cites this paper as Flavahan et al., 2016
In the citing paper
“Chromatin insulation occurs at multiple levels and leads to a hierarchical 3D nuclear organization, whereby smaller, less insulated regions (called also sub-TADs [Flavahan et al., 2016, Phillips-Cremins et al., 2013] or contact domains [Rao et al., 2014]) are nested inside TADs, which are usually bigger and more strongly insulated (Dixon et al., 2012, Nora et al., 2012, Sexton et al., 2012).”
From Multiscale 3D Genome Rewiring during Mouse Neural Development (2017) · cites this paper as Flavahan et al., 2016
In the citing paper
“Several other studies have reported the deregulation of chromatin folding structures in different cancer types11,15,16.”
From Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer (2020) · cites this paper as [16]
In the citing paper
“Accordingly, deletion of a boundary between two TADs causes ectopic contacts between previously insulated loci3 and can cause aberrant gene expression through improper enhancer-promoter contact.27,28”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [27]
In the citing paper
“Silent proto-oncogenes typically occur within insulated neighborhoods and genetic modification of the neighborhood loop anchors can cause activation of these oncogenes (Flavahan et al., 2016; Hnisz et al., 2016).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Flavahan et al., 2016
In the citing paper
“Somatic mutations occur frequently and recurrently in the loop anchors of oncogene-containing Insulated neighborhoods in a variety of cancer cells (Figure 2E).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Flavahan et al., 2016
In the citing paper
“In a dozen loci and in multiple cell types, CRISPR/Cas9 deletion of CTCF binding sites at the anchors of insulated neighborhoods have been shown to produce changes in the expression of genes within the neighborhoods and immediately adjacent to the deleted neighborhood boundary.”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Flavahan et al., 2016
In the citing paper
“These observations are consistent with the idea that mutations that alter the loop anchor sites of oncogene-containing insulated neighborhoods make an important contribution to the misregulation of gene expression that is inherent to the cancer state (Flavahan et al., 2016; Hnisz et al., 2016; Katainen et al., 2015).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Flavahan et al., 2016
In the citing paper
“DNA hypermethylation occurs in some cancer cells, and tumor-specific DNA methylation has recently been implicated in the disruption of CTCF binding, alteration of chromosome structure and dysregulation of oncogene expression (Flavahan et al., 2016).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Flavahan et al., 2016
In the citing paper
“genome-wide, high-resolution understanding of chromosome cell-cycle dynamics11 is still limited by current technologies”
From Cell-cycle dynamics of chromosomal organization at single-cell resolution (2017) · cites this paper as [10]
In the citing paper
“In addition to CD4+ T cells, an unexpected role for L-2-HG in the promotion of tumour killing acting via CD8+ T cells, cytotoxic T lymphocytes important for anti-tumour immunity, has emerged149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
In the citing paper
“Accumulation of L-2-HG altered CD8+ T cell differentiation through modulation of both the histone and DNA methylation landscape of the cell, and also via HIF stability149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
In the citing paper
“Interestingly, Tyrakis and colleagues (2016) observed a dramatic increase in L-2-HG levels, reaching up to 1.5 mM, in response to T-cell receptor triggering in mouse CD8+ T cells149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
In the citing paper
“Furthermore, exogenous treatment of CD8+ T cells with L-2-HG greatly enhanced the in vivo proliferation, persistence and anti-tumour capacity of adoptively transferred CD8+ T cells149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
In the citing paper
“Mechanistically, HIF-1α stabilisation induced LDHA expression and activity, which promiscuously converted glutamine-derived α-KG to L-2-HG149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
In the citing paper
“This increase occurred under normoxic conditions and was dependent on HIF-1α stabilisation149.”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [149]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
HiC cell-type count differs between results and Methods
MinorThe results say six cell types were examined at the PDGFRA-FIP1L1 region, but the Methods list seven cell lines for HiC analysis of that region.
“In all six cell types examined, PDGFRA and FIP1L1 reside in distinct domains, separated by one CTCF-anchored constitutive boundary (Fig. 3a, Extended Data Fig. 3).”
“5 kb resolution intra-chromosomal contact scores for Chromosome 4 for the cell lines IMR90, NHEK, KBM7, K562, HUVEC, HMEC, and GM12878 were filtered to the region between 53,700kb and 55,400kb.”
Figure 1e is assigned to two different analyses
MinorThe results describe Figure 1e as showing gene correlations in normal brain samples, while the Methods say it plots correlation differences between wildtype and IDH mutant gliomas against their significance.
“In Figure 1e, this difference in correlations is plotted against the significance of this difference (estimated by Fisher z-transformation).”
“Consistent with prior studies16, we found that genes in the same domain correlate across samples, but that genes separated by a boundary show lower correlation (Fig. 1e).”
