miRNA-877-5p inhibits malignant progression of prostate cancer by directly targeting SSFA2

Wanchun Wang(Jiangxi University of Traditional Chinese Medicine), Jun Yi(Jiangxi University of Traditional Chinese Medicine), Degang Dong(Jiangxi University of Traditional Chinese Medicine), Wenli Mao(Jiangxi University of Traditional Chinese Medicine), Xuanyu Wang(Jiangxi University of Traditional Chinese Medicine), Zhangren Yan(Jiangxi University of Traditional Chinese Medicine)
European Journal of Histochemistry
September 20, 2021
Cited by 12Open Access
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Abstract

In this study, we aimed to investigate the role of miR-877-5p in the malignant phenotypes of prostate cancer (PCa) cells and its underlying mechanism. RT-qPCR analysis was performed to examine the expression of miR-877-5p and sperm-specific antigen 2 (SSFA2) in PCa tissues and cells. Cell counting kit-8 (CCK-8) assay, 5-ethynyl-20-deoxyuridine (EdU) assay, flow cytometry, wound-healing assay, and Transwell invasion assay were performed to determine the functional roles of miR-877-5p in PCa cells. The association of miR-877-5p with SSFA2 was determined by luciferase reporter and RNA pull-down assays. In this study, we found that the expression level of miR-877-5p was decreased in PCa tissues and cells. Functionally, overexpression of miR-877-5p exerted tumor suppressor properties in PCa cells. Mechanistically, SSFA2 was identified as a target gene of miR-877-5p, while overexpression of SSFA2 could abrogate the anti-tumor effects of miR-877-5p in PCa cells. These findings demonstrated that miR-877-5p/SSFA2 axis functioned as a potential target for PCa treatment.


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