Author/Authors :
Zhao، نويسنده , , Shiguang and Liu، نويسنده , , Huailei and Liu، نويسنده , , Yaohua and Wu، نويسنده , , Jianing and Wang، نويسنده , , Chunlei and Hou، نويسنده , , Xu and Chen، نويسنده , , XiaoFeng and Yang، نويسنده , , Guang and Zhao، نويسنده , , Ling and Che، نويسنده , , Hui and Bi، نويسنده , , Yunke and Wang، نويسنده , , Hongyu and Peng، نويسنده , , Xiao-Fei and Ai، نويسنده , , Jing، نويسنده ,
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.
Keywords :
Glioblastoma stem-like cells , 2-Deoxy-d-glucose (2-DG) , glycolysis , miR-143 , Neurosphere