The goal of the Vector Core is to ensure that Center members have access to the latest and the best in vector technology they need to research the roles of specific genes in cancer. Services include consultation, production of new adenovirus, amplification and purification of existing adenovirus, production and purification of rAAV, and production of retrovirus vectors. The Core is led by Dr. R. Jude Samulski, Faculty Director and Dr. Xiaohuai Zhou, Facility Director. The Core adds value to the Center by providing members access to our standard services as well as the latest vector technologies made available through our own efforts. Some of our recent contributions in the gene delivery field are: production of Clinical grade vectors, invection of AAV alternate serotype vectors, and invention of self complementary AAV vectors for high-efficiency transduction. Highlights of research supported by the Core include: 1) Dr. Baldwin and Dr. Cance used adenovirus encoding carboxyl-terminal domain of FAK to induce the apoptosis of breast cancer cells. Dr. Baldwin also used adenovirus encoding IkappaB super-repressor to render tumor cells more susceptible to chemotherapy and radiation treatment. 2) Dr. Brenner and Dr. Lemasters used tAd dominant negative TRAF2, NIKdn, IKKldn, IKK2dn, and IkappaBsr in the elucidation of an apoptotic pathway in hepatoma cells. Future plans for the Core include the implementation of producer cell technology for rAAV production.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016086-31
Application #
7310756
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2005-12-01
Budget End
2006-11-30
Support Year
31
Fiscal Year
2006
Total Cost
$45,781
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Townsley, Loni; Yannarell, Sarah M; Huynh, Tuanh Ngoc et al. (2018) Cyclic di-AMP Acts as an Extracellular Signal That Impacts Bacillus subtilis Biofilm Formation and Plant Attachment. MBio 9:
Schulfer, Anjelique F; Battaglia, Thomas; Alvarez, Yelina et al. (2018) Intergenerational transfer of antibiotic-perturbed microbiota enhances colitis in susceptible mice. Nat Microbiol 3:234-242
Hall, Marissa G; Mendel, Jennifer R; Noar, Seth M et al. (2018) Why smokers avoid cigarette pack risk messages: Two randomized clinical trials in the United States. Soc Sci Med 213:165-172
Cholon, Deborah M; Gentzsch, Martina (2018) Recent progress in translational cystic fibrosis research using precision medicine strategies. J Cyst Fibros 17:S52-S60
Tappata, Manaswita; Eluri, Swathi; Perjar, Irina et al. (2018) Association of mast cells with clinical, endoscopic, and histologic findings in adults with eosinophilic esophagitis. Allergy 73:2088-2092
Che, Tao; Majumdar, Susruta; Zaidi, Saheem A et al. (2018) Structure of the Nanobody-Stabilized Active State of the Kappa Opioid Receptor. Cell 172:55-67.e15
Hu, Peirong; Bi, Yanmin; Ma, Hong et al. (2018) Superior lentiviral vectors designed for BSL-0 environment abolish vector mobilization. Gene Ther 25:454-472
Cranston, Ross D; Cespedes, Michelle S; Paczuski, Pawel et al. (2018) High Baseline Anal Human Papillomavirus and Abnormal Anal Cytology in a Phase 3 Trial of the Quadrivalent Human Papillomavirus Vaccine in Human Immunodeficiency Virus-Infected Individuals Older Than 26 Years: ACTG 5298. Sex Transm Dis 45:266-271
DeBono, Nathan L; Robinson, Whitney R; Lund, Jennifer L et al. (2018) Race, Menopausal Hormone Therapy, and Invasive Breast Cancer in the Carolina Breast Cancer Study. J Womens Health (Larchmt) 27:377-386
Okolie, Onyinyechukwu; Irvin, David M; Bago, Juli R et al. (2018) Intra-cavity stem cell therapy inhibits tumor progression in a novel murine model of medulloblastoma surgical resection. PLoS One 13:e0198596

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