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Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
Dang, L., White, D. W., Gross, S., Bennett, B. D., Bittinger, M. A., Driggers, E. M., Fantin, V. R., Jang, H. G., Jin, S., Keenan, M. C., et al. (2009) · Nature · doi:10.1038/nature08617 · Cited by 4,154
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Treatment of IDH-mutant glioma in the INDIGO era
Lin, M. D., Tsai, A. C.-Y., Abdullah, K. G., McBrayer, S. K., & Shi, D. D. (2024) · npj Precision Oncology · doi:10.1038/s41698-024-00646-2 · Cited by 51
Epigenetic dynamics in cancer stem cell dormancy
Ferrer, A. I., Trinidad, J. R., Sandiford, O. A., Etchegaray, J., & Rameshwar, P. (2020) · Cancer and Metastasis Reviews · doi:10.1007/s10555-020-09882-x · Cited by 44
Zhou, Z., Ibekwe, E., & Chornenkyy, Y. (2018) · Antioxidants · doi:10.3390/antiox7010016 · Cited by 44
“Flavahan and colleagues provided evidence for this hypothesis by demonstrating that DNA hypermethylation at CCCTC-binding factor (CFCF) binding sites results in reduced binding and insulator activity, causing aberrant enhancer activation of platelet-derived growth factor receptor-α (PDGFR) in gliomas [95].”
BackgroundMetabolic Signaling to Epigenetic Alterations in Cancer
Kim, J., & Yeom, Y. I. (2017) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2017.185 · Cited by 45
“…genome-wide epigenetic profiling analyses involving whole-genome bisulfite sequencing reported that high levels of DNA methylation at insulator regions can relieve the transcriptional suppression of oncogenes, such as PDGFRA (Platelet-derived growth factor receptor alpha; Flavahan et al., 2016).”
BackgroundCharacteristics of gliomas in patients with somatic IDH mosaicism
Bonnet, C., Thomas, L., Psimaras, D., Bielle, F., Vauléon, É., Loiseau, H., Cartalat‐Carel, S., Meyronet, D., Dehais, C., Honnorat, J., et al. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0302-y · Cited by 43
“2-HG competitively inhibits multiple alpha-ketoglutarate enzymes leading to histone and DNA hypermethylation, altered cell differentiation, activation of enzymes implicated in HIF degradation and PDGFRA overexpression [14, 26, 30, 47].”
BackgroundPathogenetic significance and possibility as a therapeutic target of platelet derived growth factor
Ishii, Y., Hamashima, T., Yamamoto, S., & Sasahara, M. (2017) · Pathology International · doi:10.1111/pin.12530 · Cited by 43
Beyes, S., Bediaga, N. G., & Zippo, A. (2021) · Cancers · doi:10.3390/cancers13194969 · Cited by 44
“N tably, t eatment of IDH muta t glioma cells with a demethylation agent reduced methylati at CTCF binding sites and partially restored CTCF bindi g and insulator function, which in turn resto ed PDGFRA expression [32].”
BackgroundThe Stochastic Genome and Its Role in Gene ExpressionPreprint
Bohrer, C. H., & Larson, D. R. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a040386 · Cited by 43
Hsieh, T.-H. S., Cattoglio, C., Slobodyanyuk, E., Hansen, A. S., Darzacq, X., & Tjian, R. (2021) · doi:10.1101/2021.07.14.452365 · Cited by 42
Regulatory mechanisms ensuring coordinated expression of functionally related genes
Zinani, O. Q. H., Keseroǧlu, K., & Özbudak, E. M. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.07.008 · Cited by 46
Temporal and Spatial Epigenome Editing Allows Precise Gene Regulation in Mammalian Cells
Kuscu, C., Mammadov, R., Czikora, Á., Unlu, H., Tufan, T., Fischer, N. L., Arslan, Ş., Bekiranov, S., Kanemaki, M. T., & Adli, M. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.08.001 · Cited by 42
CHESS enables quantitative comparison of chromatin contact data and automatic feature extraction
Galan, S., Machnik, N., Kruse, K., Díaz, N., Martı́-Renom, M. A., & Vaquerizas, J. M. (2020) · Nature Genetics · doi:10.1038/s41588-020-00712-y · Cited by 38
Genomic enhancers in cardiac development and disease
Anene-Nzelu, C. G., Lee, C. J. M., Tan, W. L. W., Dashi, A., & Foo, R. (2021) · Nature Reviews Cardiology · doi:10.1038/s41569-021-00597-2 · Cited by 39
DNA demethylation is associated with malignant progression of lower-grade gliomas
Nomura, M., Saito, K., Aihara, K., Nagae, G., Yamamoto, S., Tatsuno, K., Ueda, H., Fukuda, S., Umeda, T., Tanaka, S., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-38510-0 · Cited by 40
The 4D Nucleome: Genome Compartmentalization in an Evolutionary Context
Cremer, T. J., Cremer, M., & Cremer, C. G. (2018) · Biochemistry (Moscow) · doi:10.1134/s000629791804003x · Cited by 39
Hierarchical chromatin organization detected by TADpole
Soler-Vila, P., Cuscó, P., Farabella, I., Stefano, M. D., & Martı́-Renom, M. A. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa087 · Cited by 39
“Increasing evidence indicates that genome architecture regulates gene transcription (1,2) with implications on cell-fate decisions (3-5), development (6), and disease occurrences such as developmental abnormalities (7,8) and neoplastic transformations (9-11).”
