Review
Copyright ©The Author(s) 2021.
World J Virol. Sep 25, 2021; 10(5): 229-255
Published online Sep 25, 2021. doi: 10.5501/wjv.v10.i5.229
Table 1 Genetic modifications in the adenovirus
Ref.
Virus
Updates
Aim
Rojas et al[219]COVIR -7/-15Insertion of E2F-binding sites in the gene E1ASpecific targeting to the tumor cells, which express E2F and increase viral replication rate and antitumor action
Sarkar et al[220]CTV-m 7Insertion of the transgene MDA-7/IL-24Expression of the protein MDA-7/IL-24 increases the cytotoxic action in the tumor sites and lyse the metastatic cells. The studies have shown greater effectiveness in the therapy of prostate cancer
Sarkar et al[220]tCCN1 -CTV - m 7Replacement of E1A by tCCN1Specific targeting and cytotoxicity against the tumor cells, which express the promoter tCCN1 in prostate cancer
Choi et al[221]Ads armed with inhibitors of tumoral angiogenesisIncorporation of the gene FP3 Increase of the antiangiogenic capacity, which decreases the vascular endothelial growth factor production and suppresses the rate of tumor growth
Lucas et al[222]Ad5 armed with the peptide CKS17Replacement of HVR5 by the peptide CKS17Specific target to the TGFBRII in the liver cancer cells, increasing the viral cytotoxic action and decreasing the liver sequestration
Garofalo et al[223]AdV-D24-ICOSL-CD40LInsertion of D24, ICOSL and CD40 genes in the chimeric virus, AdV-D24, serotype 5/3Selectivity to infect the cancer cells through DSG-2 receptor and stimulation of the immune system by ICOSL and ICOS, both contributing to the immunogenic cell death in melanoma
Vera et al[224]VCN-01Selectivity to the pRB pathway and ability to express hyaluronidaseSpecific viral replication, decreasing the side effects and degradation of the extracellular matrix by the enzyme hyaluronidase in solid tumors
Yang et al[225]Ad5/3-CXCR4-TIMP2Replacing Ad5 knob with Ad3 knob and incorporating the gene TIMP2Selective replication in the cancer cells, which reduces the action over the normal cells and the expression of inhibitors of metalloproteinases, contributing to the degradation and remodeling of the extracellular matrix, preventing tumor growth and metastasis