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Clustering Gene Expression Regulators: New Approach to Disease Subtyping

One of the main challenges in modern medicine is to stratify different patient groups in terms of underlying disease molecular mechanisms as to develop more personalized approach to therapy. Here we propose novel method for disease subtyping based on analysis of activated expression regulators on a...

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Autores principales: Pyatnitskiy, Mikhail, Mazo, Ilya, Shkrob, Maria, Schwartz, Elena, Kotelnikova, Ekaterina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887006/
https://www.ncbi.nlm.nih.gov/pubmed/24416320
http://dx.doi.org/10.1371/journal.pone.0084955
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author Pyatnitskiy, Mikhail
Mazo, Ilya
Shkrob, Maria
Schwartz, Elena
Kotelnikova, Ekaterina
author_facet Pyatnitskiy, Mikhail
Mazo, Ilya
Shkrob, Maria
Schwartz, Elena
Kotelnikova, Ekaterina
author_sort Pyatnitskiy, Mikhail
collection PubMed
description One of the main challenges in modern medicine is to stratify different patient groups in terms of underlying disease molecular mechanisms as to develop more personalized approach to therapy. Here we propose novel method for disease subtyping based on analysis of activated expression regulators on a sample-by-sample basis. Our approach relies on Sub-Network Enrichment Analysis algorithm (SNEA) which identifies gene subnetworks with significant concordant changes in expression between two conditions. Subnetwork consists of central regulator and downstream genes connected by relations extracted from global literature-extracted regulation database. Regulators found in each patient separately are clustered together and assigned activity scores which are used for final patients grouping. We show that our approach performs well compared to other related methods and at the same time provides researchers with complementary level of understanding of pathway-level biology behind a disease by identification of significant expression regulators. We have observed the reasonable grouping of neuromuscular disorders (triggered by structural damage vs triggered by unknown mechanisms), that was not revealed using standard expression profile clustering. For another experiment we were able to suggest the clusters of regulators, responsible for colorectal carcinoma vs adenoma discrimination and identify frequently genetically changed regulators that could be of specific importance for the individual characteristics of cancer development. Proposed approach can be regarded as biologically meaningful feature selection, reducing tens of thousands of genes down to dozens of clusters of regulators. Obtained clusters of regulators make possible to generate valuable biological hypotheses about molecular mechanisms related to a clinical outcome for individual patient.
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spelling pubmed-38870062014-01-10 Clustering Gene Expression Regulators: New Approach to Disease Subtyping Pyatnitskiy, Mikhail Mazo, Ilya Shkrob, Maria Schwartz, Elena Kotelnikova, Ekaterina PLoS One Research Article One of the main challenges in modern medicine is to stratify different patient groups in terms of underlying disease molecular mechanisms as to develop more personalized approach to therapy. Here we propose novel method for disease subtyping based on analysis of activated expression regulators on a sample-by-sample basis. Our approach relies on Sub-Network Enrichment Analysis algorithm (SNEA) which identifies gene subnetworks with significant concordant changes in expression between two conditions. Subnetwork consists of central regulator and downstream genes connected by relations extracted from global literature-extracted regulation database. Regulators found in each patient separately are clustered together and assigned activity scores which are used for final patients grouping. We show that our approach performs well compared to other related methods and at the same time provides researchers with complementary level of understanding of pathway-level biology behind a disease by identification of significant expression regulators. We have observed the reasonable grouping of neuromuscular disorders (triggered by structural damage vs triggered by unknown mechanisms), that was not revealed using standard expression profile clustering. For another experiment we were able to suggest the clusters of regulators, responsible for colorectal carcinoma vs adenoma discrimination and identify frequently genetically changed regulators that could be of specific importance for the individual characteristics of cancer development. Proposed approach can be regarded as biologically meaningful feature selection, reducing tens of thousands of genes down to dozens of clusters of regulators. Obtained clusters of regulators make possible to generate valuable biological hypotheses about molecular mechanisms related to a clinical outcome for individual patient. Public Library of Science 2014-01-09 /pmc/articles/PMC3887006/ /pubmed/24416320 http://dx.doi.org/10.1371/journal.pone.0084955 Text en © 2014 Pyatnitskiy 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
Pyatnitskiy, Mikhail
Mazo, Ilya
Shkrob, Maria
Schwartz, Elena
Kotelnikova, Ekaterina
Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title_full Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title_fullStr Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title_full_unstemmed Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title_short Clustering Gene Expression Regulators: New Approach to Disease Subtyping
title_sort clustering gene expression regulators: new approach to disease subtyping
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887006/
https://www.ncbi.nlm.nih.gov/pubmed/24416320
http://dx.doi.org/10.1371/journal.pone.0084955
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