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Li Li
lli@xmu.edu.cn
English, Chinese
Fujian
Xiamen University
Life Sciences
  • 2008 - B.S. in Life Science: Xiamen University
  • 2013 - Ph.D. in Cellular and Molecular Biology: Xiamen University
  • 2015-2018 - Engineer, Xiamen University
  • 2019-Present - Assistant Professor, School of Life Sciences, Xiamen University
  • Fujian Provincial Natural Science First Prize (2017)
Discovery and mechanistic research of bioactive natural products
Functional and regulatory mechanism study on potential therapeutic targets
  • Impeding the interaction between Nur77 and p38 reduces LPS-induced inflammation., Li, L.; Liu, Y.; Chen, H. Z.; Li, F. W.; Wu, J. F.; Zhang, H. K.; He, J. P.; Xing, Y. Z.; Chen, Y.; Wang, W. J.; Tian, X. Y.; Li, A. Z.; Zhang, Q.; Huang, P. Q.; Han, J.; Lin, T.; Wu, Q., 2015
  • Pharmacological Targeting of Vacuolar H(+)-ATPase via Subunit V1G Combats Multidrug-Resistant Cancer., Wang, Y.; Zhang, L.; Wei, Y.; Huang, W.; Li, L.; Wu, A. A.; Dastur, A.; Greninger, P.; Bray, W. M.; Zhang, C. S.; Li, M.; Lian, W.; Hu, Z.; Wang, X.; Liu, G.; Yao, L.; Guh, J. H.; Chen, L.; Wang, H. R.; Zhou, D.; Lin, S. C.; Xu, Q.; Shen, Y.; Zhang, J.; Jurica, M. S.; Benes, C. H.; Deng, X., 2020
  • Tandem-Mass-Tag Based Proteomic Analysis Facilitates Analyzing Critical Factors of Porous Silicon Nanoparticles in Determining Their Biological Responses under Diseased Condition., Li, Y.; Liu, Z.; Li, L.; Lian, W.; He, Y.; Khalil, E.; Makila, E.; Zhang, W.; Torrieri, G.; Liu, X.; Su, J.; Xiu, Y.; Fontana, F.; Salonen, J.; Hirvonen, J.; Liu, W.; Zhang, H.; Santos, H. A.; Deng, X., 2020
  • The orphan receptor TR3 suppresses intestinal tumorigenesis in mice by downregulating Wnt signalling., Chen, H. Z.; Liu, Q. F.; Li, L.; Wang, W. J.; Yao, L. M.; Yang, M.; Liu, B.; Chen, W.; Zhan, Y. Y.; Zhang, M. Q.; Cai, J. C.; Zheng, Z. H.; Lin, S. C.; Li, B. A.; Wu, Q., 2012
  • A new ALK inhibitor overcomes resistance to first- and second-generation inhibitors in NSCLC., Lu, Y.; Fan, Z.; Zhu, S. J.; Huang, X.; Zhuang, Z.; Li, Y.; Deng, Z.; Gao, L.; Hong, X.; Zhang, T.; Li, L.; Sun, X.; Huang, W.; Zhang, J.; Liu, Y.; Zhang, B.; Jiang, J.; Gui, F.; Wang, Z.; Li, Q.; Song, S.; Huang, X.; Wu, Q.; Chen, L.; Zhou, D.; Zhang, J.; Yun, C. H.; Chen, L.; Deng, X., 2022
  • Pharmacological targeting PIKfyve and tubulin as an effective treatment strategy for double-hit lymphoma., Feng, L.; Chen, K.; Huang, W.; Jiang, Y.; Sun, X.; Zhou, Y.; Li, L.; Li, Y.; Deng, X.; Xu, B., 2022