BackgroundDissection of a CTCF topological boundary uncovers principles of enhancer-oncogene regulation
Kim, K. L., Rahme, G. J., Goel, V. Y., Farran, C. A. E., Hansen, A. S., & Bernstein, B. (2024) · Molecular Cell · doi:10.1016/j.molcel.2024.02.007 · Cited by 42
Self-citationRheinbay, E., Nielsen, M. M., Abascal, F., Tiao, G., Hornshøj, H., Hess, J. M., Pedersen, R. I., Feuerbach, L., Sabarinathan, R., Madsen, T. L., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/237313 · Cited by 40
“In contrast to coding regions, the observed number of mutations across the combined set of non-coding elements associated with these genes is very close to the expected number of passenger mutations, , with an excess of 71 (CI95%:22133) mutations in promoters, 32 (0-79) in 5’UTRs, and 103 (25-184) in 3’UTRs.”
BackgroundSpecific glioblastoma multiforme prognostic-subtype distinctions based on DNA methylation patterns
Ma, H., Zhao, C., Zhao, Z., Hu, L., Ye, F., Wang, H., Fang, Z., Wu, Y., & Chen, X. (2019) · Cancer Gene Therapy · doi:10.1038/s41417-019-0142-6 · Cited by 43
Impact of CDKN2A/B Homozygous Deletion on the Prognosis and Biology of IDH-Mutant Glioma
Huang, L. E. (2022) · Biomedicines · doi:10.3390/biomedicines10020246 · Cited by 43
“Although epigenomic reprogramming in IDH1-mutant glioma also results in aberrant PDGFRA expression through the dysfunction of methylation-sensitive insulator [49], whether or not this is the mechanism of IDH-mutant glioma genesis remains to be investigated.”
BackgroundLATS kinase–mediated CTCF phosphorylation and selective loss of genomic binding
Luo, H., Yu, Q., Liu, Y., Tang, M., Liang, M., Zhang, D., Xiao, T. S., Wu, L., Tan, M., Ruan, Y., et al. (2020) · Science Advances · doi:10.1126/sciadv.aaw4651 · Cited by 39
Regulation of Latency in the Human T Cell Leukemia Virus, HTLV-1
Bangham, C. R. M., Miura, M., Kulkarni, A., & Matsuoka, M. (2019) · Annual Review of Virology · doi:10.1146/annurev-virology-092818-015501 · Cited by 45
Cancer metabolism as a central driving force of glioma pathogenesis
Masui, K., Cavenee, W. K., & Mischel, P. S. (2016) · Brain Tumor Pathology · doi:10.1007/s10014-016-0265-5 · Cited by 40
“The presence of IDH mutations thus leads to a distinct subgroup of glioma with a CpG island methylator phenotype (G-CIMP) and aberrant histone methylation [36], which possibly locks differentiationrelated genes in an inactive state [26], disrupts chromosomal topology [15] and changes the landscape of enhancers [8], ev…”
Molecular Pathogenesis of Low-Grade Glioma
Bready, D., & Placantonakis, D. G. (2018) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2018.08.011 · Cited by 40
Seizures in patients with cancer
Castro, L. N. G., & Milligan, T. A. (2020) · Cancer · doi:10.1002/cncr.32708 · Cited by 42
“…D-2-hydroxyglutarate (D2-HG), an oncometabolite that, in addition to playing a role in onco-genesis through the alteration of epigenetic states, 35 has a chemical structure similar to that of glutamate and, when secreted extracellularly, is thought to produce a proepilep-tic state by…”
Background2-hydroxyglutarate inhibits MyoD-mediated differentiation by preventing H3K9 demethylation
Schvartzman, J. M., Reuter, V. P., Koche, R. P., & Thompson, C. B. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817662116 · Cited by 43
“Alteration in CTCF-binding could impair the ability of insulator regions to regulate distant promoter–enhancer interactions (29).”
BackgroundEpigenetic modulators provide a path to understanding disease and therapeutic opportunityPreprint
Honer, M. A., Ferman, B. I., Gray, Z. H., Bondarenko, E. A., & Whetstine, J. R. (2024) · Genes & Development · doi:10.1101/gad.351444.123 · Cited by 44
“2; Flavahan et al. 2016).”
