| Literature DB >> 34093749 |
Guohui Yan1,2,3, Shuidi Yan4, Jiajia Wang4, Shen Lei2, Weimin Tian5, Xin Yue6, Yang Zhang1,2,4.
Abstract
An increasing body of evidence indicates the involvement of microRNAs (miRNAs/miRs) in the initiation and progression of colorectal cancer (CRC). miR-296-5p was recently identified as a tumor suppressor in a variety of human cancer types; however, its function in CRC remains largely unknown. The present study demonstrated that the expression of miR-296-5p was significantly downregulated in CRC tissues and cell lines. The overexpression of miR-296-5p markedly inhibited proliferation, and induced cell cycle arrest and apoptosis in CRC cells. Bioinformatics analysis suggested that high mobility group AT-hook 1 (HMGA1) may be a target of miR-296-5p in CRC cells. Further experiments showed that miR-296-5p bound the 3'-untranslated region of HMGA1 and decreased its expression in CRC cells. HMGA1 was overexpressed in CRC tissues and was inversely correlated with the expression of miR-296-5p. The restoration of HMGA1 significantly reversed the inhibitory effect of miR-296-5p on the proliferation of CRC cells. Overall, the findings of the present study indicate that miR-296-5p suppressed the progression of CRC, at least partially via targeting HMGA1. Thus, miR-296-5p is a potential target for novel therapies in CRC.Entities:
Keywords: cell cycle; colorectal cancer; high mobility group AT-hook 1; microRNA-296-5p
Year: 2021 PMID: 34093749 PMCID: PMC8170657 DOI: 10.3892/etm.2021.10225
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447