Melohenine B Induces Apoptosis of HepG2 Cells via Inactivation of PI3K/Akt Pathway

被引:0
作者
Zheng, Zhibin [1 ]
Chen, Peng [2 ]
Yang, Yurou [3 ]
Hu, Mingdao [2 ]
机构
[1] Kunming Med Univ, Hepatopancreatobiliary Surg Dept, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Med Univ, Affiliated Hosp 2, Hepatopancreatobiliary Surg Dept 1, Kunming 650101, Yunnan, Peoples R China
[3] Southwest Med Univ, Affiliated Hosp, Rheumatol & Immunol Dept, Luzhou 646000, Sichuan, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2021年 / 40卷 / 03期
关键词
melohenine B; HepG2; cell; hepatocellular carcinoma; apoptosis; PI3K/Akt pathway; MITOCHONDRIA; INHIBITION; AUTOPHAGY;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hepatocellular carcinoma (HCC) is a severe solid tumor threatening human health worldwide. In the discovery of novel therapies for HCC, phytochemicals play a crucial role. In our program to search bioactive compounds for the treatment of HCC, we have evaluated melohenine B using human HCC HepG2 cells. The results showed melohenine B reduced the proliferation of HepG2 cells via inducing apoptosis. At the same time, melohenine B inhibited caspase-3 activity, disrupted mitochondrial membrane potential, down-regulated Bcl-2, and up-regulated Bax, which indicated the apoptosis underwent intrinsic pathway. Further investigations revealed inactivation of PI3K/Akt pathway was involved in the apoptosis induced by melohenine B. These findings can provide evidences for the discovery of new therapy for the treatment of HCC.
引用
收藏
页码:572 / 576
页数:5
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