| Literature DB >> 22093618 |
Masaaki Tsukigi1, Vladimir Bilim, Kaori Yuuki, Andrey Ugolkov, Sei Naito, Akira Nagaoka, Tomoyuki Kato, Teiichi Motoyama, Yoshihiko Tomita.
Abstract
Recently, we have identified GSK-3 as a new therapeutic target in renal cell cancer (RCC). miR-199a could potentially downregulate GSK-3β expression. Here, we found a decreased miR-199a expression in 59% (32 of 54) of RCCs and it was correlated with higher tumor stage (p < 0.05) and nuclear overexpression of GSK-3β (p < 0.05). We show that re-expression of miR-199a downregulates GSK-3β and suppresses cancer cell growth. Our results demonstrate low miR-199a expression as a feature of advanced RCCs, identify miR-199a as a negative regulator of GSK-3β, and suggest re-expression of pre-miR-199a as a new potential treatment of RCC.Entities:
Mesh:
Substances:
Year: 2011 PMID: 22093618 DOI: 10.1016/j.canlet.2011.10.008
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679