Principal investigator
Cancer Research Center
Personal Homepage
CONTACT
lglou@mail.shcnc.ac.cn
86-21-50806056
201203
555 Zu Chong Zhi Road , Zhang Jiang Hi-Tech Park, Pudong, Shanghai
Dr. Liguang Lou, born in 1967 in Zhejiang Province, received his master's degree in pharmacology in Henan Medical University in 1993, and Ph.D. in Shanghai Institute of Materia Medica, Chinese Academy of Sciences in 1996. He received his postdoctoral training in Shanghai Institute of Cell Biology, Chinese Academy of Sciences during 1996-1998 and in University of Pittsburgh (USA) during 2000-2002. He is now a PI in Shanghai Institute of Materia Medica, Chinese Academy of Sciences.
Dr. Lou’s lab is mainly focusing on anti-cancer drug pharmacology, especially on the discovery of new anti-tumor agents with novel mechanism of action. Through close collaboration with medicinal chemists, he has discovered a number of anti-cancer drug candidates for further development. He was awarded “National outstanding Post-doctor Award” in 2005. He has 10 patents granted and published more than 80 papers. Now he is the standing member of Shanghai Pharmacological Society, and the member of the Committee of Anticancer Drug, Chinese Pharmacological Society. He is also serving a member of editorial board in several journals.
Education
09/01/1990 - 07/31/1993 M.S., Pharmacology, Henan Medical University, M.S.
09/01/1993 - 07/31/1996 Ph.D. Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences
09/01/1996 - 07/31/1998 Postdoctoral fellow, Cell Biology, Shanghai Institute of Cell Biology, Chinese Academy of Sciences
03/01/2000 - 06/30/2002 Postdoctoral fellow, Pharmacology, University of Pittsburgh, USA
Work Experience
08/01/1985 - 07/31/1990 Teacher, Department of Anatomy, Zhejiang Quzhou Medical School
08/01/1998 - 02/28/2000 Associate Professor, Department of Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences,
07/01/2002 - 12/01/2002 Associate Professor, Department of Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences
01/01/2003 –present Professor, Department of Pharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences
1.Study on signaling transduction of tumor cell proliferation via pyridazinone-derivatives as molecular probes,PI,2009.1-2011.12, National Natural Science Foundation.
2.Pharmacological platform for anti-tumor drug innovation,PI,2009.1-2011.12, National Science & Technology Major Project
3.Molecular mechanism of PI3K inhibitor XC-302,PI,2009.1-2011.12, National Natural Science Foundation.
4.Molecular mechanism of YHHU-0632,PI,2012.1-2014.12, National Natural Science Foundation.
5.Design, synthesis, and biological activity of new platinum compounds with DNA-targeting and glycolysis inhibition,Co-PI,2012.1-2014.12, National Natural Science Foundation.
6.The molecular mechanism of a novel HSP90 inhibitor X66,PI,2012.1-2014.12, National Natural Science Foundation.
7.Preclinical study of YHHU-756,PI,2013.1-2015.12, National Science & Technology Major Project.
8.Pharmacological platform for drug innovation,PI,2013.1-2016.12, National Science & Technology Major Project.
2004-present Member of editorial board, Chinese Journal of New Drugs and Clinical Remedies
2003-present Member of editorial board, Cancer Research on Prevention and Treatment
2003-present Member of editorial board, Chinese Pharmacological Bulletin.
2000-present Standing member, Committee of Shanghai Pharmacological and Toxicological Society
1998-present Standing member, Committee for Anti-cancer Drugs, Chinese Pharmacological Society
Full Publication List
Selected Publications
1.Lei Wang, Quanren Wang, Piaopiao Xu, Li Fu, Yun Li, Haoyu Fu, Haitian Quan and* Liguang Lou*. YES1 amplification confers trastuzumab–emtansine (T-DM1) resistance in HER2-positive cancer. Br J Cancer 2020(123):1000-1011. DOI: 10.1038/s41416-020-0952-1 (SCI-E/PubMed收录,药物所名义发文)
2.Xiang-ling Chen, Peng Liu, Wei-liang Zhu and Li-guang Lou*. DCZ5248, a novel dual inhibitor of Hsp90 and autophagy,exerts antitumor activity against colon cancer. Acta Pharmacol Sin. 2021 Jan;42(1):132-141; DOI: 10.1038/s41401-020-0398-2(SCI-E/PubMed收录,药物所名义发文)
3.Chen L, Quan H, Xu Z, Wang H, Xia Y, Lou L*, Yang W*. A modular biomimetic strategy for the synthesis of macrolide P-glycoprotein inhibitors via Rh-catalyzed C-H activation. Nat Commun 2020(11):2151. DOI: 10.1038/s41467-020-16084-0(SCI-E/PubMed收录,药物所名义发文)
4.Mingzhao Gao, Hongmei Zhu, Li Fu, Yun Li, Xubin Bao, Haoyu Fu, Haitian Quan, Lei Wang*, Liguang Lou*. Pharmacologic Characterization of TQ05310, a Potent Inhibitor of Isocitrate Dehydrogenase 2 (IDH2) R140Q and R172K mutants. Cancer Science, 2019:3306-3314. DOI: 10.1111/cas.14152(SCI-E/PubMed收录,药物所名义发文)
5.Liu CP, Xie CY, Zhao JX, Ji KL, Lei XX, Sun H*, Lou LG*, Yue JM*. Dysoxylactam A: A Macrocyclolipopeptide Reverses P-Glycoprotein-Mediated Multidrug Resistance in Cancer Cells. J Am Chem Soc. 2019(141):6812-6816. DOI: 10.1021/jacs.9b02259(SCI-E/PubMed收录,药物所名义发文)
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