Abstract 1788 Small Molecule Targeting of Atypical p38 Protects Against Viral Infection
Developing therapeutics that target the host kinome is a promising strategy to support current treatments for viral infections. While multiple direct-acting antivirals (DAAs) potentially clear Hepatitis C virus (HCV) infection in most individuals, ∼2.4 million individuals are unresponsive to the current DAAs or have secondary infections/complications that impact their treatment potential. Recent studies have shown that atypical p38 activity is critical for HCV replication and may have broader functions in regulating other viruses.
Authors
- Megan G. Lloyd (ORCID: https://orcid.org/0000-0002-6034-0846)
- Reuben O. Onwe (ORCID: https://orcid.org/0000-0002-6164-8826)
- Fredejah Royer
- Jackson W. Burns (ORCID: https://orcid.org/0000-0002-0657-9426)
- Jeremy Burton (ORCID: https://orcid.org/0000-0001-8023-0866)
- Jennifer F. Moffat (ORCID: https://orcid.org/0000-0002-4371-8608)
- Neil Grimsey (ORCID: https://orcid.org/0000-0002-0481-4920)
Institutions
- Quinnipiac University (US)
Publication Details
- Journal
- Journal of Biological Chemistry
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1016/j.jbc.2025.110106
- Primary Topic
- PARP inhibition in cancer therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.00