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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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