Russell Berrie Nanotechnology Institute, Technion - Israel Institute of Technology, Haifa, 3200000, Israel; The Laboratory of Food Physical Chemistry and Biopolymeric Delivery Systems, Department of Biotechnology and Food Engineering, Technion - Israel Institute of Technology, Haifa, 3200000, Israel; The Fred Wyszkowski Cancer Research Laboratory, Department of Biology, Technion - Israel Institute of Technology, Haifa, 3200000, Israel.
Russell Berrie Nanotechnology Institute, Technion - Israel Institute of Technology, Haifa, 3200000, Israel; The Laboratory of Food Physical Chemistry and Biopolymeric Delivery Systems, Department of Biotechnology and Food Engineering, Technion - Israel Institute of Technology, Haifa, 3200000, Israel.
Drug Resist Updat. 2017 Mar;31:15-30. doi: 10.1016/j.drup.2017.05.002. Epub 2017 May 21.
Intrinsic anticancer drug resistance appearing prior to chemotherapy as well as acquired resistance due to drug treatment, remain the dominant impediments towards curative cancer therapy. Hence, novel targeted strategies to overcome cancer drug resistance constitute a key aim of cancer research. In this respect, targeted nanomedicine offers innovative therapeutic strategies to overcome the various limitations of conventional chemotherapy, enabling enhanced selectivity, early and more precise cancer diagnosis, individualized treatment as well as overcoming of drug resistance, including multidrug resistance (MDR). Delivery systems based on nanoparticles (NPs) include diverse platforms enabling a plethora of rationally designed therapeutic nanomedicines. Here we review NPs designed to enhance antitumor drug uptake and selective intracellular accumulation using strategies including passive and active targeting, stimuli-responsive drug activation or target-activated release, triggered solely in the cancer cell or in specific organelles, cutting edge theranostic multifunctional NPs delivering drug combinations for synergistic therapy, while facilitating diagnostics, and personalization of therapeutic regimens. In the current paper we review the recent findings of the past four years and discuss the advantages and limitations of the various novel NPs-based drug delivery systems. Special emphasis is put on in vivo study-based evidences supporting significant therapeutic impact in chemoresistant cancers. A future perspective is proposed for further research and development of complex targeted, multi-stage responsive nanomedical drug delivery systems for personalized cancer diagnosis and efficacious therapy.
内在的抗癌药物耐药性在化疗前出现,以及由于药物治疗而产生的获得性耐药性,仍然是治愈癌症治疗的主要障碍。因此,克服癌症药物耐药性的新靶向策略是癌症研究的一个关键目标。在这方面,靶向纳米医学为克服传统化疗的各种局限性提供了创新的治疗策略,使选择性、早期和更精确的癌症诊断、个体化治疗以及克服耐药性(包括多药耐药性)成为可能。基于纳米粒子(NPs)的递药系统包括多种平台,能够实现大量合理设计的治疗性纳米药物。在这里,我们综述了旨在通过被动和主动靶向、刺激响应性药物激活或靶向激活释放等策略来增强抗肿瘤药物摄取和选择性细胞内积累的 NPs,这些策略仅在癌细胞或特定细胞器中触发,具有最新的治疗诊断多功能 NPs,可提供联合治疗药物,同时促进诊断,并使治疗方案个性化。在本文中,我们回顾了过去四年的最新发现,并讨论了各种新型基于 NPs 的药物递药系统的优点和局限性。特别强调了支持耐药性癌症中具有显著治疗效果的基于体内研究的证据。提出了未来的研究方向,以进一步研究和开发用于个性化癌症诊断和有效治疗的复杂靶向、多阶段响应性纳米医学药物递药系统。
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