Noninvasive therapy of brain cancer using a unique systemic delivery methodology with a cancer terminator virus

Author:

Bhoopathi Praveen12,Mannangatti Padmanabhan12,Pradhan Anjan K.12,Kumar Amit12,Maji Santanu12,Lang Frederick F.3,Klibanov Alexander L.4,Madan Esha25,Cavenee Webster K.6,Keoprasert Timothy7,Sun Dong7,Bjerkvig Rolf8,Thorsen Frits8ORCID,Gogna Rajan129,Das Swadesh K.129,Emdad Luni129,Fisher Paul B.129

Affiliation:

1. Department of Human and Molecular Genetics Virginia Commonwealth University, School of Medicine Richmond Virginia USA

2. VCU Institute of Molecular Medicine Virginia Commonwealth University, School of Medicine Richmond Virginia USA

3. Department of Neurosurgery MD Anderson Cancer Center Houston Texas USA

4. Biomedical Engineering, Radiology and Medical Imaging, Department of Medicine University of Virginia Charlottesville Virginia USA

5. Department of Surgery Virginia Commonwealth University, School of Medicine Richmond Virginia USA

6. Ludwig Institute for Cancer Research University of San Diego La Jolla California USA

7. Department of Anatomy and Neurobiology Virginia Commonwealth University, School of Medicine Richmond Virginia USA

8. Department of Biomedicine, Kristian Gerhard Jebsen Brain Tumour Research Centre University of Bergen Bergen Norway

9. VCU Massey Comprehensive Cancer Center Virginia Commonwealth University, School of Medicine Richmond Virginia USA

Abstract

AbstractPrimary, glioblastoma, and secondary brain tumors, from metastases outside the brain, are among the most aggressive and therapeutically resistant cancers. A physiological barrier protecting the brain, the blood–brain barrier (BBB), functions as a deterrent to effective therapies. To enhance cancer therapy, we developed a cancer terminator virus (CTV), a unique tropism‐modified adenovirus consisting of serotype 3 fiber knob on an otherwise Ad5 capsid that replicates in a cancer‐selective manner and simultaneously produces a potent therapeutic cytokine, melanoma differentiation‐associated gene‐7/interleukin‐24 (MDA‐7/IL‐24). A limitation of the CTV and most other viruses, including adenoviruses, is an inability to deliver systemically to treat brain tumors because of the BBB, nonspecific virus trapping, and immune clearance. These obstacles to effective viral therapy of brain cancer have now been overcome using focused ultrasound with a dual microbubble treatment, the focused ultrasound‐double microbubble (FUS‐DMB) approach. Proof‐of‐principle is now provided indicating that the BBB can be safely and transiently opened, and the CTV can then be administered in a second set of complement‐treated microbubbles and released in the brain using focused ultrasound. Moreover, the FUS‐DMB can be used to deliver the CTV multiple times in animals with glioblastoma  growing in their brain thereby resulting in a further enhancement in survival. This strategy permits efficient therapy of primary and secondary brain tumors enhancing animal survival without promoting harmful toxic or behavioral side effects. Additionally, when combined with a standard of care therapy, Temozolomide, a further increase in survival is achieved. The FUS‐DMB approach with the CTV highlights a noninvasive strategy to treat brain cancers without surgery. This innovative delivery scheme combined with the therapeutic efficacy of the CTV provides a novel potential translational therapeutic approach for brain cancers.

Funder

Sherman Fairchild Foundation

Publisher

Wiley

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