The Vector Core Facility (VCF) has served, and will continue to serve, as an important component of the Cancer Center Support Grant (CCSG), by providing viral and non-viral vectors, and reagents to UPCI members. The VCF functions within the framework of the UPCI as a dynamic resource that provides state-of-the-art viral and non-viral vector technology, as well as develops novel vectors. The major emphasis of the VCF has been on the utilization of retroviral and adenoviral vectors for gene transduction. However, this facility also produces adeno-associated virus and lentivirus vectors for gene delivery; and is developing expression vectors for use in both liposome and particle-mediated gene transduction. Furthermore, the VCF is characterizing and optimizing protein transduction domains (PTDs), and can generate and provide PTD fusion proteins. The role of the VCF in the UPCI will continue to be to construct and provide the required viral and non-viral vectors expressing the appropriate genes, as required by UPCI investigators, particularly those pursuing the gene therapy of cancer. In addition, the Facility provides cell lines, viruses, packaging lines, plasmids, and protocols as needed. Furthermore, the Core provides technical assistance and training to individuals in the use of viral and non-viral vectors for gene transfer.
The specific aims of the Vector Core are: l. To provide UPCI investigators with either viral or non-viral vectors, expressing the required therapeutic gene, dlat are most appropriate and efficacious for their proposed experiments 2. To develop improved viral and non-viral vectors for more efficient gene transfer, with higher and/or regulated gene expression. 3. To assist in the development of new, state-of-the-art methods for efficient gene delivery 4. To provide technical assistance and protocols for gene therapy projects, making use of viral and non-viral gene delivery systems

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA047904-19
Application #
7279249
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
19
Fiscal Year
2006
Total Cost
$60,254
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Santos, Patricia M; Butterfield, Lisa H (2018) Next Steps for Immune Checkpoints in Hepatocellular Carcinoma. Gastroenterology 155:1684-1686
Gao, Ying; Tan, Jun; Jin, Jingyi et al. (2018) SIRT6 facilitates directional telomere movement upon oxidative damage. Sci Rep 8:5407
Krishnamurthy, Anuradha; Dasari, Arvind; Noonan, Anne M et al. (2018) Phase Ib Results of the Rational Combination of Selumetinib and Cyclosporin A in Advanced Solid Tumors with an Expansion Cohort in Metastatic Colorectal Cancer. Cancer Res 78:5398-5407
Toptan, Tuna; Abere, Bizunesh; Nalesnik, Michael A et al. (2018) Circular DNA tumor viruses make circular RNAs. Proc Natl Acad Sci U S A 115:E8737-E8745
Liu, Zuqiang; Ge, Yan; Wang, Haiyan et al. (2018) Modifying the cancer-immune set point using vaccinia virus expressing re-designed interleukin-2. Nat Commun 9:4682
Vendetti, Frank P; Karukonda, Pooja; Clump, David A et al. (2018) ATR kinase inhibitor AZD6738 potentiates CD8+ T cell-dependent antitumor activity following radiation. J Clin Invest 128:3926-3940
Lontos, Konstantinos; Tsagianni, Anastasia; Yuan, Jian-Min et al. (2018) Location matters in early stage nodal diffuse large B-cell lymphoma. Leuk Lymphoma :1-4
Correa, Andres F; Toussi, Amir; Amin, Milon et al. (2018) Small Renal Masses in Close Proximity to the Collecting System and Renal Sinus Are Enriched for Malignancy and High Fuhrman Grade and Should Be Considered for Early Intervention. Clin Genitourin Cancer 16:e729-e733
Wang, Yi-Jun; Fletcher, Rochelle; Yu, Jian et al. (2018) Immunogenic effects of chemotherapy-induced tumor cell death. Genes Dis 5:194-203
Bakkenist, Christopher J; Lee, James J; Schmitz, John C (2018) ATM Is Required for the Repair of Oxaliplatin-Induced DNA Damage in Colorectal Cancer. Clin Colorectal Cancer 17:255-257

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