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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Choe, S. E., Wang, H., Dinardo, C. D., Stein, E. M., de Botton, S., Roboz, G. J., Altman, J. K., Mims, A. S., Watts, J. M., Pollyea, D. A., et al. (2020) · Blood Advances · doi:10.1182/bloodadvances.2020001503 · Cited by 218
“In glioma, IDH1 mutations were reported to increase platelet-derived growth factor receptor a expression levels by methylation and inactivation of a nearby CCCTC-binding factor insulator site.(34) Others have observed increased AKT/mTOR signaling in mIDH1 cells.”
BackgroundMyc Regulates Chromatin Decompaction and Nuclear Architecture during B Cell Activation
Kieffer-Kwon, K.-R., Nimura, K., Rao, S. S. P., Xu, J., Jung, S., Pękowska, A., Dose, M., Stevens, E., Mathé, E. A., Dong, P., et al. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.07.013 · Cited by 210
“Architectural loops require CTCF and cohesin binding at loop anchors (Dowen et al., 2014; Flavahan et al., 2016; Guo et al., 2015; Lupiáñez et al., 2015; Rao et al., 2014; Sanborn et al., 2015; Tang et al., 2015).”
Molecular Pathways: Isocitrate Dehydrogenase Mutations in Cancer
Clark, O., Yen, K. E., & Mellinghoff, I. K. (2016) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-1333 · Cited by 210
“These findings raise the intriguing question of whether IDH mutant cancers cells might show an increased sensitivity to the DNA methyltransferase inhibitors (DNMTIs) decitabine or 5-azacytidine (53-55) or drugs targeting histone modifications.”
BackgroundReceptor tyrosine kinases and cancer: oncogenic mechanisms and therapeutic approaches
Saraon, P., Pathmanathan, S., Snider, J. D., Lyakisheva, A., Wong, V., & Štagljar, I. (2021) · Oncogene · doi:10.1038/s41388-021-01841-2 · Cited by 215
“This allows for FIP1L1 enhancer to make contacts with PDGFRA upregulating its expression in gliomas [11].”
BackgroundMcArthur, E., & Capra, J. A. (2021) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2021.01.001 · Cited by 207
“, oncogenic gene expression in gliomas.(28) We hypothesize that altering gene regulation though commonvariant disruption of transcription-factor motifs, such as CTCF, that are important in 3D structure organization contributes to the enrichment for complex-disease heritability.”
BackgroundGe, T., Gu, X., Jia, R., Ge, S., Chai, P., Zhuang, A., & Fan, X. (2022) · 癌症:英文版 · doi:10.1002/cac2.12374 · Cited by 220
“Decreased CTCF bindingwidely compromises chromosomal topology and results in oncogenes like PDGFRA aberrant activation through interaction with distant enhancers [175].”
BackgroundEpigenetic silencing of tumor suppressor genes: Paradigms, puzzles, and potential
Kazanets, A., Shorstova, T., Hilmi, K., Marques, M., & Witcher, M. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.04.001 · Cited by 203
Allen, E. K., Randolph, A. G., Bhangale, T., Dogra, P., Ohlson, M. B., Oshansky, C. M., Zamora, A. E., Shannon, J. P., Finkelstein, D., Dressen, A., et al. (2017) · Nature Medicine · doi:10.1038/nm.4370 · Cited by 195
Enhancer selectivity in space and time: from enhancer–promoter interactions to promoter activation
Yang, J. H., & Hansen, A. S. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00710-6 · Cited by 191
“P interactions causing oncogene activation and overexpression in cancer 121,122 .”
Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for Gliomagenesis
Chen, C. C. L., Deshmukh, S., Jessa, S., Hadjadj, D., Lisi, V., Andrade, A. F., Faury, D., Jawhar, W., Dali, R., Suzuki, H., et al. (2020) · Cell · doi:10.1016/j.cell.2020.11.012 · Cited by 199
“Conversely, IDH1-mutant HGGs use a distal enhancer through DNA methylation of a proximal CTCF insulator to overexpress PDGFRA (Flavahan et al., 2016), while activating mutations are more frequently observed in non-brainstem gliomas occurring in older children (14%) (Koschmann et al.”
