Warren W, Eeles R A, Ponder B A, Easton D F, Averill D, Ponder M A, Anderson K, Evans A M, DeMars R, Love R
Section of Molecular Carcinogenesis, Institute of Cancer Research, Sutton, Surrey, UK.
Oncogene. 1992 May;7(5):1043-6.
Recent studies have demonstrated that families with the Li-Fraumeni syndrome carry inherited point mutations of the p53 gene. In the present study 25 families with strong histories of breast cancer were screened for the presence of such mutations. Polymerase chain reaction products of exons 5-9 of the p53 gene were examined by single-stranded conformational polymorphism analysis and, in addition, exon 7 was further screened by direct sequencing. No mutations were detected in constitutive DNA by either method. These results indicate that familial breast cancer does not usually result from germline point mutations in the p53 gene.
最近的研究表明,患有李-弗劳梅尼综合征的家族携带p53基因的遗传性点突变。在本研究中,对25个有乳腺癌家族病史的家族进行了此类突变筛查。通过单链构象多态性分析检测p53基因外显子5-9的聚合酶链反应产物,此外,外显子7通过直接测序进一步筛查。两种方法均未在组成性DNA中检测到突变。这些结果表明,家族性乳腺癌通常并非由p53基因的种系点突变引起。