Telomerase abrogation dramatically accelerates TRF2-induced epithelial carcinogenesis
Open accessAbstract
TRF2 is a telomere-binding protein with roles in telomere protection and telomere-length regulation. The fact that TRF2 is up-regulated in some human tumors suggests a role of TRF2 in cancer. Mice that overexpress TRF2 in the skin, K5TRF2 mice, show critically short telomeres and are susceptible to UV-induced carcinogenesis as a result of deregulated XPF/ERCC1 activity, a nuclease involved in UV damage repair. Here we demonstrate that, when in combination with telomerase deficiency, TRF2 acts as a very potent oncogene in vivo. In particular, we show that telomerase deficiency dramatically accelerates TRF2-induced epithelial carcinogenesis in K5TRF2/Terc−/− mice, coinciding with increased chromosomal instability and DNA damage. Telomere recombination is also increased in these mice, suggesting that TRF2 favors the activation of alternative telomere maintenance mechanisms. Together, these results demonstrate that TRF2 increased expression is a potent oncogenic event that along with telomerase deficiency accelerates carcinogenesis, coincidental with a derepression of telomere recombination. These results are of particular relevance given that TRF2 is up-regulated in some human cancers. Furthermore, these data suggest that telomerase inhibition might not be effective to cease the growth of TRF2-overexpressing tumors.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Mice with short telomeres are resistant to tumours, with a few exceptions, arguing that telomere shortening is a potent in vivo tumour suppressor mechanism.
“Conversely, mice with short telomeres are resistant-with a few exceptions-to tumours 73 , arguing that telomere shortening represents a potent in vivo tumour suppressor mechanism.”
From The common biology of cancer and ageing (2007) · cites this paper as [73]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
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 · see citing works
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 2,855 · cited 1× · see citing works
“…with several DNA repair factors, as well as DNA damage signaling proteins, most of which are involved in human chromosome instability syndromes characterized by premature aging and increased cancer (Li et al. 2000; Zhu et al. 2000, 2003; Opresko et al. 2002; Dantzer et al. 2004; Blasco 2005).”
BackgroundTelomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
Blasco, M. A., Lee, H.-W., Hande, M. P., Samper, E., Lansdorp, P. M., DePinho, R. A., & Greider, C. W. (1997) · Cell · doi:10.1016/s0092-8674(01)80006-4 · Cited by 2,108 · see citing works
Self-citationTRF2 Protects Human Telomeres from End-to-End Fusions
van Steensel, B., Smogorzewska, A., & de Lange, T. (1998) · Cell · doi:10.1016/s0092-8674(00)80932-0 · Cited by 1,709 · see citing works
Telomeres and human disease: ageing, cancer and beyond
Blasco, M. A. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1656 · Cited by 1,690 · see citing works
Self-citationDNA Damage Foci at Dysfunctional Telomeres
Takai, H., Smogorzewska, A., & de Lange, T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00542-6 · Cited by 1,409 · see citing works
Essential role of mouse telomerase in highly proliferative organs
Lee, H.-W., Blasco, M. A., Gottlieb, G. J., Horner, J. W., Greider, C. W., & DePinho, R. A. (1998) · Nature · doi:10.1038/33345 · Cited by 1,270 · see citing works
Self-citationMolecular mechanism of nucleotide excision repair
de Laat, W. L., Jaspers, N. G. J., & Hoeijmakers, J. H. J. (1999) · Genes & Development · doi:10.1101/gad.13.7.768 · Cited by 1,122 · see citing works
Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice
Artandi, S. E., Chang, S., Lee, S.-L., Alson, S., Gottlieb, G. J., Chin, L., & DePinho, R. A. (2000) · Nature · doi:10.1038/35020592 · Cited by 1,085 · see citing works
Chin, L., Artandi, S. E., Shen, Q., Tam, A., Lee, S.-L., Gottlieb, G. J., Greider, C. W., & DePinho, R. A. (1999) · Cell · doi:10.1016/s0092-8674(00)80762-x · Cited by 979 · see citing works
Protection of mammalian telomeres
de Lange, T. (2002) · Oncogene · doi:10.1038/sj.onc.1205080 · Cited by 942 · see citing works
Telomere maintenance by recombination in human cells
Dunham, M. A., Neumann, A. A., Fasching, C. L., & Reddel, R. R. (2000) · Nature Genetics · doi:10.1038/82586 · Cited by 879 · see citing works
Control of Human Telomere Length by TRF1 and TRF2
Smogorzewska, A., van Steensel, B., Bianchi, A., Oelmann, S., Schaefer, M. R., Schnapp, G., & de Lange, T. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.5.1659-1668.2000 · Cited by 768 · see citing works
