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Expression of transforming growth factor-α (TGF-α) in cholesteatoma

Published online by Cambridge University Press:  29 June 2007

Masanori Shiwa*
Affiliation:
Department of Otorhinolaryngology, The Jikei University School of Medicine, 3-25-8 Nishishinbashi Minato-ku, Tokyo 105-0003, Japan.
Hiromi Kojima
Affiliation:
Department of Otorhinolaryngology, The Jikei University School of Medicine, 3-25-8 Nishishinbashi Minato-ku, Tokyo 105-0003, Japan.
Hiroshi Moriyama
Affiliation:
Department of Otorhinolaryngology, The Jikei University School of Medicine, 3-25-8 Nishishinbashi Minato-ku, Tokyo 105-0003, Japan.
*
Address for correspondence: Dr Masanori Shiwa, Department of Otorhinolaryngology, The Jikei University School of Medicine, 3-25-8 Nishishinbashi Minato-ku, Tokyo 105-0003, Japan. Fax: +81-3-3435-8436

Abstract

This study aims at elucidating the role of cytokines in the mechanism of proliferation of cholesteatoma epithelium by investigating the mode of expression of epidermal growth factors, such as TGF-α. The subjects of this study were patients who had undergone operation for middle ear cholesteatoma. Skins of the bone region of the externalear canal (normal skin) of the same patients were used as the negative control. The mode of expression of TGF-α was studied by immunohistochemistry and in situ hybridization. In the immunohistochemical study, there were no conspicuous differences observed between cholesteatoma tissues and normal skin. After in situ hybridization, expression of TGF-α mRNA was mainly observed in the epidermal basal cell layer in the normal skin, while in the cholesteatoma epidermis with severe inflammatory cell infiltration, expression of TFG-α mRNA was observed up to layers superior to the basal cell layer. The expression of TGF-α mRNA is greatly affected by subepithelial connective tissue, strongly suggesting involvement of paracrine regulation in proliferation of cholesteatomaepithelium.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 1998

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References

Chedid, M., Rubins, J. S., Csaky, K. G., Aaronson, S. A. (1994) Regulation of keratinocyte growth factor gene expression by interleukin 1. Journal of Biological Chemistry 269: 1075310757.Google Scholar
Coffey, R. J. Jr., Derynck, R., Wilcox, J. N., Bringman, T. S., Goustin, A. S., Moses, H. L., Pittelkow, M. R. (1987) Production and auto-induction of transforming growth factor-α in human keratinocytes. Nature 328: 817820.Google Scholar
Elder, J. T., Fisher, G. J., Lindquist, P. B., Bennett, G. L., Pittelkow, M. R., Coffey, R. J. Jr., Ellingsworth, L., Derynck, R., Voorhees, J. J. (1989) Over expression of transforming growth factor a in psoriatic epidermis. Science 243: 811814.Google Scholar
Kojima, H., Matsuhisa, A., Shiwa, M., Kamide, Y., Nakamura., M.Ohno, T., Moriyama, H. (1996) Expression ofmessenger RNA for keratinocyte growth factor in human cholesteatoma. Archives ofOtolaryngology-Head and Neck Surgery 122: 157160.Google Scholar
Kojima, H., Shiwa, M., Kamide, Y., Moriyama, H. (1994) Expression and localization of mRNA for epidermal growth factor and epidermal growth factor receptor in human cholesteatoma. Acta Otolaryngologica (Stockh) 114: 423429.Google Scholar
King, L. E. Jr, Gates, R. E., Stoscheck, C. M., Nanney, L. B. (1990) The EGF/TGFα receptor in skin. Journal of Investigative Dermatology 94: 164s170s.CrossRefGoogle Scholar
Schulz, P., Bujia, J., Shilling, V. (1993) Possible autocrine growth stimulation of cholesteatoma epithelium by transforming growth factor alpha. American Journal of Otolaryngology 14: 8287.Google Scholar
Shiwa, M., Kojima, H., Kamide, Y., Moriyama, H. (1995) Involvement of interleukin-1 in middle ear cholesteatoma. American Journal of Otolaryngology 16: 319324.Google Scholar