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 #
5P30CA016086-34
Application #
7751862
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-12-01
Budget End
2009-11-30
Support Year
34
Fiscal Year
2009
Total Cost
$99,301
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Mayer, Deborah K; Landucci, Gina; Awoyinka, Lola et al. (2018) SurvivorCHESS to increase physical activity in colon cancer survivors: can we get them moving? J Cancer Surviv 12:82-94
Huo, Dezheng; Perou, Charles M; Olopade, Olufunmilayo I (2018) Reported Biologic Differences in Breast Cancer by Race Due to Disparities in Screening-Reply. JAMA Oncol 4:883-884
Howe, Chanelle J; Robinson, Whitney R (2018) Survival-related Selection Bias in Studies of Racial Health Disparities: The Importance of the Target Population and Study Design. Epidemiology 29:521-524
Byrne, James D; Yeh, Jen Jen; DeSimone, Joseph M (2018) Use of iontophoresis for the treatment of cancer. J Control Release 284:144-151
Wilkin, Timothy J; Chen, Huichao; Cespedes, Michelle S et al. (2018) A Randomized, Placebo-Controlled Trial of the Quadrivalent Human Papillomavirus Vaccine in Human Immunodeficiency Virus-Infected Adults Aged 27 Years or Older: AIDS Clinical Trials Group Protocol A5298. Clin Infect Dis 67:1339-1346
Siegel, Marni B; He, Xiaping; Hoadley, Katherine A et al. (2018) Integrated RNA and DNA sequencing reveals early drivers of metastatic breast cancer. J Clin Invest 128:1371-1383
Ubil, Eric; Caskey, Laura; Holtzhausen, Alisha et al. (2018) Tumor-secreted Pros1 inhibits macrophage M1 polarization to reduce antitumor immune response. J Clin Invest 128:2356-2369
Hamad, Ahmad; Iweala, Onyinye I; Henderson, Cory et al. (2018) Recurrent anaphylaxis during cardiac catheterization due to ethylene oxide. J Allergy Clin Immunol Pract 6:2148-2150
Ho, G-T; Aird, R E; Liu, B et al. (2018) MDR1 deficiency impairs mitochondrial homeostasis and promotes intestinal inflammation. Mucosal Immunol 11:120-130
Pearce, Oliver M T; Delaine-Smith, Robin M; Maniati, Eleni et al. (2018) Deconstruction of a Metastatic Tumor Microenvironment Reveals a Common Matrix Response in Human Cancers. Cancer Discov 8:304-319

Showing the most recent 10 out of 1525 publications