Abstract 46: High-definition signatures of single-base substitutions in human cancer.

Abstract Cancer genomes accumulate mutations through diverse biological processes, including defective DNA repair, exposure to carcinogens, and normal aging. These processes leave characteristic patterns known as mutational signatures. Identifying these signatures in patient tumors enables researchers to understand disease mechanisms and infer past exposures.The current standard resource, COSMIC v3.5, catalogs over 90 single base substitution (SBS) signatures using the SBS-96 mutational context, which characterizes each mutation by the substituted base and one flanking nucleotide on each side. This reference is widely used across cancer genomics studies to decode the mutational processes active in tumors. However, challenges have emerged where signatures overlap and can be misassigned, leading to incorrect interpretations of the mutational processes driving individual cancers. While we showed that higher-resolution methods using extended sequence contexts can differentiate these overlapping signatures and reveal novel processes, these findings were limited to specific cancer types such as colorectal, esophageal, renal, and head and neck. Additionally, no comprehensive high-resolution reference currently exists.To address this, we developed a high-definition (HD) mutational signature SBS reference set using over 40,000 whole-genome sequences from 14 cohorts spanning diverse cancer types and non-cancer tissues, including both primary and metastatic tumors. We analyzed mutations at SBS-4608 resolution, combining extended pentanucleotide sequence contexts with strand orientation information. This represents the practical limit of current sequencing technology. Our analysis clarifies several ambiguous signatures from the existing reference, improving accuracy when identifying mutational processes in individual tumors. We also discovered novel signatures that were previously undetectable at standard resolution, revealing new insights into the mutational landscape of human cancers.This HD reference set addresses critical limitations in current mutational signature analysis, enabling more accurate interpretation of mutational processes in cancer genomes and improving the reliability of downstream biological and clinical insights. By providing a comprehensive resource that resolves signature overlaps and reveals previously hidden mutational processes, this work will enhance precision in understanding cancer biology and tumor mutagenesis. The reference will be made publicly available to the research community upon publication. Citation Format: Jessica N. Au, Marcos Diaz-Gay, Raviteja Vangara, Pilar Gallego-Garcia, Mousumy Kundu, S.M Ashiqul Islam, Maria Zhivagui, Zichen Jiang, Christopher Steele, Sarah Moody, Michael R. Stratton, Paul J. Brennan, Ludmil B. Alexandrov. High-definition signatures of single-base substitutions in human cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 46.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-46
Primary Topic
Cancer Genomics and Diagnostics
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article
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article

Abstract 46: High-definition signatures of single-base substitutions in human cancer.

SM Ashiqul Islam, Maria Zhivagui, C. Steele, Michael R. Stratton et al.
Cancer Research
Cancer Genomics and Diagnostics
article

Abstract 46: High-definition signatures of single-base substitutions in human cancer.

SM Ashiqul Islam, Maria Zhivagui, C. Steele, Michael R. Stratton, Mousumy Kundu, Jessica Au, Raviteja Vangara, Sarah Moody, Paul Brennan, Marcos Díaz-Gay, Zichen Jiang, Pilar Gallego-Garcia, Ludmil B. Alexandrov
article en

Abstract

Abstract Cancer genomes accumulate mutations through diverse biological processes, including defective DNA repair, exposure to carcinogens, and normal aging. These processes leave characteristic patterns known as mutational signatures. Identifying these signatures in patient tumors enables researchers to understand disease mechanisms and infer past exposures.The current standard resource, COSMIC v3.5, catalogs over 90 single base substitution (SBS) signatures using the SBS-96 mutational context, which characterizes each mutation by the substituted base and one flanking nucleotide on each side. This reference is widely used across cancer genomics studies to decode the mutational processes active in tumors. However, challenges have emerged where signatures overlap and can be misassigned, leading to incorrect interpretations of the mutational processes driving individual cancers. While we showed that higher-resolution methods using extended sequence contexts can differentiate these overlapping signatures and reveal novel processes, these findings were limited to specific cancer types such as colorectal, esophageal, renal, and head and neck. Additionally, no comprehensive high-resolution reference currently exists.To address this, we developed a high-definition (HD) mutational signature SBS reference set using over 40,000 whole-genome sequences from 14 cohorts spanning diverse cancer types and non-cancer tissues, including both primary and metastatic tumors. We analyzed mutations at SBS-4608 resolution, combining extended pentanucleotide sequence contexts with strand orientation information. This represents the practical limit of current sequencing technology. Our analysis clarifies several ambiguous signatures from the existing reference, improving accuracy when identifying mutational processes in individual tumors. We also discovered novel signatures that were previously undetectable at standard resolution, revealing new insights into the mutational landscape of human cancers.This HD reference set addresses critical limitations in current mutational signature analysis, enabling more accurate interpretation of mutational processes in cancer genomes and improving the reliability of downstream biological and clinical insights. By providing a comprehensive resource that resolves signature overlaps and reveals previously hidden mutational processes, this work will enhance precision in understanding cancer biology and tumor mutagenesis. The reference will be made publicly available to the research community upon publication. Citation Format: Jessica N. Au, Marcos Diaz-Gay, Raviteja Vangara, Pilar Gallego-Garcia, Mousumy Kundu, S.M Ashiqul Islam, Maria Zhivagui, Zichen Jiang, Christopher Steele, Sarah Moody, Michael R. Stratton, Paul J. Brennan, Ludmil B. Alexandrov. High-definition signatures of single-base substitutions in human cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 46.

Cancer ResearchVol. 86(7_Supplement)
Albany State University (US), University of Nevada, Las Vegas (US), Wellcome Sanger Institute (GB), University of California San Diego (US), University at Albany, State University of New York (US), Spanish National Cancer Research Centre (ES), Centre international de recherche sur le cancer (FR)
Openalex Percentile: Top 13%
Cancer Genomics and Diagnostics
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