Priority Centre for Cancer Research, Hunter Medical Research Institute and the Unviversity of Newcastle, Newcastle, New South Wales, Australia.
Division of Molecular Medicine, NSW Health Pathology North, Newcastle, New South Wales, Australia.
Clin Genet. 2021 Oct;100(4):478-483. doi: 10.1111/cge.14029. Epub 2021 Jul 26.
Inherited polyposis syndromes are predominantly caused by pathogenic variants in APC and are linked to familial adenomatous polyposis (FAP). However, after clinical screening, 20%-30% of individuals diagnosed with FAP do not carry a pathogenic variant in APC (often categorised as FAP-like). Other known inherited adenomatous polyposis syndromes such as MUTYH, POLD1/E, or NTHL1-associated polyposis only account for, 3 a fraction of the remaining cases. A cohort of 48 individuals clinically diagnosed with a FAP-like phenotype was selected based on a strong family history of colorectal cancer and no previous pathogenic variant found in APC and/or MUTYH, by genetic screening. Using whole exome sequencing, FAP-like patients were found to carry pathogenic variants in MUTYH, APC, POLE and TP53, as well as DNA-repair genes and inflammation related genes. Additionally, a comprehensive assessment of copy number variation revealed two loci of interest that appeared to be associated with polyposis risk. In total, 6 out of 48 polyposis were explained through re-sequencing. This study highlights the potential role of DNA-repair as well as inflammation-related variants towards polyp development.
遗传性息肉综合征主要由 APC 中的致病性变异引起,并与家族性腺瘤性息肉病 (FAP) 相关。然而,经过临床筛查,20%-30%被诊断为 FAP 的个体在 APC 中未携带致病性变异(通常归类为 FAP 样)。其他已知的遗传性腺瘤性息肉病综合征,如 MUTYH、POLD1/E 或 NTHL1 相关息肉病,仅占剩余病例的一部分。根据遗传筛查,选择了一组 48 名临床诊断为 FAP 样表型的个体,这些个体具有结直肠癌的强烈家族史,且 APC 和/或 MUTYH 中未发现先前的致病性变异。通过全外显子组测序,发现 FAP 样患者携带 MUTYH、APC、POLE 和 TP53 的致病性变异,以及 DNA 修复基因和炎症相关基因。此外,对拷贝数变异的全面评估揭示了两个似乎与息肉病风险相关的感兴趣位点。总共,通过重测序解释了 48 个息肉中的 6 个。这项研究强调了 DNA 修复以及炎症相关变异在息肉发展中的潜在作用。