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Donald Patrick McDonnell

Glaxo-Wellcome Distinguished Professor of Molecular Cancer Biology, in the School of Medicine
Pharmacology & Cancer Biology
Duke Box 3813, Durham, NC 27710
2138 MSRB3, 3 Genome Ct., Durham, NC 27710

Overview


Lab Website

The research in our group is focused on the development and application of mechanism based approaches to identify novel therapeutics for use in the treatment and prevention of hormonally responsive cancers. Specifically we are interested in the pharmaceutical exploitation of the estrogen and androgen receptors as therapeutic targets in breast and prostate cancers and in defining how these receptors influence the pathogenesis of these diseases. These efforts have led to the discovery of several drugs that are currently being evaluated in the clinic as cancer therapeutics, and to the identification of potential biomarkers and predictors of response that can help to target the use of these new drugs. Most recently we have explored approaches to treat triple negative breast cancer and have identified an important pathway that links obesity/dyslipidemia and cancer risk.

Current Appointments & Affiliations


Glaxo-Wellcome Distinguished Professor of Molecular Cancer Biology, in the School of Medicine · 2002 - Present Pharmacology & Cancer Biology, Basic Science Departments
Professor of Pharmacology and Cancer Biology · 2000 - Present Pharmacology & Cancer Biology, Basic Science Departments
Professor in Medicine · 2002 - Present Medicine, Endocrinology, Metabolism, and Nutrition, Medicine
Professor of Cell Biology · 2022 - Present Cell Biology, Basic Science Departments
Member of the Duke Cancer Institute · 1994 - Present Duke Cancer Institute, Institutes and Centers

In the News


Published April 8, 2025
How Duke Research Turned Failure Into Hope for Patients With Breast Cancer
Published September 9, 2024
Study Solves Testosterone’s Paradoxical Effects in Prostate Cancer
Published February 13, 2023
New Therapy for Advanced Breast Cancer Has Roots in Duke Lab

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Recent Publications


ESRRA (estrogen related receptor, alpha) induces ribosomal protein RPLP1-mediated adaptive hepatic translation during prolonged starvation.

Journal Article Autophagy · June 2025 Protein translation is an energy-intensive ribosome-driven process that is reduced during nutrient scarcity to conserve cellular resources. During prolonged starvation, cells selectively translate specific proteins to enhance their survival (adaptive trans ... Full text Link to item Cite

The Roles of Natural Killer Cells in Breast Cancer Pathobiology and their Regulation by Estrogens.

Journal Article Endocr Rev · May 9, 2025 Breast cancer remains the most commonly diagnosed malignancy among women worldwide. While breast cancer treatment outcomes have improved in recent years there remains an unmet medical need for therapeutics that can be used with curative intent in the most ... Full text Link to item Cite

Thienopyridine Based Estrogen Receptor Modulators Adopt Unique Ligand Binding Poses to Elicit Anti Proliferative Activities in ER + Breast Cancer Cells

Conference Endocrinology · April 21, 2025 Abstract TextOne in eight women will be diagnosed with breast cancer in their lifetimes. Estrogen receptor alpha (ER) drives breast cancer pathology and is expressed in approximately seventy percent of tumor ... Full text Cite
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Recent Grants


Endocrinology and Metabolism Training Program

Inst. Training Prgm or CMEMentor · Awarded by National Institutes of Health · 2024 - 2029

Duke University Program in Environmental Health

Inst. Training Prgm or CMEMentor · Awarded by National Institutes of Health · 2019 - 2029

The Duke Preparing Research scholars In bioMEdical sciences (PRIME): Cancer Research Program

ResearchPreceptor · Awarded by National Cancer Institute · 2023 - 2028

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Education, Training & Certifications


Baylor, College of Medicine · 1988 Ph.D.
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