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Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario

BACKGROUND: There is growing evidence that gene-gene interactions are ubiquitous in determining the susceptibility to common human diseases. The investigation of such gene-gene interactions presents new statistical challenges for studies with relatively small sample sizes as the number of potential...

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Autores principales: Briollais, Laurent, Wang, Yuanyuan, Rajendram, Isaac, Onay, Venus, Shi, Ellen, Knight, Julia, Ozcelik, Hilmi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976420/
https://www.ncbi.nlm.nih.gov/pubmed/17683639
http://dx.doi.org/10.1186/1741-7015-5-22
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author Briollais, Laurent
Wang, Yuanyuan
Rajendram, Isaac
Onay, Venus
Shi, Ellen
Knight, Julia
Ozcelik, Hilmi
author_facet Briollais, Laurent
Wang, Yuanyuan
Rajendram, Isaac
Onay, Venus
Shi, Ellen
Knight, Julia
Ozcelik, Hilmi
author_sort Briollais, Laurent
collection PubMed
description BACKGROUND: There is growing evidence that gene-gene interactions are ubiquitous in determining the susceptibility to common human diseases. The investigation of such gene-gene interactions presents new statistical challenges for studies with relatively small sample sizes as the number of potential interactions in the genome can be large. Breast cancer provides a useful paradigm to study genetically complex diseases because commonly occurring single nucleotide polymorphisms (SNPs) may additively or synergistically disturb the system-wide communication of the cellular processes leading to cancer development. METHODS: In this study, we systematically studied SNP-SNP interactions among 19 SNPs from 18 key genes involved in major cancer pathways in a sample of 398 breast cancer cases and 372 controls from Ontario. We discuss the methodological issues associated with the detection of SNP-SNP interactions in this dataset by applying and comparing three commonly used methods: the logistic regression model, classification and regression trees (CART), and the multifactor dimensionality reduction (MDR) method. RESULTS: Our analyses show evidence for several simple (two-way) and complex (multi-way) SNP-SNP interactions associated with breast cancer. For example, all three methods identified XPD-[Lys751Gln]*IL10-[G(-1082)A] as the most significant two-way interaction. CART and MDR identified the same critical SNPs participating in complex interactions. Our results suggest that the use of multiple statistical approaches (or an integrated approach) rather than a single methodology could be the best strategy to elucidate complex gene interactions that have generally very different patterns. CONCLUSION: The strategy used here has the potential to identify complex biological relationships among breast cancer genes and processes. This will lead to the discovery of novel biological information, which will improve breast cancer risk management.
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spelling pubmed-19764202007-09-14 Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario Briollais, Laurent Wang, Yuanyuan Rajendram, Isaac Onay, Venus Shi, Ellen Knight, Julia Ozcelik, Hilmi BMC Med Research Article BACKGROUND: There is growing evidence that gene-gene interactions are ubiquitous in determining the susceptibility to common human diseases. The investigation of such gene-gene interactions presents new statistical challenges for studies with relatively small sample sizes as the number of potential interactions in the genome can be large. Breast cancer provides a useful paradigm to study genetically complex diseases because commonly occurring single nucleotide polymorphisms (SNPs) may additively or synergistically disturb the system-wide communication of the cellular processes leading to cancer development. METHODS: In this study, we systematically studied SNP-SNP interactions among 19 SNPs from 18 key genes involved in major cancer pathways in a sample of 398 breast cancer cases and 372 controls from Ontario. We discuss the methodological issues associated with the detection of SNP-SNP interactions in this dataset by applying and comparing three commonly used methods: the logistic regression model, classification and regression trees (CART), and the multifactor dimensionality reduction (MDR) method. RESULTS: Our analyses show evidence for several simple (two-way) and complex (multi-way) SNP-SNP interactions associated with breast cancer. For example, all three methods identified XPD-[Lys751Gln]*IL10-[G(-1082)A] as the most significant two-way interaction. CART and MDR identified the same critical SNPs participating in complex interactions. Our results suggest that the use of multiple statistical approaches (or an integrated approach) rather than a single methodology could be the best strategy to elucidate complex gene interactions that have generally very different patterns. CONCLUSION: The strategy used here has the potential to identify complex biological relationships among breast cancer genes and processes. This will lead to the discovery of novel biological information, which will improve breast cancer risk management. BioMed Central 2007-08-07 /pmc/articles/PMC1976420/ /pubmed/17683639 http://dx.doi.org/10.1186/1741-7015-5-22 Text en Copyright © 2007 Briollais 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 Research Article
Briollais, Laurent
Wang, Yuanyuan
Rajendram, Isaac
Onay, Venus
Shi, Ellen
Knight, Julia
Ozcelik, Hilmi
Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title_full Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title_fullStr Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title_full_unstemmed Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title_short Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario
title_sort methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in ontario
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976420/
https://www.ncbi.nlm.nih.gov/pubmed/17683639
http://dx.doi.org/10.1186/1741-7015-5-22
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