A pan-cancer compendium of chromosomal instability

التفاصيل البيبلوغرافية
العنوان: A pan-cancer compendium of chromosomal instability
المؤلفون: Ruben M. Drews, Barbara Hernando, Maxime Tarabichi, Kerstin Haase, Tom Lesluyes, Philip S. Smith, Lena Morrill Gavarró, Dominique-Laurent Couturier, Lydia Liu, Michael Schneider, James D. Brenton, Peter Van Loo, Geoff Macintyre, Florian Markowetz
المساهمون: Drews, Ruben M [0000-0001-7360-4970], Haase, Kerstin [0000-0002-0944-5618], Lesluyes, Tom [0000-0003-2251-5884], Smith, Philip [0000-0002-9306-1747], Morrill Gavarró, Lena [0000-0002-2242-4010], Couturier, Dominique [0000-0001-5774-5036], Liu, Lydia [0000-0001-6026-3169], Brenton, James [0000-0002-5738-6683], Van Loo, Peter [0000-0003-0292-1949], Macintyre, Geoff [0000-0003-3906-467X], Markowetz, Florian [0000-0002-2784-5308], Apollo - University of Cambridge Repository
المصدر: Nature
بيانات النشر: Springer Science and Business Media LLC, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Multidisciplinary, DNA Copy Number Variations, Chromosomal Instability, Gene Expression Profiling, Neoplasms, virus diseases, Humans, Molecular Targeted Therapy, urologic and male genital diseases, Homologous Recombination, neoplasms, female genital diseases and pregnancy complications, Article
الوصف: Chromosomal instability (CIN) results in the accumulation of large-scale losses, gains, and rearrangements of DNA(1). The broad genomic complexity caused by CIN is a hallmark of cancer(2), however, there is no systematic framework to measure different types of CIN and their impact on clinical phenotypes pan-cancer. Here, we evaluate the extent, diversity and origin of chromosomal instability across 7,880 tumours representing 33 cancer types. We present a compendium of 17 copy number signatures characterising specific types of CIN, with putative aetiologies supported by multiple independent data sources. The signatures predict drug response and identify new drug targets. Our framework refines the understanding of impaired homologous recombination, one of the most therapeutically targetable types of CIN. Our results illuminate a fundamental structure underlying genomic complexity in human cancers and provide a resource to guide future CIN research.
وصف الملف: application/pdf
تدمد: 1476-4687
0028-0836
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b195b1ee3534ba28f939f59096c916b6Test
https://doi.org/10.1038/s41586-022-04789-9Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....b195b1ee3534ba28f939f59096c916b6
قاعدة البيانات: OpenAIRE