Dass Crispin R, Choong Peter F M
Departments of Orthopaedics and Surgery, University of Melbourne, St. Vincent's Hospital, Melbourne, Australia.
J Microencapsul. 2008 Jun;25(4):275-9. doi: 10.1080/02652040801970461.
With the advent of the theranostics era in biomedical research, gene therapy is poised to offer more, provided that more efficient delivery vehicles are discovered and developed. Chitosan is a biomatrix that is abundant, biocompatible, biodegradable, versatile, inexpensive and safe. These features have paved the way for its use in gene therapy, mainly for delivery of therapeutic plasmids and more recently for siRNA. Recent studies show that chitosan per se exhibits anticancer properties both in vitro and in animal models, most probably through the p21/Cip and p27/Kip pathways. This review looks at the in vivo studies using chitosan technology towards cancer gene therapy, drawing some support from non-cancer studies. The future of this promising technology lies in the evolution of new ideas for enhanced nucleic acid drug pharmacokinetics and, consequently, pharmacodynamics for cancer patients.
随着生物医学研究中治疗诊断学时代的到来,只要能发现并开发出更高效的递送载体,基因治疗有望带来更多成果。壳聚糖是一种生物基质,它储量丰富、具有生物相容性、可生物降解、用途广泛、价格低廉且安全。这些特性为其在基因治疗中的应用铺平了道路,主要用于递送治疗性质粒,最近也用于递送小干扰RNA(siRNA)。最近的研究表明,壳聚糖本身在体外和动物模型中均表现出抗癌特性,很可能是通过p21/Cip和p27/Kip途径实现的。本综述着眼于利用壳聚糖技术进行癌症基因治疗的体内研究,并从非癌症研究中获得了一些支持。这项前景广阔的技术的未来在于不断演进新的思路,以增强核酸药物的药代动力学,进而改善癌症患者的药效学。