MiRNA-183-5p promotes cell proliferation and inhibits apoptosis in human breast cancer by targeting the PDCD4

被引:90
|
作者
Cheng, Yan [1 ]
Xiang, Guixian [1 ]
Meng, Yanbo [1 ]
Dong, Runzhi [2 ]
机构
[1] Xingtai Med Coll, Dept Pharmacol, 618 Gangtie Rd, Xingtai 054000, Hebei Province, Peoples R China
[2] Xingtai Peoples Hosp, Dept Tradit Chinese Med, Xingtai 054000, Peoples R China
关键词
miR-183-5p; PDCD4; Cell proliferation; Cell cycle; Apoptosis; Breast cancer; TUMOR-SUPPRESSOR PDCD4; HEPATOCELLULAR-CARCINOMA CELLS; DEATH; 4; DOWN-REGULATION; GASTRIC-CANCER; INVASION; EXPRESSION; MIGRATION; MICRORNA; CONSEQUENCES;
D O I
10.1016/j.repbio.2016.07.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAS are often aberrantly expressed in breast cancer and postulated to play a causal role in the onset and maintenance of breast cancer by binding to its target mRNA. Here, we evaluated the effects of miRNA-183-5p on cell proliferation and apoptosis which attempted to elucidate the potential role of miR-183-5p/PDCD4 axis in human breast cancer. We found that the miR-183-5p expression level was extremely promoted in breast cancer in comparison with the adjacent normal tissues. Overexpression of miR-183-5p significantly enhanced the cell proliferation and inhibited cell apoptosis in MCF-7 and MDA-MB-231 cells. Moreover, PDCD4 was predicted as a putative target of miR-183-5p by bioinformatic approaches, and miR-183-5p negatively regulated the expression of PDCD4. Furthermore, knockdown of PDCD4 suppressed expression of p21 and p27, which was consistent with the result of the attachment of miR-183-5p. These data collectively demonstrate that miR-183-5p exerts oncomiRs effects in breast cancer, and may have broad impacts on the field of using antimiRs as anti-cancer drugs for breast cancer. (C) 2016 Published by Elsevier Sp. z o.o. on behalf of Society for Biology of Reproduction & the Institute of Animal Reproduction and Food Research of Polish Academy of Sciences in Olsztyn.
引用
收藏
页码:225 / 233
页数:9
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