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Telomere dysfunction and tumour suppression: the senescence connection
Open accessAbstract
Long-lived organisms such as humans have evolved several intrinsic tumour suppressor mechanisms to combat the slew of oncogenic somatic mutations that constantly arise in proliferating stem-cell compartments. One of these anticancer barriers is the telomere, a specialized nucleoprotein complex that caps the ends of eukaryotic chromosome. Impaired telomere function activates the canonical DNA damage response pathway that engages p53 to initiate apoptosis or replicative senescence. Here, we discuss how p53-dependent senescence induced by dysfunctional telomeres may be as potent as apoptosis in suppressing tumorigenesis in vivo.
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TL;DR
This review argues that dysfunctional telomeres activate a DNA damage response that engages p53-dependent apoptosis and replicative senescence, and that senescence can be as potent as apoptosis for suppressing tumorigenesis in vivo. Mouse models with short/dysfunctional telomeres show reduced tumor incidence and progression when p53 signaling is intact.
Key findings
- Telomere dysfunction triggers a DDR through ATM/ATR, CHK1/CHK2, p53 and p21, leading to apoptosis or replicative senescence; dysfunctional telomeres form TIFs containing γ-H2AX, 53BP1, NBS1, MDC1 and CHK2.
- In mouse cancer models, short dysfunctional telomeres suppress tumors when p53 is intact: G6 mTerc−/−;Ink4a−/− mice showed reduced tumor incidence from 64% to 31%; late-generation mTerc−/− mice produced 20-fold fewer skin tumors; late-generation mTerc−/− Eμ-myc mice had only 25% lymphoma incidence versus wild-type/early-generation mice developing B-cell lymphoma by 200 days.
- p53-dependent apoptosis appears dispensable for spontaneous tumor suppression when senescence is activated: Bcl-2-overexpressing G5/6 mTerc−/− Eμ-myc bone marrow failed to produce tumors 100 days post-transplantation, with small encapsulated tumors showing a 3-fold decrease in mitotic index and positive SA-β-Gal, p16 and p15 staining.
- In iG1 mTerc−/− p53R172P mice, which lack p53-dependent apoptosis but retain senescence, tumor formation was nearly completely suppressed: 0/23 tumors in p53P/+ and 1/9 in p53P/P mice, with robust SA-β-gal staining in multiple organs.
Methods
- This is a Perspective/review synthesizing published experimental studies; no new primary data are reported.
- Evidence comes largely from mouse models, including successive generations of telomerase knockout (mTerc−/−) mice, Eμ-myc lymphoma, p53 R172P knock-in, Ink4a−/−, ApcMin, hepatocellular carcinoma and skin carcinogenesis models, plus human cell lines and xenograft studies of telomerase inhibitors.
- Main analysis compares tumor incidence, latency, survival, cytogenetic hallmarks of telomere dysfunction, DDR markers/TIFs, and senescence markers such as SA-β-gal, p16, p15, p21 and p53.
Limitations
- Stated: anti-telomerase therapy requires an intact p53 pathway, but p53 is mutated in approximately 50% of human cancers; senescent tumor cells may secrete tumor-promoting products; and this therapy will not work in ALT tumors lacking functional telomerase.
- Stated: the role of the p16Ink4a-RB pathway in the telomere DDR is unclear, and p21 loss in late-generation mTerc−/− mice did not increase chromosomal instability or tumorigenesis, suggesting redundancy or additional p53-dependent effects.
- Evident: conclusions rely heavily on mouse models, with possible mouse–human differences in DDR wiring; the review also notes historical difficulty in reliably detecting senescent cells in vivo.
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In the paper
“However, in the setting of a competent p53 pathway, mouse models have recently shown that telomere shortening is also tumor suppressive by promoting replicative senescence to inhibit tumor formation.”
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In the paper
“We now know that the endpoint of this proliferative limit, termed replicative senescence, is due largely to erosion of telomeres, protective structures that cap the end of all eukaryotic chromosomes.”
What the sources say
- Not checked yetcites [3] Bodnar, A. G. et al. Extension of life-span by introduction of telomerase into normal human cells. Science 279, 349–352 (1998). source
- Not checked yetcites [4] Vaziri, H. & Benchimol, S. Reconstitution of telomerase activity in normal human cells leads to elongation of telomeres and extended replicative life span. Curr. Biol. 8, 279–282 (1998). source
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In the paper
“Dysfunctional telomeres activate upstream checkpoint PI3 kinases, such as ATM (ataxia-telangiectasia mutated) or ATR (ataxia-telangiectasia and Rad3 related)22, 27-30”
What the sources say
- Not checked yetcites [22] d'Adda di Fagagna, F. et al. A DNA damage checkpoint response in telomere-initiated senescence. Nature 426, 194–198 (2003). source
- Not checked yetcites [27] Guo, X. et al. Dysfunctional telomeres activate an ATM–ATR-dependent DNA damage response to suppress tumorigenesis. EMBO J. 26, 4709–4719 (2007). source
- Not checked yetcites [28] Churikov, D. & Price, C. M. Pot1 and cell cycle progression cooperate in telomere length regulation. Nature Struct. Mol. Biol. 15, 79–84 (2008). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIn the paper
“A large body of experimental evidence has demonstrated that telomere attrition contributes to tumorigenesis by promoting genome instability5.”
What the sources say
- Not checked yetcites [5] Maser, R. S. & DePinho, R. A. Connecting chromosomes, crisis, and cancer. Science 297, 565–569 (2002). source
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In the paper
“A total lifetime loss of ~2-4 kb in average telomere length has been observed in human cells8-10.”
What the sources say
- Not checked yetcites [8] Harley, C. B., Futcher, A. B. & Greider, C. W. Telomeres shorten during ageing of human fibroblasts. Nature 345, 458–460 (1990). This report links increasing telomere attrition with increased cell divisions and advancing age, suggesting that telomere shortening may be the underlying mechanism of the Hayflick limit. source
- Not checked yetcites [9] Allsopp, R. C. et al. Telomere length predicts replicative capacity of human fibroblasts. Proc. Natl Acad. Sci. USA 89, 10114–10118 (1992). source
- Not checked yetcites [10] Harley, C. B. et al. Telomerase, cell immortality, and cancer. Cold Spring Harb. Symp. Quant. Biol. 59, 307–315 (1994). source
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In the paper
“Instead, the p53-p21-dependent cellular senescence pathway is potently activated in mice bearing dysfunctional telomeres, and may be responsible for the tumor suppression observed in these animals.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIn the paper
“The fact that tumorigenesis is not increased in the context of p21 deficiency indicates that in this mouse model, p53-mediated apoptosis functions as a redundant anti-tumor barrier in response to short telomeres.”
