| Literature DB >> 27231954 |
Peng Chen1,2,3, Haibin Wang1,3, Fan Yang4, Hongwu Chen2, Wei He1, Junjian Wang2.
Abstract
Curcumin has demonstrated valuable therapeutic potential against a variety of human cancers including osteosarcoma. However, the molecular mechanisms underlying its anti-tumor effect remain to be poorly understood. By RNA sequence profiling, we found that curcumin significantly down-regulates the expression of estrogen-related receptor alpha (ERRα) in osteosarcoma cells. Overexpression of ERRα diminished curcumin-activated apoptotic cell death and scavenged curcumin-induced reactive oxygen species (ROS), while ERRα silencing sensitized osteosarcoma cells to curcumin, resulting in increased inhibition of cell proliferation. In addition, we found that curcumin suppressed the ERRα gene expression through upregulation of miR-125a. Data from this study revealed a novel mechanism for curcumin-mediated apoptotic cell death, which involves tumor cell killing via activating miR-125a/ERRα pathway. Our studies also provide further support for osteosarcoma therapy by targeting ERRα alone or in combination with curcumin. J. Cell. Biochem. 118: 74-81, 2017.Entities:
Keywords: CURCUMIN; ESTROGEN-RELATED RECEPTOR ALPHA; OSTEOSARCOMA; U2OS CELLS; miR-125a
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Year: 2016 PMID: 27231954 DOI: 10.1002/jcb.25612
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429