Serine, glycine and one-carbon units: cancer metabolism in full circle

被引:1113
|
作者
Locasale, Jason W. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Cornell Univ, Field Biochem & Mol Cell Biol, Ithaca, NY 14850 USA
[2] Cornell Univ, Field Genom Genet & Dev, Ithaca, NY 14850 USA
[3] Cornell Univ, Weill Cornell Med Coll, Triinst Program Computat Biol & Med, Ithaca, NY 14850 USA
[4] Cornell Univ, Mem Sloan Kettering Canc Inst, Ithaca, NY 14850 USA
[5] Cornell Univ, Div Nutr Sci, Ithaca, NY 14850 USA
关键词
DNA METHYLTRANSFERASE INHIBITORS; COVALENT HISTONE MODIFICATIONS; THYMIDYLATE SYNTHASE EXPRESSION; GENOME MAINTENANCE MECHANISMS; INTRACELLULAR FOLATE POOLS; MESSENGER-RNA LEVELS; PYRUVATE-KINASE M2; CELL LUNG-CANCER; COLORECTAL-CANCER; PROSTATE-CANCER;
D O I
10.1038/nrc3557
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
One-carbon metabolism involving the folate and methionine cycles integrates nutritional status from amino acids, glucose and vitamins, and generates diverse outputs, such as the biosynthesis of lipids, nucleotides and proteins, the maintenance of redox status and the substrates for methylation reactions. Long considered a 'housekeeping' process, this pathway has recently been shown to have additional complexity. Genetic and functional evidence suggests that hyperactivation of this pathway is a driver of oncogenesis and establishes a link to cellular epigenetic status. Given the wealth of clinically available agents that target one-carbon metabolism, these new findings could present opportunities for translation into precision cancer medicine.
引用
收藏
页码:572 / 583
页数:12
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