DNA processing is not required for ATM-mediated telomere damage response after TRF2 deletion
Celli, G. B., & de Lange, T. (2005) · Nature Cell Biology · doi:10.1038/ncb1275 · Cited by 623 · see citing works
DNA methyltransferases control telomere length and telomere recombination in mammalian cells
Gonzalo, S., Jaco, I., Fraga, M. F., Chen, T., Li, E., Esteller, M., & Blasco, M. A. (2006) · Nature Cell Biology · doi:10.1038/ncb1386 · Cited by 604 · see citing works
Self-citationCell-cycle-regulated association of RAD50/MRE11/NBS1 with TRF2 and human telomeres
Zhu, X., Küster, B., Mann, M., Petrini, J. H. J., & de Lange, T. (2000) · Nature Genetics · doi:10.1038/77139 · Cited by 602 · see citing works
Li, B., Oestreich, S. C., & de Lange, T. (2000) · Cell · doi:10.1016/s0092-8674(00)80858-2 · Cited by 578 · see citing works
García‐Cao, M., O’Sullivan, R. J., Peters, A. H. F. M., Jenuwein, T., & Blasco, M. A. (2003) · Nature Genetics · doi:10.1038/ng1278 · Cited by 557 · see citing works
Self-citationActivation of the mouse cellular Harvey-ras gene in chemically induced benign skin papillomas
Balmain, A., Ramsden, M., Bowden, G. T., & Smith, J. (1984) · Nature · doi:10.1038/307658a0 · Cited by 529 · see citing works
Homologous Recombination Generates T-Loop-Sized Deletions at Human Telomeres
Wang, R. C., Smogorzewska, A., & de Lange, T. (2004) · Cell · doi:10.1016/j.cell.2004.10.011 · Cited by 507 · see citing works
Telomeres in the mouse have large inter-chromosomal variations in the number of T 2 AG 3 repeats
Zijlmans, J. M. J. M., Martens, U. M., Poon, S. S. S., Raap, A. K., Tanke, H. J., Ward, R. K., & Lansdorp, P. M. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.14.7423 · Cited by 501 · see citing works
Disease states associated with telomerase deficiency appear earlier in mice with short telomeres
Herrera, E., Samper, E., Martín‐Caballero, J., Flores, J. M., Lee, H., & Blasco, M. A. (1999) · The EMBO Journal · doi:10.1093/emboj/18.11.2950 · Cited by 471 · cited 8× · see citing works
“…a normal sensitivity of K5TRF2 cells to -irradiation (Muñoz et al. 2005), and suggest that increased tumorigenesis in G2 and G3 K5TRF2/Terc−/− mice is not likely to be initiated by cancellation of the ATM pathway as a consequence of TRF2 overexpression (Karlseder et al. 2004; Bradshaw et al. 2005).”
BackgroundInfluentialSelf-citationTelomerase therapeutics for cancer: challenges and new directions
Shay, J. W., & Wright, W. E. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd2081 · Cited by 434 · see citing works
Wu, L., Multani, A. S., He, H., Cosme-Blanco, W., Deng, Y., Deng, J. M., Bachilo, O., Pathak, S., Tahara, H., Bailey, S. M., et al. (2006) · Cell · doi:10.1016/j.cell.2006.05.037 · Cited by 422 · see citing works
Karlseder, J., Hoke, K., Mirzoeva, O. K., Bakkenist, C. J., Kastan, M. B., Petrini, J. H. J., & de Lange, T. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020240 · Cited by 393 · see citing works
Telomere-binding Protein TRF2 Binds to and Stimulates the Werner and Bloom Syndrome Helicases
Opresko, P. L., von Kobbe, C., Lainé, J., Harrigan, J. A., Hickson, I. D., & Bohr, V. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205396200 · Cited by 389 · see citing works
Zhu, X., Niedernhofer, L. J., Küster, B., Mann, M., Hoeijmakers, J. H. J., & de Lange, T. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00478-7 · Cited by 382 · see citing works
González‐Suárez, E., Samper, E., Ramírez, A., Flores, J. M., Martín‐Caballero, J., Jorcano, J. L., & Blasco, M. A. (2001) · The EMBO Journal · doi:10.1093/emboj/20.11.2619 · Cited by 372 · see citing works
Self-citationShort Dysfunctional Telomeres Impair Tumorigenesis in the INK4aΔ2/3 Cancer-Prone Mouse
Greenberg, R. A., Chin, L., Femino, A., Lee, K.-H., Gottlieb, G. J., Singer, R. H., Greider, C. W., & DePinho, R. A. (1999) · Cell · doi:10.1016/s0092-8674(00)80761-8 · Cited by 367 · cited 1× · see citing works
“…activity show premature loss of organismal viability when their telomeres become critically short and are resistant to cancer (Lee et al. 1998; Greenberg et al. 1999; Herrera et al. 1999; González-Suárez et al. 2000), with the only exception of p53-deficient genetic backgrounds (Chin et al.…”
Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesis
González-Suárez, E., Samper, E., Flores, J. M., & Blasco, M. A. (2000) · Nature Genetics · doi:10.1038/79089 · Cited by 347 · see citing works
Self-citationSamper, E., Goytisolo, F. A., Slijepčević, P., van Buul, P. P. W., & Blasco, M. A. (2000) · EMBO Reports · doi:10.1093/embo-reports/kvd051 · Cited by 317 · see citing works
Self-citationNew ways not to make ends meet: telomerase, DNA damage proteins and heterochromatin