What the sources say
- Not checked yetcites [61] Choudhury, A. R. et al. Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation. Nature Genet. 39, 99–105 (2007). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In addition, up regulation of p53 was detected in late generation mTerc−/− papillomas.”
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In the paper
“Primary fibroblasts isolated from these embryos also exhibited resistance to transformation by Myc and Ras.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA 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
“Instead, the p53-p21-dependent cellular senescence pathway is potently activated in mice bearing dysfunctional telomeres, and may be responsible for the tumor suppression observed in these animals.”
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- It may state two separate claims as one. 38
- Probably not a substantial claim. 6
- The quote only partly states this claim. 2
None of the sources cited for this claim have been checked yet.
In the paper
“Activation of telomerase results in telomere elongation, abrogation of replicative senescence, a normal karyotype and cellular immortalization.”
What the sources say
- Not checked yetcites [3] Bodnar, A. G. et al. Extension of life-span by introduction of telomerase into normal human cells. Science 279, 349–352 (1998). source
- Not checked yetcites [4] Vaziri, H. & Benchimol, S. Reconstitution of telomerase activity in normal human cells leads to elongation of telomeres and extended replicative life span. Curr. Biol. 8, 279–282 (1998). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Once activated, these kinases phosphorylate downstream factors including CHK1 and CHK2 that in turn phosphorylates p5329. Phosphorylation of p53 results in the displacement of the murine double minute 2 (MDM2) protein, liberating p53 from degradation and stimulation of the expression of the cyclin-dependent kinase inhibitor p21. p21 inhibits cell cycle progression by inhibiting cyclin-dependent”
What the sources say
- Not checked yetcites [29] Gire, V., Roux, P., Wynford-Thomas, D., Brondello, J. M. & Dulic, V. DNA damage checkpoint kinase Chk2 triggers replicative senescence. EMBO J. 23, 2554–2563 (2004). source
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In the paper
“These fusions are the basis of genomic instability associated with telomere dysfunction as they lead to anaphase bridging, subsequent breakage and that requires further repair. Repetition of this fusion-bridge-breakage cycle leads to aneuploidy, further fusions and depending on how such DNA damage is resolved, it has been hypothesized that loss of heterozygosity or gene amplification could result”
What the sources say
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In the paper
“After 60-80 population doublings in culture, HDFs stop dividing and adopt a phenotype characterized by large, flat cell size, a vacuolated morphology, inability to synthesize DNA, and the presence of the senescence-associated β-galactosidase (SA-β-gal) marker2.”
What the sources say
- Not checked yetcites [1] Hayflick, L. & Moorhead, P. S. The serial cultivation of human diploid cell strains. Exp. Cell Res. 25, 585–621 (1961). A classic paper demonstrating that human cells have finite proliferative capacity in vitro (the 'Hayflick limit'). source
- Not checked yetcites [2] Dimri, G. P. et al. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proc. Natl Acad. Sci. USA 92, 9363–9367 (1995). This paper reports on the SA-β-gal assay as a way to mark senescent cells. source
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In the paper
“Mammalian telomeres associate with the shelterin complex of six core proteins — telomeric-repeat binding factor 1 (TRF1), TRF2, TRF1 interacting protein 2 (TIN2), protection of telomeres 1 (POT1), the POT1 and TIN2 interacting protein TPP1 and the transcriptional repressor/activator protein RAP115, 16”
What the sources say
- Not checked yetcites [15] de Lange, T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes Dev. 19, 2100–2110 (2005). source
- Not checked yetcites [16] Liu, D., O'Connor, M. S., Qin, J. & Songyang, Z. Telosome, a mammalian telomere-associated complex formed by multiple telomeric proteins. J. Biol. Chem. 279, 51338–51342 (2004). source
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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
“These results clearly demonstrate that telomere length determines the proliferative lifespan of HDFs, and that upregulation of telomerase activity (hence telomere length) restores proliferative capacity.”
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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
“These results suggest that both critically short telomeres and direct disruption of the shelterin structure can initiate telomere dysfunction, trigger a DDR and chromosomal fusions.”
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In the paper
“Considering that human telomeres are only 8-12 kb in length or less at birth, this degree of attrition is significant over the natural lifespan of humans, and may be responsible to elicit certain aspects of human aging phenotypes11.”
What the sources say
- Not checked yetcites [11] Blasco, M. A. Telomere length, stem cells and aging. Nature Chem. Biol. 3, 640–649 (2007). source
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In the paper
“Telomeres that can no longer exert end-protective functions are said to be dysfunctional, and these telomeres could arise either from progressive telomere attrition, or when components of the shelterin complex are perturbed, resulting in inappropriate chromosomal end-to-end fusions through the non-homologous end joining (NHEJ) or homologous recombination (HR) DNA repair pathways 17.”
What the sources say
- Not checked yetcites [17] Verdun, R. E. & Karlseder, J. Replication and protection of telomeres. Nature 447, 924–931 (2007). source
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In the paper
“Telomerase expression is low or absent in most human somatic tissues6, while it is robust in early proliferative progenitor germ and stem cells 7, 8.”
What the sources say
- Not checked yetcites [6] Masutomi, K. et al. Telomerase maintains telomere structure in normal human cells. Cell 114, 241–253 (2003). source
- Not checked yetcites [7] Wright, W. E., Piatyszek, M. A., Rainey, W. E., Byrd, W. & Shay, J. W. Telomerase activity in human germline and embryonic tissues and cells. Dev. Genet. 18, 173–179 (1996). source
- Not checked yetcites [8] Harley, C. B., Futcher, A. B. & Greider, C. W. Telomeres shorten during ageing of human fibroblasts. Nature 345, 458–460 (1990). This report links increasing telomere attrition with increased cell divisions and advancing age, suggesting that telomere shortening may be the underlying mechanism of the Hayflick limit. source
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In the paper
“These results suggest that dysfunctional telomeres are recognized as DSBs that impinge upon p53 and/or pRB tumor suppressor pathways, to induce expression of their regulators p21 and p16 Ink4a to initiate replicative senescence24-26.”
