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揭示癌症干细胞治疗的未来:对新兴创新的叙事性探索。

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.

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

癌症干细胞(CSCs)是肿瘤内的一个关键亚群,其定义为具有自我更新、分化和引发肿瘤的能力。这些独特特性促成肿瘤进展、转移以及对化疗和放疗等传统治疗的抗性,常常导致癌症复发和患者预后不良。因此,癌症干细胞已成为开发先进癌症疗法的焦点。本综述重点介绍了针对癌症干细胞的治疗进展,包括嵌合抗原受体T细胞(CAR-T)疗法、免疫疗法、分子靶向以及基于纳米颗粒的药物递送系统。探讨了植物源化合物和基因编辑技术,如成簇规律间隔短回文重复序列(CRISPR),因其具有提高精准度和最小化副作用的潜力。研究了对癌症干细胞存活至关重要的代谢途径,如线粒体动力学、线粒体自噬(由动力相关蛋白1 [DRP1]和PINK1/Parkin途径调节)、一碳代谢、氨基酸代谢(涉及谷氨酰胺酶[GLS]和谷氨酸脱氢酶[GDH]等酶)、脂质代谢以及由缺氧诱导因子(HIF-1α和HIF-2α)介导的缺氧诱导的代谢重编程,将其作为治疗靶点。讨论了癌症干细胞通过自噬、代谢灵活性以及由α-酮戊二酸、琥珀酸和富马酸等代谢物进行的表观遗传调控的适应性。此外,细胞外囊泡和烟酰胺腺嘌呤二核苷酸(NAD⁺)代谢被确定在氧化还原平衡、DNA修复和表观遗传修饰中起关键作用。应对肿瘤异质性、免疫逃逸和治疗持久性等挑战需要跨学科合作。推进针对癌症干细胞的疗法对于克服耐药性和预防癌症复发至关重要,为变革性癌症治疗铺平道路。本综述强调了利用创新技术和促进合作以彻底改变癌症治疗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c1/11929669/f588a6769f26/12672_2025_2102_Fig1_HTML.jpg

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