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(American Journal of Pathology. 2000;156:193-200.)
© 2000 American Society for Investigative Pathology


Regular Articles

Human Melanoma Progression in Skin Reconstructs

Biological Significance of bFGF

Friedegund Meier*, Mark Nesbit*, Mei-Yu Hsu*, Bernard Martin{dagger}, Patricia Van Belle{ddagger}, David E. Elder{ddagger}, Gundula Schaumburg-Lever§, Claus Garbe§, Tania Marina Walz§, Philippe Donatien*, Timothy M. Crombleholme{dagger} and Meenhard Herlyn*

From the Wistar Institute,*
Philadelphia, Pennsylvania; the Department of Surgery,{dagger}
Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania; the Department of Pathology,{ddagger}
University of Pennsylvania, Philadelphia, Pennsylvania; and the Department of Dermatology,§
University of Tuebingen, Tuebingen, Germany

Human skin reconstructs are three-dimensional in vitro models consisting of epidermal keratinocytes plated onto fibroblast-contracted collagen gels. Cells in skin reconstructs more closely recapitulate the in situ phenotype than do cells in monolayer culture. Normal melanocytes in skin reconstructs remained singly distributed at the basement membrane which separated the epidermis from the dermis. Cell lines derived from biologically early primary melanomas of the radial growth phase proliferated in the epidermis and the basement membrane was left intact. Growth and migration of the radial growth phase melanoma cells in the dermal reconstruct and tumorigenicity in vivo were only observed when cells were transduced with the basic fibroblast growth factor gene, a major autocrine growth stimulator for melanomas. Primary melanoma cell lines representing the more advanced stage vertical growth phase invaded the dermis in reconstructs and only an irregular basement membrane was formed. Metastatic melanoma cells rapidly proliferated and aggressively invaded deep into the dermis, with each cell line showing typical invasion and growth characteristics. Our results demonstrate that the growth patterns of melanoma cells in skin reconstructs closely correspond to those in situ and that basic fibroblast growth factor is critical for progression.





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