MicroRNA-19a and microRNA-19b promote the malignancy of clear cell renal cell carcinoma through targeting the tumor suppressor RhoB

被引:34
|
作者
Niu, Shaoxi [1 ,2 ]
Ma, Xin [1 ]
Zhang, Yu [1 ]
Liu, Yen-Nien [2 ,3 ]
Chen, Xufeng [2 ]
Gong, Huijie [1 ,4 ]
Yao, Yuanxin [1 ]
Liu, Kan [1 ]
Zhang, Xu [1 ]
机构
[1] Chinese PLA Med Acad, Chinese PLA Gen Hosp, Dept Urol, State Key Lab Kidney Dis, Beijing, Peoples R China
[2] Duke Univ, Dept Pathol, Durham, NC 27706 USA
[3] Taipei Med Univ, Coll Med Sci & Technol, Grad Inst Canc Biol & Drug Discovery, Taipei, Taiwan
[4] Beijing Univ Chinese Med, Dongzhimen Hosp, Dept Urol, Beijing, Peoples R China
来源
PLOS ONE | 2018年 / 13卷 / 02期
基金
国家高技术研究发展计划(863计划);
关键词
FARNESYLTRANSFERASE INHIBITORS; CANCER CELLS; INVASION; REVEALS; OVEREXPRESSION; TRANSFORMATION; PROLIFERATION; METASTASIS; PHENOTYPE; CLUSTER;
D O I
10.1371/journal.pone.0192790
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cell carcinoma, which shows high aggressiveness and lacks biomarkers. RhoB acts as a tumor suppressor that inhibits the progression of ccRCC. In the present study, we examined the effects of oncogenic microRNAs, miR-19a and miR-19b, on RhoB expression in ccRCC cells. The results showed that both miR-19a and miR-19b could directly target the 30untranslated region (3'UTR) of RhoB, resulting in the reduced expression of RhoB. With RT-PCR analysis, we detected the increased expression of miR-19a and miR-19b in ccRCC tissues compared to adjacent non-tumor renal tissues. These data also demonstrated an exclusive negative correlation between miR-19a/19b and RhoB expression in ccRCC specimens and cell lines. In addition, the knockdown of RhoB or overexpression of miR-19a and miR-19b in ccRCC cells could promote cell proliferation, migration and invasion. These data demonstrate the direct roles of miR-19a and miR-19b on the repression of RhoB and its consequences on tumorigenesis, cancer cell proliferation and invasiveness. These results suggest the potential clinical impact of miR-19a and miR-19b as molecular targets for ccRCC.
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页数:13
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