Personal profile
Research Interests
Dr Hu's research over the last 17 years has been focusing on deciphering molecular mechanisms controlling the expression and activity of UDP-glucuronosyltransferases (UGTs) in response to therapeutic drugs and signalling molecules such as sex steroid hormones. These studies discovered a series of transcriptional factors and microRNAs that control UGT expression and function in drug-metabolically relevant organs (Liver) and sex hormone-sensitive cancers (Prostate and Breast cancer). These studies have been published in over 20 articles in prestigious international journals in the fields of Pharmacology and Cancers, including Molecular pharmacology, Journal of Pharmacology and Experimental Therapeutics, Drug Metabolism and Disposition, Drug Metabolism Reviews, Pharmacology & Therapeutics, cancers, and Cancer Research.
Dr Hu's research on UGT genes also recently extends to define novel alternatively spliced UGT transcripts, including circular and chimeric transcripts that have been published in Molecular Pharmacology.
Dr Hu's research recently extends to cover ADME genes, a group of approximately 300 genes that are involved in drug Absorption, Distribution, Metabolism, Excretion (ADME). ADME genes are also involved in clearing endogenous compounds (steroids, fatty acids, bile acids, lipids). Dr Hu's published bioinformatic analysis of The Cancer Genome Atlas (TCGA) datasets reported widespread deregulation of ADME genes in cancers and their association with cancer patient survival. These discoveries highlight the potentials for ADME genes as prognostic and diagnostic biomarkers for human cancers.
Dr Hu's recent research also discovered novel androgen receptor splice variants (ARVs) and showed for the first time ARV expression in breast cancer. These discoveries are clinically relevant given their potential role in mediating anti-androgen resistance in breast cancers treated with anti-antiandrogens.
Research Areas
- Molecular biosciences
Supervisory Interests
- Molecular biology
- Drug metabolising enzymes, cytochrome P450 and UDP-glucuronosyltransferase
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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SDG 3 Good Health and Well-being
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SDG 7 Affordable and Clean Energy
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UDP-Glycosyltransferases
Hulin, J. A., Hu, D. G., Miners, J. O., Mackenzie, P. I. & Meech, R., 2026, Comprehensive Toxicology. McLean, C. A. (ed.). 4th ed. Elsevier, p. 578-607 30 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review
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Sex-specific UGT expression and function: prevalence, potential mechanisms and significance
Meech, R., Hu, D. G., Hulin, J. A. & Mackenzie, P. I., 2025, In: Expert Opinion on Drug Metabolism and Toxicology. 21, 5, p. 511-518 8 p.Research output: Contribution to journal › Article › peer-review
4 Citations (Scopus) -
A Comprehensive Bioinformatic Analysis of RNA-seq Datasets Reveals a Differential and Variable Expression of Wildtype and Variant UGT1A Transcripts in Human Tissues and Their Deregulation in Cancers
Hu, D. G., Marri, S., Hulin, J. A., McKinnon, R. A., Mackenzie, P. I. & Meech, R., 13 Jan 2024, In: Cancers. 16, 2, 23 p., 353.Research output: Contribution to journal › Article › peer-review
Open AccessFile88 Downloads (Pure) -
Activation of Cryptic Donor Splice Sites within the UDP-Glucuronosyltransferase (UGT)1A First-Exon Region Generates Variant Transcripts That Encode UGT1A Proteins with Truncated Aglycone-Binding Domains
Hu, D. G., Marri, S., Hulin, J.-A., Ansaar, R., Mackenzie, P. I., McKinnon, R. A. & Meech, R., 1 Jun 2024, In: Drug Metabolism and Disposition. 52, 6, p. 526-538 13 p.Research output: Contribution to journal › Article › peer-review
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Regulation of human UDP-glycosyltransferase (UGT) genes by miRNAs
Hu, D. G., Mackenzie, P. I., Hulin, J. A., McKinnon, R. A. & Meech, R., 2022, In: Drug Metabolism Reviews. 54, 2, p. 120-140 21 p.Research output: Contribution to journal › Review article › peer-review
14 Citations (Scopus)