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Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells

A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically...

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Autores principales: Leelatian, Nalin, Sinnaeve, Justine, Mistry, Akshitkumar M, Barone, Sierra M, Brockman, Asa A, Diggins, Kirsten E, Greenplate, Allison R, Weaver, Kyle D, Thompson, Reid C, Chambless, Lola B, Mobley, Bret C, Ihrie, Rebecca A, Irish, Jonathan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340505/
https://www.ncbi.nlm.nih.gov/pubmed/32573435
http://dx.doi.org/10.7554/eLife.56879
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author Leelatian, Nalin
Sinnaeve, Justine
Mistry, Akshitkumar M
Barone, Sierra M
Brockman, Asa A
Diggins, Kirsten E
Greenplate, Allison R
Weaver, Kyle D
Thompson, Reid C
Chambless, Lola B
Mobley, Bret C
Ihrie, Rebecca A
Irish, Jonathan M
author_facet Leelatian, Nalin
Sinnaeve, Justine
Mistry, Akshitkumar M
Barone, Sierra M
Brockman, Asa A
Diggins, Kirsten E
Greenplate, Allison R
Weaver, Kyle D
Thompson, Reid C
Chambless, Lola B
Mobley, Bret C
Ihrie, Rebecca A
Irish, Jonathan M
author_sort Leelatian, Nalin
collection PubMed
description A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically distinct cell populations, and determines whether these populations stratify patient survival. With a pilot mass cytometry dataset of 2 million cells from 28 glioblastomas, RAPID identified tumor cells whose abundance independently and continuously stratified patient survival. Statistical validation within the workflow included repeated runs of stochastic steps and cell subsampling. Biological validation used an orthogonal platform, immunohistochemistry, and a larger cohort of 73 glioblastoma patients to confirm the findings from the pilot cohort. RAPID was also validated to find known risk stratifying cells and features using published data from blood cancer. Thus, RAPID provides an automated, unsupervised approach for finding statistically and biologically significant cells using cytometry data from patient samples.
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spelling pubmed-73405052020-07-13 Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells Leelatian, Nalin Sinnaeve, Justine Mistry, Akshitkumar M Barone, Sierra M Brockman, Asa A Diggins, Kirsten E Greenplate, Allison R Weaver, Kyle D Thompson, Reid C Chambless, Lola B Mobley, Bret C Ihrie, Rebecca A Irish, Jonathan M eLife Computational and Systems Biology A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically distinct cell populations, and determines whether these populations stratify patient survival. With a pilot mass cytometry dataset of 2 million cells from 28 glioblastomas, RAPID identified tumor cells whose abundance independently and continuously stratified patient survival. Statistical validation within the workflow included repeated runs of stochastic steps and cell subsampling. Biological validation used an orthogonal platform, immunohistochemistry, and a larger cohort of 73 glioblastoma patients to confirm the findings from the pilot cohort. RAPID was also validated to find known risk stratifying cells and features using published data from blood cancer. Thus, RAPID provides an automated, unsupervised approach for finding statistically and biologically significant cells using cytometry data from patient samples. eLife Sciences Publications, Ltd 2020-06-23 /pmc/articles/PMC7340505/ /pubmed/32573435 http://dx.doi.org/10.7554/eLife.56879 Text en © 2020, Leelatian et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Leelatian, Nalin
Sinnaeve, Justine
Mistry, Akshitkumar M
Barone, Sierra M
Brockman, Asa A
Diggins, Kirsten E
Greenplate, Allison R
Weaver, Kyle D
Thompson, Reid C
Chambless, Lola B
Mobley, Bret C
Ihrie, Rebecca A
Irish, Jonathan M
Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title_full Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title_fullStr Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title_full_unstemmed Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title_short Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
title_sort unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340505/
https://www.ncbi.nlm.nih.gov/pubmed/32573435
http://dx.doi.org/10.7554/eLife.56879
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