Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
J Pathol. 2013 Jun;230(2):148-53. doi: 10.1002/path.4185.
Polymerases ε and δ are the main enzymes that replicate eukaryotic DNA. Accurate replication occurs through Watson-Crick base pairing and also through the action of the polymerases' exonuclease (proofreading) domains. We have recently shown that germline exonuclease domain mutations (EDMs) of POLE and POLD1 confer a high risk of multiple colorectal adenomas and carcinoma (CRC). POLD1 mutations also predispose to endometrial cancer (EC). These mutations are associated with high penetrance and dominant inheritance, although the phenotype can be variable. We have named the condition polymerase proofreading-associated polyposis (PPAP). Somatic POLE EDMs have also been found in sporadic CRCs and ECs, although very few somatic POLD1 EDMs have been detected. Both the germline and the somatic DNA polymerase EDMs cause an 'ultramutated', apparently microsatellite-stable, type of cancer, sometimes leading to over a million base substitutions per tumour. Here, we present the evidence for POLE and POLD1 as important contributors to the pathogenesis of CRC and EC, and highlight some of the key questions in this emerging field.
聚合酶 ε 和 δ 是复制真核 DNA 的主要酶。准确的复制是通过 Watson-Crick 碱基配对以及聚合酶的核酸外切酶(校对)结构域的作用来实现的。我们最近发现,POLE 和 POLD1 的种系核酸外切酶结构域突变(EDMs)赋予了多发性结直肠腺瘤和癌(CRC)的高风险。POLD1 突变也易患子宫内膜癌(EC)。这些突变与高外显率和显性遗传有关,尽管表型可能存在差异。我们将这种情况命名为聚合酶校对相关息肉病(PPAP)。体细胞 POLE EDMs 也已在散发性 CRC 和 EC 中发现,尽管很少检测到体细胞 POLD1 EDMs。种系和体细胞 DNA 聚合酶 EDMs 都会导致“超突变”,即微卫星稳定的癌症类型,有时每个肿瘤会导致超过一百万碱基的替换。在这里,我们提出了 POLE 和 POLD1 作为 CRC 和 EC 发病机制的重要贡献者的证据,并强调了这一新兴领域中的一些关键问题。