Schätzlein Andreas G
CRUK Centre for Oncology and Applied Pharmacology, Cancer Research UK Beatson Laboratories, University of Glasgow, Garscube Estate, Switchback Road, Bearsden, Glasgow G61 1BD, UK.
Eur J Cancer. 2006 Jun;42(9):1309-15. doi: 10.1016/j.ejca.2006.01.044. Epub 2006 May 8.
Cancer stem cells (CSCs), i.e. cancer cells that can self-renew, constitute only a minority of the cells of a tumour, but, because of their ability to initiate and repopulate tumours, failure to control CSCs can potentially lead to tumour re-growth, even though the bulk tumour may have been treated successfully. Nanomedicines improve spatio-temporal control over drug kinetics and distribution, thus opening the prospect of safer and more specific therapies to address the challenges posed by CSCs. In particular, these systems have the potential to facilitate CSC-aware therapy by overcoming resistance to conventional cytotoxic drugs and by targeting novel therapies to the tumour and CSC-marker positive cells. This review examines the implications of the CSC paradigm specifically for the development of nanomedicines, i.e. therapies based on macromolecules or supramolecular aggregates.
癌症干细胞(CSCs),即能够自我更新的癌细胞,仅占肿瘤细胞的少数,但由于它们启动和重新填充肿瘤的能力,即使大部分肿瘤可能已得到成功治疗,未能控制癌症干细胞仍可能导致肿瘤复发。纳米药物改善了对药物动力学和分布的时空控制,从而为应对癌症干细胞带来的挑战开辟了更安全、更具特异性治疗方法的前景。特别是,这些系统有可能通过克服对传统细胞毒性药物的耐药性以及将新型疗法靶向肿瘤和癌症干细胞标志物阳性细胞,来促进针对癌症干细胞的治疗。本综述专门探讨了癌症干细胞范式对纳米药物开发的影响,即基于大分子或超分子聚集体的疗法。