| Literature DB >> 26002578 |
Jie Chen1, Jinsong Zhou1,2, Xin Chen1, Baohui Yang1, Dong Wang1, Pinglin Yang1, Xijing He1, Haopeng Li3.
Abstract
Accumulating evidence reveals that miR-449a is expressed at a low level in several tumors and cancer cell lines, and acts as a tumor suppressor in several cancers. However, its role in osteosarcoma (OS) is not well understood. In the present study, we found that miR-449a was significantly downregulated in both OS tissues and cell lines. Furthermore, low expression level of miR-449a was correlated with advanced tumor stage, metastasis, and predicted a poor overall survival in OS patients. Additionally, restoration of miR-449a in OS cell lines U2OS and Saos-2 reduced cell viability, promoted cell apoptosis in vitro, and suppressed tumorigenicity in vivo. Moreover, BCL2, an antiapoptotic molecule, was identified to be a direct target of miR-449a, and the proapoptotic function of miR-449a was mainly through targeting BCL2 expression. Taken together, our results demonstrated a tumor-suppressive role of miR-449a in OS progression and suggested a potential therapeutic target for OS.Entities:
Keywords: Apoptosis; BCL2; Osteosarcoma; Tumor suppressor; miR-449a
Mesh:
Substances:
Year: 2015 PMID: 26002578 DOI: 10.1007/s13277-015-3568-y
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283