Metabolism, Epigenetics, and Causal Inference in Heart Failure
Kimball, T. H., & Vondriska, T. M. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.11.009 · Cited by 40
The kidney and hypertension: over 70 years of research
Campese, V. M., & Park, J. (2006) · Journal of Nephrology · doi:10.1093/joneph/19.6.691 · Cited by 40
Proteomics and metabolomics approach in adult and pediatric glioma diagnostics
Pienkowski, T., Kowalczyk, T., Garcia‐Romero, N., Ayuso‐Sacido, Á., & Ciborowski, M. (2022) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2022.188721 · Cited by 41
Evolving cell states and oncogenic drivers during the progression of IDH-mutant gliomas
Wu, J., Castro, L. N. G., Battaglia, S., Farran, C. A. E., D’Antonio, J. P., Miller, T. E., Suvà, M. L., & Bernstein, B. (2024) · Nature Cancer · doi:10.1038/s43018-024-00865-3 · Cited by 48
Self-citationTranscriptional dysregulation by aberrant enhancer activation and rewiring in cancer
Okabe, A., & Kaneda, A. (2021) · Cancer Science · doi:10.1111/cas.14884 · Cited by 41
Grillo, G., Keshavarzian, T., Linder, S., Arlidge, C., Mout, L., Nand, A., Teng, M., Qamra, A., Zhou, S., Kron, K. J., et al. (2023) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-0331 · Cited by 42
The potential of epigenetic therapy to target the 3D epigenome in endocrine-resistant breast cancer
Achinger-Kawecka, J., Stirzaker, C., Portman, N., Campbell, E. M., Chia, K.-M., Du, Q., Laven‐Law, G., Nair, S. S., Yong, A., Wilkinson, A., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-01181-7 · Cited by 46
“There have been limited studies to date on the role of DNA methylation in shaping the 3D genome organization 38,39 .”
BackgroundParfett, C. L. J., & Desaulniers, D. M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061179 · Cited by 41
“A similar mechanism with hypermethylation reducing CTCF affinity for its binding site explained the up-regulation of the receptor tyrosine kinase (PDGFRA) in gliaomas (with mutant IDH-2-hydroxyglutarate inhibited TET enzymes resulting in hypermethylation) [237].”
BackgroundThe impact of HTLV-1 on the cellular genome
Cook, L. B. M., Melamed, A., Yaguchi, H., & Bangham, C. R. M. (2017) · Current Opinion in Virology · doi:10.1016/j.coviro.2017.07.013 · Cited by 40
Shen, Y., Thng, D. K. H., Wong, A. L. A., & Toh, T. B. (2024) · Experimental Hematology and Oncology · doi:10.1186/s40164-024-00512-8 · Cited by 47
“…cells to establish glioma CpG island methylator phenotype (G-CIMP) [129], and potentially leads to irreversible epigenetic alterations which commit glioma cells to oncogenesis, such as the silencing of tumour suppressive microRNA, miR-148a [130], as well as activation of oncogene, PDG-FRA [131].”
BackgroundLooze, C. D., Beausang, A., Cryan, J. B., Loftus, T., Buckley, P. G., Farrell, M. A., Looby, S. T., Reilly, R. B., Brett, F. M., & KEARNEY, H. F. (2018) · Journal of Neuro-Oncology · doi:10.1007/s11060-018-2895-4 · Cited by 38
“IDH mutations occur in 70–90% of WHO grade II and III gliomas [19], following determination of WHO grade from MRI it would be desirable to also predict the IDH status of a newly diagnosed glioma.”
BackgroundKelly, A. D., Kroeger, H., Yamazaki, J., Taby, R. F., Neumann, F., Yu, S., Lee, J. T., Patel, B. G., Li, Y. C., He, R. L., et al. (2017) · Leukemia · doi:10.1038/leu.2017.12 · Cited by 40
Molecular and Genetic Determinants of Glioma Cell Invasion
Masui, K., Kato, Y., Sawada, T., Mischel, P. S., & Shibata, N. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18122609 · Cited by 38
“Alternatively, IDH mutations promote gliomagenesis by disrupting chromosomal topology and allowing aberrant regulatory interactions that induce oncogene expression such as PDGFR (platelet-derived growth factor receptor) [39], the combination of which is frequently observed in the proneural subtype of GBM [40,41].”
BackgroundmiRNA-independent function of long noncoding pri-miRNA loci
He, D. X., Wu, D., Müller, S., Wang, L., Saha, P., Ahanger, S. H., Liu, S. J., Cui, M., Hong, S. J., Jain, M., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017562118 · Cited by 35
“From a genome-scale lncRNA screen, lnc-pri-miRNA loci were enriched for function in cell proliferation, and in glioblastoma (i.e., GBM) cells with DGCR8 or DROSHA knockdown, lnc-pri-miRNA screen hits still regulated cell growth.”
BackgroundInfluentialMolecular targeted therapy: A new avenue in glioblastoma treatment (Review)
Atat, O. E., Naser, R., Abdelkhalek, M., Abi‐Habib, R. J., & El‐Sibai, M. (2022) · Oncology Letters · doi:10.3892/ol.2022.13632 · Cited by 40
Pisapia, D. J. (2017) · Archives of Pathology & Laboratory Medicine · doi:10.5858/arpa.2016-0493-ra · Cited by 43
Molecular pathogenesis and therapeutic implications in pediatric high-grade gliomas
Juratli, T. A., Qin, N., Cahill, D. P., & Filbin, M. G. (2017) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.08.006 · Cited by 36
“Interestingly, recent findings have shown that human IDH mutations in gliomas cause genome-wide hypermethylation of cohesin and CCCTCbinding factor (CTCF)-binding sites, compromising binding of this methylation-sensitive insulator protein (Flavahan et al., 2016).”
