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Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma

Reactivation of telomerase is a critical step in the development of hepatocellular carcinoma (HCC). Here we identified the frequency of mutations in telomerase reverse transcriptase (TERT) promoter was 34% in non-clear cell HCC (NCCHCC, n = 259) and 26.3% in clear cell HCC (CCHCC, n = 57). The mutat...

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Autores principales: Huang, Wan, Zhou, Weiping, Li, Can, Yang, Yuan, Shang, Yu-Kui, Chen, Changsheng, Zhang, Jing, Yao, Rui, Wang, Pei, Wen, Wen, Liu, Han-Qiang, Wang, Ling, Li, Xia, Bian, Huijie, Chen, Zhi-Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432257/
https://www.ncbi.nlm.nih.gov/pubmed/28460432
http://dx.doi.org/10.18632/oncotarget.15458
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author Huang, Wan
Zhou, Weiping
Li, Can
Yang, Yuan
Shang, Yu-Kui
Chen, Changsheng
Zhang, Jing
Yao, Rui
Wang, Pei
Wen, Wen
Liu, Han-Qiang
Wang, Ling
Li, Xia
Bian, Huijie
Chen, Zhi-Nan
author_facet Huang, Wan
Zhou, Weiping
Li, Can
Yang, Yuan
Shang, Yu-Kui
Chen, Changsheng
Zhang, Jing
Yao, Rui
Wang, Pei
Wen, Wen
Liu, Han-Qiang
Wang, Ling
Li, Xia
Bian, Huijie
Chen, Zhi-Nan
author_sort Huang, Wan
collection PubMed
description Reactivation of telomerase is a critical step in the development of hepatocellular carcinoma (HCC). Here we identified the frequency of mutations in telomerase reverse transcriptase (TERT) promoter was 34% in non-clear cell HCC (NCCHCC, n = 259) and 26.3% in clear cell HCC (CCHCC, n = 57). The mutations were independently associated with poor recurrence-free survival of HCCs. Interestingly immunohistochemical analysis demonstrated a higher positive rate of TERT cytoplasmic localization (95%) than nuclear localization (64%) in HCCs. In NCCHCCs, the mutations correlated with higher TERT nuclear expression and increased telomere-dependent telomerase activity. Higher cytoplasmic expression was found in adjacent tissues compared to tumor tissues, and was associated with tumor well-differentiation and lower level of α-fetoprotein. NCCHCCs with low nuclear as well as high cytoplasmic expression correlated with better prognosis. In CCHCCs, elevated TERT cytoplasmic expression was observed in CCHCCs harboring mutations. Higher TERT cytoplasmic expression was found in tumor tissues compared to adjacent tissues, and was associated with multiple numbers of tumors and poor prognosis of CCHCCs. In conclusion, mutations in TERT promoter disclose the significance of both nuclear and cytoplasmic TERT in HCC. Cytoplasmic TERT should also be considered when determining prognosis and treatment of HCCs.
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spelling pubmed-54322572017-05-17 Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma Huang, Wan Zhou, Weiping Li, Can Yang, Yuan Shang, Yu-Kui Chen, Changsheng Zhang, Jing Yao, Rui Wang, Pei Wen, Wen Liu, Han-Qiang Wang, Ling Li, Xia Bian, Huijie Chen, Zhi-Nan Oncotarget Research Paper Reactivation of telomerase is a critical step in the development of hepatocellular carcinoma (HCC). Here we identified the frequency of mutations in telomerase reverse transcriptase (TERT) promoter was 34% in non-clear cell HCC (NCCHCC, n = 259) and 26.3% in clear cell HCC (CCHCC, n = 57). The mutations were independently associated with poor recurrence-free survival of HCCs. Interestingly immunohistochemical analysis demonstrated a higher positive rate of TERT cytoplasmic localization (95%) than nuclear localization (64%) in HCCs. In NCCHCCs, the mutations correlated with higher TERT nuclear expression and increased telomere-dependent telomerase activity. Higher cytoplasmic expression was found in adjacent tissues compared to tumor tissues, and was associated with tumor well-differentiation and lower level of α-fetoprotein. NCCHCCs with low nuclear as well as high cytoplasmic expression correlated with better prognosis. In CCHCCs, elevated TERT cytoplasmic expression was observed in CCHCCs harboring mutations. Higher TERT cytoplasmic expression was found in tumor tissues compared to adjacent tissues, and was associated with multiple numbers of tumors and poor prognosis of CCHCCs. In conclusion, mutations in TERT promoter disclose the significance of both nuclear and cytoplasmic TERT in HCC. Cytoplasmic TERT should also be considered when determining prognosis and treatment of HCCs. Impact Journals LLC 2017-02-17 /pmc/articles/PMC5432257/ /pubmed/28460432 http://dx.doi.org/10.18632/oncotarget.15458 Text en Copyright: © 2017 Huang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Huang, Wan
Zhou, Weiping
Li, Can
Yang, Yuan
Shang, Yu-Kui
Chen, Changsheng
Zhang, Jing
Yao, Rui
Wang, Pei
Wen, Wen
Liu, Han-Qiang
Wang, Ling
Li, Xia
Bian, Huijie
Chen, Zhi-Nan
Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title_full Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title_fullStr Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title_full_unstemmed Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title_short Promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
title_sort promoter mutations and cellular distribution of telomerase in non-clear cell and clear cell hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432257/
https://www.ncbi.nlm.nih.gov/pubmed/28460432
http://dx.doi.org/10.18632/oncotarget.15458
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