Therapeutic strategies impacting cancer cell glutamine metabolism

被引:118
|
作者
Lukey, Michael J. [1 ]
Wilson, Kristin F. [1 ]
Cerione, Richard A. [1 ]
机构
[1] Cornell Univ, Dept Mol Med, Ithaca, NY 14850 USA
关键词
KIDNEY-TYPE GLUTAMINASE; PHOSPHATE-ACTIVATED GLUTAMINASE; ACUTE LYMPHOBLASTIC-LEUKEMIA; MITOCHONDRIAL GLUTAMINASE; DEFICIENT MICE; L-ASPARAGINASE; REDUCTIVE CARBOXYLATION; OXIDATIVE STRESS; GENE-EXPRESSION; INHIBITION;
D O I
10.4155/fmc.13.130
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The metabolic adaptations that support oncogenic growth can also render cancer cells dependent on certain nutrients. Along with the Warburg effect, increased utilization of glutamine is one of the metabolic hallmarks of the transformed state. Glutamine catabolism is positively regulated by multiple oncogenic signals, including those transmitted by the Rho family of GTPases and by c-Myc. The recent identification of mechanistically distinct inhibitors of glutaminase, which can selectively block cellular transformation, has revived interest in the possibility of targeting glutamine metabolism in cancer therapy. Here, we outline the regulation and roles of glutamine metabolism within cancer cells and discuss possible strategies for, and the consequences of, impacting these processes therapeutically.
引用
收藏
页码:1685 / 1700
页数:16
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