What the sources say
- Not checked yetcites [24] Wright, W. E. & Shay, J. W. The two-stage mechanism controlling cellular senescence and immortalization. Exp. Gerontol. 27, 383–389 (1992). This paper documents that DNA damage checkpoint proteins such as p53 and RB are required for cells with shortened telomeres to undergo cellular senescence. Elimination of these proteins enables these cells to immortalize. source
- Not checked yetcites [25] Kamijo, T. et al. Tumor suppression at the mouse INK4a locus mediated by the alternative reading frame product p19ARF. Cell 91, 649–659 (1997). source
- Not checked yetcites [26] Sage, J., Miller, A. L., Perez-Mancera, P. A., Wysocki, J. M. & Jacks, T. Acute mutation of retinoblastoma gene function is sufficient for cell cycle re-entry. Nature 424, 223–228 (2003). source
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In the paper
“Biochemical analyses revealed that HDFs that entered replicative senescence display molecular markers characteristic of cells bearing DNA double-strand breaks (DSBs), suggesting that dysfunctional telomeres elicit a potent DNA damage response (DDR)22.”
What the sources say
- Not checked yetcites [22] d'Adda di Fagagna, F. et al. A DNA damage checkpoint response in telomere-initiated senescence. Nature 426, 194–198 (2003). source
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In the paper
“These markers of the DDR include phosphorylated γ-H2AX, 53BP1, NBS1, MDC1 and CHK2, among others. Many of these proteins localize directly to dysfunctional telomeres to form dysfunctional telomere-induced foci (TIFs), and their inactivation in senescent cells restores cell cycle progression into S-phase22, 23.”
What the sources say
- Not checked yetcites [22] d'Adda di Fagagna, F. et al. A DNA damage checkpoint response in telomere-initiated senescence. Nature 426, 194–198 (2003). source
- Not checked yetcites [23] Takai, H., Smogorzewska, A. & de Lange, T. DNA damage foci at dysfunctional telomeres. Curr. Biol. 13, 1549–1556 (2003). References 22 and 23 report that dysfunctional telomeres activate a DDR, resulting in the accumulation of DDR proteins at telomeres. Cells with dysfunctional telomeres enter into senescence by activating a p53-dependent checkpoint response. source
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In the paper
“Analysis of telomeres from a diverse array of organisms revealed that the telomere 3′ single-stranded overhang can invade the double-stranded telomeric tracts, displacing the homologous strand of the same telomere. Consequently, a telomere forms a lasso-like structure, termed the ‘t-loop’, with a displacement (D) loop at the invasion site12, 13”
What the sources say
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In the paper
“late generation mTerc−/−, p21−/− mice do not show increased chromosomal instability nor do they succumb to increased tumorigenesis61.”
What the sources say
- Not checked yetcites [61] Choudhury, A. R. et al. Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation. Nature Genet. 39, 99–105 (2007). source
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In the paper
“The demonstration that dysfunctional telomeres could engage a senescence program to suppress tumorigenesis in vivo suggests possible future therapeutic applications63.”
What the sources say
- Not checked yetcites [63] Harley, C. B. Telomerase and cancer therapeutics. Nature Rev. Cancer 8, 167–179 (2008). source
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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
“These results suggest that progression from micro to macroadenomas was inhibited in G6 mTerc−/−ApcMin mice, presumably due to the activation of p53-dependent tumor suppressive pathways by dysfunctional telomeres.”
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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
“Together, these observations support the view that replicative senescence and crisis provide potent barriers to tumor development and, by extension, that proper telomere maintenance is an essential aspect of full malignant transformation.”
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In the paper
“However, similar treatment of G6-mTerc−/−;Ink4a−/− mice with short dysfunctional telomeres yielded a dramatic reduction in tumor incidence (from 64% to 31%) and much longer survival49.”
What the sources say
- Not checked yetcites [49] Greenberg, R. A. et al. Short dysfunctional telomeres impair tumorigenesis in the INK4aΔ2/3 cancer-prone mouse. Cell 97, 515–525 (1999). source
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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
“One explanation is that while telomere induced cellular senescence is capable of suppressing spontaneous tumorigenesis from mesenchymal tumors, it is insufficient to suppress cancer formation of epithelial tissues such as the skin.”
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In the paper
“In addition to promoting cell cycle arrest, dysfunctional telomeres can also activate p53-dependent apoptosis, since mice bearing dysfunctional telomeres show increased apoptosis in proliferative cells31-33.”
What the sources say
- Not checked yetcites [31] Lee, H. W. et al. Essential role of mouse telomerase in highly proliferative organs. Nature 392, 569–574 (1998). source
- Not checked yetcites [32] Rudolph, K. L. et al. Longevity, stress response, and cancer in aging telomerase-deficient mice. Cell 96, 701–712 (1999). source
- Not checked yetcites [33] Rajaraman, S. et al. Telomere uncapping in progenitor cells with critical telomere shortening is coupled to S-phase progression in vivo. Proc. Natl Acad. Sci. USA 104, 17747–17752 (2007). source
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In the paper
“Importantly, removal of p53 function rescued many of the cellular defects despite the presence of critically short telomeres, including growth arrest in cell culture, testicular atrophy, intestinal and germ cell apoptosis46.”
What the sources say
- Not checked yetcites [46] Chin, L. et al. p53 deficiency rescues the adverse effects of telomere loss and cooperates with telomere dysfunction to accelerate carcinogenesis. Cell 97, 527–538 (1999). source
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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
“These results suggest that dysfunctional telomeres could activate a cellular senescence pathway to suppress tumorigenesis in the absence of apoptosis to suppress tumorigenesis, while this pathway was not elicited in the tumors with competent telomeres.”
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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
“suggesting it is possible that p53-dependent but senescence- and apoptosis-independent effects of dysfunctional telomeres might account for some of the observed tumor suppression in vivo.”
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In the paper
“The telomerase deficient mouse lacks the critical RNA subunit mTerc, is viable, fertile and has no significant morphological abnormalities42.”
What the sources say
- Not checked yetcites [42] Blasco, M. A. et al. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell 91, 25–34 (1997). source
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In the paper
“Instead, loss of p21 extended organismal lifespan and rescued cellular proliferative defects due to dysfunctional telomeres, presumably due to reduced entry of proliferative cells into cellular senescence.”
What the sources say
- Not checked yetcites [61] Choudhury, A. R. et al. Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation. Nature Genet. 39, 99–105 (2007). source
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In the paper
“GRN163L is a modified oligonucleotide complementary to hTERC and a potent and specific telomerase antagonist66.”
What the sources say
- Not checked yetcites [66] Dikmen, Z. G. et al. In vivo inhibition of lung cancer by GRN163L: a novel human telomerase inhibitor. Cancer Res. 65, 7866–7873 (2005). source
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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
“Together, these findings demonstrate that telomere dysfunction promotes the development of cancer in the setting of p53 deficiency, and further reinforce the importance of an intact p53 pathway in tumor inhibition in the setting of telomere dysfunction.”