Chan, S. W.-L., & Blackburn, E. H. (2002) · Oncogene · doi:10.1038/sj.onc.1205082 · Cited by 304 · see citing works
Murillas, R., Larcher, F., Conti, C. J., Santos, M., Ullrich, A., & Jorcano, J. L. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00206.x · Cited by 250 · see citing works
Nucleotide excision repair: From E. coli to man
Petit, C. R., & Sancar, A. (1999) · Biochimie · doi:10.1016/s0300-9084(99)80034-0 · Cited by 230 · see citing works
The first molecular details of ALT in human tumor cells
Muntoni, A., & Reddel, R. R. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi266 · Cited by 226 · see citing works
Muñoz, P., Blanco, R., Flores, J. M., & Blasco, M. A. (2005) · Nature Genetics · doi:10.1038/ng1633 · Cited by 224 · see citing works
Self-citationBradshaw, P. S., Stavropoulos, D. J., & Meyn, M. S. (2005) · Nature Genetics · doi:10.1038/ng1506 · Cited by 213 · see citing works
Bailey, S. M. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh691 · Cited by 213 · see citing works
Laud, P. R., Multani, A. S., Bailey, S. M., Wu, L., Ma, J., Kingsley, C., Lebel, M., Pathak, S., DePinho, R. A., & Chang, S. (2005) · Genes & Development · doi:10.1101/gad.1321305 · Cited by 190 · see citing works
Dantzer, F., Giraud-Panis, M.-J. E., Jaco, I., Amé, J., Schultz, I., Blasco, M. A., Koering, C.-E., Gilson, É., Murcia, J. M., de MURCIA, G., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.4.1595-1607.2004 · Cited by 185 · see citing works
Self-citationBechter, O. E., Zou, Y. S., Walker, W., Wright, W. E., & Shay, J. W. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-0323 · Cited by 184 · see citing works
[1] Isolation and utilization of epidermal keratinocytes for oncogene research
Dlugosz, A. A., Glick, A. B., Tennenbaum, T., Weinberg, W. C., & Yuspa, S. H. (1995) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(95)54003-2 · Cited by 157 · see citing works
Oh, B.-K., Kim, Y., Park, C., & Park, Y. N. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)62233-x · Cited by 148 · see citing works
DNA repair: Spot(light)s on chromatin
Modesti, M., & Kanaar, R. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00112-9 · Cited by 130 · see citing works
Evolving views of telomerase and cancer
Blasco, M. (2003) · Trends in Cell Biology · doi:10.1016/s0962-8924(03)00085-0 · Cited by 123 · see citing works
Self-citationIncreased p53 activity does not accelerate telomere‐driven ageing
García‐Cao, I., García‐Cao, M., Tomás‐Loba, A., Martin‐Caballero, J., Flores, J. M., Klatt, P., Blasco, M. A., & Serrano, M. (2006) · The EMBO Reports · doi:10.1038/sj.embor.7400667 · Cited by 102 · cited 3× · see citing works
“The fact that K5TRF2 mice show increased cancer in spite of having critically short telomeres is in marked contrast to telomerase-deficient mice with short telomeres, which are resistant to skin carcinogenic treatments (González-Suárez et al. 2000).”
BackgroundSelf-citationTTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease
Garcia-Barceló, M., Ganster, R. W., Lui, V. C. H., Leon, T. Y. Y., So, M., Lau, A. M.-F., Fu, M., Sham, M. H., Knight, J., Zannini, M., et al. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddi015 · Cited by 101 · see citing works
González‐Suárez, E., Flores, J. M., & Blasco, M. A. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.20.7291-7301.2002 · Cited by 94 · see citing works
Self-citationMany ways to telomere dysfunction: in vivo studies using mouse models
Goytisolo, F. A., & Blasco, M. A. (2002) · Oncogene · doi:10.1038/sj.onc.1205085 · Cited by 94 · see citing works
Self-citationMatsutani, N., Yokozaki, H., Tahara, E., Tahara, H., Kuniyasu, H., Haruma, K., Chayama, K., Yasui, W., & Tahara, E. (2001) · International Journal of Oncology · doi:10.3892/ijo.19.3.507 · Cited by 82 · see citing works
TRF2 inhibition triggers apoptosis and reduces tumourigenicity of human melanoma cells
Biroccio, A., Rizzo, A., Elli, R., Koering, C.-E., Belleville, A., Benassi, B., Leonetti, C., Stevens, M. F. G., D’Incalci, M., Zupi, G., et al. (2006) · European Journal of Cancer · doi:10.1016/j.ejca.2006.03.010 · Cited by 67 · see citing works
Role of the TRF2 Telomeric Protein in Cancer and Aging
Muñoz, P., Blanco, R., & Blasco, M. A. (2006) · Cell Cycle · doi:10.4161/cc.5.7.2636 · Cited by 65 · see citing works
Self-citation
Flagged first, then by citations
1 of the 53 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Zijlmans, J.M., Martens, U.M., Poon, S.S., Raap, A.K., Tanke, H.J., Ward, R.K., and Lansdorp, P.M. 1997. Telomeres in the mouse have large inter-chromosomal variations in the num- ber of T2AG3 repeats. Proc. Natl. Acad. Sci. 94: 7423-7428.
Cited by
Sorted by citations
Cellular senescence in cancer and aging.
