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Long Non-coding RNA PCAT1 Drives Clear Cell Renal Cell Carcinoma by Upregulating YAP Via Sponging MiR-656 and MiR-539

Overview
Journal Cell Cycle
Specialty Cell Biology
Date 2020 Apr 15
PMID 32286142
Citations 11
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Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common RCC subtype with high metastasis, poor prognosis and conventional chemotherapy resistance. Prostate cancer associated transcript 1 (PCAT1) is an important lncRNA that was reported to be involved in cell proliferation, migration and invasion of several types of cancer cells. However, its role in ccRCC is still undetermined. This study found that PCAT1 levels were elevated in ccRCC tumors as well as several ccRCC cells, and knockdown of PCAT1 with siRNA (si-PCAT1) alleviated cell proliferation, migration and invasion of Caki-2 and ACHN cells. With bioinformatics analysis, dual-luciferase reported assay, RNA pull-down assay and Spearman's correlation analysis, we demonstrated that PCAT1 acted as a sponge for miR-656 and miR-539. Moreover, we found dual competitive interaction of miR-656/539 with PCAT1 and yes-associated protein (YAP), resulting in the identification of PCAT1-miR-656/539-YAP axis in Caki-2 and ACHN cells. With CCK-8 assay and transwell assay, miR-656/539 inhibitor or YAP overexpression could alleviate the effects of si-PCAT1 on the proliferation, migration and invasion of Caki-2 and ACHN cells. Our data indicated that PCAT1 promotes proliferation, migration and invasion of ccRCC cells by upregulating YAP via sponging miR-656 and miR-539. Taken together, this study provided a novel therapeutic target for ccRCC treatment.

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References
1.
Qi P, Du X . The long non-coding RNAs, a new cancer diagnostic and therapeutic gold mine. Mod Pathol. 2012; 26(2):155-65. DOI: 10.1038/modpathol.2012.160. View

2.
Gong J, Maia M, Dizman N, Govindarajan A, Pal S . Metastasis in renal cell carcinoma: Biology and implications for therapy. Asian J Urol. 2017; 3(4):286-292. PMC: 5730828. DOI: 10.1016/j.ajur.2016.08.006. View

3.
Wang X, Li M, Wang Z, Han S, Tang X, Ge Y . Silencing of long noncoding RNA MALAT1 by miR-101 and miR-217 inhibits proliferation, migration, and invasion of esophageal squamous cell carcinoma cells. J Biol Chem. 2014; 290(7):3925-35. PMC: 4326802. DOI: 10.1074/jbc.M114.596866. View

4.
Jiang H, Liang M, Jiang Y, Zhang T, Mo K, Su S . The lncRNA TDRG1 promotes cell proliferation, migration and invasion by targeting miR-326 to regulate MAPK1 expression in cervical cancer. Cancer Cell Int. 2019; 19:152. PMC: 6544966. DOI: 10.1186/s12935-019-0872-4. View

5.
Huang J, Deng G, Liu T, Chen W, Zhou Y . Long noncoding RNA PCAT-1 acts as an oncogene in osteosarcoma by reducing p21 levels. Biochem Biophys Res Commun. 2018; 495(4):2622-2629. DOI: 10.1016/j.bbrc.2017.12.157. View