miR-21 inhibition of LATS1 promotes proliferation and metastasis of renal cancer cells and tumor stem cell phenotype

被引:28
作者
An, Feng [1 ]
Liu, Yidong [2 ]
Hu, Yan [2 ]
机构
[1] Hebei Univ, Affiliated Hosp, Dept Urinary Surg, Baoding, Hebei 071000, Peoples R China
[2] Taian City Cent Hosp, Dept Urinary Surg, 29 Longtan Rd, Tai An 271000, Shandong, Peoples R China
关键词
miR-21; large tumor suppressor gene 1; renal cancer; tumor stem cell; HIPPO SIGNALING PATHWAY; DOWN-REGULATION; EXPRESSION; HYPERMETHYLATION; MICRORNA-21; CARCINOMA;
D O I
10.3892/ol.2017.6746
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
MicroRNA (miR)-21 has many regulatory functions in the cell, including activities in cancer cells and cancer stem cells. Large tumor suppressor gene 1 (LATS1) is a target of miR-21 that could mediate several of these phenotypes. This study explored the effect of miR-21 silencing in renal cancer cell function and LATS1 expression. Silencing of miR-21 in Caki-2 cells reached an efficiency of 55-60%. This was sufficient to detect decrease in Caki-2 cell proliferation and migration invasion capacity. miR-21 silencing increased LATS1 expression at both mRNA and protein levels. The number of tumor spheres formed by cells expressing si-miR-21 was significantly reduced and the expression of tumor stem cell markers Nanog and CT3/ 4 were significantly downregulated. miR-21 seems to regulate LATS1 expression in renal cancer Caki-2 cells, resulting in reduced proliferation, invasion, and cancer stem cell phenotype. miR-21 may promote malignant phenotype of tumor cells through LATS1 silencing, which can be regarded as a new target candidate gene for renal cancer treatment.
引用
收藏
页码:4684 / 4688
页数:5
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