Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies

Abstract The success of cancer therapy has been significantly hampered by various mechanisms of therapeutic resistance. Chief among these mechanisms is the presence of clonal heterogeneity within an individual tumor mass. The introduction of the concept of cancer stem cells (CSCs)—a rare and immature subpopulation with tumorigenic potential that contributes to intratumoral heterogeneity—has deepened our understanding of drug resistance. Given the characteristics of CSCs, such as increased drug‐efflux activity, enhanced DNA‐repair capacity, high metabolic plasticity, adaptability to oxidative stress, and/or upregulated detoxifying aldehyde dehydrogenase (ALDH) enzymes, CSCs have been recognized as a theoretical reservoir for resistant diseases. Implicit in this recognition is the possibility that CSC‐targeted therapeutic strategies might offer a breakthrough in overcoming drug resistance in cancer patients. Herein, we summarize the generation of CSCs and our current understanding of the mechanisms underlying CSC‐mediated therapeutic resistance. This extended knowledge has progressively been translated into novel anticancer therapeutic strategies and significantly enriched the available options for combination treatments, all of which are anticipated to improve clinical outcomes for patients experiencing CSC‐related relapse.

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Publication Details

Journal
MedComm – Oncology
Published
2025-01-10
DOI
https://doi.org/10.1002/mog2.70009
Citations
12
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
9.67

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article

Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies

Yunhan Tan, Edouard C. Nice, Siyuan Qin, Y. Liu et al.
12 citations
MedComm – Oncology
Epigenetics and DNA Methylation
9.67
article

Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies

Yunhan Tan, Edouard C. Nice, Siyuan Qin, Y. Liu, Yuanyuan Zhang, Bowen Li, Zhe Zhang, Jing Jing, Li Zhou
article en
12 citations

Abstract

Abstract The success of cancer therapy has been significantly hampered by various mechanisms of therapeutic resistance. Chief among these mechanisms is the presence of clonal heterogeneity within an individual tumor mass. The introduction of the concept of cancer stem cells (CSCs)—a rare and immature subpopulation with tumorigenic potential that contributes to intratumoral heterogeneity—has deepened our understanding of drug resistance. Given the characteristics of CSCs, such as increased drug‐efflux activity, enhanced DNA‐repair capacity, high metabolic plasticity, adaptability to oxidative stress, and/or upregulated detoxifying aldehyde dehydrogenase (ALDH) enzymes, CSCs have been recognized as a theoretical reservoir for resistant diseases. Implicit in this recognition is the possibility that CSC‐targeted therapeutic strategies might offer a breakthrough in overcoming drug resistance in cancer patients. Herein, we summarize the generation of CSCs and our current understanding of the mechanisms underlying CSC‐mediated therapeutic resistance. This extended knowledge has progressively been translated into novel anticancer therapeutic strategies and significantly enriched the available options for combination treatments, all of which are anticipated to improve clinical outcomes for patients experiencing CSC‐related relapse.

MedComm – OncologyVol. 4(1)
Dalian Medical University (CN), Chengdu Medical College (CN), Sichuan University (CN), West China Hospital of Sichuan University (CN), Second Affiliated Hospital of Chongqing Medical University (CN), Ministry of Public Health (MG), First Affiliated Hospital Zhejiang University (CN), State Key Laboratory of Biotherapy, Monash University (AU), Chongqing Medical University (CN)
National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 2%
Epigenetics and DNA Methylation
9.67
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