Prof. Sachin A. Gupte
New York Medical College, USA
Email: [email protected]
Qualifications
2001 M.D., Ph.D., Juntendo University School of Medicine, Japan
2000 Post-doc New York Medical College, USA
1992 M.S., University of Bombay, India
1988 B.S., University of Bombay, India
Publications (Selected)
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Signoretti, C., Matsumura, S., D'silva, M., et al. (2026). Glucose-6-phosphate dehydrogenase variants modify 3D genomic organization to suppress maladaptive and vascular disease. Journal of Biological Chemistry, 302(8), Article 113204.
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Signoretti, C., Matsumura, S., Doja, J., et al. (2026). VEGFR-2 blocker induces pulmonary vascular disease in rats with CRISPR-edited human non-deficient G6PD polymorphism: role of 3D genomic modifications and DNA methylation. British Journal of Pharmacology, 183(16), 4675–4697.
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D'silva, M., Jackson, K., Vaughan, M. T., et al. (2026). 12-Lipoxygenase (12-LOX) plays a key role in the hyperinflammatory response caused by SARS-CoV-2. mBio, 17(6), Article e00738-26.
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Signoretti, C., Fatehi, S., Drewes, R., et al. (2026). Bleomycin-induced lung fibrosis and dysfunction is exacerbated by G6PD deficiency. American Journal of Physiology-Lung Cellular and Molecular Physiology, 330(2), L145–L158.
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Signoretti, C., Matsumura, S., Fatehi, S., et al. (2024). G6pdN126D Variant Increases the Risk of Developing VEGFR (Vascular Endothelial Growth Factor Receptor) Blocker-Induced Pulmonary Vascular Disease. Journal of the American Heart Association, 13(19), Article e035174.
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Wojciak-Stothard, B., Gupte, S., & Bossone, E. (2024). Disease mechanisms and therapeutic targets in pulmonary hypertension: Key insights from the special issue of vascular pharmacology on pulmonary hypertension. Vascular Pharmacology, 156, Article 107415.
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Matsumura, S., Signoretti, C., Fatehi, S., et al. (2024). Loss-of-function G6PD variant moderated high-fat diet-induced obesity, adipocyte hypertrophy, and fatty liver in male rats. Journal of Biological Chemistry, 300(7), Article 107460.
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Krajnik, A., Nimmer, E., Brazzo, J. A., III, et al. (2023). Survivin regulates intracellular stiffness and extracellular matrix production in vascular smooth muscle cells. APL Bioengineering, 7(4), Article 046104.
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Signoretti, C., & Gupte, S. A. (2023). G6PD Orchestrates Genome-Wide DNA Methylation and Gene Expression in the Vascular Wall. International Journal of Molecular Sciences, 24(23), Article 16727.
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D'Addario, C. A., Matsumura, S., Kitagawa, A., et al. (2023). Global and endothelial G-protein coupled receptor 75 (GPR75) knockout relaxes pulmonary artery and mitigates hypoxia-induced pulmonary hypertension. Vascular Pharmacology, 153, Article 107235.
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Gupte, S. A., Bakshi, C. S., Blackham, E., et al. (2023). The severity of SARS-CoV-2 infection in K18-hACE2 mice is attenuated by a novel steroid-derivative in a gender-specific manner. British Journal of Pharmacology, 180(20), 2677–2693.
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Signoretti, C., Matsumura, S., Fatehi, S., & Gupte, S. (2023). Insight into the increased risk associated with CRISPR-generated African G6PD variant (N126D) in rat model of sugen-5416-induced pulmonary hypertension. Physiology, 38(S1).
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Jacob, C., Kitagawa, A., Signoretti, C., et al. (2022). Mediterranean G6PD variant mitigates expression of DNA methyltransferases and right heart pressure in experimental model of pulmonary hypertension. Journal of Biological Chemistry, 298(12), Article 102691.
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Matsumura, S., D'Addiaro, C., Slivano, O. J., et al. (2022). Mediterranean G6PD variant rats are protected from Angiotensin II-induced hypertension and kidney damage, but not from inflammation and arterial stiffness. Vascular Pharmacology, 145, Article 107002.
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Hashimoto, R., & Gupte, S. A. (2022). G6PD is a critical enabler of hypoxia-induced accumulation of macrophages and platelets in mice lungs and contributor to lung inflammation. Vascular Pharmacology, 144, Article 106976.
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Agostinucci, K., Hutcheson, R., Hossain, S., et al. (2022). Blockade of 20-hydroxyeicosatetraenoic acid receptor lowers blood pressure and alters vascular function in mice with smooth muscle-specific overexpression of CYP4A12-20-HETE synthase. Journal of Hypertension, 40(3), 498–511.
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D'Addario, C., Kitagawa, A., Matsumura, S., et al. (2022). Deletion Of G-Protein-Coupled Receptor 75 Prevents Hypoxia-Induced Pulmonary Vasoconstriction and Hypertension. The FASEB Journal, 36(S1).
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Stier, C. T., Jr., & Gupte, S. (2021). Commentary on Expression of Exogenous Epithelial Sodium Channel Beta Subunit in the Mouse Middle Cerebral Artery Increases Pressure-Induced Constriction COMMENT. American Journal of Hypertension, 34(11), 1143–1144.
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Kitagawa, A., Jacob, C., Jordan, A., et al. (2021). Inhibition of Glucose-6-Phosphate Dehydrogenase Activity Attenuates Right Ventricle Pressure and Hypertrophy Elicited by VEGFR Inhibitor plus Hypoxia. Journal of Pharmacology and Experimental Therapeutics, 377(2), 284–292.
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Dhagia, V., Kitagawa, A., Jacob, C., et al. (2021). G6PD activity contributes to the regulation of histone acetylation and gene expression in smooth muscle cells and to the pathogenesis of vascular diseases. American Journal of Physiology-Heart and Circulatory Physiology, 320(3), H999–H1016.
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Kitagawa, A., Kizub, I., Jacob, C., et al. (2020). CRISPR-Mediated Single Nucleotide Polymorphism Modeling in Rats Reveals Insight Into Reduced Cardiovascular Risk Associated With Mediterranean G6PD Variant. Hypertension, 76(2), 523–532.
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Gupte, R., Dhagia, V., Rocic, P., et al. (2020). Glucose-6-phosphate dehydrogenase increases Ca2+ currents by interacting with Cav1.2 and reducing intrinsic inactivation of the L-type calcium channel. American Journal of Physiology-Heart and Circulatory Physiology, 319(1), H144–H158.
Profile Details
https://www.nymc.edu/gsbms/about/leadership/program-directors/gupte-sachin-a.php?utm
https://scholar.google.com/citations?user=z_WCkPoAAAAJ&hl=en
https://www.researchgate.net/scientific-contributions/Sachin-A-Gupte-38473048
WOS ResearcherID: FYP-3572-2022