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The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review

The cell division cycle 20 homologue (CDC20) is known to regulate the cell cycle. Many studies have suggested that dysregulation of CDC20 is associated with various pathological processes in malignant solid tumors, including tumorigenesis, progression, chemoradiotherapy resistance, and poor prognosi...

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Detalles Bibliográficos
Autores principales: Xian, Feng, Zhao, Caixia, Huang, Chun, Bie, Jun, Xu, Guohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489547/
https://www.ncbi.nlm.nih.gov/pubmed/37682144
http://dx.doi.org/10.1097/MD.0000000000035038
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author Xian, Feng
Zhao, Caixia
Huang, Chun
Bie, Jun
Xu, Guohui
author_facet Xian, Feng
Zhao, Caixia
Huang, Chun
Bie, Jun
Xu, Guohui
author_sort Xian, Feng
collection PubMed
description The cell division cycle 20 homologue (CDC20) is known to regulate the cell cycle. Many studies have suggested that dysregulation of CDC20 is associated with various pathological processes in malignant solid tumors, including tumorigenesis, progression, chemoradiotherapy resistance, and poor prognosis, providing a biomarker for cancer diagnosis and prognosis. Some researchers have demonstrated that CDC20 also regulates apoptosis, immune microenvironment, and tumor angiogenesis. In this review, we have systematically summarized the biological functions of CDC20 in solid cancers. Furthermore, we briefly synthesized multiple medicines that inhibited CDC20. We anticipate that CDC20 will be a promising and effective biomarker and therapeutic target for the treatment of human cancer.
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spelling pubmed-104895472023-09-09 The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review Xian, Feng Zhao, Caixia Huang, Chun Bie, Jun Xu, Guohui Medicine (Baltimore) 5700 The cell division cycle 20 homologue (CDC20) is known to regulate the cell cycle. Many studies have suggested that dysregulation of CDC20 is associated with various pathological processes in malignant solid tumors, including tumorigenesis, progression, chemoradiotherapy resistance, and poor prognosis, providing a biomarker for cancer diagnosis and prognosis. Some researchers have demonstrated that CDC20 also regulates apoptosis, immune microenvironment, and tumor angiogenesis. In this review, we have systematically summarized the biological functions of CDC20 in solid cancers. Furthermore, we briefly synthesized multiple medicines that inhibited CDC20. We anticipate that CDC20 will be a promising and effective biomarker and therapeutic target for the treatment of human cancer. Lippincott Williams & Wilkins 2023-09-08 /pmc/articles/PMC10489547/ /pubmed/37682144 http://dx.doi.org/10.1097/MD.0000000000035038 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5700
Xian, Feng
Zhao, Caixia
Huang, Chun
Bie, Jun
Xu, Guohui
The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title_full The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title_fullStr The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title_full_unstemmed The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title_short The potential role of CDC20 in tumorigenesis, cancer progression and therapy: A narrative review
title_sort potential role of cdc20 in tumorigenesis, cancer progression and therapy: a narrative review
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489547/
https://www.ncbi.nlm.nih.gov/pubmed/37682144
http://dx.doi.org/10.1097/MD.0000000000035038
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