Ricciardiello Luigi, Goel Ajay, Mantovani Vilma, Fiorini Tania, Fossi Stefania, Chang Dong K, Lunedei Veronica, Pozzato Paolo, Zagari Rocco M, De Luca Luca, Fuccio Lorenzo, Martinelli Giuseppe N, Roda Enrico, Boland C Richard, Bazzoli Franco
Dipartimento di Medicina Interna e Gastroenterologia e Centro di Ricerca Biomedica Applicata, Università degli Studi di Bologna, 40138 Bologna, Italy.
Cancer Res. 2003 Feb 15;63(4):787-92.
The first-degree relatives of patients affected by colorectal cancer, who do not belong to familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer families, have a doubled risk of developing tumors of the large intestine. We have previously demonstrated that subjects with a single first-degree relative (SFDR) with colon cancer have a doubled risk for developing colorectal adenomas, and in these cases, polyps recur more frequently. The mechanism underlying this predisposition has not been clarified. In this study, we evaluated the frequency of microsatellite instability (MSI) using the five markers suggested by the National Cancer Institute workshop, target gene mutations, hMLH1 and hMSH2 expression, and hMLH1 promoter hypermethylation in the adenomas of patients with and without a SFDR affected by colon cancer. Seventy polyps were obtained from 70 patients: 27 with a single FDR with colon cancer and 43 without such a history. Of the 70 polyps, 12 were MSI-H (17.1%), 20 were MSI-L (28.6%), and 30 were microsatellite stable (42.9%). Of the 27 patients with positive family history, 8 polyps (29.6%) were MSI-H compared with those with negative history in which 4 polyps (9.3%) were MSI-H (P < 0.02). Of the 12 MSI-H polyps, all of the polyps obtained from patients with positive family history had loss of hMLH1 immunostaining versus one with negative family history (P < 0.02). Of the MSI-H polyps, 2 had a somatic frameshift mutation of the MBD4 gene, 1 of MSH6, 1 of BAX, and 2 of transforming growth factor betaRII. Furthermore, 6 of 8 polyps from patients with positive family history with MSI-H and loss of MLH1 had hypermethylation of the MLH1promoter versus none of the MSI-H with negative family history (P < 0.02). All 6 polyps of the 27 from SFDR positive subjects, with hMLH1 promoter hypermethylation loss of hMLH1 and MSI, were located in the right colon (P < 0.02). Hypermethylation of the promoter of hMLH1, consequent loss of hMLH1 expression, and MSI are at the basis of approximately 25% of adenomatous polyps developed in subjects with a SFDR affected by colorectal cancer.
患有结直肠癌但不属于家族性腺瘤性息肉病和遗传性非息肉病性结直肠癌家族的患者的一级亲属,患大肠肿瘤的风险会增加一倍。我们之前已经证明,有一个患结肠癌的一级亲属(SFDR)的受试者患结直肠腺瘤的风险增加一倍,并且在这些情况下,息肉复发更频繁。这种易感性的潜在机制尚未阐明。在本研究中,我们使用美国国立癌症研究所研讨会建议的五个标记评估微卫星不稳定性(MSI)的频率、靶基因突变、hMLH1和hMSH2表达以及hMLH1启动子高甲基化情况,这些研究对象为有或没有患结肠癌的SFDR的患者的腺瘤。从70名患者身上获取了70个息肉:27名患者有一个患结肠癌的FDR,43名患者没有这种病史。在这70个息肉中,12个为高度微卫星不稳定(MSI-H,17.1%),20个为低度微卫星不稳定(MSI-L,28.6%),30个微卫星稳定(42.9%)。在27名有阳性家族史的患者中,8个息肉(29.6%)为MSI-H,而在无家族史的患者中,4个息肉(9.3%)为MSI-H(P<0.02)。在12个MSI-H息肉中,所有来自有阳性家族史患者的息肉均出现hMLH1免疫染色缺失,而来自无家族史患者的息肉只有1个出现这种情况(P<0.02)。在MSI-H息肉中,2个有MBD4基因的体细胞移码突变,1个有MSH6基因的体细胞移码突变,1个有BAX基因的体细胞移码突变,2个有转化生长因子βRII的体细胞移码突变。此外,8个来自有阳性家族史且MSI-H和MLH1缺失的患者的息肉中有6个出现MLH1启动子高甲基化,而无家族史的MSI-H息肉均未出现这种情况(P<0.02)。来自SFDR阳性受试者的27个息肉中的所有6个,均出现hMLH1启动子高甲基化、hMLH1缺失和MSI,且均位于右半结肠(P<0.02)。hMLH1启动子高甲基化、随之而来的hMLH1表达缺失和MSI是约25%在有患结直肠癌的SFDR的受试者中发生的腺瘤性息肉的发病基础。