Toosendanin induces apoptosis in human gastric cancer SGC-7901 cells through mitochondrial and death receptor pathways

被引:0
作者
Fu, Xue-Peng [1 ]
He, Meng-Qi [1 ]
Miao, Chang-Jiu [1 ]
Sun, Ying-Ning [1 ,2 ]
Zhang, Wei-Wei [1 ,2 ]
Shao, Shu-Li [1 ,2 ]
机构
[1] Qiqihar Univ, Coll Life Sci & Agr & Forestry, Qiqihar 161006, Peoples R China
[2] Heilongjiang Prov Key Lab Resistance Gene Engn & P, Qiqihar 161006, Peoples R China
基金
中国国家自然科学基金;
关键词
toosendanin; SGC-7901; cells; apoptosis; gastric cancer; SUPPRESSION; GROWTH; CYCLE;
D O I
暂无
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
Toosendanin (TSN) is a triterpenoid derivative which exerts anti-cancer effects on various cancer cell lines. However, it is still not clear whether TSN has similar anti-cancer effects on gastric cancer. In the present study the effects of TSN on human gastric cancer SGC-7901 cells were investigated by trypan blue exclusion, inverted microscopy, confocal microscopy and flow cytometric analysis. The results show that TSN significantly inhibits the proliferation of SGC-7901 cells in a dose-and time-dependent manner. In addition, TSN induces the formation of apoptotic bodies, increases the apoptosis rate and decreases the mitochondrial membrane potential in the SGC-7901 cells, indicating that TSN can induce apoptosis in gastric cancer cells. Further analysis shows that expression of the genes, Bax, cytochrome c and Fas is increased by TSN, whereas Bcl-2 and PARP expression is reduced. Furthermore, the effects of TSN on activation of caspase-3, caspase-8 and caspase-9 indicate that the mitochondrial and death receptor pathways are involved in the TSN-induced apoptosis. These results suggest that TSN may be an effective candidate agent for treating gastric cancer.
引用
收藏
页码:40 / 54
页数:15
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