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Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource
BACKGROUND: Genetic alterations of somatic cells can drive non-malignant clone formation and promote cancer initiation. However, the link between these processes remains unclear and hampers our understanding of tissue homeostasis and cancer development. RESULTS: Here, we collect a literature-based r...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790917/ https://www.ncbi.nlm.nih.gov/pubmed/35078504 http://dx.doi.org/10.1186/s13059-022-02607-z |
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author | Dressler, Lisa Bortolomeazzi, Michele Keddar, Mohamed Reda Misetic, Hrvoje Sartini, Giulia Acha-Sagredo, Amelia Montorsi, Lucia Wijewardhane, Neshika Repana, Dimitra Nulsen, Joel Goldman, Jacki Pollitt, Marc Davis, Patrick Strange, Amy Ambrose, Karen Ciccarelli, Francesca D. |
author_facet | Dressler, Lisa Bortolomeazzi, Michele Keddar, Mohamed Reda Misetic, Hrvoje Sartini, Giulia Acha-Sagredo, Amelia Montorsi, Lucia Wijewardhane, Neshika Repana, Dimitra Nulsen, Joel Goldman, Jacki Pollitt, Marc Davis, Patrick Strange, Amy Ambrose, Karen Ciccarelli, Francesca D. |
author_sort | Dressler, Lisa |
collection | PubMed |
description | BACKGROUND: Genetic alterations of somatic cells can drive non-malignant clone formation and promote cancer initiation. However, the link between these processes remains unclear and hampers our understanding of tissue homeostasis and cancer development. RESULTS: Here, we collect a literature-based repertoire of 3355 well-known or predicted drivers of cancer and non-cancer somatic evolution in 122 cancer types and 12 non-cancer tissues. Mapping the alterations of these genes in 7953 pan-cancer samples reveals that, despite the large size, the known compendium of drivers is still incomplete and biased towards frequently occurring coding mutations. High overlap exists between drivers of cancer and non-cancer somatic evolution, although significant differences emerge in their recurrence. We confirm and expand the unique properties of drivers and identify a core of evolutionarily conserved and essential genes whose germline variation is strongly counter-selected. Somatic alteration in even one of these genes is sufficient to drive clonal expansion but not malignant transformation. CONCLUSIONS: Our study offers a comprehensive overview of our current understanding of the genetic events initiating clone expansion and cancer revealing significant gaps and biases that still need to be addressed. The compendium of cancer and non-cancer somatic drivers, their literature support, and properties are accessible in the Network of Cancer Genes and Healthy Drivers resource at http://www.network-cancer-genes.org/. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02607-z. |
format | Online Article Text |
id | pubmed-8790917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87909172022-01-26 Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource Dressler, Lisa Bortolomeazzi, Michele Keddar, Mohamed Reda Misetic, Hrvoje Sartini, Giulia Acha-Sagredo, Amelia Montorsi, Lucia Wijewardhane, Neshika Repana, Dimitra Nulsen, Joel Goldman, Jacki Pollitt, Marc Davis, Patrick Strange, Amy Ambrose, Karen Ciccarelli, Francesca D. Genome Biol Research BACKGROUND: Genetic alterations of somatic cells can drive non-malignant clone formation and promote cancer initiation. However, the link between these processes remains unclear and hampers our understanding of tissue homeostasis and cancer development. RESULTS: Here, we collect a literature-based repertoire of 3355 well-known or predicted drivers of cancer and non-cancer somatic evolution in 122 cancer types and 12 non-cancer tissues. Mapping the alterations of these genes in 7953 pan-cancer samples reveals that, despite the large size, the known compendium of drivers is still incomplete and biased towards frequently occurring coding mutations. High overlap exists between drivers of cancer and non-cancer somatic evolution, although significant differences emerge in their recurrence. We confirm and expand the unique properties of drivers and identify a core of evolutionarily conserved and essential genes whose germline variation is strongly counter-selected. Somatic alteration in even one of these genes is sufficient to drive clonal expansion but not malignant transformation. CONCLUSIONS: Our study offers a comprehensive overview of our current understanding of the genetic events initiating clone expansion and cancer revealing significant gaps and biases that still need to be addressed. The compendium of cancer and non-cancer somatic drivers, their literature support, and properties are accessible in the Network of Cancer Genes and Healthy Drivers resource at http://www.network-cancer-genes.org/. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02607-z. BioMed Central 2022-01-26 /pmc/articles/PMC8790917/ /pubmed/35078504 http://dx.doi.org/10.1186/s13059-022-02607-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Dressler, Lisa Bortolomeazzi, Michele Keddar, Mohamed Reda Misetic, Hrvoje Sartini, Giulia Acha-Sagredo, Amelia Montorsi, Lucia Wijewardhane, Neshika Repana, Dimitra Nulsen, Joel Goldman, Jacki Pollitt, Marc Davis, Patrick Strange, Amy Ambrose, Karen Ciccarelli, Francesca D. Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title | Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title_full | Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title_fullStr | Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title_full_unstemmed | Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title_short | Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource |
title_sort | comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the network of cancer genes (ncg) resource |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790917/ https://www.ncbi.nlm.nih.gov/pubmed/35078504 http://dx.doi.org/10.1186/s13059-022-02607-z |
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