Zhaohui (Vincent) Wang, Ph.D.
**** ********** *****, *********, ***** 76051
Cell: 682-***-****; Email: ************@*******.***
* Permanent resident of the United States
CERTIFICATION
Technologist in Molecular Biology (ASCP)
SUMMARY OF QUALIFICATIONS
Molecular assay development in support of regulatory filings to FDA
●Designed, validated and performed modified 5’ RACE-PCR assays to examine
molecular mechanism of RNA interference for animal and clinical studies (GLP
settings; products have been approved by FDA and are currently in Phase I and II)
●Developed RT-QPCR based assay to determine mRNA genotype of Ewing’s sarcoma
and quantify mRNA expression
●Developed allele-specific RT-QPCR to determine mRNA genotype of Kras
●Developed RT-QPCR to determine biomarkers in pancreatic cancer
●Designed, validated and performed RT-QPCR based microRNA assays for
biodistribution study of cancer therapeutics in animal studies and clinical studies (GLP
settings)
● Prepared documentation for IND submissions to FDA
Preclinical and clinical studies on RNA Interference and autologous vaccine
(cancer therapeutics)
●Conducted preclinical and clinical studies for regulatory filings of RNA interference
therapeutics
●Performed preclinical studies including design of RNAi drug, screening of lead RNAi,
identification of RNAi mechanism, and study of biodistribution of RNAi molecules in
vivo
●Conducted preclinical studies for regulatory filings of an autologous cancer vaccine
●Led several RNAi discovery projects aiming at silencing oncogenic genes in
melanoma, pancreatic cancer and breast cancer
Project management
●Managed and coordinated external collaborations with multiple CROs and academic
institutions
●Supervised and trained personnel (summer interns and technical staff)
●Prepared manuscripts, grants applications, SOPs, study protocols and scientific
research articles
●Presented and discussed product development in meetings and conferences
Bioinformatics
●Identified potential targets and signal pathways for cancer therapeutics by analyzing
microarray data from clinical tumor specimens
●Identified potential microRNA targets for cancer therapeutics by mining microRNA
database
●Extensive experience in GeneSpring / dChip / GSEA and other bioinformatics tools
Techniques
●Extensive experience in Real-time PCR, microarray, microRNA analysis, genotyping,
and cellular assays (fluorescence, luminescence, apoptosis, cell proliferation,
cytotoxicity and ELISA)
●Extensive experience in standard molecular biology techniques (molecular cloning,
southern/northern/western blotting, PCR and QPCR, nucleic acid extraction, and gel
electrophoresis)
●Extensive experience in establishment and application of in vitro assay (MTS assay,
LDH assay, reporter assay, flow cytometry and so on)
●Extensive experience in flow cytometer, fluorescent microscope, fluorescent
quantitative assay and immunological assay
PROFESSIONAL EXPERIENCE
2007- Present Research Associate
Gradalis Inc. (Dallas, Texas)
●Developed molecular assays to support biopharmaceutical
development from preclinical to clinical stage
●Led several RNAi discovery projects aiming at silencing oncogenic
genes in melanoma, pancreatic cancer and breast cancer
●Performed preclinical and clinical studies on RNAi-based drugs and
vaccine in support of regulatory filings for cancer therapeutics
2001-2007 Research Assistant
University of North Texas Health Science Center (Fort Worth, Texas)
●Investigated the potential roles of MAPKs in pathogenesis of age-
related macular degeneration
●Investigated the candidacy of stem-cell therapy in age-related
macular degeneration
●Developed a cataract transgenic animal model with overexpression
of the Na/Myo-Inositol Co-Transporter
2000-2001 Product Manager
Simcere Pharmaceutical Group (Nanjing, China)
●Coordinated the development of marketing strategies, advertising
and promotion programs of an osteoporosis drug and ensured their
implementation.
●Developed and conducted specialized training on new products
launched and provided technical support
1999-2000 Clinical Representative
GlaxoSmithKline Pharmaceuticals (China Division)
● Educated customers on the merits and clinical usage of company
products by giving presentations and demonstrations
● Performed clinical and library research and participated in case
reviews and clinical observation
1993-1996 Research Scientist
North China Pharmaceutical Group Corp. (China)
● Product development of anticancer recombinant proteins
EDUCATION
2001-2007 Ph.D., Biomedical Science
University of North Texas Health Science Center (Fort Worth, Texas)
● Dissertation: Molecular mechanisms of and potential therapies for
oxidative damage to the retinal pigment epithelium
1996-1999 M.S., Biopharmaceutics
China Pharmaceutical University (Nanjing, China)
1989-1993 B.S., Pharmacy
China Pharmaceutical University (Nanjing, China)
SELECTIVE HONORS AND AFFILLIATIONS
● Member of American Society of Gene & Cell Therapy (2008-present)
● Member of Sigma Xi Scientific Research Society
● Member of Association for Research in Vision and Ophthalmology (2001-2007)
● Outstanding Graduate Student Award, 1997, China Pharmaceutical University
● Merit-Based Fellowship, 1993 China Pharmaceutical University
PATENTS
1. Methods and compositions to treat cancer using bi-functional SRC3 shRNA. United
States Patent Application 201******** (2013)
2. Chemosensitization by bi-functional small hairpin RNA (bi-shRNA). United States
Patent Application 201******** (2011)
SELECTED PUBLICATIONS
1. Wang Z, Rao D, Senzer N, Nemunaitis J. Preclinical biodistribution and safety
evaluation of pbi-shSTMN1 lipoplex after subcutaneous injection in rats.(In
preparation)
2. Wang Z, Bartosh TJ, Ding M, Roque RS. (2013) MAPKs modulate Retinal
Pigment Epithelium (RPE) response to oxidative stress. J. Medical and
Bioengineering. 3(1):67-73.
