Title of article
Disruption of the ATM gene in breast cancer
Author/Authors
Lu، نويسنده , , Yong-Jie and Condie، نويسنده , , Alison and Bennett، نويسنده , , Julie D and Fry، نويسنده , , Michael J and Yuille، نويسنده , , Martin R and Shipley، نويسنده , , Janet، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
5
From page
97
To page
101
Abstract
Mutations in the ATM gene, which maps to 11q22–23, cause the multisystem recessive syndrome ataxia-telangiectasia (AT). Breast cancer has been reported in AT patients and carriers. Sporadic breast cancer is associated with loss of heterozygosity at or in the region of ATM and chromosomal abnormalities involving 11q23. We have investigated the chromosomes, nuclei and released chromatin fibers from nine primary breast carcinoma and eight cell lines by fluorescence in situ hybridization with four fluorochrome-labeled cosmids spanning the ATM gene. The ATM gene was disrupted in one primary breast carcinoma and in the cell lines MDA-MB-231 and MCF-7. The role of these aberrations in breast carcinomas, which may lead to gene dosage or dominant negative effects on gene function, requires further investigation.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2001
Journal title
Cancer Genetics and Cytogenetics
Record number
1823555
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