BackgroundDrug persistence – From antibiotics to cancer therapies
Kochanowski, K., Morinishi, L. S., Altschuler, S. J., & Wu, L. F. (2018) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2018.03.003 · Cited by 39
TAD fusion score: discovery and ranking the contribution of deletions to genome structure
Huynh, L. N., & Hormozdiari, F. (2019) · Genome biology · doi:10.1186/s13059-019-1666-7 · Cited by 35
Balasubramanian, D., Pinto, P. B., Grasso, A., Vincent, S., Tarayre, H., Lajoignie, D., & Ghavi-Helm, Y. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad1183 · Cited by 45
Active enhancers strengthen insulation by RNA-mediated CTCF binding at chromatin domain boundariesPreprint
Islam, Z., Saravanan, B., Walavalkar, K., Farooq, U., Singh, A. K., Sabarinathan, R., Thakur, J., Pandit, A., Henikoff, S., & Notani, D. (2023) · Genome Research · doi:10.1101/gr.276643.122 · Cited by 39
“…of CTCF sites at TAD boundaries affects gene expression, ranging from no effect to severe effect in the same and neighboring TADs (Narendra et al. 2015; Flavahan et al. 2016; Hanssen et al. 2017; Despang et al. 2019; Sima et al. 2019; Williamson et al. 2019; Yang et al. 2019; Kloetgen et al. 2020).”
BackgroundRevisiting 3D chromatin architecture in cancer development and progression
Feng, Y., & Pauklin, S. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa747 · Cited by 36
“DNA hypermethylation impaired CTCF binding on the loop anchors and disrupted the insulation that partitions an enhancer from PDGFRA oncogene in glioma (84), a super-enhancer from FGF4 oncogene in gastrointestinal stromal tumours (GISTs) (85), which create aberrant enhancer–promoter interactions and gene activation.”
Background3D organization of regulatory elements for transcriptional regulation in Arabidopsis
Deng, L., Zhou, Q., Zhou, J., Zhang, Q., Jia, Z.-B., Zhu, G., Cheng, S., Cheng, L., Yin, C., Yang, C., et al. (2023) · Genome Biology · doi:10.1186/s13059-023-03018-4 · Cited by 27
IGFBP2 expression predicts IDH-mutant glioma patient survival
Huang, L. E., Cohen, A. L., Colman, H., Jensen, R. L., Fults, D. W., & Couldwell, W. T. (2016) · Oncotarget · doi:10.18632/oncotarget.13329 · Cited by 37
“Furthermore, the mean PDGFRA methylation was unexpectedly decreased in IDHmutant glioma, but the mRNA levels had a modest, yet statistically insignificant, increase (Figure S2A), similar to that noted previously [22].”
ResultWei, S., Wang, J., Oyinlade, O., Ma, D., Wang, S., Kratz, L. E., Lal, B., Xu, Q., Liu, S., Shah, S. R., et al. (2018) · Oncogene · doi:10.1038/s41388-018-0334-9 · Cited by 37
Mutant IDH1 expression is associated with down-regulation of monocarboxylate transporters
Viswanath, P., Najac, C., Izquierdo-García, J. L., Pankov, A., Hong, C., Eriksson, P., Costello, J., Pieper, R. O., & Ronen, S. M. (2016) · Oncotarget · doi:10.18632/oncotarget.9006 · Cited by 35
“Indeed, a recent paper identified methylationindependent modulation of gene expression via insulator function modification in mutant IDH1 cells [66].”
From Laboratory Studies to Clinical Trials: Temozolomide Use in IDH-Mutant Gliomas
Sun, X., & Turcan, Ş. (2021) · Cells · doi:10.3390/cells10051225 · Cited by 38
“Although slower growing (at a rate of ~4–5 mm per year [6]), the majority of IDH‐mutant LGGs eventually undergo malignant progression due to activation of the PI3K/mTOR pathway as a result of PTEN loss [7,8] or enhanced PDGF signaling [9].”
BackgroundWilli, M., Yoo, K. H., Reinisch, F., Kuhns, T. M., Lee, H., Wang, C., & Hennighausen, L. G. (2017) · Nature Communications · doi:10.1038/ncomms16069 · Cited by 36
“Such regulatory neighbourhoods not only limit the search space of cis -regulatory elements to genes within the same domain but also prevent active and suppressive chromatin from spreading 7,15–18 .”
The Many Faces of Gene Regulation in Cancer: A Computational Oncogenomics Outlook
Lemus, E. H., Reyes-Gopar, H., Enríquez, J. E., & Ochoa, S. (2019) · Genes · doi:10.3390/genes10110865 · Cited by 33
Fellenberg, J., Sähr, H., Mancarella, D., Plass, C., Lindroth, A. M., Westhauser, F., Lehner, B., & Ewerbeck, V. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.02.001 · Cited by 38
Deforzh, E., Uhlmann, E. J., Das, E., Galitsyna, A. A., Arora, R., Saravanan, H., Rabinovsky, R., Wirawan, A., Teplyuk, N. M., Fatimy, R. E., et al. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.03.018 · Cited by 37
Song, M. J., & Zhong, H. (2020) · Bioinformatics · doi:10.1093/bioinformatics/btaa613 · Cited by 36
Insights about genome function from spatial organization of the genome
Roy, S. S., Mukherjee, A. K., & Chowdhury, S. (2018) · Human Genomics · doi:10.1186/s40246-018-0140-z · Cited by 32
“…boundaries and particular cancer-specific interactions within TADs could be associated with oncogenic transformation [75], and perturbation of CTCF binding by aberrant DNA methylation could cause oncogenic gene expression leading to gliomas by a mechanism similar to “ enhancer hijacking ” [76].”
