Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect

The Warburg Effect, or aerobic glycolysis, is one of the major metabolic alterations observed in cancer. Hypothesized to increase a cell's proliferative capacity via regenerating NAD+, increasing the pool of glycolytic biosynthetic intermediates, and increasing lactate production that affects t...

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Main Authors: Elizabeth K. Wiese, Taro Hitosugi
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-07-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fcell.2018.00079/full
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spelling doaj-001e8ed892ed4e54b834a4fbd1fc2b7b2020-11-25T00:04:01ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2018-07-01610.3389/fcell.2018.00079397919Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg EffectElizabeth K. Wiese0Elizabeth K. Wiese1Taro Hitosugi2Taro Hitosugi3Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, United StatesMolecular Pharmacology and Experimental Therapeutics Graduate Program, Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, MN, United StatesDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, United StatesDivision of Oncology Research, Mayo Clinic, Rochester, MN, United StatesThe Warburg Effect, or aerobic glycolysis, is one of the major metabolic alterations observed in cancer. Hypothesized to increase a cell's proliferative capacity via regenerating NAD+, increasing the pool of glycolytic biosynthetic intermediates, and increasing lactate production that affects the tumor microenvironment, the Warburg Effect is important for the growth and proliferation of tumor cells. The mechanisms by which a cell acquires the Warburg Effect phenotype are regulated by the expression of numerous oncogenes, including oncogenic tyrosine kinases. Oncogenic tyrosine kinases play a significant role in phosphorylating and regulating the activity of numerous metabolic enzymes. Tyrosine phosphorylation of glycolytic enzymes increases the activities of a majority of glycolytic enzymes, thus promoting increased glycolytic rate and tumor cell proliferation. Paradoxically however, tyrosine phosphorylation of pyruvate kinase M2 isoform (PKM2) results in decreased PKM2 activity, and this decrease in PKM2 activity promotes the Warburg Effect. Furthermore, recent studies have shown that PKM2 is also able to act as a protein kinase using phosphoenolpyruvate (PEP) as a substrate to promote tumorigenesis. Therefore, numerous recent studies have investigated both the role of the classical and non-canonical activity of PKM2 in promoting the Warburg Effect and tumor growth, which raise further interesting questions. In this review, we will summarize these recent advances revealing the importance of tyrosine kinases in the regulation of the Warburg Effect as well as the role of PKM2 in the promotion of tumor growth.https://www.frontiersin.org/article/10.3389/fcell.2018.00079/fullthe Warburg Effecttyrosine kinasesPKM2lactatepyruvate kinase
collection DOAJ
language English
format Article
sources DOAJ
author Elizabeth K. Wiese
Elizabeth K. Wiese
Taro Hitosugi
Taro Hitosugi
spellingShingle Elizabeth K. Wiese
Elizabeth K. Wiese
Taro Hitosugi
Taro Hitosugi
Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
Frontiers in Cell and Developmental Biology
the Warburg Effect
tyrosine kinases
PKM2
lactate
pyruvate kinase
author_facet Elizabeth K. Wiese
Elizabeth K. Wiese
Taro Hitosugi
Taro Hitosugi
author_sort Elizabeth K. Wiese
title Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
title_short Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
title_full Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
title_fullStr Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
title_full_unstemmed Tyrosine Kinase Signaling in Cancer Metabolism: PKM2 Paradox in the Warburg Effect
title_sort tyrosine kinase signaling in cancer metabolism: pkm2 paradox in the warburg effect
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2018-07-01
description The Warburg Effect, or aerobic glycolysis, is one of the major metabolic alterations observed in cancer. Hypothesized to increase a cell's proliferative capacity via regenerating NAD+, increasing the pool of glycolytic biosynthetic intermediates, and increasing lactate production that affects the tumor microenvironment, the Warburg Effect is important for the growth and proliferation of tumor cells. The mechanisms by which a cell acquires the Warburg Effect phenotype are regulated by the expression of numerous oncogenes, including oncogenic tyrosine kinases. Oncogenic tyrosine kinases play a significant role in phosphorylating and regulating the activity of numerous metabolic enzymes. Tyrosine phosphorylation of glycolytic enzymes increases the activities of a majority of glycolytic enzymes, thus promoting increased glycolytic rate and tumor cell proliferation. Paradoxically however, tyrosine phosphorylation of pyruvate kinase M2 isoform (PKM2) results in decreased PKM2 activity, and this decrease in PKM2 activity promotes the Warburg Effect. Furthermore, recent studies have shown that PKM2 is also able to act as a protein kinase using phosphoenolpyruvate (PEP) as a substrate to promote tumorigenesis. Therefore, numerous recent studies have investigated both the role of the classical and non-canonical activity of PKM2 in promoting the Warburg Effect and tumor growth, which raise further interesting questions. In this review, we will summarize these recent advances revealing the importance of tyrosine kinases in the regulation of the Warburg Effect as well as the role of PKM2 in the promotion of tumor growth.
topic the Warburg Effect
tyrosine kinases
PKM2
lactate
pyruvate kinase
url https://www.frontiersin.org/article/10.3389/fcell.2018.00079/full
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