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Old 04-06-2008, 08:53 AM   #1 (permalink)
 
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Cyclobutane pyrimidine dimer formation and P53 production in human skin...

Cyclobutane pyrimidine dimer formation and P53 production in human skin after repeated UV irradiation


Exp Dermatol. 2008, March 23
[My paper] Yuji Yamaguchi, Sergio G Coelho, Barbara Z Zmudzka, Kaoruko Takahashi, Janusz Z Beer, Vincent J Hearing, Sharon A Miller
Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Substantial differences in DNA damage caused by a single UV irradiation were found in our previous study on skin with different levels of constitutive pigmentation. In this study, we assessed whether facultative pigmentation induced by repeated UV irradiation is photoprotective. Three sites on the backs of 21 healthy subjects with type II-III skin were irradiated at 100-600 J/m(2) every 2-7 days over a 4- to 5-week period. The three sites received different cumulative doses of UV (1900, 2900 or 4200 J/m(2)) and were biopsied 1 day after the last irradiation. Biomarkers examined included pigment content assessed by Fontana-Masson staining, melanocyte function by expression of melanocyte-specific markers, DNA damage as cyclobutane pyrimidine dimers (CPD), nuclear accumulation of p53, apoptosis determined by TUNEL assay, and levels of p21 and Ser46-phosphorylated p53. Increases in melanocyte function and density, and in levels of apoptosis were similar among the 3 study sites irradiated with different cumulative UV doses. Levels of CPD decreased while the number of p53-positive cells increased as the cumulative dose of UV increased. These results suggest that pigmentation induced in skin by repeated UV irradiation protects against subsequent UV-induced DNA damage but not as effectively as constitutive pigmentation.

SOURCE: http://lib.bioinfo.pl/
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Old 04-07-2008, 09:08 AM   #2 (permalink)
 
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Re: Cyclobutane pyrimidine dimer formation and P53 production in human skin...

In their original study, FS Series sunlamps were used as the irradiance source. These lamps have 60% UVB (and some UVC) and almost no energy in the tanning power (UVA1) range. Assuming that the same lamps were used in this study (which I will check when I get the full paper), the results of the protective properties of the facultative pigmentation (a.k.a., a tan) were very good. Several of us tried (with no success) a few years ago to get the FDA researchers to use sunlamps typical of those used by the indoor tanning industry in their research.
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