A novel myokine, secreted protein acidic and rich in cysteine (SPARC), suppresses colon tumorigenesis via regular exercise. Issue 6 (31st July 2012)

• Record Type: Journal Article
• Authors: Aoi, Wataru; Naito, Yuji; Takagi, Tomohisa; Tanimura, Yuko; Takanami, Yoshikazu; Kawai, Yukari; Sakuma, Kunihiro; Hang, Liu Po; Mizushima, Katsura; Hirai, Yasuko; Koyama, Ryota; Wada, Sayori; Higashi, Akane; Kokura, Satoshi; Ichikawa, Hiroshi; Yoshikawa, Toshikazu
• Is Part Of: Gut. Volume 62:Issue 6(2013)
• Page Start: 882
• Page End: 889
• Publication Date: 2012-07-31
• Subjects: Skeletal muscle -- colon cancer -- apoptosis -- colorectal physiology -- colorectal cancer -- oxidative stress -- inflammatory bowel disease -- inflammatory mediators -- immunology -- ibd models -- gastric inflammation -- amino acids -- antioxidants -- cell biology -- ageing -- amino acids -- ibd -- mucosal repair -- oxidative stress; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gutjnl-2011-300776
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : Objective: Several epidemiological studies have shown that regular exercise can prevent the onset of colon cancer, although the underlying mechanism is unclear. Myokines are secreted skeletal muscle proteins responsible for some exercise-induced health benefits including metabolic improvement and anti-inflammatory effects in organs. The purpose of this study was to identify new myokines that contribute to the prevention of colon tumorigenesis. Methods: To identify novel secreted muscle-derived proteins, DNA microarrays were used to compare the transcriptome of muscle tissue in sedentary and exercised young and old mice. The level of circulating secreted protein acidic and rich in cysteine (SPARC) was measured in mice and humans that performed a single bout of exercise. The effect of SPARC on colon tumorigenesis was examined using SPARC-null mice. The secretion and function of SPARC was examined in culture experiments. Results: A single bout of exercise increased the expression and secretion of SPARC in skeletal muscle in both mice and humans. In addition, in an azoxymethane-induced colon cancer mouse model, regular low-intensity exercise significantly reduced the formation of aberrant crypt foci in wild-type mice but not in SPARC-null mice. Furthermore, regular exercise enhanced apoptosis in colon mucosal cells and increased the cleaved forms of caspase-3 and caspase-8 in wild-type mice but not in SPARC-null mice. Culture experiments showed that SPARC secretion from myocytes was induced by cyclic stretch and inhibited proliferation with apoptotic effect of colon cancer cells. Conclusions: These findings suggest that exercise stimulates SPARC secretion from muscle tissues and that SPARC inhibits colon tumorigenesis by increasing apoptosis.