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The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling

DPF3, a component of the SWI/SNF chromatin remodeling complex, has been associated with clear cell renal cell carcinoma (ccRCC) in a genome-wide association study. However, the functional role of DPF3 in ccRCC development and progression remains unknown. In this study, we demonstrate that DPF3a, the...

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Autores principales: Cui, Huanhuan, Yi, Hongyang, Bao, Hongyu, Tan, Ying, Tian, Chi, Shi, Xinyao, Gan, Diwen, Zhang, Bin, Liang, Weizheng, Chen, Rui, Zhu, Qionghua, Fang, Liang, Gao, Xin, Huang, Hongda, Tian, Ruijun, Sperling, Silke R., Hu, Yuhui, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363427/
https://www.ncbi.nlm.nih.gov/pubmed/35945219
http://dx.doi.org/10.1038/s41467-022-32472-0
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author Cui, Huanhuan
Yi, Hongyang
Bao, Hongyu
Tan, Ying
Tian, Chi
Shi, Xinyao
Gan, Diwen
Zhang, Bin
Liang, Weizheng
Chen, Rui
Zhu, Qionghua
Fang, Liang
Gao, Xin
Huang, Hongda
Tian, Ruijun
Sperling, Silke R.
Hu, Yuhui
Chen, Wei
author_facet Cui, Huanhuan
Yi, Hongyang
Bao, Hongyu
Tan, Ying
Tian, Chi
Shi, Xinyao
Gan, Diwen
Zhang, Bin
Liang, Weizheng
Chen, Rui
Zhu, Qionghua
Fang, Liang
Gao, Xin
Huang, Hongda
Tian, Ruijun
Sperling, Silke R.
Hu, Yuhui
Chen, Wei
author_sort Cui, Huanhuan
collection PubMed
description DPF3, a component of the SWI/SNF chromatin remodeling complex, has been associated with clear cell renal cell carcinoma (ccRCC) in a genome-wide association study. However, the functional role of DPF3 in ccRCC development and progression remains unknown. In this study, we demonstrate that DPF3a, the short isoform of DPF3, promotes kidney cancer cell migration both in vitro and in vivo, consistent with the clinical observation that DPF3a is significantly upregulated in ccRCC patients with metastases. Mechanistically, DPF3a specifically interacts with SNIP1, via which it forms a complex with SMAD4 and p300 histone acetyltransferase (HAT), the major transcriptional regulators of TGF-β signaling pathway. Moreover, the binding of DPF3a releases the repressive effect of SNIP1 on p300 HAT activity, leading to the increase in local histone acetylation and the activation of cell movement related genes. Overall, our findings reveal a metastasis-promoting function of DPF3, and further establish the link between SWI/SNF components and ccRCC.
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spelling pubmed-93634272022-08-11 The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling Cui, Huanhuan Yi, Hongyang Bao, Hongyu Tan, Ying Tian, Chi Shi, Xinyao Gan, Diwen Zhang, Bin Liang, Weizheng Chen, Rui Zhu, Qionghua Fang, Liang Gao, Xin Huang, Hongda Tian, Ruijun Sperling, Silke R. Hu, Yuhui Chen, Wei Nat Commun Article DPF3, a component of the SWI/SNF chromatin remodeling complex, has been associated with clear cell renal cell carcinoma (ccRCC) in a genome-wide association study. However, the functional role of DPF3 in ccRCC development and progression remains unknown. In this study, we demonstrate that DPF3a, the short isoform of DPF3, promotes kidney cancer cell migration both in vitro and in vivo, consistent with the clinical observation that DPF3a is significantly upregulated in ccRCC patients with metastases. Mechanistically, DPF3a specifically interacts with SNIP1, via which it forms a complex with SMAD4 and p300 histone acetyltransferase (HAT), the major transcriptional regulators of TGF-β signaling pathway. Moreover, the binding of DPF3a releases the repressive effect of SNIP1 on p300 HAT activity, leading to the increase in local histone acetylation and the activation of cell movement related genes. Overall, our findings reveal a metastasis-promoting function of DPF3, and further establish the link between SWI/SNF components and ccRCC. Nature Publishing Group UK 2022-08-09 /pmc/articles/PMC9363427/ /pubmed/35945219 http://dx.doi.org/10.1038/s41467-022-32472-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cui, Huanhuan
Yi, Hongyang
Bao, Hongyu
Tan, Ying
Tian, Chi
Shi, Xinyao
Gan, Diwen
Zhang, Bin
Liang, Weizheng
Chen, Rui
Zhu, Qionghua
Fang, Liang
Gao, Xin
Huang, Hongda
Tian, Ruijun
Sperling, Silke R.
Hu, Yuhui
Chen, Wei
The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title_full The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title_fullStr The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title_full_unstemmed The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title_short The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling
title_sort swi/snf chromatin remodeling factor dpf3 regulates metastasis of ccrcc by modulating tgf-β signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363427/
https://www.ncbi.nlm.nih.gov/pubmed/35945219
http://dx.doi.org/10.1038/s41467-022-32472-0
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