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Published in: Clinical and Translational Oncology 4/2017

01-04-2017 | Review Article

Telomeres and telomerase in the clinical management of colorectal cancer

Authors: C. Piñol-Felis, T. Fernández-Marcelo, J. Viñas-Salas, C. Valls-Bautista

Published in: Clinical and Translational Oncology | Issue 4/2017

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Abstract

Colorectal cancer (CRC) is the third most common cancer worldwide. Our aim is to describe the state of the art about the role of telomeres and telomerase in the clinical management of CRC and its potential utility as prognostic and diagnostic biomarkers and targets of new treatments. Telomere length could be a new diagnostic marker as an anomalous behavior is observed in peripheral blood cells when CRC patients and healthy people are compared. Moreover, telomeres and telomerase may be used as diagnostic markers considering that universal changes appear along the CRC process. Currently, new therapeutic cancer approaches are focused on inhibiting the maintenance of telomere length, choosing as targets telomerase -or its subunits- or the Shelterin complex. The goal of these therapies is the shortening of telomeres and the induction of cell senescence. Telomeres and telomerase emerge as useful molecular tools in the clinical management of CRC.
Literature
2.
go back to reference Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):359–86.CrossRef Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):359–86.CrossRef
3.
4.
5.
go back to reference Valls-Bautista C, Piñol-Felis C, Reñé-Espinet JM, Buenestado-García J, Viñas-Salas J. Telomerase activity and telomere length in the colorectal polyp-carcinoma sequence. Rev Esp Enferm Dig. 2009;101(3):179–86.PubMedCrossRef Valls-Bautista C, Piñol-Felis C, Reñé-Espinet JM, Buenestado-García J, Viñas-Salas J. Telomerase activity and telomere length in the colorectal polyp-carcinoma sequence. Rev Esp Enferm Dig. 2009;101(3):179–86.PubMedCrossRef
6.
go back to reference Engelhard M, Drullinsky P, Guillem J, Moore MA. Telomerase and telomere length in the development and progression of premalignant lesions to colorectal cancer. Clin Cancer Res. 1997;122:1141–5. Engelhard M, Drullinsky P, Guillem J, Moore MA. Telomerase and telomere length in the development and progression of premalignant lesions to colorectal cancer. Clin Cancer Res. 1997;122:1141–5.
8.
go back to reference Valls-Bautista C, Piñol-Felis C, Reñé-Espinet JM, Buenestado-García J, Viñas-Salas J. In colon cancer, normal colon tissue and blood cells have altered telomere lengths. J Surg Oncol. 2015;111(7):899–904.PubMedCrossRef Valls-Bautista C, Piñol-Felis C, Reñé-Espinet JM, Buenestado-García J, Viñas-Salas J. In colon cancer, normal colon tissue and blood cells have altered telomere lengths. J Surg Oncol. 2015;111(7):899–904.PubMedCrossRef
10.
11.
13.
go back to reference Autexier C, Greider CW. Telomerase and cancer: revisiting the telomere hypothesis. Trends Biochem Sci. 1996;21:387–91.PubMedCrossRef Autexier C, Greider CW. Telomerase and cancer: revisiting the telomere hypothesis. Trends Biochem Sci. 1996;21:387–91.PubMedCrossRef
15.
go back to reference Griffith JD, Comeau L, Rosenfield S, Stansel RM, Bianchi A, Moss H, et al. Mammalian telomeres end in a large duplex loop. Cell. 1999;97(4):503–14.PubMedCrossRef Griffith JD, Comeau L, Rosenfield S, Stansel RM, Bianchi A, Moss H, et al. Mammalian telomeres end in a large duplex loop. Cell. 1999;97(4):503–14.PubMedCrossRef
16.
go back to reference de Lange T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes Dev. 2005;19(18):2100–10 (Review).PubMedCrossRef de Lange T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes Dev. 2005;19(18):2100–10 (Review).PubMedCrossRef
17.
go back to reference Williamson JR, Raghuraman MK, Cech TR. Monovalent cation-induced structure of telomeric DNA: the G-quartet model. Cell. 1989;59:871–80.PubMedCrossRef Williamson JR, Raghuraman MK, Cech TR. Monovalent cation-induced structure of telomeric DNA: the G-quartet model. Cell. 1989;59:871–80.PubMedCrossRef
18.
go back to reference van Steensel B, de Lange T. Control of telomere length by the human telomeric protein TRF1. Nature. 1997;385(6618):740–3.PubMedCrossRef van Steensel B, de Lange T. Control of telomere length by the human telomeric protein TRF1. Nature. 1997;385(6618):740–3.PubMedCrossRef
20.
