Biography and Research Information

OverviewAI-generated summary

Martin J. Cannon's research focuses on the development and application of oncolytic viruses and immunotherapies for cancer treatment. His work investigates the potential of various viruses, including Myxoma virus and Morreton virus, as platforms for selectively targeting and destroying cancer cells. A significant portion of his research explores strategies to enhance the efficacy of these virotherapies, often in combination with other treatments like immune checkpoint blockade.

Cannon's published work includes studies on enhancing CD4 T cell-dependent antitumor immunity in ovarian cancer, the immune responses stimulated by modified Myxoma viruses in human monocytes and macrophages, and the characterization of Morreton virus as an oncolytic virotherapy platform for liver cancers. He has also explored repurposing existing vaccines, such as the MMR vaccine, for cancer immunotherapy and investigated methods to improve resectability in pancreatic cancer through enhanced neoadjuvant virotherapy by targeting the tumor stroma.

His scholarly contributions are reflected in a high h-index of 44 and over 5,800 citations across 157 publications. Cannon has secured federal funding for his research, including an NIH/National Cancer Institute grant for studying mechanisms of Th17-DC immunotherapy for ovarian cancer and an NIH/NIH Office of the Director grant as Co-PI for research on platelets in radiation-induced immune dysregulation. He collaborates with researchers at the University of Arkansas for Medical Sciences and other institutions.

Metrics

  • h-index: 44
  • Publications: 157
  • Citations: 5,866

Selected Publications

  • Multimodal reprogramming of the tumor microenvironment by MMR and dual checkpoint blockade in hepatocellular carcinoma models (2025) DOI
  • Abstract B022: Reprogramming Apoptotic Resistance in PDAC Through Synthetic Oncolytic Immunotherapy (2025) DOI
  • Pancreatic tumor microenvironment reprogramming via alloantigen-expressing virotherapy elicits tumor rejection and improves immunotherapy response (2025) DOI
  • A Replication-Defective Myxoma Virus Inducing Pro-Inflammatory Responses as Monotherapy and an Adjuvant to Chemo- and DC Immuno-Therapy for Ovarian Cancer (2025) DOI
  • Abstract 945: Live attenuated MMR vaccines modulate tumor immune cell infiltration and synergize with standard of care to prolong survival in preclinical HCC models (2025) DOI
  • Abstract 947: Engineering a synthetic oncolytic virus to overcome apoptotic resistance and induce immunogenic cell death in pancreatic ductal adenocarcinoma (2025) DOI
  • Enhancing Neoadjuvant Virotherapy’s Effectiveness by Targeting Stroma to Improve Resectability in Pancreatic Cancer (2024) DOI
  • Abstract 5004: Oncolytic Jurona-driven systemic and intratumoral immunotherapy combined with immune checkpoint blockade boost immune response and survival in hepatocellular carcinoma models (2024) DOI
  • Th17-inducing dendritic cell vaccines stimulate effective CD4 T cell-dependent antitumor immunity in ovarian cancer that overcomes resistance to immune checkpoint blockade (2023) DOI
  • Supplemental Figures 1-9 and Table S1 from Gastrointestinal Tract Dysbiosis Enhances Distal Tumor Progression through Suppression of Leukocyte Trafficking (2023) DOI
  • Supplemental Figures 1-9 and Table S1 from Gastrointestinal Tract Dysbiosis Enhances Distal Tumor Progression through Suppression of Leukocyte Trafficking (2023) DOI
  • Repurposing live attenuated trivalent MMR vaccine as cost-effective cancer immunotherapy (2022) DOI
  • Myxoma virus lacking the host range determinant M062 stimulates cGAS-dependent type 1 interferon response and unique transcriptomic changes in human monocytes/macrophages (2022) DOI
  • Characterization of Morreton virus as an oncolytic virotherapy platform for liver cancers (2022) DOI
  • Abstract 3529: T-cell trafficking and extravasation is suppressed in distal tumors during gastrointestinal tract dysbiosis (2022) DOI

Federal Grants 2 $872,121 total

NIH/National Cancer Institute Contact PI Mar 2024 - Feb 2027

Mechanisms of Th17-DC immunotherapy for ovarian cancer

National Cancer Institute $178,819 R21
NIH/NIH Office of the Director Co-PI Jul 2022 - May 2027

Platelets in radiation-induced immune dysregulation

NIH Office of the Director $693,302 U01

Grants & Funding

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