| Literature DB >> 28105233 |
Haidong Xu1, Xiaozhou Liu1, Juan Zhou1, Xiaoyun Chen1, Jianning Zhao1.
Abstract
Human osteosarcoma is the most common primary bone malignancy sarcoma that affects primarily children and people <20 years old. In the present study, it was demonstrated that miR-574-3p was downregulated in human osteosarcoma U2OS, SAOS and MG63 cells lines as well as in osteosarcoma tissue compared with the normal tissues. Downregulation of miR-574-3p by antisense miR-574-3p, inhibited cell growth and induced cell apoptosis. Overexpression of miR-574-3p by transfection with miR-574-3p mimics promoted the growth of U2OS cells. The present study then identified mothers against decapentaplegic homolog 4 (SMAD4) as a target of miR-574-3p and SMAD4 was suppressed in miR-574-3p transfected cells. Overexpression of SMAD4 could rescue the promoting effects of miR-574-3p on cancer cell growth. In conclusion, miR-574-3p exerts tumor-promoting roles by targeting the tumor-suppressing gene SMAD4 and its downstream signaling in human osteosarcoma, which provides a novel target for the treatment.Entities:
Keywords: SMAD4; miR-574-3p; oncogene; osteosarcoma
Year: 2016 PMID: 28105233 PMCID: PMC5228465 DOI: 10.3892/ol.2016.5355
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967