go back to reference Zhao Z, Pan X, Liu L, Liu N. Telomere length maintenance, shortening, and lengthening. J Cell Physiol. 2014;229(10):1323–9 (Review).PubMedCrossRef Zhao Z, Pan X, Liu L, Liu N. Telomere length maintenance, shortening, and lengthening. J Cell Physiol. 2014;229(10):1323–9 (Review).PubMedCrossRef
21.
go back to reference Kim SH, Beausejour C, Davalos AR, Kaminker P, Heo SJ, Campisi J. TIN2 mediates functions of TRF2 at human telomeres. J Biol Chem. 2004;279(42):43799–804.PubMedCrossRef Kim SH, Beausejour C, Davalos AR, Kaminker P, Heo SJ, Campisi J. TIN2 mediates functions of TRF2 at human telomeres. J Biol Chem. 2004;279(42):43799–804.PubMedCrossRef
22.
go back to reference Rodier F, Kim SH, Nijjar T, Yaswen P, Campisi J. Cancer and aging: the importance of telomeres in genome maintenance. Int J Biochem Cell Biol. 2005;37:977–90.PubMedCrossRef Rodier F, Kim SH, Nijjar T, Yaswen P, Campisi J. Cancer and aging: the importance of telomeres in genome maintenance. Int J Biochem Cell Biol. 2005;37:977–90.PubMedCrossRef
24.
25.
go back to reference Farnung BO, Brun CM, Arora R, Lorenzi LE, Azzalin CM. Telomerase efficiently elongates highly transcribing telomeres in human cancer cells. PLoS One. 2012;7(4):e35714.PubMedPubMedCentralCrossRef Farnung BO, Brun CM, Arora R, Lorenzi LE, Azzalin CM. Telomerase efficiently elongates highly transcribing telomeres in human cancer cells. PLoS One. 2012;7(4):e35714.PubMedPubMedCentralCrossRef
26.
go back to reference Gomez DE, Armando RG, Farina HG, Menna PL, Cerrudo CS, Ghiringhelli PD, et al. Telomere structure and telomerase in health and disease (review). Int J Oncol. 2012;41(5):1561–9.PubMedPubMedCentral Gomez DE, Armando RG, Farina HG, Menna PL, Cerrudo CS, Ghiringhelli PD, et al. Telomere structure and telomerase in health and disease (review). Int J Oncol. 2012;41(5):1561–9.PubMedPubMedCentral
27.
go back to reference Greider CW, Blackburn EH. Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell. 1985;43:405–13.PubMedCrossRef Greider CW, Blackburn EH. Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell. 1985;43:405–13.PubMedCrossRef
28.
go back to reference Shay JW, Zou Y, Hiyama E, Wright WE. Telomerase and cancer. Hum Mol Gen. 2001;346:677–85.CrossRef Shay JW, Zou Y, Hiyama E, Wright WE. Telomerase and cancer. Hum Mol Gen. 2001;346:677–85.CrossRef
29.
go back to reference Nakamura TM, Morin GB, Chapman KB, Weinrich SL, Andrews WH, Lingner J, et al. Telomerase catalytic subunit homologs from fission yeast and human. Science. 1997;277(5328):955–9.PubMedCrossRef Nakamura TM, Morin GB, Chapman KB, Weinrich SL, Andrews WH, Lingner J, et al. Telomerase catalytic subunit homologs from fission yeast and human. Science. 1997;277(5328):955–9.PubMedCrossRef
30.
go back to reference Meyerson M, Counter CM, Eaton EN, Ellisen LW, Steiner P, Caddle SD, et al. hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization. Cell. 1997;90(4):785–95.PubMedCrossRef Meyerson M, Counter CM, Eaton EN, Ellisen LW, Steiner P, Caddle SD, et al. hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization. Cell. 1997;90(4):785–95.PubMedCrossRef
31.
go back to reference Guilleret I, Yan P, Grange F, Braunschweig R, Bosman FT, Benhattar J. Hypermethylation of the human telomerase catalytic subunit (hTERT) gene correlates with telomerase activity. Int J Cancer. 2002;101(4):335–41.PubMedCrossRef Guilleret I, Yan P, Grange F, Braunschweig R, Bosman FT, Benhattar J. Hypermethylation of the human telomerase catalytic subunit (hTERT) gene correlates with telomerase activity. Int J Cancer. 2002;101(4):335–41.PubMedCrossRef
32.
go back to reference Kyo S, Takakura M, Fujiwara T, Inoue M. Understanding and exploiting hTERT promoter regulation for diagnosis and treatment of human cancers. Cancer Sci. 2008;99(8):1528–38 (Review).PubMedCrossRef Kyo S, Takakura M, Fujiwara T, Inoue M. Understanding and exploiting hTERT promoter regulation for diagnosis and treatment of human cancers. Cancer Sci. 2008;99(8):1528–38 (Review).PubMedCrossRef
33.
