Integrins are cell adhesion receptors overexpressed in tumor cells. A direct inhibition of integrins was investigated, but the best inhibitors performed poorly in clinical trials. A gained attention towards these receptors arouse because they could be target for a selective transport of cytotoxic agents. Several active-targeting systems have been developed to use integrins as a selective cell entrance for some antitumor agents. The aim of this review paper is to report on the most recent results on covalent conjugates between integrin ligands and antitumor drugs. Cytotoxic drugs thus conjugated through specific linker to integrin ligands, mainly RGD peptides, demonstrated that the covalent conjugates were more selective against tumor cells and hopefully with fewer side effects than the free drugs.

Cirillo M., Giacomini D. (2021). Molecular delivery of cytotoxic agents via integrin activation. CANCERS, 13(2), 1-25 [10.3390/cancers13020299].

Molecular delivery of cytotoxic agents via integrin activation

Cirillo M.
Primo
Writing – Review & Editing
;
Giacomini D.
Ultimo
Writing – Original Draft Preparation
2021

Abstract

Integrins are cell adhesion receptors overexpressed in tumor cells. A direct inhibition of integrins was investigated, but the best inhibitors performed poorly in clinical trials. A gained attention towards these receptors arouse because they could be target for a selective transport of cytotoxic agents. Several active-targeting systems have been developed to use integrins as a selective cell entrance for some antitumor agents. The aim of this review paper is to report on the most recent results on covalent conjugates between integrin ligands and antitumor drugs. Cytotoxic drugs thus conjugated through specific linker to integrin ligands, mainly RGD peptides, demonstrated that the covalent conjugates were more selective against tumor cells and hopefully with fewer side effects than the free drugs.
2021
Cirillo M., Giacomini D. (2021). Molecular delivery of cytotoxic agents via integrin activation. CANCERS, 13(2), 1-25 [10.3390/cancers13020299].
Cirillo M.; Giacomini D.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/806245
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