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家族性腺瘤性息肉病:疾病多样性和基因异质性的更多证据。

Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.

作者信息

Scott R J, Meldrum C, Crooks R, Spigelman A D, Kirk J, Tucker K, Koorey D

机构信息

Hunter Area Pathology Service, Locked Bag No 1, Hunter Regional Mail Centre, Newcastle NSW 2310, Australia.

出版信息

Gut. 2001 Apr;48(4):508-14. doi: 10.1136/gut.48.4.508.

DOI:10.1136/gut.48.4.508
PMID:11247895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1728257/
Abstract

Familial adenomatous polyposis (FAP) is characterised by the presence of profuse colonic carpeting of adenomas throughout the entire colon and rectum. The genetic basis of FAP has been shown to be primarily associated with germline mutations in the APC gene. Notwithstanding, several reports have been published indicating that there is genetic heterogeneity in FAP and that the most likely explanation is the existence of another gene. In this report we further delineate the genotype/phenotype correlation in families that harbour germline mutations in the APC gene and identify some previously unreported changes in the APC gene which predispose to an attenuated disease phenotype. From 53 index patients diagnosed with either FAP or attenuated FAP, 27 harboured changes in the APC gene. The remaining 26 patients were further subgrouped according to their colonic phenotype. There were nine patients with a mixed hyperplastic/adenomatous colonic phenotype and there were 17 patients with an adenomatous colonic phenotype. Evaluation of the disease characteristics of these patients and their families is presented which may aid in the identification of new genes associated with colonic polyposis.

摘要

家族性腺瘤性息肉病(FAP)的特征是在整个结肠和直肠中存在大量腺瘤性息肉。FAP的遗传基础已被证明主要与APC基因的种系突变有关。尽管如此,已有多篇报道表明FAP存在遗传异质性,最可能的解释是存在另一个基因。在本报告中,我们进一步描述了携带APC基因种系突变的家族中的基因型/表型相关性,并鉴定了一些先前未报道的APC基因变化,这些变化易导致疾病表型减弱。在53例被诊断为FAP或轻度FAP的索引患者中,27例携带APC基因变化。其余26例患者根据其结肠表型进一步分组。有9例患者具有增生性/腺瘤性混合结肠表型,17例患者具有腺瘤性结肠表型。本文介绍了对这些患者及其家族疾病特征的评估,这可能有助于识别与结肠息肉病相关的新基因。

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本文引用的文献

1
Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development.Apc1638T:一种描绘参与肿瘤发生和发展的腺瘤性息肉病大肠杆菌蛋白关键结构域的小鼠模型。
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The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.APC基因变异体I1307K和E1317Q与结肠直肠肿瘤相关,但并不总是与家族病史相关。
Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10722-7. doi: 10.1073/pnas.95.18.10722.
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Genotype-phenotype correlations in attenuated adenomatous polyposis coli.attenuated adenomatous polyposis coli的基因型-表型相关性
Am J Hum Genet. 1998 Jun;62(6):1290-301. doi: 10.1086/301883.
6
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.由于APC基因中一个高度可变区域导致的德系犹太人遗传性结直肠癌。
Nat Genet. 1997 Sep;17(1):79-83. doi: 10.1038/ng0997-79.
7
Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.由APC基因3'端复发性突变引起的家族性浸润性纤维瘤病(韧带样瘤)(MIM135290)
Hum Mol Genet. 1996 Dec;5(12):1921-4. doi: 10.1093/hmg/5.12.1921.
8
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.由于APC基因第1924位密码子发生移码突变导致的遗传性硬纤维瘤病。
Am J Hum Genet. 1996 Dec;59(6):1193-201.
9
Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.APC外显子15 3'端的种系突变不会导致截短蛋白的产生,且与弱化的腺瘤性息肉病相关。
Hum Genet. 1996 Dec;98(6):727-34. doi: 10.1007/s004390050293.
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Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene.家族性腺瘤性息肉病(FAP)患者结肠外表现的发展与APC基因第1403密码子以外的突变之间的相关性。
J Med Genet. 1996 Apr;33(4):274-80. doi: 10.1136/jmg.33.4.274.