BackgroundHuang, H., Zhu, Q., Jussila, A., Han, Y., Bintu, B., Kern, C., Conte, M., Zhang, Y., Bianco, S., Chiariello, A. M., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00863-6 · Cited by 187
Involvement of platelet‐derived growth factor ligands and receptors in tumorigenesis
Heldin, C. ‐., Lennartsson, J., & Westermark, B. (2018) · Journal of Internal Medicine · doi:10.1111/joim.12690 · Cited by 181
Hallmarks of glioblastoma: a systematic review
Nørøxe, D. S., Poulsen, H. S., & Lassen, U. (2016) · ESMO Open · doi:10.1136/esmoopen-2016-000144 · Cited by 189
Circulating tumor cells: from new biological insights to clinical practice
Gu, X., Wei, S., & Lv, X. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01938-6 · Cited by 204
“404,405 An explanation for the observed correlation between increased CCNE1 expression in gastric cancer primary tumors and CCNE1 rearrangement in response to changed TAD borders and interactions has been found.”
BackgroundAldape, K., Amin, S. B., Ashley, D. M., Barnholtz‐Sloan, J. S., Bates, A. J., Beroukhim, R., Bock, C., Brat, D. J., Claus, E. B., Costello, J., et al. (2018) · Neuro-Oncology · doi:10.1093/neuonc/noy020 · Cited by 179
Oncometabolites: Unconventional triggers of oncogenic signalling cascades
Sciacovelli, M., & Frezza, C. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.025 · Cited by 184
“This hypothesis has been recently corroborated by the fi nding that DNA hypermethylation causes reduced CCCTC-binding factor (CTCF) binding to DNA, leading to aberrant activation of the oncogene Platelet-derived growth factor receptor ( PDGFRA ) [81] in gliomas.”
BackgroundGlioblastoma cancer stem cell biology: Potential theranostic targets
Sharifzad, F., Ghavami, S., Verdi, J., Mardpour, S., Sisakht, M. M., Azizi, Z., Taghikhani, A., Łoś, M., Fakharian, E., Ebrahimi, M., et al. (2019) · Drug Resistance Updates · doi:10.1016/j.drup.2018.03.003 · Cited by 186
Systematic identification of silencers in human cells
Pang, B., & Snyder, M. P. (2020) · Nature Genetics · doi:10.1038/s41588-020-0578-5 · Cited by 183
Qu, K., Zaba, L. C., Satpathy, A. T., Giresi, P. G., Li, R., Jin, Y., Armstrong, R. J., Chen, J., Schmitt, N., Rahbar, Z., et al. (2017) · Cancer Cell · doi:10.1016/j.ccell.2017.05.008 · Cited by 175
“…to several of these factors or their upstream regulators have been developed, such as JNK inhibitors (Zhang et al., 2012), Aza-C for CTCF (Flavahan et al., 2016), or BRD4 inhibitors for Myc deactivation (Filippakopoulos et al., 2010), knowledge of the dominant regulators in each patient…”
Greater Than the Sum of Parts: Complexity of the Dynamic Epigenome
Soshnev, A. A., Josefowicz, S. Z., & Allis, C. D. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.05.004 · Cited by 181
Reprogramming of Meiotic Chromatin Architecture during Spermatogenesis
Wang, Y., Wang, H., Zhang, Y., Du, Z., Si, W., Fan, S., Qin, D., Wang, M., Duan, Y., Li, L., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2018.11.019 · Cited by 172
Lio, C.-W., Zhang, J., González-Avalos, E., Hogan, P. G., Chang, X., & Rao, A. (2016) · eLife · doi:10.7554/elife.18290 · Cited by 170
“Notably, consistent with a previous study (Benner et al., 2015), a fraction of the commonly accessible regions (especially those with the lowest ATAC-seq signals) corresponded to regions with significant CTCF binding in pro-B cells (Lin et al., 2010), suggesting these regions are potent insulators (Song et al., 2011).”
