sample-level enrichment analysis unravels shared stress phenotypes among multiple cancer typessample-level浓缩拆解分析共享压力多种癌症类型之间的表型.pdfVIP
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sample-level enrichment analysis unravels shared stress phenotypes among multiple cancer typessample-level浓缩拆解分析共享压力多种癌症类型之间的表型
Gundem and Lopez-Bigas Genome Medicine 2012, 4:28
/content/4/3/28
RESEARCH Open Access
Sample-level enrichment analysis unravels shared
stress phenotypes among multiple cancer types
Gunes Gundem1,2* and Nuria Lopez-Bigas1,3*
Abstract
Background: Adaptation to stress signals in the tumor microenvironment is a crucial step towards carcinogenic
phenotype. The adaptive alterations attained by cells to withstand different types of insults are collectively referred
to as the stress phenotypes of cancers. In this manuscript we explore the interrelation of different stress
phenotypes in multiple cancer types and ask if these phenotypes could be used to explain prognostic differences
among tumor samples.
Methods: We propose a new approach based on enrichment analysis at the level of samples (sample-level
enrichment analysis - SLEA) in expression profiling datasets. Without using a priori phenotypic information about
samples, SLEA calculates an enrichment score per sample per gene set using z-test. This score is used to determine
the relative importance of the corresponding pathway or module in different patient groups.
Results: Our analysis shows that tumors significantly upregulating genes related to chromosome instability
strongly correlate with worse prognosis in breast cancer. Moreover, in multiple tumor types, these tumors
upregulate a senescence-bypass transcriptional program and exhibit similar stress phenotypes.
Conclusions: Using SLEA we are able to find relationships between stress phenotype pathways across multiple
cancer types. Moreover we show that SLEA enables the identification of gene sets in correlation with clinical
characteristics such as survival, as well as the identification of biological pathways/processes that underlie the
pathology of different cancer subgroups.
Background
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