瓦博格效应
过剩1
胶质瘤
糖酵解
小RNA
癌症研究
癌细胞
细胞生物学
生物能学
厌氧糖酵解
医学
氧化磷酸化
葡萄糖转运蛋白
癌症
新陈代谢
线粒体
生物化学
生物
内科学
基因
胰岛素
作者
Sheng Nie,Keqin Li,Yi Huang,Qinle Hu,Xiang Gao,Jie Sun
标识
DOI:10.1097/scs.0000000000001385
摘要
Cancer cell metabolism is often characterized by a shift from an oxidative to a glycolytic bioenergetics pathway, a phenomenon known as the Warburg effect. Whether the deregulation of microRNAs contributes to the Warburg effect remains largely unknown. Here, we show that miR-495 expression is decreased and thus induces a metabolic shift in glioma cells. miR-495 performs this function by increasing the expression of Glut1, leading to the increase of glucose uptake and lactate production. The altered metabolism induced by miR-495 results in the rapid growth of cancer cells. These results identify miR-495 as a molecular switch involved in the orchestration of the Warburg effect in glioma cells via targeting the expression of Glut1.
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