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Wnt/β-catenin signaling in cancers and targeted therapies

Wnt/β-catenin signaling has been broadly implicated in human cancers and experimental cancer models of animals. Aberrant activation of Wnt/β-catenin signaling is tightly linked with the increment of prevalence, advancement of malignant progression, development of poor prognostics, and even ascendenc...

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Autores principales: Yu, Fanyuan, Yu, Changhao, Li, Feifei, Zuo, Yanqin, Wang, Yitian, Yao, Lin, Wu, Chenzhou, Wang, Chenglin, Ye, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403677/
https://www.ncbi.nlm.nih.gov/pubmed/34456337
http://dx.doi.org/10.1038/s41392-021-00701-5
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author Yu, Fanyuan
Yu, Changhao
Li, Feifei
Zuo, Yanqin
Wang, Yitian
Yao, Lin
Wu, Chenzhou
Wang, Chenglin
Ye, Ling
author_facet Yu, Fanyuan
Yu, Changhao
Li, Feifei
Zuo, Yanqin
Wang, Yitian
Yao, Lin
Wu, Chenzhou
Wang, Chenglin
Ye, Ling
author_sort Yu, Fanyuan
collection PubMed
description Wnt/β-catenin signaling has been broadly implicated in human cancers and experimental cancer models of animals. Aberrant activation of Wnt/β-catenin signaling is tightly linked with the increment of prevalence, advancement of malignant progression, development of poor prognostics, and even ascendence of the cancer-associated mortality. Early experimental investigations have proposed the theoretical potential that efficient repression of this signaling might provide promising therapeutic choices in managing various types of cancers. Up to date, many therapies targeting Wnt/β-catenin signaling in cancers have been developed, which is assumed to endow clinicians with new opportunities of developing more satisfactory and precise remedies for cancer patients with aberrant Wnt/β-catenin signaling. However, current facts indicate that the clinical translations of Wnt/β-catenin signaling-dependent targeted therapies have faced un-neglectable crises and challenges. Therefore, in this study, we systematically reviewed the most updated knowledge of Wnt/β-catenin signaling in cancers and relatively targeted therapies to generate a clearer and more accurate awareness of both the developmental stage and underlying limitations of Wnt/β-catenin-targeted therapies in cancers. Insights of this study will help readers better understand the roles of Wnt/β-catenin signaling in cancers and provide insights to acknowledge the current opportunities and challenges of targeting this signaling in cancers.
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spelling pubmed-84036772021-09-15 Wnt/β-catenin signaling in cancers and targeted therapies Yu, Fanyuan Yu, Changhao Li, Feifei Zuo, Yanqin Wang, Yitian Yao, Lin Wu, Chenzhou Wang, Chenglin Ye, Ling Signal Transduct Target Ther Review Article Wnt/β-catenin signaling has been broadly implicated in human cancers and experimental cancer models of animals. Aberrant activation of Wnt/β-catenin signaling is tightly linked with the increment of prevalence, advancement of malignant progression, development of poor prognostics, and even ascendence of the cancer-associated mortality. Early experimental investigations have proposed the theoretical potential that efficient repression of this signaling might provide promising therapeutic choices in managing various types of cancers. Up to date, many therapies targeting Wnt/β-catenin signaling in cancers have been developed, which is assumed to endow clinicians with new opportunities of developing more satisfactory and precise remedies for cancer patients with aberrant Wnt/β-catenin signaling. However, current facts indicate that the clinical translations of Wnt/β-catenin signaling-dependent targeted therapies have faced un-neglectable crises and challenges. Therefore, in this study, we systematically reviewed the most updated knowledge of Wnt/β-catenin signaling in cancers and relatively targeted therapies to generate a clearer and more accurate awareness of both the developmental stage and underlying limitations of Wnt/β-catenin-targeted therapies in cancers. Insights of this study will help readers better understand the roles of Wnt/β-catenin signaling in cancers and provide insights to acknowledge the current opportunities and challenges of targeting this signaling in cancers. Nature Publishing Group UK 2021-08-30 /pmc/articles/PMC8403677/ /pubmed/34456337 http://dx.doi.org/10.1038/s41392-021-00701-5 Text en © The Author(s) 2021 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 Review Article
Yu, Fanyuan
Yu, Changhao
Li, Feifei
Zuo, Yanqin
Wang, Yitian
Yao, Lin
Wu, Chenzhou
Wang, Chenglin
Ye, Ling
Wnt/β-catenin signaling in cancers and targeted therapies
title Wnt/β-catenin signaling in cancers and targeted therapies
title_full Wnt/β-catenin signaling in cancers and targeted therapies
title_fullStr Wnt/β-catenin signaling in cancers and targeted therapies
title_full_unstemmed Wnt/β-catenin signaling in cancers and targeted therapies
title_short Wnt/β-catenin signaling in cancers and targeted therapies
title_sort wnt/β-catenin signaling in cancers and targeted therapies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403677/
https://www.ncbi.nlm.nih.gov/pubmed/34456337
http://dx.doi.org/10.1038/s41392-021-00701-5
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