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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.
Afiliação
  • Leelatian N; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United States.
  • Sinnaeve J; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
  • Mistry AM; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, United States.
  • Barone SM; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United States.
  • Brockman AA; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
  • Diggins KE; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
  • Greenplate AR; Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, United States.
  • Weaver KD; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United States.
  • Thompson RC; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United States.
  • Chambless LB; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
  • Mobley BC; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United States.
  • Ihrie RA; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
  • Irish JM; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, United States.
Elife ; 92020 06 23.
Article em En | MEDLINE | ID: mdl-32573435
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Aprendizado de Máquina não Supervisionado Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Aprendizado de Máquina não Supervisionado Idioma: En Ano de publicação: 2020 Tipo de documento: Article