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Sci Rep. 2016 May 26;6:26786. doi: 10.1038/srep26786.

First-in-class small molecule potentiators of cancer virotherapy.

Author information

1
Departments of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada.
2
Centre for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
3
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ontario, Canada.
4
Department of Chemistry and Institute of Biochemistry, Carleton University, Ottawa, Ontario, Canada.

Abstract

The use of engineered viral strains such as gene therapy vectors and oncolytic viruses (OV) to selectively destroy cancer cells is poised to make a major impact in the clinic and revolutionize cancer therapy. In particular, several studies have shown that OV therapy is safe and well tolerated in humans and can infect a broad range of cancers. Yet in clinical studies OV therapy has highly variable response rates. The heterogeneous nature of tumors is widely accepted to be a major obstacle for OV therapeutics and highlights a need for strategies to improve viral replication efficacy. Here, we describe the development of a new class of small molecules for selectively enhancing OV replication in cancer tissue. Medicinal chemistry studies led to the identification of compounds that enhance multiple OVs and gene therapy vectors. Lead compounds increase OV growth up to 2000-fold in vitro and demonstrate remarkable selectivity for cancer cells over normal tissue ex vivo and in vivo. These small molecules also demonstrate enhanced stability with reduced electrophilicity and are highly tolerated in animals. This pharmacoviral approach expands the scope of OVs to include resistant tumors, further potentiating this transformative therapy. It is easily foreseeable that this approach can be applied to therapeutically enhance other attenuated viral vectors.

PMID:
27226390
PMCID:
PMC4880900
DOI:
10.1038/srep26786
[Indexed for MEDLINE]
Free PMC Article

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