Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jul 15, 2003; 9(7): 1567-1570
Published online Jul 15, 2003. doi: 10.3748/wjg.v9.i7.1567
Role of NF-κB and cytokine in experimental cancer cachexia
Wei Zhou, Zhi-Wei Jiang, Jie Tian, Jun Jiang, Ning Li, Jie-Shou Li
Wei Zhou, Zhi-Wei Jiang, Jun Jiang, Ning Li, Jie-Shou Li, Department of Surgery, School of Medicine, Nanjing University, Nanjing 210002, Jiangsu Province, China
Jie Tian, Department of Anaesthesiology, School of Life Sciences, Nanjing University, Nanjing 210002, Jiangsu Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Wei Zhou, Department of Surgery, Jinling Hospital, 305 East Zhongshan Road, Nanjing 210002, Jiangsu Province, China. nuzw@sohu.com
Telephone: +86-25-3685194 Fax: +86-25-4803956
Received: March 2, 2003
Revised: March 14, 2003
Accepted: March 29, 2003
Published online: July 15, 2003
Abstract

AIM: To assess the putative involvement of NF-κB and pro-inflammatory cytokines in the pathogenesis of cancer cachexia and the therapeutic efficacy of indomethacin (IND) on cachexia.

METHODS: Thirty young male BABL/c mice were divided randomly into five groups: (a) control, (b) tumor-bearing plus saline, (c) tumor-bearing plus IND (0.25 mg•kg-1), (d) tumor-bearing plus IND (0.5 mg•kg-1), and (e) tumor-bearing plus IND (2 mg•kg-1). Colon 26 adenocarcinoma cells of murine were inoculated subcutaneously to induce cachexia. Saline and IND were given intraperitoneally daily for 7 d from the onset of cachexia to sacrifice. Food intake and body composition were documented, serum levels of TNF-α and IL-6 and activity of NF-κB in the spleen were investigated in all animals.

RESULTS: Weight loss was observed in all tumor-bearing mice. By day 16, body weights of non-tumor mice were about 72% of healthy controls (P < 0.01), and the weight of gastrocnemius was decreased by 28.7% (P < 0.01). No difference was found between groups in food intake (P > 0.05). Gastrocnemius weight was increased markedly (P < 0.01) after treatment of IND (0.5 mg•kg-1), while the non-tumor body weights were not significantly elevated. Tumor-bearing caused a 2-3 fold increase in serum levels of both TNF-α and IL-6 (P < 0.01). The concentration of TNF-α (P < 0.05) and IL-6 (P < 0.01) in tumor-bearing mice was reduced after administration of 0.5 mg•kg-1 IND for 7 d. But the level of IL-6 was slightly elevated following treatment of IND 2.0 mg•kg-1. NF-κB activation in the spleen was increased in tumor-bearing mice in comparison with controls in electrophoretic mobility shift assay (EMSA). NF-κB activity was reduced in mice treated with 0.5 mg•kg-1 of IND, whereas a higher NF-κB activity was observed in mice treated with 2.0 mg•kg-1 of IND.

CONCLUSION: Colon 26 adenocarcinoma cells can induce severe cancer cachexia experimentally, and the mechanism may be partially due to the enhanced TNF-α and IL-6 in tumor-bearing animals, which is controlled by NF-κB. Low dose of indomethacin alleviates the cachexia, decreases the activation of NF-κB and the serum levels of TNF-α and IL-6, and prevents body weight loss and muscle atrophy, while no further effect is gained by a higher dosage.

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