BackgroundEffective normalization for copy number variation in Hi-C data
Servant, N., Varoquaux, N., Heard, E., Barillot, E., & Vert, J.-P. (2017) · BMC Bioinformatics · doi:10.1186/s12859-018-2256-5 · Cited by 34
“[22] link insulator dysfunctions to oncogene activation in cancer.”
BackgroundEnhancer reprogramming in tumor progression: a new route towards cancer cell plasticity
Fagnocchi, L., Poli, V., & Zippo, A. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2820-1 · Cited by 38
TERT and DNMT1 expression predict sensitivity to decitabine in gliomas
Park, J., Sahm, F., Steffl, B., Arrillaga‐Romany, I., Cahill, D. P., Monje, M., Herold‐Mende, C. C., Wick, W., & Turcan, Ş. (2020) · Neuro-Oncology · doi:10.1093/neuonc/noaa207 · Cited by 35
Roles of CTCF in conformation and functions of chromosome
Liu, F., Wu, D., & Wang, X. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.07.021 · Cited by 38
Therapeutic approaches to modulate the immune microenvironment in gliomas
Sarantopoulos, A., Ene, C., & Aquilanti, E. (2024) · npj Precision Oncology · doi:10.1038/s41698-024-00717-4 · Cited by 36
Functional interrogation of non-coding DNA through CRISPR genome editing
Canver, M. C., Bauer, D. E., & Orkin, S. H. (2017) · Methods · doi:10.1016/j.ymeth.2017.03.008 · Cited by 36
“These studies have demonstrated that disrupting these CTCF binding sites with indels results in aberrant enhancer activity, changes in gene expression, and disruption of genomic topology [46,47].”
BackgroundWang, M., Sunkel, B. D., Ray, W. C., & Stanton, B. Z. (2022) · BMC Molecular and Cell Biology · doi:10.1186/s12860-022-00433-6 · Cited by 37
“Connecting altered CpG methylation and altered tumor metabolism, a recent report revealed DNA hypermethylation at CpG islands in IDH-driven gliomas [48].”
BackgroundInfluentialLee, D.-I., & Roy, S. (2021) · Genome biology · doi:10.1186/s13059-021-02378-z · Cited by 34
“Although the relationship between TADs and changes in gene expression is debated [12–14], these units have been shown to be conserved across species [5, 15] and also associated with developmental [16] and disease processes [11, 17–19].”
A comparison of topologically associating domain callers over mammals at high resolution
Sefer, E. (2022) · BMC Bioinformatics · doi:10.1186/s12859-022-04674-2 · Cited by 37
Shi, T., Guo, D., Xu, H., Su, G., Chen, J., Zhao, Z., Shi, J., Wedemeyer, M. A., Attenello, F. J., Zhang, L., et al. (2020) · Molecular Biology Reports · doi:10.1007/s11033-020-05371-0 · Cited by 33
Stalled oligodendrocyte differentiation in IDH-mutant gliomas
Wei, Y., Li, G., Feng, J. H., Wu, F., Zhao, Z., Bao, Z., Zhang, W., Su, X., Li, J., Qi, X., et al. (2023) · Genome Medicine · doi:10.1186/s13073-023-01175-6 · Cited by 36
Xie, T., Danieli‐Mackay, A., Buccarelli, M., Barbieri, M., Papadionysiou, I., D’Alessandris, Q. G., Robens, C., Übelmesser, N., Vinchure, O. S., Lauretti, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48053-2 · Cited by 36
“Notably, in gliomas with IDH gain-of-function mutations, hypermethylation of CTCF sites at insulator ele-mentspreventsbindingtoalsodisruptboundaryformation 22 .”
BackgroundDNA methylation and histone variants in aging and cancer
Mangelinck, A., & Mann, C. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.06.002 · Cited by 35
Galupa, R., & Heard, É. (2017) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2017.82.035030 · Cited by 30
“CTCF sites can also be affected by DNA hypermethylation, as observed in a subset of gliomas, where this is associated with impaired CTCF binding, loss of insulation between TADs and aberrant oncogene activation (Flavahan et al. 2016).”
BackgroundInfluentialThe 3D Genome as a Target for Anticancer Therapy
Kantidze, O. L., Gurova, K. V., Studitsky, V. M., & Razin, S. V. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.09.011 · Cited by 36
“At the 3D genome organization level, it is also possible to unite several individual enhancers in a common activating complex, as in the case of super-enhancers (SEs), composed of several functional enhancers [15].”
