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Repair of UV Dimers in Skin DNA of Patients with Basal Cell Carcinoma

¹ Department of Biosciences and Nutrition, Karolinska Institute, Huddinge, Sweden; ² Department of Dermatology, Päijät-Häme Central Hospital, Lahti, Finland; and ³ Division of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany

Requests for reprints: Dan Segerbäck, Department of Biosciences and Nutrition, Karolinska Institute, Novum S-141 57, Huddinge, Sweden. Phone: 46-8-58583779; Fax: 46-8-7116659. E-mail: dan.segerback{at}biosci.ki.se

Epidemiologic studies suggest that exposure to sunlight is the primary etiologic agent for basal cell carcinoma. Formation of UV-induced DNA damage is believed to be a crucial event in the process leading to skin cancer. In this study, repair of photoproducts in DNA was followed in the skin of patients with basal cell carcinoma and control subjects. The subjects were exposed to 800 J/m² Commission Internationale de 1'Éclairag of solar-simulating radiation on buttock skin. Biopsies were taken at 0 hour, 24 hours, and 3 weeks after the exposure. Two cyclobutane pyrimidine dimers, TT=C and TT=T, were measured using a sensitive ³²P-postlabeling assay. Initial levels of both TT=C and TT=T differed between individuals in both groups. The levels of TT=T in patients with basal cell carcinoma and controls were similar (9.9 ± 4.0 and 9.2 ± 2.9 products per 10⁶ normal nucleotides), whereas the level of TT=C was significantly lower in controls than in patients with basal cell carcinoma (6.2 ± 3.1 versus 10.9 ± 4.5 products per 10⁶ normal nucleotides). The fractions of TT=T remaining after 24 hours and 3 weeks were significantly higher in patients with basal cell carcinoma (72% and 11%) compared with controls (48% and 5%). A slower removal in patients with basal cell carcinoma than in controls was indicated also for TT=C (52% versus 42% remaining at 24 hours); however, the difference between groups was not significant. When including data from our previously reported small-scale study, the fraction of dimers remaining at 24 hours was significantly higher in patients with basal cell carcinoma for both TT=C and TT=T. The data suggest that patients with basal cell carcinoma have a reduced capacity to repair UV-induced DNA lesions. (Cancer Epidemiol Biomarkers Prev 2008;17(9):2388–92)