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Nanoparticles for Immune Cytokine TRAIL-Based Cancer Therapy

Journal

ACS NANO
Volume 12, Issue 2, Pages 912-931

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.7b05876

Keywords

nanotechnology; cancer therapy; oncology; metastasis; biological barriers; drug delivery; gene therapy; immunotherapy; biomaterials; tumor targeting

Funding

  1. Fulbright Canada Killam Fellowship
  2. Cancer Center Support (core) from the National Cancer Institute [P30-CA14051]
  3. Burroughs Wellcome Fund Career Award at the Scientific Interface
  4. National Institutes of Health (NIH)
  5. Leslie Misrock Cancer Nanotechnology Postdoctoral Fellowship
  6. Koch Institute for Integrative Cancer Research at MIT
  7. Koch Institute's Marble Center for Cancer Nanomedicine
  8. Fundacao Estudar
  9. Burroughs Wellcome Fund [1015145]
  10. National Cancer Institute
  11. Max Planck Society
  12. National Institutes of Health (NIH) [F32CA200351]
  13. Dana-Farber/Harvard Cancer Center
  14. NATIONAL CANCER INSTITUTE [P30CA014051, F32CA200351] Funding Source: NIH RePORTER

Ask authors/readers for more resources

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.

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