1 Giovanni Paolo II Oncological Centre, Laboratory of Medical Genetics, Lecce Hospital - Italy.
Int J Biol Markers. 2013 Dec 17;28(4):e405-8. doi: 10.5301/jbm.5000042.
Familial adenomatous polyposis (FAP) is an autosomal dominant disorder related to germline mutations of the adenomatous polyposis coli (APC) gene. It is characterized by the detection of numerous adenomatous polyps that, if untreated, develop into colorectal cancer. We studied an Italian family with FAP history and the related colorectal tumor sample of the proband. Sequencing analysis of blood samples revealed the presence of a never-reported germline mutation in the APC gene (exon 15): an heterozygous G deletion at position c.2126 resulting in a premature stop codon (p.Gly721GlufsX6) and in a truncated protein. This mutation was also identified in the colorectal tumor tissue, together with a second known pathogenic heterozygotic somatic mutation, c.4348C>T (p.Arg1450X), which generates a premature truncated protein. The novel identified germline mutation is therefore related to FAP and, in accordance with Knudson's "two hit" hypothesis, can be considered the first event predisposing to the insurgence of colorectal cancer in these patients. The somatic hit inactivating the second allele of the APC gene is located in the mutation cluster region of the gene; this is not a random event since it depends on the position of the germline mutation. The inactivation of APC generates the neoplastic growth advantage to the cell.
家族性腺瘤性息肉病(FAP)是一种常染色体显性遗传疾病,与腺瘤性结肠息肉病 APC 基因的种系突变有关。其特征是检测到大量腺瘤性息肉,如果不治疗,这些息肉会发展成结直肠癌。我们研究了一个有 FAP 病史的意大利家族和先证者的相关结直肠肿瘤样本。对血液样本的测序分析显示,APC 基因(外显子 15)中存在一个从未报道过的种系突变:c.2126 位置的杂合性 G 缺失导致提前终止密码子(p.Gly721GlufsX6)和截短蛋白。该突变也在结直肠肿瘤组织中被发现,同时还存在第二个已知的致病性杂合性体细胞突变 c.4348C>T(p.Arg1450X),导致提前截短蛋白。因此,新发现的种系突变与 FAP 有关,并且符合 Knudson 的“两次打击”假说,可以被认为是导致这些患者结直肠癌发生的第一个事件。失活 APC 基因的第二个等位基因的体细胞打击位于基因的突变簇区域;这不是一个随机事件,因为它取决于种系突变的位置。APC 的失活赋予了细胞肿瘤生长的优势。