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Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis
Biomarkers of osteoarthritis (OA) that can accurately diagnose the disease at the earliest stage would significantly support efforts to develop treatments for prevention and early intervention. We have sought to determine the time course of alterations in peripheral blood gene expression profile ass...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512050/ https://www.ncbi.nlm.nih.gov/pubmed/28758108 http://dx.doi.org/10.1155/2017/1746426 |
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author | Korostyński, Michał Małek, Natalia Piechota, Marcin Starowicz, Katarzyna |
author_facet | Korostyński, Michał Małek, Natalia Piechota, Marcin Starowicz, Katarzyna |
author_sort | Korostyński, Michał |
collection | PubMed |
description | Biomarkers of osteoarthritis (OA) that can accurately diagnose the disease at the earliest stage would significantly support efforts to develop treatments for prevention and early intervention. We have sought to determine the time course of alterations in peripheral blood gene expression profile associated with the development of OA. Blood samples were collected from a tail vein of individual rats with monosodium iodoacetate- (MIA-) induced OA (2, 14, 21, and 28 days after the treatment). We used whole-genome microarrays to reveal OA-related transcriptional alterations of 72 transcripts. Three main groups of coexpressed genes revealed diverse time-dependent profiles of up- and downregulation. Functional links that connect expression of the gradually downregulated genes to the G13 signaling pathway were indicated. The mRNA abundance levels of the identified transcripts were further analyzed in publicly available gene expression dataset obtained from a GARP study cohort of OA patients. We revealed three-gene signature differentially expressed in both rat and human blood (TNK2, KCTD2, and WDR37). The alterations in expression of the selected transcripts in peripheral blood samples of the patients indicate heterogeneity of the OA profiles potentially related to disease progress and severity of clinical symptoms. Our study identifies several potential stage-specific biomarkers of OA progression. |
format | Online Article Text |
id | pubmed-5512050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-55120502017-07-30 Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis Korostyński, Michał Małek, Natalia Piechota, Marcin Starowicz, Katarzyna Int J Genomics Research Article Biomarkers of osteoarthritis (OA) that can accurately diagnose the disease at the earliest stage would significantly support efforts to develop treatments for prevention and early intervention. We have sought to determine the time course of alterations in peripheral blood gene expression profile associated with the development of OA. Blood samples were collected from a tail vein of individual rats with monosodium iodoacetate- (MIA-) induced OA (2, 14, 21, and 28 days after the treatment). We used whole-genome microarrays to reveal OA-related transcriptional alterations of 72 transcripts. Three main groups of coexpressed genes revealed diverse time-dependent profiles of up- and downregulation. Functional links that connect expression of the gradually downregulated genes to the G13 signaling pathway were indicated. The mRNA abundance levels of the identified transcripts were further analyzed in publicly available gene expression dataset obtained from a GARP study cohort of OA patients. We revealed three-gene signature differentially expressed in both rat and human blood (TNK2, KCTD2, and WDR37). The alterations in expression of the selected transcripts in peripheral blood samples of the patients indicate heterogeneity of the OA profiles potentially related to disease progress and severity of clinical symptoms. Our study identifies several potential stage-specific biomarkers of OA progression. Hindawi 2017 2017-07-03 /pmc/articles/PMC5512050/ /pubmed/28758108 http://dx.doi.org/10.1155/2017/1746426 Text en Copyright © 2017 Michał Korostyński et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Korostyński, Michał Małek, Natalia Piechota, Marcin Starowicz, Katarzyna Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title | Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title_full | Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title_fullStr | Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title_full_unstemmed | Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title_short | Blood Transcriptional Signatures for Disease Progression in a Rat Model of Osteoarthritis |
title_sort | blood transcriptional signatures for disease progression in a rat model of osteoarthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512050/ https://www.ncbi.nlm.nih.gov/pubmed/28758108 http://dx.doi.org/10.1155/2017/1746426 |
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