| Literature DB >> 27294355 |
Fei Geng1,2, Jian-Lin Wu1,2, Gui-Feng Lu3, Zhi-Ping Liang1,2, Zhuo-Li Duan1,2, Xi Gu4,5.
Abstract
Gliomas are highly malignant tumors, the most common of which are astrocytomas. A growing number of studies suggest that dysregulation of miRNAs is a frequent event contributing to the pathogenesis of gliomas. In this study, we found that over-expression of miR-132 inhibited cell proliferation and migration and triggered apoptosis, while knockdown of miR-132 showed opposite effects. PEA-15 was identified as a direct target of miR-132. Reintroduction of PEA-15 without 3'UTR region reversed the inhibitory effects of miR-132 on cell proliferation, migration, and apoptosis. MiR-132 was inversely correlated with the PEA-15 expression. CREB (cAMP response element binding protein) and KLF (Krüppel-like factor 8) were conformed as transcription factors of miR-132, which bidirectionally regulate the expression of miR-132. Our study suggests that miR-132 is an important tumor suppressor of astrocytoma progression by targeting PEA-15, while CREB and KLF can modulate the expression of miR-132, thus providing new insight into the molecular mechanisms underlying astrocytoma progression in vitro.Entities:
Keywords: Astrocytoma; CREB; Glioma; KLF; MiR-132; PEA-15
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Year: 2016 PMID: 27294355 DOI: 10.1007/s11060-016-2173-2
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130