go back to reference Goueli BS, Janknecht R. Regulation of telomerase reverse transcriptase gene activity by upstream stimulatory factor. Oncogene. 2003;22(39):8042–7.PubMedCrossRef Goueli BS, Janknecht R. Regulation of telomerase reverse transcriptase gene activity by upstream stimulatory factor. Oncogene. 2003;22(39):8042–7.PubMedCrossRef
34.
go back to reference Poole JC, Andrews LG, Tollefsbol TO. Activity, function, and gene regulation of the catalytic subunit of telomerase (hTERT). Gene. 2001;269:1–12.PubMedCrossRef Poole JC, Andrews LG, Tollefsbol TO. Activity, function, and gene regulation of the catalytic subunit of telomerase (hTERT). Gene. 2001;269:1–12.PubMedCrossRef
35.
go back to reference Renaud S, Loukinov D, Bosman FT, Lobanenkov V, Benhattar J. CTCF binds the proximal exonic region of hTERT and inhibits its transcription. Nucleic Acids Res. 2005;33:6850–60.PubMedPubMedCentralCrossRef Renaud S, Loukinov D, Bosman FT, Lobanenkov V, Benhattar J. CTCF binds the proximal exonic region of hTERT and inhibits its transcription. Nucleic Acids Res. 2005;33:6850–60.PubMedPubMedCentralCrossRef
36.
go back to reference Valls C, Piñol C, Reñé JM, Buenestado J, Viñas J. Telomere length is a prognostic factor for overall survival in colorectal cancer. Colorectal Dis. 2011;13:1265–72.PubMedCrossRef Valls C, Piñol C, Reñé JM, Buenestado J, Viñas J. Telomere length is a prognostic factor for overall survival in colorectal cancer. Colorectal Dis. 2011;13:1265–72.PubMedCrossRef
38.
go back to reference Reddel RR. Alternative lengthening of telomeres, telomerase and cancer. Cancer Lett. 2003;194:155–62.PubMedCrossRef Reddel RR. Alternative lengthening of telomeres, telomerase and cancer. Cancer Lett. 2003;194:155–62.PubMedCrossRef
39.
go back to reference Cerone MA, Londono-Vallejo JA, Bacchetti S. Telomere maintenance by telomerase and by recombination can coexist in human cells. Hum Mol Genet. 2001;18:1945–52.CrossRef Cerone MA, Londono-Vallejo JA, Bacchetti S. Telomere maintenance by telomerase and by recombination can coexist in human cells. Hum Mol Genet. 2001;18:1945–52.CrossRef
40.
go back to reference Xu L, Li S, Stohr BA. The role of telomere biology in cancer. Annu Rev Pathol. 2013;8:49–78 (Review).PubMedCrossRef Xu L, Li S, Stohr BA. The role of telomere biology in cancer. Annu Rev Pathol. 2013;8:49–78 (Review).PubMedCrossRef
41.
go back to reference Muntoni A, Reddel RR. The first molecular details of ALT in human tumor cells. Hum Mol Genet. 2005;14(Spec No. 2):R191–6 (Review).PubMedCrossRef Muntoni A, Reddel RR. The first molecular details of ALT in human tumor cells. Hum Mol Genet. 2005;14(Spec No. 2):R191–6 (Review).PubMedCrossRef
42.
go back to reference Artandi SE, Attardi LD. Pathways connecting telomeres and p53 in senescence, apoptosis, and cancer. Biochem Biophys Res Commun. 2005;331(3):881–90 (Review).PubMedCrossRef Artandi SE, Attardi LD. Pathways connecting telomeres and p53 in senescence, apoptosis, and cancer. Biochem Biophys Res Commun. 2005;331(3):881–90 (Review).PubMedCrossRef
43.
go back to reference De Cian A, Lacroix L, Douarre C, Temime-Smaali N, Trentesaux C, Riou JF, et al. Targeting telomeres and telomerase. Biochimie. 2008;90(1):131–55 (Review).PubMedCrossRef De Cian A, Lacroix L, Douarre C, Temime-Smaali N, Trentesaux C, Riou JF, et al. Targeting telomeres and telomerase. Biochimie. 2008;90(1):131–55 (Review).PubMedCrossRef
44.
go back to reference Flores I, Benetti R, Blasco MA. Telomerase regulation and stem cell behaviour. Curr Opin Cell Biol. 2006;18(3):254–60 (Review).PubMedCrossRef Flores I, Benetti R, Blasco MA. Telomerase regulation and stem cell behaviour. Curr Opin Cell Biol. 2006;18(3):254–60 (Review).PubMedCrossRef
45.
go back to reference Harley CB. Telomere loss: mitotic clock or genetic time bomb? Mutat Res. 1991;256(2–6):271–82 (Review).PubMedCrossRef Harley CB. Telomere loss: mitotic clock or genetic time bomb? Mutat Res. 1991;256(2–6):271–82 (Review).PubMedCrossRef
46.
