Meyer A, Auernheimer J, Modlinger A, Kessler H
Department Chemie, Lehrstuhl II für Organische Chemie, Technische Universität München, Lichtenbergstrasse 4, 85747 Garching, Germany.
Curr Pharm Des. 2006;12(22):2723-47. doi: 10.2174/138161206777947740.
Integrins constitute an important class of cell adhesion receptors responsible not only for cell-matrix adhesion but also for signaling bidirectionally across the membrane. Integrins are involved in many biological processes such as angiogenesis, thrombosis, inflammation, osteoporosis and cancer. Integrins thus play a key role in many severe human diseases. In this review we will describe recent research and development of RGD-containing integrin ligands for medical applications including drug design, radiolabeling, drug targeting, as well as biomaterial research. Many ligands have been developed for targeting the avb3 integrin in order to block angiogenesis or osteoporosis, but there are also other integrins like avb5 and a5b1 which become more and more interesting for similar purposes. aIIbb3 constitutes a potent target in thrombosis therapy; but the search for suitable ligands is still ongoing. We will reconstruct the drug development process for these integrin subtypes considering selected examples with focus on structure based design. Different structural requirements are pointed out concerning integrin activity and particularly the selectivity towards the distinct integrin types. Furthermore, we will show recent progress in tumor and thrombosis imaging based on radiolabeled RGD-containing ligands binding avb3 or aIIbb3, respectively. Additionally further advances in biomaterial research are presented. We describe the coating of different implant materials with various avb3 recognizing ligands for the purpose of increasing cell attachment and biocompatibility.
整合素是一类重要的细胞黏附受体,不仅负责细胞与基质的黏附,还能在细胞膜两侧进行双向信号传导。整合素参与许多生物过程,如血管生成、血栓形成、炎症、骨质疏松和癌症。因此,整合素在许多严重的人类疾病中起着关键作用。在这篇综述中,我们将描述含RGD的整合素配体在医学应用方面的最新研究进展,包括药物设计、放射性标记、药物靶向以及生物材料研究。为了阻断血管生成或骨质疏松,已经开发了许多靶向αvβ3整合素的配体,但还有其他整合素,如αvβ5和α5β1,也因类似目的而变得越来越受关注。αIIbβ3是血栓形成治疗中的一个有效靶点;但寻找合适配体的工作仍在进行中。我们将以基于结构的设计为例,重建这些整合素亚型的药物开发过程。指出了关于整合素活性特别是对不同整合素类型选择性的不同结构要求。此外,我们将展示基于分别与αvβ3或αIIbβ3结合的放射性标记含RGD配体的肿瘤和血栓成像的最新进展。此外,还介绍了生物材料研究的进一步进展。我们描述了用各种识别αvβ3的配体对不同植入材料进行涂层,以增加细胞附着和生物相容性。