In the Functional Genomics & Virology Core, we have brought together a diverse group of NIH-fundedinvestigators from basic science and clinical medicine. These investigators have a common interest in usingstate-of-the-art technologies to better understand the molecular mechanisms underlying the progressionfrom HCV infection to end-stage liver disease. The Center has made great strides in defining global geneexpression signatures associated with HCV infection, including the identification of gene expression patternsspecifically associated with fibrosis progression. While the Center continues to exploit recurrent HCV afterliver transplantation as an investigative tool, we now include a greater emphasis on AIDS, includingHCV/HIV-1 co-infection and in vitro HIV infection systems. We have also initiated collaborations withEvergreen Treatment Services to investigate the impact of intravenous drug abuse on HCV-associated liverdisease and treatment.
The Specific Aims of this Core are to: 1) Supply biological samples, including clinical,in vitro and animal model systems, for microarray, proteomic, and molecular virological analysis. Supportservices will include sample preparation, RNA and protein isolation, and preparation of materials for genomicand proteomic analyses. Model systems for HCV infection will include, but not be limited to, the SCIDbeige/Alb-uPA mouse model and the HCV 2a in vitro infection system. AIDS-related studies will include theanalysis of liver biopsies from patients co-infected with HCV and HIV-1 and from in vitro HIV-1 infection andin vivo SIV infection systems. 2) Use oligonucleotide microarrays, proteomics, laser/confocal microscopy,and molecular virology to profile the cellular events that occur during HCV-infection, HCV/HIV-1 co-infection,and liver disease and AIDS progression. The overall goal of this Core is to have an integrated systemsbiology approach to understand the host response to virus infection utlizing genomics tools and classicalvirological and histological assays. Our ability to integrate gene expression data (this Core) with proteomicdata (Proteomics Core) and sophisticated bioinformatic techniques (Bioinformatics & Biostatistics Core) willprovide insight into the molecular mechanisms associated with liver disease and AIDS. Ultimately, this willimprove patient care by yielding improved diagnostic methods, markers of disease progression, and novelapproaches for therapeutic intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Center Core Grants (P30)
Project #
2P30DA015625-06
Application #
7285801
Study Section
Special Emphasis Panel (ZDA1-RXL-E (02))
Project Start
2007-06-01
Project End
2012-06-30
Budget Start
2007-06-01
Budget End
2008-06-30
Support Year
6
Fiscal Year
2007
Total Cost
$791,307
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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