BackgroundInfluentialTommasini-Ghelfi, S., Murnan, K., Kouri, F. M., Mahajan, A., May, J., & Stegh, A. H. (2019) · Science Advances · doi:10.1126/sciadv.aaw4543 · Cited by 166
Enhancer Logic and Mechanics in Development and Disease
Rickels, R. A., & Shilatifard, A. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.04.003 · Cited by 171
Wang, K., & Chang, H. Y. (2018) · Circulation Research · doi:10.1161/circresaha.118.310998 · Cited by 180
“In fact, 3D domain disruption of TAD and sub-TAD boundaries via mutations, deletions, or genetic rearrangements has been linked to aberrant activation of genes via ectopic looping of enhancers in limb malformation syndromes(70) and cancer.(71) Mutations affecting proper function of architectural proteins, such as cohe…”
Rinzema, N. J., Sofiadis, K., Tjalsma, S. J. D., Verstegen, M. J. A. M., Oz, Y., Valdes-Quezada, C., Felder, A.-K., Filipovska, T., van der Elst, S., de Andrade dos Ramos, Z., et al. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00787-7 · Cited by 166
Kmt1e regulates a large neuron-specific topological chromatin domain
Jiang, Y., Loh, Y., Rajarajan, P., Hirayama, T., Liao, W., Kassim, B. S., Javidfar, B., Hartley, B., Kleofas, L., Park, R. B., et al. (2017) · Nature Genetics · doi:10.1038/ng.3906 · Cited by 128
Achinger-Kawecka, J., Valdés-Mora, F., Luu, P.-L., Giles, K., Caldon, C. E., Qu, W., Nair, S., Soto, S., Locke, W. J., Yeo-Teh, N. S., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14098-x · Cited by 136
Polycomb Group Proteins Regulate Chromatin Architecture in Mouse Oocytes and Early Embryos
Du, Z., Zheng, H., Kawamura, Y., Zhang, K., Gassler, J., Powell, S. T., Xu, Q., Lin, Z., Xu, K., Zhou, Q., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.11.011 · Cited by 163
Kaaij, L. J. T., Mohn, F., van der Weide, R. H., de Wit, E., & Bühler, M. (2019) · Cell · doi:10.1016/j.cell.2019.08.007 · Cited by 161
Thandapani, P. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.02.014 · Cited by 167
Metabolic coordination of cell fate by α-ketoglutarate-dependent dioxygenases
Baksh, S. C., & Finley, L. W. S. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2020.09.010 · Cited by 165
“In both mtIDH gliomas and SDH-deficient gastrointestinal stromal tumors, hypermethylation of CTCF binding sites is associated with increased interactions between key receptor tyrosine kinase (RTK) genes and constitutive lineage-specific enhancers normally outside of their domains, resulting in elevated RTK expression…”
BackgroundTopologically associating domain boundaries are required for normal genome function
Rajderkar, S., Barozzi, I., Zhu, Y., Hu, R., Zhang, Y., Li, B., Alcaina‐Caro, A., Fukuda-Yuzawa, Y., Kelman, G., Akeza, A., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-04819-w · Cited by 172
“…by the overall depletion of structural variants at TAD boundaries observed in the general human population 26 , while disruptions and rearrangements of TAD structure have been implicated in the mis-expression of genes and are associated with developmental and cancer phenotypes 1 – 3, 29, 30 .”
Systemic Loss and Gain of Chromatin Architecture throughout Zebrafish Development
Kaaij, L. J. T., van der Weide, R. H., Ketting, R. F., & de Wit, E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.003 · Cited by 156
The Epigenetic Hallmarks of Cancer
Esteller, M., Dawson, M. A., Kadoch, C., Rassool, F. V., Jones, P. A., & Baylin, S. B. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-24-0296 · Cited by 202
Von Hippel–Lindau disease: insights into oxygen sensing, protein degradation, and cancer
Kaelin, W. G. (2022) · Journal of Clinical Investigation · doi:10.1172/jci162480 · Cited by 187
“In this regard, there is evidence that IDH mutations might act in a “hit and run” manner in glioma, setting in motion a feed-forward cycle that promotes transformation (96, 97).”