Collado, M., Blasco, M. A., & Serrano, M. (2007) · Cell · doi:10.1016/j.cell.2007.07.003 · Cited by 1,708 · see citing works
Self-citationTelomeres: protecting chromosomes against genome instability
O’Sullivan, R. J., & Karlseder, J. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2848 · Cited by 994 · see citing works
Mammalian Telomeres Resemble Fragile Sites and Require TRF1 for Efficient Replication
Sfeir, A., Kosiyatrakul, S. T., Hockemeyer, D., MacRae, S. L., Karlseder, J., Schildkraut, C. L., & de Lange, T. (2009) · Cell · doi:10.1016/j.cell.2009.06.021 · Cited by 990 · see citing works
The common biology of cancer and ageing
Finkel, T., Serrano, M., & Blasco, M. A. (2007) · Nature · doi:10.1038/nature05985 · Cited by 988 · see citing works
Self-citationTelomere length, stem cells and aging
Blasco, M. A. (2007) · Nature Chemical Biology · doi:10.1038/nchembio.2007.38 · Cited by 747 · see citing works
Self-citationThe epigenetic regulation of mammalian telomeres
Blasco, M. A. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2047 · Cited by 668 · see citing works
Self-citationTargeting telomeres and telomerase
Cian, A. D., Lacroix, L., Douarre, C., Temime‐Smaali, N., Trentesaux, C., Riou, J., & Mergny, J. (2007) · Biochimie · doi:10.1016/j.biochi.2007.07.011 · Cited by 571 · see citing works
Telomeric and extra-telomeric roles for telomerase and the telomere-binding proteins
Martínez, P., & Blasco, M. A. (2011) · Nature reviews. Cancer · doi:10.1038/nrc3025 · Cited by 530 · see citing works
Self-citationTelomere dysfunction and tumour suppression: the senescence connection
Deng, Y., Chan, S. S., & Chang, S. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2393 · Cited by 411 · see citing works
Martínez, P., Thanasoula, M., Muñoz, P., Liao, C., Tejera, Á. M., McNees, C. J., Flores, J. M., Fernández-Capetillo, Ó., Tarsounas, M., & Blasco, M. A. (2009) · Genes & Development · doi:10.1101/gad.543509 · Cited by 367 · see citing works
Self-citationSerrano, L., Martínez‐Redondo, P., Marazuela-Duque, A., Vázquez, B. N., Dooley, S., Voigt, P., Beck, D. B., Kane‐Goldsmith, N., Tong, Q., Rabanal, R. M., et al. (2013) · Genes & Development · doi:10.1101/gad.211342.112 · Cited by 282 · see citing works
Self-citationMartínez, P., Thanasoula, M., Carlos, A. R., Goméz-López, G., Tejera, Á. M., Schoeftner, S., Domı́nguez, O., Pisano, D. G., Tarsounas, M., & Blasco, M. A. (2010) · Nature Cell Biology · doi:10.1038/ncb2081 · Cited by 257 · see citing works
Self-citationSIRT1 contributes to telomere maintenance and augments global homologous recombination
Palacios, J., Herranz, D., Bonis, M. L. D., Velasco, S., Serrano, M., & Blasco, M. A. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201005160 · Cited by 254 · see citing works
Self-citationTelomere Dynamics in Mice and Humans
Calado, R. T., & Dumitriu, B. (2013) · Seminars in Hematology · doi:10.1053/j.seminhematol.2013.03.030 · Cited by 214 · see citing works
Assessing cell and organ senescence biomarkers
de Jesus, B. B., & Blasco, M. A. (2012) · Circulation Research · doi:10.1161/circresaha.111.247866 · Cited by 187 · see citing works
Self-citationCancer and ageing: convergent and divergent mechanisms
Serrano, M., & Blasco, M. A. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2242 · Cited by 182 · see citing works
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 162 · see citing works
Self-citationBRCA2 acts as a RAD51 loader to facilitate telomere replication and capping
Badie, S., Escandell, J. M., Bouwman, P., Carlos, A. R., Thanasoula, M., Gallardo, M. M., Suram, A., Jaco, I., Benitez, J. J., Herbig, U., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1943 · Cited by 164 · see citing works
Self-citationTejera, Á. M., d’Alcontres, M. S., Thanasoula, M., Marión, R. M., Martínez, P., Liao, C., Flores, J. M., Tarsounas, M., & Blasco, M. A. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.03.011 · Cited by 144 · see citing works
Self-citationDAMPs, ageing, and cancer: The ‘DAMP Hypothesis’
Huang, J., Xie, Y., Sun, X., Zeh, H. J., Kang, R., Lotze, M. T., & Tang, D. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2014.10.004 · Cited by 144 · see citing works
Radiation damage and radioprotectants: new concepts in the era of molecular medicine
Koukourakis, M. I. (2012) · British Journal of Radiology · doi:10.1259/bjr/16386034 · Cited by 142 · see citing works
TRF2 inhibits a cell-extrinsic pathway through which natural killer cells eliminate cancer cells
