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Strategic Combinations: The Future of Oncolytic Virotherapy with Reovirus
- Source :
- Molecular Cancer Therapeutics. 15:767-773
- Publication Year :
- 2016
- Publisher :
- American Association for Cancer Research (AACR), 2016.
-
Abstract
- The dominant cancer treatment modalities such as chemotherapy, radiotherapy, and even targeted kinase inhibitors and mAbs are limited by low efficacy, toxicity, and treatment-resistant tumor subclones. Oncolytic viral therapy offers a novel therapeutic strategy that has the potential to dramatically improve clinical outcomes. Reovirus, a double-stranded benign human RNA virus, is a leading candidate for therapeutic development and currently in phase III trials. Reovirus selectively targets transformed cells with activated Ras signaling pathways; Ras genes are some of the most frequently mutated oncogenes in human cancer and it is estimated that at least 30% of all human tumors exhibit aberrant Ras signaling. By targeting Ras-activated cells, reovirus can directly lyse cancer cells, disrupt tumor immunosuppressive mechanisms, reestablish multicellular immune surveillance, and generate robust antitumor responses. Reovirus therapy is currently being tested in combination with radiotherapy, chemotherapy, immunotherapy, and surgery. In this review, we discuss the current successes of these combinatorial therapeutic strategies and emphasize the importance of prioritizing combination oncolytic viral therapy as reovirus-based treatments progress in clinical development. Mol Cancer Ther; 15(5); 767–73. ©2016 AACR.
- Subjects :
- 0301 basic medicine
Cancer Research
viruses
medicine.medical_treatment
Genetic Vectors
Biology
Reoviridae
Virus Replication
03 medical and health sciences
0302 clinical medicine
Neoplasms
Antineoplastic Combined Chemotherapy Protocols
medicine
Animals
Humans
Combined Modality Therapy
Oncolytic Virotherapy
Chemotherapy
Radiotherapy
Cancer
Immunotherapy
medicine.disease
Oncolytic virus
Radiation therapy
Oncolytic Viruses
030104 developmental biology
Oncology
Viral replication
030220 oncology & carcinogenesis
Immunology
Cancer cell
Cancer research
Signal Transduction
Subjects
Details
- ISSN :
- 15388514 and 15357163
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Molecular Cancer Therapeutics
- Accession number :
- edsair.doi.dedup.....8e729142ee53a8b24019dfec5bf518f6
- Full Text :
- https://doi.org/10.1158/1535-7163.mct-15-0695