| Literature DB >> 23376635 |
Shiguang Zhao1, Huailei Liu, Yaohua Liu, Jianing Wu, Chunlei Wang, Xu Hou, Xiaofeng Chen, Guang Yang, Ling Zhao, Hui Che, Yunke Bi, Hongyu Wang, Fei Peng, Jing Ai.
Abstract
Glioblastomas rely mainly on aerobic glycolysis to sustain proliferation and growth; however, little is known about the regulatory mechanisms of metabolism in glioblastoma stem cells. We show that miR-143 is significantly down-regulated in glioma tissues and glioblastoma stem-like cells (GSLCs), while miR-143 over-expression inhibits glycolysis by directly targeting hexokinase 2, and promotes differentiation of GSLCs. Moreover, miR-143 inhibits proliferation of GSLCs under hypoxic conditions and decreases tumor formation capacity of GSLCs in vivo. We also show that a combination of miR-143 and 2-DG, a widely used glycolysis inhibitor, has synergistic effects against GSLCs. miR-143 is a potential therapeutic target for glioblastoma treatment.Entities:
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Year: 2013 PMID: 23376635 DOI: 10.1016/j.canlet.2013.01.039
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679