3. Rao DD, Wang Z, Senzer N, Nemunaitis J. (2013) RNA interference and
personalized cancer therapy. Discov Med. 15(81):101-10.
4. Rao DD, Senzer N, Wang Z, Kumar P, Jay CM, Nemunaitis J. (2013) Bi-functional
Short Hairpin RNA (bi-shRNA): Design and Pathway to Clinical Application.
Methods in Molecular Biology. 942:259-78.
5. Liu SH, Rao DD, Nemunaitis J, Senzer N, Zhou G, Dawson D, Gingras MC, Wang
Z, Gibbs R, Norman M, Templeton NS, Demayo FJ, O'Malley B, Sanchez R,
Fisher WE, Brunicardi FC.(2012) PDX-1 is a therapeutic target for pancreatic
cancer, insulinoma and islet neoplasia using a novel RNA interference platform.
PLoS One. 7(8).
6. Senzer N, Barve M, Kuhn J, Melnyk A, Beitsch P, Lazar M, Lifshitz S, Magee M,
Oh J, Mill SW, Bedell C, Higgs C, Kumar P, Yu Y, Norvell F, Phalon C, Taquet N,
Rao DD, Wang Z, Jay CM, Pappen BO, Wallraven G, Brunicardi FC, Shanahan
DM, Maples PB, Nemunaitis J. (2012) Phase I Trial of “bi-shRNAifurin/GMCSF
DNA/Autologous Tumor Cell” Vaccine (FANG) in Advanced Cancer. Mol Ther.
20(3):679-86.
7. Wang Z, Rao D, Senzer N, Nemunaitis J. (2011) RNA Interference and Cancer
Therapy. Pharmaceutical Research, 28(12), 2983-2995. (Invited Review)
8. Phadke AP, Jay CM, Wang Z, Chen S, Liu S, et al. (2011) In vivo safety and
antitumor efficacy of bifunctional small hairpin RNAs specific for the human
Stathmin 1 oncoprotein. DNA Cell Biol. 30(9):715-26.
9. Rao D, Maples PB, Senzer N, Kumar P, Wang Z, et al. (2010) Enhanced Target
Gene Knockdown by a Bifunctional shRNA: A Novel Approach of RNA
Interference. Cancer Gene Ther. 17(11):780-91.
10. Maples PB, Kumar P, Yu Y, Wang Z, Jay CM, et al. (2009) Fang Vaccine:
Autologous Tumor Cell Vaccine Genetically Modified to Express GM-CSF and
Block Production of Furin. BioProcess. J. 8(4): 4-14.
11. Phadke AP, Jay C, Chen SJ, Haddock C, Wang Z, Yu Y, et al. (2009) Safety and
in vivo Expression of a GNE-Transgene: A Novel Treatment Approach for
Hereditary Inclusion Body Myopathy-2. Gene Regul Syst Bio. (3) 89–101.
12. Bartosh TJ, Wang Z, Rosales AA, Dimitrijevich SD, Roque RS. (2008) 3D-model
of adult cardiac stem cells promotes differentiation and resistance to oxidative
stress. J. Cellular Biochemistry. 105(2):612-23.
13. Srinivasan B, Wang Z, Brun-Zinkernagel AM, Collier RJ, Chao M, Black, RA,
Frank SJ, Barker PA, Roque RS. (2007) Photic injury promotes cleavage of
p75NTR by TACE and nuclear trafficking of the p75 intracellular domain. Mol.
Cell. Neurosci. 36(4):449-61
14. Sheedlo HJ, Bartosh TJ, Wang Z, Srinivasan B, Brun-Zinkernagel AM, Roque RS.
(2007) RPE-derived factors modulate photoreceptor differentiation: a possible role
in the retinal stem cell niche. In Vitro Cell Dev Biol Anim. 43(10):361-70.
15. Cammarata PR, Chu S, Moor A, Wang Z. (2004) Subcellular distribution of native
estrogen receptor α and β subtypes in cultured human lens epithelial cells. Exp.
Eye Res. 78: 867-871.
16. Wang Z, Ding M, Liu J. (1999) Synthesis, cloning and fusion Expression of the
hPTH N-terminus 34 Peptide Gene. Journal of China Pharmaceutical
University 30(3): 216-9.