Abstract
Loss of muscle mass related to anti-cancer therapy is a major concern in cancer patients, being associated with important clinical endpoints including survival, treatment toxicity and patient-related outcomes. We investigated effects of voluntary exercise during cisplatin treatment on body weight, food intake as well as muscle mass, strength and signalling. Mice were treated weekly with 4 mg/kg cisplatin or saline for 6 weeks, and randomized to voluntary wheel running or not. Cisplatin treatment induced loss of body weight (29.8%, P < 0.001), lean body mass (20.6%, P = 0.001), as well as anorexia, impaired muscle strength (22.5% decrease, P < 0.001) and decreased glucose tolerance. In addition, cisplatin impaired Akt-signalling, induced genes related to protein degradation and inflammation, and reduced muscle glycogen content. Voluntary wheel running during treatment attenuated body weight loss by 50% (P < 0.001), maintained lean body mass (P < 0.001) and muscle strength (P < 0.001), reversed anorexia and impairments in Akt and protein degradation signalling. Cisplatin-induced muscular inflammation was not prevented by voluntary wheel running, nor was glucose tolerance improved. Exercise training may preserve muscle mass in cancer patients receiving cisplatin treatment, potentially improving physical capacity, quality of life and overall survival.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anorexia / chemically induced
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Anorexia / metabolism
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Anorexia / physiopathology
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Anorexia / prevention & control*
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Body Weight / drug effects
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Cisplatin / pharmacology*
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Female
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Gene Expression
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Glucose Intolerance / chemically induced
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Glucose Intolerance / metabolism
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Glucose Intolerance / physiopathology
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Glycogen / antagonists & inhibitors
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Glycogen / biosynthesis
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Mice
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Muscle Strength / drug effects
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Muscle Strength / physiology
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Muscle, Skeletal / drug effects*
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Muscle, Skeletal / physiology
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Muscular Atrophy / chemically induced
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Muscular Atrophy / metabolism
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Muscular Atrophy / physiopathology
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Muscular Atrophy / prevention & control*
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Physical Conditioning, Animal*
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Proto-Oncogene Proteins c-akt / genetics
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Proto-Oncogene Proteins c-akt / metabolism
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Running / physiology
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Signal Transduction
Substances
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Glycogen
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Proto-Oncogene Proteins c-akt
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Cisplatin
Grants and funding
CIM is supported by a grant from the Danish National Research Foundation (DNRF55). CFAS is supported by a grant from Trygfonden. This study was further supported by grants from the Danish Council for Independent Research and by grants from the Novo Nordic Foundation, Lundbeck Foundation, and Fabrikant Einar Willumsens legat. JG is a Royal Swedish Academy of Sciences Research Fellow supported by a grant from the Acta Oncologica Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.