Habitual myofibrillar protein synthesis is normalin patients with upper GI cancer cachexia

  • Alisdair J. MacDonald
  • , Neil Johns
  • , Nathan Stephens
  • , Carolyn Greig
  • , James A. Ross
  • , Alexandra C. Small
  • , Holger Husi
  • , Kenneth C.H. Fearon
  • , Tom Preston

Research output: Journal PublicationArticlepeer-review

63 Citations (Scopus)

Abstract

Purpose: Skeletal muscle wasting and weight loss are characteristic features of cancer cachexia and contribute to impaired function, increased morbidity, and poor tolerance of chemotherapy. This study used a novel technique to measure habitual myofibrillar protein synthesis in patients with cancer compared with healthy controls. Experimental design: An oral heavy water (87.5 g deuterium oxide) tracer was administered as a single dose. Serum samples were taken over the subsequent week followed by a quadriceps muscle biopsy. Deuterium enrichment was measured in body water, serum alanine, and alanine in the myofibrillar component of muscle using gas chromatography-pyrolysis-isotope ratio mass spectrometry and the protein synthesis rate calculated from the rate of tracer incorporation. Net change in muscle mass over the preceding 3 months was calculated from serial CT scans and allowed estimation of protein breakdown. Results: Seven healthy volunteers, 6 weight-stable, and 7 weight-losing (≥5% weight loss) patients undergoing surgery for upper gastrointestinal cancer were recruited. Serial CT scans were available in 10 patients, who lost skeletal muscle mass preoperatively at a rate of 5.6%/100 days. Myofibrillar protein fractional synthetic rate was 0.058%, 0.061%, and 0.073%/hour in controls, weight-stable, and weight-losing patients, respectively. Weight-losing patients had higher synthetic rates than controls (P = 0.03). Conclusion: Contrary to previous studies, there was no evidence of suppression of myo fibrillar protein synthesis in patients with cancer cachexia. Our finding implies a small increase in muscle breakdown may account for muscle wasting.

Original languageEnglish
Pages (from-to)1734-1740
Number of pages7
JournalClinical Cancer Research
Volume21
Issue number7
DOIs
Publication statusPublished - 1 Apr 2015
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

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