Ribavirin as an anti-cancer therapy: acute myeloid leukemia and beyond? - PubMed (original) (raw)

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Ribavirin as an anti-cancer therapy: acute myeloid leukemia and beyond?

Katherine L B Borden et al. Leuk Lymphoma. 2010 Oct.

Abstract

Ribavirin was discovered nearly 40 years ago as a broad-spectrum antiviral drug. Recent data suggest that ribavirin may also be an effective cancer therapy. In this case, ribavirin targets an oncogene, the eukaryotic translation initiation factor eIF4E, elevated in approximately 30% of cancers including many leukemias and lymphomas. Specifically, ribavirin impedes eIF4E mediated oncogenic transformation by acting as an inhibitor of eIF4E. In a phase II clinical trial, ribavirin treatment led to substantial clinical benefit in patients with poor-prognosis acute myeloid leukemia (AML). Here molecular targeting of eIF4E correlated with clinical response. Ribavirin also targets a key enzyme in the guanosine biosynthetic pathway, inosine monophosphate dehydrogenase (IMPDH), and also modulates immunity. Parallels with known antiviral mechanisms could be informative; however, after 40 years, these are not entirely clear. The antiviral effects of ribavirin appear cell-type specific. This variation likely arises for many reasons, including cell specific variations in ribavirin metabolism as well as virus specific factors. Thus, it seems that the mechanisms for ribavirin action in cancer therapy may also vary in terms of the cancer/tissue under study. Here we review the anticancer activities of ribavirin and discuss the possible utility of incorporating ribavirin into diverse cancer therapeutic regimens.

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Figures

Figure 1

Figure 1. 3H ribavirin associates with eIF4E in living cells

A. 0.7 uM 3H ribavirin was incubated with eIF4E for 24 hours, FaDu cells were washed, crosslinked with formaldehyde (1% formaldehyde for 15 minutes), lysed and immunoprecipitated (IP) with IgG or anti-eIF4E antibody according to [66]. The ribavirin was tritiated at the 5 position of the triazole ring (Moravek Pharmaceuticals). The extent of ribavirin binding was assessed by scintillation counting. Note that IPs were washed six times prior to scintillation counting and the sixth wash (W) was also examined for 3H ribavirin content. B. Western blot analysis confirmed that eIF4E was present in the eIF4E IP but not in the IgG control. These are taken from the same cells used for scintillation counting.

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