Myxoma virus and oncolytic virotherapy: a new biologic weapon in the war against cancer

被引:60
作者
Stanford, Marianne M.
McFadden, Grant [1 ]
机构
[1] Univ Florida, Dept Mol Genet & Microbiol, Gainesville, FL 32610 USA
[2] Univ Western Ontario, Dept Microbiol & Immunol, Biotherapeut Res Grp, Robarts Res Inst, London, ON N6G 2V4, Canada
关键词
Akt; mTOR; oncolysis; poxvirus; rapamycin; virotherapy;
D O I
10.1517/14712598.7.9.1415
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Oncolytic virotherapy is an innovative alternative to more conventional cancer therapies. The ability of some viruses to specifically target and kill malignant cancerous cells while leaving normal tissue unscathed has opened a large repertoire of new and selective cancer killing therapeutic candidates. Poxviruses, such as vaccinia virus, have a long history of use in humans as live vaccines and have more recently been studied as potential platforms for delivery of immunotherapeutics and attenuated variants of vaccinia have been explored as oncolytic candidates. In contrast, the poxvirus myxoma virus is a novel oncolytic candidate that has no history of use in humans directly, as it has a distinct and absolute host species tropism to lagomorphs (rabbits). Myxoma virus has been recently shown to be able to also selectively infect and kill human tumor cells, a unique tropism that is linked to dysregulated intracellular signalling pathways found in the majority of human cancers. This review outlines the existing knowledge on the tropism of myxoma virus for human cancer cells, as well as preclinical data exhibiting its ability to infect and clear tumors in animal models of cancer. This is an exciting new therapeutic option for treating cancer, and myxoma virus joins a growing group of oncolytic virus candidates that are being developed as a new class of cancer therapies in man.
引用
收藏
页码:1415 / 1425
页数:11
相关论文
共 101 条
  • [71] Cell-based delivery of oncolytic viruses: A new strategic alliance for a cancer
    Power, Anthony T.
    Bell, John C.
    [J]. MOLECULAR THERAPY, 2007, 15 (04) : 660 - 665
  • [72] Carrier cell-based delivery of an oncolytic virus circumvents antiviral immunity
    Power, Anthony T.
    Wang, Jiahu
    Falls, Theresa J.
    Paterson, Jennifer M.
    Parato, Kelley A.
    Lichty, Brian D.
    Stojdl, David F.
    Forsyth, Peter A. J.
    Atkins, Harry
    Bell, John C.
    [J]. MOLECULAR THERAPY, 2007, 15 (01) : 123 - 130
  • [73] Vaccinia as a vector for tumor-directed gene therapy: Biodistribution of a thymidine kinase-deleted mutant
    Puhlmann, M
    Brown, CK
    Gnant, M
    Huang, J
    Libutti, SK
    Alexander, HR
    Bartlett, DL
    [J]. CANCER GENE THERAPY, 2000, 7 (01) : 66 - 73
  • [74] Varicella-zoster virus requires a functional PI3K/Akt/GSK-3α/β signaling cascade for efficient replication
    Rahaus, Markus
    Desloges, Nathalie
    Wolff, Manfred H.
    [J]. CELLULAR SIGNALLING, 2007, 19 (02) : 312 - 320
  • [75] Ries Stefan J, 2005, Future Oncol, V1, P763, DOI 10.2217/14796694.1.6.763
  • [76] Roberts MS, 2006, CURR OPIN MOL THER, V8, P314
  • [77] Rogulski KR, 2000, CANCER RES, V60, P1193
  • [78] Extensive syncytium formation mediated by the reovirus FAST proteins triggers apoptosis-induced membrane instability
    Salsman, J
    Top, D
    Boutilier, J
    Duncan, R
    [J]. JOURNAL OF VIROLOGY, 2005, 79 (13) : 8090 - 8100
  • [79] TOR, a central controller of cell growth
    Schmelzle, T
    Hall, MN
    [J]. CELL, 2000, 103 (02) : 253 - 262
  • [80] Fighting cancer with vaccinia virus: Teaching new tricks to an old dog
    Shen, YQ
    Nemunaitis, J
    [J]. MOLECULAR THERAPY, 2005, 11 (02) : 180 - 195