Upregulation of Limk1 caused by microRNA-138 loss aggravates the metastasis of ovarian cancer by activation of Limk1/cofilin signaling

被引:53
|
作者
Chen, Puxiang [1 ]
Zeng, Mengjun [1 ]
Zhao, Yan [1 ]
Fang, Xiaolin [1 ]
机构
[1] Cent S Univ, Dept Gynecol & Obstet, Xiangya Hosp 2, Changsha 410011, Hunan, Peoples R China
关键词
ovarian cancer; LIM kinase 1; miR-138; metastasis; cofilin; Talen technology; SQUAMOUS-CELL CARCINOMA; DOWN-REGULATION; KINASE; INVASION; MIR-138; GROWTH; LINES; CHEMOTHERAPY; MIGRATION; PATHWAY;
D O I
10.3892/or.2014.3461
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
LIM kinase 1 (Limk1) is associated with cell proliferation and metastasis and its dysregulated expression has been observed in many types of cancer. The present study aimed to examine the role of Limk1 in the development of ovarian cancer, as well as the underlying molecular mechanism involved. The results showed that increased Limk1 and decreased miR-138 expression co-existed in ovarian cancer. Furthermore, knockout of Limk1 or the overexpression of miR-138 resulted in reduced cell invasion and migration, while silencing of miR-138 led to enhancement of the invasion and migration of ovarian cancer cells. Cell growth was inhibited by the overexpression of miR-138, although not by the knockout of Limk1. miR-138 directly targeted Limk1 and inhibited ovarian cancer cell growth by PCNA and Bc1-2. Moreover, Limk1/cofilin/p-cofilin is likely a critical signaling pathway involving in miR-138 modulation of ovarian cancer cell metastasis. The results provide evidence supporting miR-138/Limk1 as a novel diagnostic or therapeutic target for ovarian cancer.
引用
收藏
页码:2070 / 2076
页数:7
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