  • Biosynthesis and Chemical Diversification of Verucopeptin Leads to Structural and Functional Versatility., Zhang, L.; Wang, Y.; Huang, W.; Wei, Y.; Jiang, Z.; Kong, L.; Wu, A. A.; Hu, Z.; Huang, H.; Xu, Q.; Li, L.; Deng, X., 2020
  • Blocking PPARgamma interaction facilitates Nur77 interdiction of fatty acid uptake and suppresses breast cancer progression., Yang, P. B.; Hou, P. P.; Liu, F. Y.; Hong, W. B.; Chen, H. Z.; Sun, X. Y.; Li, P.; Zhang, Y.; Ju, C. Y.; Luo, L. J.; Wu, S. F.; Zhou, J. X.; Wang, Z. J.; He, J. P.; Li, L.; Zhao, T. J.; Deng, X.; Lin, T.; Wu, Q., 2020
  • Discovery of 4-methyl-N- (4-((4-methylpiperazin-1-yl)methyl) -3- (trifluoromethyl)phenyl) -3- ((6-(pyridin-3-yl) -1H-pyrazolo [3,4-d] pyrimidin-4-yl)-oxy)benzamide as a potent inhibitor of RET and its gatekeeper mutant., Li, X.; Su, J.; Yang, Y.; Lian, W.; Deng, Z.; Yang, Z.; Chen, G.; Zhang, B.; Dong, C.; Liu, X.; Li, L.; Wang, Z.; Hu, Z.; Xu, Q.; Deng, X., 2020
  • Targeting RIPK3 oligomerization blocks necroptosis without inducing apoptosis., Li, W.; Ni, H.; Wu, S.; Han, S.; Chen, C.; Li, L.; Li, Y.; Gui, F.; Han, J.; Deng, X., 2020
  • Discovery of methyl 3-((2-((1-(dimethylglycyl)-5-methoxyindolin-6-yl)amino)-5-(trifluoro-methyl) pyrimidin-4-yl)amino)thiophene-2-carboxylate as a potent and selective polo-like kinase 1 (PLK1) inhibitor for combating hepatocellular carcinoma., Deng, Z.; Chen, G.; Liu, S.; Li, Y.; Zhong, J.; Zhang, B.; Li, L.; Huang, H.; Wang, Z.; Xu, Q.; Deng, X., 2020
  • Discovery and optimization of 4-oxo-2-thioxo-thiazolidinones as NOD-like receptor (NLR) family, pyrin domain-containing protein 3 (NLRP3) inhibitors., Chen, Y.; He, H.; Jiang, H.; Li, L.; Hu, Z.; Huang, H.; Xu, Q.; Zhou, R.; Deng, X., 2020
  • Pharmacological Targeting of STK19 Inhibits Oncogenic NRAS-Driven Melanomagenesis., Yin, C.; Zhu, B.; Zhang, T.; Liu, T.; Chen, S.; Liu, Y.; Li, X.; Miao, X.; Li, S.; Mi, X.; Zhang, J.; Li, L.; Wei, G.; Xu, Z. X.; Gao, X.; Huang, C.; Wei, Z.; Goding, C. R.; Wang, P.; Deng, X.; Cui, R., 2019
  • A cell-based high-throughput screening method based on a ubiquitin-reference technique for identifying modulators of E3 ligases., Tian, M.; Zeng, T.; Liu, M.; Han, S.; Lin, H.; Lin, Q.; Li, L.; Jiang, T.; Li, G.; Lin, H.; Zhang, T.; Kang, Q.; Deng, X.; Wang, H. R., 2019
  • Close-loop dynamic nanohybrids on collagen-ark with in situ gelling transformation capability for biomimetic stage-specific diabetic wound healing., Liu, Z. H.; Li, Y. Z.; Li, W.; Lian, W. H.; Kemell, M.; Hietala, S.; Figueiredo, P.; Li, L.; Makila, E.; Ma, M.; Salonen, J.; Hirvonen, J. T.; Liu, D. F.; Zhang, H. B.; Deng, X. M.; Santos, H. A., 2019
