Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

被引:15
作者
Cleton-Jansen, AM
Moerland, EW
Pronk, JC
van Berkel, CGM
Apostolou, S
Crawford, J
Savoia, A
Auerbach, AD
Mathew, CG
Callen, DF
Cornelisse, CJ
机构
[1] Leiden Univ, Med Ctr, Dept Pathol, NL-2300 RC Leiden, Netherlands
[2] Free Univ Amsterdam, Dept Human Genet, Amsterdam, Netherlands
[3] Adelaides Women & Childrens Hosp, Dept Cytogenet & Mol Genet, N Adelaide, SA, Australia
[4] Osped Casa Sollievo Sofferenza, Foggia, Italy
[5] Rockefeller Univ, Lab Human Genet & Hematol, New York, NY 10021 USA
[6] United Med & Dent Sch Guys & St Thomas, Guys Hosp, Div Med & Mol Genet, London SE1 7EH, England
关键词
Fanconi anaemia; breast cancer; allelic imbalance; tumour suppressor gene; chromosome; 16;
D O I
10.1038/sj.bjc.6690168
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The recently identified Fanconi anaemia A (FAA) gene is located on chromosomal band 16q24.3 within a region that has been frequently reported to show loss of heterozygosity (LOH) in breast cancer. FAA mutation analysis of 19 breast tumours with specific LOH at 16q24.3 was performed. Single-stranded conformational polymorphism (SSCP) analysis on cDNA and genomic DNA, and Southern blotting failed to identify any tumour-specific mutations. Five polymorphisms were identified, but frequencies of occurrence did not deviate from those in a normal control population. Therefore, the FAA gene is not the gene targeted by LOH at 16q24.3 in breast cancer. Another tumour suppressor gene in this chromosomal region remains to be identified.
引用
收藏
页码:1049 / 1052
页数:4
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