Rui Su Lab
Research Lab Overview
Three overarching questions drive the Rui Su lab research program:
- How do RNA modifications and RBPs coordinate gene expression at the post-transcriptional level?
- Whether the dysregulation of RNA modifications or RBPs is associated with tumorigenesis?
- Can we develop novel therapeutic approaches targeting RNA modifications or RBPs to treat tumors?
Dr. Su's prior studies have determined the oncogenic role of FTO in AML as a demethylase of N6-methyladenosine (m6A, the most abundant modification in mRNA) (Cancer Cell, 2017). In addition, she discovered that FTO could act as a druggable target for leukemia therapy (Cell, 2018) and developed selective and effective novel small-molecule inhibitors targeting FTO to treat leukemia via attenuating leukemia stem cell self-renewal, reprogramming leukemia metabolism, and potentiating immunotherapy (Cancer Cell, 2019 & 2020; Molecular Cell, 2021). More recently, Dr. Su currently leads another study to reveal the robust oncogenic role and methyltransferase-independent mechanism of METTL16 in HCC (Nature Cell Biology, 2022).
Several foundation awards fund Dr. Su’s research program, including The Margaret E. Early Medical Research Trust, the Leukemia Research Foundation, and the American Association for the Study of Liver Disease Foundation. She also contributes to several NIH R01 grants as a co-investigator.
An assistant professor in the Department of Systems Biology, Rui Su, Ph.D., conducts research on RNA modification(s) and RNA-binding proteins (RBPs)-mediated post-transcriptional gene regulation in tumorigenesis.
Lab Members
Research Focus RNA-binding proteins and RNA granules in
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Research Focus
- RNA-binding proteins and RNA granules in leukemogenesis
Research Focus Targeting RNA modification for leukemia therapy
Research Focus
- Targeting RNA modification for leukemia therapy
Research FocusTumorigenesis mechanism and new treatment
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Research Focus
- Tumorigenesis mechanism and new treatment strategies exploring for leukemia
Education
- Doctor of Medicine
Publications
- Venetoclax with hypomethylating agents versus intensive chemotherapy in newly diagnosed acute myeloid leukemia with myelodysplasia related changes: a propensity score matched analysis based on International Consensus Classification. Blood Cancer J, 2024;14:144
- Investigations of the prognostic value of RUNX1 mutation in acute myeloid leukemia patients: Data from a real-world study. Leuk Res, 2024;139:107483
- Venetoclax combined with azacitidine as an effective and safe salvage regimen for relapsed or refractory T-cell acute lymphoblastic leukemia: a case series. Leuk Lymphoma, 2021, 62(13):3300-3303
Research FocusRNA-binding proteins in tumor progression and
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Research Focus
- RNA-binding proteins in tumor progression and therapeutic resistance, particularly in gynecologic cancers
- Organoid-based modeling and translational research in solid tumors
Research Focus Mitochondrial RNA-binding proteins in
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Research Focus
- Mitochondrial RNA-binding proteins in tumorigenesis
Research Focus RNA-binding proteins in regulating mRNA
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Research Focus
- RNA-binding proteins in regulating mRNA translation and tumor metabolism
Research FocusRNA-binding protein and RNA modification in
...
Research Focus
- RNA-binding protein and RNA modification in leukemogenesis.
Partnerships
We collaborate with organizations in progressing the development of new treatments in our specialized areas of research.
Our Publications
Li Z*, Weng H*, Su R*, Weng X*, Zuo Z*, Li C, Huang H, Nachtergaele S, Dong L, Hu C, Qin X, Tang L, Wang Y, Hong GM, Huang H, Wang X, Chen P, Gurbuxani S, Arnovitz S, Li Y, Li S, Strong J, Neilly MB, Larson RA, Jiang X, Zhang P, Jin J, He C, Chen J. Cancer Cell. 2017 Jan 9;31(1):127-141. PMCID: PMC5234852. **Cover Story of this issue of Cancer Cell ***Highlighted (Research Watch) by Cancer Discovery (2017 Feb;7(2): OF9)
Su R*, Dong L*, Li C*, Nachtergaele S*, Wunderlich M, Qing Y, Deng X, Wang Y, Weng X, Hu C, Yu M, Skibbe J, Dai Q, Zou D, Wu T, Yu K, Weng H, Huang H, Ferchen K, Qin X, Zhang B, Qi J, Sasaki AT, Plas D, Bradner JE, Wei M, Marcucci G, Jiang X, Mulloy J, Jin J, He C, Chen J. Cell. 2018 Jan 11;172(1-2):90-105. ** Highlighted (Research Highlights) by Nature Reviews Cancer (2018 Jan 25;18(2):66.); ***Highlighted (Research Watch) by Cancer Discovery (2018 Feb;8(2):137).
Weng H, Huang H, Wu H, Qin X, Zhao BS, Dong L, Shi H, Skibbe J, Shen C, Hu C, Sheng Y, Wang Y, Wunderlich M, Zhang B, Dore L, Su R, Deng X, Ferchen K, Li C, Sun M, Lu Z, Jiang X, Marcucci G, Mulloy J, Yang J, Qian, Z, Wei M, He C, Chen J. Cell Stem Cell. 2018 Feb 1;22(2):191-205.
Huang H, Weng H, Sun W, Qin X, Shi H, Wu H, Zhao BS, Mesquita A, Liu C, Yuan CL, Hu YC, Hüttelmaier S, Skibbe J, Su R, Deng X, Dong L, Sun M, Li C, Nachtergaele S, Wang Y, Hu C, Ferchen K, Greis KD, Jiang X, Wei M, Qu L, Guan JL, He C, Yang J, Chen J. Nature Cell Biology. 2018 Mar;20(3):285-295.
Huang H, Weng H, Zhou K, Wu T, Zhao BS, Sun M, Chen Z, Deng X, Xiao G, Auer F, Klemm L, Wu H, Zuo Z, Qin X, Dong Y, Zhou Y, Qin H, Tao S, Du J, Liu J, Lu Z, Yin H, Mesquita A, Yuan CL, Hu YC, Sun W, Su R, Dong L, Shen C, Li C, Qing Y, Jiang X, Wu X, Sun M, Guan JL, Qu LH, Wei M, Müschen M, Huang G, He C, Yang JH, Chen J. Nature. 2019 Mar 21;567(7748):414-419.
Latest Research News
Contact Information
34.1293409, -117.971358
Duarte, CA 91010