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Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data
BACKGROUND: Wound healing involves careful coordination among various cell types carrying out unique or even multifaceted functions. The abstraction of this complex dynamic process into four primary wound stages is essential to the study of wound care for timing treatment and tracking wound progress...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127407/ https://www.ncbi.nlm.nih.gov/pubmed/37098473 http://dx.doi.org/10.1186/s12859-023-05295-z |
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author | Zlobina, Ksenia Malekos, Eric Chen, Han Gomez, Marcella |
author_facet | Zlobina, Ksenia Malekos, Eric Chen, Han Gomez, Marcella |
author_sort | Zlobina, Ksenia |
collection | PubMed |
description | BACKGROUND: Wound healing involves careful coordination among various cell types carrying out unique or even multifaceted functions. The abstraction of this complex dynamic process into four primary wound stages is essential to the study of wound care for timing treatment and tracking wound progression. For example, a treatment that may promote healing in the inflammatory stage may prove detrimental in the proliferative stage. Additionally, the time scale of individual responses varies widely across and within the same species. Therefore, a robust method to assess wound stages can help advance translational work from animals to humans. RESULTS: In this work, we present a data-driven model that robustly identifies the dominant wound healing stage using transcriptomic data from biopsies gathered from mouse and human wounds, both burn and surgical. A training dataset composed of publicly available transcriptomic arrays is used to derive 58 shared genes that are commonly differentially expressed. They are divided into 5 clusters based on temporal gene expression dynamics. The clusters represent a 5-dimensional parametric space containing the wound healing trajectory. We then create a mathematical classification algorithm in the 5-dimensional space and demonstrate that it can distinguish between the four stages of wound healing: hemostasis, inflammation, proliferation, and remodeling. CONCLUSIONS: In this work, we present an algorithm for wound stage detection based on gene expression. This work suggests that there are universal characteristics of gene expression in wound healing stages despite the seeming disparities across species and wounds. Our algorithm performs well for human and mouse wounds of both burn and surgical types. The algorithm has the potential to serve as a diagnostic tool that can advance precision wound care by providing a way of tracking wound healing progression with more accuracy and finer temporal resolution compared to visual indicators. This increases the potential for preventive action. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05295-z. |
format | Online Article Text |
id | pubmed-10127407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101274072023-04-26 Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data Zlobina, Ksenia Malekos, Eric Chen, Han Gomez, Marcella BMC Bioinformatics Research BACKGROUND: Wound healing involves careful coordination among various cell types carrying out unique or even multifaceted functions. The abstraction of this complex dynamic process into four primary wound stages is essential to the study of wound care for timing treatment and tracking wound progression. For example, a treatment that may promote healing in the inflammatory stage may prove detrimental in the proliferative stage. Additionally, the time scale of individual responses varies widely across and within the same species. Therefore, a robust method to assess wound stages can help advance translational work from animals to humans. RESULTS: In this work, we present a data-driven model that robustly identifies the dominant wound healing stage using transcriptomic data from biopsies gathered from mouse and human wounds, both burn and surgical. A training dataset composed of publicly available transcriptomic arrays is used to derive 58 shared genes that are commonly differentially expressed. They are divided into 5 clusters based on temporal gene expression dynamics. The clusters represent a 5-dimensional parametric space containing the wound healing trajectory. We then create a mathematical classification algorithm in the 5-dimensional space and demonstrate that it can distinguish between the four stages of wound healing: hemostasis, inflammation, proliferation, and remodeling. CONCLUSIONS: In this work, we present an algorithm for wound stage detection based on gene expression. This work suggests that there are universal characteristics of gene expression in wound healing stages despite the seeming disparities across species and wounds. Our algorithm performs well for human and mouse wounds of both burn and surgical types. The algorithm has the potential to serve as a diagnostic tool that can advance precision wound care by providing a way of tracking wound healing progression with more accuracy and finer temporal resolution compared to visual indicators. This increases the potential for preventive action. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05295-z. BioMed Central 2023-04-25 /pmc/articles/PMC10127407/ /pubmed/37098473 http://dx.doi.org/10.1186/s12859-023-05295-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zlobina, Ksenia Malekos, Eric Chen, Han Gomez, Marcella Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title | Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title_full | Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title_fullStr | Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title_full_unstemmed | Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title_short | Robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
title_sort | robust classification of wound healing stages in both mice and humans for acute and burn wounds based on transcriptomic data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127407/ https://www.ncbi.nlm.nih.gov/pubmed/37098473 http://dx.doi.org/10.1186/s12859-023-05295-z |
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