Ginkgolic acid inhibits proliferation and migration of human hepatocellular carcinoma cells by inducing G0/G1 cell cycle arrest

被引:13
作者
Chen, Jiayu [1 ,2 ,3 ]
Wang, Rui [1 ,2 ]
Li, Ying [1 ,2 ,4 ]
Li, Chunhe [5 ]
Liu, Tao [5 ]
Xin, Yi [6 ]
Li, Yiling [3 ]
Zhang, Dianbao [1 ,2 ]
机构
[1] China Med Univ, Dept Stem Cells & Regenerat Med, Key Lab Cell Biol, Natl Hlth Commiss China, Shenyang 110122, Peoples R China
[2] China Med Univ, Key Lab Med Cell Biol, Minist Educ China, Shenyang 110122, Peoples R China
[3] China Med Univ, Dept Med, Div Gastroenterol, Affiliated Hosp 1, Shenyang 110015, Peoples R China
[4] Affiliated Hosp Jining Med Univ, Dept Pathol, Jining 272029, Peoples R China
[5] China Med Univ, Sch Pharm, Dept Nat Prod Chem, Shenyang 110122, Peoples R China
[6] Tianjin Univ Tradit Chinese Med, Sch Management, Tianjin 301617, Peoples R China
来源
SCIENCEASIA | 2021年 / 47卷 / 01期
基金
中国国家自然科学基金;
关键词
ginkgolic acid; hepatocellular carcinoma; G0/G1 cell cycle arrest; p38; MAPK; TUMOR PROGRESSION; SIGNAL TRANSDUCER; CANCER; PATHWAYS; KINASE; SUPPRESSES; SORAFENIB; MORTALITY; APOPTOSIS; AUTOPHAGY;
D O I
10.2306/scienceasia1513-1874.2021.001
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatocellular carcinoma (HCC) is a common cancer worldwide with high morbidity and mortality. Ginkgolic acid (GA) is a natural compound obtained from leaves and seed coats of Ginkgo biloba L., and it has been reported to have various bioactivities. However, the effects of GA on HCC cell cycle distribution and the mechanisms involved are still unknown. By CCK-8 assay and Transwell assay, the cell viability and migration of HCC cells were shown to be inhibited significantly by GA in a concentration-dependent manner. By cell cycle analysis and western blot, the cell cycle arrest at G0/G1 phase was shown to contribute to the inhibitory effects of GA. Furthermore, the phosphorylation of p38 MAPK was found to be elevated upon GA treatment as analyzed by western blot. Thus, GA inhibited cell proliferation and migration of HCC cells by inducing G0/G1 cell cycle arrest via p38 MAPK activation, indicating GA as an agent candidate for HCC treatment.
引用
收藏
页码:11 / 18
页数:8
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