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ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression

Prostate cancer is still one of the most common malignancies in men all around the world. The mechanism of how prostate cancer initiates and develops is still not clear. Here in this study, we show that tumor suppressor ZBTB38 could suppress the migration and proliferation of prostate cancer cells....

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Autores principales: Ding, Guanxiong, Lu, Wei, Zhang, Qing, Li, Kai, Zhou, Huihui, Wang, Fei, Zhao, Chunchun, Fan, Caibin, Wang, Jianqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546125/
https://www.ncbi.nlm.nih.gov/pubmed/34697293
http://dx.doi.org/10.1038/s41419-021-04278-3
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author Ding, Guanxiong
Lu, Wei
Zhang, Qing
Li, Kai
Zhou, Huihui
Wang, Fei
Zhao, Chunchun
Fan, Caibin
Wang, Jianqing
author_facet Ding, Guanxiong
Lu, Wei
Zhang, Qing
Li, Kai
Zhou, Huihui
Wang, Fei
Zhao, Chunchun
Fan, Caibin
Wang, Jianqing
author_sort Ding, Guanxiong
collection PubMed
description Prostate cancer is still one of the most common malignancies in men all around the world. The mechanism of how prostate cancer initiates and develops is still not clear. Here in this study, we show that tumor suppressor ZBTB38 could suppress the migration and proliferation of prostate cancer cells. We find lower ZBTB38 expression in prostate cancer tissues, which also strongly predicts a poorer prognosis of prostate cancer. ZBTB38 binds DKK1 (Dickkopf WNT signaling pathway inhibitor 1) locus and promotes DKK1 expression in prostate cancer cell lines. Consistently, reduction of DKK1 expression significantly restores ZBTB38-mediated suppression of migration and proliferation of prostate cancer cell lines. Mechanistically, we find that ZBTB38 primarily binds the promoters of target genes, and differentially regulates the expression of 1818 genes. We also identify PRKDC (protein kinase, DNA-activated, catalytic subunit) as a ZBTB38-interacting protein that could repress the function of ZBTB38 in suppressing migration and proliferation of prostate cancer cells. Taken together, our results indicate that ZBTB38 could repress cell migration and proliferation in prostate cancer via promoting DKK1 expression, and also provide evidence supporting ZBTB38 as a potential prognosis marker for prostate cancer.
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spelling pubmed-85461252021-10-29 ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression Ding, Guanxiong Lu, Wei Zhang, Qing Li, Kai Zhou, Huihui Wang, Fei Zhao, Chunchun Fan, Caibin Wang, Jianqing Cell Death Dis Article Prostate cancer is still one of the most common malignancies in men all around the world. The mechanism of how prostate cancer initiates and develops is still not clear. Here in this study, we show that tumor suppressor ZBTB38 could suppress the migration and proliferation of prostate cancer cells. We find lower ZBTB38 expression in prostate cancer tissues, which also strongly predicts a poorer prognosis of prostate cancer. ZBTB38 binds DKK1 (Dickkopf WNT signaling pathway inhibitor 1) locus and promotes DKK1 expression in prostate cancer cell lines. Consistently, reduction of DKK1 expression significantly restores ZBTB38-mediated suppression of migration and proliferation of prostate cancer cell lines. Mechanistically, we find that ZBTB38 primarily binds the promoters of target genes, and differentially regulates the expression of 1818 genes. We also identify PRKDC (protein kinase, DNA-activated, catalytic subunit) as a ZBTB38-interacting protein that could repress the function of ZBTB38 in suppressing migration and proliferation of prostate cancer cells. Taken together, our results indicate that ZBTB38 could repress cell migration and proliferation in prostate cancer via promoting DKK1 expression, and also provide evidence supporting ZBTB38 as a potential prognosis marker for prostate cancer. Nature Publishing Group UK 2021-10-25 /pmc/articles/PMC8546125/ /pubmed/34697293 http://dx.doi.org/10.1038/s41419-021-04278-3 Text en © The Author(s) 2021 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
Ding, Guanxiong
Lu, Wei
Zhang, Qing
Li, Kai
Zhou, Huihui
Wang, Fei
Zhao, Chunchun
Fan, Caibin
Wang, Jianqing
ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title_full ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title_fullStr ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title_full_unstemmed ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title_short ZBTB38 suppresses prostate cancer cell proliferation and migration via directly promoting DKK1 expression
title_sort zbtb38 suppresses prostate cancer cell proliferation and migration via directly promoting dkk1 expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546125/
https://www.ncbi.nlm.nih.gov/pubmed/34697293
http://dx.doi.org/10.1038/s41419-021-04278-3
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