Novel Target Molecules Research Group, Department of Biotechnology and Molecular Medicine, A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Integr Biol (Camb). 2010 Aug;2(7-8):326-37. doi: 10.1039/c0ib00013b. Epub 2010 Jul 26.
Each normal organ and pathological condition appear to contain organ- or disease-specific molecular tags on its vasculature, which constitute a vascular "zip code" system. In vivo phage display has been exploited to profile this vascular heterogeneity and a number of peptides that home specifically to various normal organs or pathological conditions have been identified. These peptides have been used for targeted delivery of oligonucleotides, drugs, imaging agents, inorganic nanoparticles, liposomes, and viruses. Identification of the receptor molecules for the homing peptides has revealed novel biomarkers for target organs. In tumors many of these receptors seem to play a functional role in tumor angiogenesis. Recently, tumor homing peptides have entered clinical trials. Results from several Phase I and II trials have been reported, and a number of trials are currently ongoing or recruiting patients. In these trials no dose-limiting toxicity has occurred and all combinations of peptide-targeted therapies have been well tolerated.
每个正常器官和病理状况似乎在其血管中都含有器官或疾病特异性的分子标记,这些标记构成了一个血管“邮政编码”系统。体内噬菌体展示技术被用来描述这种血管异质性,已经鉴定出了许多专门针对各种正常器官或病理状况的肽。这些肽已被用于靶向递送寡核苷酸、药物、成像剂、无机纳米粒子、脂质体和病毒。对归巢肽的受体分子的鉴定揭示了靶器官的新型生物标志物。在肿瘤中,这些受体中的许多似乎在肿瘤血管生成中发挥功能作用。最近,肿瘤归巢肽已进入临床试验。已经报道了几项 I 期和 II 期试验的结果,并且目前正在进行或招募患者的多项试验。在这些试验中,没有发生剂量限制毒性,并且所有肽靶向治疗的组合都耐受良好。