Rethinking the Warburg Effect with Myc Micromanaging Glutamine Metabolism

被引:305
作者
Dang, Chi V. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Hematol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
CELL-CYCLE ENTRY; MITOCHONDRIAL BIOGENESIS; TUMOR METABOLISM; CANCER; HYPOXIA; EXPRESSION; NETWORKS; LACTATE; GENES;
D O I
10.1158/0008-5472.CAN-09-3556
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The MYC oncogene, which is frequently deregulated in human cancers, encodes a master transcription factor c-Myc (herein termed Myc) that integrates cell proliferation with metabolism through its regulation of thousands of genes including microRNAs (miRNA). In addition to its known function in regulating the cell cycle and glucose metabolism, recent studies document a role for Myc in stimulating glutamine catabolism, in part through the repression of miRNAs miR-23a and miR-23b. These observations suggest an additional level of complexity in tumor metabolism, which includes the commensal metabolic relationship between hypoxic and nonhypoxic regions of tumors as well as the surrounding stroma. Thus, a reevaluation of cancer metabolism considering glutamine catabolism with a better understanding of the tumor histological complexity is needed before cancer metabolism can be effectively targeted in therapy. Cancer Res; 70(3); 859-62. (C)2010 AACR.
引用
收藏
页码:859 / 862
页数:4
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