D. Terlouw, A. Boot, Q. R. Ducarmon, S. Nooij, M. A. Jessurun, M. E. van Leerdam, C. M. Tops, A. M. J. Langers, H. Morreau, T. van Wezel, M. Nielsen
{"title":"NTHL1肿瘤综合征和MUTYH相关息肉病患者的大肠杆菌素突变特征。","authors":"D. Terlouw, A. Boot, Q. R. Ducarmon, S. Nooij, M. A. Jessurun, M. E. van Leerdam, C. M. Tops, A. M. J. Langers, H. Morreau, T. van Wezel, M. Nielsen","doi":"10.1002/gcc.23208","DOIUrl":null,"url":null,"abstract":"<p>Polyketide synthase (<i>pks</i>) island harboring <i>Escherichia coli</i> are, under the right circumstances, able to produce the genotoxin colibactin. Colibactin is a risk factor for the development of colorectal cancer and associated with mutational signatures SBS88 and ID18. This study explores colibactin-associated mutational signatures in biallelic <i>NTHL1</i> and <i>MUTYH</i> patients. Targeted Next Generation Sequencing (NGS) was performed on colorectal adenomas and carcinomas of one biallelic <i>NTHL</i> and 12 biallelic <i>MUTYH</i> patients. Additional fecal metagenomics and genome sequencing followed by mutational signature analysis was conducted for the <i>NTHL1</i> patient. Targeted NGS of the <i>NTHL1</i> patient showed somatic <i>APC</i> variants fitting SBS88 which was confirmed using WGS. Furthermore, fecal metagenomics revealed <i>pks</i> genes. Also, in 1 out of 11 <i>MUTYH</i> patient a somatic variant was detected fitting SBS88. This report shows that colibactin may influence development of colorectal neoplasms in predisposed patients.</p>","PeriodicalId":12700,"journal":{"name":"Genes, Chromosomes & Cancer","volume":"63 1","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2023-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gcc.23208","citationCount":"0","resultStr":"{\"title\":\"Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients\",\"authors\":\"D. Terlouw, A. Boot, Q. R. Ducarmon, S. Nooij, M. A. Jessurun, M. E. van Leerdam, C. M. Tops, A. M. J. Langers, H. Morreau, T. van Wezel, M. Nielsen\",\"doi\":\"10.1002/gcc.23208\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Polyketide synthase (<i>pks</i>) island harboring <i>Escherichia coli</i> are, under the right circumstances, able to produce the genotoxin colibactin. Colibactin is a risk factor for the development of colorectal cancer and associated with mutational signatures SBS88 and ID18. This study explores colibactin-associated mutational signatures in biallelic <i>NTHL1</i> and <i>MUTYH</i> patients. Targeted Next Generation Sequencing (NGS) was performed on colorectal adenomas and carcinomas of one biallelic <i>NTHL</i> and 12 biallelic <i>MUTYH</i> patients. Additional fecal metagenomics and genome sequencing followed by mutational signature analysis was conducted for the <i>NTHL1</i> patient. Targeted NGS of the <i>NTHL1</i> patient showed somatic <i>APC</i> variants fitting SBS88 which was confirmed using WGS. Furthermore, fecal metagenomics revealed <i>pks</i> genes. Also, in 1 out of 11 <i>MUTYH</i> patient a somatic variant was detected fitting SBS88. This report shows that colibactin may influence development of colorectal neoplasms in predisposed patients.</p>\",\"PeriodicalId\":12700,\"journal\":{\"name\":\"Genes, Chromosomes & Cancer\",\"volume\":\"63 1\",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2023-10-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/gcc.23208\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes, Chromosomes & Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/gcc.23208\",\"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.23208","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients
Polyketide synthase (pks) island harboring Escherichia coli are, under the right circumstances, able to produce the genotoxin colibactin. Colibactin is a risk factor for the development of colorectal cancer and associated with mutational signatures SBS88 and ID18. This study explores colibactin-associated mutational signatures in biallelic NTHL1 and MUTYH patients. Targeted Next Generation Sequencing (NGS) was performed on colorectal adenomas and carcinomas of one biallelic NTHL and 12 biallelic MUTYH patients. Additional fecal metagenomics and genome sequencing followed by mutational signature analysis was conducted for the NTHL1 patient. Targeted NGS of the NTHL1 patient showed somatic APC variants fitting SBS88 which was confirmed using WGS. Furthermore, fecal metagenomics revealed pks genes. Also, in 1 out of 11 MUTYH patient a somatic variant was detected fitting SBS88. This report shows that colibactin may influence development of colorectal neoplasms in predisposed patients.
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.