Qingping Dou

Position Title

Professor
Basic Science

Office Location

Karmanos Cancer Institute
4100 John R
Hudson-Webber Cancer Research Center RM 540.1
Mail Code: HW05AO
Detroit, MI 48201

Office Phone

313-576-8301

Office Fax

313-576-8307

Education Training

Education
(1988)  Ph.D. Chemistry, Rutgers University, Piscataway, NJ
(1981)  B.S. Chemistry, Shandong University, Jinan, Shandong, People's Republic of China

Postgraduate Training
(1988-1993)  Postdoctoral Research Fellow, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

Professional Experience

Faculty Appointments
(2010-Present)  Professor, Department of Oncology, Wayne State University School of Medicine, Detroit, MI
(2009-Present)  Professor, Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI
(2003-Present)  Professor, Department of Pathology, Wayne State University School of Medicine, Detroit, MI
(2000-2003)  Associate Professor, Department of Interdisciplinary Oncology, University of SouthFloridaCollege of Medicine, Tampa, FL
(1998-2003)  Associate Professor, Department of Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, FL
(1993-1998)  Assistant Professor, Department of Pharmacology, University of PittsburghSchool of Medicine, Pittsburgh, PA

Hospital or Other Professional Appointments
(2012-Present) Scientific Member, Molecular Therapeutics Program, Barbara Ann Karmanos Cancer Institute, Detroit, MI
(2010-2011) Co-Program Leader and Scientific Member, Developmental Therapeutics Program, Barbara Ann Karmanos Cancer Institute, Detroit, MI
(2003-2010) Co-Program Leader and Scientific Member, Population Studies and Prevention Program, Barbara Ann Karmanos Cancer Institute, Detroit, MI
(1998-2003) Member in Residence (Scientific Member), Drug Discovery Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL
(1993-1998) Member, Experimental Therapeutic Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA

Major Professional Societies

American Association for Cancer Research, Inc.
American Association for the Advancement of Science
American Society for Pharmacology and Experimental Therapeutics
American Chemistry Society

Honors and Awards

(2007)  WayneStateUniversitySchool of Medicine Research Excellence Award Nominee
(2006)  Karmanos Cancer Center Director's Award (for the article published by Yang HJ, Chen D, Cui QC, Yuan X, and Dou QP in Cancer Research 66, 4758-4765, 2006).
(2000)  Moffitt Cancer Center & Research Institute Director's Award (for the article published by Li B and Dou QP in Proc. Natl. Acad. Sci. USA, 2000; 97:3850-3855)

Courses taught

CB 7210: Fundamentals of Cancer Biology
CB 7460: Mechanisms of Neoplasia: Alterations to Cellular Signaling
CB 7700: Cancer Biology Journal Club
CB 7890: Cancer Biology Student Seminars

Research Interests

The main objective in this laboratory is to discover molecular targets of natural products in pre-clinical studies, followed by validation in targeted cancer intervention clinical trials. Dr. Dou's laboratory is one of the first to report that proteasome inhibitors rapidly induce tumor cell apoptosis, selectively activate the cell death program in oncogene-transformed, but not normal or untransformed cells, and are able to trigger apoptotic death in human cancer cells that are resistant to various anticancer agents. Possible molecular mechanisms involve, at least in part, accumulation of the cyclin-dependent kinase inhibitor p27kip and the apoptosis inducer Bax. Dr. Dou's laboratory has also shown that some tea polyphenols and medicinal compounds potently and specifically inhibit the chymotrypsin-like activity of the proteasome in vitro and in vivo at physiological concentrations. Furthermore, his laboratory has established, for the first time, a computational molecular model that shows how these natural compounds bind and target the proteasome chymotrypsin subunit. This innovative computational model has been validated by comparison of predicted and actual activities of various analogs, either naturally occurring or rationally designed and synthesized. Recently, Dr. Dou and collaborators have reported that certain copper-binding drugs (such as the antialcoholism drug Disulfiram) can convert the pro-angiogenic copper to a specific cancer cell death inducer, and that environmental toxic organotins target the proteasome in human cells and proteasome inhibition by organotins contributes to their cellular toxicity.