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- Rests on an assumption: Findings from mouse models of telomere dysfunction and cancer are informative about human tumor suppression and tumorigenesis.
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In the paper
“Cells harboring this mutation (p53P/P) are incapable of activating p53-dependent apoptosis59, but the p53-dependent cellular senescence pathway is intact as induction of telomere dysfunction through overexpression of TRF2-DN in these cells led to dramatic reduction of cellular proliferation and the appearance of senescent cells that stain positive for SA-β-Gal58.”
What the sources say
- Not checked yetcites [58] Cosme-Blanco, W. et al. Telomere dysfunction suppresses spontaneous tumorigenesis in vivo by initiating p53-dependent cellular senescence. EMBO Rep. 8, 497–503 (2007). Using telomerase-knockout mouse models in a setting in which the apoptotic function of p53 is eliminated, references 57 and 58 document for the first time that activation of the cellular senescence programme could potently inhibit tumour initiation and progression in vivo. source
- Not checked yetcites [59] Liu, G. et al. Chromosome stability, in the absence of apoptosis, is critical for suppression of tumorigenesis in Trp53 mutant mice. Nature Genet. 36, 63–68 (2004). source
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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
“However, transplantation of G5/6 mTerc−/−, Eμ-myc, Bcl-2 bone marrow failed to produce any tumors 100 days post-transplantation.”
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In the paper
“Interestingly, TIF formation correlated with delocalization of POT1 and was antagonized by overexpression of POT1 or TRF2.”
What the sources say
- Not checked yetcites [71] Salvati, E. et al. Telomere damage induced by the G-quadruplex ligand RHPS4 has an antitumor effect. J. Clin. Invest. 117, 3236–3247 (2007). source
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Similar findings were observed in vivo, where the progressive decline in telomere function correlated with increased tumor incidence and decreased survival.”
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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
“In contrast, iG1 mTerc−/− p53P/+ and iG1 mTerc−/− p53P/P cells possessed a 6-8 fold increase in p-p arm fusions and a 3-fold increase in the formation of anaphase bridges, both hallmarks of telomere dysfunction.”
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In the paper
“The upregulation of telomerase in most human cancers and its requirement for proliferation makes anti-telomerase compounds a potential means to induce telomere shortening and initiation of a senescence program in tumor cells64.”
What the sources say
- Not checked yetcites [64] Shay, J. W. & Keith, W. N. Targeting telomerase for cancer therapeutics. Br. J. Cancer 98, 677–683 (2008). source
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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
“Therefore, it is not surprising that p53 loss results in a permissive environment that favors proliferation and survival of genomically damaged cells and the eventual progression to cancer.”
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Crisis serves as the second checkpoint in tumor suppression and is characterized by multiple chromosomal fusions36.”
What the sources say
- Not checked yetcites [36] Counter, C. M. et al. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 11, 1921–1929 (1992). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“treatment of HT1080 fibrosarcoma cell lines with the telomerase inhibitor BIBR1532 results in progressive telomere shortening, induction of a senescence phenotype and inhibition of tumor growth when transplanted into recipient mice65.”
What the sources say
- Not checked yetcites [65] Damm, K. et al. A highly selective telomerase inhibitor limiting human cancer cell proliferation. EMBO J. 20, 6958–6968 (2001). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“GRN163L effectively inhibits telomerase activity of various human cancer cell lines67-70, resulting in progressive telomere shortening and induction of cellular senescence to suppress tumor cell growth in vitro.”
What the sources say
- Not checked yetcites [67] Djojosubroto, M. W. et al. Telomerase antagonists GRN163 and GRN163L inhibit tumor growth and increase chemosensitivity of human hepatoma. Hepatology 42, 1127–1136 (2005). source
- Not checked yetcites [68] Hochreiter, A. E. et al. Telomerase template antagonist GRN163L disrupts telomere maintenance, tumor growth, and metastasis of breast cancer. Clin. Cancer Res. 12, 3184–3192 (2006). source
- Not checked yetcites [69] Jackson, S. R. et al. Antiadhesive effects of GRN163L — an oligonucleotide N3′→P5′ thio-phosphoramidate targeting telomerase. Cancer Res. 67, 1121–1129 (2007). source
- Not checked yetcites [70] Ozawa, T. et al. Antitumor effects of specific telomerase inhibitor GRN163 in human glioblastoma xenografts. Neuro Oncol. 6, 218–226 (2004). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Similar results were observed in p53-competent mouse models of hepatocellular carcinoma, in which dysfunctional telomeres served to initiate tumor growth, but also limited the size of these tumors (progression) by activating apoptosis53.”
What the sources say
- Not checked yetcites [53] Farazi, P. A. et al. Differential impact of telomere dysfunction on initiation and progression of hepatocellular carcinoma. Cancer Res. 63, 5021–5027 (2003).
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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In the paper
“Virally transformed human cells that eliminate p53 and/or pRB function can escape crisis at very low frequencies, and invariably adopt telomere-maintenance programs: 80-90% of human tumors possess some telomerase activity, while the remainder maintain telomeres via a recombination-mediated process termed ALT (for Alternative Lengthening of Telomeres)37-40.”
What the sources say
- Not checked yetcites [37] Shay, J. W., Van Der Haegen, B. A., Ying, Y. & Wright, W. E. The frequency of immortalization of human fibroblasts and mammary epithelial cells transfected with SV40 large T-antigen. Exp. Cell Res. 209, 45–52 (1993). source
- Not checked yetcites [38] Kim, N. W. et al. Specific association of human telomerase activity with immortal cells and cancer. Science 266, 2011–2015 (1994). source
- Not checked yetcites [39] Bryan, T. M., Englezou, A., Dalla-Pozza, L., Dunham, M. A. & Reddel, R. R. Evidence for an alternative mechanism for maintaining telomere length in human tumors and tumor-derived cell lines. Nature Med. 3, 1271–1274 (1997). source
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
“In carcinomas, perhaps activation of both senescence and apoptotic pathways are required to enforce tumor suppression.”
Tests✗ Asserted: fails✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The authors may not put it forward as true. The paper may give no reason why it holds. The quote only partly states this claim.
In the paper
“One must also be concerned about the possibility that tumor cells rendered senescent would yield secretory products that might itself be tumor promoting77.”
