Wang Junfeng, Sun Dawei, Wang Yanbo, Ren Fenghai, Pang Sainan, Wang Dandan, Xu Shidong
The Department of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
PLoS One. 2014 Nov 6;9(11):e112150. doi: 10.1371/journal.pone.0112150. eCollection 2014.
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.
Fos相关抗原2(FRA-2/FOSL2)属于AP-1转录因子家族。尽管已表明FOSL2参与多种生理和病理过程,但对于调节FOSL2表达的信号通路以及FOSL2发挥功能的机制却知之甚少。在此,我们表明FOSL2的表达受转化生长因子-β1(TGF-β1)调控,且FOSL2是TGF-β1诱导迁移所必需的。我们证明FOSL2在体外和体内均与Smad3相互作用,从而上调TGF-β1诱导的信号反应。从机制上讲,FOSL2促进P300与Smad3结合以及P300介导的Smad3乙酰化。此外,我们发现FOSL2的表达与临床非小细胞肺癌(NSCLC)样本中活化的Smad3表达相关。总之,本研究表明FOSL2通过与NSCLC中的Smad3相互作用促进TGF-β1诱导的迁移,并提示FOSL2作为NSCLC的潜在治疗靶点。