Biroccio, A., Cherfils‐Vicini, J., Augereau, A., Pinte, S., Bauwens, S., Ye, J., Simonet, T., Horard, B., Jamet, K., Cervera, L., et al. (2013) · Nature Cell Biology · doi:10.1038/ncb2774 · Cited by 136 · see citing works
Causes and consequences of nuclear envelope alterations in tumour progression
Bell, E. S., & Lammerding, J. (2016) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2016.06.007 · Cited by 110 · see citing works
Telomeres in aging and disease: lessons from zebrafish
Carneiro, M. C., de Castro, I. P., & Ferreira, M. G. (2016) · Disease Models & Mechanisms · doi:10.1242/dmm.025130 · Cited by 105 · see citing works
Telomere instability and cancer
Londoño‐Vallejo, A. (2007) · Biochimie · doi:10.1016/j.biochi.2007.07.009 · Cited by 97 · see citing works
Telomerase and drug resistance in cancer
Lipińska, N., Romaniuk-Drapała, A., Paszel-Jaworska, A., Totoń, E., Kopczyński, P., & Rubiś, B. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2573-2 · Cited by 99 · see citing works
TRF1 Controls Telomere Length and Mitotic Fidelity in Epithelial Homeostasis
Muñoz, P., Blanco, R., de Cárcer, G., Schoeftner, S., Benetti, R., Flores, J. M., Malumbres, M., & Blasco, M. A. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01339-08 · Cited by 89 · see citing works
Self-citationThe 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 · see citing works
Shelterin Complex at Telomeres: Implications in Ageing
Mir, S. M., Tehrani, S. S., Goodarzi, G., Jamalpoor, Z., Asadi, J., Khelghati, N., Qujeq, D., & Maniati, M. (2020) · Clinical Interventions in Aging · doi:10.2147/cia.s256425 · Cited by 93 · see citing works
Frías-López, C., García-Aranda, C., de Juan, C., Morán, A., Ortega, P., Gómez, A., Hernándo, F., López-Asenjo, J. A., Torres, A.-J., Benito, M., et al. (2008) · Lung Cancer · doi:10.1016/j.lungcan.2007.11.001 · Cited by 82 · see citing works
Telomere regulation and function during meiosis
Siderakis, M., & Tarsounas, M. (2007) · Chromosome Research · doi:10.1007/s10577-007-1149-7 · Cited by 74 · see citing works
Hussain, T., Saha, D., Purohit, G., Kar, A., Mukherjee, A. K., Sharma, S., Sengupta, S., Dhapola, P., Maji, B., Sreekanth, V., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-11177-1 · Cited by 70 · see citing works
Varela, E., Muñoz-Lorente, M. A., Tejera, Á. M., Ortega, S., & Blasco, M. A. (2016) · Nature Communications · doi:10.1038/ncomms11739 · Cited by 67 · see citing works
Self-citationSurace, C., Piazzolla, S., Sirleto, P., Digilio, M., Roberti, M. C., Lombardo, A., D’Elia, G., Tomaiuolo, A. C., Petrocchi, S., Capolino, R., et al. (2009) · Clinical Genetics · doi:10.1111/j.1399-0004.2009.01203.x · Cited by 63 · see citing works
The shelterin complex and hematopoiesis
Jones, M., Bisht, K. K., Savage, S. A., Nandakumar, J., Keegan, C. E., & Maillard, I. P. (2016) · Journal of Clinical Investigation · doi:10.1172/jci84547 · Cited by 61 · see citing works
Zizza, P., Dinami, R., Porru, M., Cingolani, C., Salvati, E., Rizzo, A., D’Angelo, C., Petti, E., Amoreo, C. A., Mottolese, M., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz041 · Cited by 56 · see citing works
Human XPF controls TRF2 and telomere length maintenance through distinctive mechanisms
Wu, Y., Mitchell, T. R. H., & Zhu, X. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.08.004 · Cited by 58 · see citing works
New Insights into the Role of Epithelial–Mesenchymal Transition during Aging
Santos, F. D. S., Moreira, C., Pereira, S. N., & de Jesus, B. B. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040891 · Cited by 57 · see citing works
Telomere shortening relaxes X chromosome inactivation and forces global transcriptome alterations
Schoeftner, S., Blanco, R., de Silanes, I. L., Muñoz, P., Goméz-López, G., Flores, J. M., & Blasco, M. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909265106 · Cited by 57 · see citing works
Self-citationMiR-103 regulates hepatocellular carcinoma growth by targeting AKAP12
Xia, W., Ni, J., Zhuang, J., Qian, L., Wang, P., & Wang, J. (2015) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2015.11.017 · Cited by 56 · see citing works
da Silva-Diz, V., Solé‐Sánchez, S., Valdés, A., Urpí, M., Riba-Artés, D., Penin, R. M., Pascual, G., González‐Suárez, E., Casanovas, O., Viñals, F., et al. (2012) · Oncogene · doi:10.1038/onc.2012.375 · Cited by 54 · see citing works
Self-citationLack of TRF2 in ALT cells causes PML-dependent p53 activation and loss of telomeric DNA