What the sources say
- Not checked yetcites [77] Krtolica, A., Parrinello, S., Lockett, S., Desprez, P. Y. & Campisi, J. Senescent fibroblasts promote epithelial cell growth and tumorigenesis: a link between cancer and aging. Proc. Natl Acad. Sci. USA 98, 12072–12077 (2001). source
Tests✓ 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
“Finally, this therapy will not work in ALT tumors which lack functional telomerase.”
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
None of the sources cited for this claim have been checked yet.
In the paper
“Recent observations indicate that both telomere dysfunction73, 74 and the DDR75, 76 are activated at the earliest stages in many human carcinomas.”
What the sources say
- Not checked yetcites [73] Chin, K. et al. In situ analyses of genome instability in breast cancer. Nature Genet. 36, 984–988 (2004). source
- Not checked yetcites [74] Meeker, A. K. et al. Telomere length abnormalities occur early in the initiation of epithelial carcinogenesis. Clin. Cancer Res. 10, 3317–3326 (2004). source
- Not checked yetcites [75] Bartkova, J. et al. DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis. Nature 434, 864–870 (2005). source
- Not checked yetcites [76] Gorgoulis, V. G. et al. Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions. Nature 434, 907–913 (2005). source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
Long-lived organisms such as humans have evolved intrinsic tumor suppressor mechanisms to combat oncogenic somatic mutations that arise in proliferating stem cell compartments.
“Long lived organisms such as humans have evolved several intrinsic tumor suppressor mechanisms to combat the slew of oncogenic somatic mutations that constantly arise in proliferating stem cell compartments.”
The paper relies on this without support.
Findings from mouse models of telomere dysfunction and cancer are informative about human tumor suppression and tumorigenesis.
“late generation mTerc−/− p53+/− mice emerged with a tumor spectrum that strikingly resembled those of aged humans: carcinomas of the skin, breast, and intestine with cytogenetic hallmarks of telomere dysfunction emerged as the largest group of tumors47.”
The paper relies on this without support.
p53 is mutated in approximately 50% of all human cancers.
“p53 is mutated in approximately 50% of all human cancers.”
The paper relies on this without support.
The G-rich strand of telomeric DNA can fold into a 4-stranded G-quadruplex (G4), whose stabilization perturbs telomere function.
“The G-rich strand of telomeric DNA can fold into a 4-stranded G-quadruplex (G4), whose stabilization perturbs telomere function.”
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
“although in most mouse studies, short telomeres have been found to be cancer-protective rather than cancer-promoting80.”
From The telomere syndromes (2012) · cites this paper as [80]
Citations
Cites
The serial cultivation of human diploid cell strains
Hayflick, L., & Moorhead, P. S. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90192-6 · Cited by 8,508
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., & Pereira-Smith, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9363 · Cited by 7,477
Specific Association of Human Telomerase Activity with Immortal Cells and Cancer
Kim, N. W., Piatyszek, M. A., Prowse, K. R., Harley, C. B., West, M. D., Ho, P. L. C., Coviello, G. M., Wright, W. E., Weinrich, S. L., & Shay, J. W. (1994) · Science · doi:10.1126/science.7605428 · Cited by 7,091
Telomeres shorten during ageing of human fibroblasts
Harley, C. B., Futcher, A. B., & Greider, C. W. (1990) · Nature · doi:10.1038/345458a0 · Cited by 5,750
Extension of Life-Span by Introduction of Telomerase into Normal Human Cells
Bodnar, A. G., Ouellette, M., Frolkis, M., Holt, S. E., Chiu, C.-P., Morin, G. B., Harley, C. B., Shay, J. W., Lichtsteiner, S., & Wright, W. E. (1998) · Science · doi:10.1126/science.279.5349.349 · Cited by 4,975
Shelterin: the protein complex that shapes and safeguards human telomeres
de Lange, T. (2005) · Genes & Development · doi:10.1101/gad.1346005 · Cited by 3,056
A DNA damage checkpoint response in telomere-initiated senescence
Fagagna, F. D. D., Reaper, P. M., Clay-Farrace, L., Fiegler, H., Carr, P., von Zglinicki, T., Saretzki, G., Carter, N. P., & Jackson, S. P. (2003) · Nature · doi:10.1038/nature02118 · Cited by 2,917
A survey of telomerase activity in human cancer
Shay, J. W., & Bacchetti, S. (1997) · European Journal of Cancer · doi:10.1016/s0959-8049(97)00062-2 · Cited by 2,794
DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis
Bartkova, J., Hořejší, Z., Koed, K., Krämer, A., Tort, F., Zieger, K., Guldberg, P., Sehested, M., Nesland, J. M., Lukas, C., et al. (2005) · Nature · doi:10.1038/nature03482 · Cited by 2,688
Mammalian Telomeres End in a Large Duplex Loop
Griffith, J. D., Comeau, L., Rosenfield, S., Stansel, R. M., Bianchi, A., Moss, H., & de Lange, T. (1999) · Cell · doi:10.1016/s0092-8674(00)80760-6 · Cited by 2,447
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Blinded by the Light: The Growing Complexity of p53
Vousden, K. H., & Prives, C. (2009) · Cell · doi:10.1016/j.cell.2009.04.037 · Cited by 3,163
Bonner, W. M., Redon, C. E., Dickey, J. S., Nakamura, A. J., Sedelnikova, O. A., Solier, S., & Pommier, Y. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2523 · Cited by 1,623
Senescence in tumours: evidence from mice and humans
Collado, M., & Serrano, M. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2772 · Cited by 1,124
P53 in survival, death and metabolic health: a lifeguard with a licence to kill.
