Ahmed M, Rahman N
Section of Cancer Genetics, Institute of Cancer Research, Sutton, UK.
Oncogene. 2006 Sep 25;25(43):5906-11. doi: 10.1038/sj.onc.1209873.
ATM was originally identified by positional cloning as the gene that underlies the autosomal recessive condition ataxia-telangiectasia. The encoded protein plays a central role in the complex processes that repair DNA double-strand breaks. Nearly 20 years ago, epidemiological surveys of relatives of ataxia-telangiectasia cases suggested that female relatives were at modestly increased risk of breast cancer. Subsequently, many studies have tried to clarify the role of ATM in breast cancer susceptibility, but have produced inconclusive and/or inconsistent results. Recently, large epidemiological and molecular studies have finally provided conclusive evidence that ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.
ATM最初是通过定位克隆被鉴定为常染色体隐性共济失调毛细血管扩张症所依据的基因。该编码蛋白在修复DNA双链断裂的复杂过程中起核心作用。近20年前,对共济失调毛细血管扩张症病例亲属的流行病学调查表明,女性亲属患乳腺癌的风险略有增加。随后,许多研究试图阐明ATM在乳腺癌易感性中的作用,但结果尚无定论且/或相互矛盾。最近,大规模的流行病学和分子研究终于提供了确凿证据,表明导致共济失调毛细血管扩张症的ATM突变是乳腺癌易感等位基因。