Alessi Patrizia, Ebbinghaus Christina, Neri Dario
Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology Zurich, Building 36 M14, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Biochim Biophys Acta. 2004 Mar 4;1654(1):39-49. doi: 10.1016/j.bbcan.2003.08.001.
The majority of pharmacological approaches for the treatment of solid tumors suffer from poor selectivity, thus limiting dose escalation (i.e., the doses of drug which are required to kill tumor cells cause unacceptable toxicities to normal tissues). The situation is made more dramatic by the fact that the majority of anticancer drugs accumulate preferentially in normal tissues rather than in neoplastic sites, due to the irregular vasculature and to the high interstitial pressure of solid tumors. One avenue towards the development of more efficacious and better tolerated anti-cancer drugs relies on the targeted delivery of therapeutic agents to the tumor environment, thus sparing normal tissues. Molecular markers which are selectively expressed in the stroma and in neo-vascular sites of aggressive solid tumors appear to be particularly suited for ligand-based tumor targeting strategies. Tumor blood vessels are accessible to agents coming from the bloodstream, and their occlusion may result in an avalanche of tumor cell death. Furthermore, endothelial cells and stromal cells are genetically more stable than tumor cells and can produce abundant markers, which are ideally suited for tumor targeting strategies. This review focuses on recent advances in the development of ligands for the selective targeting of tumor blood vessels and new blood vessels in other angiogenesis-related diseases.
大多数用于治疗实体瘤的药理学方法都存在选择性差的问题,从而限制了剂量的增加(即杀死肿瘤细胞所需的药物剂量会对正常组织造成不可接受的毒性)。由于实体瘤的血管不规则以及间质压力高,大多数抗癌药物优先在正常组织而非肿瘤部位蓄积,这使得情况更加严峻。开发更有效且耐受性更好的抗癌药物的一个途径是将治疗剂靶向递送至肿瘤环境,从而使正常组织免受影响。在侵袭性实体瘤的基质和新生血管部位选择性表达的分子标志物似乎特别适合基于配体的肿瘤靶向策略。来自血流的药物可以作用于肿瘤血管,阻断这些血管可能导致大量肿瘤细胞死亡。此外,内皮细胞和基质细胞在基因上比肿瘤细胞更稳定,并且可以产生丰富的标志物,这非常适合肿瘤靶向策略。本综述重点关注用于选择性靶向肿瘤血管以及其他血管生成相关疾病中的新生血管的配体开发的最新进展。