Kruiswijk, F., Labuschagne, C. F., & Vousden, K. H. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4007 · Cited by 1,080
Armanios, M., & Blackburn, E. H. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3246 · Cited by 982
Senescence-messaging secretome: SMS-ing cellular stress
Kuilman, T., & Peeper, D. S. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2560 · Cited by 909
Oxidative stress response and Nrf2 signaling in aging
Zhang, H., Davies, K. J. A., & Forman, H. J. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.05.036 · Cited by 804
Stability and kinetics of G-quadruplex structures
Lane, A. N., Chaires, J. B., Gray, R. D., & Trent, J. O. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn517 · Cited by 736
Radiation-induced cell death mechanisms
Eriksson, D., & Stigbrand, T. I. (2010) · Tumor Biology · doi:10.1007/s13277-010-0042-8 · Cited by 704
The effects of aging in the hippocampus and cognitive decline
Bettio, L. E. B., Rajendran, L., & Gil‐Mohapel, J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.04.030 · Cited by 700
Pro-senescence therapy for cancer treatment
Nardella, C., Clohessy, J. G., Alimonti, A., & Pandolfi, P. P. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3057 · Cited by 437
Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease
Mora, A. L., Rojas, M., Pardo, A., & Selman, M. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.170 · Cited by 406
Telomeres and age-related disease: how telomere biology informs clinical paradigms
Armanios, M. Y. (2013) · Journal of Clinical Investigation · doi:10.1172/jci66370 · Cited by 352
Chemistry in human telomere biology: structure, function and targeting of telomere DNA/RNA
Xu, Y. (2011) · Chemical Society Reviews · doi:10.1039/c0cs00134a · Cited by 326
miR-22 represses cancer progression by inducing cellular senescence
Xu, D., Takeshita, F., Hino, Y., Fukunaga, S., Kudo, Y., Tamaki, A., Matsunaga, J., Takahashi, R., Takata, T., Shimamoto, A., et al. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201010100 · Cited by 297
Telomere biology in healthy aging and disease
Oeseburg, H., de Boer, R. A., van Gilst, W. H., & van der Harst, P. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0728-1 · Cited by 279
Connecting obesity, aging and diabetes
Ahima, R. S. (2009) · Nature Medicine · doi:10.1038/nm0909-996 · Cited by 270
Cohesin acetylation speeds the replication fork
Terret, M., Sherwood, R., Rahman, S., Qin, J., & Jallepalli, P. V. (2009) · Nature · doi:10.1038/nature08550 · Cited by 258
The role of telomeres and telomerase in cirrhosis and liver cancer
Nault, J., Ningarhari, M., Rebouissou, S., & Zucman‐Rossi, J. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0165-3 · Cited by 255
The Rate of Increase of Short Telomeres Predicts Longevity in Mammals
Vera, E., de Jesus, B. B., Foronda, M., Flores, J. M., & Blasco, M. A. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.08.023 · Cited by 228
NKG2D-CAR T cells eliminate senescent cells in aged mice and nonhuman primates
Yang, D., Sun, B., Li, S., Wei, W., Liu, X., Cui, X., Zhang, X., Liu, N., Yan, L., Deng, Y., et al. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.add1951 · Cited by 217
Self-citationCusanelli, E., & Chartrand, P. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00143 · Cited by 219
Shariat, S. F., Milowsky, M. I., & Droller, M. J. (2009) · Urologic Oncology Seminars and Original Investigations · doi:10.1016/j.urolonc.2009.07.020 · Cited by 205
Multiple roles for MRE11 at uncapped telomeres
Deng, Y., Guo, X., Ferguson, D. O., & Chang, S. S. (2009) · Nature · doi:10.1038/nature08196 · Cited by 204
Self-citationRai, R., Zheng, H., He, H., Luo, Y., Multani, A. S., Carpenter, P. B., & Chang, S. S. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.142 · Cited by 200
Self-citationChen, J., Zhang, B., Wong, N., Lo, A. W. I., To, K., Chan, A. W. H., Ng, M. H. L., Ho, C. Y. S., Cheng, S.-H., Lai, P. B. S., et al. (2011) · Cancer Research · doi:10.1158/0008-5472.can-10-4274 · Cited by 191
Ageing, telomeres, senescence, and liver injury
Hoare, M., Das, T., & Alexander, G. (2010) · Journal of Hepatology · doi:10.1016/j.jhep.2010.06.009 · Cited by 184
Deng, Z., Wang, Z., Stong, N., Plasschaert, R. N., Moczan, A., Chen, H.-S., Hu, S., Wickramasinghe, P., Davuluri, R. V., Bartolomei, M. S., et al. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.266 · Cited by 174
Mice with hyper-long telomeres show less metabolic aging and longer lifespans
Muñoz-Lorente, M. A., Cano-Martin, A. C., & Blasco, M. A. (2019) · Nature Communications · doi:10.1038/s41467-019-12664-x · Cited by 184
Gu, P., Min, J., Wang, Y., Huang, C., Peng, T., Chai, W., & Chang, S. S. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.96 · Cited by 162
Self-citationRole of shelterin in cancer and aging
Martínez, P., & Blasco, M. A. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00596.x · Cited by 136
Molckovsky, A., & Siu, L. L. (2008) · Journal of Hematology & Oncology · doi:10.1186/1756-8722-1-20 · Cited by 161
Jia, L., Li, H., & Sun, Y. (2011) · Neoplasia · doi:10.1593/neo.11420 · Cited by 155
Exploring the multiple roles of guardian of the genome: P53
Feroz, W., & Sheikh, A. M. A. (2020) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-020-00089-x · Cited by 172
In Search of Adrenocortical Stem and Progenitor Cells
Kim, A. C., Barlaskar, F. M., Heaton, J. H., Else, T., Kelly, V. R., Krill, K. T., Scheys, J. O., Simon, D. P., Trovato, A., Yang, W., et al. (2009) · Endocrine Reviews · doi:10.1210/er.2008-0039 · Cited by 136
The diagnosis and treatment of dyskeratosis congenita: a review
Feldstein, J. T., & Garcia, S. F. (2014) · Journal of Blood Medicine · doi:10.2147/jbm.s47437 · Cited by 140
Role of the inflammation-autophagy-senescence integrative network in osteoarthritis
Vinatier, C., Domínguez, E., Guicheux, J., & Caramés, B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00706 · Cited by 135
Zhi-yin, S., Wang, X., Cheng, S.-Q., Su, X., & Ou, T. (2019) · Molecules · doi:10.3390/molecules24030396 · Cited by 142
New insights into p53 activation
Brooks, C. L., & Gu, W. (2010) · Cell Research · doi:10.1038/cr.2010.53 · Cited by 102
The cancer biology of whole-chromosome instability
Duijf, P. H. G., & Benezra, R. (2013) · Oncogene · doi:10.1038/onc.2012.616 · Cited by 125
TERRA-Reinforced Association of LSD1 with MRE11 Promotes Processing of Uncapped Telomeres
Porro, A., Feuerhahn, S., & Lingner, J. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.01.022 · Cited by 128
Jia, L., Soengas, M. S., & Sun, Y. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-4671 · Cited by 128