48.
go back to reference Allsopp RC, Harley CB. Evidence for a critical telomere length in senescent human fibroblasts. Exp Cell Res. 1995;219(1):130–6.PubMedCrossRef Allsopp RC, Harley CB. Evidence for a critical telomere length in senescent human fibroblasts. Exp Cell Res. 1995;219(1):130–6.PubMedCrossRef
49.
go back to reference Counter CM, Avilion AA, LeFeuvre CE, Stewart NG, Greider CW, Harley CB, et al. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 1992;11(5):1921–9.PubMedPubMedCentral Counter CM, Avilion AA, LeFeuvre CE, Stewart NG, Greider CW, Harley CB, et al. Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity. EMBO J. 1992;11(5):1921–9.PubMedPubMedCentral
50.
go back to reference Brunori M, Luciano P, Gilson E, Géli V. The telomerase cycle: normal and pathological aspects. J Mol Med (Berl). 2005;83(4):244–57 (Review).CrossRef Brunori M, Luciano P, Gilson E, Géli V. The telomerase cycle: normal and pathological aspects. J Mol Med (Berl). 2005;83(4):244–57 (Review).CrossRef
51.
go back to reference Swiderska M, Choromańska B, Dąbrowska E, Konarzewska-Duchnowska E, Choromańska K, Szczurko G, et al. The diagnostics of colorectal cancer. Contemp Oncol. 2014;18(1):1–6 (Review). Swiderska M, Choromańska B, Dąbrowska E, Konarzewska-Duchnowska E, Choromańska K, Szczurko G, et al. The diagnostics of colorectal cancer. Contemp Oncol. 2014;18(1):1–6 (Review).
52.
go back to reference Sagaert X. Prognostic biomarkers in colorectal cancer: where do we stand? Virchows Arch. 2014;464(3):379–91 (Review).PubMedCrossRef Sagaert X. Prognostic biomarkers in colorectal cancer: where do we stand? Virchows Arch. 2014;464(3):379–91 (Review).PubMedCrossRef
53.
go back to reference Bolocan A, Ion D, Ciocan DN, Paduraru DN. Prognostic and predictive factors in colorectal cancer. Chirurgia. 2012;107(5):555–63 (Review).PubMed Bolocan A, Ion D, Ciocan DN, Paduraru DN. Prognostic and predictive factors in colorectal cancer. Chirurgia. 2012;107(5):555–63 (Review).PubMed
54.
go back to reference Bannura G, Cumsille MA, Contreras J, Barrera A, Melo C, Soto D. Carcinoembryonic antigen (CEA) as an independent prognostic factor in colorectal carcinoma. Rev Med Chil. 2004;132(6):691–700.PubMedCrossRef Bannura G, Cumsille MA, Contreras J, Barrera A, Melo C, Soto D. Carcinoembryonic antigen (CEA) as an independent prognostic factor in colorectal carcinoma. Rev Med Chil. 2004;132(6):691–700.PubMedCrossRef
55.
go back to reference Yamashita K, Watanabe M. Clinical significance of tumor markers and an emerging perspective on colorectal cancer. Cancer Sci. 2009;100(2):195–9 (Review).PubMedCrossRef Yamashita K, Watanabe M. Clinical significance of tumor markers and an emerging perspective on colorectal cancer. Cancer Sci. 2009;100(2):195–9 (Review).PubMedCrossRef
56.
go back to reference Kim NW, Piatyszek MA, Weinrich SL, Hiyama K, Hiyama E, Wright WE, et al. Detection of telomerase activity in human cells and tumors by a telomeric repeat amplification protocol (TRAP). Methods Cell Sci. 1995;17:1–15.CrossRef Kim NW, Piatyszek MA, Weinrich SL, Hiyama K, Hiyama E, Wright WE, et al. Detection of telomerase activity in human cells and tumors by a telomeric repeat amplification protocol (TRAP). Methods Cell Sci. 1995;17:1–15.CrossRef
57.
go back to reference Brown T, Aldous W, Lance R, Blaser J, Baker T, Williard W. The association between telomerase, p53 and clinical staging in colorectal cancer. Am J Surg. 1998;175:364–6.PubMedCrossRef Brown T, Aldous W, Lance R, Blaser J, Baker T, Williard W. The association between telomerase, p53 and clinical staging in colorectal cancer. Am J Surg. 1998;175:364–6.PubMedCrossRef
58.