 

 

Publications

1. Schmitt SM, Neslund-Dudas C, Shen M, Cui QZ, Mitro B, and Dou QP. Involvement of ALAD-20S Proteasome Complexes in Ubiquitination and Acetylation of Proteasomal α2 Subunits. Journal of Cellular Biochemistry (2014 Impact Factor 3.368). 2016 Jan;117(1):144-51. doi: 10.1002/jcb.25259. (first published: 19 November 2015) doi: 10.1002/jcb.25259.

2. Deshmukh RR, Dou QP. Proteasome inhibitors induce AMPK activation via CaMKKβ in human breast cancer cells. Breast Cancer Research and Treatment. (2014 Impact Factor 3.940) 2015 Aug;153(1):79-88. doi: 10.1007/s10549-015-3512-2. Epub 2015 Jul 31.

3. Lu L, Shi W, Deshmukh RR, Long J, Cheng X, Ji W, Zeng G, Chen X, Zhang Y, Dou QP. Tumor necrosis factor-α sensitizes breast cancer cells to natural products with proteasome-inhibitory activity leading to apoptosis. PLoS ONE (IF 4.537). 2014 Nov 24;9(11):e113783. doi: 10.1371/journal.pone.0113783. eCollection 2014.

4. Nardon C, Schmitt SM, Yang H, Zuo J, Fregona, Dou QP. Gold(III)-dithiocarbamato Peptidomimetics in the Forefront of the TargetedAnticancer Therapy: Preclinical Studies against Human Breast Neoplasia. PLoS ONE (IF 4.537). 2014 Jan 2;9(1):e84248. doi: 10.1371/journal.pone.0084248. eCollection 2014

5. Shen M, Zhang Z, Ratnam M, Dou QP. The Interplay of AMP-activated Protein Kinase and Androgen Receptor in Prostate Cancer Cells. Journal of Cellular Physiology (Rapid Communications) (IF 4.257), 2014 Jun;229(6):688-95. doi: 10.1002/jcp.24494

6. Buac D, Kona FR, Seth AK, Dou QP. Regulation of Metformin Response by Breast Cancer Associated Gene 2 (BCA2). Neoplasia (IF 5.470), 2013; 15: 1379-1390

7. Li X, Liu S, Huang H, Liu N, Zhao C, Liao S, Yang C, Liu Y, Zhao C, Li S, Lu X, Liu C, Guan S, Zhao K, Shi X, Song W, Zhou P, Dong X, Guo H, Wen G, Zhang C, Jiang L, Ma N, Li B, Wang S, Tan H, Wang X, Dou QP (co-corresponding author) and Liu J (co-corresponding author).Gambogic Acid is a Tissue-Specific Proteasome Inhibitor in vitro and in vivo. Cell Reports (a new open-access, online-only journal from Cell Press). 2013 Jan 31;3(1):211-22. doi: 10.1016/j.celrep.2012.11.023

8. Frezza M, Dou QP* (Co-corresponding author), Xiao Y, Samouei H, Rashidi M*, Samari F, Hemmateenejad F* (Co-corresponding author). In vitro and In vivo Anti-tumor Activities and DNA Binding Mode of Five Coordinated Cyclometallated Organoplatinum(II) Complexes Containing Biphosphine Ligands. Journal of Medicinal Chemistry (IF 5.248), 2011 Sep 22;54(18):6166-76. Epub 2011 Aug 24.

9. Dou QP. Proteasome inhibition and cancer therapy. Poster Review. Nature Reviews Cancer (2010 Impact Factor 37.178), the December issue of 2011.http://www.nature.com/nrc/posters/proteasome/proteasome_poster.pdf

10. Milacic V and Dou QP. The tumor proteasome as a novel target for gold(III) compounds: implications in breast cancer therapy (invited review). Coordination Chemistry Reviews (Impact Factor 10.566), 2009; 253:1649-1660.
 

http://www.ncbi.nlm.nih.gov/pubmed/?term=qp+dou

 

 

 

 

 

Faculty Status

Basic Science

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