Related Experiment Video
Updated: Oct 19, 2025

Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
Epitranscriptomics modifier pentostatin indirectly triggers Toll-like receptor 3 and can enhance immune infiltration
Marina Tusup1, Thomas M Kündig2, Steve Pascolo2
1University Hospital of Zürich, Department of Dermatology, Raemistrasse 100, 8091 Zürich, Switzerland; Faculty of Science, University of Zurich, Zürich, Switzerland.
Abstract:
The adenosine deaminase inhibitor 2'-deoxycoformycin (pentostatin, Nipent) has been used since 1982 to treat leukemia and lymphoma, but its mode of action is still unknown. Pentostatin was reported to decrease methylation of cellular RNA. We discovered that RNA extracted from pentostatin-treated cells or mice has enhanced immunostimulating capacities. Accordingly, we demonstrated in mice that the anticancer activity of pentostatin required Toll-like receptor 3, the type I interferon receptor, and T cells. Upon systemic administration of pentostatin, type I interferon is produced locally in tumors, resulting in immune cell infiltration. We combined pentostatin with immune checkpoint inhibitors and observed synergistic anti-cancer activities. Our work identifies pentostatin as a new class of an anticancer immunostimulating drug that activates innate immunity within tumor tissues and synergizes with systemic T cell therapies.
More Related Videos
Related Concept Videos
Tumor Immunotherapy
The Tumor Microenvironment
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

