Tao Ming-Zhu, Gao Xia, Zhou Tie-Jun, Guo Qing-Xi, Zhang Qiang, Yang Cheng-Wan
Department of Oncology, The Affiliated Hospital of Luzhou Medical College, Luzhou, 646000, People's Republic of China.
Department of Pathology, The Affiliated Hospital of Luzhou Medical College, 25 Taiping Street, Jiangyang District, Luzhou, 646000, Sichuan, People's Republic of China.
Cell Biochem Biophys. 2015 Dec;73(3):737-41. doi: 10.1007/s12013-015-0673-x.
To investigate the effects of TGF-β1 on the proliferation and apoptosis of cervical cancer Hela cells in vitro. Human cervical cancer Hela cells were cultured in vitro and divided into the experimental and control groups. In the experimental groups, Hela cells were stimulated with different concentrations of TGF-β1 (0.01, 0.1, 1, and 10 ng/mL), while Hela cells cultured in serum-free medium without TGF-β1 were used as controls. The CCK8 method was adopted to detect the effect of TGF-β1 on Hela cell proliferation, and flow cytometry was used to determine cell apoptosis 72 h after TGF-β1 treatment. Compared with the control group, the CCK-8 tests showed that different concentrations of TGF-β1 had no obvious effect on Hela cell proliferation 24 h after treatment (P > 0.05). However, upon 48 or 72 h of treatment, TGF-β1 significantly inhibited the proliferation of Hela cells in a time- and dose-dependent manner (P < 0.05). The flow cytometry results indicated that TGF-β1 influenced the apoptosis of human cervical cancer Hela cells in a dose-dependent manner after 72 h of treatment (P < 0.05). TGF-β1 significantly inhibited the growth and induced the apoptosis of human cervical Hela cells in vitro.
探讨转化生长因子-β1(TGF-β1)对宫颈癌Hela细胞体外增殖和凋亡的影响。体外培养人宫颈癌Hela细胞并分为实验组和对照组。实验组中,用不同浓度的TGF-β1(0.01、0.1、1和10 ng/mL)刺激Hela细胞,而将在无TGF-β1的无血清培养基中培养的Hela细胞用作对照。采用CCK8法检测TGF-β1对Hela细胞增殖的影响,并在TGF-β1处理72小时后用流式细胞术测定细胞凋亡情况。与对照组相比,CCK-8检测显示,处理24小时后不同浓度的TGF-β1对Hela细胞增殖无明显影响(P>0.05)。然而,处理48或72小时后,TGF-β1以时间和剂量依赖性方式显著抑制Hela细胞的增殖(P<0.05)。流式细胞术结果表明,处理72小时后,TGF-β1以剂量依赖性方式影响人宫颈癌Hela细胞的凋亡(P<0.05)。TGF-β1在体外显著抑制人宫颈Hela细胞的生长并诱导其凋亡。