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iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue
BACKGROUND: A hypertrophic scar is a unique fibrotic disease that only exists in humans. Despite advances in burn care and rehabilitation, as well as progress in the management during these decades, the hypertrophic scar remains hard to cure following surgical methods and drugs for treatment. In thi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964291/ https://www.ncbi.nlm.nih.gov/pubmed/27574659 http://dx.doi.org/10.1186/s41038-015-0016-6 |
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author | Tan, Jianglin He, Weifeng Luo, Gaoxing Wu, Jun |
author_facet | Tan, Jianglin He, Weifeng Luo, Gaoxing Wu, Jun |
author_sort | Tan, Jianglin |
collection | PubMed |
description | BACKGROUND: A hypertrophic scar is a unique fibrotic disease that only exists in humans. Despite advances in burn care and rehabilitation, as well as progress in the management during these decades, the hypertrophic scar remains hard to cure following surgical methods and drugs for treatment. In this study, we are looking forward to finding the multitude of possible traumatic mechanisms and the underlying molecular signal ways in the formation of the hypertrophic scar. METHODS: We used isobaric tags for relative and absolute quantitation (iTRAQ) labeling technology, followed by high-throughput 2D LC-MS/MS, to determine relative quantitative differential proteins between the hypertrophic scar and normal skin tissue. RESULTS: A total of 3166 proteins were identified with a high confidence (≥95 % confidence). And, a total of 89 proteins were identified as the differential proteins between the hypertrophic scar and normal skin, among which 41 proteins were up-regulated and 48 proteins were down-regulated in the hypertrophic scar. GO-Analysis indicated the up-regulated proteins were involved in extracellular matrix, whereas the down-regulated proteins were involved in dynamic junction and structural molecule activity. CONCLUSIONS: In our study, we demonstrate 89 proteins present differently in the hypertrophic scar compared to normal skin by iTRAQ technology, which might indicate the pathologic process of hypertrophic scar formation and guide us to propose new strategies against the hypertrophic scar. |
format | Online Article Text |
id | pubmed-4964291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49642912016-08-29 iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue Tan, Jianglin He, Weifeng Luo, Gaoxing Wu, Jun Burns Trauma Research Article BACKGROUND: A hypertrophic scar is a unique fibrotic disease that only exists in humans. Despite advances in burn care and rehabilitation, as well as progress in the management during these decades, the hypertrophic scar remains hard to cure following surgical methods and drugs for treatment. In this study, we are looking forward to finding the multitude of possible traumatic mechanisms and the underlying molecular signal ways in the formation of the hypertrophic scar. METHODS: We used isobaric tags for relative and absolute quantitation (iTRAQ) labeling technology, followed by high-throughput 2D LC-MS/MS, to determine relative quantitative differential proteins between the hypertrophic scar and normal skin tissue. RESULTS: A total of 3166 proteins were identified with a high confidence (≥95 % confidence). And, a total of 89 proteins were identified as the differential proteins between the hypertrophic scar and normal skin, among which 41 proteins were up-regulated and 48 proteins were down-regulated in the hypertrophic scar. GO-Analysis indicated the up-regulated proteins were involved in extracellular matrix, whereas the down-regulated proteins were involved in dynamic junction and structural molecule activity. CONCLUSIONS: In our study, we demonstrate 89 proteins present differently in the hypertrophic scar compared to normal skin by iTRAQ technology, which might indicate the pathologic process of hypertrophic scar formation and guide us to propose new strategies against the hypertrophic scar. BioMed Central 2015-08-27 /pmc/articles/PMC4964291/ /pubmed/27574659 http://dx.doi.org/10.1186/s41038-015-0016-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Tan, Jianglin He, Weifeng Luo, Gaoxing Wu, Jun iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title | iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title_full | iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title_fullStr | iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title_full_unstemmed | iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title_short | iTRAQ-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
title_sort | itraq-based proteomic profiling reveals different protein expression between normal skin and hypertrophic scar tissue |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964291/ https://www.ncbi.nlm.nih.gov/pubmed/27574659 http://dx.doi.org/10.1186/s41038-015-0016-6 |
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