Identification of miR-200a as a novel suppressor of connexin 43 in breast cancer cells

被引:15
|
作者
Ming, Jia [1 ]
Zhou, Yan [2 ]
Du, Junze [2 ]
Fan, Shenghao [1 ]
Pan, Beibei [1 ]
Wang, Yinhuan [1 ]
Fan, Lingjun [2 ]
Jiang, Jun [2 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 2, Dept Breast Thyroid & Pancreas Surg, Chongqing 400010, Peoples R China
[2] Third Mil Med Univ, Affiliated Hosp 1, Breast Dis Ctr, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; connexin 43 (Cx43); metastasis; micro ribonucleic acid (miR)-200a; micro ribonucleic acid (miR)-1; 3 '-untranslated region (3 '-UTR); LYMPH-NODE METASTASES; EXPRESSION; MIGRATION; MICRORNAS; NETWORK; PROTEIN; CX43; RNA;
D O I
10.1042/BSR20150153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both miRNAs (miRs) and connexin 43 (Cx43) were important regulators of the metastasis of breast cancer, whereas the miRs regulating Cx43 expression in breast cancer cells were still obscure. In the present study, we scanned and found miR-1, miR-206, miR-200a, miR-381, miR-23a/b and miR-186 were functional suppressors of human Cx43 mRNA and protein expression. Specially, we demonstrated that only miR-200a could directly target the 3'-untranslated region (3'-UTR) of human Cx43 gene. Functionally, overexpression of Cx43 in MCF cells potentiated the migration activity, whereas additional miR-200a treatment notably prevented this effect. Finally, we demonstrated that decreased levels of miR-200a and elevated expression of Cx43 in the metastatic breast cancer tissues compared with the primary ones. Thus, we are the first to identify miR-200a as a novel and direct suppressor of human Cx43, indicating that miR200a/Cx43 axis might be a useful diagnostic and therapeutic target of metastatic breast cancer.
引用
收藏
页数:9
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