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首页> 外文期刊>International immunopharmacology >Involvement of melatonin in autophagy-mediated mouse hepatoma H22 cell survival
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Involvement of melatonin in autophagy-mediated mouse hepatoma H22 cell survival

机译:褪黑素参与自噬介导的小鼠肝癌H22细胞存活

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The role of autophagy in cancer is controversial. Melatonin has been linked to several aspects of cancer progression and also to regulation of autophagy. Whether melatonin is involved in an autophagy-induced tumor suppressor mechanism or a cyto-protective mechanism is unknown. Therefore, we investigated the effects of melatonin on autophagy and its upstream regulator. We found that melatonin triggers an autophagic process by enhancing Beclin 1 expression and inducing a conversion of microtubule-associated protein 1 light chain 3(LC3)-I to LC3-II, the protein associated with the autophagosome membrane, in hepatoma H22 tumor-bearing mice. Moreover, melatonin inhibits the phosphorylation of the mammalian target of the rapamycin (mTOR) and Akt. Knockdown of Beclin 1 by either RNA interference or co-treatment with the autophagy inhibitor, 3-methyladenine(3-MA), significantly enhanced the melatonin-induced apoptosis in mouse hepatoma H22 cells. Our data provides the first evidence that melatonin induces protective autophagy that prevents mouse hepatoma H22 cells from undergoing apoptosis. A combination of melatonin with an autophagy inhibitor might be a useful therapeutic strategy for hepatocellular carcinoma.
机译:自噬在癌症中的作用是有争议的。褪黑激素与癌症进展的几个方面以及自噬的调节有关。褪黑素是否参与自噬诱导的肿瘤抑制机制或细胞保护机制尚不清楚。因此,我们研究了褪黑激素对自噬及其上游调节剂的影响。我们发现褪黑素通过增强Beclin 1的表达并诱导微管相关蛋白1轻链3(LC3)-I转化为LC3-II(与自噬体膜相关的蛋白)而转化为自噬,这在肝癌H22肿瘤中老鼠。此外,褪黑激素抑制雷帕霉素(mTOR)和Akt的哺乳动物靶标的磷酸化。通过RNA干扰或与自噬抑制剂3-甲基腺嘌呤(3-MA)共同处理来抑制Beclin 1,显着增强了褪黑素诱导的小鼠肝癌H22细胞凋亡。我们的数据提供了第一个证据,褪黑素可诱导保护性自噬,阻止小鼠肝癌H22细胞凋亡。褪黑素与自噬抑制剂的组合可能是治疗肝细胞癌的有效策略。

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