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EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis
SMAD3 plays a central role in cancer metastasis, and its hyperactivation is linked to poor cancer outcomes. Thus, it is critical to understand the upstream signaling pathways that govern SMAD3 activation. Here, we report that SMAD3 underwent methylation at K53 and K333 (K53/K333) by EZH2, a process...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884901/ https://www.ncbi.nlm.nih.gov/pubmed/35085106 http://dx.doi.org/10.1172/JCI152394 |
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author | Huang, Changsheng Hu, Fuqing Song, Da Sun, Xuling Liu, Anyi Wu, Qi She, Xiaowei Chen, Yaqi Chen, Lisheng Hu, Fayong Xu, Feng Luo, Xuelai Feng, Yongdong Yang, Xiangping Hu, Junbo Wang, Guihua |
author_facet | Huang, Changsheng Hu, Fuqing Song, Da Sun, Xuling Liu, Anyi Wu, Qi She, Xiaowei Chen, Yaqi Chen, Lisheng Hu, Fayong Xu, Feng Luo, Xuelai Feng, Yongdong Yang, Xiangping Hu, Junbo Wang, Guihua |
author_sort | Huang, Changsheng |
collection | PubMed |
description | SMAD3 plays a central role in cancer metastasis, and its hyperactivation is linked to poor cancer outcomes. Thus, it is critical to understand the upstream signaling pathways that govern SMAD3 activation. Here, we report that SMAD3 underwent methylation at K53 and K333 (K53/K333) by EZH2, a process crucial for cell membrane recruitment, phosphorylation, and activation of SMAD3 upon TGFB1 stimulation. Mechanistically, EZH2-triggered SMAD3 methylation facilitated SMAD3 interaction with its cellular membrane localization molecule (SARA), which in turn sustained SMAD3 phosphorylation by the TGFB receptor. Pathologically, increased expression of EZH2 expression resulted in the accumulation of SMAD3 methylation to facilitate SMAD3 activation. EZH2-mediated SMAD3 K53/K333 methylation was upregulated and correlated with SMAD3 hyperactivation in breast cancer, promoted tumor metastasis, and was predictive of poor survival outcomes. We used 2 TAT peptides to abrogate SMAD3 methylation and therapeutically inhibit cancer metastasis. Collectively, these findings reveal the complicated layers involved in the regulation of SMAD3 activation coordinated by EZH2-mediated SMAD3 K53/K333 methylation to drive cancer metastasis. |
format | Online Article Text |
id | pubmed-8884901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-88849012022-03-08 EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis Huang, Changsheng Hu, Fuqing Song, Da Sun, Xuling Liu, Anyi Wu, Qi She, Xiaowei Chen, Yaqi Chen, Lisheng Hu, Fayong Xu, Feng Luo, Xuelai Feng, Yongdong Yang, Xiangping Hu, Junbo Wang, Guihua J Clin Invest Research Article SMAD3 plays a central role in cancer metastasis, and its hyperactivation is linked to poor cancer outcomes. Thus, it is critical to understand the upstream signaling pathways that govern SMAD3 activation. Here, we report that SMAD3 underwent methylation at K53 and K333 (K53/K333) by EZH2, a process crucial for cell membrane recruitment, phosphorylation, and activation of SMAD3 upon TGFB1 stimulation. Mechanistically, EZH2-triggered SMAD3 methylation facilitated SMAD3 interaction with its cellular membrane localization molecule (SARA), which in turn sustained SMAD3 phosphorylation by the TGFB receptor. Pathologically, increased expression of EZH2 expression resulted in the accumulation of SMAD3 methylation to facilitate SMAD3 activation. EZH2-mediated SMAD3 K53/K333 methylation was upregulated and correlated with SMAD3 hyperactivation in breast cancer, promoted tumor metastasis, and was predictive of poor survival outcomes. We used 2 TAT peptides to abrogate SMAD3 methylation and therapeutically inhibit cancer metastasis. Collectively, these findings reveal the complicated layers involved in the regulation of SMAD3 activation coordinated by EZH2-mediated SMAD3 K53/K333 methylation to drive cancer metastasis. American Society for Clinical Investigation 2022-03-01 2022-03-01 /pmc/articles/PMC8884901/ /pubmed/35085106 http://dx.doi.org/10.1172/JCI152394 Text en © 2022 Huang et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Huang, Changsheng Hu, Fuqing Song, Da Sun, Xuling Liu, Anyi Wu, Qi She, Xiaowei Chen, Yaqi Chen, Lisheng Hu, Fayong Xu, Feng Luo, Xuelai Feng, Yongdong Yang, Xiangping Hu, Junbo Wang, Guihua EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title | EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title_full | EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title_fullStr | EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title_full_unstemmed | EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title_short | EZH2-triggered methylation of SMAD3 promotes its activation and tumor metastasis |
title_sort | ezh2-triggered methylation of smad3 promotes its activation and tumor metastasis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884901/ https://www.ncbi.nlm.nih.gov/pubmed/35085106 http://dx.doi.org/10.1172/JCI152394 |
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