Journal
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY
Volume 12, Issue 2, Pages 148-168Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1574892812666170203151930
Keywords
Cancer; drug-conjugates; drug delivery; integrins; peptidomimetics; tumor targeting
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Funding
- Associazione Italiana per la Ricerca sul Cancro, Milan (AIRC IG) [15333]
- Fondazione I. Monzino
- MIUR (PRIN project) [20157WW5EH]
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Background: Integrins are heterodimeric cell surface receptors that mediate cell-cell and cell-extracellular matrix adhesion. These molecules play a role in processes such as cell growth and proliferation, differentiation, migration, cell trafficking, besides contributing to angiogenesis and tumor development. Given their biological role, integrins have been proposed as amenable targets in medicinal chemistry. In particular, alpha(nu)beta(3), alpha(nu)beta(5), alpha(nu)beta(6) and alpha(5)beta(1), integrins involved in tumor angiogenesis and metastasis, have been the subject of studies aimed at the discovery of novel cancer therapeutics. A large number of peptides and peptidomimetics based on the RGD (Arg-Gly-Asp) recognition sequence were developed in the past two decades as integrin ligands. Though such ligands have not been satisfactory as anti-angiogenic agents, their use as tools to achieve selective tumor targeting of anticancer drugs has been explored. Objective: In this review, we summarize recent literature and patent applications in which integrin peptidic and peptidomimetic ligands were conjugated to chemotherapeutic agents both with stable or cleavable bonds to achieve tumor targeted drug delivery. Methods: Relevant recent patents and literature in this field have been considered spanning the search from 2000 to 2016. Literature and patents were examined according to the different classes of cytotoxic drug targeted to integrins. Conclusion: In spite of the promising features of the conjugates, none of them has entered clinical trials. New efforts are focused on innovative approaches in the field such as the synthesis of new integrin ligands able to target a single integrin type or the employment of nanoparticles based drug delivery systems.
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