d’Alcontres, M. S., Méndez-Bermúdez, A., Foxon, J. L., Royle, N. J., & Salomoni, P. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200703020 · Cited by 51 · see citing works
Siegl‐Cachedenier, I., Muñoz, P., Flores, J. M., Klatt, P., & Blasco, M. A. (2007) · Genes & Development · doi:10.1101/gad.430107 · Cited by 50 · see citing works
Self-citationAugereau, A., de Roodenbeke, C. T., Simonet, T., Bauwens, S., Horard, B., Callanan, M. B., Leroux, D., Jallades, L., Salles, G., Gilson, É., et al. (2011) · Blood · doi:10.1182/blood-2010-07-295774 · Cited by 49 · see citing works
MiR‐182‐3p targets TRF2 and impairs tumor growth of triple‐negative breast cancer
Dinami, R., Pompili, L., Petti, E., Porru, M., D’Angelo, C., Vito, S. D., Rizzo, A., Campani, V., Rosa, G. D., Bruna, A., et al. (2022) · EMBO Molecular Medicine · doi:10.15252/emmm.202216033 · Cited by 48 · see citing works
Martínez, P., Goméz-López, G., Pisano, D. G., Flores, J. M., & Blasco, M. A. (2016) · Aging Cell · doi:10.1111/acel.12517 · Cited by 47 · see citing works
Self-citationThe Shelterin Protein TRF2 Inhibits Chk2 Activity at Telomeres in the Absence of DNA Damage
Buscemi, G., Zannini, L., Fontanella, E., Lecis, D., Lisanti, S., & Delia, D. (2009) · Current Biology · doi:10.1016/j.cub.2009.03.064 · Cited by 47 · see citing works
Molecular targeting of TRF2 suppresses the growth and tumorigenesis of glioblastoma stem cells
Bai, Y., Lathia, J. D., Zhang, P., Flavahan, W. A., Rich, J. N., & Mattson, M. P. (2014) · Glia · doi:10.1002/glia.22708 · Cited by 46 · see citing works
Elevated TRF2 in advanced breast cancers with short telomeres
Diehl, M. C., Idowu, M. O., Kimmelshue, K. N., York, T. P., Jackson‐Cook, C. K., Turner, K. C., Holt, S. E., & Elmore, L. W. (2010) · Breast Cancer Research and Treatment · doi:10.1007/s10549-010-0988-7 · Cited by 41 · see citing works
Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients
Joksić, I., Vujić, D., Guć‐Šćekić, M., Leskovac, A. R., Petrović, S. Ž., Ojani, M., Trujillo‐Quintero, J. P., Surrallés, J., Živković, M., Stanković, A., et al. (2012) · Genome Integrity · doi:10.1186/2041-9414-3-6 · Cited by 40 · see citing works
MSH2 deficiency abolishes the anticancer and pro‐aging activity of short telomeres
Martínez, P., Siegl‐Cachedenier, I., Flores, J. M., & Blasco, M. A. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00441.x · Cited by 39 · see citing works
Self-citationTargeting DNA binding proteins for cancer therapy
Shiroma, Y., Takahashi, R.-U., Yamamoto, Y., & Tahara, H. (2020) · Cancer Science · doi:10.1111/cas.14355 · Cited by 34 · see citing works
Telomere Length and Telomerase Activity Impact the UV Sensitivity Syndrome Xeroderma Pigmentosum C
Stout, G. J., & Blasco, M. A. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-3125 · Cited by 35 · see citing works
Self-citationZhang, P., Potts, R. C., Precht, P., Jiang, H., Liu, Y., Pazin, M. J., & Mattson, M. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106906108 · Cited by 36 · see citing works
Fan, H., Chang, F.-W., Tsai, J., Lin, K., Chen, C., Lin, S., Liu, C.-A., & Harn, H. (2021) · Life · doi:10.3390/life11121405 · Cited by 37 · see citing works
Squelching Glioblastoma Stem Cells by Targeting REST for Proteasomal Degradation
Zhang, P.-S., Lathia, J., Flavahan, W. A., Rich, J., & Mattson, M. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.07.005 · Cited by 34 · see citing works
Low oxygen delays fibroblast senescence despite shorter telomeres
Betts, D. H., Perrault, S. D., & King, W. A. (2007) · Biogerontology · doi:10.1007/s10522-007-9113-7 · Cited by 34 · see citing works
Dong, W., Shen, R., Wang, Q., Gao, Y., Qi, X., Jiang, H., Yao, J., Lin, X., Wu, Y., & Wang, L. (2009) · Cancer Biology & Therapy · doi:10.4161/cbt.8.22.9880 · Cited by 34 · see citing works
Shading the TRF2 Recruiting Function: A New Horizon in Drug Development
Maro, S. D., Zizza, P., Salvati, E., Luca, V. D., Capasso, C., Fotticchia, I., Pagano, B., Marinelli, L., Gilson, É., Novellino, E., et al. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5080773 · Cited by 33 · see citing works
Telomeric impact of conventional chemotherapy
Lu, Y., Leong, W., Guérin, O., Gilson, É., & Ye, J. (2013) · Frontiers of Medicine · doi:10.1007/s11684-013-0293-z · Cited by 32 · see citing works
ERK1/2/MAPK pathway-dependent regulation of the telomeric factor TRF2
Picco, V., Coste, I., Giraud-Panis, M.-J. E., Renno, T., Gilson, É., & Pagès, G. (2016) · Oncotarget · doi:10.18632/oncotarget.10316 · Cited by 31 · see citing works
