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Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer

PBX1 is a transcription factor that regulates a variety of genes, involved in intracellular lipid metabolism, cell proliferation, and other pathways. The promoting and inhibiting function of PBX1 in various cancer types was extensively discussed, however, there have been no studies on PBX1 proteins...

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Autores principales: Dai, Weigang, Liu, Yinan, Zhang, Tianhao, Huang, Zhixin, Xu, Xiang, Zhao, Zeyu, Liu, Jianqiu, Zhai, Ertao, Cai, Shirong, Chen, Jianhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899229/
https://www.ncbi.nlm.nih.gov/pubmed/36739270
http://dx.doi.org/10.1038/s41389-023-00448-4
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author Dai, Weigang
Liu, Yinan
Zhang, Tianhao
Huang, Zhixin
Xu, Xiang
Zhao, Zeyu
Liu, Jianqiu
Zhai, Ertao
Cai, Shirong
Chen, Jianhui
author_facet Dai, Weigang
Liu, Yinan
Zhang, Tianhao
Huang, Zhixin
Xu, Xiang
Zhao, Zeyu
Liu, Jianqiu
Zhai, Ertao
Cai, Shirong
Chen, Jianhui
author_sort Dai, Weigang
collection PubMed
description PBX1 is a transcription factor that regulates a variety of genes, involved in intracellular lipid metabolism, cell proliferation, and other pathways. The promoting and inhibiting function of PBX1 in various cancer types was extensively discussed, however, there have been no studies on PBX1 proteins in colorectal cancer (CRC). This study aimed to reveal the anti-tumor function of PBX1 in CRC and the underlying molecular mechanism. Bioinformatics analysis revealed that PBX1 is downregulated in CRC, indicating that is a potential antioncogene in CRC. Overexpression of PBX1 suppresses tumor growth and metastasis in vitro and in vivo. Mechanistically, we found that PBX1 acted as a transcription factor that suppressed DCDC2 expression and inhibited spindle function. Moreover, the PBX1-DCDC2 axis controlled the Wnt pathway in CRC cells. Overexpression of DCDC2 restored CRC proliferation, metastasis abilities and Wnt pathway. In conclusion, this study suggests that PBX1 acts as a transcription factor to suppress DCDC2 expression and inhibit cell proliferation and metastasis by disrupting spindle function and the Wnt pathway in CRC.
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spelling pubmed-98992292023-02-06 Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer Dai, Weigang Liu, Yinan Zhang, Tianhao Huang, Zhixin Xu, Xiang Zhao, Zeyu Liu, Jianqiu Zhai, Ertao Cai, Shirong Chen, Jianhui Oncogenesis Article PBX1 is a transcription factor that regulates a variety of genes, involved in intracellular lipid metabolism, cell proliferation, and other pathways. The promoting and inhibiting function of PBX1 in various cancer types was extensively discussed, however, there have been no studies on PBX1 proteins in colorectal cancer (CRC). This study aimed to reveal the anti-tumor function of PBX1 in CRC and the underlying molecular mechanism. Bioinformatics analysis revealed that PBX1 is downregulated in CRC, indicating that is a potential antioncogene in CRC. Overexpression of PBX1 suppresses tumor growth and metastasis in vitro and in vivo. Mechanistically, we found that PBX1 acted as a transcription factor that suppressed DCDC2 expression and inhibited spindle function. Moreover, the PBX1-DCDC2 axis controlled the Wnt pathway in CRC cells. Overexpression of DCDC2 restored CRC proliferation, metastasis abilities and Wnt pathway. In conclusion, this study suggests that PBX1 acts as a transcription factor to suppress DCDC2 expression and inhibit cell proliferation and metastasis by disrupting spindle function and the Wnt pathway in CRC. Nature Publishing Group UK 2023-02-04 /pmc/articles/PMC9899229/ /pubmed/36739270 http://dx.doi.org/10.1038/s41389-023-00448-4 Text en © The Author(s) 2023 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
Dai, Weigang
Liu, Yinan
Zhang, Tianhao
Huang, Zhixin
Xu, Xiang
Zhao, Zeyu
Liu, Jianqiu
Zhai, Ertao
Cai, Shirong
Chen, Jianhui
Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title_full Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title_fullStr Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title_full_unstemmed Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title_short Spindle function and Wnt pathway inhibition by PBX1 to suppress tumor progression via downregulating DCDC2 in colorectal cancer
title_sort spindle function and wnt pathway inhibition by pbx1 to suppress tumor progression via downregulating dcdc2 in colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899229/
https://www.ncbi.nlm.nih.gov/pubmed/36739270
http://dx.doi.org/10.1038/s41389-023-00448-4
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