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SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis

Endometrial epithelial cells carry distinct cancer-associated alterations that may be more susceptible to endometriosis. Mouse models have shown that overexpression of SIRT1 associated with oncogene activation contributes to the pathogenesis of endometriosis, but the underlying reason remains elusiv...

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Autores principales: Wang, Minghua, Wu, Yongqi, He, Yunbiao, Liu, Jing, Chen, Yingxing, Huang, Jieqiong, Qi, Guolong, Li, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296487/
https://www.ncbi.nlm.nih.gov/pubmed/35853978
http://dx.doi.org/10.1038/s41598-022-16629-x
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author Wang, Minghua
Wu, Yongqi
He, Yunbiao
Liu, Jing
Chen, Yingxing
Huang, Jieqiong
Qi, Guolong
Li, Ping
author_facet Wang, Minghua
Wu, Yongqi
He, Yunbiao
Liu, Jing
Chen, Yingxing
Huang, Jieqiong
Qi, Guolong
Li, Ping
author_sort Wang, Minghua
collection PubMed
description Endometrial epithelial cells carry distinct cancer-associated alterations that may be more susceptible to endometriosis. Mouse models have shown that overexpression of SIRT1 associated with oncogene activation contributes to the pathogenesis of endometriosis, but the underlying reason remains elusive. Here, we used integrated systems biology analysis and found that enrichment of endometrial stromal fibroblasts in endometriosis and their cellular abundance correlated negatively with epithelial cells in clinical specimens. Furthermore, endometrial epithelial cells were characterized by significant overexpression of SIRT1, which is involved in triggering the EMT switch by escaping damage or oncogene-induced induced senescence in clinical specimens and in vitro human cell line models. This observation supports that genetic and epigenetic incident favors endometrial epithelia cells escape from senescence and fuel EMT process in endometriosis, what could be overcome by downregulation of SIRT1.
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spelling pubmed-92964872022-07-21 SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis Wang, Minghua Wu, Yongqi He, Yunbiao Liu, Jing Chen, Yingxing Huang, Jieqiong Qi, Guolong Li, Ping Sci Rep Article Endometrial epithelial cells carry distinct cancer-associated alterations that may be more susceptible to endometriosis. Mouse models have shown that overexpression of SIRT1 associated with oncogene activation contributes to the pathogenesis of endometriosis, but the underlying reason remains elusive. Here, we used integrated systems biology analysis and found that enrichment of endometrial stromal fibroblasts in endometriosis and their cellular abundance correlated negatively with epithelial cells in clinical specimens. Furthermore, endometrial epithelial cells were characterized by significant overexpression of SIRT1, which is involved in triggering the EMT switch by escaping damage or oncogene-induced induced senescence in clinical specimens and in vitro human cell line models. This observation supports that genetic and epigenetic incident favors endometrial epithelia cells escape from senescence and fuel EMT process in endometriosis, what could be overcome by downregulation of SIRT1. Nature Publishing Group UK 2022-07-19 /pmc/articles/PMC9296487/ /pubmed/35853978 http://dx.doi.org/10.1038/s41598-022-16629-x Text en © The Author(s) 2022 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
Wang, Minghua
Wu, Yongqi
He, Yunbiao
Liu, Jing
Chen, Yingxing
Huang, Jieqiong
Qi, Guolong
Li, Ping
SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title_full SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title_fullStr SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title_full_unstemmed SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title_short SIRT1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
title_sort sirt1 upregulation promotes epithelial-mesenchymal transition by inducing senescence escape in endometriosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296487/
https://www.ncbi.nlm.nih.gov/pubmed/35853978
http://dx.doi.org/10.1038/s41598-022-16629-x
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