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Evidence for the involvement of interleukin 6 in experimental cancer cachexia.

Open access
Strassmann, G, Fong, M, Kenney, J S, Jacob, C O·1992·Journal of Clinical Investigation

Abstract

In this report we describe an experimental model of cachexia that fulfills the criteria of an early effect with a small tumor mass not related to the growth rate of the tumor, and progressive wasting of muscle and fat without a detectable loss of appetite. C-26.IVX is a cell line derived from murine colon-26 adenocarcinoma which retains the transplantability of the original tumor and induces true cachexia in syngeneic hosts. Evidence is presented to support a role for interleukin (IL-6) as a cachectic factor in the development of cancer cachexia in this model system. Thus, increasing levels of IL-6 in C-26.IVX-bearing mice correlate with the development of cachexia. If the primary tumors were resected, mice gained weight and the levels of IL-6 in the serum were reduced significantly. Moreover, monoclonal antibody to murine IL-6 (but not anti-tumor necrosis factor antibody) was able to significantly suppress the development of key parameters of cachexia in tumor bearing mice.

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Metadata

Authors
Strassmann, G., Fong, M., Kenney, J. S., & Jacob, C. O.
Venue
Journal of Clinical Investigation
Published
1992-05-01
Volume
89
Issue
5
Pages
1681-1684
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2126540916
Cited by
658
References
0
FWCI
13.20
Type
journal article
Language
en
Open access
bronze

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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