中国癌症杂志 ›› 2014, Vol. 24 ›› Issue (7): 517-520.doi: 10.3969/j.issn.1007-3969.2014.07.007

• 论著 • 上一篇    下一篇

miR-340对乳腺癌MDA-MB231细胞增殖和凋亡的影响

欧阳倩雯,曹亚丽   

  1. 江西省南昌市第三医院乳腺科,江西 南昌 330009
  • 出版日期:2014-07-30 发布日期:2014-07-29
  • 通信作者: 曹亚丽 E-mail:364590189@qq.com

The effect of miR-340 on proliferation and apoptosis of breast cancer cell MDA-MB231

OUYANG Qian-wen,CAO Ya-li   

  1. Department of Breast Surgery, the Third Hospital of Nanchang, Nanchang Jiangxi 330009, China
  • Published:2014-07-30 Online:2014-07-29
  • Contact: CAO Ya-li E-mail: 364590189@qq.com

摘要:

背景与目的:既往研究表明,微小RNA-340(miR-340)能负性调控多种肿瘤的进展,但其在乳腺癌细胞增殖和凋亡中的研究较少,本研究旨在探讨miR-340对乳腺癌MDA-MB231细胞增殖和凋亡的作用。方法:利用脂质体LipofectamineTM2000pre-miR-340anti-miR-340瞬时转染至乳腺癌MDA-MB231细胞,通过RT-PCR检测miR-340 mRNA的水平,蛋白质印迹法(Western blot)检测cleaved-caspase-3蛋白的表达,MTT比色法检测细胞增殖的抑制情况,流式细胞仪检测细胞凋亡。结果:Pre-miR-340增加了MDA-MB231细胞中miR-340表达,同时增加cleaved-caspase-3蛋白表达、抑制MDA-MB231细胞增殖并促进其凋亡。而anti-miR-340抑制了MDAMB231细胞中miR-340表达,并且抑制cleaved-caspase-3蛋白表达,促进了MDA-MB231细胞增殖,抑制了MDAMB231细胞的凋亡。结论:miR-340转染后能上调MDA-MB231细胞中cleaved-caspase-3蛋白的表达从而抑制细胞增殖,促进其凋亡。

关键词: 乳腺癌MDA-MB231细胞, miR-340, 增殖, 凋亡

Abstract:

Background and purpose: MicroRNA-340 (miR-340) has been demonstrated to play a role of negative regulation in many kinds of tumor, however, there are few reports about the relationship between miR-340 in proliferation and apoptosis of breast cancer cell. This study was aimed to explore the effect of miR-340 on proliferation and apoptosis of breast cancer cell MDA-MB231. Methods: The pre-miR-340 or anti-miR-340 were transiently transfected into breast cancer cell MDA-MB231 with LipofectamineTM2000. miR-340 level was detected by RT-PCR. The Western blot was performed to detect the protein level of cleaved-caspase-3. The inhibition rate of cell proliferation was evaluated by MTT assay. The cell apoptosis was studied by flow cytometry. Results: The pre-miR-340 facilitated the expression of miR-340 in MDA-MB231 cells. The pre-miR-340 enhanced the protein level of cleaved-caspase-3, inhibited the proliferation of MDA-MB231 cells and increased its apoptosis. On the contrary, the expression of miR-340 was inhibited by anti-miR-340 in MDA-MB231 cells. The protein level of cleaved-caspase-3 was reduced after the antimiR-340-transfected MDA-MB231 cells. Anti-miR-340 promoted the proliferation of MDA-MB231 cells. Decreased apoptosis of MDA-MB231 cells was observed by flow cytometry. Conclusion: The overexpression of miR-340 can effectively inhibit the proliferation and increase the apoptosis of MDA-MB231 cells, which may be explained by upregulating of protein cleaved-caspase-3 level.

Key words: Breast cancer cell MDA-MB231, miR-340, Proliferation, Apoptosis