Lectins play diverse roles in physiological processes as biological recognition molecules. In this report, a gene encoding Lectin (TTL) was inserted into an oncolytic vaccinia virus (oncoVV) vector to form oncoVV-TTL, which showed significant antitumor activity in a hepatocellular carcinoma mouse model. Furthermore, TTL enhanced oncoVV replication through suppressing antiviral factors expression such as interferon-inducible protein 16 (IFI16), mitochondrial antiviral signaling protein (MAVS) and interferon-beta (IFN-β). Further investigations revealed that oncoVV-TTL replication was highly dependent on ERK activity. This study might provide insights into a novel way of the utilization of TTL in oncolytic viral therapies.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025575 | PMC |
http://dx.doi.org/10.3390/md16060200 | DOI Listing |
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