LACK OF MUTATIONS IN THE P53 GENE EXON-5 TO EXON-8 IN ATAXIA-TELANGIECTASIA

被引:4
作者
JONVEAUX, P [1 ]
BERGER, R [1 ]
机构
[1] HOP ST LOUIS,HEMATOL LAB,F-75010 PARIS,FRANCE
关键词
D O I
10.1016/0165-4608(93)90242-E
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Alterations of the TP53 tumor suppressor gene are present in various human malignancies and in the dominantly inherited Li-Fraumeni syndrome. Recently, a cell cycle checkpoint pathway involving p53 and GADD45 has been identified as defective in ataxia-telangiectasia. Using single strand conformation polymorphism analysis of PCR products, we looked for TP53 mutations in DNA of patients with AT. We did not find any mutation in 6 patients, suggesting that TP53 mutations are not directly involved in the cancer susceptibility observed in AT.
引用
收藏
页码:128 / 129
页数:2
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