| Literature DB >> 29378114 |
Pedro P G Guimarães1,2, Stephanie Gaglione1, Tomasz Sewastianik3,4, Ruben D Carrasco3,5, Robert Langer1, Michael J Mitchell2.
Abstract
The immune cytokine tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has received significant attention as a cancer therapeutic due to its ability to selectively trigger cancer cell apoptosis without causing toxicity in vivo. While TRAIL has demonstrated significant promise in preclinical studies in mice as a cancer therapeutic, challenges including poor circulation half-life, inefficient delivery to target sites, and TRAIL resistance have hindered clinical translation. Recent advances in drug delivery, materials science, and nanotechnology are now being exploited to develop next-generation nanoparticle platforms to overcome barriers to TRAIL therapeutic delivery. Here, we review the design and implementation of nanoparticles to enhance TRAIL-based cancer therapy. The platforms we discuss are diverse in their approaches to the delivery problem and provide valuable insight into guiding the design of future nanoparticle-based TRAIL cancer therapeutics to potentially enable future translation into the clinic.Entities:
Keywords: biological barriers; biomaterials; cancer therapy; drug delivery; gene therapy; immunotherapy; metastasis; nanotechnology; oncology; tumor targeting
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Year: 2018 PMID: 29378114 PMCID: PMC5834400 DOI: 10.1021/acsnano.7b05876
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881