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A statistical framework for assessing pharmacological responses and biomarkers using uncertainty estimates.
Wang, Dennis; Hensman, James; Kutkaite, Ginte; Toh, Tzen S; Galhoz, Ana; Dry, Jonathan R; Saez-Rodriguez, Julio; Garnett, Mathew J; Menden, Michael P; Dondelinger, Frank.
Afiliação
  • Wang D; Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, United Kingdom.
  • Hensman J; Department of Computer Science, University of Sheffield, Sheffield, United Kingdom.
  • Kutkaite G; PROWLER.io, Cambridge, United Kingdom.
  • Toh TS; Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.
  • Galhoz A; Department of Biology, Ludwig-Maximilians University Munich, Martinsried, Germany.
  • Dry JR; Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.
  • Saez-Rodriguez J; Department of Biology, Ludwig-Maximilians University Munich, Martinsried, Germany.
  • Garnett MJ; Wellcome Sanger Institute, Cambridge, United Kingdom.
  • Menden MP; Research and Early Development, Oncology R&D, AstraZeneca, Boston, United States.
  • Dondelinger F; Institute of Computational Biomedicine,Faculty of Medicine,Heidelberg Universityand Heidelberg University Hospital, Bioquant, Heidelberg, Germany.
Elife ; 92020 12 04.
Article em En | MEDLINE | ID: mdl-33274713
ABSTRACT
High-throughput testing of drugs across molecular-characterised cell lines can identify candidate treatments and discover biomarkers. However, the cells' response to a drug is typically quantified by a summary statistic from a best-fit dose-response curve, whilst neglecting the uncertainty of the curve fit and the potential variability in the raw readouts. Here, we model the experimental variance using Gaussian Processes, and subsequently, leverage uncertainty estimates to identify associated biomarkers with a new Bayesian framework. Applied to in vitro screening data on 265 compounds across 1074 cancer cell lines, our models identified 24 clinically established drug-response biomarkers, and provided evidence for six novel biomarkers by accounting for association with low uncertainty. We validated our uncertainty estimates with an additional drug screen of 26 drugs, 10 cell lines with 8 to 9 replicates. Our method is applicable to any dose-response data without replicates, and improves biomarker discovery for precision medicine.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Estatística como Assunto / Descoberta de Drogas / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Estatística como Assunto / Descoberta de Drogas / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article