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 #
5P30CA047904-18
Application #
7111833
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
18
Fiscal Year
2005
Total Cost
$58,498
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Lee, Young-Sun; Lee, Dae-Hee; Choudry, Haroon A et al. (2018) Ferroptosis-Induced Endoplasmic Reticulum Stress: Cross-talk between Ferroptosis and Apoptosis. Mol Cancer Res 16:1073-1076
Tong, Jingshan; Zheng, Xingnan; Tan, Xiao et al. (2018) Mcl-1 Phosphorylation without Degradation Mediates Sensitivity to HDAC Inhibitors by Liberating BH3-Only Proteins. Cancer Res 78:4704-4715
Menk, Ashley V; Scharping, Nicole E; Rivadeneira, Dayana B et al. (2018) 4-1BB costimulation induces T cell mitochondrial function and biogenesis enabling cancer immunotherapeutic responses. J Exp Med 215:1091-1100
Wang, Yue; Wang, Zehua; Xu, Jieni et al. (2018) Systematic identification of non-coding pharmacogenomic landscape in cancer. Nat Commun 9:3192
Saydmohammed, Manush; Vollmer, Laura L; Onuoha, Ezenwa O et al. (2018) A High-Content Screen Reveals New Small-Molecule Enhancers of Ras/Mapk Signaling as Probes for Zebrafish Heart Development. Molecules 23:
Gough, Albert; Shun, Tong Ying; Taylor, D Lansing et al. (2018) Integrating Analysis of Cellular Heterogeneity in High-Content Dose-Response Studies. Methods Mol Biol 1745:25-46
Fletcher, Rochelle; Wang, Yi-Jun; Schoen, Robert E et al. (2018) Colorectal cancer prevention: Immune modulation taking the stage. Biochim Biophys Acta Rev Cancer 1869:138-148
Caves, Elizabeth A; Cook, Sarah A; Lee, Nara et al. (2018) Air-Liquid Interface Method To Study Epstein-Barr Virus Pathogenesis in Nasopharyngeal Epithelial Cells. mSphere 3:
Singh, Renu; Mehrotra, Shailly; Gopalakrishnan, Mathangi et al. (2018) Population pharmacokinetics and exposure-response assessment of veliparib co-administered with temozolomide in patients with myeloid leukemias. Cancer Chemother Pharmacol :
Li, Changfeng; Zhang, Ying; Cheng, Xing et al. (2018) PINK1 and PARK2 Suppress Pancreatic Tumorigenesis through Control of Mitochondrial Iron-Mediated Immunometabolism. Dev Cell 46:441-455.e8

Showing the most recent 10 out of 1187 publications