Di Jia, Ph.D.
Vascular Biology Program, Boston Children’s Hospital
Department of Surgery, Harvard Medical School
12.007F, Karp Family Research Building
*** ******** ******, ******, ** 02115
Immigration Status: Permanent Resident of US
Cell: 765-***-**** Fax: 617-***-****
Email: **.***@*********.*******.***
Summary of Qualifications
Passionate scientist with broad expertise in molecular biology / cell biology and extensive experience in
translating clinical observations into scientific research in order to find therapeutic and diagnostic tools
for human diseases. Lead a team effort to identify key processes in tumor angiogenesis and tumor
dormancy using cancer cell and primary cell based assays. Successfully managed multiple
collaborations with cross-functional teams of biologists, biostatistitians, and clinicians to discover
biomarkers for endometriosis. Demonstrated excellent scientific communication and presentation skills
in both research meetings and fundraising events. Mentored Harvard undergraduate student for his
honors thesis which received multiple prestigious awards.
Research Experience
Postdoctoral Research Fellow, Vascular Biology Program, Boston Children’s Hospital; Department of
Surgery, Harvard Medical School 2008-Present
Principle Investigator: Marsha A. Moses, Ph.D.
Deciphered the molecular mechanisms by which ZNF24 represses VEGF expression by
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combining molecular biology techniques and primary / cancer cell studies
Collaborated extensively with laboratories at Boston Children's Hospital and at
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University of Florida to identify the in vivo function of ZNF24 using animal models for breast
cancer tumor angiogenesis
Demonstrated the efficiency of targeted cancer drug delivery using nanoparticles in
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collaboration with Harvard School of Engineering and Applied Sciences
Designed studies based on clinical data to identify novel non-invasive biomarkers for
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endometriosis with a multidisciplinary team of scientists and clinicians at Boston Children's
Hospital and Boston Center for Endometriosis
Mentored Harvard undergraduate student for his honors thesis which was awarded the
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prestigious Thomas T. Hoopes Prize, the highest honor for undergraduate thesis writing at
Harvard University
Supervised his thesis research work which was presented at 104th Annual Meeting of
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AACR and won honorary mention at the Eighth Annual Undergraduate Student Caucus and
Poster Competition
Graduate Research Fellow, Department of Biological Sciences, Purdue University 2002-2008
Principle Investigator: Stephen F. Konieczny, Ph.D.
Dissertation: “Functional analysis of the bHLH transcription factor Mist1 during pancreatic development”
Discovered the growth inhibitory function of a bHLH transcription factor Mist1 in pancreatic
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cancer cells and identified the p21CIP1/WAF1 as the downstream target of Mist1
Lead a multidisciplinary team to identify Mist1 interacting proteins in pancreatic cancer cells by
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Mass-Spec analyses
Validated functions of Mist1 interacting proteins in regulating downstream target genes
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associated with pancreatic cell proliferation and differentiation using innovative approaches
Determined the in vivo function of Mist1 in pancreatic development and pancreatic cancer
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using genetically modified mouse models
Collaborated with scientists at School of Engineering at Purdue University to determine the
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optimal architecture of nanoparticles for siRNA drug delivery
Education
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Ph.D., Biochemistry and Molecular Biology/Biophysics 2008
Purdue University, West Lafayette, IN
Bachelor of Science, Biotechnology 2001
Shanghai Jiaotong University, Shanghai, China
Di Jia, Ph.D.
Technical Expertise
Molecular biology techniques: protein and nucleic acid isolation, characterization of protein-
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protein and protein-nucleic acid interactions
Molecular cloning techniques: generating mammalian & zebrafish expression vectors,
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lentiviral expression vectors and promoter luciferase constructs, mutagenesis, lentiviral production
Gene expression analyses: gene overexpression and knockdown using DNA transfection and
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viral delivery systems, RNAi, SyberGreen and Taqman based quantitative RT-PCR, luciferase
assays, chromatin immunoprecipitation assays, transcriptomic analyses
Immunological assays: immunoblot, ELISA assays, multiplex immunoassays, coimmuno-
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precipitation assays, Immunohistochemistry, immunofluorescence staining
Enzyme-based assays: substrate gel electrophoresis
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Cell-based assays: cancer cell and primary cell culture, proliferation assays, FACS analyses,
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migration assays, invasion assays, cell fractionation and cell organelle isolation, generation of stable
cell lines
Imaging: light and fluorescent microscopy, Xenogen bioluminescence imaging
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Small animal techniques: zebrafish embryo microinjection, rodent subcutaneous and
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intraperitoneal injection, tissue harvesting and processing, animal models for breast
cancer tumor dormancy
Publications
Peer Reviewed Research Articles
Jia D., Huang L., Bischoff J., and Moses MA. An endogenous zinc finger transcription factor, ZNF24,
modulates the angiogenic potential of human microvascular endothelial cells. (In revision at FASEB
Journal)
Guo P, Huang J, Wang L, Jia D, Yang J, You J, Dillon D, Zurakowski D, Moses MA, and August DT.
Triple negative breast cancer specific targeted magnetic nanoparticles enhance tumor imaging. (In
revision at Proc Natl Acad Sci U S A.)
Guo P, You JO, Yang Y, Jia D, Moses MA., and Auguste DT. Inhibiting breast cancer cell migration via
multi-targeted siRNA delivery. (In Press at Molecular Pharmaceutics)
Jia D., Hasso S.M., Chan J., Filingeri D., D’Amore P. A., Rice L., Pampo C., Siemann D. W., Zurakowski
D., Rodig S. J., and Moses M.A. Transcriptional repression of VEGF by ZNF24: mechanistic studies
and vascular consequences in vivo. Blood. 2013 Jan 24;121(4):707-15. Featured as cover artwork.
