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Function and mechanism of MCM8 in the development and progression of colorectal cancer

Colorectal cancer (CRC) has become a global health problem which has almost highest morbidity and mortality in all types of cancers. This study aimed to uncover the biological functions and underlying mechanism of MCM8 in the development and progression of CRC. The expression level of MCM8 was found...

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Autores principales: Yu, Shaojun, Dai, Weixing, Zhao, Senlin, Yang, Yongzhi, Xu, Ye, Wang, Jianwei, Deng, Qun, He, Jinghu, Shi, Debing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503009/
https://www.ncbi.nlm.nih.gov/pubmed/37710286
http://dx.doi.org/10.1186/s12967-023-04084-9
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author Yu, Shaojun
Dai, Weixing
Zhao, Senlin
Yang, Yongzhi
Xu, Ye
Wang, Jianwei
Deng, Qun
He, Jinghu
Shi, Debing
author_facet Yu, Shaojun
Dai, Weixing
Zhao, Senlin
Yang, Yongzhi
Xu, Ye
Wang, Jianwei
Deng, Qun
He, Jinghu
Shi, Debing
author_sort Yu, Shaojun
collection PubMed
description Colorectal cancer (CRC) has become a global health problem which has almost highest morbidity and mortality in all types of cancers. This study aimed to uncover the biological functions and underlying mechanism of MCM8 in the development and progression of CRC. The expression level of MCM8 was found to be upregulated in CRC tissues and significantly associated with tumor grade and patients’ survival. Knocking down MCM8 expression in CRC cells could restrain cell growth and cell motility while promoting cell apoptosis in vitro, as well as inhibit tumor growth in xenograft mice model. Based on the RNA screening performing on CRC cells with or without MCM8 knockdown and the following IPA analysis, CHSY1 was identified as a potential target of MCM8 in CRC, whose expression was also found to be higher in tumor tissues than in normal tissues. Moreover, it was demonstrated that MCM8 may regulate the expression of CHSY1 through affecting its NEDD4-mediated ubiquitination, both of which synergistically execute tumor promotion effects on CRC. In conclusion, the outcomes of our study showed the first evidence that MCM8 act as a tumor promotor in CRC, and may be a promising therapeutic target of CRC treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04084-9.
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spelling pubmed-105030092023-09-16 Function and mechanism of MCM8 in the development and progression of colorectal cancer Yu, Shaojun Dai, Weixing Zhao, Senlin Yang, Yongzhi Xu, Ye Wang, Jianwei Deng, Qun He, Jinghu Shi, Debing J Transl Med Research Colorectal cancer (CRC) has become a global health problem which has almost highest morbidity and mortality in all types of cancers. This study aimed to uncover the biological functions and underlying mechanism of MCM8 in the development and progression of CRC. The expression level of MCM8 was found to be upregulated in CRC tissues and significantly associated with tumor grade and patients’ survival. Knocking down MCM8 expression in CRC cells could restrain cell growth and cell motility while promoting cell apoptosis in vitro, as well as inhibit tumor growth in xenograft mice model. Based on the RNA screening performing on CRC cells with or without MCM8 knockdown and the following IPA analysis, CHSY1 was identified as a potential target of MCM8 in CRC, whose expression was also found to be higher in tumor tissues than in normal tissues. Moreover, it was demonstrated that MCM8 may regulate the expression of CHSY1 through affecting its NEDD4-mediated ubiquitination, both of which synergistically execute tumor promotion effects on CRC. In conclusion, the outcomes of our study showed the first evidence that MCM8 act as a tumor promotor in CRC, and may be a promising therapeutic target of CRC treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04084-9. BioMed Central 2023-09-14 /pmc/articles/PMC10503009/ /pubmed/37710286 http://dx.doi.org/10.1186/s12967-023-04084-9 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yu, Shaojun
Dai, Weixing
Zhao, Senlin
Yang, Yongzhi
Xu, Ye
Wang, Jianwei
Deng, Qun
He, Jinghu
Shi, Debing
Function and mechanism of MCM8 in the development and progression of colorectal cancer
title Function and mechanism of MCM8 in the development and progression of colorectal cancer
title_full Function and mechanism of MCM8 in the development and progression of colorectal cancer
title_fullStr Function and mechanism of MCM8 in the development and progression of colorectal cancer
title_full_unstemmed Function and mechanism of MCM8 in the development and progression of colorectal cancer
title_short Function and mechanism of MCM8 in the development and progression of colorectal cancer
title_sort function and mechanism of mcm8 in the development and progression of colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503009/
https://www.ncbi.nlm.nih.gov/pubmed/37710286
http://dx.doi.org/10.1186/s12967-023-04084-9
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