Age-Related Changes in Subtelomeric Methylation in the Normal Japanese Population
Maeda, T., Guan, J. Z., Oyama, J.-I., Higuchi, Y., & Makino, N. (2009) · The Journals of Gerontology Series A · doi:10.1093/gerona/gln057 · Cited by 28 · see citing works
da Silva-Diz, V., Simón-Extremera, P., Bernat‐Peguera, A., de Sostoa, J., Urpí, M., Penin, R. M., Sidelnikova, D. P., Bermejo, O., Viñals, J. M., Rodolosse, A., et al. (2016) · Cancer Research · doi:10.1158/0008-5472.can-15-1631 · Cited by 28 · see citing works
Self-citationIncreased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice
Parra, D., Manils, J., Castellana, B., Viña‐Vilaseca, A., Morán‐Salvador, E., Vázquez‐Villoldo, N., Tarancón, G., Borràs, M., Sancho, S., Benito, C., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1208 · Cited by 27 · see citing works
Marión, R. M., Schotta, G., Ortega, S., & Blasco, M. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025680 · Cited by 26 · see citing works
Self-citationDefending the end zone: Studying the players involved in protecting chromosome ends
Chan, S., & Chang, S. S. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.06.016 · Cited by 26 · see citing works
Güneş, Ç., Avila, A. I., & Rudolph, K. L. (2017) · Differentiation · doi:10.1016/j.diff.2017.12.004 · Cited by 26 · see citing works
Wang, Z., & Wu, X. (2021) · Oncology Reports · doi:10.3892/or.2021.8135 · Cited by 23 · see citing works
Low-level infrared laser modulates muscle repair and chromosome stabilization genes in myoblasts
Trajano, L. A. D. S. N., Stumbo, A. C., da Silva, C. L., Mencalha, A. L., & da Fonseca, A. D. S. (2016) · Lasers in Medical Science · doi:10.1007/s10103-016-1956-1 · Cited by 22 · see citing works
Jaskelioff, M., Song, W., Xia, J., Liu, C., Kramer, J., Koido, S., Gendler, S. J., Calderwood, S. K., & Gong, J. (2009) · Oncogene · doi:10.1038/onc.2009.268 · Cited by 21 · see citing works
TRF2 cooperates with CTCF for controlling the oncomiR-193b-3p in colorectal cancer
Dinami, R., Petti, E., Porru, M., Rizzo, A., Ganci, F., Sacconi, A., Ostano, P., Chiorino, G., Trusolino, L., Blandino, G., et al. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.215607 · Cited by 21 · see citing works
The telomere proteins in tumorigenesis and clinical outcomes of oral squamous cell carcinoma
Benhamou, Y., Picco, V., & Pagès, G. (2016) · Oral Oncology · doi:10.1016/j.oraloncology.2016.04.006 · Cited by 21 · see citing works
Stout, G. J., & Blasco, M. A. (2009) · Disease Models & Mechanisms · doi:10.1242/dmm.002121 · Cited by 21 · see citing works
Self-citationMaeda, T., Oyama, J., Sasaki, M., Arima, T., & Makino, N. (2010) · The journal of nutrition health & aging · doi:10.1007/s12603-010-0137-3 · Cited by 19 · see citing works
Ponsot, E., Echaniz‐Laguna, A., Delis, A. M., & Kadi, F. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2011.063818 · Cited by 19 · see citing works
PinX1: a sought-after major tumor suppressor at human chromosome 8p23
Zhou, X. Z. (2011) · Oncotarget · doi:10.18632/oncotarget.339 · Cited by 18 · see citing works
Metabolic Alterations at the Crossroad of Aging and Oncogenesis
Raffaghello, L., & Longo, V. D. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.01.003 · Cited by 18 · see citing works
Retraction: Human telomeric G‐quadruplex: targeting with small molecules
Arora, A., Kumar, N., Agarwal, T., & Maiti, S. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07461.x · Cited by 18 · see citing works
RetractedUpregulation and CpG Island Hypomethylation of the TRF2 Gene in Human Gastric Cancer
Dong, W., Wang, L., Chen, X., Sun, P.-H., & Wu, Y. (2009) · Digestive Diseases and Sciences · doi:10.1007/s10620-009-0810-8 · Cited by 17 · see citing works
Dynamics of telomeric chromatin at the crossroads of aging and cancer
Ye, J., Wu, Y., & Gilson, É. (2010) · Essays in Biochemistry · doi:10.1042/bse0480147 · Cited by 15 · see citing works
Interactions of TRF2 with model telomeric ends
Khan, S. J., Yanez, G., Seldeen, K. L., Wang, H., Lindsay, S. M., & Fletcher, T. M. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.08.122 · Cited by 16 · see citing works
The long and the short of TRF2 in neurogenesis
Grammatikakis, I., Zhang, P., Mattson, M. P., & Gorospe, M. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1222339 · Cited by 16 · see citing works
Gemcitabine causes telomere attrition by stabilizing TRF2
Su, C.-H., Chu, W.-C., Lan, K., Li, C., Chao, Y., Lin, H.-C., Lee, S., Tsai, Y.-C., & Lee, W. (2012) · European Journal of Cancer · doi:10.1016/j.ejca.2012.04.015 · Cited by 14 · see citing works
