4.8 Article

Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas

Journal

CELL REPORTS
Volume 23, Issue 1, Pages 172-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2018.03.046

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Funding

  1. Gordon and Betty Moore Foundation [GBMF 4552]
  2. NIH [R01 NS095411, T32 HG000046]
  3. U.S. National Cancer Institute of TCGA [U54 HG003273, U54 HG003067, U54 HG003079, U24 CA143799, U24 CA143835, U24 CA143840, U24 CA143843, U24 CA143845, U24 CA143848, U24 CA143858, U24 CA143866, U24 CA143867, U24 CA143882, U24 CA143883, U24 CA144025, P30 CA016672]

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Precision oncology uses genomic evidence to match patients with treatment but often fails to identify all patients who may respond. The transcriptome of these hidden responders'' may reveal responsive molecular states. We describe and evaluate a machine-learning approach to classify aberrant pathway activity in tumors, which may aid in hidden responder identification. The algorithm integrates RNA-seq, copy number, and mutations from 33 different cancer types across The Cancer Genome Atlas (TCGA) PanCanAtlas project to predict aberrant molecular states in tumors. Applied to the Ras pathway, the method detects Ras activation across cancer types and identifies phenocopying variants. The model, trained on human tumors, can predict response to MEK inhibitors in wild-type Ras cell lines. We also present data that suggest that multiple hits in the Ras pathway confer increased Ras activity. The transcriptome is underused in precision oncology and, combined with machine learning, can aid in the identification of hidden responders.

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