BIOGRAPHICAL SKETCH |
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NAME Paul
Christopher Roberts |
POSITION TITLE Associate
Professor, Dept. of Biomedical Sciences and Pathobiology, Virginia Maryland
Regional College of Veterinary Medicine, Virginia Tech, VA |
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eRA COMMONS USER
NAME |
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EDUCATION/TRAINING |
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INSTITUTION AND LOCATION |
DEGREE (if
applicable) |
YEAR(s) |
FIELD OF STUDY |
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Davidson
College (Davidson, NC) |
BS |
1984 |
Biology |
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Philipps-Universität
Marburg (Marburg, Germany) |
MS |
1988 |
Microbiology |
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Philipps-Universität
Marburg (Marburg, Germany) |
PhD |
1992 |
Microbiology/Virology |
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Emory
University (Atlanta, GA) |
Postdoctoral |
1992-1996 |
Microbiology/Virology |
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1992 -
1996 Research Associate, Emory
University School of Medicine, Atlanta, GA
1996 –
1999 Senior Research Associate, Emory
University School of Medicine, Atlanta, GA
1999
- 2007 Assistant
Professor, Department of Immunology and Microbiology, Wayne State University
School of Medicine, Detroit, MI.
2007-Present Associate Professor, Biomedical Science and
Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine,
Virginia Tech, Blacksburg, VA
2002 Wayne State University, School of Medicine Teaching Award
2006 Wayne State University, School of Medicine Teaching Award
2003 Member, NIH Study Section VR-3,
July
2005-2006 Member, NIH Study Section ZRG1 IDM-B
2006 Member, DOD OC-1 Study Section,
May
2006-Present Member, NIH Study Section ZRG1 IDM-10 “Bugs
and Drugs”
Professional
Societies: American Society
of Virology, American Association of Cancer Research, American Society of
Microbiology.
Reviewer: Journal of Virology, Virology,
Virus Research, Cell Motility and Cytoskeleton, and European Journal of Cancer.
Patents:
Virus vaccines comprising envelope-bound
immunomodulatory proteins and methods of use thereof. Inventors: Sundick, RS,
Yang, Y, Roberts, PC. US Provisional filed 7/8/2005
B.
Selected peer-reviewed publications, abstracts and review articles.
Stieneke-Grober,
A., M. Vey, H. Angliker, E. Shaw, G. Thomas, P.C. Roberts, H.-D. Klenk and W. Garten. 1992. Influenza virus hemagglutinin with a
multibasic cleavage site is activated by furin, a subtilisin-like
endoprotease. EMBO J., 11:2407-2414.
Roberts, P.C., W. Garten and H.-D.
Klenk. 1993. The role of conserved glycosylation sites in
maturation and transport of influenza A virus hemagglutinin. J. Virol., 67:3048-3060.
Hughey,
P.G., P.C. Roberts, L.J. Holsinger,
S.L. Zebedee, R.A. Lamb and R.W. Compans.
1995. Effects of antibody to the
influenza A virus M2 protein on M2 surface expression and virus assembly. Virology 212:411-421.
Roberts, P.C., P.G. Hughey, L.J.
Holsinger, R.A. Lamb and R.W. Compans.
1996. Effect of influenza A virus
M2 protein on virus assembly and release.
In: “Options for the Control of Influenza III”. (eds. L.E. Brown, A.W. Hampson and R.G.
Webster), International Conference Series, Elsevier, pp 351-356.
Marschall,
M., A. Shuler, A. Hechtfischer, A. Helten, C. Boswald, H. Meier-Ewert, D.M.
Blau, P.C. Roberts and R.W.
Compans. 1996. A tissue culture model of viral persistence
for an orthomyxovirus. In: “Options for
the Control of Influenza III”. (eds.
L.E. Brown, A.W. Hampson and R.G. Webster), International Conference Series,
Elsevier, pp 455-560.
Roberts, P.C., A. Lamb and R.W.
Compans. 1998. The M1 and M2 proteins of influenza A virus
are important determinants of virus morphology.
Virology 240:127-137.
Schmelz,
E.-M., M. Dombrink-Kurtzman, Roberts,
P.C., Y. Kozutsumi, T. Kawasaki and A.H. Merrill, Jr. 1998.
Induction of apoptosis by fumonisin B1 in HT29 cells is
mediated by accumulation of free sphingoid bases. Toxicol. Appl. Pharmacol., 148:252-260.
Roberts, P.C. and R.W.
Compans. 1998. Host cell dependence of virus morphology.
Proc. Natl. Acad. Sci. USA, 95:5746-5751.
Roberts, P. C., T. Kipperman, R. W.
Compans. (1999). The VSV G protein
acquires pH-independent fusion activity during transport in a polarized
endometrial cell line. J. Virol. 73, 10447-10457.
S.
Balachandran**, P. C. Roberts**, T. Kipperman,
R. W. Compans, D. R. Archer, K. N. Bhalla, and G. N. Barber. (2000).
Alpha/Beta interferons potentiate virus-induced apoptosis through
activation of the FADD/Caspase-8 Death Signaling pathway. J. Virol. 74: 1513-1523.
**First two authors contributed equally.
S.