p53-Dependent Translational Control of Senescence and Transformation via 4E-BPs
Petroulakis, E., Parsyan, A. E., Dowling, R. J. O., Bacquer, O. L., Martineau, Y., Bidinosti, M., Larsson, O. S., Alain, T., Rong, L., Mamane, Y., et al. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.09.025 · Cited by 122
Lafferty‐Whyte, K., Cairney, C. J., Jamieson, N. B., Oien, K. A., & Keith, W. N. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.02.003 · Cited by 120
Roles and mechanisms of cellular senescence in regulation of tissue homeostasis
Ohtani, N., & Hara, E. (2013) · Cancer Science · doi:10.1111/cas.12118 · Cited by 122
Erratum: Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease
Mora, A. L., Rojas, M., Pardo, A., & Selman, M. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.225 · Cited by 122
Cellular senescence: Its role in tumor suppression and aging
Ohtani, N., Mann, D. J., & Hara, E. (2009) · Cancer Science · doi:10.1111/j.1349-7006.2009.01123.x · Cited by 119
The Genetic Basis of Natural Variation in Caenorhabditis elegans Telomere Length
Cook, D. E., Zdraljevic, S., Tanny, R. E., Seo, B., Riccardi, D., Noble, L. M., Rockman, M. V., Alkema, M. J., Braendle, C., Kammenga, J. E., et al. (2016) · Genetics · doi:10.1534/genetics.116.191148 · Cited by 112
Poly(ADP-ribose) polymerase enzymes and the maintenance of genome integrity
Eisemann, T., & Pascal, J. M. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03366-0 · Cited by 116
Beyond average: potential for measurement of short telomeres
Vera, E., & Blasco, M. A. (2012) · Aging · doi:10.18632/aging.100462 · Cited by 112
Lansdorp, P. M. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.172 · Cited by 109
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Maehara, K., Takahashi, K., & Saitoh, S. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01318-09 · Cited by 117
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Fujita, K., Horikawa, I., Mondal, A. M., Jenkins, L. M. M., Appella, E., Vojtěšek, B., Bourdon, J., Lane, D. P., & Harris, C. C. (2010) · Nature Cell Biology · doi:10.1038/ncb2123 · Cited by 111
Binet, R., Ythier, D., Robles, A. I., Collado, M., Larrieu, D., Fonti, C., Brambilla, E., Brambilla, C., Serrano, M., Harris, C. C., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1016 · Cited by 101
He, H., Wang, Y., Guo, X., Ramchandani, S., Ma, J., Shen, M., Garcia, D. A., Deng, Y., Multani, A. S., You, M. J., et al. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01400-08 · Cited by 103
Self-citationHypoxia and Senescence: The Impact of Oxygenation on Tumor Suppression
Welford, S. M., & Giaccia, A. J. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-11-0065 · Cited by 103
Zhou, G., Liu, X., Li, Y., Xu, S., Ma, C., Wu, X., Cheng, Y., Yu, Z., Zhao, G., & Chen, Y. (2016) · Oncotarget · doi:10.18632/oncotarget.7483 · Cited by 107
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Behl, T., Sharma, A., Sharma, L. K., Sehgal, A., Zengin, G., Brata, R. D., Frățilă, O., & BUNGAU, S. G. (2020) · Biomedicines · doi:10.3390/biomedicines8120571 · Cited by 100
Inflammation, Aging, and Cancer: Tumoricidal Versus Tumorigenesis of Immunity
Khatami, M. (2009) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-009-9059-2 · Cited by 100
TERT promoter mutations in primary liver tumors
Nault, J., & Zucman‐Rossi, J. (2015) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2015.07.006 · Cited by 104
Gray, R. D., Petraccone, L., Trent, J. O., & Chaires, J. B. (2009) · Biochemistry · doi:10.1021/bi901357r · Cited by 98
Cellular senescence in gastrointestinal diseases: from pathogenesis to therapeutics
Frey, N., Venturelli, S., Zender, L., & Bitzer, M. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.146 · Cited by 97
mTOR and Aging: An Old Fashioned Dress
Stallone, G., Infante, B., Prisciandaro, C., & Grandaliano, G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112774 · Cited by 97
Wei, D., & Sun, Y. (2010) · Genes & Cancer · doi:10.1177/1947601910382776 · Cited by 98
Restoration of senescent human diploid fibroblasts by modulation of the extracellular matrix
Choi, H. R., Cho, K. A., Kang, H. T., Lee, J. B., Kaeberlein, M., Suh, Y., Chung, I. K., & Park, S. C. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2010.00654.x · Cited by 84
The Telomeric Protein TRF2 Regulates Angiogenesis by Binding and Activating the PDGFRβ Promoter
Maï, M. E., Wagner, K., Michiels, J., Ambrosetti, D., Borderie, A., Destree, S., Renault, V. M., Djerbi, N., Giraud-Panis, M.-J. E., Gilson, É., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.09.038 · Cited by 89
Shorter telomeres precede population extinction in wild lizards
Dupoué, A., Rutschmann, A., Galliard, J. L., Clobert, J., Angelier, F., Marciau, C., Ruault, S., Miles, D. B., & Meylan, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-17323-z · Cited by 90
Using naturally occurring tumours in dogs and cats to study telomerase and cancer stem cell biology
Pang, L. Y., & Argyle, D. J. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.02.010 · Cited by 92
Telomere Maintenance as a Target for Drug Discovery
Sekaran, V. G., Soares, J., & Jarstfer, M. B. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm400528t · Cited by 94
Wong, L. S. M., Oeseburg, H., de Boer, R. A., van Gilst, W. H., van Veldhuisen, D. J., & van der Harst, P. (2008) · Cardiovascular Research · doi:10.1093/cvr/cvn337 · Cited by 88
Nicholls, C., Pinto, A. R., Li, H., Li, L., Wang, L., Simpson, R. J., & Liu, J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206672109 · Cited by 86
Senescence and immortality in hepatocellular carcinoma
Öztürk, M., Arslan-Ergül, A., Baǧışlar, S., Şentürk, Ş., & Yuzugullu, H. (2008) · Cancer Letters · doi:10.1016/j.canlet.2008.10.048 · Cited by 89
Cellular Senescence: The Trojan Horse in Chronic Lung Diseases
Hamsanathan, S., Alder, J. K., Sellarés, J., Rojas, M. M., Gurkar, A. U., & Mora, A. L. (2019) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2018-0410tr · Cited by 89
Telomere attrition and candidate gene mutations preceding monosomy 7 in aplastic anemia
Dumitriu, B., Feng, X., Townsley, D. M., Ueda, Y., Yoshizato, T., Calado, R. T., Yang, Y., Wakabayashi, Y., Kajigaya, S., Ogawa, S., et al. (2014) · Blood · doi:10.1182/blood-2014-10-607572 · Cited by 88
Building immunity to cancer with radiation therapy
Haikerwal, S. J., Hagekyriakou, J., MacManus, M. P., Martin, O. A., & Haynes, N. M. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.01.009 · Cited by 83
The ageing epigenome: Damaged beyond repair?