59.
go back to reference Abe N, Watanabe T, Nakashima M, Masaki T, Mori T, Sugiyama M, et al. Quantitative analysis of telomerase activity: a potential diagnostic tool for colorectal cancer. Hepatogastroenterology. 2001;48:692–5.PubMed Abe N, Watanabe T, Nakashima M, Masaki T, Mori T, Sugiyama M, et al. Quantitative analysis of telomerase activity: a potential diagnostic tool for colorectal cancer. Hepatogastroenterology. 2001;48:692–5.PubMed
60.
go back to reference Shoji Y, Yoshinaga K, Inoue A, Iwasaki A, Sugihara K. Quantification of telomerase activity in sporadic colorectal carcinoma: association with tumor growth and venous invasion. Cancer. 2000;88:1304–9.PubMedCrossRef Shoji Y, Yoshinaga K, Inoue A, Iwasaki A, Sugihara K. Quantification of telomerase activity in sporadic colorectal carcinoma: association with tumor growth and venous invasion. Cancer. 2000;88:1304–9.PubMedCrossRef
61.
go back to reference Boldrini L, Faviana P, Gisfredi S, Zucconi Y, Di Quirico D, Donati V, et al. Evaluation of telomerase in the development and progression of colon cancer. Int J Mol Med. 2002;10:589–92.PubMed Boldrini L, Faviana P, Gisfredi S, Zucconi Y, Di Quirico D, Donati V, et al. Evaluation of telomerase in the development and progression of colon cancer. Int J Mol Med. 2002;10:589–92.PubMed
62.
go back to reference Yan P, Saraga EP, Bouzourene H, Bosman FT, Benhattar J. Telomerase activation in colorectal carcinogenesis. J Pathol. 1999;189:207–12.PubMedCrossRef Yan P, Saraga EP, Bouzourene H, Bosman FT, Benhattar J. Telomerase activation in colorectal carcinogenesis. J Pathol. 1999;189:207–12.PubMedCrossRef
63.
go back to reference Ghori A, Usselman B, Ferryman S, Morris A, Fraser I. Telomerase expression of malignant epithelial cells correlates with Duke’s stage in colorectal cancer. Colorectal Dis. 2002;4:441–6.PubMedCrossRef Ghori A, Usselman B, Ferryman S, Morris A, Fraser I. Telomerase expression of malignant epithelial cells correlates with Duke’s stage in colorectal cancer. Colorectal Dis. 2002;4:441–6.PubMedCrossRef
64.
go back to reference Tang R, Cheng AJ, Wang JY, Wang TC. Close correlation between telomerase expression and adenomatous polyp progression in multistep colorectal carcinogenesis. Cancer Res. 1998;58(18):4052–4.PubMed Tang R, Cheng AJ, Wang JY, Wang TC. Close correlation between telomerase expression and adenomatous polyp progression in multistep colorectal carcinogenesis. Cancer Res. 1998;58(18):4052–4.PubMed
65.
go back to reference Chadeneau C, Hay K, Hirte HW, Gallinger S, Bacchetti S. Telomerase activity associated with acquisition of malignancy in human colorectal cancer. Cancer Res. 1995;55(12):2533–6.PubMed Chadeneau C, Hay K, Hirte HW, Gallinger S, Bacchetti S. Telomerase activity associated with acquisition of malignancy in human colorectal cancer. Cancer Res. 1995;55(12):2533–6.PubMed
66.
go back to reference Sanz-Casla MT, Vidaurreta M, Sanchez-Rueda D, Maestro ML, Arroyo M, Cerdán FJ. Telomerase activity as a prognostic factor in colorectal cancer. Onkologie. 2005;28(11):553–7.PubMed Sanz-Casla MT, Vidaurreta M, Sanchez-Rueda D, Maestro ML, Arroyo M, Cerdán FJ. Telomerase activity as a prognostic factor in colorectal cancer. Onkologie. 2005;28(11):553–7.PubMed
67.
go back to reference Garcia-Aranda C, de Juan C, Diaz-Lopez A, Sanchez-Pernaute A, Torres AJ, Diaz-Rubio E, et al. Correlations of telomere length, telomerase activity and telomeric-repeat binding factor 1 expression in colorectal carcinoma. Cancer. 2006;106:541–51.PubMedCrossRef Garcia-Aranda C, de Juan C, Diaz-Lopez A, Sanchez-Pernaute A, Torres AJ, Diaz-Rubio E, et al. Correlations of telomere length, telomerase activity and telomeric-repeat binding factor 1 expression in colorectal carcinoma. Cancer. 2006;106:541–51.PubMedCrossRef
68.
go back to reference Kawanishi-Tabata R, López F, Fratantonio S, Kim N, Goldblum J, Tubbs R, et al. Telomerase activity in stage II colorectal cancer. Cancer. 2002;95:1834–9.PubMedCrossRef Kawanishi-Tabata R, López F, Fratantonio S, Kim N, Goldblum J, Tubbs R, et al. Telomerase activity in stage II colorectal cancer. Cancer. 2002;95:1834–9.PubMedCrossRef
69.
