Hadiloo Kaveh, Mostanadi Parsa, Asadzadeh Ali, Taremi Siavash, Esmaeilzadeh Abdolreza
Department of Surgery, Velayat Clinical Research Development Unit, Qazvin University of Medical Sciences, Qazvin, Iran.
Student Research Committee, Department of Immunology, Zanjan University of Medical Science, Zanjan, Iran.
Cancer Cell Int. 2025 Jul 28;25(1):289. doi: 10.1186/s12935-025-03846-3.
Cancer stem cells (CSCs) are pivotal in tumor initiation, progression, and relapse, underscoring the need for targeted therapies to achieve lasting responses. This review delves into CSC biology, highlighting their tumor-initiating potential demonstrated through limiting dilution assays and their role in resistance to therapies. Although successful CAR therapies, such as anti-CD19 CAR T-cells, can induce complete responses without directly targeting CSCs, CAR strategies focusing on CSCs may offer promising avenues to prevent recurrence. We assess CAR therapies targeting CSC-specific antigens, including CD133 and GD2, in preclinical and clinical contexts, emphasizing their effectiveness against glioblastoma, breast cancer, and other malignancies. Nevertheless, challenges such as marker specificity and suppression by the tumor microenvironment (TME) persist. Future strategies, which may include dual-targeting and AI-driven marker discovery, aim to improve CSC elimination and advance personalized cancer immunotherapy.
癌症干细胞(CSCs)在肿瘤的起始、进展和复发中起着关键作用,这凸显了采用靶向疗法以实现持久疗效的必要性。本综述深入探讨了癌症干细胞生物学,强调了通过有限稀释分析所证明的它们的肿瘤起始潜能以及它们在治疗抗性中的作用。尽管成功的嵌合抗原受体(CAR)疗法,如抗CD19 CAR T细胞,可以在不直接靶向癌症干细胞的情况下诱导完全缓解,但专注于癌症干细胞的CAR策略可能为预防复发提供有前景的途径。我们评估了在临床前和临床环境中靶向癌症干细胞特异性抗原(包括CD133和GD2)的CAR疗法,强调了它们对胶质母细胞瘤、乳腺癌和其他恶性肿瘤的有效性。然而,诸如标志物特异性和肿瘤微环境(TME)抑制等挑战仍然存在。未来的策略,可能包括双靶点治疗和人工智能驱动的标志物发现,旨在改善癌症干细胞的清除并推进个性化癌症免疫治疗。