Cargando…

Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer

Genome-wide association studies (GWAS) explore the genetic causes of complex diseases. However, classical approaches ignore the biological context of the genetic variants and genes under study. To address this shortcoming, one can use biological networks, which model functional relationships, to sea...

Descripción completa

Detalles Bibliográficos
Autores principales: Climente-González, Héctor, Lonjou, Christine, Lesueur, Fabienne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Azencott, Chloé-Agathe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009366/
https://www.ncbi.nlm.nih.gov/pubmed/33735170
http://dx.doi.org/10.1371/journal.pcbi.1008819
_version_ 1783672859535605760
author Climente-González, Héctor
Lonjou, Christine
Lesueur, Fabienne
Stoppa-Lyonnet, Dominique
Andrieu, Nadine
Azencott, Chloé-Agathe
author_facet Climente-González, Héctor
Lonjou, Christine
Lesueur, Fabienne
Stoppa-Lyonnet, Dominique
Andrieu, Nadine
Azencott, Chloé-Agathe
author_sort Climente-González, Héctor
collection PubMed
description Genome-wide association studies (GWAS) explore the genetic causes of complex diseases. However, classical approaches ignore the biological context of the genetic variants and genes under study. To address this shortcoming, one can use biological networks, which model functional relationships, to search for functionally related susceptibility loci. Many such network methods exist, each arising from different mathematical frameworks, pre-processing steps, and assumptions about the network properties of the susceptibility mechanism. Unsurprisingly, this results in disparate solutions. To explore how to exploit these heterogeneous approaches, we selected six network methods and applied them to GENESIS, a nationwide French study on familial breast cancer. First, we verified that network methods recovered more interpretable results than a standard GWAS. We addressed the heterogeneity of their solutions by studying their overlap, computing what we called the consensus. The key gene in this consensus solution was COPS5, a gene related to multiple cancer hallmarks. Another issue we observed was that network methods were unstable, selecting very different genes on different subsamples of GENESIS. Therefore, we proposed a stable consensus solution formed by the 68 genes most consistently selected across multiple subsamples. This solution was also enriched in genes known to be associated with breast cancer susceptibility (BLM, CASP8, CASP10, DNAJC1, FGFR2, MRPS30, and SLC4A7, P-value = 3 × 10(−4)). The most connected gene was CUL3, a regulator of several genes linked to cancer progression. Lastly, we evaluated the biases of each method and the impact of their parameters on the outcome. In general, network methods preferred highly connected genes, even after random rewirings that stripped the connections of any biological meaning. In conclusion, we present the advantages of network-guided GWAS, characterize their shortcomings, and provide strategies to address them. To compute the consensus networks, implementations of all six methods are available at https://github.com/hclimente/gwas-tools.
format Online
Article
Text
id pubmed-8009366
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-80093662021-04-07 Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer Climente-González, Héctor Lonjou, Christine Lesueur, Fabienne Stoppa-Lyonnet, Dominique Andrieu, Nadine Azencott, Chloé-Agathe PLoS Comput Biol Research Article Genome-wide association studies (GWAS) explore the genetic causes of complex diseases. However, classical approaches ignore the biological context of the genetic variants and genes under study. To address this shortcoming, one can use biological networks, which model functional relationships, to search for functionally related susceptibility loci. Many such network methods exist, each arising from different mathematical frameworks, pre-processing steps, and assumptions about the network properties of the susceptibility mechanism. Unsurprisingly, this results in disparate solutions. To explore how to exploit these heterogeneous approaches, we selected six network methods and applied them to GENESIS, a nationwide French study on familial breast cancer. First, we verified that network methods recovered more interpretable results than a standard GWAS. We addressed the heterogeneity of their solutions by studying their overlap, computing what we called the consensus. The key gene in this consensus solution was COPS5, a gene related to multiple cancer hallmarks. Another issue we observed was that network methods were unstable, selecting very different genes on different subsamples of GENESIS. Therefore, we proposed a stable consensus solution formed by the 68 genes most consistently selected across multiple subsamples. This solution was also enriched in genes known to be associated with breast cancer susceptibility (BLM, CASP8, CASP10, DNAJC1, FGFR2, MRPS30, and SLC4A7, P-value = 3 × 10(−4)). The most connected gene was CUL3, a regulator of several genes linked to cancer progression. Lastly, we evaluated the biases of each method and the impact of their parameters on the outcome. In general, network methods preferred highly connected genes, even after random rewirings that stripped the connections of any biological meaning. In conclusion, we present the advantages of network-guided GWAS, characterize their shortcomings, and provide strategies to address them. To compute the consensus networks, implementations of all six methods are available at https://github.com/hclimente/gwas-tools. Public Library of Science 2021-03-18 /pmc/articles/PMC8009366/ /pubmed/33735170 http://dx.doi.org/10.1371/journal.pcbi.1008819 Text en © 2021 Climente-González et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Climente-González, Héctor
Lonjou, Christine
Lesueur, Fabienne
Stoppa-Lyonnet, Dominique
Andrieu, Nadine
Azencott, Chloé-Agathe
Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title_full Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title_fullStr Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title_full_unstemmed Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title_short Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
title_sort boosting gwas using biological networks: a study on susceptibility to familial breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009366/
https://www.ncbi.nlm.nih.gov/pubmed/33735170
http://dx.doi.org/10.1371/journal.pcbi.1008819
work_keys_str_mv AT climentegonzalezhector boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT lonjouchristine boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT lesueurfabienne boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT stoppalyonnetdominique boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT andrieunadine boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer
AT azencottchloeagathe boostinggwasusingbiologicalnetworksastudyonsusceptibilitytofamilialbreastcancer