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Pathogenesis of muscle wasting in cancer cachexia: targeted anabolic and anticatabolic therapies. | LitMetric

AI Article Synopsis

  • Cancer-related muscle loss, known as cachexia, affects about 2 million lives globally, leading to decreased quality of life and shorter survival rates.
  • Cytokines like tumor necrosis factor-alpha activate pathways that break down muscle, but androgen treatment may reduce inflammation and enhance muscle-building.
  • Combining androgens and amino acids could be an effective strategy to combat cachexia, with further research needed to pinpoint specific therapeutic targets for treatment.

Article Abstract

Purpose Of Review: Cancer-related muscle loss, or cachexia, is the cause of death for approximately 2 million people worldwide and severely reduces quality of life. The degree of cachexia is inversely correlated with survival time; however, the exact mechanisms behind cancer-induced muscle wasting remain under investigation.

Recent Findings: Cytokines such as tumor necrosis factor-alpha trigger degradatory pathways through nuclear factor-kappaB signaling that activate the ubiquitin-proteasome system and muscle proteolysis. Androgen treatment has been shown to reduce inflammatory cytokines and even stimulate anti-inflammatory cytokine production. Amino acid supplementation has been shown to induce muscle protein synthesis in ovarian cancer patients.

Summary: Targeted anabolic therapies aimed at preventing or reversing cancer cachexia might involve the combined use of androgens and amino acids working concurrently to enhance muscle protein synthesis and reduce muscle protein breakdown. Additional focused clinical studies are needed to identify muscle-specific targets or biomarkers for defined therapeutic approaches to slow or prevent cancer cachexia. In this review, we summarize the pathogenesis of cancer-related muscle wasting and discuss potential interventions at reversing or preventing cancer-related muscle loss.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618842PMC
http://dx.doi.org/10.1097/MCO.0b013e328339fdd2DOI Listing

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