| Literature DB >> 30675254 |
Pengfei Zhang1, Jikai Yin1, Lijuan Yuan1, Qing Wang1, Xilin Du1, Rui Dong1, Chengguo Wang1, Qiangshan Bai1, Ling Ji2, Guizhi Zhang3, Jianguo Lu1.
Abstract
microRNAs (miRNAs) have been determined to be associated with cancer progression and metastasis. Mir-139 is located on 11q13.4 and exhibits anti-oncogenic and anti-metastatic activity in human cancers. It is downregulated in various malignant tumor types. In the present study, the potential functions and targets of miR-139 in hepatocellular carcinoma (HCC) were explored. Using a combinational analysis of four miRNA target prediction tools and biological experiments, it was determined that Topoisomerase I (TOP1) is a direct target of miR-139 in HCC. Several traditional topoisomerase inhibitors have demonstrated anticancer activity, but their side effects outnumbered their anticancer potential. The present study determined that overexpression of miR-139 significantly inhibits HCC cell proliferation (P<0.05) and migration (P<0.05), which is largely due to TOP1 downregulation. The present study indicated that miR-139 exerts a tumor-suppressive effect during hepatocarcinogenesis via the suppression of expression of TOP1; therefore, miR-139 is a promising target for the treatment of HCC.Entities:
Keywords: Topoisomerase I; hepatocellular carcinoma; miR-139; microRNA; migration; proliferation
Year: 2018 PMID: 30675254 PMCID: PMC6341805 DOI: 10.3892/ol.2018.9746
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967