You Jijun, He Xuejun, Ding Haibing, Zhang Tingrong
Department of Cardiothoracic Surgery, Taizhou Second People's Hospital, No. 27 Jiankang Road, Taizhou, 225599, China.
Cell Biochem Biophys. 2015 Jan;71(1):465-72. doi: 10.1007/s12013-014-0226-8.
Breast cancer metastasis suppressor 1 (BRMS1) was originally identified as a metastasis suppressor gene in human breast cancer. Previous studies have reported that loss of BRMS1 expression correlates with tumor progression, and poor prognosis in NSCLC. However, the role of BRMS1 in NSCLC is not fully understood. In this study, we found that expression of BRMS1 in A549 cells did not affect cell growth under normal culture conditions but sensitized cells to apoptosis induced by serum deprivation. Consistently, knockdown of endogenous BRMS1 expression in H1299 cells suppressed cell apoptosis. We identified that BRMS1 regulate apoptosis in NSCLC cells by modulating Stat3 activation. Taken together, our results show that BRMS1 sensitizes NSCLC cells to apoptosis through Stat3 signaling pathway, suggesting a potential role of BRMS1 in regulating NSCLC apoptosis and metastasis.
乳腺癌转移抑制因子1(BRMS1)最初被鉴定为人类乳腺癌中的一种转移抑制基因。先前的研究报道,BRMS1表达缺失与肿瘤进展以及非小细胞肺癌(NSCLC)的不良预后相关。然而,BRMS1在NSCLC中的作用尚未完全明确。在本研究中,我们发现,在正常培养条件下,BRMS1在A549细胞中的表达不影响细胞生长,但使细胞对血清剥夺诱导的凋亡敏感。同样,敲低H1299细胞中内源性BRMS1的表达可抑制细胞凋亡。我们确定BRMS1通过调节Stat3激活来调控NSCLC细胞的凋亡。综上所述,我们的结果表明,BRMS1通过Stat3信号通路使NSCLC细胞对凋亡敏感,提示BRMS1在调控NSCLC凋亡和转移中具有潜在作用。