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ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer

BACKGROUND: Protein kinases are a large and diverse family of enzymes that are genomically altered in many human cancers. Targeted cancer genome sequencing efforts have unveiled the mutational profiles of protein kinase genes from many different cancer types. While mutational data on protein kinases...

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Autores principales: Gosal, Gurinder, Kochut, Krys J., Kannan, Natarajan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237543/
https://www.ncbi.nlm.nih.gov/pubmed/22194913
http://dx.doi.org/10.1371/journal.pone.0028782
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author Gosal, Gurinder
Kochut, Krys J.
Kannan, Natarajan
author_facet Gosal, Gurinder
Kochut, Krys J.
Kannan, Natarajan
author_sort Gosal, Gurinder
collection PubMed
description BACKGROUND: Protein kinases are a large and diverse family of enzymes that are genomically altered in many human cancers. Targeted cancer genome sequencing efforts have unveiled the mutational profiles of protein kinase genes from many different cancer types. While mutational data on protein kinases is currently catalogued in various databases, integration of mutation data with other forms of data on protein kinases such as sequence, structure, function and pathway is necessary to identify and characterize key cancer causing mutations. Integrative analysis of protein kinase data, however, is a challenge because of the disparate nature of protein kinase data sources and data formats. RESULTS: Here, we describe ProKinO, a protein kinase-specific ontology, which provides a controlled vocabulary of terms, their hierarchy, and relationships unifying sequence, structure, function, mutation and pathway information on protein kinases. The conceptual representation of such diverse forms of information in one place not only allows rapid discovery of significant information related to a specific protein kinase, but also enables large-scale integrative analysis of protein kinase data in ways not possible through other kinase-specific resources. We have performed several integrative analyses of ProKinO data and, as an example, found that a large number of somatic mutations (∼288 distinct mutations) associated with the haematopoietic neoplasm cancer type map to only 8 kinases in the human kinome. This is in contrast to glioma, where the mutations are spread over 82 distinct kinases. We also provide examples of how ontology-based data analysis can be used to generate testable hypotheses regarding cancer mutations. CONCLUSION: We present an integrated framework for large-scale integrative analysis of protein kinase data. Navigation and analysis of ontology data can be performed using the ontology browser available at: http://vulcan.cs.uga.edu/prokino.
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spelling pubmed-32375432011-12-22 ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer Gosal, Gurinder Kochut, Krys J. Kannan, Natarajan PLoS One Research Article BACKGROUND: Protein kinases are a large and diverse family of enzymes that are genomically altered in many human cancers. Targeted cancer genome sequencing efforts have unveiled the mutational profiles of protein kinase genes from many different cancer types. While mutational data on protein kinases is currently catalogued in various databases, integration of mutation data with other forms of data on protein kinases such as sequence, structure, function and pathway is necessary to identify and characterize key cancer causing mutations. Integrative analysis of protein kinase data, however, is a challenge because of the disparate nature of protein kinase data sources and data formats. RESULTS: Here, we describe ProKinO, a protein kinase-specific ontology, which provides a controlled vocabulary of terms, their hierarchy, and relationships unifying sequence, structure, function, mutation and pathway information on protein kinases. The conceptual representation of such diverse forms of information in one place not only allows rapid discovery of significant information related to a specific protein kinase, but also enables large-scale integrative analysis of protein kinase data in ways not possible through other kinase-specific resources. We have performed several integrative analyses of ProKinO data and, as an example, found that a large number of somatic mutations (∼288 distinct mutations) associated with the haematopoietic neoplasm cancer type map to only 8 kinases in the human kinome. This is in contrast to glioma, where the mutations are spread over 82 distinct kinases. We also provide examples of how ontology-based data analysis can be used to generate testable hypotheses regarding cancer mutations. CONCLUSION: We present an integrated framework for large-scale integrative analysis of protein kinase data. Navigation and analysis of ontology data can be performed using the ontology browser available at: http://vulcan.cs.uga.edu/prokino. Public Library of Science 2011-12-14 /pmc/articles/PMC3237543/ /pubmed/22194913 http://dx.doi.org/10.1371/journal.pone.0028782 Text en Gosal 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gosal, Gurinder
Kochut, Krys J.
Kannan, Natarajan
ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title_full ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title_fullStr ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title_full_unstemmed ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title_short ProKinO: An Ontology for Integrative Analysis of Protein Kinases in Cancer
title_sort prokino: an ontology for integrative analysis of protein kinases in cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237543/
https://www.ncbi.nlm.nih.gov/pubmed/22194913
http://dx.doi.org/10.1371/journal.pone.0028782
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