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Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model
Tissue fibrosis is a major driver of pathology in aging and is involved in numerous age-related diseases. The lungs are particularly susceptible to fibrotic pathology which is currently difficult to treat. The mouse bleomycin-induced fibrosis model was developed to investigate lung fibrosis and wide...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481473/ https://www.ncbi.nlm.nih.gov/pubmed/34588506 http://dx.doi.org/10.1038/s41598-021-98674-6 |
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author | Toren, Dmitri Yanai, Hagai Abu Taha, Reem Bunu, Gabriela Ursu, Eugen Ziesche, Rolf Tacutu, Robi Fraifeld, Vadim E |
author_facet | Toren, Dmitri Yanai, Hagai Abu Taha, Reem Bunu, Gabriela Ursu, Eugen Ziesche, Rolf Tacutu, Robi Fraifeld, Vadim E |
author_sort | Toren, Dmitri |
collection | PubMed |
description | Tissue fibrosis is a major driver of pathology in aging and is involved in numerous age-related diseases. The lungs are particularly susceptible to fibrotic pathology which is currently difficult to treat. The mouse bleomycin-induced fibrosis model was developed to investigate lung fibrosis and widely used over the years. However, a systematic analysis of the accumulated results has not been performed. We undertook a comprehensive data mining and subsequent manual curation, resulting in a collection of 213 genes (available at the TiRe database, www.tiredb.org), which when manipulated had a clear impact on bleomycin-induced lung fibrosis. Our meta-analysis highlights the age component in pulmonary fibrosis and strong links of related genes with longevity. The results support the validity of the bleomycin model to human pathology and suggest the importance of a multi-target therapeutic strategy for pulmonary fibrosis treatment. |
format | Online Article Text |
id | pubmed-8481473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84814732021-10-01 Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model Toren, Dmitri Yanai, Hagai Abu Taha, Reem Bunu, Gabriela Ursu, Eugen Ziesche, Rolf Tacutu, Robi Fraifeld, Vadim E Sci Rep Article Tissue fibrosis is a major driver of pathology in aging and is involved in numerous age-related diseases. The lungs are particularly susceptible to fibrotic pathology which is currently difficult to treat. The mouse bleomycin-induced fibrosis model was developed to investigate lung fibrosis and widely used over the years. However, a systematic analysis of the accumulated results has not been performed. We undertook a comprehensive data mining and subsequent manual curation, resulting in a collection of 213 genes (available at the TiRe database, www.tiredb.org), which when manipulated had a clear impact on bleomycin-induced lung fibrosis. Our meta-analysis highlights the age component in pulmonary fibrosis and strong links of related genes with longevity. The results support the validity of the bleomycin model to human pathology and suggest the importance of a multi-target therapeutic strategy for pulmonary fibrosis treatment. Nature Publishing Group UK 2021-09-29 /pmc/articles/PMC8481473/ /pubmed/34588506 http://dx.doi.org/10.1038/s41598-021-98674-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Toren, Dmitri Yanai, Hagai Abu Taha, Reem Bunu, Gabriela Ursu, Eugen Ziesche, Rolf Tacutu, Robi Fraifeld, Vadim E Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title | Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title_full | Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title_fullStr | Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title_full_unstemmed | Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title_short | Systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
title_sort | systems biology analysis of lung fibrosis-related genes in the bleomycin mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481473/ https://www.ncbi.nlm.nih.gov/pubmed/34588506 http://dx.doi.org/10.1038/s41598-021-98674-6 |
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