Abstract
The development of resistance to chemotherapy is a major obstacle for lasting effective treatment of cancer. Here, we demonstrate that endogenous mesenchymal stem cells (MSCs) become activated during treatment with platinum analogs and secrete factors that protect tumor cells against a range of chemotherapeutics. Through a metabolomics approach, we identified two distinct platinum-induced polyunsaturated fatty acids (PIFAs), 12-oxo-5,8,10-heptadecatrienoic acid (KHT) and hexadeca-4,7,10,13-tetraenoic acid (16:4(n-3)), that in minute quantities induce resistance to a broad spectrum of chemotherapeutic agents. Interestingly, blocking central enzymes involved in the production of these PIFAs (cyclooxygenase-1 and thromboxane synthase) prevents MSC-induced resistance. Our findings show that MSCs are potent mediators of resistance to chemotherapy and reveal targets to enhance chemotherapy efficacy in patients.
Copyright © 2011 Elsevier Inc. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antineoplastic Agents / pharmacology*
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Apoptosis / drug effects
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Carboplatin / administration & dosage
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Carboplatin / pharmacology
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Cisplatin / administration & dosage
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Cisplatin / pharmacology
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Cyclooxygenase 1 / metabolism*
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Cyclooxygenase Inhibitors
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Drug Resistance, Neoplasm*
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Fatty Acids / metabolism*
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Fatty Acids, Unsaturated / metabolism*
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Humans
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Mass Spectrometry
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Mesenchymal Stem Cells / metabolism*
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Metabolomics
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Organoplatinum Compounds / administration & dosage
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Organoplatinum Compounds / pharmacology
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Oxaliplatin
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Platinum Compounds / pharmacology*
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Thromboxane-A Synthase / antagonists & inhibitors
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Thromboxane-A Synthase / metabolism*
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Tumor Cells, Cultured
Substances
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Antineoplastic Agents
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Cyclooxygenase Inhibitors
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Fatty Acids
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Fatty Acids, Unsaturated
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Organoplatinum Compounds
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Platinum Compounds
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hexadeca-4,7,10,13-tetraenoic acid
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Oxaliplatin
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12-keto-5,8,10-heptadecatrienoic acid
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Carboplatin
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Cyclooxygenase 1
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Thromboxane-A Synthase
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Cisplatin