The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences and Medical Center, University of Science & Technology of China, Hefei, Anhui 230027, PR China.
The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences and Medical Center, University of Science & Technology of China, Hefei, Anhui 230027, PR China.
Biomaterials. 2016 Jan;74:1-18. doi: 10.1016/j.biomaterials.2015.09.037. Epub 2015 Sep 28.
Circumstantial evidence suggests that most tumours are heterogeneous and contain a small population of cancer stem cells (CSCs) that exhibit distinctive self-renewal, proliferation and differentiation capabilities, which are believed to play a crucial role in tumour progression, drug resistance, recurrence and metastasis in multiple malignancies. Given that the existence of CSCs is a primary obstacle to cancer therapy, a tremendous amount of effort has been put into the development of anti-CSC strategies, and several potential approaches to kill therapeutically-resistant CSCs have been explored, including inhibiting ATP-binding cassette transporters, blocking essential signalling pathways involved in self-renewal and survival of CSCs, targeting CSCs surface markers and destroying the tumour microenvironment. Meanwhile, an increasing number of therapeutic agents (e.g. small molecule drugs, nucleic acids and antibodies) to selectively target CSCs have been screened or proposed in recent years. Drug delivery technology-based approaches hold great potential for tackling the limitations impeding clinical applications of CSC-specific agents, such as poor water solubility, short circulation time and inconsistent stability. Properly designed nanocarrier-based therapeutic agents (or nanomedicines) offer new possibilities of penetrating CSC niches and significantly increasing therapeutic drug accumulation in CSCs, which are difficult for free drug counterparts. In addition, intelligent nanomedicine holds great promise to overcome pump-mediated multidrug resistance which is driven by ATP and to decrease detrimental effects on normal somatic stem cells. In this review, we summarise the distinctive biological processes related to CSCs to highlight strategies against inherently drug-resistant CSCs. We then focus on some representative examples that give a glimpse into state-of-the-art nanomedicine approaches developed for CSCs elimination. A perspective on innovative therapeutic strategies and the potential direction of nanomedicine-based CSC therapy in the near future is also presented.
有间接证据表明,大多数肿瘤是异质性的,其中包含一小部分癌症干细胞(CSC),它们具有独特的自我更新、增殖和分化能力,被认为在多种恶性肿瘤的肿瘤进展、耐药性、复发和转移中起关键作用。鉴于 CSC 的存在是癌症治疗的主要障碍,人们已经投入大量精力开发针对 CSC 的策略,并且已经探索了几种潜在的杀死治疗耐药性 CSC 的方法,包括抑制 ATP 结合盒转运蛋白、阻断涉及 CSC 自我更新和存活的关键信号通路、针对 CSC 表面标记物以及破坏肿瘤微环境。同时,近年来,越来越多的治疗剂(例如小分子药物、核酸和抗体)被筛选或提出用于选择性靶向 CSC。基于药物递送技术的方法为解决阻碍 CSC 特异性药物临床应用的局限性提供了巨大的潜力,例如较差的水溶性、短循环时间和不一致的稳定性。适当设计的基于纳米载体的治疗剂(或纳米药物)为穿透 CSC 生态位并显著增加 CSC 中治疗药物积累提供了新的可能性,这对于游离药物难以实现。此外,智能纳米医学有望克服由 ATP 驱动的泵介导的多药耐药性,并减少对正常体细胞干细胞的有害影响。在这篇综述中,我们总结了与 CSC 相关的独特生物学过程,以突出针对固有耐药性 CSC 的策略。然后,我们重点介绍了一些有代表性的例子,这些例子让我们对为消除 CSC 而开发的最先进的纳米医学方法有了一些了解。本文还对创新治疗策略和基于纳米医学的 CSC 治疗的潜在方向进行了展望。