FENG Hong-lei, et al. The effects of BMP9 expressions on proliferation and apoptosis of human breast cancer cell line MDA-MB-231. [J]. Journal of Chongqing Medical University 35(11):1619-1623(2010)
FENG Hong-lei, et al. The effects of BMP9 expressions on proliferation and apoptosis of human breast cancer cell line MDA-MB-231. [J]. Journal of Chongqing Medical University 35(11):1619-1623(2010) DOI: 10.13406/j.cnki.cyxb.2010.11.032.
The effects of BMP9 expressions on proliferation and apoptosis of human breast cancer cell line MDA-MB-231
腺病毒感染后第3 d MDA-MB-231/BMP9组细胞凋亡百分率(31.55%±8.26%)明显高于MDA-MB-231/GFP组(3.80%±0.46%)(P<0.05)。结论:提示BMP9可通过阻滞细胞周期进程和诱导细胞凋亡来抑制乳腺癌细胞MDA-MB-231的增殖。
Abstract
Objective:To investigate the effects of bone morphogenetic protein 9 on the proliferation
cell cycle and apoptosis of breast cancer cell line MDA-MB-231.Methods:The expression of BMP9 in high-metastatic cell line MDA-MB-231 and low-metastatic cell line MCF-7 were detected by Semi-quantitative PCR respectively
MDA-MB-231 were transfected with AdBMP9(as experimental groups) and AdGFP(as control groups) respectively
Then the ability of cell proliferation was detected by MTT
cell cycle and apoptosis were detected by flow cytometry.Results:The BMP9 mRNA was not detected in human breast cancer cell line MDA-MB-231.After transfection with AdBMP9
the MDA-MB-231 cells showed an inhibited proliferation
On the fifth day
the growth rate of experimental groups(0.886 0±0.053 2)was significantly lower than that of control groups(1.224 0±0.103 1)(P<0.05);The results of flow cytometry showed that
BMP9 could induce the cell cycle arrest in MDA-MB-231
On the second day and third day after transfection
the cell number of G2/M phase increased significantly
which were 3.2 fold and 2.4 fold that of control groups respectively;It’s also found that after 72h treatment
the apoptosis rate of experimental groups(31.55%±8.26%) was significantly higher than that of control group(3.80%±0.46%)(P<0.05).Conclusion:These data demonstrated that BMP9 could inhibit the proliferation of MDA-MB-231 by blocking cell cycle and inducing apoptosis.