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Finding biological process modifications in cancer tissues by mining gene expression correlations

BACKGROUND: Through the use of DNA microarrays it is now possible to obtain quantitative measurements of the expression of thousands of genes from a biological sample. This technology yields a global view of gene expression that can be used in several ways. Functional insight into expression profile...

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Autores principales: Gamberoni, Giacomo, Storari, Sergio, Volinia, Stefano
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360676/
https://www.ncbi.nlm.nih.gov/pubmed/16401337
http://dx.doi.org/10.1186/1471-2105-7-6
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author Gamberoni, Giacomo
Storari, Sergio
Volinia, Stefano
author_facet Gamberoni, Giacomo
Storari, Sergio
Volinia, Stefano
author_sort Gamberoni, Giacomo
collection PubMed
description BACKGROUND: Through the use of DNA microarrays it is now possible to obtain quantitative measurements of the expression of thousands of genes from a biological sample. This technology yields a global view of gene expression that can be used in several ways. Functional insight into expression profiles is routinely obtained by using Gene Ontology terms associated to the cellular genes. In this paper, we deal with functional data mining from expression profiles, proposing a novel approach that studies the correlations between genes and their relations to Gene Ontology (GO). By using this "functional correlations comparison" we explore all possible pairs of genes identifying the affected biological processes by analyzing in a pair-wise manner gene expression patterns and linking correlated pairs with Gene Ontology terms. RESULTS: We apply here this "functional correlations comparison" approach to identify the existing correlations in hepatocarcinoma (161 microarray experiments) and to reveal functional differences between normal liver and cancer tissues. The number of well-correlated pairs in each GO term highlights several differences in genetic interactions between cancer and normal tissues. We performed a bootstrap analysis in order to compute false detection rates (FDR) and confidence limits. CONCLUSION: Experimental results show the main advantage of the applied method: it both picks up general and specific GO terms (in particular it shows a fine resolution in the specific GO terms). The results obtained by this novel method are highly coherent with the ones proposed by other cancer biology studies. But additionally they highlight the most specific and interesting GO terms helping the biologist to focus his/her studies on the most relevant biological processes.
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spelling pubmed-13606762006-02-10 Finding biological process modifications in cancer tissues by mining gene expression correlations Gamberoni, Giacomo Storari, Sergio Volinia, Stefano BMC Bioinformatics Methodology Article BACKGROUND: Through the use of DNA microarrays it is now possible to obtain quantitative measurements of the expression of thousands of genes from a biological sample. This technology yields a global view of gene expression that can be used in several ways. Functional insight into expression profiles is routinely obtained by using Gene Ontology terms associated to the cellular genes. In this paper, we deal with functional data mining from expression profiles, proposing a novel approach that studies the correlations between genes and their relations to Gene Ontology (GO). By using this "functional correlations comparison" we explore all possible pairs of genes identifying the affected biological processes by analyzing in a pair-wise manner gene expression patterns and linking correlated pairs with Gene Ontology terms. RESULTS: We apply here this "functional correlations comparison" approach to identify the existing correlations in hepatocarcinoma (161 microarray experiments) and to reveal functional differences between normal liver and cancer tissues. The number of well-correlated pairs in each GO term highlights several differences in genetic interactions between cancer and normal tissues. We performed a bootstrap analysis in order to compute false detection rates (FDR) and confidence limits. CONCLUSION: Experimental results show the main advantage of the applied method: it both picks up general and specific GO terms (in particular it shows a fine resolution in the specific GO terms). The results obtained by this novel method are highly coherent with the ones proposed by other cancer biology studies. But additionally they highlight the most specific and interesting GO terms helping the biologist to focus his/her studies on the most relevant biological processes. BioMed Central 2006-01-09 /pmc/articles/PMC1360676/ /pubmed/16401337 http://dx.doi.org/10.1186/1471-2105-7-6 Text en Copyright © 2006 Gamberoni et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Gamberoni, Giacomo
Storari, Sergio
Volinia, Stefano
Finding biological process modifications in cancer tissues by mining gene expression correlations
title Finding biological process modifications in cancer tissues by mining gene expression correlations
title_full Finding biological process modifications in cancer tissues by mining gene expression correlations
title_fullStr Finding biological process modifications in cancer tissues by mining gene expression correlations
title_full_unstemmed Finding biological process modifications in cancer tissues by mining gene expression correlations
title_short Finding biological process modifications in cancer tissues by mining gene expression correlations
title_sort finding biological process modifications in cancer tissues by mining gene expression correlations
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360676/
https://www.ncbi.nlm.nih.gov/pubmed/16401337
http://dx.doi.org/10.1186/1471-2105-7-6
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