  • A non-covalent inhibitor XMU-MP-3 overrides ibrutinib-resistant Btk(C481S) mutation in B-cell malignancies., Gui, F.; Jiang, J.; He, Z.; Li, L.; Li, Y.; Deng, Z.; Lu, Y.; Wu, X.; Chen, G.; Su, J.; Song, S.; Zhang, Y. M.; Yun, C. H.; Huang, X.; Weisberg, E.; Zhang, J.; Deng, X., 2019
  • Discovery and Identification of Small Molecules as Methuosis Inducers with in Vivo Antitumor Activities., Huang, W.; Sun, X.; Li, Y.; He, Z.; Li, L.; Deng, Z.; Huang, X.; Han, S.; Zhang, T.; Zhong, J.; Wang, Z.; Xu, Q.; Zhang, J.; Deng, X., 2018
  • Mycoepoxydiene suppresses HeLa cell growth by inhibiting glycolysis and the pentose phosphate pathway., Jin, K.; Li, L.; Sun, X.; Xu, Q.; Song, S.; Shen, Y.; Deng, X., 2017
  • Targeting BRK-Positive Breast Cancers with Small-Molecule Kinase Inhibitors., Jiang, J.; Gui, F.; He, Z.; Li, L.; Li, Y.; Li, S.; Wu, X.; Deng, Z.; Sun, X.; Huang, X.; Huang, W.; Han, S.; Zhang, T.; Wang, Z.; Jiao, B.; Song, S.; Wang, H.; Chen, L.; Zhou, D.; Liu, Q.; Ren, R.; Zhang, J.; Deng, X., 2017
  • Structure Determinants of Lagunamide A for Anticancer Activity and Its Molecular Mechanism of Mitochondrial Apoptosis., Huang, X.; Huang, W.; Li, L.; Sun, X.; Song, S.; Xu, Q.; Zhang, L.; Wei, B. G.; Deng, X., 2016
  • Enhancement of hypothalamic STAT3 acetylation by nuclear receptor Nur77 dictates leptin sensitivity., Chen, Y.; Wu, R.; Chen, H. Z.; Xiao, Q.; Wang, W. J.; He, J. P.; Li, X. X.; Yu, X. W.; Li, L.; Wang, P.; Wan, X. C.; Tian, X. H.; Li, S. J.; Yu, X.; Wu, Q., 2015
  • Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway., Wang, W. J.; Wang, Y.; Chen, H. Z.; Xing, Y. Z.; Li, F. W.; Zhang, Q.; Zhou, B.; Zhang, H. K.; Zhang, J.; Bian, X. L.; Li, L.; Liu, Y.; Zhao, B. X.; Chen, Y.; Wu, R.; Li, A. Z.; Yao, L. M.; Chen, P.; Zhang, Y.; Tian, X. Y.; Beermann, F.; Wu, M.; Han, J.; Huang, P. Q.; Lin, T.; Wu, Q., 2014
  • Diindolylmethane analogs bind NR4A1 and are NR4A1 antagonists in colon cancer cells., Lee, S. O.; Li, X.; Hedrick, E.; Jin, U. H.; Tjalkens, R. B.; Backos, D. S.; Li, L.; Zhang, Y.; Wu, Q.; Safe, S., 2014
  • Prolyl isomerase Pin1 stabilizes and activates orphan nuclear receptor TR3 to promote mitogenesis., Chen, H. Z.; Li, L.; Wang, W. J.; Du, X. D.; Wen, Q.; He, J. P.; Zhao, B. X.; Li, G. D.; Zhou, W.; Xia, Y.; Yang, Q. Y.; Hew, C. L.; Liou, Y. C.; Wu, Q., 2012
  • Akt phosphorylates the TR3 orphan receptor and blocks its targeting to the mitochondria., Chen, H. Z.; Zhao, B. X.; Zhao, W. X.; Li, L.; Zhang, B.; Wu, Q., 2008
Natural Products Drug Development Biosynthetic Approaches Chemoproteomic Therapeutic Targets Small Molecules Kinases Epigenetic Enzymes Lead Compounds Molecular Mechanisms

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