Jiyan Yu, Chunhe Yang, Xintao Zhu, Zhankun Wang, Boping Xu, Ye Cai, Jingbo Zhao, Ruijian Guo, Wuzhou Yuan, Jianqing Wang, Bohao Dong, Frank Ron Zheng, Shuang Yang
{"title":"一种用于临床的DNA改变和甲基化联合检测方法。","authors":"Jiyan Yu, Chunhe Yang, Xintao Zhu, Zhankun Wang, Boping Xu, Ye Cai, Jingbo Zhao, Ruijian Guo, Wuzhou Yuan, Jianqing Wang, Bohao Dong, Frank Ron Zheng, Shuang Yang","doi":"10.1038/s44321-025-00259-7","DOIUrl":null,"url":null,"abstract":"<p><p>Traditional approaches for capturing genomic alterations and DNA methylation require separate assays, complicating clinical workflows and limiting sample utilization, particularly with low-input materials like cell-free DNA. To address these challenges, we introduce a streamlined approach combining mutation and methylation profiling via mutation-protective strand synthesis with modified deoxycytidine triphosphates, demonstrating high concordance with standard enzymatic methyl-seq and DNA-seq in both whole-genome sequencing of cell lines and targeted sequencing of clinical samples. In potential clinical contexts, incorporating multi-omics information with this approach modestly improve circulating tumor DNA (ctDNA) detection by ~12% in pre-treatment lung cancer patients (N = 26) while preserving specificity in healthy controls (N = 13), and reveal relationships between homologous recombination repair (HRR) gene function and homologous recombination deficiency (HRD) mediated by promoter methylation-driven biallelic loss of HRR genes in gynecologic cancer patients (N = 27). For practical convenience, this method was also implemented on qPCR platform with high performance (0.5% limit of detection). With its adaptability and potential utility in ctDNA detection and treatment, this approach holds promise for advancing clinical diagnostics.</p>","PeriodicalId":11597,"journal":{"name":"EMBO Molecular Medicine","volume":" ","pages":"1825-1841"},"PeriodicalIF":8.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12254327/pdf/","citationCount":"0","resultStr":"{\"title\":\"A DNA alteration and methylation co-detection method for clinical purpose.\",\"authors\":\"Jiyan Yu, Chunhe Yang, Xintao Zhu, Zhankun Wang, Boping Xu, Ye Cai, Jingbo Zhao, Ruijian Guo, Wuzhou Yuan, Jianqing Wang, Bohao Dong, Frank Ron Zheng, Shuang Yang\",\"doi\":\"10.1038/s44321-025-00259-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Traditional approaches for capturing genomic alterations and DNA methylation require separate assays, complicating clinical workflows and limiting sample utilization, particularly with low-input materials like cell-free DNA. To address these challenges, we introduce a streamlined approach combining mutation and methylation profiling via mutation-protective strand synthesis with modified deoxycytidine triphosphates, demonstrating high concordance with standard enzymatic methyl-seq and DNA-seq in both whole-genome sequencing of cell lines and targeted sequencing of clinical samples. In potential clinical contexts, incorporating multi-omics information with this approach modestly improve circulating tumor DNA (ctDNA) detection by ~12% in pre-treatment lung cancer patients (N = 26) while preserving specificity in healthy controls (N = 13), and reveal relationships between homologous recombination repair (HRR) gene function and homologous recombination deficiency (HRD) mediated by promoter methylation-driven biallelic loss of HRR genes in gynecologic cancer patients (N = 27). For practical convenience, this method was also implemented on qPCR platform with high performance (0.5% limit of detection). With its adaptability and potential utility in ctDNA detection and treatment, this approach holds promise for advancing clinical diagnostics.</p>\",\"PeriodicalId\":11597,\"journal\":{\"name\":\"EMBO Molecular Medicine\",\"volume\":\" \",\"pages\":\"1825-1841\"},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12254327/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EMBO Molecular Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s44321-025-00259-7\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EMBO Molecular Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s44321-025-00259-7","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/4 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
A DNA alteration and methylation co-detection method for clinical purpose.
Traditional approaches for capturing genomic alterations and DNA methylation require separate assays, complicating clinical workflows and limiting sample utilization, particularly with low-input materials like cell-free DNA. To address these challenges, we introduce a streamlined approach combining mutation and methylation profiling via mutation-protective strand synthesis with modified deoxycytidine triphosphates, demonstrating high concordance with standard enzymatic methyl-seq and DNA-seq in both whole-genome sequencing of cell lines and targeted sequencing of clinical samples. In potential clinical contexts, incorporating multi-omics information with this approach modestly improve circulating tumor DNA (ctDNA) detection by ~12% in pre-treatment lung cancer patients (N = 26) while preserving specificity in healthy controls (N = 13), and reveal relationships between homologous recombination repair (HRR) gene function and homologous recombination deficiency (HRD) mediated by promoter methylation-driven biallelic loss of HRR genes in gynecologic cancer patients (N = 27). For practical convenience, this method was also implemented on qPCR platform with high performance (0.5% limit of detection). With its adaptability and potential utility in ctDNA detection and treatment, this approach holds promise for advancing clinical diagnostics.
期刊介绍:
EMBO Molecular Medicine is an open access journal in the field of experimental medicine, dedicated to science at the interface between clinical research and basic life sciences. In addition to human data, we welcome original studies performed in cells and/or animals provided they demonstrate human disease relevance.
To enhance and better specify our commitment to precision medicine, we have expanded the scope of EMM and call for contributions in the following fields:
Environmental health and medicine, in particular studies in the field of environmental medicine in its functional and mechanistic aspects (exposome studies, toxicology, biomarkers, modeling, and intervention).
Clinical studies and case reports - Human clinical studies providing decisive clues how to control a given disease (epidemiological, pathophysiological, therapeutic, and vaccine studies). Case reports supporting hypothesis-driven research on the disease.
Biomedical technologies - Studies that present innovative materials, tools, devices, and technologies with direct translational potential and applicability (imaging technologies, drug delivery systems, tissue engineering, and AI)