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FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies

Drug therapy, including chemotherapy, targeted therapy, immunotherapy, and endocrine therapy, stands as the foremost therapeutic approach for contemporary human malignancies. However, increasing drug resistance during antineoplastic therapy has become a substantial barrier to favorable outcomes in c...

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Autores principales: Wang, Wanqing, Jiang, Kaipeng, Liu, Xue, Li, Ju, Zhou, Wenshuo, Wang, Chang, Cui, Jiuwei, Liang, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680170/
https://www.ncbi.nlm.nih.gov/pubmed/38027013
http://dx.doi.org/10.3389/fphar.2023.1278056
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author Wang, Wanqing
Jiang, Kaipeng
Liu, Xue
Li, Ju
Zhou, Wenshuo
Wang, Chang
Cui, Jiuwei
Liang, Tingting
author_facet Wang, Wanqing
Jiang, Kaipeng
Liu, Xue
Li, Ju
Zhou, Wenshuo
Wang, Chang
Cui, Jiuwei
Liang, Tingting
author_sort Wang, Wanqing
collection PubMed
description Drug therapy, including chemotherapy, targeted therapy, immunotherapy, and endocrine therapy, stands as the foremost therapeutic approach for contemporary human malignancies. However, increasing drug resistance during antineoplastic therapy has become a substantial barrier to favorable outcomes in cancer patients. To enhance the effectiveness of different cancer therapies, an in-depth understanding of the unique mechanisms underlying tumor drug resistance and the subsequent surmounting of antitumor drug resistance is required. Recently, F-box and WD Repeat Domain-containing-7 (FBXW7), a recognized tumor suppressor, has been found to be highly associated with tumor therapy resistance. This review provides a comprehensive summary of the underlying mechanisms through which FBXW7 facilitates the development of drug resistance in cancer. Additionally, this review elucidates the role of FBXW7 in therapeutic resistance of various types of human tumors. The strategies and challenges implicated in overcoming tumor therapy resistance by targeting FBXW7 are also discussed.
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spelling pubmed-106801702023-11-13 FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies Wang, Wanqing Jiang, Kaipeng Liu, Xue Li, Ju Zhou, Wenshuo Wang, Chang Cui, Jiuwei Liang, Tingting Front Pharmacol Pharmacology Drug therapy, including chemotherapy, targeted therapy, immunotherapy, and endocrine therapy, stands as the foremost therapeutic approach for contemporary human malignancies. However, increasing drug resistance during antineoplastic therapy has become a substantial barrier to favorable outcomes in cancer patients. To enhance the effectiveness of different cancer therapies, an in-depth understanding of the unique mechanisms underlying tumor drug resistance and the subsequent surmounting of antitumor drug resistance is required. Recently, F-box and WD Repeat Domain-containing-7 (FBXW7), a recognized tumor suppressor, has been found to be highly associated with tumor therapy resistance. This review provides a comprehensive summary of the underlying mechanisms through which FBXW7 facilitates the development of drug resistance in cancer. Additionally, this review elucidates the role of FBXW7 in therapeutic resistance of various types of human tumors. The strategies and challenges implicated in overcoming tumor therapy resistance by targeting FBXW7 are also discussed. Frontiers Media S.A. 2023-11-13 /pmc/articles/PMC10680170/ /pubmed/38027013 http://dx.doi.org/10.3389/fphar.2023.1278056 Text en Copyright © 2023 Wang, Jiang, Liu, Li, Zhou, Wang, Cui and Liang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wang, Wanqing
Jiang, Kaipeng
Liu, Xue
Li, Ju
Zhou, Wenshuo
Wang, Chang
Cui, Jiuwei
Liang, Tingting
FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title_full FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title_fullStr FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title_full_unstemmed FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title_short FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
title_sort fbxw7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680170/
https://www.ncbi.nlm.nih.gov/pubmed/38027013
http://dx.doi.org/10.3389/fphar.2023.1278056
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