BackgroundThe spatial organization of transcriptional control
Hafner, A., & Boettiger, A. N. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00526-0 · Cited by 158
Independence of chromatin conformation and gene regulation during Drosophila dorsoventral patterning
Ing-Simmons, E., Vaid, R., Bing, X. Y., Levine, M., Mannervik, M., & Vaquerizas, J. M. (2021) · Nature Genetics · doi:10.1038/s41588-021-00799-x · Cited by 159
Miller, T. E., Lareau, C. A., Verga, J. A., DePasquale, E. A. K., Liu, V., Ssozi, D., Sándor, K., Yin, Y., Ludwig, L. S., Farran, C. A. E., et al. (2022) · Nature Biotechnology · doi:10.1038/s41587-022-01210-8 · Cited by 150
Self-citationIsocitrate dehydrogenase‐mutant glioma: Evolving clinical and therapeutic implications
Miller, J. J., Shih, H. A., Andronesi, O. C., & Cahill, D. P. (2017) · Cancer · doi:10.1002/cncr.31039 · Cited by 154
“It is interesting to note that IDH1-mutant-associated hypermethylation recently was shown to occur at cohesion and CCCTC-binding factor (CTCF)-binding sites, which play a role in the formation of chromatin loops and in the maintenance of chromosomal topology.(34) Normally, CTCF-binding proteins serve as insulators to…”
BackgroundLooking beyond the genes: the role of non-coding variants in human disease
Spielmann, M., & Mundlos, S. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw205 · Cited by 154
Mitigation of off-target toxicity in CRISPR-Cas9 screens for essential non-coding elements
Tycko, J., Wainberg, M., Marinov, G. K., Ursu, O., Hess, G. T., Ego, B. K., Aradhana, Li, A., Truong, A., Trevino, A. E., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11955-7 · Cited by 150
Guo, Y. A., Chang, M. M., Huang, W., Ooi, W. F., Xing, M., Tan, P. B. O., & Skanderup, A. J. (2018) · Nature Communications · doi:10.1038/s41467-018-03828-2 · Cited by 149
Isocitrate Dehydrogenase Mutations in Glioma: From Basic Discovery to Therapeutics Development
Huang, J., Yu, J., Tu, L., Huang, N., Li, H., & Luo, Y. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00506 · Cited by 147
The Roles of 2-Hydroxyglutarate
Du, X., & Hu, H. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.651317 · Cited by 160
Collier, M. D., Sungalee, S., Zufferey, M., Tavernari, D., Katanayeva, N., Battistello, E., Mina, M., Douglass, K. M., Rey, T., Raynaud, F., et al. (2019) · Nature Genetics · doi:10.1038/s41588-018-0338-y · Cited by 150
Greenwald, W. W. Y., Li, H., Benaglio, P., Jakubosky, D. A., Matsui, H., Schmitt, A. D., Selvaraj, S., D’Antonio, M., D’Antonio‐Chronowska, A., Smith, E. N., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08940-5 · Cited by 144
Gong, Y., Lazaris, C., Sakellaropoulos, T., Lozano, A. C., Kambadur, P., Ntziachristos, P., Aifantis, I., & Tsirigos, A. (2018) · Nature Communications · doi:10.1038/s41467-018-03017-1 · Cited by 143
The BET Protein BRD2 Cooperates with CTCF to Enforce Transcriptional and Architectural Boundaries
Hsu, S. C., Gilgenast, T. G., Bartman, C., Edwards, C. R., Stonestrom, A. J., Huang, P., Emerson, D. J., Evans, P., Werner, M. T., Keller, C. A., et al. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.02.027 · Cited by 143
“For example, in some cases, genes within TADs exhibit more correlated expression patterns with each other than with genes in other domains (Flavahan et al., 2016; Nora et al., 2012), and enhancers typically exert their activity within TAD boundaries (Symmons et al.”
