Department of Nanoengineering and Moores Cancer Center, University of California San Diego, La Jolla, 92093, USA.
Curr Drug Metab. 2009 Oct;10(8):836-41. doi: 10.2174/138920009790274540.
This review focuses on the application of drug-loaded nanoparticles (NPs), also called therapeutic NPs, to combat cancer chemoresistance. Many cancer patients have encouraging response to first line chemotherapies but end up with cancer progression or cancer recurrence that requires further treatment. Response to subsequent chemotherapies with various agents usually drops significantly due to formidable cancer chemoresistance. A number of mechanisms have been postulated to account for cancer chemoresistance or poor response to chemotherapy. The best studied mechanism of resistance is mediated through the alteration in the drug efflux proteins responsible for the removal of many commonly used anticancer drugs. Therapeutic NPs have emerged as an innovative and promising alternative of the conventional small molecule chemotherapies to combat cancer drug resistance and have shown enhanced therapeutic efficacy and reduced adverse side effects as compared to their small molecule counterparts. Here the possible mechanisms of therapeutic NPs to combat cancer chemoresistance are reviewed, including prolonging drug systemic circulation lifetime, targeted drug delivery, stimuli-responsive drug release, endocytic uptake of drugs and co-delivering chemo-sensitizing agents. We also call attention to the current challenges and needs of developing therapeutic NPs to combat cancer drug resistance.
这篇综述专注于载药纳米颗粒(NPs),也称为治疗性 NPs,在克服癌症化疗耐药性方面的应用。许多癌症患者对一线化疗有令人鼓舞的反应,但最终癌症进展或复发需要进一步治疗。由于癌症化疗耐药性,许多不同药物的后续化疗反应通常显著下降。已经提出了许多机制来解释癌症耐药性或对化疗反应不佳的原因。研究最多的耐药机制是通过改变负责清除许多常用抗癌药物的药物外排蛋白来介导的。治疗性 NPs 已成为对抗癌症药物耐药性的常规小分子化疗的一种创新和有前途的替代方法,与小分子相比,它们显示出增强的治疗效果和降低的不良反应。本文综述了治疗性 NPs 克服癌症化疗耐药性的可能机制,包括延长药物系统循环寿命、靶向药物递送、刺激响应性药物释放、内吞摄取药物和共递送化疗增敏剂。我们还提请注意开发治疗性 NPs 以对抗癌症药物耐药性所面临的当前挑战和需求。