| Literature DB >> 25581432 |
Rudolf S N Fehrmann1, Juha M Karjalainen2, Małgorzata Krajewska3, Harm-Jan Westra2, David Maloney4, Anton Simeonov4, Tune H Pers5, Joel N Hirschhorn6, Ritsert C Jansen7, Erik A Schultes8, Herman H H B M van Haagen9, Elisabeth G E de Vries3, Gerard J te Meerman2, Cisca Wijmenga2, Marcel A T M van Vugt3, Lude Franke2.
Abstract
Many cancer-associated somatic copy number alterations (SCNAs) are known. Currently, one of the challenges is to identify the molecular downstream effects of these variants. Although several SCNAs are known to change gene expression levels, it is not clear whether each individual SCNA affects gene expression. We reanalyzed 77,840 expression profiles and observed a limited set of 'transcriptional components' that describe well-known biology, explain the vast majority of variation in gene expression and enable us to predict the biological function of genes. On correcting expression profiles for these components, we observed that the residual expression levels (in 'functional genomic mRNA' profiling) correlated strongly with copy number. DNA copy number correlated positively with expression levels for 99% of all abundantly expressed human genes, indicating global gene dosage sensitivity. By applying this method to 16,172 patient-derived tumor samples, we replicated many loci with aberrant copy numbers and identified recurrently disrupted genes in genomically unstable cancers.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25581432 DOI: 10.1038/ng.3173
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330