LncRNA ADAMTS9-AS2 inhibits cell proliferation and decreases chemoresistance in clear cell renal cell carcinoma via the miR-27a-3p/FOXO1 axis

被引:46
|
作者
Song, Er-lin [1 ]
Xing, Li [2 ]
Wang, Liang [3 ]
Song, Wen-ting [4 ]
Li, Dan-bin [1 ]
Wang, Yi [1 ]
Gu, Yi-wei [1 ]
Liu, Ming-ming [5 ]
Ni, Wen-jun [1 ]
Zhang, Peng [6 ]
Ma, Xin [6 ]
Zhang, Xu [6 ]
Yao, Jie [7 ]
Chen, Yang [8 ]
An, Rui-hua [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Urinary Surg, Harbin 150007, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 1, Dept Nephrol, Harbin 150007, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Affiliated Hosp 1, Med Dept, Harbin 150007, Heilongjiang, Peoples R China
[4] Harbin Med Univ, Heilongjiang Acad Med Sci, Harbin 150081, Heilongjiang, Peoples R China
[5] Harbin Med Univ, Affiliated Hosp 1, Dept Endocrinol, Harbin 150007, Heilongjiang, Peoples R China
[6] Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Med Acad, Dept Urol, Beijing 100036, Peoples R China
[7] Wuhan Univ, Zhongnan Hosp, Dept Urol Surg, Wuhan 430071, Hubei, Peoples R China
[8] Beijing ChuiYangLiu Hosp, Dept Hematol & Med Oncol, Beijing 100022, Peoples R China
来源
AGING-US | 2019年 / 11卷 / 15期
基金
中国博士后科学基金;
关键词
ADAMTS9-AS2; miR-27a-3p; renal cell carcinoma; chemoresistance; proliferation; FOXO1; LONG NONCODING RNAS; CANCER; EXPRESSION; PROMOTES; INVASION; FOXO1; METASTASIS; BIOMARKERS; RESISTANCE; MIGRATION;
D O I
10.18632/aging.102154
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Accumulating evidence reveals the principal role of long noncoding RNAs in the progression of clear cell renal cell carcinoma (ccRCC). However, little is known about the underlying mechanism of ADAM metallopeptidase with thrombospondin type 1 motif, 9 antisense RNA 2 (ADAMTS9-AS2) in ccRCC. Here, bioinformatics analyses verified ADAMTS9-AS2 is a long noncoding RNA and its high expression was associated with better prognosis of ccRCC. ADAMTS9-AS2 was clearly downregulated in ccRCC clinical samples and cell lines. Clinical data showed low-expressed ADAMTS9-AS2 was correlated with worse overall survival in ccRCC patients. Next, miR-27a-3p was identified as an inhibitory target of ADAMTS9-AS2 by dual-luciferase reporter and RNA immunoprecipitation assays. Both overexpressed ADAMTS9-AS2 and underexpressed miR-27a-3p in ccRCC cell lines led to the inhibition of cell proliferation and the reduction of chemoresistance. Additionally, Forkhead Box Protein O1 (FOXO1) was confirmed as the inhibitory target of miR-27a-3p. Induced by ADAMTS9-AS2 overexpression, cell proliferation and chemoresistance exhibited an obvious reduction, FOXO1 expression showed an evident increase, but all were reversed after miR-27a-3p was simultaneously overexpressed. Collectively, these results suggest ADAMTS9-AS2 inhibits the progression and impairs the chemoresistance of ccRCC via miR-27a-3p-mediated regulation of FOXO1 and may serve as a prognostic biomarker and therapeutic target for ccRCC.
引用
收藏
页码:5705 / 5725
页数:21
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