Wang Hai-Yan, Yu Hai-Zhong, Huang Sheng-Mou, Zheng Yu-Lan
Department of Chemical Engineering and Food Science, Hubei University of Arts and Science, Xiangyang, Hubei 441053, P.R. China.
Department of Respiratory Disease, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, Hubei 441021, P.R. China.
Mol Med Rep. 2016 Oct;14(4):3855-61. doi: 10.3892/mmr.2016.5696. Epub 2016 Aug 31.
The present study aimed to investigate the effects of berberine hydrochloride on the proliferation and apoptosis of HeLa229 human cervical cancer cells. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was performed to examine the cytotoxicity of berberine hydrochloride against HeLa229 cells. The effects of berberine hydrochloride on the apoptosis of HeLa229 cells was detected by immunofluorescence and flow cytometry, and the mRNA expression levels of p53, B‑cell lymphoma 2 (Bcl‑2) and cyclooxygenase‑2 (cox‑2) were analyzed by reverse transcription-quantitative polymerase chain reaction. Berberine hydrochloride inhibited the proliferation of HeLa229 cells in a dose‑dependent manner; minimum cell viability (3.61%) was detected following treatment with 215.164 µmol/l berberine hydrochloride and the half maximal inhibitory concentration value was 42.93 µmol/l following treatment for 72 h. In addition, berberine hydrochloride induced apoptosis in HeLa229 cells in a dose‑ and time‑dependent manner. Berberine hydrochloride upregulated the mRNA expression levels of p53, and downregulated mRNA expression levels of Bcl‑2 and cox‑2, in a dose‑dependent manner. In conclusion, berberine hydrochloride inhibited the proliferation and induced apoptosis of HeLa229 cells, potentially via the upregulation of p53 and the downregulation of Bcl‑2 and cox‑2 mRNA expression levels.
本研究旨在探讨盐酸小檗碱对HeLa229人宫颈癌细胞增殖和凋亡的影响。采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐法检测盐酸小檗碱对HeLa229细胞的细胞毒性。通过免疫荧光和流式细胞术检测盐酸小檗碱对HeLa229细胞凋亡的影响,并采用逆转录-定量聚合酶链反应分析p53、B细胞淋巴瘤2(Bcl-2)和环氧合酶-2(cox-2)的mRNA表达水平。盐酸小檗碱以剂量依赖性方式抑制HeLa229细胞的增殖;用215.164 μmol/l盐酸小檗碱处理后检测到最低细胞活力(3.61%),处理72 h后的半数最大抑制浓度值为42.93 μmol/l。此外,盐酸小檗碱以剂量和时间依赖性方式诱导HeLa229细胞凋亡。盐酸小檗碱以剂量依赖性方式上调p53的mRNA表达水平,下调Bcl-2和cox-2的mRNA表达水平。综上所述,盐酸小檗碱可能通过上调p53以及下调Bcl-2和cox-2 mRNA表达水平来抑制HeLa229细胞的增殖并诱导其凋亡。