Teresa Fan

Professor

University of Kentucky

United States

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About

Dr. Teresa Fan is a Professor at the University of Kentucky in the United States. Her research focuses on metabolic reprogramming in cancer, with recent articles discussing topics such as patient-derived tissue cultures, spatially resolved metabolism, and the role of cell-matrix interactions in cancer biology. Additionally, she explores various metabolic pathways and their implications in diseases such as breast and lung cancer.

Articles (14)

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2025

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

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UNITED STATES

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Teresa Fan

Research Interests

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About

Articles (14)

Patient-derived organotypic tissue cultures as a platform to evaluate metabolic reprogramming in breast cancer patients

Challenges of Spatially Resolved Metabolism in Cancer Research

Differential Inhibition of Anaplerotic Pyruvate Carboxylation and Glutaminolysis-Fueled Anabolism Underlies Distinct Toxicity of Selenium Agents in Human Lung Cancer

Metabolic reprogramming driven by EZH2 inhibition depends on cell-matrix interactions.

Cyclin D1 extensively reprograms metabolism to support biosynthetic pathways in hepatocytes

Polarization and β-Glucan Reprogram Immunomodulatory Metabolism in Human Macrophages and Ex Vivo in Human Lung Cancer Tissues

Resolving Enantiomers of 2-Hydroxy Acids by Nuclear Magnetic Resonance

A Micro-Scale Analytical Method for Determining Glycogen Turnover by NMR and FTMS

Tissue-Specific Downregulation of Fatty Acid Synthase Suppresses Intestinal Adenoma Formation via Coordinated Reprograming of Transcriptome and Metabolism in the Mouse Model of Apc-Driven Colorectal Cancer

Ultrahigh resolution MS1/MS2-based reconstruction of metabolic networks in mammalian cells reveals changes for selenite and arsenite action

NMR Analysis of Carboxylate Isotopomers of 13C-Metabolites by Chemoselective Derivatization with 15N-Cholamine

6-Phosphogluconate dehydrogenase (6PGD), a key checkpoint in reprogramming of regulatory T cells metabolism and function

Rapid analysis of S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) isotopologues in stable isotope-resolved metabolomics (SIRM) using direct infusion nanoelectrospray ultra-high-resolution Fourier transform mass spectrometry (DI-nESI-UHR-FTMS)

Innate immune activation by checkpoint inhibition in human patient-derived lung cancer tissues

Collaborators (8)

Saeed Daneshmandi

Ramon Sun

Pawel Lorkiewicz

Andrew Lane

Richard Higashi

Matthew Gentry

Christine Brainson

Mark Klein

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