Hydralazine inhibits cysteamine dioxygenase to treat preeclampsia and senesce glioblastoma

Hydralazine (HYZ), a treatment for preeclampsia and hypertensive crisis, is listed by the World Health Organization as an essential medicine. Its mode of action has remained unknown through its seven decades of clinical use. Here, we identify 2-aminoethanethiol dioxygenase (ADO), a key mediator of targeted protein degradation, as a selective HYZ target. The drug chelates ADO's metallocofactor and can alkylate one of its ligands. The resultant inactivation stabilizes regulators of G protein signaling (RGS4 and RGS5) that ADO normally marks for proteolysis, explaining the drug's vasodilatory activity and comporting with observations of diminished RGS levels in both clinical preeclampsia and a mouse model thereof. Its inhibition of ADO suggested use of HYZ against glioblastoma (GBM); indeed, a single dose robustly senesces cultured GBM cells. By establishing ADO as a nexus for GBM and preeclampsia and connecting it to HYZ, the results create opportunities for directed tailoring of the old drug for new therapies.

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Publication Details

Journal
Science Advances
Published
2025-10-15
DOI
https://doi.org/10.1126/sciadv.adx7687
Primary Topic
Biomedical Research and Pathophysiology
Type
article
Field-Weighted Citation Impact
0.00
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article

Hydralazine inhibits cysteamine dioxygenase to treat preeclampsia and senesce glioblastoma

Kyosuke Shishikura, Nate R. McKnight, Kelly Hicks, Zev A. Binder et al.
Science Advances
Biomedical Research and Pathophysiology
article

Hydralazine inhibits cysteamine dioxygenase to treat preeclampsia and senesce glioblastoma

Kyosuke Shishikura, Nate R. McKnight, Kelly Hicks, Zev A. Binder, Zongtao Lin, Jiasong Li, Eric W. Barr, Thomas P. Keeley, Kirill A. Martemyanov, Aimin Liu, Donald M. O’Rourke, J. Martin Bollinger, Megan L. Matthews, William H. Parsons, Katelyn A. Bustin, Mahaa Ayub, Yiming Chen, Xie Wang, Sun Woo Kim, HU Ren-ming, Snehil R. Chilkamari
article en

Abstract

Hydralazine (HYZ), a treatment for preeclampsia and hypertensive crisis, is listed by the World Health Organization as an essential medicine. Its mode of action has remained unknown through its seven decades of clinical use. Here, we identify 2-aminoethanethiol dioxygenase (ADO), a key mediator of targeted protein degradation, as a selective HYZ target. The drug chelates ADO's metallocofactor and can alkylate one of its ligands. The resultant inactivation stabilizes regulators of G protein signaling (RGS4 and RGS5) that ADO normally marks for proteolysis, explaining the drug's vasodilatory activity and comporting with observations of diminished RGS levels in both clinical preeclampsia and a mouse model thereof. Its inhibition of ADO suggested use of HYZ against glioblastoma (GBM); indeed, a single dose robustly senesces cultured GBM cells. By establishing ADO as a nexus for GBM and preeclampsia and connecting it to HYZ, the results create opportunities for directed tailoring of the old drug for new therapies.

Science AdvancesVol. 11(42)
Scripps Research Institute (US), Pennsylvania State University (US), Thomas Jefferson University (US), Cardiovascular Institute of the South (US), Ludwig Cancer Research (GB), Translational Therapeutics (United States) (US), The University of Texas at San Antonio (US), Oberlin College (US), University of Pennsylvania (US)
Openalex Percentile: Top 59%
Biomedical Research and Pathophysiology
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