RETRACTED: MiR-137 suppresses tumor growth and metastasis in clear cell renal cell carcinoma (Retracted Article)

被引:13
|
作者
Wang, Meizhi [1 ]
Gao, Hui [2 ]
Qu, Haijun [3 ]
Li, Jing [3 ]
Liu, Kaili [2 ]
Han, Zhiwu [3 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Crit Care Med, Qingdao, Peoples R China
[2] Qingdao Univ, Sch Pharm, Dept Pharmacol, Qingdao, Peoples R China
[3] Qingdao Univ, Affiliated Hosp, Dept Pharm, Qingdao, Peoples R China
关键词
miR-137; ccRCC; RLIP76; INHIBITS PROLIFERATION; INTERFERON-ALPHA; MELANOMA-CELLS; RLIP76; LUNG; TRANSPORT; EXPRESSION; SUNITINIB; APOPTOSIS; INVASION;
D O I
10.1016/j.pharep.2018.04.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The most frequent type of renal cell carcinoma is called clear-cell renal cell carcinoma (ccRCC) which is associated with a poor prognosis. It has been observed that miR-137 is aberrantly expressed in many different kinds of human malignancies including ccRCC. This research aims to examine the role of miR-137 in ccRCC. Methods: Quantitative RT-PCR (qRT-PCR) was applied to measure miR-137 expression in ccRCC and adjacent noncancerous tissue. Gene expression was determined by western blot. Cell Counting Kit-8 (CCK-8) assay, flow cytometry and Transwell assay were used to determine the effects of miR-137 on cell growth, apoptosis and invasion, respectively. Moreover, xenograft and pulmonary metastasis animal models were established to investigate the role of miR-137 in vivo. Results: Our findings show that there was significant downregulation of miR-137 in ccRCC tissue relative to corresponding non-cancerous tissue. Ectopic miR-137 expression in ccRCC cells led to suppression of cell growth and invasion, as well as apoptosis induction. In contrast, knockdown of miR-137 enhances proliferation and invasion, inhibits apoptosis. It also confirms that miR-137 plays a tumor supressor role in vivo. Mechanically, miR-137 directly targets the 30-UTR of RLIP76 which is an established oncogene in ccRCC. Conclusion: MiR-137 serves as a tumor suppressor, which can be considered a potential therapeutic target in ccRCC. (c) 2018 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:963 / 971
页数:9
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