Balachandran, P. C. Roberts, D. R.
Archer, K. N. Bhalla, and G. N. Barber.
(2000). Essential role for the dsRNA-dependent protein kinase, PKR, in
innate immunity to viral infection. Immunity, 13: 129-141.
Schmelz,
E.M., Roberts, P.C., Kustin, E.M.,
Lemonnier, L.A, Sullards, M.C., Dillehay, D.L., and Merrill, A.H., Jr. (2001)
Modulation of intracellular ß-catenin localization and intestinal tumorigenesis
in vivo and in vitro by sphingolipids. Cancer
Res. 61: 6723-6729.
L.
Gregoire, E.M. Schmelz, A. Munkarah, R. Rabbah, P. C. Roberts, and W. D. Lancaster.
(2001). Spontaneous Malignant Transformation of Human Ovarian Surface
Epithelial Cells in Vitro. Clinical
Cancer Research 7: 4280-4287.
Prachi
P. Trivedi, Paul C. Roberts, Norbert
A. Wolf, and Robert H. Swanborg.
(2005). NK Cells Inhibit T Cell
Proliferation via p21-Mediated Cell Cycle Arrest. J. Immunol. Volume 174 / No.
8/April 15th.
Roberts, P.C., Mottillo, E.P.,
Baxa, A., Reale, N., Gregoire, L., Rabah, R., Lancaster, W.D., and Schmelz,
E.M. (2005) Sequential molecular and cellular events during neoplastic
progression: a mouse syngeneic ovarian cancer model. Neoplasia 7 (10) 944-956.
Lin
Tang, Paul C. Roberts, Janice M.
Kraniak, Qunfang Li, , and Michael A.
Tainsky. (2006). STAT1 expression is not sufficient to
regulate interferon-signaling pathway in cellular immortalization. J Interferon and Cytokine Res. 26 (1) 14-26.
Aviva
Levine Fridman, L. Tang, O. I. Kulaeva, B. Y., Q. Li, P.
C. Roberts, J. Abrams, M. A. Tainsky. (2006).
Expression Profiling Identifies Three Pathways Altered in Cellular
Immortalization: Interferon, Cell Cycle
and Cytoskeleton., J
Gerontol A Biol Sci Med Sci, 61 (9) 879-89.
Prachi
P. Trivedi, Taba K. Amouzegar, Paul C.
Roberts, Norbert A. Wolf, and Robert H. Swanborg. (2006). Regulation of
Adaptive Immunity by cells of the the innate immune system: Bone marrow natural
killer cells inhibit T cell proliferation. "Crossroads between Innate and
Adaptive Immunity", Proceedings of the Aegean Conference, in Advances in
Experimental Medicine and Biology,
Springer Verlag.
Janice
Speshock, N. Doyon-Reale, R. Rabah, M. Neely and P.C. Roberts. (2007). Filamentous influenza A virus infection
predisposes mice to fatal septicemia following superinfection with Streptococcus pneumoniae (serotype 3). Infection and Immunity 75 (6)
3102-3111.
Amouzegar, T. K. Trivedi, P.P, N.A. Wolf, P.C. Roberts, R. H. Swanborg. (2008). A Unique Subset
of Bone Marrow-Derived Natural Killer Cells Regulates T Cell Activation. (J. Leukocyte
Biology; in press)
Yufang Yang, David Legget, Andrew
Herbert, Roy S. Sundick and Paul C.
Roberts. (2008). A novel method to incorporate cytokines as adjuvants on
the surface of whole, virus vaccines. (submitted to J. Interferon and Cytokine
Research)
Andrew Herbert, Nicole Doyon-Reale, Roy
S. Sundick and Paul C. Roberts.
(2008). Membrane-bound Cytokines Augment Influenza Virus Vaccines and Protect
Against Lethal Challenge in Mice. (submitted to J. Interferon and Cytokine
Research)
C. Research Support.
NIH R21-AI065591 4/01/06-3/31/2009
PI: Paul Christopher Roberts (25% Effort)
Avian
Influenza Virus Vaccines Bearing Immunomodulators.
The major goals are to assess the in vivo efficacy of novel inactivated
influenza vaccines bearing chicken derived membrane-bound cytokines. The animal challenge model is chicken.
USDA Hatch Program 7/1/07-6/30/08
PI: Paul Christopher Roberts (5% Effort)
Novel Influenza Virus Vaccines bearing human-specific
Immunomodulators.
Co-I: RM Gogal and S
Witonsky.
NCI/NIH R01-CA109019 (PI: EM Schmelz) 8/1/05-
7/30/2010
Co-I: Paul Christopher Roberts (10% Effort)
Tumor Suppression by sphingolipids: role of b-catenin.
The major goal is to
define how sphingolipids regulate the beta catenin signaling pathway in colon
cancer.
NCI/NIH R01-CA118846 (PI: EM Schmelz) 7/1/07-6/30/11
Co-PI:
Paul Christopher Roberts (20% Effort)
Regulation
of Gene Silencing by Exogenous Sphingosine.
This
project determines the mechanisms of how exogeneous sphingosine regulates gene
silencing in a progressive model of mouse ovarian cancer that was developed in
our laboratory.