Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients

IF 3.1 2区 医学 Q2 GENETICS & HEREDITY
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
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Abstract

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.

Abstract Image

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。
在适当的情况下,携带大肠杆菌的聚酮合酶(pks)岛能够产生基因毒素大肠杆菌素。大肠杆菌素是结直肠癌癌症发展的危险因素,并与突变特征SBS88和ID18相关。本研究探讨了双等位基因NTHL1和MUTYH患者中大肠杆菌素相关的突变特征。对1例双等位基因NTHL和12例双等基因MUTYH患者的结直肠腺瘤和癌进行了靶向下一代测序(NGS)。对NTHL1患者进行了额外的粪便宏基因组学和基因组测序,然后进行了突变特征分析。NTHL1患者的靶向NGS显示出符合SBS88的体细胞APC变体,这是使用WGS确认的。此外,粪便宏基因组学揭示了pks基因。此外,在11名MUTYH患者中有1名患者检测到符合SBS88的体细胞变体。本报告显示大肠杆菌素可能影响易感患者结肠肿瘤的发展。
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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.
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