期刊
ENVIRONMENTAL TOXICOLOGY
卷 31, 期 12, 页码 1899-1908出版社
WILEY-BLACKWELL
DOI: 10.1002/tox.22191
关键词
bidemethoxycurcumin; mitochondria; ER stress; apoptosis; NCI H-460 cells
资金
- China Medical University Hospital [DMR-101-051]
Curcuminoids are the major natural phenolic compounds found in the rhizome of many Curcuma species. Curcuminoids consist of a mixture of curcumin, demethoxycurcumin (DMC), and bisdemethoxycurcumin (BDMC). Although numerous studies have shown that curcumin induced cell apoptosis in many human cancer cells, however, mechanisms of BDMC-inhibited cell growth and - induced apoptosis in human lung cancer cells still remain unclear. Herein, we investigated the effect of BDMC on the cell death via the cell cycle arrest and induction of apoptosis in NCI H460 human lung cancer cells. Flow cytometry assay was used to measure viable cells, cell cycle distribution, the productions of reactive oxygen species (ROS) and Ca2+, mitochondrial membrane potential (Delta Psi(m)) and caspase-3, -8 and -9 activity. DNA damage and condension were assayed by Comet assay and DAPI staining, respectively. Western blotting was used to measure the changes of cell cycle and apoptosis associated protein expressions. Results indicated that BDMC significantly induced cell death through induced S phase arrest and induced apoptosis. Moreover, DMC induced DNA damage and condension, increased ROS and Ca2+ productions and decreased the levels of Delta Psi(m) and promoted activities caspase-3, -8, and -9. Western blotting results showed that BDMC inhibited Cdc25A, cyclin A and E for causing S phase arrest, furthermore, promoted the expression of AIF, Endo G and PARP and the levels of Fas ligand (Fas L) and Fas were also upregulated. Results also indicated that BDMC increased ER stress associated protein expression such as GRP78, GADD153, IRE1 alpha, IRE1 beta, ATF-6 alpha, ATF-6 beta, and caspase-4. Taken together, we suggest that BDMC induced cell apoptosis through multiple signal pathways such as extrinsic, intrinsic and ES tress pathway. (C) 2015 Wiley Periodicals, Inc.
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