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Expression of a murine homolog of apoptosis-inducing human IL-24/MDA-7 in murine tumors fails to induce apoptosis or produce anti-tumor effects.

Abstract
Expression of human interleukin (IL)-24 in tumors achieved anti-tumor effects through apoptosis. IL-24 also induced secretion of proinflammatory cytokines, suggesting the role in immunity. We showed that murine IL-24 transcripts started from the second initiation codon and that expressed mIL-24 in tumors failed to induce apoptosis. Proliferation of murine cells expressing mIL-24 was the same as that of the parent cells and inoculation of the mIL-24-expressing tumors into syngeneic mice did not produce anti-tumor effects. Secretory mIL-24 did not induce the expression of the IL-6, TNF-α or IFN-γ gene in spleen cells. Expression of mIL-24 receptor subunits, IL-22R and IL-20R1, was undetectable in spleen cells even though they were stimulated by anti-CD3, anti-CD40 antibody or concanavalin A. Transduction of murine tumors with adenoviruses expressing the human IL-24 gene however suppressed the viability and decreased the tumor growth. These data suggest that mIL-24 is functionally irrelevant to the human counterpart.
AuthorsHiroyasu Nagakawa, Osamu Shimozato, Ling Yu, Akihiko Wada, Kiyoko Kawamura, Quanhai Li, Sunil Chada, Yuji Tada, Yuichi Takiguchi, Koichiro Tatsumi, Masatoshi Tagawa
JournalCellular immunology (Cell Immunol) 2012 Jan-Feb Vol. 275 Issue 1-2 Pg. 90-7 ISSN: 1090-2163 [Electronic] Netherlands
PMID22475191 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Cytokines
  • Il24 protein, mouse
  • Interleukins
  • interleukin-24
Topics
  • Amino Acid Sequence
  • Animals
  • Apoptosis
  • Cell Line
  • Cytokines (chemistry, genetics, immunology)
  • Female
  • Gene Expression Regulation
  • Humans
  • Interleukins (genetics, immunology)
  • Mice
  • Molecular Sequence Data
  • Neoplasms (genetics, immunology, pathology)
  • Sequence Alignment

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