首页> 外文期刊>Journal of cellular and molecular medicine. >Suppression of LETM1 inhibits the proliferation and stemness of colorectal cancer cells through reactive oxygen species–induced autophagy
【24h】

Suppression of LETM1 inhibits the proliferation and stemness of colorectal cancer cells through reactive oxygen species–induced autophagy

机译:抑制Letm1通过反应性氧物种诱导的自噬抑制结肠直肠癌细胞的增殖和茎

获取原文
获取外文期刊封面目录资料

摘要

Leucine zipper‐EF‐hand–containing transmembrane protein 1 (LETM1) is a mitochondrial inner membrane protein that is highly expressed in various cancers. Although LETM1 is known to be associated with poor prognosis in colorectal cancer (CRC), its roles in autophagic cell death in CRC have not been explored. In this study, we examined the mechanisms through which LETM1 mediates autophagy in CRC. Our results showed that LETM1 was highly expressed in CRC tissues and that down‐regulation of LETM1 inhibited cell proliferation and induced S‐phase arrest. LETM1 silencing also suppressed cancer stem cell–like properties and induced autophagy in CRC cells. Additionally, the autophagy inhibitor 3‐methyladenine reversed the inhibitory effects of LETM1 silencing on proliferation and stemness, whereas the autophagy activator rapamycin had the opposite effects. Mechanistically, suppression of LETM1 increased the levels of reactive oxygen species (ROS) and mitochondrial ROS by regulation of SOD2, which in turn activated AMP‐activated protein kinase (AMPK)/mammalian target of rapamycin (mTOR), initiated autophagy, and inhibited proliferation and stemness. Our findings suggest that silencing LETM1 induced autophagy in CRC cells by triggering ROS‐mediated AMPK/mTOR signalling, thus blocking CRC progression, which will enhance our understanding of the molecular mechanism of LETM1 in CRC.
机译:亮氨酸Zipper-EF手工跨膜蛋白1(Letm1)是一种线粒体内膜蛋白,其在各种癌症中高度表达。虽然已知遗体1与结肠直肠癌(CRC)的预后差有关,但其在CRC中的自噬细胞死亡中的作用尚未探讨。在这项研究中,我们检查了别致的机制,通过该机制在CRC中介导自噬。我们的研究结果表明,遗体1在CRC组织中高度表达,遗体的下调抑制细胞增殖和诱导的S-阶段停滞。 Letm1沉默还抑制了癌症干细胞样特性并在CRC细胞中诱导自噬。另外,自噬抑制剂3-甲基腺嘌呤反转莴苣对增殖和茎的抑制作用,而自噬活性剂雷帕霉素具有相反的效果。机械地,通过调节SOD2的SOD2抑制Letm1增加了活性氧物质(ROS)和线粒体RO的水平,这反过来活化的AMP活化蛋白激酶(AMPK)/哺乳动物的雷帕霉素(MTOR),引发的自噬和抑制增殖和茎。我们的研究结果表明,通过触发ROS介导的AMPK / MTOR信号传导,诱导遗体1在CRC细胞中诱导自噬,从而阻断CRC进展,这将提高我们对CRC中遗体的分子机制的理解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号