UV-induced DNA damage and melanin content in human skin differing in racial/ethnic origin

被引:256
作者
Tadokoro, T
Kobayashi, N
Zmudzka, BZ
Ito, S
Wakamatsu, K
Yamaguchi, Y
Korossy, KS
Miller, SA
Beer, JZ
Hearing, VJ
机构
[1] NCI, Cell Biol Lab, NIH, Bethesda, MD 20892 USA
[2] US FDA, Ctr Devices & Radiol Hlth, Rockville, MD 20852 USA
[3] Fujita Hlth Univ, Sch Hlth Sci, Dept Chem, Aichi 4701192, Japan
关键词
melanocytes; skin color; photocarcinogenesis; cyclobutane pyrimidine dimers;
D O I
10.1096/fj.02-0865fje
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA damage induced by UV radiation is a critical event in skin photocarcinogenesis. However, the role of racial/ethnic origin in determining individual UV sensitivity remains unclear. In this study, we examined the relationships between melanin content and DNA damage induced by UV exposure in situ in normal human skin of different racial/ethnic groups, phototypes, and UV sensitivities. The minimal erythema dose (MED) was established for each subject exposed to UVA/UVB radiation, and skin was biopsied before as well as 7 min, 1 day, and 1 wk after UV exposure. There was great variation among individuals in the amount of DNA damage incurred and rates of its removal. The results show that after exposure to 1 MED of UV, the skin of subjects from all groups suffered significant DNA damage, and that increasing content of constitutive melanin inversely correlated with the amount of DNA damage. It is clear from these results that measured erythemal UV sensitivity of the skin (MED) is a more useful predictor of DNA photodamage than is racial/ethnic origin or skin phototype and that rates of DNA damage removal following UV radiation may be the critical determinant of the UV sensitivity (including predisposition to cancer) of the skin.
引用
收藏
页码:1177 / +
页数:22
相关论文
共 52 条
[31]  
MONTAGNA W, 1972, PIGMENTATION ITS GEN, P1
[32]   INDUCTION AND REPAIR OF UVB-INDUCED CYCLOBUTANE PYRIMIDINE DIMERS AND (6-4) PHOTOPRODUCTS IN ORGAN-CULTURED NORMAL HUMAN SKIN [J].
MURAMATSU, T ;
KOBAYASHI, N ;
TADA, H ;
YAMAJI, M ;
SHIRAI, T ;
MORI, T ;
OHNISHI, T .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1992, 284 (04) :232-237
[33]  
Nordlund J. J., 2008, The pigmentary system: Physiology and pathophysiology
[34]  
Pathak MA, 1971, BIOL NORMAL ABNORMAL, P149
[35]   NONMELANOMA CANCERS OF THE SKIN [J].
PRESTON, DS ;
STERN, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (23) :1649-1662
[36]   Pigment cell research: What directions? [J].
Prota, G .
PIGMENT CELL RESEARCH, 1997, 10 (1-2) :5-11
[37]   Free radical scavenging properties of melanin interaction of eu- and pheo-melanin models with reducing and oxidising radicals [J].
Rózanowska, M ;
Sarna, T ;
Land, EJ ;
Truscott, TG .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (5-6) :518-525
[38]   REPAIR DEFICIENT HUMAN DISORDERS AND CANCER [J].
SETLOW, RB .
NATURE, 1978, 271 (5647) :713-717
[39]   WAVELENGTHS EFFECTIVE IN INDUCTION OF MALIGNANT-MELANOMA [J].
SETLOW, RB ;
GRIST, E ;
THOMPSON, K ;
WOODHEAD, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) :6666-6670
[40]  
Smit NPM, 2001, PHOTOCHEM PHOTOBIOL, V74, P424, DOI 10.1562/0031-8655(2001)074<0424:MOPAIO>2.0.CO