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Chromosome arm aneuploidies shape tumour evolution and drug response

Chromosome arm aneuploidies (CAAs) are pervasive in cancers. However, how they affect cancer development, prognosis and treatment remains largely unknown. Here, we analyse CAA profiles of 23,427 tumours, identifying aspects of tumour evolution including probable orders in which CAAs occur and CAAs p...

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Autores principales: Shukla, Ankit, Nguyen, Thu H. M., Moka, Sarat B., Ellis, Jonathan J., Grady, John P., Oey, Harald, Cristino, Alexandre S., Khanna, Kum Kum, Kroese, Dirk P., Krause, Lutz, Dray, Eloise, Fink, J. Lynn, Duijf, Pascal H. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978319/
https://www.ncbi.nlm.nih.gov/pubmed/31974379
http://dx.doi.org/10.1038/s41467-020-14286-0
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author Shukla, Ankit
Nguyen, Thu H. M.
Moka, Sarat B.
Ellis, Jonathan J.
Grady, John P.
Oey, Harald
Cristino, Alexandre S.
Khanna, Kum Kum
Kroese, Dirk P.
Krause, Lutz
Dray, Eloise
Fink, J. Lynn
Duijf, Pascal H. G.
author_facet Shukla, Ankit
Nguyen, Thu H. M.
Moka, Sarat B.
Ellis, Jonathan J.
Grady, John P.
Oey, Harald
Cristino, Alexandre S.
Khanna, Kum Kum
Kroese, Dirk P.
Krause, Lutz
Dray, Eloise
Fink, J. Lynn
Duijf, Pascal H. G.
author_sort Shukla, Ankit
collection PubMed
description Chromosome arm aneuploidies (CAAs) are pervasive in cancers. However, how they affect cancer development, prognosis and treatment remains largely unknown. Here, we analyse CAA profiles of 23,427 tumours, identifying aspects of tumour evolution including probable orders in which CAAs occur and CAAs predicting tissue-specific metastasis. Both haematological and solid cancers initially gain chromosome arms, while only solid cancers subsequently preferentially lose multiple arms. 72 CAAs and 88 synergistically co-occurring CAA pairs multivariately predict good or poor survival for 58% of 6977 patients, with negligible impact of whole-genome doubling. Additionally, machine learning identifies 31 CAAs that robustly alter response to 56 chemotherapeutic drugs across cell lines representing 17 cancer types. We also uncover 1024 potential synthetic lethal pharmacogenomic interactions. Notably, in predicting drug response, CAAs substantially outperform  mutations and focal deletions/amplifications combined. Thus, CAAs predict cancer prognosis, shape tumour evolution, metastasis and drug response, and may advance precision oncology.
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spelling pubmed-69783192020-01-27 Chromosome arm aneuploidies shape tumour evolution and drug response Shukla, Ankit Nguyen, Thu H. M. Moka, Sarat B. Ellis, Jonathan J. Grady, John P. Oey, Harald Cristino, Alexandre S. Khanna, Kum Kum Kroese, Dirk P. Krause, Lutz Dray, Eloise Fink, J. Lynn Duijf, Pascal H. G. Nat Commun Article Chromosome arm aneuploidies (CAAs) are pervasive in cancers. However, how they affect cancer development, prognosis and treatment remains largely unknown. Here, we analyse CAA profiles of 23,427 tumours, identifying aspects of tumour evolution including probable orders in which CAAs occur and CAAs predicting tissue-specific metastasis. Both haematological and solid cancers initially gain chromosome arms, while only solid cancers subsequently preferentially lose multiple arms. 72 CAAs and 88 synergistically co-occurring CAA pairs multivariately predict good or poor survival for 58% of 6977 patients, with negligible impact of whole-genome doubling. Additionally, machine learning identifies 31 CAAs that robustly alter response to 56 chemotherapeutic drugs across cell lines representing 17 cancer types. We also uncover 1024 potential synthetic lethal pharmacogenomic interactions. Notably, in predicting drug response, CAAs substantially outperform  mutations and focal deletions/amplifications combined. Thus, CAAs predict cancer prognosis, shape tumour evolution, metastasis and drug response, and may advance precision oncology. Nature Publishing Group UK 2020-01-23 /pmc/articles/PMC6978319/ /pubmed/31974379 http://dx.doi.org/10.1038/s41467-020-14286-0 Text en © The Author(s) 2020 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/.
spellingShingle Article
Shukla, Ankit
Nguyen, Thu H. M.
Moka, Sarat B.
Ellis, Jonathan J.
Grady, John P.
Oey, Harald
Cristino, Alexandre S.
Khanna, Kum Kum
Kroese, Dirk P.
Krause, Lutz
Dray, Eloise
Fink, J. Lynn
Duijf, Pascal H. G.
Chromosome arm aneuploidies shape tumour evolution and drug response
title Chromosome arm aneuploidies shape tumour evolution and drug response
title_full Chromosome arm aneuploidies shape tumour evolution and drug response
title_fullStr Chromosome arm aneuploidies shape tumour evolution and drug response
title_full_unstemmed Chromosome arm aneuploidies shape tumour evolution and drug response
title_short Chromosome arm aneuploidies shape tumour evolution and drug response
title_sort chromosome arm aneuploidies shape tumour evolution and drug response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978319/
https://www.ncbi.nlm.nih.gov/pubmed/31974379
http://dx.doi.org/10.1038/s41467-020-14286-0
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