Mechanism-based peroxiredoxin 3 inhibitors exploit a covalent warhead for cancer therapy

Covalent inhibitors that are approved and marketed drugs exploit a wide array of warheads and reactions with amino acid side chain-based nucleophiles. Thiostrepton (TS) inhibits the peroxidase activity of the mitochondrial antioxidant protein peroxiredoxin 3 by forming a covalent crosslink between the two active site cysteine residues. Peroxiredoxin 3 inactivation increases reactive oxygen species levels, induces cancer cell death in preclinical models, and shows promise in an ongoing clinical trial for malignant mesothelioma using direct pleural infusion. We report the identification of the minimal fragment of TS that contains tandem dehydro-alanine (DHA) moieties and maintains anticancer activity while losing interactions with three alternative targets of intact TS. Biochemical, kinetic, cellular, and structural studies demonstrate that this fragment is a mechanism-based peroxiredoxin inhibitor. These findings represent a promising start toward a pro-oxidant approach for cancer therapy. Moreover, the data support that the DHA moiety should be added to the covalent warhead arsenal.

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Publication Details

Journal
Science Advances
Published
2025-10-31
DOI
https://doi.org/10.1126/sciadv.ady4492
Citations
1
Primary Topic
Redox biology and oxidative stress
Type
article
Field-Weighted Citation Impact
0.81
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article

Mechanism-based peroxiredoxin 3 inhibitors exploit a covalent warhead for cancer therapy

Terrence L. Smalley, Terri Messier, Kimberly Nelson, Robert J. Hondal et al.
1 citations
Science Advances
Redox biology and oxidative stress
0.81
article

Mechanism-based peroxiredoxin 3 inhibitors exploit a covalent warhead for cancer therapy

Terrence L. Smalley, Terri Messier, Kimberly Nelson, Robert J. Hondal, Hannah I. Hoffman, Aida Habibovic, Victoria Gibson, R. Gumpena, Brian Cunniff, W. Todd Lowther, Uma Gandhi
article en
1 citations

Abstract

Covalent inhibitors that are approved and marketed drugs exploit a wide array of warheads and reactions with amino acid side chain-based nucleophiles. Thiostrepton (TS) inhibits the peroxidase activity of the mitochondrial antioxidant protein peroxiredoxin 3 by forming a covalent crosslink between the two active site cysteine residues. Peroxiredoxin 3 inactivation increases reactive oxygen species levels, induces cancer cell death in preclinical models, and shows promise in an ongoing clinical trial for malignant mesothelioma using direct pleural infusion. We report the identification of the minimal fragment of TS that contains tandem dehydro-alanine (DHA) moieties and maintains anticancer activity while losing interactions with three alternative targets of intact TS. Biochemical, kinetic, cellular, and structural studies demonstrate that this fragment is a mechanism-based peroxiredoxin inhibitor. These findings represent a promising start toward a pro-oxidant approach for cancer therapy. Moreover, the data support that the DHA moiety should be added to the covalent warhead arsenal.

Science AdvancesVol. 11(44)
University of Vermont (US), Atrium Health Wake Forest Baptist (US), Wake Forest University (US)
Openalex Percentile: Top 22%
Redox biology and oxidative stress
0.81
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Mechanism-based peroxiredoxin 3 inhibitors exploit a covalent warhead for cancer therapy — Terrence L. Smalley, Terri Messier, et al. · Science Advances (2025) | TGRS Research Map | TGRS