Targeting RGD recognizing integrins: Drug development, biomaterial research, tumor imaging and targeting

A. Meyer, J. Auernheimer, A. Modlinger, Horst Kessler

Research output: Contribution to journalReview articlepeer-review

274 Scopus citations

Abstract

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 αvβ3 integrin in order to block angiogenesis or osteoporosis, but there are also other integrins like αvβ3 and α5β1 which become more and more interesting for similar purposes. αIIbβ3 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 αvβ3 or αIIbβ3, respectively. Additionally further advances in biomaterial research are presented. We describe the coating of different implant materials with various αvβ3 recognizing ligands for the purpose of increasing cell attachment and biocompatibility.

Original languageEnglish
Pages (from-to)2723-2747
Number of pages25
JournalCurrent Pharmaceutical Design
Volume12
Issue number22
DOIs
StatePublished - Aug 2006

Keywords

  • Biomaterial
  • Drug Targeting
  • Integrin ligands
  • RGD peptides
  • Radiolabeling
  • Structure based drug design
  • Tumor imaging

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