Constitutional alterations of the ATM gene in early onset sporadic breast cancer
Open Access
- 1 October 2002
- journal article
- letter
- Published by BMJ in Journal of Medical Genetics
- Vol. 39 (10) , 751-753
- https://doi.org/10.1136/jmg.39.10.751
Abstract
Ataxia-telangiectasia (AT) is a recessive disorder caused by mutations in the ATM gene (ataxia-telangiectasia mutated) located on chromosome 11q22-23 (OMIM 208900). AT is characterised by progressive cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, radiosensitivity, and cancer predisposition with a predominance of lymphoid tumours and less frequently other tumours including breast cancer. The 13 kb mRNA of ATM is assembled from 66 exons distributed across a genomic region of 150 kb. It codes for a 350 kDa protein with a C-terminus phosphatidylinositol 3-kinase domain involved in the recognition and repair of radiation induced DNA double strand breaks.1–5 Oncoproteins, including the tumour suppressors p53, BRCA1, and CHK2, are regulated by ATM.6 Epidemiological evidence suggests that ATM heterozygotes, representing 0.5-1% of the general population, have a 5 to 8-fold increased risk of developing breast cancer.7,8 These estimations raised the possibility that germline mutations of ATM may account for ∼5% of all breast cancer cases. Furthermore, since breast cancer reported in obligate carriers among AT family members affects predominantly younger women, an age specific relative risk model has been proposed.9 In this model, up to 8% of breast cancer diagnosed in women under the age of 40 may arise in ATM mutation carriers, compared with 2% of cases diagnosed between 40 and 59 years. However, recent data suggest that this model may overestimate the true allele frequency in women with breast cancer.10–12 Moreover, direct molecular examination of ATM in selected breast cancer patients outside AT families has led to conflicting results. Fitzgerald et al 13 showed that ATM mutations were present in only 2/401 (0.5%) women with early onset breast cancer, but they only looked for truncating mutations. In a recent study, Broeks et al 14 identified seven germline ATM truncating mutations among 82 patients who developed breast …Keywords
This publication has 21 references indexed in Scilit:
- Dominant Negative ATM Mutations in Breast Cancer FamiliesJNCI Journal of the National Cancer Institute, 2002
- Cancer Risk in ATM Heterozygotes: A Model of Phenotypic and Mechanistic Differences between Missense and Truncating MutationsMolecular Genetics and Metabolism, 1999
- ATM is usually rearranged in T-cell prolymphocytic leukaemiaOncogene, 1998
- ATM Mutations and Phenotypes in Ataxia-Telangiectasia Families in the British Isles: Expression of Mutant ATM and the Risk of Leukemia, Lymphoma, and Breast CancerAmerican Journal of Human Genetics, 1998
- Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemiaNature Genetics, 1997
- Heterozygous ATM mutations do not contribute to early onset of breast cancerNature Genetics, 1997
- Genomic Organization of the ATM GeneGenomics, 1996
- A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 KinaseScience, 1995
- Incidence of Cancer in 161 Families Affected by Ataxia–TelangiectasiaNew England Journal of Medicine, 1991
- Breast and Other Cancers in Families with Ataxia-TelangiectasiaNew England Journal of Medicine, 1987