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Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo

Objective: To investigate the correlation between estrogen-related receptor a (ERRα) expression level and gastric cancer (GC). Methods: We collected GC and adjacent normal tissues from 50 patients. The parameters of the patients were summarized, and correlation with the expression level of ERRα was...

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Autores principales: Zhong, Yuejiao, He, Kang, Shi, Lin, Chen, Lingxiang, Zhou, Bin, Ma, Rong, Yu, Hui, Zhang, Jia, Shuai, You, Fei, Yan, Lu, Jianwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7950300/
https://www.ncbi.nlm.nih.gov/pubmed/33591949
http://dx.doi.org/10.18632/aging.202508
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author Zhong, Yuejiao
He, Kang
Shi, Lin
Chen, Lingxiang
Zhou, Bin
Ma, Rong
Yu, Hui
Zhang, Jia
Shuai, You
Fei, Yan
Lu, Jianwei
author_facet Zhong, Yuejiao
He, Kang
Shi, Lin
Chen, Lingxiang
Zhou, Bin
Ma, Rong
Yu, Hui
Zhang, Jia
Shuai, You
Fei, Yan
Lu, Jianwei
author_sort Zhong, Yuejiao
collection PubMed
description Objective: To investigate the correlation between estrogen-related receptor a (ERRα) expression level and gastric cancer (GC). Methods: We collected GC and adjacent normal tissues from 50 patients. The parameters of the patients were summarized, and correlation with the expression level of ERRα was calculated. Downregulated ERRα using lentivirus was designed and transfected to SGC-7901 and MGC-803 cells. Cell migration, invasion and wound assays were conducted to determine the correlation between ERRα and capacity for cell migration and invasion. The expression level of the genes involved in epithelial–mesenchymal transition, including E-cadherin, γ-catenin, N-cadherin and vimentin, was determined via real-time or quantitative polymerase chain reaction(qPCR) and Western blot analysis. Results: The expression of ERRα tends to be higher in GC tissues than in adjacent normal tissues. Analyses ofthe expression level of ERRα and patient parameters show that the ERRα level is significantly correlated with TNM staging and patient survival (P<0.05). The downregulation of ERRα can inhibit cell invasion and migration, which was proven by Transwell and cell wound assays. The levels of E-cadherin and γ-catenin increased by conducting qPCR and Western blot analysis. Meanwhile, the levels of N-cadherin and vimentin decreased when ERRα expression was reduced. Conclusion: ERRα is highly expressed in GC tissues and can promote the migration and invasion of cancer cells. It can be a potential marker for GC diagnosis.
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spelling pubmed-79503002021-03-23 Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo Zhong, Yuejiao He, Kang Shi, Lin Chen, Lingxiang Zhou, Bin Ma, Rong Yu, Hui Zhang, Jia Shuai, You Fei, Yan Lu, Jianwei Aging (Albany NY) Research Paper Objective: To investigate the correlation between estrogen-related receptor a (ERRα) expression level and gastric cancer (GC). Methods: We collected GC and adjacent normal tissues from 50 patients. The parameters of the patients were summarized, and correlation with the expression level of ERRα was calculated. Downregulated ERRα using lentivirus was designed and transfected to SGC-7901 and MGC-803 cells. Cell migration, invasion and wound assays were conducted to determine the correlation between ERRα and capacity for cell migration and invasion. The expression level of the genes involved in epithelial–mesenchymal transition, including E-cadherin, γ-catenin, N-cadherin and vimentin, was determined via real-time or quantitative polymerase chain reaction(qPCR) and Western blot analysis. Results: The expression of ERRα tends to be higher in GC tissues than in adjacent normal tissues. Analyses ofthe expression level of ERRα and patient parameters show that the ERRα level is significantly correlated with TNM staging and patient survival (P<0.05). The downregulation of ERRα can inhibit cell invasion and migration, which was proven by Transwell and cell wound assays. The levels of E-cadherin and γ-catenin increased by conducting qPCR and Western blot analysis. Meanwhile, the levels of N-cadherin and vimentin decreased when ERRα expression was reduced. Conclusion: ERRα is highly expressed in GC tissues and can promote the migration and invasion of cancer cells. It can be a potential marker for GC diagnosis. Impact Journals 2021-02-11 /pmc/articles/PMC7950300/ /pubmed/33591949 http://dx.doi.org/10.18632/aging.202508 Text en Copyright: © 2021 Zhong et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhong, Yuejiao
He, Kang
Shi, Lin
Chen, Lingxiang
Zhou, Bin
Ma, Rong
Yu, Hui
Zhang, Jia
Shuai, You
Fei, Yan
Lu, Jianwei
Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title_full Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title_fullStr Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title_full_unstemmed Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title_short Down-regulation of estrogen-related receptor alpha (ERRα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
title_sort down-regulation of estrogen-related receptor alpha (errα) inhibits gastric cancer cell migration and invasion in vitro and in vivo
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7950300/
https://www.ncbi.nlm.nih.gov/pubmed/33591949
http://dx.doi.org/10.18632/aging.202508
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