生物能学
黑色素瘤
小眼畸形相关转录因子
重编程
氧化磷酸化
生物
线粒体
细胞生物学
PTEN公司
癌症研究
厌氧糖酵解
糖酵解
新陈代谢
PI3K/AKT/mTOR通路
生物化学
基因
信号转导
转录因子
作者
Cecilie Abildgaard,Per Guldberg
标识
DOI:10.1016/j.molmed.2014.12.007
摘要
The development of metastatic melanoma is accompanied by distinct changes in cellular metabolism, most notably a change in strategy for energy production from mitochondrial oxidative phosphorylation to cytoplasmic aerobic glycolysis. This bioenergetic switch occurs at the expense of less-efficient utilization of glucose, but is required for melanoma cells to meet their bioenergetic and biosynthetic demands. Recent work has implicated well-established melanoma drivers such as BRAF, PTEN, MITF, and ARF in the regulation of cellular energy metabolism. The metabolic changes in melanoma cells offer new opportunities for therapeutic intervention. However, inter- and intratumor bioenergetic heterogeneity caused by variation in genetic driver profiles and mitochondrial performance may impact on the effectiveness of treatment.
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