Abstract | BACKGROUND: METHODS: Age- and weight-matched female mice were injected with SCCF/VII cells. Daily food intake and weights were measured. Body composition and analysis of circulating cytokines was performed. At the completion of experiments, hind legs were weighed. Muscle atrophy was detected using analysis for muscle ring finger 1 (MuRF1). The tumor-derived lipid mobilizing factor (LMF) was measured. RESULTS: Despite increased food intake, tumor-bearing mice lost weight and experienced reduced hind leg weights. Interleukin-1beta (IL-1beta) was increased and MuRF1 was present in tumor-bearing mice but not controls. LMF was present in SCCF/VII cells. CONCLUSION: In this immunocompetent murine model, we demonstrated the development of cancer cachexia in mice inoculated with SCCF cells, which express LMF. There was increased serum IL-1beta, weight loss, and muscle wasting and atrophy in tumor-bearing mice.
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Authors | Trinitia Cannon, Carol Shores, Xiaoying Yin, Jason Dahlman, Denis Guttridge, Victor Lai, Jonathan George, Petra Buzkova, Marion Couch |
Journal | Head & neck
(Head Neck)
Vol. 30
Issue 3
Pg. 320-6
(Mar 2008)
ISSN: 1043-3074 [Print] United States |
PMID | 17657796
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | (c) 2007 Wiley Periodicals, Inc. Head Neck 2008. |
Chemical References |
- Interleukin-1alpha
- Interleukin-1beta
- Muscle Proteins
- Peptides
- Tripartite Motif Proteins
- lipid mobilizing substance
- TRIM63 protein, human
- Ubiquitin-Protein Ligases
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Topics |
- Animals
- Cachexia
(etiology)
- Carcinoma, Squamous Cell
(complications, metabolism)
- Cell Line, Tumor
- Disease Models, Animal
- Female
- Head and Neck Neoplasms
(complications, metabolism)
- Hindlimb
- Immunocompetence
- Interleukin-1alpha
(blood)
- Interleukin-1beta
(blood)
- Mice
- Mice, Inbred C3H
- Muscle Proteins
(metabolism)
- Muscle, Skeletal
(metabolism)
- Muscular Atrophy
(etiology)
- Neoplasm Transplantation
- Peptides
(metabolism)
- Tripartite Motif Proteins
- Ubiquitin-Protein Ligases
(metabolism)
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