Zhijian Qian Lab
Research Lab Overview
The Qian Laboratory is dedicated to uncovering the molecular and cellular mechanisms that drive the initiation and progression of myeloid malignancies, with a primary focus on myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). These disorders develop from hematopoietic stem and progenitor cells that acquire genetic and epigenetic alterations, ultimately disrupting normal hematopoiesis and promoting leukemic transformation. Our overarching goal is to define the molecular complexity underlying this process and to identify novel regulatory networks that control hematopoietic stem cell (HSC) fate decisions, leukemic stem cell (LSC) maintenance and disease evolution.
Our research integrates multiple disciplines — cancer stem cell biology, RNA biology and the epigenetic and transcriptional regulation of gene expression — to provide a systems-level understanding of leukemia pathogenesis. We are particularly interested in how transcriptional, epigenetic and epitranscriptomic mechanisms converge to reprogram HSCs during malignant transformation. Using state-of-the-art genomic, transcriptomic and functional approaches in both mouse models and patient-derived samples, we aim to dissect the interplay between oncogenic signaling, RNA modification pathways and chromatin regulation that sustains the self-renewal and therapy resistance of LSCs.
Beyond blood cancers, we are expanding our research to explore whether similar mechanisms operate in solid tumors, aiming to uncover shared principles of cancer stem cell regulation. By translating these discoveries into new therapeutic strategies, our long-term vision is to develop targeted treatments that selectively eliminate cancer stem cells while preserving normal stem cell function — ultimately improving outcomes for patients with cancer.
Principle Investigator: Zhijian Qian, Ph.D.
Zhijian Qian, Ph.D., joined the Beckman Research Institute at City of Hope® as a professor and vice chair of the Department of Systems Biology in August 2025. His research spans various tumor types, including acute leukemia, myelodysplastic syndromes and lung cancer, and is currently supported by funding from the National Cancer Institute, National Heart, Lung, and Blood Institute and National Institute of Diabetes and Digestive and Kidney Diseases.
Lab Members
Research FocusOn deciphering the function and mechanism of RNA
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Research Focus
- On deciphering the function and mechanism of RNA modifiers in leukemia and hematopoiesis
Research Focus Role of RNA binding proteins (RBPs) in
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Research Focus
- Role of RNA binding proteins (RBPs) in hematopoiesis and leukemogenesis
- Hematopoietic malignancies targeted therapy
Research FocusRole of RNA binding proteins and RNA modifiers
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Research Focus
- Role of RNA binding proteins and RNA modifiers during AML tumorigenesis.
- Therapeutic value of small molecular inhibitors targeting tumorigenic RNA binding proteins and RNA modifiers.
Research Focus Integrin signaling in leukemia stem cell
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Research Focus
- Integrin signaling in leukemia stem cell regulation
My research focuses on how integrin-mediated adhesion and signaling pathways regulate leukemia stem cell survival, proliferation, and interaction with the bone marrow microenvironment. - Epigenetic regulation of germline development by TET1
I study how TET1-mediated DNA demethylation influences germline cell fate determination and epigenetic reprogramming during early development
Research FocusInvestigate the molecular mechanisms, including
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Research Focus
- Investigate the molecular mechanisms, including transcriptional regulation, RNA processing, and stress response pathways, that drive the initiation and progression of hematopoietic malignancies, including leukemia and myelodysplastic syndromes.
- Use in vivo models and multi-omics approaches to uncover key regulators of hematopoietic stem cells and identify potential therapeutic targets.
Research FocusInvestigate the molecular mechanism of RNA
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Research Focus
Investigate the molecular mechanism of RNA regulators during Leukemogenesis.
Our Publications
Yu F, Zheng S, Yu C, Gao S, Shen Z, Nar R, Liu Z, Huang S, Wu L, Gu T, Qian Z*. J Clin Invest 2025 Feb 4;135(6):e185149. doi: 10.1172/JCI185149. PMID: 39960727
Nar R, Wu Z, Li Y, Smith A, Zhang Y, Wang J, Yu F, Gao S, Yu C, Huo Z, Zheng G, Qian Z*. Genes Dis. 2024 Nov 7;12(4):101452. doi: 10.1016/j.gendis.2024.101452. eCollection 2025 Jul. PMID: 40453361
Qian Z* and Yu F. Blood. 2024 Jul 4;144(1):6-7. doi: 10.1182/blood.2024024685.PMID: 38963670
Yu F, Liu S, Zhu AC, He C, Qian Z*. STAR Protoc. 2024 Mar 15;5(1):102855. 2024.102855. PMID: 38300798
Yu F, Zhu A, Liu S, Wang Y, Khudaverdyann N, Yu C, Wu Q, Jiang Y, Song J, Jin L, He C and Qian Z*. Mol Cell 2023 Jun 15;83(12):2003-2019.e6. PMID: 37257451 DOI: 10.1016/j.molcel.2023.05.010
Yu C, Sheng Y, Ni H, Qiu A, Huang Y and Qian Z*. J Clin Invest. 2023 Aug 1;133(15):e163911. doi: 10.1172/JCI163911.
Yu F. Qian Z*. J Clin Invest. 2023 Jun 15;133(12):e171104. doi: 10.1172/JCI171104.
Dang Q, Wu Q, Yu F, Sheng Y, Yu C, Song G, Paulsen K, Lyu J and Qian Z*. Hematologica. 2022 Aug1: 107(8). 1922 doi: 10.3324/haematol.2021.279300. PMID: 34818872
Sheng Y, Wei J, Yu F, Yu C, Wu Q, Liu Y, Li L, Cui X, Gu X, Shen B, Li W, He C* and Qian Z*. Blood. 2021 Dec 30;138(26):2838-2852. doi: 10.1182/blood.2021011707. PMID: 34255814
Yu F, Wei J, Cui X, Yu C, Ni W, Bungert J, Wu L, He C, Qian Z*. Nucleic Acids Res. 2021 Jun 4;49(10):5779-5797. doi: 10.1093/nar/gkab415. PMID: 34048572