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.

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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
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Abstract 1788 Small Molecule Targeting of Atypical p38 Protects Against Viral Infection

Megan G. Lloyd, Reuben O. Onwe, Fredejah Royer, Jackson W. Burns et al.
Journal of Biological Chemistry
PARP inhibition in cancer therapy
article

Abstract 1788 Small Molecule Targeting of Atypical p38 Protects Against Viral Infection

Megan G. Lloyd, Reuben O. Onwe, Fredejah Royer, Jackson W. Burns, Jeremy Burton, Jennifer F. Moffat, Neil Grimsey
article en

Abstract

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.

Journal of Biological ChemistryVol. 301(5)
Quinnipiac University (US)
Zero hunger
Openalex Percentile: Top 79%
PARP inhibition in cancer therapy
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