Inferring tumour purity and stromal and immune cell admixture from expression data

Kosuke Yoshihara(Niigata University), Maria Shahmoradgoli(The University of Texas MD Anderson Cancer Center), Emmanuel Martínez(Tecnológico de Monterrey), Rahulsimham Vegesna(The University of Texas MD Anderson Cancer Center), Hoon Kim(The University of Texas MD Anderson Cancer Center), Wandaliz Torres‐García(The University of Texas MD Anderson Cancer Center), Víctor Treviño(Tecnológico de Monterrey), Hui Shen(University of Southern California), Peter W. Laird(University of California, Los Angeles), Douglas A. Levine(Memorial Sloan Kettering Cancer Center), Scott L. Carter(Broad Institute), Gad Getz(Broad Institute), Katherine Stemke‐Hale(The University of Texas MD Anderson Cancer Center), Gordon B. Mills(The University of Texas MD Anderson Cancer Center), Roel G.W. Verhaak(The University of Texas MD Anderson Cancer Center)
Nature Communications
October 11, 2013
Cited by 10,670Open Access
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Abstract

Infiltrating stromal and immune cells form the major fraction of normal cells in tumour tissue and not only perturb the tumour signal in molecular studies but also have an important role in cancer biology. Here we describe ‘Estimation of STromal and Immune cells in MAlignant Tumours using Expression data’ (ESTIMATE)—a method that uses gene expression signatures to infer the fraction of stromal and immune cells in tumour samples. ESTIMATE scores correlate with DNA copy number-based tumour purity across samples from 11 different tumour types, profiled on Agilent, Affymetrix platforms or based on RNA sequencing and available through The Cancer Genome Atlas. The prediction accuracy is further corroborated using 3,809 transcriptional profiles available elsewhere in the public domain. The ESTIMATE method allows consideration of tumour-associated normal cells in genomic and transcriptomic studies. An R-library is available on https://sourceforge.net/projects/estimateproject/ . Tumour biopsies contain contaminating normal cells and these can influence the analysis of tumour samples. In this study, Yoshihara et al.develop an algorithm based on gene expression profiles from The Cancer Genome Atlas to estimate the number of contaminating normal cells in tumour samples.


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