2010Journal of Hunan Normal UniversityRequires access

Induction of Apoptosis in Human Cervical Cancer HeLa Cells by Casticin

Sheng Xi

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Abstract

Objective To investigate the effects of casticin(CAS) on apoptosis of human cervical cancer HeLa cell line.Methods Human cervical cancer HeLa cells were cultured in vitro.Histone/DNA fragments in medium were determined using ELISA assay.The percentage of the sub-G1 population was determined by flow cytometry of PI fluorescence staining.Caspase-3 activity in HeLa cells was examined using ELISA assay.Results CAS significantly increased leakage of the histone/DNA fragments in HeLa cell line(P0.05),in a concentration-dependent manner.Meanwhile,CAS significantly promoted the increase of the percentage of the sub-G1 cell population in human cervical cancer HeLa cells(P0.05).CAS effectively activated Caspase-3 in human cervical cancer HeLa cells(P 0.05),in a concentration-dependent manner.Conclusion CAS can effectively induce apoptosis of human cervical cancer HeLa cells.

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Objective To investigate the effects of casticin(CAS) on apoptosis of human cervical cancer HeLa cell line.Methods Human cervical cancer HeLa cells were cultured in vitro.Histone/DNA fragments in medium were determined using ELISA assay.The percentage of the sub-G1 population was determined by flow cytometry of PI fluorescence staining.Caspase-3 activity in HeLa cells was examined using ELISA assay.Results CAS significantly increased leakage of the histone/DNA fragments in HeLa cell line(P0.05),in a concentration-dependent manner.Meanwhile,CAS significantly promoted the increase of the percentage of the sub-G1 cell population in human cervical cancer HeLa cells(P0.05).CAS effectively activated Caspase-3 in human cervical cancer HeLa cells(P 0.05),in a concentration-dependent manner.Conclusion CAS can effectively induce apoptosis of human cervical cancer HeLa cells.

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Available abstract

Objective To investigate the effects of casticin(CAS) on apoptosis of human cervical cancer HeLa cell line.Methods Human cervical cancer HeLa cells were cultured in vitro.Histone/DNA fragments in medium were determined using ELISA assay.The percentage of the sub-G1 population was determined by flow cytometry of PI fluorescence staining.Caspase-3 activity in HeLa cells was examined using ELISA assay.Results CAS significantly increased leakage of the histone/DNA fragments in HeLa cell line(P0.05),in a concentration-dependent manner.Meanwhile,CAS significantly promoted the increase of the percentage of the sub-G1 cell population in human cervical cancer HeLa cells(P0.05).CAS effectively activated Caspase-3 in human cervical cancer HeLa cells(P 0.05),in a concentration-dependent manner.Conclusion CAS can effectively induce apoptosis of human cervical cancer HeLa cells.

Key concepts: HeLa, Apoptosis, Flow cytometry, Molecular biology, Population, Cell culture, Cell, Cervical cancer

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