go back to reference Lukman K, Maskoen AM, Achmad TH, Hanafi B, Kamadihadja W. Telomerase activity in different clinical staging of colorectal adenocarcinoma. Gan To Kagaku Ryoho. 2000;27:491–7.PubMed Lukman K, Maskoen AM, Achmad TH, Hanafi B, Kamadihadja W. Telomerase activity in different clinical staging of colorectal adenocarcinoma. Gan To Kagaku Ryoho. 2000;27:491–7.PubMed
70.
go back to reference Bautista CV, Felis CP, Espinet JM, Garcia JB, Salas JV. Telomerase activity is a prognostic factor for recurrence and survival in rectal cancer. Dis Colon Rectum. 2007;50:611–20.PubMedCrossRef Bautista CV, Felis CP, Espinet JM, Garcia JB, Salas JV. Telomerase activity is a prognostic factor for recurrence and survival in rectal cancer. Dis Colon Rectum. 2007;50:611–20.PubMedCrossRef
71.
go back to reference Roig AI, Wright WE, Shay JW. Is telomerase a novel target for metastatic colon cancer? Current Colorectal Cancer Rep. 2009;5(4):203–8.CrossRef Roig AI, Wright WE, Shay JW. Is telomerase a novel target for metastatic colon cancer? Current Colorectal Cancer Rep. 2009;5(4):203–8.CrossRef
72.
go back to reference Bertorelle R, Rampazzo E, Pucciarelli S, Nitti D, De Rossi A. Telomeres, telomerase and colorectal cancer. World J Gastroenterol. 2014;20(8):1940–50.PubMedPubMedCentralCrossRef Bertorelle R, Rampazzo E, Pucciarelli S, Nitti D, De Rossi A. Telomeres, telomerase and colorectal cancer. World J Gastroenterol. 2014;20(8):1940–50.PubMedPubMedCentralCrossRef
73.
go back to reference Ayiomamitis GD, Notas G, Zaravinos A, Zizi-Sermpetzoglou A, Georgiadou M, Sfakianaki O, et al. Differences in telomerase activity between colon and rectal cancer. Can J Surg. 2014;57(3):199–208.PubMedPubMedCentralCrossRef Ayiomamitis GD, Notas G, Zaravinos A, Zizi-Sermpetzoglou A, Georgiadou M, Sfakianaki O, et al. Differences in telomerase activity between colon and rectal cancer. Can J Surg. 2014;57(3):199–208.PubMedPubMedCentralCrossRef
74.
go back to reference Kapiteijn E, Liefers GJ, Los LC, Kranenbarg EK, Hermans J, Tollenaar RA, et al. Mechanisms of oncogenesis in colon versus rectal cancer. J Pathol. 2001;195(2):171–8.PubMedCrossRef Kapiteijn E, Liefers GJ, Los LC, Kranenbarg EK, Hermans J, Tollenaar RA, et al. Mechanisms of oncogenesis in colon versus rectal cancer. J Pathol. 2001;195(2):171–8.PubMedCrossRef
75.
go back to reference Russo A, Bazan V, Iacopetta B, Kerr D, Soussi T, Gebbia N. The TP53 colorectal cancer international collaborative study on the prognostic and predictive significance of p53 mutation: influence of tumor site, type of mutation, and adjuvant treatment. TP53-CRC Collaborative Study Group. J Clin Oncol. 2005;23(30):7518–28 (Review).PubMedCrossRef Russo A, Bazan V, Iacopetta B, Kerr D, Soussi T, Gebbia N. The TP53 colorectal cancer international collaborative study on the prognostic and predictive significance of p53 mutation: influence of tumor site, type of mutation, and adjuvant treatment. TP53-CRC Collaborative Study Group. J Clin Oncol. 2005;23(30):7518–28 (Review).PubMedCrossRef
76.
go back to reference Tatsumoto N, Hiyama E, Murakami Y, Imamura Y, Shay JW, Matsuura Y, et al. High telomerase activity is an independent prognostic indicator of poor outcome in colorectal cancer. Clin Cancer Res. 2000;6(7):2696–701.PubMed Tatsumoto N, Hiyama E, Murakami Y, Imamura Y, Shay JW, Matsuura Y, et al. High telomerase activity is an independent prognostic indicator of poor outcome in colorectal cancer. Clin Cancer Res. 2000;6(7):2696–701.PubMed
77.
go back to reference Vidaurreta M, Maestro ML, Rafael S, Veganzones S, Sanz-Casla MT, Cerdán J, et al. Telomerase activity in colorectal cancer, prognostic factor and implications in the microsatellite instability pathway. World J Gastroenterol. 2007;13(28):3868–72.PubMedPubMedCentralCrossRef Vidaurreta M, Maestro ML, Rafael S, Veganzones S, Sanz-Casla MT, Cerdán J, et al. Telomerase activity in colorectal cancer, prognostic factor and implications in the microsatellite instability pathway. World J Gastroenterol. 2007;13(28):3868–72.PubMedPubMedCentralCrossRef
78.
