Cassidy Jim, Schätzlein Andreas G
Centre for Oncology and Applied Pharmacology, Cancer Research UK Beatson Laboratories, Division of Cancer Sciences and Molecular Pathology, University of Glasgow, Glasgow, G61 1BD, UK.
Expert Rev Mol Med. 2004 Sep 13;6(19):1-17. doi: 10.1017/S1462399404008269.
Delivery systems for tumour targeting fall into two basic categories: drug conjugate systems, in which individual drug molecules are chemically modified to target them directly to the tumour; and carrier-based systems, in which the drug or gene is first packaged non-covalently into a synthetic carrier that is then targeted to the tumour. In both cases, the objective is to maximise exposure of the target cells to the drug yet minimise side effects that result from nonspecific toxicity in normal tissues. The creation of such dose differentials is based on phenotypic differences between the tumour and the rest of the body. However, although a wide range of such changes have been linked to the transformation of normal cells to cancer cells, no single common feature exists to allow unambiguous targeting to the tumour. In addition, the tumour microenvironment creates physical barriers that significantly impair transport within the tumour. It is therefore important to match the delivery requirements of the drug to the capabilities of the delivery system. In this review, a brief overview is given of the underlying concepts and principles that help guide the development of such tumour-targeting strategies.
药物偶联系统,即将单个药物分子进行化学修饰,使其直接靶向肿瘤;以及基于载体的系统,即先将药物或基因非共价包装到合成载体中,然后将该载体靶向肿瘤。在这两种情况下,目标都是使靶细胞对药物的暴露最大化,同时将正常组织中非特异性毒性导致的副作用最小化。产生这种剂量差异的依据是肿瘤与身体其他部位之间的表型差异。然而,尽管多种此类变化已与正常细胞向癌细胞的转变相关联,但不存在单一的共同特征来实现对肿瘤的明确靶向。此外,肿瘤微环境会形成物理屏障,严重阻碍肿瘤内的转运。因此,将药物的递送需求与递送系统的能力相匹配非常重要。在本综述中,将简要概述有助于指导此类肿瘤靶向策略发展的基本概念和原理。