TY - JOUR
T1 - RNA viruses as virotherapy agents
AU - Russell, Stephen J.
N1 - Funding Information:
This work was supported by the Harold W Siebens Foundation, the George W Eisenberg Foundation, and NIH Grants PO1 HL66958-02 and RO1 CA83181-03. We would also like to thank Maureen Craft for her secretarial support.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - RNA viruses are rapidly emerging as extraordinarily promising agents for oncolytic virotherapy. Integral to the lifecycles of all RNA viruses is the formation of double-stranded RNA, which activates a spectrum of cellular defense mechanisms including the activation of PKR and the release of interferon. Tumors are frequently defective in their PKR signaling and interferon response pathways, and therefore provide a relatively permissive substrate for the propagation of RNA viruses. For most of the oncolytic RNA viruses currently under study, tumor specificity is either a natural characteristic of the virus, or a serendipitous consequence of adapting the virus to propagate in human tumor cell lines. Further refinement and optimization of these oncolytic agents can be achieved through virus engineering. This article provides a summary of the current status of oncolytic virotherapy efforts for seven different RNA viruses, namely, mumps, Newcastle disease virus, measles virus, vesicular stomatitis virus, influenza, reovirus, and poliovirus.
AB - RNA viruses are rapidly emerging as extraordinarily promising agents for oncolytic virotherapy. Integral to the lifecycles of all RNA viruses is the formation of double-stranded RNA, which activates a spectrum of cellular defense mechanisms including the activation of PKR and the release of interferon. Tumors are frequently defective in their PKR signaling and interferon response pathways, and therefore provide a relatively permissive substrate for the propagation of RNA viruses. For most of the oncolytic RNA viruses currently under study, tumor specificity is either a natural characteristic of the virus, or a serendipitous consequence of adapting the virus to propagate in human tumor cell lines. Further refinement and optimization of these oncolytic agents can be achieved through virus engineering. This article provides a summary of the current status of oncolytic virotherapy efforts for seven different RNA viruses, namely, mumps, Newcastle disease virus, measles virus, vesicular stomatitis virus, influenza, reovirus, and poliovirus.
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U2 - 10.1038/sj.cgt.7700535
DO - 10.1038/sj.cgt.7700535
M3 - Review article
C2 - 12522435
AN - SCOPUS:0036905014
SN - 0929-1903
VL - 9
SP - 961
EP - 966
JO - Cancer Gene Therapy
JF - Cancer Gene Therapy
IS - 12
ER -