Chen, L., Zhu, X., Zou, Y., Xing, J., Gilson, É., Lu, Y., & Ye, J. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00321.2014 · Cited by 13 · see citing works
Bojović, B., Ho, H.-Y., Wu, J., & Crowe, D. L. (2012) · Oncogene · doi:10.1038/onc.2012.555 · Cited by 12 · see citing works
Altered telomere homeostasis and resistance to skin carcinogenesis in Suv39h1 transgenic mice
Petti, E., Jordi, F., Buemi, V., Dinami, R., Benetti, R., Blasco, M. A., & Schoeftner, S. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1021517 · Cited by 11 · see citing works
Self-citationLagunas, A. M., Wu, J., & Crowe, D. L. (2017) · Oncotarget · doi:10.18632/oncotarget.20960 · Cited by 11 · see citing works
Mouse models in modeling aging and cancer
Li, H., Wei, C., Zhou, R., Wang, B., Zhang, Y., Shao, C., & Luo, Y. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.03.002 · Cited by 11 · see citing works
Sherin, D. R., Manojkumar, T. K., Prakash, R. C., & Sobha, V. N. (2020) · Materials Today Proceedings · doi:10.1016/j.matpr.2020.10.675 · Cited by 10 · see citing works
Chronic Obstructive Pulmonary Disease: From Injury to Genomic Stability
Sergio, L. P. D. S., de Paoli, F., Mencalha, A. L., & da Fonseca, A. D. S. (2017) · COPD Journal of Chronic Obstructive Pulmonary Disease · doi:10.1080/15412555.2017.1332025 · Cited by 9 · see citing works
Super-telomeres in transformed human fibroblasts
Chiodi, I., Belgiovine, C., Zongaro, S., Ricotti, R., Horard, B., Lossani, A., Focher, F., Gilson, É., Giulotto, E., & Mondello, C. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.03.030 · Cited by 9 · see citing works
de Castro, A., Minty, F., Hattinger, E., Wolf, R., & Parkinson, E. K. (2014) · Longevity & Healthspan · doi:10.1186/2046-2395-3-8 · Cited by 9 · see citing works
Maeda, T., Oyama, J., Higuchi, Y., Nishiyama, Y., Kudo, Y., Yamori, T., Nakazono, T., Arima, T., Mimori, K., & Makino, N. (2010) · Gerontology · doi:10.1159/000314633 · Cited by 9 · see citing works
Begemann, S., Galimi, F., & Karlseder, J. (2009) · Aging · doi:10.18632/aging.100015 · Cited by 9 · see citing works
Lu, Y., Wei, B., Zhang, T., Chen, Z., & Ye, J. (2013) · Protein & Cell · doi:10.1007/s13238-013-3002-4 · Cited by 8 · see citing works
Maeda, T., Oyama, J., Higuchi, Y., Koyanagi, M., Sasaki, M., Arima, T., Mimori, K., & Makino, N. (2010) · The Aging Male · doi:10.3109/13685538.2010.502270 · Cited by 8 · see citing works
Sameni, S., Viswanathan, R., Ng, G. Y.-Q., Martínez-López, W., & Hande, M. P. (2023) · Genome Integrity · doi:10.14293/genint.14.1.003 · Cited by 6 · see citing works
Ng, Y. B., & Akıncılar, S. C. (2024) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2024.102460 · Cited by 6 · see citing works
Maeda, T., Oyama, J., Higuchi, Y., Arima, T., Mimori, K., & Makino, N. (2010) · The journal of nutrition health & aging · doi:10.1007/s12603-010-0136-4 · Cited by 6 · see citing works
Sergio, L. P. S., Lucinda, L. M. F., Reboredo, M. M., de Paoli, F., da Fonseca, L. M. C., Pinheiro, B. V., Mencalha, A. L., & da Fonseca, A. D. S. (2018) · Experimental Lung Research · doi:10.1080/01902148.2017.1422158 · Cited by 6 · see citing works
- Authors
- Blanco, R., Muñoz, P., Flores, J. M., Klatt, P., & Blasco, M. A.
- Affiliations
- Spanish National Cancer Research Centre (ES)
- Universidad Complutense de Madrid (ES)
- ORCID
- Flores, Juana M.
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2007-01-15
- Volume
- 21
- Issue
- 2
- Pages
- 206-220
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC1770903
- OpenAlex
- W2049151391
- Cited by
- 135
- References
- 53
- Citations by year
- 2025: 3 · 2024: 2 · 2023: 5 · 2022: 4 · 2021: 2 · 2020: 4 · 2019: 3 · 2018: 2 · 2017: 7 · 2016: 10 · 2015: 5 · 2014: 9 · 2013: 8 · 2012: 10
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › 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
- TRF2, telomerase deficiency, telomere-binding proteins, epithelial carcinogenesis, oncogenes, chromosomal instability, telomere recombination, UV-induced carcinogenesis, telomere length, DNA damage, telomerase inhibition
- MeSH terms
- Animals, Animals, Newborn, Disease Models, Animal, DNA Damage, Recombination, Genetic, Skin, Skin Neoplasms, Specific Pathogen-Free Organisms, Ultraviolet Rays, 9,10-Dimethyl-1,2-benzanthracene, Keratinocytes, Telomere, Telomerase, Telomeric Repeat Binding Protein 2, Chromosomal Instability, Mice, Keratin-5, Keratin-15
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review