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The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis

The present study aimed to investigate the potential effect of fibronectin (FN) in adenomyosis progression. Small guide RNAs were designed to knock down FN expression in Ishikawa cells. The impact of FN on the proliferation, apoptosis, migration, and invasion of the cells was assessed. Cell prolifer...

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Detalles Bibliográficos
Autores principales: Gao, Jiangman, Guo, Wei, Li, Rong, Qiao, Jie, Long, Xiaoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10558947/
https://www.ncbi.nlm.nih.gov/pubmed/37809570
http://dx.doi.org/10.1016/j.heliyon.2023.e19674
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author Gao, Jiangman
Guo, Wei
Li, Rong
Qiao, Jie
Long, Xiaoyu
author_facet Gao, Jiangman
Guo, Wei
Li, Rong
Qiao, Jie
Long, Xiaoyu
author_sort Gao, Jiangman
collection PubMed
description The present study aimed to investigate the potential effect of fibronectin (FN) in adenomyosis progression. Small guide RNAs were designed to knock down FN expression in Ishikawa cells. The impact of FN on the proliferation, apoptosis, migration, and invasion of the cells was assessed. Cell proliferation was detected using a Celigo Imaging Cytometer system; apoptosis was quantified by flow cytometry; and cell migration and invasion were investigated via transwell assays. Cell proliferation was markedly suppressed in the FN knockout (KO) group compared with the control group, while apoptosis significantly increased. The levels of cell migration and invasion in the KO group were significantly decreased compared with the control group. Our study revealed that downregulation of FN expression is likely to restrain cell proliferation, migration, and invasion in endometrial cells in adenomyosis.
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spelling pubmed-105589472023-10-08 The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis Gao, Jiangman Guo, Wei Li, Rong Qiao, Jie Long, Xiaoyu Heliyon Research Article The present study aimed to investigate the potential effect of fibronectin (FN) in adenomyosis progression. Small guide RNAs were designed to knock down FN expression in Ishikawa cells. The impact of FN on the proliferation, apoptosis, migration, and invasion of the cells was assessed. Cell proliferation was detected using a Celigo Imaging Cytometer system; apoptosis was quantified by flow cytometry; and cell migration and invasion were investigated via transwell assays. Cell proliferation was markedly suppressed in the FN knockout (KO) group compared with the control group, while apoptosis significantly increased. The levels of cell migration and invasion in the KO group were significantly decreased compared with the control group. Our study revealed that downregulation of FN expression is likely to restrain cell proliferation, migration, and invasion in endometrial cells in adenomyosis. Elsevier 2023-08-30 /pmc/articles/PMC10558947/ /pubmed/37809570 http://dx.doi.org/10.1016/j.heliyon.2023.e19674 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Gao, Jiangman
Guo, Wei
Li, Rong
Qiao, Jie
Long, Xiaoyu
The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title_full The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title_fullStr The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title_full_unstemmed The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title_short The impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
title_sort impact of fibronectin knockout on invasion and migration of endometrial cell in adenomyosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10558947/
https://www.ncbi.nlm.nih.gov/pubmed/37809570
http://dx.doi.org/10.1016/j.heliyon.2023.e19674
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