Proteases in cancer drug delivery

• Published in: Advanced drug delivery reviews Vol. 97; pp. 144 - 155
• Main Authors: Vandooren, Jennifer, Opdenakker, Ghislain, Loadman, Paul M., Edwards, Dylan R.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.02.2016
• Subjects: Animals; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - therapeutic use; Cathepsin; Drug Delivery Systems; Legumain; Metalloproteinase; Nanoparticles; Neoplasms - drug therapy; Neoplasms - metabolism; Peptide Hydrolases - metabolism; Prodrug; Prodrugs - administration & dosage; Prodrugs - therapeutic use; Urokinase; BD; NP; Prodrug; ECM; ABP; Nanoparticles; MMP; Urokinase; Cathepsin; PEG; Legumain; Metalloproteinase; ACPP; MMPI; PAP
• ISSN: 0169-409X; 1872-8294; 1872-8294
• DOI: 10.1016/j.addr.2015.12.020

Whereas protease inhibitors have been developed successfully against hypertension and viral infections, they have failed thus far as cancer drugs. With advances in cancer profiling we now better understand that the tumor “degradome” (i.e. the repertoire of proteases and their natural inhibitors and interaction partners) forms a complex network in which specific nodes determine the global outcome of manipulation of the protease web. However, knowing which proteases are active in the tumor micro-environment, we may tackle cancers with the use of Protease-Activated Prodrugs (PAPs). Here we exemplify this concept for metallo-, cysteine and serine proteases. PAPs not only exist as small molecular adducts, containing a cleavable substrate sequence and a latent prodrug, they are presently also manufactured as various types of nanoparticles. Although the emphasis of this review is on PAPs for treatment, it is clear that protease activatable probes and nanoparticles are also powerful tools for imaging purposes, including tumor diagnosis and staging, as well as visualization of tumor imaging during microsurgical resections. [Display omitted]