BackgroundInfluentialOncogenic Activities of IDH1/2 Mutations: From Epigenetics to Cellular Signaling
Gagné, L. M., Boulay, K., Topisirović, I., Huot, M., & Mallette, F. A. (2017) · Trends in Cell Biology · doi:10.1016/j.tcb.2017.06.002 · Cited by 143
PDGF receptor mutations in human diseases
Guérit, E. M., Arts, F. A., Dachy, G., Boulouadnine, B., & Demoulin, J. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03753-y · Cited by 146
Genome control by SMC complexes
Hoencamp, C., & Rowland, B. D. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00609-8 · Cited by 147
Poleshko, A. S., Smith, C. L., Nguyen, S. C., Sivaramakrishnan, P., Wong, K. G., Murray, J. I., Lakadamyali, M., Joyce, E. F., Jain, R., & Epstein, J. A. (2019) · eLife · doi:10.7554/elife.49278 · Cited by 143
“…and the requirement for chromatin to allow nuclear membranes to reform in daughter cells after mitosis (Gerace and Blobel, 1980, Newport, 1987, Foisner and Gerace, 1993, Burke and Gerace, 1986, Wei et al., 1999, Prigent and Dimitrov, 2003, Wandke and Kutay, 2013, Haraguchi et al., 2008).”
BackgroundDevelopmentally regulated Shh expression is robust to TAD perturbations
Williamson, I., Kane, L., Devenney, P. S., Flyamer, I. M., Anderson, E., Kilanowski, F. M., Hill, R. E., Bickmore, W. A., & Lettice, L. A. (2019) · Development · doi:10.1242/dev.179523 · Cited by 148
“Moreover, a number of recent studies have suggested that changes to TAD structure can disrupt gene regulation through enhancer-rewiring in human disease (Flavahan et al., 2016; Franke et al., 2016; Lupiáñez et al., 2015).”
BackgroundA critical assessment of topologically associating domain prediction tools
Dali, R., & Blanchette, M. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx145 · Cited by 144
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Mazor, T., Chesnelong, C., Pankov, A., Jalbert, L. E., Hong, C., Hayes, J. L., Smirnov, I. V., Marshall, R. E., de Souza, C. F., Shen, Y., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1708914114 · Cited by 139
Methylation across the central dogma in health and diseases: new therapeutic strategies
Liu, R., Zhao, E., Yu, H., Yuan, C., Abbas, M. N., & Cui, H. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01528-y · Cited by 155
TET Enzymes and 5hmC in Adaptive and Innate Immune Systems
Lio, C. J., & Rao, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00210 · Cited by 144
“In addition, 5hmC may act as a bookmark to label CpG sites in cis-elements such as promoters, enhancers and insulators marked by CTCF binding (5, 98, 99) for subsequent demethylation upon cell division, thus affecting gene expression patterns in the daughter cells (a latent effect).”
BackgroundMultimodal 3D DenseNet for IDH Genotype Prediction in Gliomas
Liang, S., Zhang, R., Liang, D., Song, T., Ai, T., Chen, X., Xia, L., & Wang, Y. (2018) · Genes · doi:10.3390/genes9080382 · Cited by 137
“However, when IDH is mutated, the isocitrate will be converted to 2-hydroxyglutarate, which can inhibit the activity of man α -ketoglutarate-dependent dioxygenases, including, but are not limited, to histone demethylases [7].”
