Basal Cell Carcinomas in Mice Overexpressing Sonic Hedgehog

Author:

Oro Anthony E.123,Higgins Kay M.123,Hu Zhilan123,Bonifas Jeannette M.123,Epstein Ervin H.123,Scott Matthew P.123

Affiliation:

1. A. E. Oro, Howard Hughes Medical Institute, Departments of Dermatology, Developmental Biology, and Genetics, Stanford University School of Medicine, Stanford, CA 94305–5427, USA.

2. K. M. Higgins and M. P. Scott, Howard Hughes Medical Institute, Departments of Developmental Biology and Genetics, Stanford University School of Medicine, Stanford, CA 94305–5427, USA.

3. Z. Hu, J. M. Bonifas, E. H. Epstein Jr., Department of Dermatology, San Francisco General Hospital, University of California, San Francisco, CA 94110, USA.

Abstract

Mutations in the tumor suppressor gene PATCHED ( PTC ) are found in human patients with the basal cell nevus syndrome, a disease causing developmental defects and tumors, including basal cell carcinomas. Gene regulatory relationships defined in the fruit fly Drosophila suggest that overproduction of Sonic hedgehog (SHH), the ligand for PTC, will mimic loss of ptc function. It is shown here that transgenic mice overexpressing SHH in the skin develop many features of basal cell nevus syndrome, demonstrating that SHH is sufficient to induce basal cell carcinomas in mice. These data suggest that SHH may have a role in human tumorigenesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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