| Literature DB >> 29969627 |
Ying Zheng1, Yong Sun2, Yi Liu1, Xianlong Zhang1, Fayin Li1, Lin Li1, Jiayu Wang1.
Abstract
MicroRNAs were thought to play a regulatory role through complementarity to target messenger RNA (mRNA). Our previous study revealed a miR-31-SOX10 axis that regulated tumor growth and resistance to chemotherapy of melanoma. Up-regulation of SOX10 and down-regulation of miR-31 were found in melanoma tissues. SOX10 was further identified as a target of miR-31. Overexpression of SOX10 dramatically promoted melanoma cell proliferation and chemotherapy resistance both in vitro and in vivo. While enforced miR-31 expression suppressed cell growth and enhanced the chemosensitivity of melanoma cells, the re-expression of SOX10 rescued these effects by activating PI3K/AKT signaling pathway. In conclusion, our results demonstrated that SOX10 acted as an oncogene and was negatively regulated by miR-31, which supports the potential therapeutic strategy against melanoma by targeting the miR-31-SOX10 axis.Entities:
Keywords: Dacarbazine (DTIC); Melanoma; Oncogene; SOX10; miR-31
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Year: 2018 PMID: 29969627 DOI: 10.1016/j.bbrc.2018.06.175
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575