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Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer

Colorectal cancer (CRC) is the third most common malignant tumor in humans. Chemotherapy is used for the treatment of CRC. However, the effect of chemotherapy remains unsatisfactory due to drug resistance. Growing evidence has shown that the presence of highly metastatic tumor stem cells, regulation...

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Autores principales: Zhu, Gui-Xian, Gao, Dian, Shao, Zhao-Zhao, Chen, Li, Ding, Wen-Jie, Yu, Qiong-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723170/
https://www.ncbi.nlm.nih.gov/pubmed/33300082
http://dx.doi.org/10.3892/mmr.2020.11744
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author Zhu, Gui-Xian
Gao, Dian
Shao, Zhao-Zhao
Chen, Li
Ding, Wen-Jie
Yu, Qiong-Fang
author_facet Zhu, Gui-Xian
Gao, Dian
Shao, Zhao-Zhao
Chen, Li
Ding, Wen-Jie
Yu, Qiong-Fang
author_sort Zhu, Gui-Xian
collection PubMed
description Colorectal cancer (CRC) is the third most common malignant tumor in humans. Chemotherapy is used for the treatment of CRC. However, the effect of chemotherapy remains unsatisfactory due to drug resistance. Growing evidence has shown that the presence of highly metastatic tumor stem cells, regulation of non-coding RNAs and the tumor microenvironment contributes to drug resistance mechanisms in CRC. Wnt/β-catenin signaling mediates the chemoresistance of CRC in these three aspects. Therefore, the present study analyzed the abundant evidence of the contribution of Wnt/β-catenin signaling to the development of drug resistance in CRC and discussed its possible role in improving the chemosensitivity of CRC, which may provide guidelines for its clinical treatment.
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spelling pubmed-77231702020-12-23 Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer Zhu, Gui-Xian Gao, Dian Shao, Zhao-Zhao Chen, Li Ding, Wen-Jie Yu, Qiong-Fang Mol Med Rep Review Colorectal cancer (CRC) is the third most common malignant tumor in humans. Chemotherapy is used for the treatment of CRC. However, the effect of chemotherapy remains unsatisfactory due to drug resistance. Growing evidence has shown that the presence of highly metastatic tumor stem cells, regulation of non-coding RNAs and the tumor microenvironment contributes to drug resistance mechanisms in CRC. Wnt/β-catenin signaling mediates the chemoresistance of CRC in these three aspects. Therefore, the present study analyzed the abundant evidence of the contribution of Wnt/β-catenin signaling to the development of drug resistance in CRC and discussed its possible role in improving the chemosensitivity of CRC, which may provide guidelines for its clinical treatment. D.A. Spandidos 2021-02 2020-12-01 /pmc/articles/PMC7723170/ /pubmed/33300082 http://dx.doi.org/10.3892/mmr.2020.11744 Text en Copyright: © Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Zhu, Gui-Xian
Gao, Dian
Shao, Zhao-Zhao
Chen, Li
Ding, Wen-Jie
Yu, Qiong-Fang
Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title_full Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title_fullStr Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title_full_unstemmed Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title_short Wnt/β-catenin signaling: Causes and treatment targets of drug resistance in colorectal cancer
title_sort wnt/β-catenin signaling: causes and treatment targets of drug resistance in colorectal cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723170/
https://www.ncbi.nlm.nih.gov/pubmed/33300082
http://dx.doi.org/10.3892/mmr.2020.11744
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