Hall Janet
DNA Repair Team, International Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon cedex, France.
Cancer Lett. 2005 Sep 28;227(2):105-14. doi: 10.1016/j.canlet.2004.12.001. Epub 2005 Jan 8.
The role of the Ataxia-telangiectaisa mutated (ATM) gene, as a risk factor for breast cancer has been a consistent theme in the literature since the first reports by Swift and colleagues who reported that ATM heterozygotes in AT families had increased risks of developing breast cancer. Loss of heterozygosity at the ATM locus has been reported in 30-40% of breast tumours and 50-70% show altered ATM protein levels. Germline ATM sequence variants have been reported in breast cancer cases, however, it is difficult to fully evaluate the increased risk associated with their presence. The potential role of such variants needs to be further assessed, together with functional studies to model their impact on ATM function.
自斯威夫特及其同事首次报告共济失调毛细血管扩张症突变(ATM)基因作为乳腺癌风险因素以来,该基因一直是文献中的一个持续主题。他们报告称,共济失调毛细血管扩张症(AT)家族中的ATM杂合子患乳腺癌的风险增加。据报道,30%-40%的乳腺肿瘤存在ATM基因座杂合性缺失,50%-70%的乳腺肿瘤显示ATM蛋白水平改变。乳腺癌病例中已报告了种系ATM序列变异,然而,很难全面评估其存在所带来的增加风险。此类变异的潜在作用需要进一步评估,同时需要进行功能研究以模拟其对ATM功能的影响。