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Tanapoxvirus: From discovery towards oncolytic immunovirotherapy


1 Department of Molecular Medicine, Mayo Clinic College of Medicine, Rochester, MN; Department of Biological Sciences, Laboratory of Virology, Western Michigan University, Kalamazoo, MI, USA
2 Department of Biological Sciences, Laboratory of Virology, Western Michigan University, Kalamazoo, MI; Toni Stephenson Lymphoma Center, City of Hope, CA, USA
3 Department of Biology, Kalamazoo College, Kalamazoo, MI, USA
4 Department of Biological Sciences, Laboratory of Virology, Western Michigan University, Kalamazoo, MI, USA

Correspondence Address:
Karim Essani,
Department of Biological Sciences, Laboratory of Virology, Western Michigan University, Kalamazoo, MI 49008-5410
USA
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/jcrt.JCRT_157_18

 > Abstract 


Insufficiency of standard cancer therapeutic agents and a high degree of toxicity associated with chemotherapy and radiotherapy have created a dearth of therapeutic options for metastatic cancers. Oncolytic viruses (OVs) are an emerging therapeutic option for the treatment of various human cancers. Several OVs, including poxviruses, are currently in preclinical and clinical studies and have shown to be effective in treating metastatic cancer types. Tanapoxvirus (TANV), a member of the Poxviridae family, is being developed as an OV for different human cancers due to its desirable safety and efficacy features. TANV causes a mild self-limiting febrile disease in humans, does not spread human to human, and its large genome makes it a relatively safer OV for use in humans. TANV is relatively well characterized at both molecular and clinical levels. Some of the TANV-encoded proteins that are a part of the virus' immune evasion strategy are also characterized. TANV replicates considerably slower than vaccinia virus. TANV has been shown to replicate in different human cancer cells in vitro and regresses human tumors in a nude mouse model. TANV is currently being developed as a therapeutic option for several human cancers including breast cancer, ovarian cancer, colorectal cancer, pancreatic cancer, retinoblastoma, and melanoma. This review provides a comprehensive summary from the discovery to the development of TANV as an OV candidate for a wide array of human cancers.

Keywords: Breast cancer, colorectal cancer, melanoma, oncolytic virus, poxvirus, tanapoxvirus



How to cite this URL:
Suryawanshi YR, Zhang T, Razi F, Essani K. Tanapoxvirus: From discovery towards oncolytic immunovirotherapy. J Can Res Ther [Epub ahead of print] [cited 2019 May 19]. Available from: http://www.cancerjournal.net/preprintarticle.asp?id=244439

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