BackgroundDe novo pyrimidine synthesis is a targetable vulnerability in IDH mutant glioma
Shi, D. D., Savani, M. R., Levitt, M. M., Wang, A. C., Endress, J. E., Bird, C. E., Buehler, J., Stopka, S. A., Regan, M. S., Lin, Y., et al. (2022) · Cancer Cell · doi:10.1016/j.ccell.2022.07.011 · Cited by 140
Youssef, G., & Miller, J. J. (2020) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-020-01040-8 · Cited by 144
The three-dimensional genome: regulating gene expression during pluripotency and development
Andrey, G., & Mundlos, S. (2017) · Development · doi:10.1242/dev.148304 · Cited by 134
Epigenetic programming, early life nutrition and the risk of metabolic disease
Block, T., & El-Osta, A. (2017) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2017.09.003 · Cited by 130
Metabolic Reprogramming in Brain Tumors
Venneti, S., & Thompson, C. B. (2017) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012615-044329 · Cited by 139
Multiplexed Gene Editing and Protein Overexpression Using a Tobacco mosaic virus Viral Vector
Cody, W. B., Scholthof, H. B., & Mirkov, T. E. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00411 · Cited by 129
“…which are not necessarily accessible when using VIGS screening, such as targeting promoters, enhancers, and insulator sequences, is now feasible for understanding functionality within the context of a native gene environment (Zhang et al., 2016; Flavahan et al., 2016; Basak and Nithin, 2015).”
BackgroundParadoxical association of TET loss of function with genome-wide DNA hypomethylation
López-Moyado, I. F., Tsagaratou, A., Yuita, H., Seo, H., Delatte, B., Heinz, S., Benner, C. W., & Rao, A. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903059116 · Cited by 130
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CTCF shapes chromatin structure and gene expression in health and disease
Dehingia, B., Milewska, M., Janowski, M., & Pękowska, A. (2022) · EMBO Reports · doi:10.15252/embr.202255146 · Cited by 141
“The resulting epimutations lead to loss of CTCF binding and disruption of TAD boundaries (Flavahan et al , 2016) accompanied by aberrant gene expression as exemplified at the locus coding PDGFRA , a glioma oncogene.”
Characterization of gliomas: from morphology to molecules
Ferris, S. P., Hofmann, J. W., Solomon, D. A., & Perry, A. (2017) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-017-2181-4 · Cited by 130
“The precise role of IDH mutations in glioma pathogenesis is not completely understood, but there is strong evidence that IDHmutation results in epigenetic changes (global hypermethylation, termed the glioma-CpG island methylator phenotype (G-CIMP)) through production of 2-hydroxyglutarate (2-HG), which inhibits enzyme…”
Gene signature driving invasive mucinous adenocarcinoma of the lung
Guo, M., Tomoshige, K., Meister, M. A., Muley, T., Fukazawa, T., Tsuchiya, T., Karns, R. A., Warth, A., Fink-Baldauf, I. M., Nagayasu, T., et al. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201606711 · Cited by 124
“CRISPR/Cas9-mediated deletion (4–13 bp) of the insulator CTCF binding site in the PDGFRA locus induced the expression of PDGFRA by 1.6-fold in human glioblastoma cells (Flavahan et al, 2016).”
BackgroundInfluentialNew Molecular Considerations for Glioma: IDH, ATRX, BRAF, TERT, H3 K27M
Karsy, M. J., Guan, J., Cohen, A. L., Jensen, R. L., & Colman, H. (2017) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-017-0722-5 · Cited by 128
Mitochondrial metabolism supports resistance to IDH mutant inhibitors in acute myeloid leukemia
Stuani, L., Sabatier, M., Wang, F., Poupin, N., Bosc, C., Saland, E., Castelli, F. A., Gales, L., Montersino, C., Boët, E., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20200924 · Cited by 143
“Through the production of (R)-2-HG, IDH mutations directly impact histone/DNAmethylation and gene expression (Figueroa et al., 2010; Turcan et al., 2018; Guilhamon et al., 2013; Flavahan et al., 2016), cell proliferation, and differentiation bias (Losman et al.”
