4.4 Review

Buy One Get One Free: Armed Viruses for the Treatment of Cancer Cells and their Microenvironment

Journal

CURRENT GENE THERAPY
Volume 9, Issue 5, Pages 341-355

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/156652309789753329

Keywords

Oncolytic viruses; tumor microenvironment; angiogenesis; extracellular matrix; cytokines

Funding

  1. NINDS/NIH [1R01NS064607, 1K01NS059575, 1R21NS066299]
  2. NCI/NIH [R21CA133663, R01CA 114004]
  3. NIH/NCI [P01CA089248]
  4. NIH/NIMH [R21MH082421]
  5. NIH/NINDS [R21NS063290, U01NS061811]
  6. Alliance for Cancer Gene Therapy
  7. NATIONAL CANCER INSTITUTE [R01CA114004, R01CA150153, R21CA133663, P01CA069246] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF MENTAL HEALTH [R21MH082421] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [K01NS059575, R21NS063290, R21NS056203, R01NS064607, R21NS066299, U01NS061811] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Oncolytic viral therapy is a promising biological therapy for the treatment of cancer. Recent advances in genetic engineering have facilitated the construction of custom-built oncolytic viruses that can be exquisitely targeted to tumors by exploiting each cancer's unique biology and their efficacy can be further enhanced by arming them with additional therapeutic genes. Such an approach allows the virus to unload its therapeutic cargo at the tumor site, thereby enhancing its anti-neoplastic properties. While several clever strategies have been recently described using genes that can induce cellular apoptosis/suicide and/or facilitate tumor/virus imaging, viruses armed with genes that also affect the tumor microenvironment present an exciting and promising approach to therapy. In this review we discuss recently developed oncolytic viruses armed with genes encoding for angiostatic factors, inflammatory cytokines, or proteases that modulate the extracellular matrix to regulate tumor vascularization, anti-tumor immune responses and viral spread throughout the solid tumor.

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