Hypermutability of UV-treated plasmids in dysplastic nevus/familial melanoma cell lines

被引:0
|
作者
Moriwaki, SI
Tarone, RE
Tucker, MA
Goldstein, AM
Kraemer, KH
机构
[1] NCI,MOL CARCINOGENESIS LAB,BETHESDA,MD 20892
[2] NCI,BIOSTAT BRANCH,BETHESDA,MD 20892
[3] NCI,GENET EPIDEMIOL BRANCH,BETHESDA,MD 20892
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D O I
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Members of cutaneous melanoma (CM) families with dysplastic nevi (DN) are at high risk of developing CM. Using a shuttle vector plasmid, pSP189, cell lints from three patients with CM plus DN were previously found to have elevated post-UV plasmid mutability, To investigate familial occurrence of this cellular phenotype, we examined post-UV plasmid mutability in 31 lymphoblastoid cell lines from 6 familial CM kindreds. In comparison to 16 normal control lines, we found an abnormally elevated post-UV plasmid mutability in cell lines from 13 of 13 patients with CM plus DN (P = 1.5 x 10(-8)) and from 5 of 8 patients with DN only (P = 0.001), Elevated spontaneous plasmid mutation frequency (MF) was also present in cell lines from six of the CM plus DN patients (P = 0.002) and three of the DN-only patients (P = 0.028), However, cell lines from two patients with CM without DN had normal post-UV plasmid MF, Although not specific for CM patients, of 27 cell lines with elevated post-UV plasmid MF, only 8 were from donors who did not have CM + DN or DN (19 of 24 versus 8 of 28; P = 0.0003), This study indicates that post-UV plasmid hypermutability is a laboratory marker for members of melanoma-prone families and suggests that patients with familial CM have a defective mechanism for handling UV-induced DNA damage.
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页码:4637 / 4641
页数:5
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