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Unveiling the future of cancer stem cell therapy: a narrative exploration of emerging innovations.

作者信息

Obisi Joseph Nhyira, Abimbola Abike Ndidiamaka Josephine, Babaleye Oluwasegun Adesina, Atidoglo Peter Kwame, Usin Saviour God'swealth, Nwanaforo Eudora Obioma, Patrick-Inezi Faith Sutu, Fasogbon Ilemobayo Victor, Chimezie Joseph, Dare Christianah Adebimpe, Kuti Oluwadoyinsayemi Oluwadamilare, Uti Daniel Ejim, Omeoga Humphrey Chukwudi

机构信息

Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Department of Environmental Chemistry, University of Ibadan, Ibadan, Nigeria.

出版信息

Discov Oncol. 2025 Mar 22;16(1):373. doi: 10.1007/s12672-025-02102-4.


DOI:10.1007/s12672-025-02102-4
PMID:40120008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11929669/
Abstract

Cancer stem cells (CSCs), are a critical subpopulation within tumours, and are defined by their capacity for self-renewal, differentiation, and tumour initiation. These unique traits contribute to tumour progression, metastasis, and resistance to conventional treatments like chemotherapy and radiotherapy, often resulting in cancer recurrence and poor patient outcomes. As such, CSCs have become focal points in developing advanced cancer therapies. This review highlights progress in CSC-targeted treatments, including chimeric antigen receptor T-cell (CAR-T) therapy, immunotherapy, molecular targeting, and nanoparticle-based drug delivery systems. Plant-derived compounds and gene-editing technologies, such as clustered regularly interspaced short palindromic repeats (CRISPR), are explored for their potential to enhance precision and minimize side effects. Metabolic pathways integral to CSC survival, such as mitochondrial dynamics, mitophagy (regulated by dynamin-related protein 1 [DRP1] and the PINK1/Parkin pathway), one-carbon metabolism, amino acid metabolism (involving enzymes like glutaminase (GLS) and glutamate dehydrogenase (GDH]), lipid metabolism, and hypoxia-induced metabolic reprogramming mediated by hypoxia-inducible factors (HIF-1α and HIF-2α), are examined as therapeutic targets. The adaptability of CSCs through autophagy, metabolic flexibility, and epigenetic regulation by metabolites like α-ketoglutarate, succinate, and fumarate is discussed. Additionally, extracellular vesicles and nicotinamide adenine dinucleotide (NAD⁺) metabolism are identified as pivotal in redox balance, DNA repair, and epigenetic modifications. Addressing challenges such as tumour heterogeneity, immune evasion, and treatment durability requires interdisciplinary collaboration. Advancing CSC-targeted therapies is essential for overcoming drug resistance and preventing cancer relapse, paving the way for transformative cancer treatments. This review underscores the importance of leveraging innovative technologies and fostering collaboration to revolutionize cancer treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/2f0d4195db8b/12672_2025_2102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/f588a6769f26/12672_2025_2102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/7a266fce3605/12672_2025_2102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/6f2018fa0f82/12672_2025_2102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/6ca634a85ac6/12672_2025_2102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/2f0d4195db8b/12672_2025_2102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/f588a6769f26/12672_2025_2102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/7a266fce3605/12672_2025_2102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/6f2018fa0f82/12672_2025_2102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/6ca634a85ac6/12672_2025_2102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/2f0d4195db8b/12672_2025_2102_Fig5_HTML.jpg

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[1]
Unveiling the future of cancer stem cell therapy: a narrative exploration of emerging innovations.

Discov Oncol. 2025-3-22

[2]
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[3]
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引用本文的文献

[1]
Epitranscriptomic alterations induced by environmental toxins: implications for RNA modifications and disease.

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本文引用的文献

[1]
Eicosapentaenoic acid enhances intestinal stem cell-mediated colonic epithelial regeneration by activating the LSD1-WNT signaling pathway.

J Adv Res. 2024-12-30

[2]
Revisiting immune checkpoint inhibitors: new strategies to enhance efficacy and reduce toxicity.

Front Immunol. 2024-12-10

[3]
Types of cell death in diabetic cardiomyopathy: insights from animal models.

Acta Biochim Biophys Sin (Shanghai). 2024-12-25

[4]
Comprehensive review of drug resistance in mammalian cancer stem cells: implications for cancer therapy.

Cancer Cell Int. 2024-12-18

[5]
Metabolic reprogramming, sensing, and cancer therapy.

Cell Rep. 2024-12-24

[6]
Exosome crosstalk between cancer stem cells and tumor microenvironment: cancer progression and therapeutic strategies.

Stem Cell Res Ther. 2024-11-22

[7]
Utilizing Indigenous Flora in East Africa for Breast Cancer Treatment: An Overview.

Anticancer Agents Med Chem. 2025

[8]
Biological Functions and Therapeutic Potential of NAD Metabolism in Gynecological Cancers.

Cancers (Basel). 2024-9-5

[9]
Defining and modeling dynamic spatial heterogeneity within tumor microenvironments.

Curr Opin Cell Biol. 2024-10

[10]
Role of Autophagy and AMPK in Cancer Stem Cells: Therapeutic Opportunities and Obstacles in Cancer.

Int J Mol Sci. 2024-8-8

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