| Literature DB >> 24616104 |
Takeshi Chiyomaru1, Shinichiro Fukuhara, Sharanjot Saini, Shahana Majid, Guoren Deng, Varahram Shahryari, Inik Chang, Yuichiro Tanaka, Hideki Enokida, Masayuki Nakagawa, Rajvir Dahiya, Soichiro Yamamura.
Abstract
HOTAIR is a long non-coding RNA that interacts with the polycomb repressive complex and suppresses its target genes. HOTAIR has also been demonstrated to promote malignancy. MicroRNA-141 (miR-141) has been reported to play a role in the epithelial to mesenchymal transition process, and the expression of miR-141 is inversely correlated with tumorigenicity and invasiveness in several human cancers. We found that HOTAIR expression is inversely correlated to miR-141 expression in renal carcinoma cells. HOTAIR promotes malignancy, including proliferation and invasion, whereas miR-141 suppresses malignancy in human cancer cells. miR-141 binds to HOTAIR in a sequence-specific manner and suppresses HOTAIR expression and functions, including proliferation and invasion. Both HOTAIR and miR-141 were associated with the immunoprecipitated Ago2 (Argonaute2) complex, and the Ago2 complex cleaved HOTAIR in the presence of miR-141. These results demonstrate that HOTAIR is suppressed by miR-141 in an Ago2-dependent manner.Entities:
Keywords: Cancer Biology; Cell Growth; Gene Regulation; Genistein; HOTAIR; Invasion; Long Non-coding RNA; MicroRNA; Renal Carcinoma; miR-141
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Year: 2014 PMID: 24616104 PMCID: PMC4007447 DOI: 10.1074/jbc.M113.488593
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157