Mario Ćuk , Busra Unal , Connor P. Hayes , McKenzie Walker , Anđela Bevanda , Viktorija Antolović , Arezou A. Ghazani
{"title":"全基因组联合分析发现,ATM:C.1564_1565del 变体与共济失调-特朗吉特氏病和乳腺癌存在分离关系。","authors":"Mario Ćuk , Busra Unal , Connor P. Hayes , McKenzie Walker , Anđela Bevanda , Viktorija Antolović , Arezou A. Ghazani","doi":"10.1016/j.cancergen.2024.07.002","DOIUrl":null,"url":null,"abstract":"<div><p><em>ATM</em> gene is implicated in the development of breast cancer in the heterozygous state, and Ataxia-telangiectasia (A-T) in a homozygous or compound heterozygous state. Ataxia-telangiectasia (A-T) is a rare cerebellar ataxia syndrome presenting with progressive neurologic impairment, telangiectasia, and an increased risk of leukemia and lymphoma.</p><p>Although the role of <em>ATM,</em> separately, in association with A-T and breast cancer is well documented, there is a limited number of studies investigating <em>ATM</em> variants when segregating with both phenotypes in the same family. Here, using joint analysis and whole genome sequencing, we investigated <em>ATM</em> c.1564_1565del in a family with one homozygous member presenting with A-T (OMIM # <span><span>208900</span><svg><path></path></svg></span>) and three heterozygous members, of whom one had breast cancer (OMIM #<span><span>114480</span><svg><path></path></svg></span>). To our knowledge, this is the first study of <em>ATM</em> c.1564_1565del segregation with both A-T and breast cancer phenotypes within the same kindred. This study highlights the need for a comprehensive genomic approach in the appropriate cancer risk management of heterozygote carriers of <em>ATM</em> in families with A-T.</p></div>","PeriodicalId":49225,"journal":{"name":"Cancer Genetics","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Whole genome joint analysis reveals ATM:C.1564_1565del variant segregating with Ataxia-Telangiectasia and breast cancer\",\"authors\":\"Mario Ćuk , Busra Unal , Connor P. Hayes , McKenzie Walker , Anđela Bevanda , Viktorija Antolović , Arezou A. Ghazani\",\"doi\":\"10.1016/j.cancergen.2024.07.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>ATM</em> gene is implicated in the development of breast cancer in the heterozygous state, and Ataxia-telangiectasia (A-T) in a homozygous or compound heterozygous state. Ataxia-telangiectasia (A-T) is a rare cerebellar ataxia syndrome presenting with progressive neurologic impairment, telangiectasia, and an increased risk of leukemia and lymphoma.</p><p>Although the role of <em>ATM,</em> separately, in association with A-T and breast cancer is well documented, there is a limited number of studies investigating <em>ATM</em> variants when segregating with both phenotypes in the same family. Here, using joint analysis and whole genome sequencing, we investigated <em>ATM</em> c.1564_1565del in a family with one homozygous member presenting with A-T (OMIM # <span><span>208900</span><svg><path></path></svg></span>) and three heterozygous members, of whom one had breast cancer (OMIM #<span><span>114480</span><svg><path></path></svg></span>). To our knowledge, this is the first study of <em>ATM</em> c.1564_1565del segregation with both A-T and breast cancer phenotypes within the same kindred. This study highlights the need for a comprehensive genomic approach in the appropriate cancer risk management of heterozygote carriers of <em>ATM</em> in families with A-T.</p></div>\",\"PeriodicalId\":49225,\"journal\":{\"name\":\"Cancer Genetics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2210776224000309\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Genetics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210776224000309","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Whole genome joint analysis reveals ATM:C.1564_1565del variant segregating with Ataxia-Telangiectasia and breast cancer
ATM gene is implicated in the development of breast cancer in the heterozygous state, and Ataxia-telangiectasia (A-T) in a homozygous or compound heterozygous state. Ataxia-telangiectasia (A-T) is a rare cerebellar ataxia syndrome presenting with progressive neurologic impairment, telangiectasia, and an increased risk of leukemia and lymphoma.
Although the role of ATM, separately, in association with A-T and breast cancer is well documented, there is a limited number of studies investigating ATM variants when segregating with both phenotypes in the same family. Here, using joint analysis and whole genome sequencing, we investigated ATM c.1564_1565del in a family with one homozygous member presenting with A-T (OMIM # 208900) and three heterozygous members, of whom one had breast cancer (OMIM #114480). To our knowledge, this is the first study of ATM c.1564_1565del segregation with both A-T and breast cancer phenotypes within the same kindred. This study highlights the need for a comprehensive genomic approach in the appropriate cancer risk management of heterozygote carriers of ATM in families with A-T.
期刊介绍:
The aim of Cancer Genetics is to publish high quality scientific papers on the cellular, genetic and molecular aspects of cancer, including cancer predisposition and clinical diagnostic applications. Specific areas of interest include descriptions of new chromosomal, molecular or epigenetic alterations in benign and malignant diseases; novel laboratory approaches for identification and characterization of chromosomal rearrangements or genomic alterations in cancer cells; correlation of genetic changes with pathology and clinical presentation; and the molecular genetics of cancer predisposition. To reach a basic science and clinical multidisciplinary audience, we welcome original full-length articles, reviews, meeting summaries, brief reports, and letters to the editor.