Straume O, Shimamura T, Lampa M, Carretero J, Øyan A, Jia D, Borgman C, Downing S, Short S,
Kang SY, Watnick R, Chen L, Collett K, Bachmann I, Wong KK., Shapiro G, Kalland K, Folkman J,
Akslen L, and Naumov G. Suppression of Heat Shock Protein 27 induces long-term dormancy in
human breast cancer. Proc Natl Acad Sci U S A. 2012 May 29;109(22):8699-704.
Gary DJ, Lee H, Sharma R, Lee JS, Kim Y, Cui ZY, Jia D, Bowman VD., Chipman PR., Wan L, Zou
Y, Mao G, Park K, Herbert BS, Konieczny SF, and Won YY. Influence of Nano-Carrier
Architecture on in Vitro siRNA Delivery Performance and in Vivo Biodistribution: Polyplexes
vs Micelleplexes. ACS Nano. 2011 May 24;5(5):3493-505.
Jia D, Sun Y, and Konieczny SF. The bHLH transcription factor Mist1 modulates pancreatic acinar cell
proliferation through induction of p21CIP1/WAF1. Gastroenterology 2008 135: 1687-1697.
Tran T, Jia D, Sun Y, and Konieczny SF. The bHLH domain of Mist1 is sufficient to activate gene
transcription. Gene Expr. 2007 13: 241-53.
Liao C, Zhao M, Zhao J, Jia D, Song H, and Li T. Over-expression of LPTS-L in hepatocellular
carcinoma cell line SMMC-7721 induces crisis. World J Gastroenterol. 2002 8:1050-2.
Book Chapters
Jia D, Roy R, and Moses MA. Matrix Metalloproteinases as potential therapeutic targets in human
cancer. In Press.
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Moses MA. and Jia D. Neovascularization. Encyclopedia of Systems Biology. August, 2013.
Moses MA. and Jia D. Regulation of Tumor Angiogenesis. Encyclopedia of Systems Biology. August,
2013.
Moses MA. and Jia D. Therapeutic Targeting of the Vasculature. Encyclopedia of Systems Biology.
August, 2013.
Di Jia, Ph.D.
Relavant Presentations at Conferences
Oral Presentations
Jia D. Transcriptional repression of VEGF by ZNF24: mechanistic studies and vascular consequences
in vivo. November 2012, Boston Angiogenesis Meeting, Boston, MA.
Poster Presentations
Jia D, Huang L, Bischoff J, and Moses MA. Modulating the angiogenic potential of human microvascular
endothelial cells by an endogenous transcription factor, ZNF24. April 2014, American Association
for Cancer Research (AACR) 105th Annual Meeting, San Diego, CA
Stein EJ, Jia D, and Moses MA. BATF3 is a novel regulator of breast cancer cell invasion. April 2013,
American Association for Cancer Research (AACR) 104th Annual Meeting, Washington, DC
Jia D and Moses MA. ZNF24 may modulate microvascular endothelial cell invasion through regulating
MMP2 transcription. April 2013, AACR 104th Annual Meeting, Washington, DC
Jia D and Moses MA. ZNF24 may regulate normal mammary epithelial cell proliferation through
transcriptional repression of CDKN1A. March 2012, DF/HCC Breast and Gynecologic Cancer
Symposium, Boston, MA
Jia D, Hasso SM., Chan J, D’Amore PA, Zurakowski D, Rodig SJ, and Moses MA. Transcriptional
repression of VEGF by ZNF24: Mechanistic studies and vascular consequences in vivo. April 2011,
AACR 102nd Annual Meeting, Orlando, FL
Jia D and Konieczny SF. The basic helix-loop-helix transcription factor Mist1 modulates pancreatic
acinar cell proliferation through induction of p21 CIP1/WAF1. April 2007, The 46th Annual Midwest
Developmental Biology Meeting, The University of Chicago, IL; August 2006, Transcriptional
Regulation During Cell Growth, Differentiation, & Development; FASEB Summer Research
Conference, Saxtons River, VT
Presentations at Fundraising Events
Demonstrated the latest discoveries in biomarker research for cancer detection at fundraising events
organized by Boston Children’s Hospital Trust
Boston Investment Conference, Boston, MA
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November 2012
Circle of Care Fall Reception, Boston, MA
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October 2012
Shoe & Tell Stuart Weitzman Event, New York, NY
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April 2012
Honors & Awards
Research Grant, Purdue Research Foundation, Purdue University 2005-2007
Undergraduate Student Research Grant, Tang Zhongying Fund, Shanghai Jiaotong University, China
2001
Merit Student Award, Shanghai Jiaotong University, China 1997-2001
Mentoring & Supervisory Experience
Research Supervisor of Undergraduate Honors Thesis for Harvard Undergraduate Student, Harvard
Medical School 2011- 2013
Research Supervisor for MIT Undergraduate Student, Harvard Medical School 2009-2010
Research Supervisor for 4 rotating graduate students, Purdue University 2004-2007
Teaching Assistant - Laboratory in Animal Cell Culture, Purdue University 2005
Teaching Assistant - Bioenergetics, Purdue University 2003
Professional Affiliations
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American Association for Cancer Research 2010-present
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