Elias Quijano, PhD; Diana Martinez-Saucedo, PhD; Zaira Ianniello, PhD; and Natasha Pinto-Medici, PhD, there are 25 other contributors, most from Yale's Department of Therapeutic Radiology and from the departments of genetics, molecular biophysics and biochemistry, biomedical engineering, pathology, and medical oncology and three from the University of Illinois Urbana-Champaign.
Specifically, animal models of three types of "cold" tumors that are usually resistant to standard treatments and the best immunotherapies—pancreatic cancer, medulloblastoma (a type of brain cancer), and melanoma (skin cancer)—had significant responses to the precision treatment, that homed in on cancerous cells, largely avoiding healthy tissue. Results:
• In the animal model for pancreatic ductal adenocarcinoma the treatment significantly reduced the size of the tumors and extended survival by boosting the presence of CD8+ T cells that attack cancer cells.
• The medulloblastoma animal models responded similarly. The treatment made it past the blood-brain barrier to reach and shrink the tumors and extended survival, without triggering an immune reaction that can be caused by collateral treatment of healthy tissue.
• Pronounced suppressed tumor growth and an absence of severe side effects or toxicities were noted in the animal models with melanoma.
Researchers used computer modeling to modify the antibody, enabling it to bind to RNA, and also "humanized" it so the body wouldn't attack it as an invader, a step toward possible clinical use.
"This work lays the foundation for translating RNA-based therapies into the clinic. By achieving targeted delivery to tumor cells without systemic toxicity, we open the possibility of developing treatments that are not only tumor-specific but also adaptable to the immunologic context of each patient's cancer," says Luisa Escobar-Hoyos, PhD, senior author and a YSM associate professor of therapeutic radiology and molecular biophysics and biochemistry.
"With further development, this platform could support personalized immuno-RNA therapies and move toward first-in-human clinical trials."
Quijano, E., et al. (2025). Systemic administration of an RNA binding and cell-penetrating antibody targets therapeutic RNA to multiple mouse models of cancer. Science Translational Medicine. doi.org/10.1126/scitranslmed.adk1868.
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