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Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells

Drug resistance remains the greatest challenge in improving outcomes for cancer patients who receive chemotherapy and targeted therapy. Surmounting evidence suggests that a subpopulation of cancer cells could escape intense selective drug treatment by entering a drug‐tolerant state without genetic v...

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Autores principales: Song, Xiaohai, Lan, Yang, Zheng, Xiuli, Zhu, Qianyu, Liao, Xuliang, Liu, Kai, Zhang, Weihan, Peng, QiangBo, Zhu, Yunfeng, Zhao, Linyong, Chen, Xiaolong, Shu, Yang, Yang, Kun, Hu, Jiankun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449058/
https://www.ncbi.nlm.nih.gov/pubmed/37638338
http://dx.doi.org/10.1002/mco2.342
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author Song, Xiaohai
Lan, Yang
Zheng, Xiuli
Zhu, Qianyu
Liao, Xuliang
Liu, Kai
Zhang, Weihan
Peng, QiangBo
Zhu, Yunfeng
Zhao, Linyong
Chen, Xiaolong
Shu, Yang
Yang, Kun
Hu, Jiankun
author_facet Song, Xiaohai
Lan, Yang
Zheng, Xiuli
Zhu, Qianyu
Liao, Xuliang
Liu, Kai
Zhang, Weihan
Peng, QiangBo
Zhu, Yunfeng
Zhao, Linyong
Chen, Xiaolong
Shu, Yang
Yang, Kun
Hu, Jiankun
author_sort Song, Xiaohai
collection PubMed
description Drug resistance remains the greatest challenge in improving outcomes for cancer patients who receive chemotherapy and targeted therapy. Surmounting evidence suggests that a subpopulation of cancer cells could escape intense selective drug treatment by entering a drug‐tolerant state without genetic variations. These drug‐tolerant cells (DTCs) are characterized with a slow proliferation rate and a reversible phenotype. They reside in the tumor region and may serve as a reservoir for resistant phenotypes. The survival of DTCs is regulated by epigenetic modifications, transcriptional regulation, mRNA translation remodeling, metabolic changes, antiapoptosis, interactions with the tumor microenvironment, and activation of signaling pathways. Thus, targeting the regulators of DTCs opens a new avenue for the treatment of therapy‐resistant tumors. In this review, we first provide an overview of common characteristics of DTCs and the regulating networks in DTCs development. We also discuss the potential therapeutic opportunities to target DTCs. Last, we discuss the current challenges and prospects of the DTC‐targeting approach to overcome acquired drug resistance. Reviewing the latest developments in DTC research could be essential in discovering of methods to eliminate DTCs, which may represent a novel therapeutic strategy for preventing drug resistance in the future.
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spelling pubmed-104490582023-08-25 Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells Song, Xiaohai Lan, Yang Zheng, Xiuli Zhu, Qianyu Liao, Xuliang Liu, Kai Zhang, Weihan Peng, QiangBo Zhu, Yunfeng Zhao, Linyong Chen, Xiaolong Shu, Yang Yang, Kun Hu, Jiankun MedComm (2020) Reviews Drug resistance remains the greatest challenge in improving outcomes for cancer patients who receive chemotherapy and targeted therapy. Surmounting evidence suggests that a subpopulation of cancer cells could escape intense selective drug treatment by entering a drug‐tolerant state without genetic variations. These drug‐tolerant cells (DTCs) are characterized with a slow proliferation rate and a reversible phenotype. They reside in the tumor region and may serve as a reservoir for resistant phenotypes. The survival of DTCs is regulated by epigenetic modifications, transcriptional regulation, mRNA translation remodeling, metabolic changes, antiapoptosis, interactions with the tumor microenvironment, and activation of signaling pathways. Thus, targeting the regulators of DTCs opens a new avenue for the treatment of therapy‐resistant tumors. In this review, we first provide an overview of common characteristics of DTCs and the regulating networks in DTCs development. We also discuss the potential therapeutic opportunities to target DTCs. Last, we discuss the current challenges and prospects of the DTC‐targeting approach to overcome acquired drug resistance. Reviewing the latest developments in DTC research could be essential in discovering of methods to eliminate DTCs, which may represent a novel therapeutic strategy for preventing drug resistance in the future. John Wiley and Sons Inc. 2023-08-24 /pmc/articles/PMC10449058/ /pubmed/37638338 http://dx.doi.org/10.1002/mco2.342 Text en © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Song, Xiaohai
Lan, Yang
Zheng, Xiuli
Zhu, Qianyu
Liao, Xuliang
Liu, Kai
Zhang, Weihan
Peng, QiangBo
Zhu, Yunfeng
Zhao, Linyong
Chen, Xiaolong
Shu, Yang
Yang, Kun
Hu, Jiankun
Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title_full Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title_fullStr Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title_full_unstemmed Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title_short Targeting drug‐tolerant cells: A promising strategy for overcoming acquired drug resistance in cancer cells
title_sort targeting drug‐tolerant cells: a promising strategy for overcoming acquired drug resistance in cancer cells
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449058/
https://www.ncbi.nlm.nih.gov/pubmed/37638338
http://dx.doi.org/10.1002/mco2.342
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