FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.

Fos-related antigen 2 (FRA-2/FOSL2) belongs to the AP-1 transcription factor family. Although FOSL2 has been shown to be involved in diverse physiological and pathological processes, very little is known about the signalling pathways that regulate FOSL2 expression and the mechanisms of FOSL2 functio...

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Main Authors: Junfeng Wang, Dawei Sun, Yanbo Wang, Fenghai Ren, Sainan Pang, Dandan Wang, Shidong Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4223012?pdf=render
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spelling doaj-5176fda66b5243368a43f35aed233e652020-11-24T21:11:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11215010.1371/journal.pone.0112150FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.Junfeng WangDawei SunYanbo WangFenghai RenSainan PangDandan WangShidong XuFos-related antigen 2 (FRA-2/FOSL2) belongs to the AP-1 transcription factor family. Although FOSL2 has been shown to be involved in diverse physiological and pathological processes, very little is known about the signalling pathways that regulate FOSL2 expression and the mechanisms of FOSL2 function. Here, we show that FOSL2 expression is regulated by TGF-β1 and that FOSL2 is required for TGF-β1-induced migration. We demonstrate that FOSL2 interacts with Smad3 in vitro and in vivo and thus up-regulates TGF-β1-induced signalling responses. Mechanistically, FOSL2 promotes P300 binding to Smad3 and the acetylation of Smad3 by P300. Furthermore, we show that the expression of FOSL2 correlates with activated Smad3 expression in clinical non-small cell lung cancer (NSCLC) samples. In summary, the present study indicates that FOSL2 facilitates TGF-β1-induced migration by interaction with Smad3 in NSCLC and suggests FOSL2 as a potential therapeutic target for NSCLC.http://europepmc.org/articles/PMC4223012?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Junfeng Wang
Dawei Sun
Yanbo Wang
Fenghai Ren
Sainan Pang
Dandan Wang
Shidong Xu
spellingShingle Junfeng Wang
Dawei Sun
Yanbo Wang
Fenghai Ren
Sainan Pang
Dandan Wang
Shidong Xu
FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
PLoS ONE
author_facet Junfeng Wang
Dawei Sun
Yanbo Wang
Fenghai Ren
Sainan Pang
Dandan Wang
Shidong Xu
author_sort Junfeng Wang
title FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
title_short FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
title_full FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
title_fullStr FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
title_full_unstemmed FOSL2 positively regulates TGF-β1 signalling in non-small cell lung cancer.
title_sort fosl2 positively regulates tgf-β1 signalling in non-small cell lung cancer.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Fos-related antigen 2 (FRA-2/FOSL2) belongs to the AP-1 transcription factor family. Although FOSL2 has been shown to be involved in diverse physiological and pathological processes, very little is known about the signalling pathways that regulate FOSL2 expression and the mechanisms of FOSL2 function. Here, we show that FOSL2 expression is regulated by TGF-β1 and that FOSL2 is required for TGF-β1-induced migration. We demonstrate that FOSL2 interacts with Smad3 in vitro and in vivo and thus up-regulates TGF-β1-induced signalling responses. Mechanistically, FOSL2 promotes P300 binding to Smad3 and the acetylation of Smad3 by P300. Furthermore, we show that the expression of FOSL2 correlates with activated Smad3 expression in clinical non-small cell lung cancer (NSCLC) samples. In summary, the present study indicates that FOSL2 facilitates TGF-β1-induced migration by interaction with Smad3 in NSCLC and suggests FOSL2 as a potential therapeutic target for NSCLC.
url http://europepmc.org/articles/PMC4223012?pdf=render
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