由不常见基因变异引起的遗传性结直肠癌和息肉病综合征。

IF 3.1 2区 医学 Q2 GENETICS & HEREDITY
Ahmed Bouras, Aurélie Fabre, Hélène Zattara, Sandrine Handallou, Françoise Desseigne, Caroline Kientz, Fabienne Prieur, Magalie Peysselon, Clémentine Legrand, Laura Calavas, Jean-Christophe Saurin, Qing Wang
{"title":"由不常见基因变异引起的遗传性结直肠癌和息肉病综合征。","authors":"Ahmed Bouras,&nbsp;Aurélie Fabre,&nbsp;Hélène Zattara,&nbsp;Sandrine Handallou,&nbsp;Françoise Desseigne,&nbsp;Caroline Kientz,&nbsp;Fabienne Prieur,&nbsp;Magalie Peysselon,&nbsp;Clémentine Legrand,&nbsp;Laura Calavas,&nbsp;Jean-Christophe Saurin,&nbsp;Qing Wang","doi":"10.1002/gcc.23263","DOIUrl":null,"url":null,"abstract":"<p>A substantial number of hereditary colorectal cancer (CRC) and colonic polyposis cannot be explained by alteration in confirmed predisposition genes, such as mismatch repair (MMR) genes, <i>APC</i> and <i>MUTYH</i>. Recently, a certain number of potential predisposition genes have been suggested, involving each a small number of cases reported so far. Here, we describe the detection of rare variants in the <i>NTLH1</i>, <i>AXIN2</i>, <i>RNF43</i>, <i>BUB1</i>, and <i>TP53</i> genes in nine unrelated patients who were suspected for inherited CRC and/or colonic polyposis. Seven of them were classified as pathogenic or likely pathogenic variants (PV/LPV). Clinical manifestations of carriers were largely consistent with reported cases with, nevertheless, distinct characteristics. PV/LPV in these uncommon gene can be responsible for up to 2.7% of inherited CRC or colonic polyposis syndromes. Our findings provide supporting evidence for the role of these genes in cancer predisposition, and contribute to the determination of related cancer spectrum and cancer risk for carriers, allowing for the establishment of appropriate screening strategy and genetic counseling in affected families.</p>","PeriodicalId":12700,"journal":{"name":"Genes, Chromosomes & Cancer","volume":"63 8","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gcc.23263","citationCount":"0","resultStr":"{\"title\":\"Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes\",\"authors\":\"Ahmed Bouras,&nbsp;Aurélie Fabre,&nbsp;Hélène Zattara,&nbsp;Sandrine Handallou,&nbsp;Françoise Desseigne,&nbsp;Caroline Kientz,&nbsp;Fabienne Prieur,&nbsp;Magalie Peysselon,&nbsp;Clémentine Legrand,&nbsp;Laura Calavas,&nbsp;Jean-Christophe Saurin,&nbsp;Qing Wang\",\"doi\":\"10.1002/gcc.23263\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A substantial number of hereditary colorectal cancer (CRC) and colonic polyposis cannot be explained by alteration in confirmed predisposition genes, such as mismatch repair (MMR) genes, <i>APC</i> and <i>MUTYH</i>. Recently, a certain number of potential predisposition genes have been suggested, involving each a small number of cases reported so far. Here, we describe the detection of rare variants in the <i>NTLH1</i>, <i>AXIN2</i>, <i>RNF43</i>, <i>BUB1</i>, and <i>TP53</i> genes in nine unrelated patients who were suspected for inherited CRC and/or colonic polyposis. Seven of them were classified as pathogenic or likely pathogenic variants (PV/LPV). Clinical manifestations of carriers were largely consistent with reported cases with, nevertheless, distinct characteristics. PV/LPV in these uncommon gene can be responsible for up to 2.7% of inherited CRC or colonic polyposis syndromes. Our findings provide supporting evidence for the role of these genes in cancer predisposition, and contribute to the determination of related cancer spectrum and cancer risk for carriers, allowing for the establishment of appropriate screening strategy and genetic counseling in affected families.</p>\",\"PeriodicalId\":12700,\"journal\":{\"name\":\"Genes, Chromosomes & Cancer\",\"volume\":\"63 8\",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-08-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gcc.23263\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes, Chromosomes & Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/gcc.23263\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes, Chromosomes & Cancer","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/gcc.23263","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

相当多的遗传性结直肠癌(CRC)和结肠息肉病无法用已证实的易感基因(如错配修复(MMR)基因、APC 和 MUTYH)的改变来解释。最近,人们提出了一些潜在的易感基因,但迄今为止,这些基因只涉及少数病例。在此,我们描述了在 9 例疑似遗传性 CRC 和/或结肠息肉病的非亲属患者中检测到的 NTLH1、AXIN2、RNF43、BUB1 和 TP53 基因的罕见变异。其中 7 个变异被归类为致病变异或可能致病变异(PV/LPV)。携带者的临床表现与已报道的病例基本一致,但具有不同的特征。这些不常见基因的 PV/LPV 可导致高达 2.7% 的遗传性 CRC 或结肠息肉病综合征。我们的研究结果为这些基因在癌症易感性中的作用提供了支持性证据,并有助于确定相关癌症谱和携带者的癌症风险,从而为受影响的家庭制定适当的筛查策略和遗传咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes

Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes

A substantial number of hereditary colorectal cancer (CRC) and colonic polyposis cannot be explained by alteration in confirmed predisposition genes, such as mismatch repair (MMR) genes, APC and MUTYH. Recently, a certain number of potential predisposition genes have been suggested, involving each a small number of cases reported so far. Here, we describe the detection of rare variants in the NTLH1, AXIN2, RNF43, BUB1, and TP53 genes in nine unrelated patients who were suspected for inherited CRC and/or colonic polyposis. Seven of them were classified as pathogenic or likely pathogenic variants (PV/LPV). Clinical manifestations of carriers were largely consistent with reported cases with, nevertheless, distinct characteristics. PV/LPV in these uncommon gene can be responsible for up to 2.7% of inherited CRC or colonic polyposis syndromes. Our findings provide supporting evidence for the role of these genes in cancer predisposition, and contribute to the determination of related cancer spectrum and cancer risk for carriers, allowing for the establishment of appropriate screening strategy and genetic counseling in affected families.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Genes, Chromosomes & Cancer
Genes, Chromosomes & Cancer 医学-遗传学
CiteScore
7.00
自引率
8.10%
发文量
94
审稿时长
4-8 weeks
期刊介绍: Genes, Chromosomes & Cancer will offer rapid publication of original full-length research articles, perspectives, reviews and letters to the editors on genetic analysis as related to the study of neoplasia. The main scope of the journal is to communicate new insights into the etiology and/or pathogenesis of neoplasia, as well as molecular and cellular findings of relevance for the management of cancer patients. While preference will be given to research utilizing analytical and functional approaches, descriptive studies and case reports will also be welcomed when they offer insights regarding basic biological mechanisms or the clinical management of neoplastic disorders.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信