Original Article
Subject Category: Tumor Biology
Journal of Investigative Dermatology (2005) 124, 263–267; doi:10.1111/j.0022-202X.2004.23573.x
Anti-Rejection Drug Treatment Increases Basal Cell Carcinoma Burden in Ptch1+/- Mice
Annika Vogt*,1, Jennifer Hebert*, Jimmy Hwang†, Ying Lu† and Ervin H Epstein Jr*,†
- *Department of Dermatology, UCSF Comprehensive Cancer Center, University of California, San Francisco, California, USA
- †UCSF Comprehensive Cancer Center, University of California, San Francisco, California, USA
Correspondence: Ervin Epstein Jr, University of California San Francisco, San Francisco General Hospital, 1001 Potrero Avenue, Building 100 – Room 269, San Francisco, CA 94110, USA. Email: epsteine@derm.ucsf.edu
1Current address: Department of Dermatology, University Medical Center Charite, Berlin, Germany.
Received 7 June 2004; Revised 21 September 2004; Accepted 4 October 2004; Published online 21 December 2004.
Abstract
The development of extensive and severe non-melanoma skin cancer is an extremely common complication of organ transplantation and is assumed to be caused by long-term treatment with anti-rejection drugs (ARD). Despite this florid clinical problem, ARD treatments have been reported to affect experimental murine skin carcinogenesis only weakly. We report here that treatment of cesium-137-irradiated Ptch1+/- mice with immunosuppressive doses of cyclosporine A plus prednisolone for 4-1/2 mo increased basal cell carcinoma burden by 2.5-fold. Thus, these mice provide a good model for study of the effects of long-term administration of ARD on at least one type of non-melanoma skin cancer.
Keywords:
basal cell carcinoma, cyclosporine A, hedgehog, organ transplantation, patched
Abbreviations:
ARD, anti-rejection drug; BCC, basal cell carcinoma; BSA, bovine serum albumin; CsA, cyclosporine A; DTH, delayed type hypersensitivity; OTR, organ transplant recipient
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