Role of intracellular interleukin-1 receptor antagonist in skin carcinogenesis

Mol Carcinog. 2001 Apr;30(4):218-23. doi: 10.1002/mc.1031.

Abstract

Interleukin 1 (IL-1) is a major mediator of inflammation and exerts pleiotropic effects on many systems. To elucidate the role of its endogenous inhibitor, intracellular IL-1 receptor antagonist (icIL-1Ra), in mouse skin, we produced an icIL-1Ra-overexpressing skin carcinoma cell line (icIL-1Ra-JWF2). Altered expression of icIL-1Ra did not change IL-1alpha mRNA levels in these transfected cells. In icIL-1Ra-JWF2 cells, however, cyclooxygenase-2 mRNA levels were dramatically reduced and shown to be transcriptionally regulated by icIL-1Ra. To determine the effect of icIL-1Ra on cell proliferation, cell counts were done 24 h after plating equal numbers of cells. Cells from three icIL-1Ra-JWF2 clones showed significantly reduced growth rates compared with parental JWF2 cells. We subcutaneously injected five independent clones of icIL-1Ra-JWF2 cells into nude mice and measured the tumor doubling time by weekly measurements of tumor volume. IcIL-1Ra appeared to significantly slow the growth of tumors in vivo. Collectively these observations suggest that IL-1Ra has antiproliferative effects in murine skin carcinoma cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blotting, Northern
  • Carcinogenicity Tests / methods*
  • Carcinoma, Squamous Cell / metabolism*
  • Cell Division
  • Cyclooxygenase 2
  • Female
  • In Vitro Techniques
  • Interleukin 1 Receptor Antagonist Protein
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Keratinocytes / metabolism*
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Sialoglycoproteins / genetics
  • Sialoglycoproteins / metabolism*
  • Skin Neoplasms / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Il1rn protein, mouse
  • Interleukin 1 Receptor Antagonist Protein
  • Isoenzymes
  • Sialoglycoproteins
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases