Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.

PTEN-Long is a translational variant of PTEN (Phosphatase and Tensin Homolog). Like PTEN, PTEN-Long is able to antagonize the PI3K-Akt pathway and inhibits tumor growth. In this study, we investigated the role PTEN-Long plays in the development and progression of clear cell renal cell carcinoma (ccR...

Full description

Bibliographic Details
Main Authors: Hui Wang, Peng Zhang, Chunhua Lin, Qingxia Yu, Jitao Wu, Lin Wang, Yupeng Cui, Ke Wang, Zhenli Gao, Hong Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4340966?pdf=render
id doaj-27c368f170cf4fe1887fdf2028f4b185
record_format Article
spelling doaj-27c368f170cf4fe1887fdf2028f4b1852020-11-24T21:27:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01102e11425010.1371/journal.pone.0114250Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.Hui WangPeng ZhangChunhua LinQingxia YuJitao WuLin WangYupeng CuiKe WangZhenli GaoHong LiPTEN-Long is a translational variant of PTEN (Phosphatase and Tensin Homolog). Like PTEN, PTEN-Long is able to antagonize the PI3K-Akt pathway and inhibits tumor growth. In this study, we investigated the role PTEN-Long plays in the development and progression of clear cell renal cell carcinoma (ccRCC) and explored the therapeutic possibility using proteinaceous PTEN-Long to treat ccRCC. We found that the protein levels of PTEN-Long were drastically reduced in ccRCC, which was correlated with increased levels of phosphorylated Akt (pAkt). Gain of function experiments showed overexpression of PTEN-Long in the ccRCC cell line 786-0 suppressed PI3K-Akt signaling, inhibited cell proliferation, migration and invasion, and eventually induced cell death. When purified PTEN-Long was added into cultured 786-0 cells, it entered cells, blocked Akt activation, and induced apoptosis involving Caspase 3 cleavage. Furthermore, PTEN-Long inhibited proliferation of 786-0 cells in xenograft mouse model. Our results implicated that understanding the roles of PTEN-Long in renal cell carcinogenesis has therapeutic significance.http://europepmc.org/articles/PMC4340966?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hui Wang
Peng Zhang
Chunhua Lin
Qingxia Yu
Jitao Wu
Lin Wang
Yupeng Cui
Ke Wang
Zhenli Gao
Hong Li
spellingShingle Hui Wang
Peng Zhang
Chunhua Lin
Qingxia Yu
Jitao Wu
Lin Wang
Yupeng Cui
Ke Wang
Zhenli Gao
Hong Li
Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
PLoS ONE
author_facet Hui Wang
Peng Zhang
Chunhua Lin
Qingxia Yu
Jitao Wu
Lin Wang
Yupeng Cui
Ke Wang
Zhenli Gao
Hong Li
author_sort Hui Wang
title Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
title_short Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
title_full Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
title_fullStr Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
title_full_unstemmed Relevance and therapeutic possibility of PTEN-long in renal cell carcinoma.
title_sort relevance and therapeutic possibility of pten-long in renal cell carcinoma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description PTEN-Long is a translational variant of PTEN (Phosphatase and Tensin Homolog). Like PTEN, PTEN-Long is able to antagonize the PI3K-Akt pathway and inhibits tumor growth. In this study, we investigated the role PTEN-Long plays in the development and progression of clear cell renal cell carcinoma (ccRCC) and explored the therapeutic possibility using proteinaceous PTEN-Long to treat ccRCC. We found that the protein levels of PTEN-Long were drastically reduced in ccRCC, which was correlated with increased levels of phosphorylated Akt (pAkt). Gain of function experiments showed overexpression of PTEN-Long in the ccRCC cell line 786-0 suppressed PI3K-Akt signaling, inhibited cell proliferation, migration and invasion, and eventually induced cell death. When purified PTEN-Long was added into cultured 786-0 cells, it entered cells, blocked Akt activation, and induced apoptosis involving Caspase 3 cleavage. Furthermore, PTEN-Long inhibited proliferation of 786-0 cells in xenograft mouse model. Our results implicated that understanding the roles of PTEN-Long in renal cell carcinogenesis has therapeutic significance.
url http://europepmc.org/articles/PMC4340966?pdf=render
work_keys_str_mv AT huiwang relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT pengzhang relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT chunhualin relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT qingxiayu relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT jitaowu relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT linwang relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT yupengcui relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT kewang relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT zhenligao relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
AT hongli relevanceandtherapeuticpossibilityofptenlonginrenalcellcarcinoma
_version_ 1725976139908775936