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Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells
In this study, we identified ret finger protein-like 3 (RFPL3) as a hTERT promoter binding protein in lung cancer cells. The high hTERT promoter-binding activity of RFPL3 was detected in lung cancer cells compared to normal cells. Chromatin immunoprecipitation confirmed RFPL3 as a tumor-specific hTE...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322990/ https://www.ncbi.nlm.nih.gov/pubmed/25481043 |
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author | Chen, Wangbing Lu, Jianjun Qin, Yu Wang, Jingshu Tian, Yun Shi, Dingbo Wang, Shusen Xiao, Yao Dai, Meng Liu, Lu Wei, Guo Wu, Taihua Jin, Bilian Xiao, Xiangsheng Kang, Tie-Bang Huang, Wenlin Deng, Wuguo |
author_facet | Chen, Wangbing Lu, Jianjun Qin, Yu Wang, Jingshu Tian, Yun Shi, Dingbo Wang, Shusen Xiao, Yao Dai, Meng Liu, Lu Wei, Guo Wu, Taihua Jin, Bilian Xiao, Xiangsheng Kang, Tie-Bang Huang, Wenlin Deng, Wuguo |
author_sort | Chen, Wangbing |
collection | PubMed |
description | In this study, we identified ret finger protein-like 3 (RFPL3) as a hTERT promoter binding protein in lung cancer cells. The high hTERT promoter-binding activity of RFPL3 was detected in lung cancer cells compared to normal cells. Chromatin immunoprecipitation confirmed RFPL3 as a tumor-specific hTERT promoter binding protein. Overexpression of RFPL3 activated hTERT promoter and up-regulated hTERT expression and telomerase activity. Inhibition of RFPL3 expression by siRNA suppressed hTERT promoter activation and telomerase activity. Inhibition of RFPL3 by siRNA or shRNA also significantly inhibited tumor cell growth in vitro and in a xenograft mouse model in vivo. Immunohistochemical analysis of 181 human lung adenocarcinomas specimens showed a significant correlation between RFPL3 and hTERT expression. The overexpression of RFPL3 was also associated significantly with lymph node metastasis. Univariate and multivariate Cox model analyses of NSCLC clinical specimens revealed a strong correlation between RFPL3 expression and overall survival. These results demonstrate that RFPL3 is an important cellular factor which promotes lung cancer growth by activating hTERT expression and may be a potential novel therapeutic target for lung cancer. |
format | Online Article Text |
id | pubmed-4322990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-43229902015-02-10 Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells Chen, Wangbing Lu, Jianjun Qin, Yu Wang, Jingshu Tian, Yun Shi, Dingbo Wang, Shusen Xiao, Yao Dai, Meng Liu, Lu Wei, Guo Wu, Taihua Jin, Bilian Xiao, Xiangsheng Kang, Tie-Bang Huang, Wenlin Deng, Wuguo Oncotarget Research Paper In this study, we identified ret finger protein-like 3 (RFPL3) as a hTERT promoter binding protein in lung cancer cells. The high hTERT promoter-binding activity of RFPL3 was detected in lung cancer cells compared to normal cells. Chromatin immunoprecipitation confirmed RFPL3 as a tumor-specific hTERT promoter binding protein. Overexpression of RFPL3 activated hTERT promoter and up-regulated hTERT expression and telomerase activity. Inhibition of RFPL3 expression by siRNA suppressed hTERT promoter activation and telomerase activity. Inhibition of RFPL3 by siRNA or shRNA also significantly inhibited tumor cell growth in vitro and in a xenograft mouse model in vivo. Immunohistochemical analysis of 181 human lung adenocarcinomas specimens showed a significant correlation between RFPL3 and hTERT expression. The overexpression of RFPL3 was also associated significantly with lymph node metastasis. Univariate and multivariate Cox model analyses of NSCLC clinical specimens revealed a strong correlation between RFPL3 expression and overall survival. These results demonstrate that RFPL3 is an important cellular factor which promotes lung cancer growth by activating hTERT expression and may be a potential novel therapeutic target for lung cancer. Impact Journals LLC 2014-11-13 /pmc/articles/PMC4322990/ /pubmed/25481043 Text en Copyright: © 2014 Chen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Paper Chen, Wangbing Lu, Jianjun Qin, Yu Wang, Jingshu Tian, Yun Shi, Dingbo Wang, Shusen Xiao, Yao Dai, Meng Liu, Lu Wei, Guo Wu, Taihua Jin, Bilian Xiao, Xiangsheng Kang, Tie-Bang Huang, Wenlin Deng, Wuguo Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title | Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title_full | Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title_fullStr | Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title_full_unstemmed | Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title_short | Ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
title_sort | ret finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322990/ https://www.ncbi.nlm.nih.gov/pubmed/25481043 |
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