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GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification
Epithelial-mesenchymal transition (EMT), a biological process by which polarized epithelial cells convert into a mesenchymal phenotype, has been implicated to contribute to the molecular heterogeneity of epithelial ovarian cancer (EOC). Here we report that a transcription factor—Grainyhead-like 2 (G...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757891/ https://www.ncbi.nlm.nih.gov/pubmed/26887977 http://dx.doi.org/10.1038/srep19943 |
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author | Chung, Vin Yee Tan, Tuan Zea Tan, Ming Wong, Meng Kang Kuay, Kuee Theng Yang, Zhe Ye, Jieru Muller, Julius Koh, Cheryl M. Guccione, Ernesto Thiery, Jean Paul Huang, Ruby Yun-Ju |
author_facet | Chung, Vin Yee Tan, Tuan Zea Tan, Ming Wong, Meng Kang Kuay, Kuee Theng Yang, Zhe Ye, Jieru Muller, Julius Koh, Cheryl M. Guccione, Ernesto Thiery, Jean Paul Huang, Ruby Yun-Ju |
author_sort | Chung, Vin Yee |
collection | PubMed |
description | Epithelial-mesenchymal transition (EMT), a biological process by which polarized epithelial cells convert into a mesenchymal phenotype, has been implicated to contribute to the molecular heterogeneity of epithelial ovarian cancer (EOC). Here we report that a transcription factor—Grainyhead-like 2 (GRHL2) maintains the epithelial phenotype. EOC tumours with lower GRHL2 levels are associated with the Mes/Mesenchymal molecular subtype and a poorer overall survival. shRNA-mediated knockdown of GRHL2 in EOC cells with an epithelial phenotype results in EMT changes, with increased cell migration, invasion and motility. By ChIP-sequencing and gene expression microarray, microRNA-200b/a is identified as the direct transcriptional target of GRHL2 and regulates the epithelial status of EOC through ZEB1 and E-cadherin. Our study demonstrates that loss of GRHL2 increases the levels of histone mark H3K27me3 on promoters and GRHL2-binding sites at miR-200b/a and E-cadherin genes. These findings support GRHL2 as a pivotal gatekeeper of EMT in EOC via miR-200-ZEB1. |
format | Online Article Text |
id | pubmed-4757891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47578912016-02-26 GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification Chung, Vin Yee Tan, Tuan Zea Tan, Ming Wong, Meng Kang Kuay, Kuee Theng Yang, Zhe Ye, Jieru Muller, Julius Koh, Cheryl M. Guccione, Ernesto Thiery, Jean Paul Huang, Ruby Yun-Ju Sci Rep Article Epithelial-mesenchymal transition (EMT), a biological process by which polarized epithelial cells convert into a mesenchymal phenotype, has been implicated to contribute to the molecular heterogeneity of epithelial ovarian cancer (EOC). Here we report that a transcription factor—Grainyhead-like 2 (GRHL2) maintains the epithelial phenotype. EOC tumours with lower GRHL2 levels are associated with the Mes/Mesenchymal molecular subtype and a poorer overall survival. shRNA-mediated knockdown of GRHL2 in EOC cells with an epithelial phenotype results in EMT changes, with increased cell migration, invasion and motility. By ChIP-sequencing and gene expression microarray, microRNA-200b/a is identified as the direct transcriptional target of GRHL2 and regulates the epithelial status of EOC through ZEB1 and E-cadherin. Our study demonstrates that loss of GRHL2 increases the levels of histone mark H3K27me3 on promoters and GRHL2-binding sites at miR-200b/a and E-cadherin genes. These findings support GRHL2 as a pivotal gatekeeper of EMT in EOC via miR-200-ZEB1. Nature Publishing Group 2016-02-18 /pmc/articles/PMC4757891/ /pubmed/26887977 http://dx.doi.org/10.1038/srep19943 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chung, Vin Yee Tan, Tuan Zea Tan, Ming Wong, Meng Kang Kuay, Kuee Theng Yang, Zhe Ye, Jieru Muller, Julius Koh, Cheryl M. Guccione, Ernesto Thiery, Jean Paul Huang, Ruby Yun-Ju GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title | GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title_full | GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title_fullStr | GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title_full_unstemmed | GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title_short | GRHL2-miR-200-ZEB1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
title_sort | grhl2-mir-200-zeb1 maintains the epithelial status of ovarian cancer through transcriptional regulation and histone modification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757891/ https://www.ncbi.nlm.nih.gov/pubmed/26887977 http://dx.doi.org/10.1038/srep19943 |
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