Abstract |
We have developed a 32P-postlabelling method for quantifying ultraviolet irradiation (UV)-induced cyclobutane dimers and 6-4 photoproducts in human skin in situ. We review the application of the method in studies with human volunteers, demonstrating dose-response relationships over a wide range of administered doses, repair kinetics of UV-damaged DNA among healthy individuals and melanoma patients, and modulation by sunscreens, tan and constitutive pigmentation of damage induction. A notable finding is the wide interindividual variation in DNA damage immediately after irradiation and in its repair. Moreover, the protective effects of sunscreens against erythema and DNA damage also show wide interindividual variation. These results cannot be explained by variation in the experimental methods used. The worst-case scenario is that the differences between individuals are multiplicative, resulting in 1000-fold differences in sensitivity in the population, which would be likely to translate into differences in risk of skin cancer.
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Authors | K Hemminki, G Xu, F Le Curieux |
Journal | IARC scientific publications
(IARC Sci Publ)
Vol. 154
Pg. 69-79
( 2001)
ISSN: 0300-5038 [Print] France |
PMID | 11220670
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Biomarkers, Tumor
- DNA Adducts
- Phosphorus Radioisotopes
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Topics |
- Biomarkers, Tumor
(analysis, genetics)
- Chromatography, High Pressure Liquid
(methods)
- DNA Adducts
(analysis)
- DNA Damage
(physiology)
- Humans
- Phosphorus Radioisotopes
(metabolism)
- Skin
(radiation effects)
- Skin Neoplasms
(genetics, prevention & control)
- Ultraviolet Rays
(adverse effects)
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