| Literature DB >> 29556270 |
Peijie Chen1,2,3, Jing Quan1,3, Lu Jin1,3, Canbin Lin1,2,3, Weijie Xu1, Jinling Xu1, Xin Guan1, Zebo Chen1, Liangchao Ni1, Shangqi Yang1, Yun Chen4, Yongqing Lai1,3.
Abstract
MiR-216a-5p has been acknowledged as an oncogene and is known to be involved in the progression and metastasis of numerous cancer subtypes. However, the potential role of miR-216a-5p in renal cell carcinoma (RCC) remains to be elucidated. In the present study, reverse transcription-quantitative polymerase chain reaction was performed to detect the expression levels of miR-216a-5p in RCC tissues. Cell counting kit-8, MTT, wound scratch, Transwell and flow cytometric assays were performed to establish the biological functions of miR-216a-5p in RCC. Functional experiments demonstrated that the expression of miR-216a-5p was upregulated in RCC (P<0.05) and miR-216a-5p mimics promoted cellular proliferation, viability and motility, and suppressed apoptosis. Conversely, miR-216a-5p inhibitor suppressed cellular proliferation, viability, motility and induced apoptosis. Based on these findings, it was concluded that miR-216a-5p may function as an oncogene in RCC. MiR-216a-5p target genes need to be explored and the potential of miR-216a-5p to be used as a diagnostic or a prognostic biomarker for RCC needs to be validated by future research.Entities:
Keywords: miR-216a-5p; microRNA; oncogene; renal cell carcinoma
Year: 2018 PMID: 29556270 PMCID: PMC5844176 DOI: 10.3892/etm.2018.5881
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447