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Matthew Hirschey

Associate Professor of Medicine
Medicine, Endocrinology, Metabolism, and Nutrition
104775, Room 50-201, Durham, NC 27701
300 N. Duke Street, 50-201, Durham, NC 27701

Overview


The Hirschey Lab in the Duke Molecular Physiology Institute, and the Departments of Medicine and Pharmacology & Cancer Biology at Duke University studies different aspects of metabolic control, mitochondrial signaling, and cellular processes regulating human health and disease.

Current Appointments & Affiliations


Associate Professor of Medicine · 2019 - Present Medicine, Endocrinology, Metabolism, and Nutrition, Medicine
Associate Professor in Pharmacology and Cancer Biology · 2019 - Present Pharmacology & Cancer Biology, Basic Science Departments
Associate Professor of Cell Biology · 2022 - Present Cell Biology, Basic Science Departments
Member of Sarah W. Stedman Nutrition and Metabolism Center · 2011 - Present Sarah Stedman Nutrition & Metabolism Center, Duke Molecular Physiology Institute
Member of the Duke Cancer Institute · 2012 - Present Duke Cancer Institute, Institutes and Centers

In the News


Published February 8, 2024
The AI Explosion, Explained
Published July 10, 2023
New University Course Offers a Technical and Ethical Exploration of Our Data-Centric World
Published May 12, 2023
Navigating AI at Duke

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Recent Publications


Targeting androgen receptor signaling to enhance cancer immunotherapy.

Journal Article Trends Pharmacol Sci · December 3, 2025 Men experience higher cancer incidence and mortality than women, and accumulating evidence implicates androgen receptor (AR) signaling as a key biological driver of these sex-based disparities. AR signaling can suppress adaptive anticancer immunity. Precli ... Full text Link to item Cite

Cysteine S-acetylation is a widespread post-translational modification on metabolic proteins

Journal Article Npj Metabolic Health and Disease · December 1, 2025 Protein acetylation is a fundamental regulatory mechanism occurring primarily on lysine amino acids. Here we report systematic in vivo characterization of cysteine S-acetylation as a widespread post-translational modification in mammalian tissues. By devel ... Full text Cite

Pathway coessentiality mapping reveals complex II is required for de novo purine biosynthesis in acute myeloid leukaemia.

Journal Article Nat Metab · December 2025 Understanding how cellular pathways interact is crucial for treating complex diseases like cancer. Individual gene-gene interaction studies have provided valuable insights, but may miss pathways working together. Here we develop a multi-gene approach to pa ... Full text Link to item Cite
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Recent Grants


Pharmacological Sciences Training Program

Inst. Training Prgm or CMEPreceptor · Awarded by National Institutes of Health · 2025 - 2030

Unified Program for Therapeutics in Children

Inst. Training Prgm or CMEPreceptor · Awarded by National Institutes of Health · 2025 - 2030

Stimulating Access to Research in Residency (StARR) - NIAID

Inst. Training Prgm or CMEPreceptor · Awarded by National Institute of Allergy and Infectious Diseases · 2018 - 2029

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Education, Training & Certifications


University of California, Santa Barbara · 2006 Ph.D.