go back to reference Dessain SK, Yu HY, Reddel RR, Beijersbergen RL, Weinberg RA. Methylation of the human telomerase gene CpG island. Cancer Res. 2000;60:537–41.PubMed Dessain SK, Yu HY, Reddel RR, Beijersbergen RL, Weinberg RA. Methylation of the human telomerase gene CpG island. Cancer Res. 2000;60:537–41.PubMed
79.
go back to reference Devereux TR, Horikawa I, Anna CH, Annab LA, Afshari CA, Barrett JC. DNA methylation analysis of the promoter region of the human telomerase reverse transcriptase (hTERT) gene. Cancer Res. 1999;59:6087–90.PubMed Devereux TR, Horikawa I, Anna CH, Annab LA, Afshari CA, Barrett JC. DNA methylation analysis of the promoter region of the human telomerase reverse transcriptase (hTERT) gene. Cancer Res. 1999;59:6087–90.PubMed
80.
go back to reference Bertorelle R, Briarava M, Rampazzo E, Biasini L, Agostini M, Maretto I, et al. Telomerase is an independent prognostic marker of overall survival in patients with colorectal cancer. Br J Cancer. 2013;108(2):278–84.PubMedPubMedCentralCrossRef Bertorelle R, Briarava M, Rampazzo E, Biasini L, Agostini M, Maretto I, et al. Telomerase is an independent prognostic marker of overall survival in patients with colorectal cancer. Br J Cancer. 2013;108(2):278–84.PubMedPubMedCentralCrossRef
81.
go back to reference Terrin L, Rampazzo E, Pucciarelli S, Agostini M, Bertorelle R, Esposito G, et al. Relationship between tumor and plasma levels of hTERT mRNA in patients with colorectal cancer: implications for monitoring of neoplastic disease. Clin Cancer Res. 2008;14(22):7444–51.PubMedCrossRef Terrin L, Rampazzo E, Pucciarelli S, Agostini M, Bertorelle R, Esposito G, et al. Relationship between tumor and plasma levels of hTERT mRNA in patients with colorectal cancer: implications for monitoring of neoplastic disease. Clin Cancer Res. 2008;14(22):7444–51.PubMedCrossRef
82.
go back to reference Gertler R, Rosenberg R, Stricker D, Friederichs J, Hoos A, Werner M, et al. Telomere length and human telomerase reverse transcriptase expression as markers for progression and prognosis of colorectal carcinoma. J Clin Oncol. 2004;22:1807–14.PubMedCrossRef Gertler R, Rosenberg R, Stricker D, Friederichs J, Hoos A, Werner M, et al. Telomere length and human telomerase reverse transcriptase expression as markers for progression and prognosis of colorectal carcinoma. J Clin Oncol. 2004;22:1807–14.PubMedCrossRef
83.
go back to reference Takagi S, Kinouchi Y, Hiwatashi N, Nagashima F, Chida M, Takahashi S, et al. Relationship between microsatellite instability and telomere shortening in colorectal cancer. Dis Colon Rectum. 2000;43(10 Suppl):S12–7.PubMedCrossRef Takagi S, Kinouchi Y, Hiwatashi N, Nagashima F, Chida M, Takahashi S, et al. Relationship between microsatellite instability and telomere shortening in colorectal cancer. Dis Colon Rectum. 2000;43(10 Suppl):S12–7.PubMedCrossRef
85.
go back to reference Fernández-Marcelo T, Sánchez-Pernaute A, Pascua I, De Juan C, Head J, Torres-García AJ, et al. Clinical Relevance of Telomere Status and Telomerase Activity in Colorectal Cancer. PLoS One. 2016;11(2):e0149626.PubMedPubMedCentralCrossRef Fernández-Marcelo T, Sánchez-Pernaute A, Pascua I, De Juan C, Head J, Torres-García AJ, et al. Clinical Relevance of Telomere Status and Telomerase Activity in Colorectal Cancer. PLoS One. 2016;11(2):e0149626.PubMedPubMedCentralCrossRef
86.
go back to reference Friedrich U, Griese E, Schwab M, Fritz P, Thon K, Klotz U. Telomere length in different tissues of elderly patients. Mech Ageing Dev. 2000;119(3):89–99.PubMedCrossRef Friedrich U, Griese E, Schwab M, Fritz P, Thon K, Klotz U. Telomere length in different tissues of elderly patients. Mech Ageing Dev. 2000;119(3):89–99.PubMedCrossRef
87.
