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索拉非尼联合葡萄糖限制通过损害 SIAH1 介导的线粒体自噬抑制体内外肝癌。

Simultaneous treatment with sorafenib and glucose restriction inhibits hepatocellular carcinoma in vitro and in vivo by impairing SIAH1-mediated mitophagy.

机构信息

Department of Physiology, School of Basic Medical Sciences, Guangxi Medical University, 530021, Nanning, Guangxi Province, P. R. China.

Department of Physiology, National University of Singapore, Singapore, 117593, Singapore.

出版信息

Exp Mol Med. 2022 Nov;54(11):2007-2021. doi: 10.1038/s12276-022-00878-x. Epub 2022 Nov 16.

Abstract

Transarterial chemoembolization (TACE) is the first-line treatment for unresectable intermediate-stage hepatocellular carcinoma (HCC). It is of high clinical significance to explore the synergistic effect of TACE with antiangiogenic inhibitors and the molecular mechanisms involved. This study determined that glucose, but not other analyzed nutrients, offered significant protection against cell death induced by sorafenib, as indicated by glucose deprivation sensitizing cells to sorafenib-induced cell death. Next, this synergistic effect was found to be specific to sorafenib, not to lenvatinib or the chemotherapeutic drugs cisplatin and doxorubicin. Mechanistically, sorafenib-induced mitophagy, as indicated by PINK1 accumulation, increased the phospho-poly-ubiquitination modification, accelerated mitochondrial membrane protein and mitochondrial DNA degradation, and increased the amount of mitochondrion-localized mKeima-Red engulfed by lysosomes. Among several E3 ubiquitin ligases tested, SIAH1 was found to be essential for inducing mitophagy; that is, SIAH1 silencing markedly repressed mitophagy and sensitized cells to sorafenib-induced death. Notably, the combined treatment of glucose restriction and sorafenib abolished ATP generation and mitophagy, which led to a high cell death rate. Oligomycin and antimycin, inhibitors of electron transport chain complexes, mimicked the synergistic effect of sorafenib with glucose restriction to promote cell death mediated via mitophagy inhibition. Finally, inhibition of the glucose transporter by canagliflozin (a clinically available drug used for type-II diabetes) effectively synergized with sorafenib to induce HCC cell death in vitro and to inhibit xenograft tumor growth in vivo. This study demonstrates that simultaneous treatment with sorafenib and glucose restriction is an effective approach to treat HCC, suggesting a promising combination strategy such as transarterial sorafenib-embolization (TASE) for the treatment of unresectable HCC.

摘要

经导管动脉化疗栓塞术(TACE)是不可切除的中期肝细胞癌(HCC)的一线治疗方法。探讨 TACE 与抗血管生成抑制剂的协同作用及其相关分子机制具有重要的临床意义。本研究确定葡萄糖(而不是其他分析的营养素)可显著保护细胞免受索拉非尼诱导的细胞死亡,因为葡萄糖剥夺使细胞对索拉非尼诱导的细胞死亡敏感。接下来,发现这种协同作用是索拉非尼特有的,而不是仑伐替尼或化疗药物顺铂和阿霉素。从机制上讲,如 PINK1 积累所表明的,索拉非尼诱导的线粒体自噬增加了磷酸多泛素化修饰,加速了线粒体膜蛋白和线粒体 DNA 的降解,并增加了溶酶体吞噬的定位于线粒体的 mKeima-Red 的量。在所测试的几种 E3 泛素连接酶中,发现 SIAH1 对于诱导线粒体自噬是必不可少的;也就是说,SIAH1 沉默明显抑制了线粒体自噬并使细胞对索拉非尼诱导的死亡敏感。值得注意的是,葡萄糖限制和索拉非尼的联合治疗消除了 ATP 的产生和线粒体自噬,导致细胞死亡率很高。寡霉素和安密妥,电子传递链复合物的抑制剂,模拟了索拉非尼与葡萄糖限制的协同作用,通过抑制线粒体自噬来促进细胞死亡。最后,用坎格列净(一种用于 II 型糖尿病的临床可用药物)抑制葡萄糖转运体可有效与索拉非尼协同诱导 HCC 细胞死亡,并抑制体内异种移植肿瘤的生长。本研究表明,同时给予索拉非尼和葡萄糖限制是治疗 HCC 的有效方法,提示联合 TACE 治疗不可切除 HCC 具有潜在的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c37c/9723179/9c639594f450/12276_2022_878_Fig1_HTML.jpg

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