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  • Dongmei Ren
  • Dongmei Ren, Ph.D, Professor

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    ADDRESS:

    School of Pharmaceutical Sciences
    Shandong University
    No.44, Wenhuaxi Road, Jinan, 250012
    P.R.China
    Tel: 0086-531-88382012

    E-mail: rendom@sdu.edu.cn

    EDUCATION:

    1988--1992: Shandong Medical University , Bachelor

    1992--1995: Shandong Traditional Chinese Medicine University , Master

    2003--2007: Shandong University, Ph. D

     

    PROFESSIOAN EXPERIENCE:
    2010-present:
    Shandong University, Professor

    2015-2016: Center for Drug Evaluation, China Food and Drug Administration

    2009-2010: University of Arizona, Research associate

    2004-2010: Shandong University, Associate professor

    2005: Center for Drug Evaluation, China Food and Drug Administration

    1997-2004: Shandong University, Lecturer

    1995-1997: Shandong Medical University, Teaching assistant


    RESEARCH INTERESTS:
    1. Isolation and identification of bioactive natural compounds targeting Nrf2-Keap1 pathway

    2. Bioactivity evaluation of Nrf2 activators for cancer chemoprevention

    3. Develpoment of novel traditional chinese medicine originated from herbs 

     

    RESEARCH FOUNDING:

    1. Investigation of quassinoids targeting Nrf2 from Brucea javanica, National Natural Science Foundation, No:81173528,¥580000, PI.

    2. Flavonoidal alkaloids from Dracocephalum rupestre, National Natural Science Foundation, No. 30672611, ¥280000, PI.

    3. Nrf2 activators from Dracocephalum plants, National Natural Science Foundation No. 30973622, ¥320000, PI.

    4. Total flavonoids from Dracocephalum moldavica,Shandong Key Technologies R & D Program, No. 2006GG2202058,PI,¥100000

    5. Flavonoidal alkaloids from Dracocephalum plants, Foundation for Excellent Young Scientists in Shandong Province,No. 2008BS02015,PI,¥60000

    7. Flavonoidal alkaloids from Dracocephalum plants,China Postdoctoral Science Foundation,No. 20080441137,PI, ¥30000  6. Phytochemicals targeting ARE-Nrf2-Keep1 pathway,Independent Innovation Foundation of Shandong University, No. 2012TS203, ¥100000, PI,


    RECENT PUBLICATION:

    1. Zhao LJ#, Wen Q#, Yang GT, Huang ZQ, Shen T, Li HZ, Ren DM*. (2016) Apoptosis induction of dehydrobruceine B on two kinds of human lung cancer cell lines through mitochondrial-dependent pathway. Phytomedicine. 23(2): 114-122.

    2. Li HZ, Hou Z, Li C, Zhang Y, Shen T, Hu QW, Ren DM *. (2015) Three pairs of diastereoisomeric flavanone glycosides from Viscum articulatum. Fitoterapia. 102:156-162.

    3. Yang S, Shen T, Zhao LJ, Li C, Zhang Y, Lou HX, Ren DM*. (2014) Chemical constituents of Lobelia chinensis. Fitoterapia. 93, 168-174.

    4. Shen T, Chen XM, Harder B, Long M, Wang XN, Lou HX, Wondark G, Ren DM*, Zhang D*. (2014) Plant extracts of the family Lauraceae: A potential resource for chemopreventive agents that activate the Nrf2/ARE pathway. Planta Med. 80 (5), 426-434

    5. Yang S, Li C, Wang SQ, Zhao LJ, Hou Z, Lou HX, Ren DM*. (2013) Chiral separation of two diastereomeric pairs of enantiomers of novel alkaloid-lignan hybrids from Lobelia chinensis and determination of the tentative absolute configuration. J Chromatogr A. 1311, 134-139.

    6. Yang S, Wang LM, Guo XJ, Lou HX and Ren DM*. (2013) A new flavonoid glycoside and other constituents from Dracocephalum moldavica. Nat. Prod. Res. 27(3), 201-207

    7. Jing X§, Ren DM§ (co-first author), Wei XB, Shi HY, Zhang XM, Perez R.G., Lou HY*,

    Lou HX. (2013) Eriodictyol-7-O-glucoside activates Nrf2 and protects against cerebral ischemic injury. Toxicol. Appl. Pharmacol. 273(3), 672-679.

    8. Wang LM, Wang SQ, Yang S, Guo XJ, Lou HX and Ren DM*. (2012) Phenolic alkaloids from the aerial parts of Dracocephalum heterophyllum. Phytochemistry. 82, 166-171.

    9. Hu QW, Zhang DD, Wang LM, Lou HX and Ren DM*. (2012) Eriodictyol-7-O-glucoside, a novel Nrf2 activator, confers protection against cisplatin-induced toxicity. Food Chem. Toxicol. 50, 1927-1932.

    10. Ren DM, Villeneuve NF, Jiang T, Wu TD, Lau A, Toppin AH and Zhang DD*. (2011) Brusatol enhances the efficacy of chemotherapy by inhibiting the Nrf2-mediated defense mechanism. Proc Natl Acad Sci U S A 108 (4), 1433 – 8. 

     


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