Department of Medicine
Faculty Profiles by Division

Department of Medicine

Faculty Profiles

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photo Wei Du, MD, PhD


Division of Hematology/Oncology

Member, Genome Stability Program, UPMC Hillman Cancer Center

Member, Molecular Pharmacology Graduate Program

Member, Molecular Genetics & Developmental Biology Program


Phone: 412-623-2211

Office: Hillman Cancer Center, Research Pavillion
5117 Centre Ave, Suite G5.c
Pittsburgh, PA
Phone: 412-623-2211
Fax: 412-623-1010
Administrative Assistant:
Brenda Atoo
Phone: 412-623-1012
Fax: 412-623-1010
Education and Training
PhD, Tohoku University, School of Medicine, Sendal, Japan
MD, North China University of Science and Technology, China
Postdoctoral Fellow, EHCB, CCHMC, Cincinnati, Ohio, USA
Fanconi Anemia Research Foundation Fellow, Cincinnati, Ohio, USA
NIH/NCI T32 Postdoctoral Fellow, EHCB, CCHMC, Cincinnati, Ohio, USA
Research Associate: Experimental Hematology Cancer Biology, CCHMC, Cincinnati, Ohio, USA
Research Interest
Dr. Du's research is centered on pathophysiology of hematologic diseases such as bone marrow (BM) failure and leukemia. Dr. Du has a broad background in hematopoiesis, stem cell biology & aging, cellular metabolism and tumor microenvironment, with specific training and expertise in DNA damage response/repair, mouse modeling, metabolite profiling, and in vivo disease modeling. She has been investigating the mechanism of hematopoietic stem cell (HSC) mobilization and BM niche engraftment as well as the factors implicated in cell proliferation and apoptosis. She has identified functional interactions between certain factors implicated in cell polarity, adhesion/migration, stem cell metabolism and aging. These studies led to 44 peer-reviewed scientific papers in high-impact scientific journals in the field of Hematology, including 6 Blood and 6 Leukemia papers. Her current research interests include: 1) Define the molecular and functional collaboration between a major cell signaling (FA) pathway and immunometabolic regulation in HSCs; 2) Target stem cell-niche interaction for improved therapy for patients with bone marrow failure and leukemia; 3) Study a novel interplay between DDR and immune responses in FA leukemogenesis; 4) Study on the systemic immune effects of persistent DNA damage using mouse and human models of DNA repair deficiency and aging; 5) Molecular mechanism and therapeutic potential of synthetic lethal targeting our newly identified PRMT5-CtIP-FANCD2 complex in homologous recombination repair-competent cancers; and 6) Mechanistic and functional elucidation of the role of a novel paracrine Wnt5a-Prox1 signaling axis in regulating HSC regeneration under conditions of injury and aging.
For my complete bibliography, Click Here.
Selected Publications:
Wu, L, Li, X, Lin, Q, Chowdhury, F, Mazumder MH, Du, W. FANCD2 and HES1 suppress inflammation-induced PPAR gamma to prevent haematopoietic stem cell exhaustion. British Journal of Hematology. 2021; 192(3): 652-663.
Lin, Q, Wu, L, Ma, Z, Chowdhury, FA, Mazumder, MHH, Du, W. Persistent DNA damage-induced NLRP12 improves hematopoietic stem cell function. Journal of Clinical Investigation Insight. 2020; 5(10): e133365.
Wu, L, Lin, Q, Ma, Z, Chowdhury, FA, Mazumder, MHH, Du, W. Mesenchymal PGD 2 activates an ILC2-Treg axis to promote proliferation of normal and malignant HSPCs. Leukemia. 2020; 34(11): 3028-3041.
Ma, Z, Xu, J, Wu, L, Wang, J, Lin, Q, Chowdhury, FA, Mazumder MHH, Li, X, Du, W. Hes1 deficiency causes hematopoietic stem cell exhaustion. Stem Cells. 2020; 38(6): 756-768.
Li, X, Wu, L, Zopp, M, Kopelov, S, Du, W. p53-TIGAR axis-mediated glycolytic suppression attenuates DNA damage and chromosomal instability in Fanconi Anemia hematopoietic stem cells. Stem Cells. 2019; 37(7): 937-947.
Du, W, Liu, W, Mizukawa B,, Shang, X, Sipple, J, Wunderlich, M, Geiger, H, Davies, S, Mulloy, J, Pang, Q, Zheng, Y. A non-myeloablative conditioning approach for hematopoietic stem cell engraftment in mouse models. Leukemia. 2018; 32(9): 2041-2046.
Du, W, Amarachintha, S, Erden, O, Wilson, A, Pang, Q. The immune receptors Trem1 cooperates with diminished DNA damage response to induce preleukemic stem cell expansion. Leukemia. 2017; 31(2): 423-433.
Li, X, Erden, O, Li, L, Ye, Q, Wilson, A, Du, W. Binding to WGR domain by salidroside activates PARP1 and protects hematopoietic stem cells from oxidative stress. Antioxidant Redox Signal. 2014; 20(12): 1853-65.
Li, X, Sipple, J, Pang, Q, Du, W. Salidroside stimulates DNA repair enzyme Parp-1 activity in mouse HSC maintenance. Blood. 2012; 119(18): 4142-51.
Du, W, Rani, R, Sipple, J, Schick,J, Myers, KC, Mehta, P, Andreassen, PR, Davies, SM, Pang, Q. The FA pathway counteracts oxidative stress through selective protection of antioxidant defense gene promoters. Blood. 2012; 119(18): 4142-51.
Notable Achievements
NIH/NHLBI R01HL151390 Grant, 2020-2024
NIH/NIGMS P20GM121322 Grant, 2018-2020
American Cancer Society (ACS) Pilot Grant, 2017-2018
WVU School of Pharmacy Incentive Award, 2018-2020
WVU Health Science Center Faculty Research Award, 2018
Leukemia Research Foundation New Investigator Award, 2018
NIH T32 Postdoctoral Training Award, 2011-2013
ASH Abstract Achievement Award, 2008, 2009, 2011, 2013
Fanconi Anemia research Fund Research Award, 2008-2010
Fujino Incentive Award, 2007