| Literature DB >> 27613090 |
Yikai Zhang1, Chengwu Zeng2, Shuai Lu3, Tianyu Qin4, Lijian Yang4, Shaohua Chen4, Jie Chen5, Yangqiu Li6.
Abstract
Acute promyelocytic leukemia (APL) is characterized by the presence of the PML-RARα fusion protein. We have previously found that PML-RARα-regulated miR-125b is highly expressed in APL; however, the characteristics of the regulatory effects and mechanisms of miR-125b involved in APL proliferation have yet to be clarified. In this study, we demonstrate that miR-125b promotes the proliferation of APL cells with the involvement of the PI3K/Akt and MAPK signaling pathways. Furthermore, we identified BTG2, MAP3K11, RPS6KA1 and PRDM1 as putative targets of miR-125b, which we verified using luciferase reporter constructs. Moreover, we demonstrate that the expression of miR-125b targets is downregulated in leukemic cells in patients with APL. Thus, our results provide evidence that miR-125b can modulate multiple oncogenic cell proliferation pathways and may be a novel therapeutic target for APL.Entities:
Keywords: 3′-untranslated regions; Acute promyelocytic leukemia; MicroRNAs; PML-RARα; Proliferation; Small non-coding RNAs
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Year: 2016 PMID: 27613090 DOI: 10.1016/j.bbrc.2016.09.020
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575