Effect and Underlying Mechanism of Piperlongumine on Proliferation and Apoptosis of Human Gastric Cancer Cell Line MKN45
10.3969/j.issn.1008-7125.2016.02.002
- VernacularTitle:荜茇酰胺对人胃癌细胞株 MKN45增殖、凋亡的影响及其机制研究
- Author:
Chaoqin DUAN
;
Chao DENG
;
Xiaoping ZOU
- Publication Type:Journal Article
- Keywords:
Piperlongumine;
Reactive Oxygen Species;
Tumor Suppressor Protein p53;
Caspases;
Apoptosis;
Stomach Neoplasms
- From:
Chinese Journal of Gastroenterology
2016;21(2):69-74
- CountryChina
- Language:Chinese
-
Abstract:
Background:Recently,studies have shown that piperlongumine( PL)selectively killed cancer cells by elevating reactive oxygen species(ROS)in various cancers. However,the effect of PL on gastric cancer cells remained to be further studied. Aims:To investigate the effect of PL on proliferation and apoptosis of human gastric cancer cell line MKN45 and its underlying mechanism. Methods:MKN45 cells were treated with different doses of PL,caspase inhibitor,antioxidant, and their combinations,respectively. Cell viability was assessed by CCK-8 assay;cell cycle,apoptosis and intracellular ROS level were measured by flow cytometry;and Western blotting was employed to determine the expression of apoptosis-related proteins( XIAP,cleaved-caspase3,7,9 and cleaved-PARP),p53 and its downstream target genes( p21, GADD45α and PUMA). Results:PL inhibited the proliferation of MKN45 cells in a dose- and time-dependent manner. In MKN45 cells treated with PL,the proportion of cells in G1 phase,apoptotic rate and intracellular ROS level were significantly increased,the expression of inhibitor of apoptosis protein XIAP was down-regulated,and the caspase-dependent apoptosis pathway,p53 and its downstream target genes were activated. Pretreatment with antioxidant NAC or Z-VAD-FMK, a general caspase inhibitor could partially abolish the effect of PL on ROS production and its antitumor effect. Conclusions:PL can inhibit cell proliferation and induce cell cycle G1 phase arrest and apoptosis in MKN45 cells. Its antitumor effect may be associated with a ROS-mediated p53 activation and subsequent triggering of caspases cascade of cell apoptosis.
