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Protein kinase function of pyruvate kinase M2 and cancer

Journal

CANCER CELL INTERNATIONAL
Volume 20, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12935-020-01612-1

Keywords

Pyruvate kinase M2; Protein kinase; Glycolytic pathway; Non-metabolic function; Tumorigenesis

Categories

Funding

  1. National Natural Science Foundation of China [81873711, 31670788]
  2. Open Fund of Guangdong Key Laboratory of Pharmaceutical Functional Genes [2014B030301028, 2017B030314021]

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Pyruvate kinase is a terminal enzyme in the glycolytic pathway, where it catalyzes the conversion of phosphoenolpyruvate to pyruvate and production of ATP via substrate level phosphorylation. PKM2 is one of four isoforms of pyruvate kinase and is widely expressed in many types of tumors and associated with tumorigenesis. In addition to pyruvate kinase activity involving the metabolic pathway, increasing evidence demonstrates that PKM2 exerts a non-metabolic function in cancers. PKM2 has been shown to be translocated into nucleus, where it serves as a protein kinase to phosphorylate various protein targets and contribute to multiple physiopathological processes. We discuss the nuclear localization of PKM2, its protein kinase function and association with cancers, and regulation of PKM2 activity.

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