BackgroundLoop stacking organizes genome folding from TADs to chromosomes
Hafner, A., Park, M., Berger, S. E., Murphy, S. E., Nora, E. P., & Boettiger, A. N. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.04.008 · Cited by 126
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Characterization of noncoding regulatory DNA in the human genome
Elkon, R., & Agami, R. (2017) · Nature Biotechnology · doi:10.1038/nbt.3863 · Cited by 132
BORIS promotes chromatin regulatory interactions in treatment-resistant cancer cells
Debruyne, D. N., Dries, R., Sengupta, S., Seruggia, D., Gao, Y., Sharma, B., Huang, H., Moreau, L. A., McLane, M., Day, D. S., et al. (2019) · Nature · doi:10.1038/s41586-019-1472-0 · Cited by 126
Advances in Chromatin Imaging at Kilobase-Scale Resolution
Boettiger, A. N., & Murphy, S. E. (2020) · Trends in Genetics · doi:10.1016/j.tig.2019.12.010 · Cited by 121
Connections Between Metabolism and Epigenetics in Programming Cellular Differentiation
Chisolm, D. A., & Weinmann, A. S. (2018) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042617-053127 · Cited by 133
The nuclear matrix protein HNRNPU maintains 3D genome architecture globally in mouse hepatocytesPreprint
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Cancer epigenetics: Past, present and future
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Principles of Chromosome Architecture Revealed by Hi-C
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In silico prediction of high-resolution Hi-C interaction matrices
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“These long-range interactions can have major roles in tissue4 specific expression [1–3] and how regulatory sequence variants impact complex phenotypes [4, 5], in5 cluding diseases such as cancer, diabetes and obesity [6, 7].”
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Clustered CTCF binding is an evolutionary mechanism to maintain topologically associating domains
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“Local TAD disruptions may also lead to disease (Flavahan et al., 2016; Ibn-Salem et al., 2014; Lupiáñez et 40 al., 2015, 2016).”
BackgroundInfluentialDNA Methylation and Genetic Aberrations in Gastric Cancer
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Cancer-specific CTCF binding facilitates oncogenic transcriptional dysregulation
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“The functional importance of CTCF is highlighted in disruptions to CTCF binding coupled with alterations in gene expression, which have been widely observed[19-22].”
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“The use of various specific surface markers or molecular mediators such as CD133, CD90, CD44, L1CAM, A2B5, and GPD1 is a common method to identify GSCs and define lineagespecific subpopulations within the tumor, although the cause of their reproducibility and accuracy is still unclear (29, 30, 72).”
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Mutant IDH1 Promotes Glioma Formation In Vivo
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“previously demonstrated aberrant PDGFRA gene activation in cells harboringmutant IDH as a result of hypermethylation at cohesin and CCCTC-binding factor (CTCF)-binding sites, which disrupted binding of CTCF, a methylation-sensitive insulator protein (Flavahan et al., 2016).”
CTCF and R-loops are boundaries of cohesin-mediated DNA looping
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Integrative Analysis Defines Distinct Prognostic Subgroups of Intrahepatic Cholangiocarcinoma
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The chromosome folding problem and how cells solve it
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Glioma diagnosis and therapy: Current challenges and nanomaterial-based solutions
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The classification of gliomas based on a Pyramid dilated convolution resnet model
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Molecular mechanisms in colitis-associated colorectal cancer
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“In glioma and gastrointestinal stromal tumors (GISTs), 2-HG displacement of CTCF allows enhancers once insulated from nearby proto-oncogenes to activate their expression to promote tumor growth and progression [75, 76].”
BackgroundEpigenetic regulation in cancer
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“78 The studies into chromatin structure in IDH and SDH mutant tumors illuminate the broader implications of chromatin remodeling.”
BackgroundInfluentialAccelerating the understanding of cancer biology through the lens of genomics
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Epigenomic Reprogramming as a Driver of Malignant Glioma
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“DNA methylation can in certain circumstances prevent CTCF binding and indeed loss of these insulation sites in an IDH mutant glioma model increased expression of the PDGFRA oncogene, potentially by abrogating the TAD boundary and permitting the PDGFRA gene access to an active enhancer in a distinct domain (Flavahan et…”
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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