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
Ancevski Hunter, Katerina; Socinski, Mark A; Villaruz, Liza C (2018) PD-L1 Testing in Guiding Patient Selection for PD-1/PD-L1 Inhibitor Therapy in Lung Cancer. Mol Diagn Ther 22:1-10
Luu, Thehang; Kim, Kyu-Pyo; Blanchard, Suzette et al. (2018) Phase IB trial of ixabepilone and vorinostat in metastatic breast cancer. Breast Cancer Res Treat 167:469-478
Menk, Ashley V; Scharping, Nicole E; Moreci, Rebecca S et al. (2018) Early TCR Signaling Induces Rapid Aerobic Glycolysis Enabling Distinct Acute T Cell Effector Functions. Cell Rep 22:1509-1521
Redner, Robert L; Beumer, Jan H; Kropf, Patricia et al. (2018) A phase-1 study of dasatinib plus all-trans retinoic acid in acute myeloid leukemia. Leuk Lymphoma 59:2595-2601
Shayan, Gulidanna; Kansy, Benjamin A; Gibson, Sandra P et al. (2018) Phase Ib Study of Immune Biomarker Modulation with Neoadjuvant Cetuximab and TLR8 Stimulation in Head and Neck Cancer to Overcome Suppressive Myeloid Signals. Clin Cancer Res 24:62-72
Frahm, Krystle A; Waldman, Jacob K; Luthra, Soumya et al. (2018) A comparison of the sexually dimorphic dexamethasone transcriptome in mouse cerebral cortical and hypothalamic embryonic neural stem cells. Mol Cell Endocrinol 471:42-50
Pulopulos, Matias M; Vanderhasselt, Marie-Anne; De Raedt, Rudi (2018) Association between changes in heart rate variability during the anticipation of a stressful situation and the stress-induced cortisol response. Psychoneuroendocrinology 94:63-71
Shiffman, Saul; Scholl, Sarah M (2018) Three approaches to quantifying cigarette consumption: Data from nondaily smokers. Psychol Addict Behav 32:249-254
Samuelsson, Laura B; Bovbjerg, Dana H; Roecklein, Kathryn A et al. (2018) Sleep and circadian disruption and incident breast cancer risk: An evidence-based and theoretical review. Neurosci Biobehav Rev 84:35-48
Chen, Dongshi; Ni, Hong-Min; Wang, Lei et al. (2018) PUMA induction mediates acetaminophen-induced necrosis and liver injury. Hepatology :

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