Lee Haksoo, Kim Byeongsoo, Park Junhyeong, Park Sujin, Yoo Gaeun, Yum Soomin, Kang Wooseok, Lee Jae-Myung, Youn HyeSook, Youn BuHyun
Department of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Institute for Future Earth, Pusan National University, Busan, Republic of Korea.
Signal Transduct Target Ther. 2025 Aug 5;10(1):248. doi: 10.1038/s41392-025-02360-2.
Cancer stem cells (CSCs) constitute a highly plastic and therapy-resistant cell subpopulation within tumors that drives tumor initiation, progression, metastasis, and relapse. Their ability to evade conventional treatments, adapt to metabolic stress, and interact with the tumor microenvironment makes them critical targets for innovative therapeutic strategies. Recent advances in single-cell sequencing, spatial transcriptomics, and multiomics integration have significantly improved our understanding of CSC heterogeneity and metabolic adaptability. Metabolic plasticity allows CSCs to switch between glycolysis, oxidative phosphorylation, and alternative fuel sources such as glutamine and fatty acids, enabling them to survive under diverse environmental conditions. Moreover, interactions with stromal cells, immune components, and vascular endothelial cells facilitate metabolic symbiosis, further promoting CSC survival and drug resistance. Despite substantial progress, major hurdles remain, including the lack of universally reliable CSC biomarkers and the challenge of targeting CSCs without affecting normal stem cells. The development of 3D organoid models, CRISPR-based functional screens, and AI-driven multiomics analysis is paving the way for precision-targeted CSC therapies. Emerging strategies such as dual metabolic inhibition, synthetic biology-based interventions, and immune-based approaches hold promise for overcoming CSC-mediated therapy resistance. Moving forward, an integrative approach combining metabolic reprogramming, immunomodulation, and targeted inhibition of CSC vulnerabilities is essential for developing effective CSC-directed therapies. This review discusses the latest advancements in CSC biology, highlights key challenges, and explores future perspectives on translating these findings into clinical applications.
癌症干细胞(CSCs)是肿瘤内高度可塑性且具有治疗抗性的细胞亚群,驱动肿瘤的起始、进展、转移和复发。它们逃避传统治疗、适应代谢应激以及与肿瘤微环境相互作用的能力,使其成为创新治疗策略的关键靶点。单细胞测序、空间转录组学和多组学整合的最新进展显著提高了我们对CSC异质性和代谢适应性的理解。代谢可塑性使CSCs能够在糖酵解、氧化磷酸化以及谷氨酰胺和脂肪酸等替代燃料来源之间切换,使其能够在不同的环境条件下存活。此外,与基质细胞、免疫成分和血管内皮细胞的相互作用促进了代谢共生,进一步促进了CSC的存活和耐药性。尽管取得了重大进展,但主要障碍仍然存在,包括缺乏普遍可靠的CSC生物标志物以及在不影响正常干细胞的情况下靶向CSCs的挑战。三维类器官模型、基于CRISPR的功能筛选和人工智能驱动的多组学分析的发展为精准靶向CSC治疗铺平了道路。双重代谢抑制、基于合成生物学的干预措施和基于免疫的方法等新兴策略有望克服CSC介导的治疗抗性。展望未来,将代谢重编程、免疫调节和靶向抑制CSC脆弱性相结合的综合方法对于开发有效的CSC定向治疗至关重要。本综述讨论了CSC生物学的最新进展,强调了关键挑战,并探讨了将这些发现转化为临床应用的未来前景。