The emerging role and targetability of the TCA cycle in cancer metabolism

ABSTRACT The tricarboxylic acid (TCA) cycle is a central route for oxidative phosphorylation in cells, and fulfills their bioenergetic, biosynthetic, and redox balance requirements. Despite early dogma that cancer cells bypass the TCA cycle and primarily utilize aerobic glycolysis, emerging evidence...

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Main Authors: Nicole M. Anderson, Patrick Mucka, Joseph G. Kern, Hui Feng
Format: Article
Language:English
Published: SpringerOpen 2017-07-01
Series:Protein & Cell
Subjects:
Online Access:http://link.springer.com/article/10.1007/s13238-017-0451-1
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spelling doaj-95ec30fd4d80421e927f1fb612740eef2020-11-24T21:09:59ZengSpringerOpenProtein & Cell1674-800X1674-80182017-07-019221623710.1007/s13238-017-0451-1The emerging role and targetability of the TCA cycle in cancer metabolismNicole M. Anderson0Patrick Mucka1Joseph G. Kern2Hui Feng3Abramson Family Cancer Research Institute, University of PennsylvaniaDepartments of Pharmacology and Medicine, The Center for Cancer Research, Section of Hematology and Medical Oncology, Boston University School of MedicineProgram in Biomedical Sciences, Boston University School of MedicineDepartments of Pharmacology and Medicine, The Center for Cancer Research, Section of Hematology and Medical Oncology, Boston University School of MedicineABSTRACT The tricarboxylic acid (TCA) cycle is a central route for oxidative phosphorylation in cells, and fulfills their bioenergetic, biosynthetic, and redox balance requirements. Despite early dogma that cancer cells bypass the TCA cycle and primarily utilize aerobic glycolysis, emerging evidence demonstrates that certain cancer cells, especially those with deregulated oncogene and tumor suppressor expression, rely heavily on the TCA cycle for energy production and macromolecule synthesis. As the field progresses, the importance of aberrant TCA cycle function in tumorigenesis and the potentials of applying small molecule inhibitors to perturb the enhanced cycle function for cancer treatment start to evolve. In this review, we summarize current knowledge about the fuels feeding the cycle, effects of oncogenes and tumor suppressors on fuel and cycle usage, common genetic alterations and deregulation of cycle enzymes, and potential therapeutic opportunities for targeting the TCA cycle in cancer cells. With the application of advanced technology and in vivo model organism studies, it is our hope that studies of this previously overlooked biochemical hub will provide fresh insights into cancer metabolism and tumorigenesis, subsequently revealing vulnerabilities for therapeutic interventions in various cancer types.http://link.springer.com/article/10.1007/s13238-017-0451-1glutaminolysisthe TCA cyclecancer metabolismglycolysis
collection DOAJ
language English
format Article
sources DOAJ
author Nicole M. Anderson
Patrick Mucka
Joseph G. Kern
Hui Feng
spellingShingle Nicole M. Anderson
Patrick Mucka
Joseph G. Kern
Hui Feng
The emerging role and targetability of the TCA cycle in cancer metabolism
Protein & Cell
glutaminolysis
the TCA cycle
cancer metabolism
glycolysis
author_facet Nicole M. Anderson
Patrick Mucka
Joseph G. Kern
Hui Feng
author_sort Nicole M. Anderson
title The emerging role and targetability of the TCA cycle in cancer metabolism
title_short The emerging role and targetability of the TCA cycle in cancer metabolism
title_full The emerging role and targetability of the TCA cycle in cancer metabolism
title_fullStr The emerging role and targetability of the TCA cycle in cancer metabolism
title_full_unstemmed The emerging role and targetability of the TCA cycle in cancer metabolism
title_sort emerging role and targetability of the tca cycle in cancer metabolism
publisher SpringerOpen
series Protein & Cell
issn 1674-800X
1674-8018
publishDate 2017-07-01
description ABSTRACT The tricarboxylic acid (TCA) cycle is a central route for oxidative phosphorylation in cells, and fulfills their bioenergetic, biosynthetic, and redox balance requirements. Despite early dogma that cancer cells bypass the TCA cycle and primarily utilize aerobic glycolysis, emerging evidence demonstrates that certain cancer cells, especially those with deregulated oncogene and tumor suppressor expression, rely heavily on the TCA cycle for energy production and macromolecule synthesis. As the field progresses, the importance of aberrant TCA cycle function in tumorigenesis and the potentials of applying small molecule inhibitors to perturb the enhanced cycle function for cancer treatment start to evolve. In this review, we summarize current knowledge about the fuels feeding the cycle, effects of oncogenes and tumor suppressors on fuel and cycle usage, common genetic alterations and deregulation of cycle enzymes, and potential therapeutic opportunities for targeting the TCA cycle in cancer cells. With the application of advanced technology and in vivo model organism studies, it is our hope that studies of this previously overlooked biochemical hub will provide fresh insights into cancer metabolism and tumorigenesis, subsequently revealing vulnerabilities for therapeutic interventions in various cancer types.
topic glutaminolysis
the TCA cycle
cancer metabolism
glycolysis
url http://link.springer.com/article/10.1007/s13238-017-0451-1
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