The study of the apoptosis induced by EPA on human colon cancer SW480 cells
Xiangqun Wang, Lijuan Chen, Qing Hua Zhang, Dan Wu, Junhua Luo
Abstract
Xiangqun Wang, Lijuan Chen, Qing Hua Zhang, Dan Wu, Junhua Luo
Abstract
Objective To investigate the effect of eicosapentaenoic acid(EPA) on the apoptosis of human colon cancer SW480 cells and the mechanisms. Methods Mitochondrial membrane potential was detected, the quantity of cytochrome C was analyzed by Elisa kit, and the expression of cleaved caspase-9 and caspase-3 was detected by Western Blot. Results After treatment with EPA(0μg/mL, 42.1μg/mL, 84.2μg/mL, 168.4μg/mL), the mitochondrial membrane potential(Δψm) of SW480 cells were declined(P<0.05), the values were (99.71±0.04)%, (95.04±0.10)%, (88.65±0.41)% and (73.60±1.20)%(t=5.161, 6.302, 4.601, 5.198, all P<0.05). The quantity of cytochrome C in cytosol was increased significantly compared with no treatment group, and the values were (12.8±1.2)ng/mL, (115.5±3.5)ng/mL, (290.5±5.2)ng/mL and (262.0±12.5)ng/mL in different EPA treatment groups(t=6.345, 6.013, 5.846, 4.613, all P<0.01). The expression of cleaved caspase-9 and caspase-3 were significantly increased. Conclusion EPA inhibits SW480 cells growth and induces apoptosis in a dose dependent manner.This action may be mediated by mitochondria-mediated intrinsic apoptosis pathway, cytochrome C release, and caspase-9 and caspase-3 activation. Key words: Colon tumor; Twenty carbon five acid; SW480 cells; Cell apoptosis
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the effect of eicosapentaenoic acid(EPA) on the apoptosis of human colon cancer SW480 cells and the mechanisms. Methods Mitochondrial membrane potential was detected, the quantity of cytochrome C was analyzed by Elisa kit, and the expression of cleaved caspase-9 and caspase-3 was detected by Western Blot. Results After treatment with EPA(0μg/mL, 42.1μg/mL, 84.2μg/mL, 168.4μg/mL), the mitochondrial membrane potential(Δψm) of SW480 cells were declined(P<0.05), the values were (99.71±0.04)%, (95.04±0.10)%, (88.65±0.41)% and (73.60±1.20)%(t=5.161, 6.302, 4.601, 5.198, all P<0.05). The quantity of cytochrome C in cytosol was increased significantly compared with no treatment group, and the values were (12.8±1.2)ng/mL, (115.5±3.5)ng/mL, (290.5±5.2)ng/mL and (262.0±12.5)ng/mL in different EPA treatment groups(t=6.345, 6.013, 5.846, 4.613, all P<0.01). The expression of cleaved caspase-9 and caspase-3 were significantly increased. Conclusion EPA inhibits SW480 cells growth and induces apoptosis in a dose dependent manner.This action may be mediated by mitochondria-mediated intrinsic apoptosis pathway, cytochrome C release, and caspase-9 and caspase-3 activation. Key words: Colon tumor; Twenty carbon five acid; SW480 cells; Cell apoptosis
Key concepts: Cytochrome c, Apoptosis, Western blot, Eicosapentaenoic acid, Mitochondrion, Molecular biology, Medicine, Caspase-9