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Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2
MicroRNAs (miRNAs) are frequently dysregulated in a variety of human cancers, including gastric carcinoma. To improve our understanding of the role of miRNAs in gastric carcinoma and potential identify novel biomarkers or therapeutic agents, we performed microarray analysis to identify differentiall...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461178/ https://www.ncbi.nlm.nih.gov/pubmed/30923258 http://dx.doi.org/10.18632/aging.101877 |
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author | Wang, Gui-Jun Jiao, Bao-Ping Liu, Yang-Jun Li, Yan-Rong Deng, Bei-Bei |
author_facet | Wang, Gui-Jun Jiao, Bao-Ping Liu, Yang-Jun Li, Yan-Rong Deng, Bei-Bei |
author_sort | Wang, Gui-Jun |
collection | PubMed |
description | MicroRNAs (miRNAs) are frequently dysregulated in a variety of human cancers, including gastric carcinoma. To improve our understanding of the role of miRNAs in gastric carcinoma and potential identify novel biomarkers or therapeutic agents, we performed microarray analysis to identify differentially expressed miRNAs in gastric carcinoma, compared with paired non-cancerous gastric tissues. We identified significantly differentially expressed miRNAs in gastric carcinoma tissues, including miR-506. We validated the microarray results by quantitative reverse transcription polymerase chain reaction in 26 specimens and confirmed significant downregulation of miR-506 in gastric carcinoma. Bioinformatics analysis predicted ZEB2 (zinc finger E-box-binding homeobox 2) as a potential target of miR-506. MiR-506 levels and ZEB2 levels were inversely correlated in gastric carcinoma, and low miR-506 levels in gastric carcinoma were associated with poor prognosis. Overexpression of miR-506 in gastric carcinoma cells significantly inhibited cell migration and invasion, while depletion of miR-506 in gastric carcinoma cells significantly increased cell migration and invasion. Transplantation of miR-506-overexpressing gastric carcinoma cells developed significantly smaller tumor, compared to the control. Thus, our results suggest that miR-506 may function as a tumor suppressor and targets and inhibits ZEB2 in gastric carcinoma. |
format | Online Article Text |
id | pubmed-6461178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-64611782019-04-19 Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 Wang, Gui-Jun Jiao, Bao-Ping Liu, Yang-Jun Li, Yan-Rong Deng, Bei-Bei Aging (Albany NY) Research Paper MicroRNAs (miRNAs) are frequently dysregulated in a variety of human cancers, including gastric carcinoma. To improve our understanding of the role of miRNAs in gastric carcinoma and potential identify novel biomarkers or therapeutic agents, we performed microarray analysis to identify differentially expressed miRNAs in gastric carcinoma, compared with paired non-cancerous gastric tissues. We identified significantly differentially expressed miRNAs in gastric carcinoma tissues, including miR-506. We validated the microarray results by quantitative reverse transcription polymerase chain reaction in 26 specimens and confirmed significant downregulation of miR-506 in gastric carcinoma. Bioinformatics analysis predicted ZEB2 (zinc finger E-box-binding homeobox 2) as a potential target of miR-506. MiR-506 levels and ZEB2 levels were inversely correlated in gastric carcinoma, and low miR-506 levels in gastric carcinoma were associated with poor prognosis. Overexpression of miR-506 in gastric carcinoma cells significantly inhibited cell migration and invasion, while depletion of miR-506 in gastric carcinoma cells significantly increased cell migration and invasion. Transplantation of miR-506-overexpressing gastric carcinoma cells developed significantly smaller tumor, compared to the control. Thus, our results suggest that miR-506 may function as a tumor suppressor and targets and inhibits ZEB2 in gastric carcinoma. Impact Journals 2019-03-28 /pmc/articles/PMC6461178/ /pubmed/30923258 http://dx.doi.org/10.18632/aging.101877 Text en Copyright © 2019 Wang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Wang, Gui-Jun Jiao, Bao-Ping Liu, Yang-Jun Li, Yan-Rong Deng, Bei-Bei Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title | Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title_full | Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title_fullStr | Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title_full_unstemmed | Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title_short | Reactivation of microRNA-506 inhibits gastric carcinoma cell metastasis through ZEB2 |
title_sort | reactivation of microrna-506 inhibits gastric carcinoma cell metastasis through zeb2 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461178/ https://www.ncbi.nlm.nih.gov/pubmed/30923258 http://dx.doi.org/10.18632/aging.101877 |
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