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Pan-cancer atlas of somatic core and linker histone mutations

Recent genomic data points to a growing role for somatic mutations altering core histone and linker histone-encoding genes in cancer. However, the prevalence and the clinical and biological implications of histone gene mutations in malignant tumors remain incompletely defined. To address these knowl...

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Autores principales: Bonner, Erin R., Dawood, Adam, Gordish-Dressman, Heather, Eze, Augustine, Bhattacharya, Surajit, Yadavilli, Sridevi, Mueller, Sabine, Waszak, Sebastian M., Nazarian, Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462747/
https://www.ncbi.nlm.nih.gov/pubmed/37640703
http://dx.doi.org/10.1038/s41525-023-00367-8
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author Bonner, Erin R.
Dawood, Adam
Gordish-Dressman, Heather
Eze, Augustine
Bhattacharya, Surajit
Yadavilli, Sridevi
Mueller, Sabine
Waszak, Sebastian M.
Nazarian, Javad
author_facet Bonner, Erin R.
Dawood, Adam
Gordish-Dressman, Heather
Eze, Augustine
Bhattacharya, Surajit
Yadavilli, Sridevi
Mueller, Sabine
Waszak, Sebastian M.
Nazarian, Javad
author_sort Bonner, Erin R.
collection PubMed
description Recent genomic data points to a growing role for somatic mutations altering core histone and linker histone-encoding genes in cancer. However, the prevalence and the clinical and biological implications of histone gene mutations in malignant tumors remain incompletely defined. To address these knowledge gaps, we analyzed somatic mutations in 88 linker and core histone genes across 12,743 tumors from pediatric, adolescent and young adult (AYA), and adult cancer patients. We established a pan-cancer histone mutation atlas contextualized by patient age, survival outcome, and tumor location. Overall, 11% of tumors harbored somatic histone mutations, with the highest rates observed among chondrosarcoma (67%), pediatric high-grade glioma (pHGG, >60%), and lymphoma (>30%). Previously unreported histone mutations were discovered in pHGG and other pediatric brain tumors, extending the spectrum of histone gene alterations associated with these cancers. Histone mutation status predicted patient survival outcome in tumor entities including adrenocortical carcinoma. Recurrent pan-cancer histone mutation hotspots were defined and shown to converge on evolutionarily conserved and functional residues. Moreover, we studied histone gene mutations in 1700 pan-cancer cell lines to validate the prevalence and spectrum of histone mutations seen in primary tumors and derived histone-associated drug response profiles, revealing candidate drugs targeting histone mutant cancer cells. This study presents the first-of-its-kind atlas of both core and linker histone mutations across pediatric, AYA, and adult cancers, providing a framework by which specific cancers may be redefined in the context of histone and chromatin alterations.
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spelling pubmed-104627472023-08-30 Pan-cancer atlas of somatic core and linker histone mutations Bonner, Erin R. Dawood, Adam Gordish-Dressman, Heather Eze, Augustine Bhattacharya, Surajit Yadavilli, Sridevi Mueller, Sabine Waszak, Sebastian M. Nazarian, Javad NPJ Genom Med Article Recent genomic data points to a growing role for somatic mutations altering core histone and linker histone-encoding genes in cancer. However, the prevalence and the clinical and biological implications of histone gene mutations in malignant tumors remain incompletely defined. To address these knowledge gaps, we analyzed somatic mutations in 88 linker and core histone genes across 12,743 tumors from pediatric, adolescent and young adult (AYA), and adult cancer patients. We established a pan-cancer histone mutation atlas contextualized by patient age, survival outcome, and tumor location. Overall, 11% of tumors harbored somatic histone mutations, with the highest rates observed among chondrosarcoma (67%), pediatric high-grade glioma (pHGG, >60%), and lymphoma (>30%). Previously unreported histone mutations were discovered in pHGG and other pediatric brain tumors, extending the spectrum of histone gene alterations associated with these cancers. Histone mutation status predicted patient survival outcome in tumor entities including adrenocortical carcinoma. Recurrent pan-cancer histone mutation hotspots were defined and shown to converge on evolutionarily conserved and functional residues. Moreover, we studied histone gene mutations in 1700 pan-cancer cell lines to validate the prevalence and spectrum of histone mutations seen in primary tumors and derived histone-associated drug response profiles, revealing candidate drugs targeting histone mutant cancer cells. This study presents the first-of-its-kind atlas of both core and linker histone mutations across pediatric, AYA, and adult cancers, providing a framework by which specific cancers may be redefined in the context of histone and chromatin alterations. Nature Publishing Group UK 2023-08-28 /pmc/articles/PMC10462747/ /pubmed/37640703 http://dx.doi.org/10.1038/s41525-023-00367-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bonner, Erin R.
Dawood, Adam
Gordish-Dressman, Heather
Eze, Augustine
Bhattacharya, Surajit
Yadavilli, Sridevi
Mueller, Sabine
Waszak, Sebastian M.
Nazarian, Javad
Pan-cancer atlas of somatic core and linker histone mutations
title Pan-cancer atlas of somatic core and linker histone mutations
title_full Pan-cancer atlas of somatic core and linker histone mutations
title_fullStr Pan-cancer atlas of somatic core and linker histone mutations
title_full_unstemmed Pan-cancer atlas of somatic core and linker histone mutations
title_short Pan-cancer atlas of somatic core and linker histone mutations
title_sort pan-cancer atlas of somatic core and linker histone mutations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462747/
https://www.ncbi.nlm.nih.gov/pubmed/37640703
http://dx.doi.org/10.1038/s41525-023-00367-8
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