go back to reference Allsopp RC, Vaziri H, Patterson C, Goldstein S, Younglai EV, Futcher AB, et al. Telomere length predicts replicative capacity of human fibroblasts. Proc Natl Acad Sci USA. 1998;95:5607–10.CrossRef Allsopp RC, Vaziri H, Patterson C, Goldstein S, Younglai EV, Futcher AB, et al. Telomere length predicts replicative capacity of human fibroblasts. Proc Natl Acad Sci USA. 1998;95:5607–10.CrossRef
88.
go back to reference Hastie ND, Dempster M, Dunlop MG, Thompson AM, Green DK, Allshire RC. Telomere reduction in human colorectal carcinoma and with ageing. Nature. 1990;346(6287):866–8.PubMedCrossRef Hastie ND, Dempster M, Dunlop MG, Thompson AM, Green DK, Allshire RC. Telomere reduction in human colorectal carcinoma and with ageing. Nature. 1990;346(6287):866–8.PubMedCrossRef
89.
go back to reference Riegert-Johnson DL, Boardman LA, Crook JE, Thomas CS, Johnson RA, Roberts ME. Shorter peripheral blood telomeres are a potential biomarker for patients with advanced colorectal adenomas. Int J Biol Markers. 2012;27(4):375–80.CrossRef Riegert-Johnson DL, Boardman LA, Crook JE, Thomas CS, Johnson RA, Roberts ME. Shorter peripheral blood telomeres are a potential biomarker for patients with advanced colorectal adenomas. Int J Biol Markers. 2012;27(4):375–80.CrossRef
90.
go back to reference Cui Y, Gao YT, Cai Q, Qu S, Cai H, Li HL, et al. Associations of leukocyte telomere length with body anthropometric indices and weight change in Chinese women. Obesity. 2013;21(12):2582–8.PubMedPubMedCentralCrossRef Cui Y, Gao YT, Cai Q, Qu S, Cai H, Li HL, et al. Associations of leukocyte telomere length with body anthropometric indices and weight change in Chinese women. Obesity. 2013;21(12):2582–8.PubMedPubMedCentralCrossRef
91.
go back to reference Weischer M, Nordestgaard BG, Cawthon RM, Freiberg JJ, Tybjærg-Hansen A, Bojesen SE. Short telomere length, cancer survival, and cancer risk in 47102 individuals. J Natl Cancer Inst. 2013;105(7):459–68.PubMedCrossRef Weischer M, Nordestgaard BG, Cawthon RM, Freiberg JJ, Tybjærg-Hansen A, Bojesen SE. Short telomere length, cancer survival, and cancer risk in 47102 individuals. J Natl Cancer Inst. 2013;105(7):459–68.PubMedCrossRef
92.
go back to reference Kaszubowska L. Telomere shortening and ageing of the immune system. J Physiol Pharmacol. 2008;59(Suppl 9):169–86 (Review).PubMed Kaszubowska L. Telomere shortening and ageing of the immune system. J Physiol Pharmacol. 2008;59(Suppl 9):169–86 (Review).PubMed
93.
go back to reference Queisser A, Heeg S, Thaler M, von Werder A, Opitz OG. Inhibition of telomerase induces alternative lengthening of telomeres during human esophageal carcinogenesis. Cancer Genet. 2013;206(11):374–86.PubMedCrossRef Queisser A, Heeg S, Thaler M, von Werder A, Opitz OG. Inhibition of telomerase induces alternative lengthening of telomeres during human esophageal carcinogenesis. Cancer Genet. 2013;206(11):374–86.PubMedCrossRef
94.
go back to reference Agrawal A, Dang S, Gabrani R. Recent patents on anti-telomerase cancer therapy. Recent Pat Anticancer Drug Discov. 2012;7(1):102–17 (Review).PubMedCrossRef Agrawal A, Dang S, Gabrani R. Recent patents on anti-telomerase cancer therapy. Recent Pat Anticancer Drug Discov. 2012;7(1):102–17 (Review).PubMedCrossRef
95.
go back to reference Augustine TA, Baig M, Sood A, Budagov T, Atzmon G, Mariadason JM, et al. Telomere length is a novel predictive biomarker of sensitivity to anti-EGFR therapy in metastatic colorectal cancer. Br J Cancer. 2015;112(2):313–8.PubMedCrossRef Augustine TA, Baig M, Sood A, Budagov T, Atzmon G, Mariadason JM, et al. Telomere length is a novel predictive biomarker of sensitivity to anti-EGFR therapy in metastatic colorectal cancer. Br J Cancer. 2015;112(2):313–8.PubMedCrossRef
Metadata
Title
Telomeres and telomerase in the clinical management of colorectal cancer
Authors
C. Piñol-Felis
T. Fernández-Marcelo
J. Viñas-Salas
C. Valls-Bautista
Publication date
01-04-2017
Publisher
Springer International Publishing
Published in
Clinical and Translational Oncology / Issue 4/2017
Print ISSN: 1699-048X
Electronic ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-016-1559-0

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