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ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin
EGFR is required for animal development, and dysregulation of EGFR is critically implicated in malignant transformation. However, the molecular mechanism underlying the regulation of EGFR expression remains poorly explored. Here we report that the zinc-finger protein ZNF516 is a transcription repres...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612949/ https://www.ncbi.nlm.nih.gov/pubmed/28947780 http://dx.doi.org/10.1038/s41467-017-00702-5 |
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author | Li, Lifang Liu, Xinhua He, Lin Yang, Jianguo Pei, Fei Li, Wanjin Liu, Shumeng Chen, Zhe Xie, Guojia Xu, Bosen Ting, Xia Zhang, Zihan Jin, Tong Liu, Xujun Zhang, Wenting Yuan, Shuai Yang, Ziran Wu, Chongyang Zhang, Yu Yang, Xiaohan Yi, Xia Liang, Jing Shang, Yongfeng Sun, Luyang |
author_facet | Li, Lifang Liu, Xinhua He, Lin Yang, Jianguo Pei, Fei Li, Wanjin Liu, Shumeng Chen, Zhe Xie, Guojia Xu, Bosen Ting, Xia Zhang, Zihan Jin, Tong Liu, Xujun Zhang, Wenting Yuan, Shuai Yang, Ziran Wu, Chongyang Zhang, Yu Yang, Xiaohan Yi, Xia Liang, Jing Shang, Yongfeng Sun, Luyang |
author_sort | Li, Lifang |
collection | PubMed |
description | EGFR is required for animal development, and dysregulation of EGFR is critically implicated in malignant transformation. However, the molecular mechanism underlying the regulation of EGFR expression remains poorly explored. Here we report that the zinc-finger protein ZNF516 is a transcription repressor. ZNF516 is physically associated with the CtBP/LSD1/CoREST complex and transcriptionally represses a cohort of genes including EGFR that are critically involved in cell proliferation and motility. We demonstrate that the ZNF516–CtBP/LSD1/CoREST complex inhibits the proliferation and invasion of breast cancer cells in vitro and suppresses breast cancer growth and metastasis in vivo. Significantly, low expression of ZNF516 is positively associated with advanced pathological staging and poor survival of breast carcinomas. Our data indicate that ZNF516 is a transcription repressor and a potential suppressor of EGFR, adding to the understanding of EGFR-related breast carcinogenesis and supporting the pursuit of ZNF516 as a potential therapeutic target for breast cancer. |
format | Online Article Text |
id | pubmed-5612949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56129492017-09-27 ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin Li, Lifang Liu, Xinhua He, Lin Yang, Jianguo Pei, Fei Li, Wanjin Liu, Shumeng Chen, Zhe Xie, Guojia Xu, Bosen Ting, Xia Zhang, Zihan Jin, Tong Liu, Xujun Zhang, Wenting Yuan, Shuai Yang, Ziran Wu, Chongyang Zhang, Yu Yang, Xiaohan Yi, Xia Liang, Jing Shang, Yongfeng Sun, Luyang Nat Commun Article EGFR is required for animal development, and dysregulation of EGFR is critically implicated in malignant transformation. However, the molecular mechanism underlying the regulation of EGFR expression remains poorly explored. Here we report that the zinc-finger protein ZNF516 is a transcription repressor. ZNF516 is physically associated with the CtBP/LSD1/CoREST complex and transcriptionally represses a cohort of genes including EGFR that are critically involved in cell proliferation and motility. We demonstrate that the ZNF516–CtBP/LSD1/CoREST complex inhibits the proliferation and invasion of breast cancer cells in vitro and suppresses breast cancer growth and metastasis in vivo. Significantly, low expression of ZNF516 is positively associated with advanced pathological staging and poor survival of breast carcinomas. Our data indicate that ZNF516 is a transcription repressor and a potential suppressor of EGFR, adding to the understanding of EGFR-related breast carcinogenesis and supporting the pursuit of ZNF516 as a potential therapeutic target for breast cancer. Nature Publishing Group UK 2017-09-25 /pmc/articles/PMC5612949/ /pubmed/28947780 http://dx.doi.org/10.1038/s41467-017-00702-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Lifang Liu, Xinhua He, Lin Yang, Jianguo Pei, Fei Li, Wanjin Liu, Shumeng Chen, Zhe Xie, Guojia Xu, Bosen Ting, Xia Zhang, Zihan Jin, Tong Liu, Xujun Zhang, Wenting Yuan, Shuai Yang, Ziran Wu, Chongyang Zhang, Yu Yang, Xiaohan Yi, Xia Liang, Jing Shang, Yongfeng Sun, Luyang ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title | ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title_full | ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title_fullStr | ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title_full_unstemmed | ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title_short | ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin |
title_sort | znf516 suppresses egfr by targeting the ctbp/lsd1/corest complex to chromatin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612949/ https://www.ncbi.nlm.nih.gov/pubmed/28947780 http://dx.doi.org/10.1038/s41467-017-00702-5 |
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