Sinclair, D. A., & Oberdoerffer, P. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.04.004 · Cited by 86
Bar, C., Huber, N., Beier, F., & Blasco, M. A. (2015) · Haematologica · doi:10.3324/haematol.2015.129239 · Cited by 81
Telomere capping in non‐dividing yeast cells requires Yku and Rap1
Vodenicharov, M. D., Laterreur, N., & Wellinger, R. J. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.155 · Cited by 87
Short-term gain, long-term pain: the senescence life cycle and cancer
Chan, A. S. L., & Narita, M. (2019) · Genes & Development · doi:10.1101/gad.320937.118 · Cited by 80
Beier, F., Foronda, M., Martinez, P., & Blasco, M. A. (2012) · Blood · doi:10.1182/blood-2012-03-418038 · Cited by 79
Rübe, C. E., Bäumert, C., Schuler, N., Isermann, A., Schmal, Z., Glanemann, M., Mann, C., & Scherthan, H. (2021) · npj Aging and Mechanisms of Disease · doi:10.1038/s41514-021-00060-z · Cited by 76
NEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis
Zhou, J., Chan, J., Lambelé, M., Yusufzai, T. M., Stumpff, J. K., Opresko, P. L., Thali, M., & Wallace, S. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.020 · Cited by 79
Epithelial cell senescence: an adaptive response to pre-carcinogenic stresses?
Abbadie, C., Pluquet, O., & Pourtier, A. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2587-9 · Cited by 77
Cellular senescence: a hitchhiker’s guide
Aravinthan, A. D. (2015) · Human Cell · doi:10.1007/s13577-015-0110-x · Cited by 83
Yu, S., Wang, X., Geng, P., Tang, X.-D., Xiang, L., Lu, X., Li, J., Ruan, Z., Chen, J., Xie, G., et al. (2017) · Journal of Pineal Research · doi:10.1111/jpi.12405 · Cited by 72
Dyrk2-associated EDD-DDB1-VprBP E3 Ligase Inhibits Telomerase by TERT Degradation
Jung, H., Wang, X., Jun, S., & Park, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.416792 · Cited by 72
Saha, D., Singh, A., Hussain, T., Srivastava, V. K., Sengupta, S., Kar, A., Dhapola, P., Dhople, V. M., Ummanni, R., & Chowdhury, S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.792077 · Cited by 71
Change in Peripheral Blood Leukocyte Telomere Length and Mortality in Breast Cancer Survivors
Duggan, C. R., Risques, R. A., Alfano, C. M., Prunkard, D. E., Imayama, I., Holte, S., Baumgartner, K. B., Baumgartner, R., Bernstein, L., Ballard-Barbash, R. R., et al. (2014) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/dju035 · Cited by 70
p21 Expression in Colon Cancer and Modifying Effects of Patient Age and Body Mass Index on Prognosis
Ogino, S., Nosho, K., Shima, K., Baba, Y., Irahara, N., Kirkner, G. J., Hazra, A., Vivo, I. D., Giovannucci, E. L., Meyerhardt, J. A., et al. (2009) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-09-0451 · Cited by 69
RECQL1 and WRN Proteins Are Potential Therapeutic Targets in Head and Neck Squamous Cell Carcinoma
Arai, A., Chano, T., Futami, K., Furuichi, Y., Ikebuchi, K., Inui, T., Tameno, H., Ochi, Y., Shimada, T., Hisa, Y., et al. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-0320 · Cited by 70
Breastfeeding effects on DNA methylation in the offspring: A systematic literature review
Hartwig, F. P., de Mola, C. L., Davies, N. M., Victora, C. G., & Relton, C. L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173070 · Cited by 69
Paulino, A. C., Constine, L. S., Rubin, P., & Williams, J. P. (2009) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2009.08.003 · Cited by 67
Li, Q., Du, J., Feng, R., Xu, Y., Wang, H., Sang, Q., Xing, Q., Zhao, X., Li, J., He, L., et al. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-3685 · Cited by 66
Varela, E., Muñoz-Lorente, M. A., Tejera, Á. M., Ortega, S., & Blasco, M. A. (2016) · Nature Communications · doi:10.1038/ncomms11739 · Cited by 72
Telomere Length Maintenance, Shortening, and Lengthening
Zhao, Z., Pan, X., Liu, L., & Liu, N. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24537 · Cited by 66
Macleod, K. F. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2504 · Cited by 68
Zaki, M. B., Abd‐Elmawla, M. A., Elimam, H., El-Din, H. G., Fawzy, A., Abulsoud, A. I., & Rizk, S. M. (2023) · Non-coding RNA Research · doi:10.1016/j.ncrna.2023.03.004 · Cited by 65
Mir‐23a induces telomere dysfunction and cellular senescence by inhibiting TRF 2 expression
Luo, Z., Feng, X., Wang, H., Xu, W., Zhao, Y. B., Ma, W., Jiang, S., Liu, D., Huang, J., & Songyang, Z. (2015) · Aging Cell · doi:10.1111/acel.12304 · Cited by 67
Short telomeres are preferentially elongated by telomerase in human cells
Britt‐Compton, B., Capper, R., Rowson, J., & Baird, D. M. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.08.029 · Cited by 64
Metadata
- Authors
- Deng, Y., Chan, S. S., & Chang, S.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Corresponding author
- Chang, Sandy
- Venue
- Nature Reviews Cancer
- Published
- 2008-06
- Volume
- 8
- Issue
- 6
- Pages
- 450-458
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- PMC
- PMC3688269
- OpenAlex
- W2036639619
- Semantic Scholar
- 75f734a34472ae400620f2bd295550ba3267f262
- Cited by
- 411
- References
- 98
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 9 · 2023: 9 · 2022: 11 · 2021: 16 · 2020: 13 · 2019: 22 · 2018: 18 · 2017: 28 · 2016: 18 · 2015: 31 · 2014: 22 · 2013: 31 · 2012: 30
- FWCI
- 4.85
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Abraham J. and Phyllis Katz Foundation
- National Institutes of Health
- National Institute on Aging (R01AG028888)
- National Cancer Institute (K01CA124461, R01CA129037)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- telomere dysfunction, replicative senescence, tumor suppression, apoptosis, DNA damage response, telomeres, carcinogenesis, stem cells
- MeSH terms
- Animals, DNA Damage, Humans, Neoplasms, Tumor Suppressor Protein p53, Retinoblastoma Protein, Telomere, Cellular Senescence, Apoptosis, Telomerase, Cyclin-Dependent Kinase Inhibitor p21
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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