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A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance

BACKGROUND: Mutational signatures are somatic mutation patterns enriching operational mutational processes, which can provide abundant information about the mechanism of cancer. However, understanding of the pathogenic biological processes is still limited, such as the association between mutational...

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Autores principales: Li, Zhenzhang, Liang, Haihua, Zhang, Shaoan, Luo, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636515/
https://www.ncbi.nlm.nih.gov/pubmed/35575002
http://dx.doi.org/10.1002/cam4.4717
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author Li, Zhenzhang
Liang, Haihua
Zhang, Shaoan
Luo, Wen
author_facet Li, Zhenzhang
Liang, Haihua
Zhang, Shaoan
Luo, Wen
author_sort Li, Zhenzhang
collection PubMed
description BACKGROUND: Mutational signatures are somatic mutation patterns enriching operational mutational processes, which can provide abundant information about the mechanism of cancer. However, understanding of the pathogenic biological processes is still limited, such as the association between mutational signatures and genes. METHODS: We developed a simple and practical R package called RNMF (https://github.com/zhenzhang‐li/RNMF) for mutational signature analysis, including a key model of cumulative contribution abundance (CCA), which was designed to highlight the association between mutational signatures and genes and then applying it to a meta‐analysis of 1073 individuals with esophageal squamous cell carcinoma (ESCC). RESULTS: We revealed a number of known and previously undescribed SBS or ID signatures, and we found that APOBEC signatures (SBS2* and SBS13*) were closely associated with PIK3CA mutation, especially the E545k mutation. Furthermore, we found that age signature is closely related to the frequent mutation of TP53, of which R342* is highlighted due to strongly linked to age signature. In addition, the CCA matrix image data of genes in the signatures New, SBS3*, and SBS17b* were helpful for the preliminary evaluation of shortened survival outcome. These results can be extended to estimate the distribution of mutations or features, and study the potential impact of clinical factors. CONCLUSIONS: In a word, RNMF can successfully achieve the correlation analysis of mutational signatures and genes, proving a strong theoretical basis for the study of mutational processes during tumor development.
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spelling pubmed-96365152022-11-07 A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance Li, Zhenzhang Liang, Haihua Zhang, Shaoan Luo, Wen Cancer Med Method BACKGROUND: Mutational signatures are somatic mutation patterns enriching operational mutational processes, which can provide abundant information about the mechanism of cancer. However, understanding of the pathogenic biological processes is still limited, such as the association between mutational signatures and genes. METHODS: We developed a simple and practical R package called RNMF (https://github.com/zhenzhang‐li/RNMF) for mutational signature analysis, including a key model of cumulative contribution abundance (CCA), which was designed to highlight the association between mutational signatures and genes and then applying it to a meta‐analysis of 1073 individuals with esophageal squamous cell carcinoma (ESCC). RESULTS: We revealed a number of known and previously undescribed SBS or ID signatures, and we found that APOBEC signatures (SBS2* and SBS13*) were closely associated with PIK3CA mutation, especially the E545k mutation. Furthermore, we found that age signature is closely related to the frequent mutation of TP53, of which R342* is highlighted due to strongly linked to age signature. In addition, the CCA matrix image data of genes in the signatures New, SBS3*, and SBS17b* were helpful for the preliminary evaluation of shortened survival outcome. These results can be extended to estimate the distribution of mutations or features, and study the potential impact of clinical factors. CONCLUSIONS: In a word, RNMF can successfully achieve the correlation analysis of mutational signatures and genes, proving a strong theoretical basis for the study of mutational processes during tumor development. John Wiley and Sons Inc. 2022-05-16 /pmc/articles/PMC9636515/ /pubmed/35575002 http://dx.doi.org/10.1002/cam4.4717 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Li, Zhenzhang
Liang, Haihua
Zhang, Shaoan
Luo, Wen
A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title_full A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title_fullStr A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title_full_unstemmed A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title_short A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
title_sort practical framework rnmf for exploring the association between mutational signatures and genes using gene cumulative contribution abundance
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636515/
https://www.ncbi.nlm.nih.gov/pubmed/35575002
http://dx.doi.org/10.1002/cam4.4717
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