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A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles

Patient-derived cell lines are often used in pre-clinical cancer research, but some cell lines are too different from tumors to be good models. Comparison of genomic and expression profiles can guide the choice of pre-clinical models, but typically not all features are equally relevant. We present T...

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Detalles Bibliográficos
Autores principales: Sinha, Rileen, Luna, Augustin, Schultz, Nikolaus, Sander, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017219/
https://www.ncbi.nlm.nih.gov/pubmed/35475239
http://dx.doi.org/10.1016/j.crmeth.2021.100039
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author Sinha, Rileen
Luna, Augustin
Schultz, Nikolaus
Sander, Chris
author_facet Sinha, Rileen
Luna, Augustin
Schultz, Nikolaus
Sander, Chris
author_sort Sinha, Rileen
collection PubMed
description Patient-derived cell lines are often used in pre-clinical cancer research, but some cell lines are too different from tumors to be good models. Comparison of genomic and expression profiles can guide the choice of pre-clinical models, but typically not all features are equally relevant. We present TumorComparer, a computational method for comparing cellular profiles with higher weights on functional features of interest. In this pan-cancer application, we compare ∼600 cell lines and ∼8,000 tumor samples of 24 cancer types, using weights to emphasize known oncogenic alterations. We characterize the similarity of cell lines and tumors within and across cancers by using multiple datum types and rank cell lines by their inferred quality as representative models. Beyond the assessment of cell lines, the weighted similarity approach is adaptable to patient stratification in clinical trials and personalized medicine.
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spelling pubmed-90172192022-04-25 A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles Sinha, Rileen Luna, Augustin Schultz, Nikolaus Sander, Chris Cell Rep Methods Article Patient-derived cell lines are often used in pre-clinical cancer research, but some cell lines are too different from tumors to be good models. Comparison of genomic and expression profiles can guide the choice of pre-clinical models, but typically not all features are equally relevant. We present TumorComparer, a computational method for comparing cellular profiles with higher weights on functional features of interest. In this pan-cancer application, we compare ∼600 cell lines and ∼8,000 tumor samples of 24 cancer types, using weights to emphasize known oncogenic alterations. We characterize the similarity of cell lines and tumors within and across cancers by using multiple datum types and rank cell lines by their inferred quality as representative models. Beyond the assessment of cell lines, the weighted similarity approach is adaptable to patient stratification in clinical trials and personalized medicine. Elsevier 2021-06-21 /pmc/articles/PMC9017219/ /pubmed/35475239 http://dx.doi.org/10.1016/j.crmeth.2021.100039 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sinha, Rileen
Luna, Augustin
Schultz, Nikolaus
Sander, Chris
A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title_full A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title_fullStr A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title_full_unstemmed A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title_short A pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
title_sort pan-cancer survey of cell line tumor similarity by feature-weighted molecular profiles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017219/
https://www.ncbi.nlm.nih.gov/pubmed/35475239
http://dx.doi.org/10.1016/j.crmeth.2021.100039
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