4.6 Review

Metabolic Kinases Moonlighting as Protein Kinases

期刊

TRENDS IN BIOCHEMICAL SCIENCES
卷 43, 期 4, 页码 301-310

出版社

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tibs.2018.01.006

关键词

-

资金

  1. National Cancer Institute [2R01 CA109035, 1R01 CA169603, 1R01 CA204996, CA014195, CA080100, CA082683, CA194584]
  2. National Institute of Neurological Disorders and Stroke [1R01 NS089754]
  3. National Institutes of Health/National Cancer Institute MD Anderson Support Grant [P30CA016672]
  4. National Institutes of Health Brain Cancer Specialized Program of Research Excellence [2P50 CA127001]

向作者/读者索取更多资源

Protein kinases regulate every aspect of cellular activity, whereas metabolic enzymes are responsible for energy production and catabolic and anabolic processes. Emerging evidence demonstrates that some metabolic enzymes, such as pyruvate kinase M2 (PKM2), phosphoglycerate kinase 1 (PGK1), ketohexokinase (KHK) isoform A (KHK-A), hexokinase (HK), and nucleoside diphosphate kinase 1 and 2 (NME1/2), that phosphorylate soluble metabolites can also function as protein kinases and phosphorylate a variety of protein substrates to regulate the Warburg effect, gene expression, cell cycle progression and proliferation, apoptosis, autophagy, exosome secretion, T cell activation, iron transport, ion channel opening, and many other fundamental cellular functions. The elevated protein kinase functions of these moonlighting metabolic enzymes in tumor development make them promising therapeutic targets for cancer.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据