Use of cell fusion proteins to enhance adenoviral vector efficacy as an anti-cancer therapeutic.
Joshua Del PapaRyan G ClarkinRobin J ParksPublished in: Cancer gene therapy (2020)
Oncolytic viruses are designed to replicate in and kill cancer cells, and have shown tremendous promise in preclinical and clinical studies. Indeed, several oncolytic viruses are available to patients in a number of different countries around the world. However, most oncolytic viruses show a poor ability to spread throughout the tumor mass, frequently leading to only a partial response and regrowth of the tumor. One approach to improve spread of the viral effect throughout the tumor mass is to arm the oncolytic virus with a fusogenic protein. In this manner, a single infected cell can fuse with many adjacent uninfected cells, essentially amplifying the anti-tumor effects. In this review, we discuss the development and use of fusogenic proteins to enhance the efficacy of human adenovirus-based vectors for cancer therapy.
Keyphrases
- end stage renal disease
- cancer therapy
- cell therapy
- single cell
- chronic kidney disease
- endothelial cells
- ejection fraction
- newly diagnosed
- induced apoptosis
- hiv infected
- sars cov
- peritoneal dialysis
- prognostic factors
- stem cells
- machine learning
- bone marrow
- big data
- mesenchymal stem cells
- oxidative stress
- protein protein
- small molecule
- deep learning
- cell cycle arrest
- genetic diversity
- cell proliferation
- artificial intelligence
- endoplasmic reticulum stress