Literature DB >> 21660860

Oral resveratrol therapy inhibits cancer-induced skeletal muscle and cardiac atrophy in vivo.

Scott Shadfar1, Marion E Couch, Kibwei A McKinney, Lisa J Weinstein, Xiaoying Yin, Jessica E Rodríguez, Denis C Guttridge, Monte Willis.   

Abstract

The mechanism by which cancer mediates muscle atrophy has been delineated in the past 3 decades and includes a prominent role of tumor-derived cytokines, such as IL-6, TNFα, and IL-1. These cytokines interact with their cognate receptors on muscle to activate the downstream transcription factor NF-κB and induce sarcomere proteolysis. Experimentally, inhibiting NF-κB signaling largely prevents cancer-induced muscle wasting, indicating its prominent role in muscle atrophy. Resveratrol, a natural phytoalexin found in the skin of grapes, has recently been shown to inhibit NF-κB in cancer cells, which led us to hypothesize that it might have a protective role in cancer cachexia. Therefore, we investigated whether daily oral resveratrol could protect against skeletal muscle loss and cardiac atrophy in an established mouse model. We demonstrate resveratrol inhibits skeletal muscle and cardiac atrophy induced by C26 adenocarcinoma tumors through its inhibition of NF-κB (p65) activity in skeletal muscle and heart. These studies demonstrate for the first time the utility of oral resveratrol therapy to provide clinical benefit in cancer-induced atrophy through the inhibition of NF-κB in muscle. These findings may have application in the treatment of diseases with parallel pathophysiologies such as muscular dystrophy and heart failure.

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Year:  2011        PMID: 21660860      PMCID: PMC3623008          DOI: 10.1080/01635581.2011.563032

Source DB:  PubMed          Journal:  Nutr Cancer        ISSN: 0163-5581            Impact factor:   2.900


  61 in total

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Review 3.  Interleukin 6 as a key regulator of muscle mass during cachexia.

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5.  Altered expression of skeletal muscle myosin isoforms in cancer cachexia.

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6.  Identification of ubiquitin ligases required for skeletal muscle atrophy.

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9.  Role of NF-kappaB and cytokine in experimental cancer cachexia.

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  35 in total

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Review 5.  Nuclear factor-κB signalling and transcriptional regulation in skeletal muscle atrophy.

Authors:  Robert W Jackman; Evangeline W Cornwell; Chia-Ling Wu; Susan C Kandarian
Journal:  Exp Physiol       Date:  2012-07-30       Impact factor: 2.969

6.  Metabolic derangements in the gastrocnemius and the effect of Compound A therapy in a murine model of cancer cachexia.

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Review 7.  F-BOX proteins in cancer cachexia and muscle wasting: Emerging regulators and therapeutic opportunities.

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8.  Both aerobic exercise and resveratrol supplementation attenuate doxorubicin-induced cardiac injury in mice.

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9.  Post-translationally modified muscle-specific ubiquitin ligases as circulating biomarkers in experimental cancer cachexia.

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10.  Baicalin, a component of Scutellaria baicalensis, alleviates anorexia and inhibits skeletal muscle atrophy in experimental cancer cachexia.

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