| Literature DB >> 21435336 |
Hailin Tang1, Xiaoping Liu, Zeyou Wang, Xiaoling She, Xi Zeng, Min Deng, Qianjin Liao, Xiaofang Guo, Rong Wang, Xiaoling Li, Fang Zeng, Minghua Wu, Guiyuan Li.
Abstract
LRRC4 is not only a brain-specific gene, but it has also been identified as a tumor suppressor gene for glioma. Promoter methylation of LRRC4 is frequently involved in the inactivation in glioma. MiRNA-mediated gene regulation has recently been demonstrated to play an important role in multiple biological processes related to cancer, including glioma. In this study, we demonstrated that a small regulatory microRNA, hsa-miR-381, an "oncomir", had a major role in glioma progression and that LRRC4 was a target of hsa-miR-381. By regulating LRRC4, hsa-miR-381 increased the in vitro and in vivo proliferation of glioma cells, and this action was associated with decreased inhibition of MEK/ERK and AKT signaling. Conversely, LRRC4, as a glioma suppressor, inhibited the endogenous expression of hsa-miR-381 and decreased cell proliferation and tumor growth. The interaction of hsa-miR-381 and LRRC4 is involved in the pathogenesis of glioma. In addition, the stable expression of hsa-miR-381 in blood provides a novel and promising diagnostic biomarker, and anti-hsa-miR-381 "antagomir" may be an ideal target for glioma therapy.Entities:
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Year: 2011 PMID: 21435336 DOI: 10.1016/j.brainres.2011.03.034
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252