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Tumor inoculation site affects the development of cancer cachexia and muscle wasting
Authors:Tatsuzo Matsuyama  Takeshi Ishikawa  Tetsuya Okayama  Kaname Oka  Satoko Adachi  Katsura Mizushima  Reiko Kimura  Manabu Okajima  Hiromi Sakai  Naoyuki Sakamoto  Kazuhiro Katada  Kazuhiro Kamada  Kazuhiko Uchiyama  Osamu Handa  Tomohisa Takagi  Satoshi Kokura  Yuji Naito  Yoshito Itoh
Affiliation:1. Department of Molecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan;2. Department of Cancer ImmunoCell Regulation, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan;3. Faculty of Health Medicine, Kyoto Gakuen University, Kyoto, Japan
Abstract:The phenotype and severity of cancer cachexia differ among tumor types and metastatic site in individual patients. In this study, we evaluated if differences in tumor microenvironment would affect the development of cancer cachexia in a murine model, and demonstrated that body weight, adipose tissue and gastrocnemius muscle decreased in tumor‐bearing mice. Interestingly, a reduction in heart weight was observed in the intraperitoneal tumor group but not in the subcutaneous group. We evaluated 23 circulating cytokines and members of the TGF‐β family, and found that levels of IL‐6, TNF‐α and activin A increased in both groups of tumor‐bearing mice. Eotaxin and G‐CSF levels in the intraperitoneal tumor group were higher than in the subcutaneous group. Atrogin 1 and MuRF1 mRNA expressions in the gastrocnemius muscle increased significantly in both groups of tumor‐bearing mice, however, in the myocardium, expression of these mRNAs increased in the intraperitoneal group but not in subcutaneous group. Based on these results, we believe that differences in microenvironment where tumor cells develop can affect the progression and phenotype of cancer cachexia through alterations in various circulating factors derived from the tumor microenvironment.
Keywords:cancer cachexia  muscle wasting  tumor microenvironment  cytokine  colorectal cancer
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