Abstract
Tumor progression and resistance to treatment are often accompanied by the polarization of malignant cells towards a mesenchymal or poorly differentiated state. Such a transition generates an accrued vulnerability to the induction of ferroptosis, potentially paving the way to novel therapeutic strategies for targeting residual disease in patients with cancer.
Keywords:
epithelial-to-mesenchymal transition; glutathione; lipid peroxidation; polyunsaturated fatty acids; regulated cell death; statins.
Copyright © 2017 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Antineoplastic Agents / metabolism*
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Antineoplastic Agents / pharmacology
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Antineoplastic Agents / therapeutic use
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Apoptosis / drug effects
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Apoptosis / physiology*
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Cell Death / drug effects
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Cell Death / physiology
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Cell Differentiation / drug effects
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Cell Differentiation / physiology
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Drug Resistance, Neoplasm / drug effects
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Drug Resistance, Neoplasm / physiology*
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Glutathione Peroxidase / antagonists & inhibitors
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Glutathione Peroxidase / metabolism
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Humans
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Iron / metabolism*
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Neoplasms / drug therapy
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Neoplasms / metabolism*
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Neoplasms / pathology
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Phospholipid Hydroperoxide Glutathione Peroxidase
Substances
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Antineoplastic Agents
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Iron
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Phospholipid Hydroperoxide Glutathione Peroxidase
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Glutathione Peroxidase