MicroRNA-375 Suppresses the Tumor Aggressive Phenotypes of Clear Cell Renal Cell Carcinomas through Regulating YWHAZ.
- Author:
Xiang ZHANG
1
;
Nai-Dong XING
2
;
Cheng-Jun LAI
3
,
4
;
Rui LIU
5
;
Wei JIAO
1
;
Jue WANG
6
;
Jie SONG
7
,
8
;
Zhong-Hua XU
1
Author Information
- Publication Type:Journal Article
- Keywords: Clear Cell Renal Cell Carcinoma; MicroRNA-375; Proliferation; YWHAZ
- MeSH: 14-3-3 Proteins; metabolism; Carcinoma, Renal Cell; pathology; Cell Line, Tumor; Cell Movement; Cell Proliferation; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; Humans; Kidney Neoplasms; pathology; MicroRNAs; physiology; Phenotype
- From: Chinese Medical Journal 2018;131(16):1944-1950
- CountryChina
- Language:English
-
Abstract:
Background:MicroRNAs (miRNAs) are key regulators during tumor initiation and progression. MicroRNA-375 (MiR-375) has been proven to play a tumor-suppressive role in various types of human malignancies; however, its biological role in clear cell renal cell carcinoma (ccRCC) remains unclear. The purpose of this study was to explore the biologic role as well as the underlying mechanism of miR-375 in ccRCC progression.
Methods:Quantitative polymerase chain reaction (qPCR) was applied to test the expression of miR-375 in tissues and cell lines by t-test. Functional experiments were used to investigate the biological role of miR-375 utilizing a gain-of-function strategy. The target of miR-375 was investigated by bioinformatic analysis and further verified by luciferase reporter assay, qPCR, Western blotting, and functional experiments in vitro.
Results:Our study demonstrated that miR-375 was significantly downregulated in ccRCC tissues (cancer vs. normal, 0.804 ± 0.079 vs. 1.784 ± 0.200, t = 5.531 P < 0.0001) and cell lines, and loss of miR-375 expression significantly associated with advanced Fuhrman nuclear grades (Grade III and IV vs. Grade I and II, 1.000 ± 0.099 vs. 1.731 ± 0.189, t = 3.262 P = 0.003). Functional studies demonstrated that miR-375 suppressed ccRCC cell proliferation, migration, and invasion (all P < 0.05 in both 786-O and A498 cell lines). Multiple miRNA target prediction algorithms indicated the well-studied oncogene YWHAZ as a direct target of miR-375, which was further confirmed by the luciferase reporter assay, qPCR, and Western blotting. Moreover, restoration of YWHAZ could rescue the antiproliferation effect of miR-375.
Conclusions:The data provide the solid evidence that miR-375 plays a tumor-suppressive role in ccRCC progression, partially through regulating YWHAZ. This study expands the antitumor profile of miR-375, and supports its role as a potential therapeutic target in ccRCC treatment.
