miR-3188 Regulates Cell Proliferation, Apoptosis, and Migration in Breast Cancer by Targeting TUSC5 and Regulating the p38 MAPK Signaling Pathway

被引:21
|
作者
Chen, Xiaowen [1 ]
Chen, Jianli [2 ]
机构
[1] Guangdong Med Coll, Affiliated Hosp, Dept Oncol Ctr, Zhanjiang, Guangdong, Peoples R China
[2] Xinxiang Med Univ, Affiliated Hosp 3, Dept Med Oncol 3, 679 Xiangyang Rd, Xinxiang 453000, Henan, Peoples R China
关键词
Breast cancer; miR-3188; Cell proliferation; Cell migration; Apoptosis; MESSENGER-RNA; EXPRESSION; METASTASIS; SURVIVAL; DISEASE; GENES; ALPHA; PTEN; P27;
D O I
10.3727/096504017X14953948675421
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study intended to investigate the effects of miR-3188 on breast cancer and to reveal the possible molecular mechanisms. miR-3188 was upregulated and TUSC5 was downregulated in breast cancer tissues and MCF-7 cells compared to normal tissue and MCF-10 cells. After MCF-7 cells were transfected with miR-3188 inhibitor. cell proliferation and migration were inhibited, whereas apoptosis was promoted. Luciferase reporter assay suggested that TUSC5 was a target gene of miR-3188. In addition, miR-3188 overexpression increased the p-p38 expression, while miR-3188 suppression decreased the p-p38 expression significantly. miR-3188 regulated breast cancer progression via the p38 MAPK signaling pathway. In conclusion. miR-3188 affects breast cancer cell proliferation, apoptosis, and migration by targeting TUSC5 and activating the p38 MAPK signaling pathway. miR-3188 may serve as a potential therapeutic agent for the treatment of breast cancer.
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页码:363 / 372
页数:10
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