| Literature DB >> 30867721 |
Hui Yue1, Lin Liu1, Zhenguo Song1.
Abstract
MicroRNA-212 (miR-212) is dysregulated in numerous tissues and cancer types and serves a role in the progression of human cancer. However, the function and mechanism of miR-212 in the development of pancreatic ductal adenocarcinoma (PDAC) remain unknown, particularly in a hypoxic microenvironment. In the present study, miR-212 expression was observed to be significantly upregulated in PDAC tissues compared with normal tissues. Clinical data analysis indicated that miR-212 was positively associated with a large tumor size, Tumor-Node-Metastasis stage, lymph node metastasis and vessel invasion, and influenced the overall survival time. Notably, there was a positive association between the expression of hypoxia-inducible factor-1α (HIF-1α) and miR-212 in vivo and in vitro in hypoxic conditions. Mechanistically, HIF-1α bound directly to a hypoxia response element in the miR-212 promoter region and activated miR-212 expression in PDAC cells. Collectively, these results demonstrated that HIF-1α positively regulated miR-212 expression and resulted in PDAC progression.Entities:
Keywords: hypoxia-inducible factor-1α; microRNA-212; pancreatic cancer; progression
Year: 2019 PMID: 30867721 PMCID: PMC6396010 DOI: 10.3892/etm.2019.7213
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447