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iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis

OBJECTIVE: We performed comprehensive proteomic analyses of articular cartilage by using the isobaric tags for relative and absolute quantitation (iTRAQ) method, and searched for candidate biomarkers for osteoarthritis (OA). METHODS: Articular cartilage was collected from patients with OA or femoral...

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Autores principales: Ikeda, Daiki, Ageta, Hiroshi, Tsuchida, Kunihiro, Yamada, Harumoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa UK Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836424/
https://www.ncbi.nlm.nih.gov/pubmed/23937207
http://dx.doi.org/10.3109/1354750X.2013.810667
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author Ikeda, Daiki
Ageta, Hiroshi
Tsuchida, Kunihiro
Yamada, Harumoto
author_facet Ikeda, Daiki
Ageta, Hiroshi
Tsuchida, Kunihiro
Yamada, Harumoto
author_sort Ikeda, Daiki
collection PubMed
description OBJECTIVE: We performed comprehensive proteomic analyses of articular cartilage by using the isobaric tags for relative and absolute quantitation (iTRAQ) method, and searched for candidate biomarkers for osteoarthritis (OA). METHODS: Articular cartilage was collected from patients with OA or femoral neck fracture for the control group. Molecular variations were detected by the iTRAQ method, and quantitative analyses were performed by western blot. RESULTS: Using the iTRAQ method, we identified 76 proteins with different expression levels in OA patients and the control group. Among these proteins, we selected LECT2 (leukocyte cell-derived chemotaxin-2), BAALC (brain and acute leukemia, cytoplasmic), and PRDX6 (peroxiredoxin-6), which had not been reported as biomarkers for OA. CONCLUSIONS: Use of these proteins in combination with conventional OA biomarkers may better reflect the grade and prognosis of OA.
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spelling pubmed-38364242013-11-22 iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis Ikeda, Daiki Ageta, Hiroshi Tsuchida, Kunihiro Yamada, Harumoto Biomarkers Research Article OBJECTIVE: We performed comprehensive proteomic analyses of articular cartilage by using the isobaric tags for relative and absolute quantitation (iTRAQ) method, and searched for candidate biomarkers for osteoarthritis (OA). METHODS: Articular cartilage was collected from patients with OA or femoral neck fracture for the control group. Molecular variations were detected by the iTRAQ method, and quantitative analyses were performed by western blot. RESULTS: Using the iTRAQ method, we identified 76 proteins with different expression levels in OA patients and the control group. Among these proteins, we selected LECT2 (leukocyte cell-derived chemotaxin-2), BAALC (brain and acute leukemia, cytoplasmic), and PRDX6 (peroxiredoxin-6), which had not been reported as biomarkers for OA. CONCLUSIONS: Use of these proteins in combination with conventional OA biomarkers may better reflect the grade and prognosis of OA. Informa UK Ltd. 2013-11 2013-08-12 /pmc/articles/PMC3836424/ /pubmed/23937207 http://dx.doi.org/10.3109/1354750X.2013.810667 Text en © 2013 Informa UK Ltd. All rights reserved: reproduction in whole or part not permitted http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Research Article
Ikeda, Daiki
Ageta, Hiroshi
Tsuchida, Kunihiro
Yamada, Harumoto
iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title_full iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title_fullStr iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title_full_unstemmed iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title_short iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis
title_sort itraq-based proteomics reveals novel biomarkers of osteoarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836424/
https://www.ncbi.nlm.nih.gov/pubmed/23937207
http://dx.doi.org/10.3109/1354750X.2013.810667
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