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miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model

BACKGROUND: Intrauterine adhesions (IUAs) are one of the most common reproductive system diseases in women worldwide. Emerging evidence has demonstrated that the upregulation or downregulation of genes plays an important role in IUAs. The aim of this study was to evaluate the role of NUS1 in IUAs in...

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Autores principales: Liu, Min, Zhao, Dapeng, Wu, Xingguo, Guo, Song, Yan, Li, Zhao, Shan, Li, Hua, Wang, Yongmei, Rong, Fengnian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561142/
https://www.ncbi.nlm.nih.gov/pubmed/31154456
http://dx.doi.org/10.12659/MSM.914202
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author Liu, Min
Zhao, Dapeng
Wu, Xingguo
Guo, Song
Yan, Li
Zhao, Shan
Li, Hua
Wang, Yongmei
Rong, Fengnian
author_facet Liu, Min
Zhao, Dapeng
Wu, Xingguo
Guo, Song
Yan, Li
Zhao, Shan
Li, Hua
Wang, Yongmei
Rong, Fengnian
author_sort Liu, Min
collection PubMed
description BACKGROUND: Intrauterine adhesions (IUAs) are one of the most common reproductive system diseases in women worldwide. Emerging evidence has demonstrated that the upregulation or downregulation of genes plays an important role in IUAs. The aim of this study was to evaluate the role of NUS1 in IUAs in a rat model. MATERIAL/METHODS: The expression of miR-466 in intrauterine adhesions tissues was detected by using RT-qPCR assay. RT-qPCR, IHC, and Western blot were used to investigate mRNA and proteins expression, respectively, of NUS1. MTT and colony-formation assays were used to evaluate cell growth. Transwell assays were used to detect cell migration and invasion. To investigate miR-466 and NUS1 functions in vivo, we established a rat model. The level of epithelial-to-mesenchymal transition (EMT)-related markers was analyzed by Western blot assay. RESULTS: NUS1 was upregulated in IUAs tissues, and the high expression level of NUS1 was positively correlated with the severity of IUAs. NUS1 promoted cell proliferation in vitro. NUS1 overexpression on cell migration and invasion promoted the EMT process in vitro and in vivo. NUS1 acted as a target of miR-466 and played the stimulative role by regulating AKT/NFκB pathway. CONCLUSIONS: Our data suggest that miR-466 and NUS1 regulate proliferation and the EMT process through the AKT/NFκB pathway in IUAs in a rat model.
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spelling pubmed-65611422019-06-26 miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model Liu, Min Zhao, Dapeng Wu, Xingguo Guo, Song Yan, Li Zhao, Shan Li, Hua Wang, Yongmei Rong, Fengnian Med Sci Monit Lab/In Vitro Research BACKGROUND: Intrauterine adhesions (IUAs) are one of the most common reproductive system diseases in women worldwide. Emerging evidence has demonstrated that the upregulation or downregulation of genes plays an important role in IUAs. The aim of this study was to evaluate the role of NUS1 in IUAs in a rat model. MATERIAL/METHODS: The expression of miR-466 in intrauterine adhesions tissues was detected by using RT-qPCR assay. RT-qPCR, IHC, and Western blot were used to investigate mRNA and proteins expression, respectively, of NUS1. MTT and colony-formation assays were used to evaluate cell growth. Transwell assays were used to detect cell migration and invasion. To investigate miR-466 and NUS1 functions in vivo, we established a rat model. The level of epithelial-to-mesenchymal transition (EMT)-related markers was analyzed by Western blot assay. RESULTS: NUS1 was upregulated in IUAs tissues, and the high expression level of NUS1 was positively correlated with the severity of IUAs. NUS1 promoted cell proliferation in vitro. NUS1 overexpression on cell migration and invasion promoted the EMT process in vitro and in vivo. NUS1 acted as a target of miR-466 and played the stimulative role by regulating AKT/NFκB pathway. CONCLUSIONS: Our data suggest that miR-466 and NUS1 regulate proliferation and the EMT process through the AKT/NFκB pathway in IUAs in a rat model. International Scientific Literature, Inc. 2019-06-02 /pmc/articles/PMC6561142/ /pubmed/31154456 http://dx.doi.org/10.12659/MSM.914202 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Liu, Min
Zhao, Dapeng
Wu, Xingguo
Guo, Song
Yan, Li
Zhao, Shan
Li, Hua
Wang, Yongmei
Rong, Fengnian
miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title_full miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title_fullStr miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title_full_unstemmed miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title_short miR-466 and NUS1 Regulate the AKT/Nuclear Factor kappa B (NFκB) Signaling Pathway in Intrauterine Adhesions in a Rat Model
title_sort mir-466 and nus1 regulate the akt/nuclear factor kappa b (nfκb) signaling pathway in intrauterine adhesions in a rat model
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561142/
https://www.ncbi.nlm.nih.gov/pubmed/31154456
http://dx.doi.org/10.12659/MSM.914202
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