Abstract
Cancer cells undergo significant metabolic adaptation. Cellular transformation enhances both glycolysis and mitochondrial respiration efficiency through the induction of HIF-1α and HIF-2α. In this process, energy production and synthesis of macromolecules are maximized with minimal ROS accumulation. Furthermore, a series of antioxidant enzymes are induced to mitigate the damaging effects of ROS. Examination of these metabolic changes provides rationale for a synergistic approach to combination anti-cancer therapy; targeted inhibition of HIF and inhibition of cellular defenses against oxidative stress.
Published by Elsevier Ltd.
MeSH terms
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Antineoplastic Agents / pharmacology
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Antioxidants / metabolism
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Basic Helix-Loop-Helix Transcription Factors / metabolism*
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Gene Expression Regulation*
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Glucose / metabolism
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Glycolysis
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Humans
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Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
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Macromolecular Substances
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Mitochondria / metabolism
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Models, Biological
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Neoplasms / metabolism*
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Oxidative Stress
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Reactive Oxygen Species*
Substances
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Antineoplastic Agents
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Antioxidants
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Basic Helix-Loop-Helix Transcription Factors
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HIF1A protein, human
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Hypoxia-Inducible Factor 1, alpha Subunit
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Macromolecular Substances
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Reactive Oxygen Species
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endothelial PAS domain-containing protein 1
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Glucose