BackgroundMethodInfluentialZhang, G., Tanaka, S., Jiapaer, S., Sabit, H., Tamai, S., Kinoshita, M., & Nakada, M. (2020) · Cancer Science · doi:10.1111/cas.14642 · Cited by 32
Role of CTCF in DNA damage response
Tanwar, V. S., Jose, C. C., & Cuddapah, S. (2018) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2018.02.002 · Cited by 34
Mortenson, K. L., Dawes, C., Wilson, E. R., Patchen, N. E., Johnson, H. E., Gertz, J., Bailey, S. D., Yang, J., Varley, K. E., & Zhang, X. (2024) · Nature Communications · doi:10.1038/s41467-024-50387-w · Cited by 35
“In this study, we focus on trans-enhancer hijacking events because they are more likely caused by structural alterations than cis-enhancer hijacking events that may be caused by other types alterations such as epigenetic loss of TAD boundaries 38,39 .”
Regulation and Dysregulation of Chromosome Structure in Cancer
Hnisz, D., Schuijers, J., Li, C. H., & Young, R. A. (2017) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030617-050134 · Cited by 31
“10 neighborhood boundary alterations occur at oncogene loci in leukemia and gliomas (Flavahan et al., 2016; Hnisz et al., 2013) suggests that neighborhoods with recurrently altered boundaries can identify new oncogenic drivers.”
BackgroundInfluentialDissecting super-enhancer hierarchy based on chromatin interactions
(2017) · doi:10.1101/149583 · Cited by 32
Crosstalk between metabolic and epigenetic modifications during cell carcinogenesis
Gao, Y., Zhang, S., Zhang, X., Du, Y., Ni, T., & Hao, S. (2024) · iScience · doi:10.1016/j.isci.2024.111359 · Cited by 42
Properties of gene expression and chromatin structure with mechanically regulated elongation
Sevier, S. A., & Levine, H. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky382 · Cited by 29
“These include mechanical transduction of gene expression and cell differentiation (31), diseases related to changes in mechanical properties of the cell (32) as well as direct changes in the constraints and structure of chromatin itself such as been recently observed in cancer (33).”
BackgroundDisease gene classification with metagraph representations
Ata, S. K., Fang, Y., Wu, M., Li, X., & Xiao, X. (2017) · Methods · doi:10.1016/j.ymeth.2017.06.036 · Cited by 32
“Despite recent advances in identifying the functions of genes and proteins [1, 2, 3, 4, 5, 6], it still remains a challenging research issue to understand their interactions and pathways in the context of many diseases.”
BackgroundTETology: Epigenetic Mastermind in Action
Seethy, A. A., Pethusamy, K., Chattopadhyay, I., Sah, R., Chopra, A., Dhar, R., & Karmakar, S. (2021) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-021-03537-5 · Cited by 31
Topological isolation of developmental regulators in mammalian genomes
Wu, H., Landshammer, A., Stamenova, E. K., Bolondi, A., Kretzmer, H., Meissner, A., & Michor, F. (2021) · Nature Communications · doi:10.1038/s41467-021-24951-7 · Cited by 29
Topography of transcriptionally active chromatin in glioblastoma
Xu, L., Chen, Y., Huang, Y., Sandanaraj, E., Yu, J. S., Lin, R. Y., Dakle, P., Ke, X., Chong, Y. K., Koh, L., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd4676 · Cited by 35
Dynamic Runx1 chromatin boundaries affect gene expression in hematopoietic development
Owens, D. D. G., Anselmi, G., Oudelaar, A. M., Downes, D. J., Cavallo, A., Harman, J. R., Schweßinger, R., Bucakci, A., Greder, L. V., Ornellas, S. D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28376-8 · Cited by 33
Epigenetic Reprogramming for Targeting IDH-Mutant Malignant Gliomas
Park, J., & Turcan, Ş. (2019) · Cancers · doi:10.3390/cancers11101616 · Cited by 33
“Majority of secondary GBMs harbor IDH mutations and platelet-derived growth factor receptor A (PDGFRA) alterations [70].”
BackgroundInfluentialFurther understanding of the pathology of glioma: implications for the clinic
Camelo-Piragua, S. I., & Kesari, S. (2016) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2016.1194755 · Cited by 29
“demonstrated that loss of CTCF allows a constitutive enhancer to interact aberrantly with receptor tyrosine kinase (RTK) (PDGFRA), a potent oncogene, suggesting this as a mechanism of gliomagenesis in mutIDH gliomas [40].”
