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lncRNA SLCO4A1-AS1 promotes growth and invasion of bladder cancer through sponging miR-335-5p to upregulate OCT4

Authors Yang Y, Wang F, Huang H, Zhang Y, Xie H, Men T

Received 22 October 2018

Accepted for publication 3 January 2019

Published 18 February 2019 Volume 2019:12 Pages 1351—1358

DOI https://doi.org/10.2147/OTT.S191740

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Andrew Yee

Peer reviewer comments 2

Editor who approved publication: Dr Leo Jen-Liang Su


Yu Yang,1 Feng Wang,2 Hang Huang,2 Yan Zhang,3 Hui Xie,2 Tongyi Men1

1Department of Urology, Qianfoshan Hospital Affiliated to Shandong University, Jinan 250014, China; 2Department of Urology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, China; 3Transplant Section, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, China

Background: Bladder cancer (BC) is among the most frequently occurring cancer types in the urinary system. In recent years, the importance of lncRNAs in BC has been acknowledged. SLCO4A1-AS1 is an oncogene in colorectal cancer. However, the role of SLCO4A1-AS1 in BC remains unknown.
Materials and methods: The expression levels of SLCO4A1-AS1 in BC tissues were analyzed by qRT-PCR. The effects of SLCO4A1-AS1 knockdown on proliferation were determined by CCK8 assay. Transwell assay was used to evaluate the role of SLCO4A1-AS1 on migration and invasion. Furthermore, xenograft assay was utilized to test the effect of SLCO4A1-AS1 on BC growth in vivo.
Results: SLCO4A1-AS1 expression was more upregulated in BC tissues than in adjacent normal tissues. Moreover, SLCO4A1-AS1 level was positively correlated with the advanced stage and metastasis in BC. The upregulation of SLCO4A1-AS1 indicates poor prognosis in BC patients. The knockdown of SLCO4A1-AS1 downregulated the proliferation, migration, and invasion of EJ and T24 cells in vitro. In addition, the loss of SLCO4A1-AS1 prevented BC growth in vivo. Mechanistic investigation showed that SLCO4A1-AS1 was the sponge for miR-335-5p, and miR-335-5p modulated OCT4 expression.
Conclusion: High SLCO4A1-AS1 expression level was associated with the progression of BC, and SLCO4A1-AS1 promoted the malignant phenotypes of BC cells through the miR-335-5p/OCT4 axis.

Keywords: bladder cancer, lncRNA, SLCO4A1-AS1, proliferation, invasion
 

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