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来源于植物舞草(Glyccsmis pentaphylla (Retz) correa)的甲基格尔文。通过激活线粒体和内质网应激信号以及抑制 AKT 和 STAT3 通路来介导抗肝癌作用。

Methylgerambullin derived from plant Glyccsmis pentaphylla (Retz) correa. Mediates anti-hepatocellular carcinoma cancer effect by activating mitochondrial and endoplasmic reticulum stress signaling and inhibiting AKT and STAT3 pathways.

机构信息

School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan, 430074, China.

Hotian Uygur Pharmaceutical Co., Ltd, Hotian, 848200, China.

出版信息

Food Chem Toxicol. 2021 Mar;149:112031. doi: 10.1016/j.fct.2021.112031. Epub 2021 Jan 30.

Abstract

Hepatocellular carcinoma (HCC) is one of the most common fatal malignant tumors. Glycosmis pentaphylla is used by traditional medical practitioners worldwide to treat various diseases. We isolated and identified a chemical component with potential anti-hepatocellular carcinoma (HCC) effects. Methylgerambullin is a sulfur containing amine and has significant antihepatoma activity in vitro and in vivo. Methylgerambullin was significantly cytotoxic to HCC cells and induces apoptosis in HCC cells. In addition, methylgerambullin is able to inhibit the growth of transplanted tumors in nude mice without significant toxicity. Regarding the anti-cancer mechanism of methylgerambullin, treatment with methylgerambullin increased the expression of caspase-3, caspase-9 and Bax in vitro and in vivo and reduce the expression of B-cell lymphoma-2 (Bcl-2). Simultaneously, methylgerambullin can also affect ERS-related proteins, inhibit Protein Kinase B (Akt) activity, cause dephosphorylation of downstream Bad, and inhibit the expression of the Signal Transducer and Activator of Transcription 3 (STAT3) protein to inhibit HCC cells proliferation. Overall, these results suggest that methylgerambullin can inhibit HCC cells proliferation by inducing mitochondrial apoptosis, activating ERS signaling pathways and inhibiting the Akt and STAT3 pathways.

摘要

肝细胞癌 (HCC) 是最常见的致命恶性肿瘤之一。全世界的传统医学从业者都使用五叶甘藤来治疗各种疾病。我们分离并鉴定出一种具有潜在抗肝癌 (HCC) 作用的化学物质成分。甲基格尔文宁是一种含硫胺,具有显著的体外和体内抗肝癌活性。甲基格尔文宁对肝癌细胞具有显著的细胞毒性,并诱导肝癌细胞凋亡。此外,甲基格尔文宁能够抑制裸鼠移植瘤的生长,而没有明显的毒性。关于甲基格尔文宁的抗癌机制,用甲基格尔文宁处理可增加体外和体内 caspase-3、caspase-9 和 Bax 的表达,并降低 B 细胞淋巴瘤-2 (Bcl-2) 的表达。同时,甲基格尔文宁还可以影响 ERS 相关蛋白,抑制蛋白激酶 B (Akt) 的活性,引起下游 Bad 的去磷酸化,抑制信号转导和转录激活因子 3 (STAT3) 蛋白的表达,从而抑制 HCC 细胞的增殖。总的来说,这些结果表明,甲基格尔文宁通过诱导线粒体凋亡、激活 ERS 信号通路以及抑制 Akt 和 STAT3 通路,抑制 HCC 细胞的增殖。

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