BackgroundInfluentialEpigenetic Mechanisms Regulating Adaptive Responses to Targeted Kinase Inhibitors in Cancer
Angus, S. P., Zawistowski, J. S., & Johnson, G. L. (2017) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010617-052954 · Cited by 32
Structure–function relationships explain CTCF zinc finger mutation phenotypes in cancer
Bailey, C. G., Gupta, S. K., Metierre, C., Amarasekera, P. M. S., O’Young, P., Kyaw, W., Laletin, T., Francis, H., Semaan, C., Tabar, M. S., et al. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03946-z · Cited by 31
Nuclear genome organization in fungi: from gene folding to Rabl chromosomes
Torres, D. E., Reckard, A. T., Klocko, A. D., & Seidl, M. F. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad021 · Cited by 29
“…ganizes the genome in the nucleus, or are essential for genome function (Beagan and Phillips-Cr emins 2020 ), possibl y r equir ed to r egulate gene expr ession by increasing the contact probability of distant enhancers/silencers with cognate promoters (Flavahan et al. 2016 , Dixon et al. 2018 ).”
Super-enhancers and novel therapeutic targets in colorectal cancer
Liu, Q., Guo, L., Lou, Z., Xiang, X., & Shao, J. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04673-4 · Cited by 31
Sim, N., Carter, J.-M., Deka, K., Tan, B. K. T., Sim, Y., Tan, S., & Li, Y. (2024) · Nature Communications · doi:10.1038/s41467-024-50071-z · Cited by 37
“…TWEAK/Fn14 activation drives enhancer-promoter looping associated with TNBC dependency genes Distal enhancers and SEs have been shown to activate the transcription of cancer driver genes through enhancer-promoter cis -regulatory interactions in various malignancies including TNBCs 52 – 54 .”
Effects of super-enhancers in cancer metastasis: mechanisms and therapeutic targets
Liu, S., Dai, W., Jin, B., Jiang, F., Huang, H., Hou, W., Lan, J., Jin, Y., Peng, W., & Pan, J. (2024) · Molecular Cancer · doi:10.1186/s12943-024-02033-8 · Cited by 35
“This permitted aberrant activation of PDGFRA gene, a prominent glioma oncogene, by a potent enhancer that was previously isolated from the gene’s promoter [61].”
BackgroundRole of succinate dehydrogenase deficiency and oncometabolites in gastrointestinal stromal tumors
Zhao, Y., Feng, F., Guo, Q., Wang, Y., & Zhao, R. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i34.5074 · Cited by 35
The Emergence of Pan-Cancer CIMP and Its Elusive Interpretation
Miller, B., Sánchez-Vega, F., & Elnitski, L. L. (2016) · Biomolecules · doi:10.3390/biom6040045 · Cited by 33
“Methylation of CpGs in CTCF binding motifs can disrupt genome topology and lead to activation of oncogenes, at least in IDH-mutant gliomas [87].”
BackgroundQuiroga, I. Y., Ahn, J. H., Wang, G. G., & Phanstiel, D. H. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101901 · Cited by 32
CTCF: A misguided jack-of-all-trades in cancer cells
Segueni, J., & Noordermeer, D. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.05.044 · Cited by 31
“In gliomas, this permits the PDGFRA oncogene to hijack the FIP1L1 enhancer [105], whereas in GISTs the FGF4 and KIT oncogenes establish inappropriate contacts with super-enhancers in fused TADs as well [106].”
Background
Metadata
- Authors
- Flavahan, W. A., Drier, Y., Liau, B. B., Gillespie, S. M., Venteicher, A. S., Stemmer-Rachamimov, A. O., Suvà, M. L., & Bernstein, B. E.
- Affiliations
- Broad Institute (US)
- Harvard University (US)
- Corresponding author
- Bernstein, Bradley E.
- ORCID
- Venue
- Nature
- Published
- 2015-12-23
- Volume
- 529
- Issue
- 7584
- Pages
- 110-114
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4831574
- OpenAlex
- W2222531233
- Semantic Scholar
- 749f7a7a14c60dad4fd2f91895fe8ba804d72f81
- Cited by
- 1,288
- References
- 44
- Citations by year
- 2026: 71 · 2025: 81 · 2024: 106 · 2023: 119 · 2022: 142 · 2021: 144 · 2020: 139 · 2019: 147 · 2018: 110 · 2017: 135 · 2016: 89 · 2015: 1
- FWCI
- 62.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Human Genome Research Institute (U54HG006991)
- National Cancer Institute (DP1CA216873, P50CA165962)
- Topics
- Health Sciences › Medicine › Oncology › Glioma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- IDH-mutant glioma, CTCF, PDGFRA, chromatin topology, topologically associating domains, DNA methylation, 2-hydroxyglutarate, TET enzymes, G-CIMP, enhancer-promoter interactions, hypomethylating agents, gliomagenesis
- MeSH terms
- CCCTC-Binding Factor, Cohesins, Base Sequence, Binding Sites, Cell Transformation, Neoplastic, Cells, Cultured, Chromatin, Chromosomal Proteins, Non-Histone, Enhancer Elements, Genetic, Glioma, Glutarates, Humans, Isocitrate Dehydrogenase, Mutation, Oncogenes, Phenotype, Protein Binding, Repressor Proteins, Down-Regulation, Up-Regulation, Gene Expression Regulation, Neoplastic, Cell Cycle Proteins, CpG Islands, DNA Methylation, Receptor, Platelet-Derived Growth Factor alpha, Insulator Elements, Epigenesis, Genetic, Cell Proliferation, CRISPR-Cas Systems
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