Abstract / Description of output
The ability to target specific cell types to achieve optimal distribution of therapeutic entities into diseased tissues, while limiting possible adverse off-target effects, has long been a goal of many research groups and pharmaceutical organizations. This review focuses on peptidic tissue-specific biomarkers that allow peptides to act as homing devices for specific tissue types or organs, with a focus on homing peptides (HPs) and cell-penetrating homing peptides (CPHPs). These HPs, in addition to promoting cellular uptake, can deliver a variety of cargos (drugs, oligonucleotides and nanoparticles) into cells. Two such peptides that have entered clinical trials are the tumor-homing peptide asparagine-glycine-arginine (NGR) (fused to human tumor necrosis factor), which selectively binds CD13, an aminopeptidase that is overexpressed on tumor blood vessels, and cyclo[Arg-Gly-Asp-D-Phe-(NMeVal)] (cRGD, cilengitide), an anti-angiogenic agent that targets the alpha(v)beta(3) and alpha(v)beta(5) integrins.
Original language | English |
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Pages (from-to) | 186-192 |
Number of pages | 7 |
Journal | Trends in Pharmacological Sciences |
Volume | 33 |
Issue number | 4 |
Early online date | 15 Mar 2012 |
DOIs | |
Publication status | Published - Apr 2012 |
Keywords / Materials (for Non-textual outputs)
- HUMAN IMMUNODEFICIENCY VIRUS
- ADVANCED SOLID TUMORS
- VIVO PHAGE DISPLAY
- IN-VIVO
- PENETRATING PEPTIDE
- PHASE-II
- ENDOTHELIAL-CELLS
- HOMING PEPTIDE
- PHENOTYPIC HETEROGENEITY
- GLIOBLASTOMA-MULTIFORME