The Effect Induced by Arsenic Trioxide on Human Cervical Carcinoma Hela Cell Lines
Chen Zhong-dong
Abstract
Chen Zhong-dong
Abstract
Objective To study the effect induced by 1.0,2.0,3.0 μmol/L arsenic trioxide(As2O3) on human cervical carcinoma Hela cell lines.Methods Hela cell lines were treated by 1.0,2.0,3.0 μmol/L As2O3.Cell proliferation was evaluated by MTT assay.Flow cytometry was used to examine apoptosis on cervical carcinoma Hela cell lines.The expression of Bcl-2 protein and Bax protein were investigated by immunohistochemical SABC techniques.Results MTT assay showed that As2O3 inhibited human cervical carcinoma Hela cell lines growth in vitro in a dose and time-dependent manner.Flow cytometry showed that As2O3 induced the apoptosis in a dose and time-dependent manner(P0.05).Immunohistochemical SABC techniques showed that As2O3 can downregulate the expression of Bcl-2 protein and upregulate the expression of Bax protein(P0.05).Conclusions As2O3 can significantly inhibit Hela cells growth and p roliferation and induce their apoptosis.The reason of these changes may be the downregulation expression of Bcl-2 protein and upregulation expression of Bax protein.
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 study the effect induced by 1.0,2.0,3.0 μmol/L arsenic trioxide(As2O3) on human cervical carcinoma Hela cell lines.Methods Hela cell lines were treated by 1.0,2.0,3.0 μmol/L As2O3.Cell proliferation was evaluated by MTT assay.Flow cytometry was used to examine apoptosis on cervical carcinoma Hela cell lines.The expression of Bcl-2 protein and Bax protein were investigated by immunohistochemical SABC techniques.Results MTT assay showed that As2O3 inhibited human cervical carcinoma Hela cell lines growth in vitro in a dose and time-dependent manner.Flow cytometry showed that As2O3 induced the apoptosis in a dose and time-dependent manner(P0.05).Immunohistochemical SABC techniques showed that As2O3 can downregulate the expression of Bcl-2 protein and upregulate the expression of Bax protein(P0.05).Conclusions As2O3 can significantly inhibit Hela cells growth and p roliferation and induce their apoptosis.The reason of these changes may be the downregulation expression of Bcl-2 protein and upregulation expression of Bax protein.
Key concepts: HeLa, Arsenic trioxide, Apoptosis, Flow cytometry, Downregulation and upregulation, Immunohistochemistry, MTT assay, Cell culture