Farrington Susan M, Tenesa Albert, Barnetson Rebecca, Wiltshire Alice, Prendergast James, Porteous Mary, Campbell Harry, Dunlop Malcolm G
Colon Cancer Genetics Group, School of Clinical and Molecular Medicine, University of Edinburgh, United Kingdom.
Am J Hum Genet. 2005 Jul;77(1):112-9. doi: 10.1086/431213. Epub 2005 May 3.
DNA repair is a key process in the maintenance of genome integrity. Here, we present a large, systematically collected population-based association study (2,239 cases; 1,845 controls) that explores the contribution to colorectal cancer incidence of inherited defects in base-excision repair (BER) genes. We show that biallelic MUTYH defects impart a 93-fold (95% CI 42-213) excess risk of colorectal cancer, which accounts for 0.8% of cases aged <55 years and 0.54% of the entire cohort. Penetrance for homozygous carriers was almost complete by age 60 years. Significantly more biallelic carriers had coexisting adenomatous polyps. However, notably, 36% of biallelic carriers had no polyps. Three patients with heterozygous MUTYH defects carried monoallelic mutations in other BER genes (OGG1 and MTH1). Recessive inheritance accounted for the elevated risk for those aged <55 years. However, there was also a 1.68-fold (95% CI 1.07-2.95) excess risk for heterozygous carriers aged >55 years, with a population attributable risk in this age group of 0.93% (95% CI 0%-2.0%). These data provide the strongest evidence to date for a causative role of BER defects in colorectal cancer etiology and show, to our knowledge for the first time, that heterozygous MUTYH mutations predispose to colorectal cancer later in life. These findings have clinical relevance for BER gene testing for patients with colorectal cancer and for genetic counseling of their relatives.
DNA修复是维持基因组完整性的关键过程。在此,我们开展了一项大规模、系统收集的基于人群的关联研究(2239例病例;1845例对照),以探究碱基切除修复(BER)基因的遗传性缺陷对结直肠癌发病率的影响。我们发现,双等位基因MUTYH缺陷使患结直肠癌的风险增加93倍(95%置信区间42 - 213),在年龄小于55岁的病例中占0.8%,在整个队列中占0.54%。纯合子携带者到60岁时的外显率几乎达到100%。双等位基因携带者同时存在腺瘤性息肉的比例显著更高。然而,值得注意的是,36%的双等位基因携带者没有息肉。3例携带杂合子MUTYH缺陷的患者在其他BER基因(OGG1和MTH1)中携带单等位基因突变。隐性遗传导致年龄小于55岁者风险升高。然而,年龄大于55岁的杂合子携带者患癌风险也增加了1.68倍(95%置信区间1.07 - 2.95),该年龄组人群归因风险为0.93%(95%置信区间0% - 2.0%)。这些数据提供了迄今为止关于BER缺陷在结直肠癌病因中致病作用的最有力证据,并且据我们所知首次表明,杂合子MUTYH突变会使人在晚年易患结直肠癌。这些发现对于结直肠癌患者的BER基因检测及其亲属的遗传咨询具有临床意义。