Department of Medical Oncology, The Military General Hospital of Beijing PLA, Beijing, China.
Int Immunopharmacol. 2012 Feb;12(2):394-401. doi: 10.1016/j.intimp.2011.12.012. Epub 2012 Jan 2.
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.
自噬在癌症中的作用存在争议。褪黑素与癌症进展的几个方面有关,也与自噬的调节有关。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,我们研究了褪黑素对自噬及其上游调节因子的影响。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 向 LC3-II 的转化,从而触发肝癌 H22 荷瘤小鼠的自噬过程,LC3-II 是与自噬体膜相关的蛋白。此外,褪黑素抑制哺乳动物雷帕霉素靶蛋白(mTOR)和 Akt 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,Beclin 1 的敲低显著增强了褪黑素诱导的小鼠肝癌 H22 细胞凋亡。我们的数据首次提供了证据,表明褪黑素诱导保护性自噬,防止小鼠肝癌 H22 细胞发生凋亡。褪黑素与自噬抑制剂的联合应用可能是治疗肝细胞癌的一种有效治疗策略。