Fred Bunz
Stress-activated pathways and anti-cancer therapies
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Associate Professor
Department of Radiation Oncology and Molecular Radiation Sciences
School of Medicine
Research Overview
Dr. Bunz’s research objective is to understand how stress-activated signaling pathways affect the cellular responses to anti-cancer therapy. A longstanding interest is p53, a central node within a complex network of DNA damage-response pathways involved in tumor suppression. Cancer associated p53 mutations impact the efficacy of DNA damage-based anticancer therapies, but mutant p53 proteins can also serve as targets for new immune-based therapies.
Recent work in the lab is focused on understanding the mechanistic basis for p53 function, and on the development of therapeutic viral agents that can stimulate neoantigen-specific anti-cancer immune responses. The long-term goal is to better understand how current therapies work, and to develop new and improved cancer treatments.
Selected Publications
- Miciak JJ, Petrova L, Sajwan R, Pandya A, Deckard M, Munoz AJ, Bunz F. Robust p53 phenotypes and prospective downstream targets in telomerase-immortalized human cells. Oncotarget. 2025.
- Jang Y, Bunz F. Dynamic Modulation of IRE1α-XBP1 Signaling by Adenovirus. Pathogens, 2025.
- Bunz, Fred. Principles of cancer genetics, 3rd Edition (textbook). Springer, 2022.
- Jang Y, Bunz F. AdenoBuilder: A platform for the modular assembly of recombinant adenoviruses. STAR Protocols, 2022.
- Miciak J, Bunz F. Long story short: p53 mediates innate immunity. Biochimica et Biophysica acta, 2016.