): The objective of this program is to provide high quality training at the predoctoral and postdoctoral levels and to prepare outstanding individuals for careers in research and teaching in Molecular and Viral Oncology. The applicants have developed a multidisciplinary, multi-departmental, group of seventeen investigators with proven expertise and research interests in these areas. The ongoing research programs of these faculty members include the investigation of the genetics and replication of oncogenic RNA and DNA viruses, studies on the maturation and development of various components of the immune response and aberrations that occur during oncogenesis in this system, regulation of gene expression through studies on DNA structure and regulatory elements, the role of oncogenes in carcinogenesis and molecular studies of the host immune response. The faculty members in this proposal occupy laboratories that are well-equipped and well-funded for all phases of the research. The participating faculty believes that this represents an excellent environment for providing outstanding predoctoral and postdoctoral training in the area of Molecular and Viral Oncology. Predoctoral trainees are required to meet the admission and graduation standards of an innovative multi- departmental program entitled the """"""""Cellular and Molecular Biology (CMB) Graduate Program"""""""" or a highly selective M.D./Ph.D. program. Specific requirements for students enrolled in the Molecular and Viral Oncology Program include participation in an advanced level course in viral and molecular oncology as well as journal clubs and attendance at seminars relevant to the various aspects of this discipline. Selected course offerings, journal clubs, seminars, and discussion groups will be attended by postdoctoral trainees also. In addition to research activities and courses the training program includes participation in local, regional and national scientific meetings. Recruitment of both predoctoral and postdoctoral trainees will be at the national level through a variety of recruitment programs and will encourage recruitment of minority participants.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA009467-20
Application #
6497346
Study Section
Subcommittee G - Education (NCI)
Program Officer
Eckstein, David J
Project Start
1983-09-01
Project End
2005-01-31
Budget Start
2002-02-01
Budget End
2005-01-31
Support Year
20
Fiscal Year
2002
Total Cost
$249,560
Indirect Cost
Name
University of Alabama Birmingham
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Robb, Caroline M; Kour, Smit; Contreras, Jacob I et al. (2018) Characterization of CDK(5) inhibitor, 20-223 (aka CP668863) for colorectal cancer therapy. Oncotarget 9:5216-5232
Van Tine, Brian A; Dao, Luan D; Wu, Shwu-Yuan et al. (2004) Human papillomavirus (HPV) origin-binding protein associates with mitotic spindles to enable viral DNA partitioning. Proc Natl Acad Sci U S A 101:4030-5
Levasseur, Dana N; Ryan, Thomas M; Reilly, Michael P et al. (2004) A recombinant human hemoglobin with anti-sickling properties greater than fetal hemoglobin. J Biol Chem 279:27518-24
Kim, Hyung-Gyoon; de Guzman, Cristina G; Swindle, C Scott et al. (2004) The ETS family transcription factor PU.1 is necessary for the maintenance of fetal liver hematopoietic stem cells. Blood 104:3894-900
Stansell, Elizabeth; Tytler, Ewan; Walter, Mark R et al. (2004) An early stage of Mason-Pfizer monkey virus budding is regulated by the hydrophobicity of the Gag matrix domain core. J Virol 78:5023-31
Levasseur, Dana N; Ryan, Thomas M; Pawlik, Kevin M et al. (2003) Correction of a mouse model of sickle cell disease: lentiviral/antisickling beta-globin gene transduction of unmobilized, purified hematopoietic stem cells. Blood 102:4312-9
Sfakianos, Jeffrey N; LaCasse, Rachel A; Hunter, Eric (2003) The M-PMV cytoplasmic targeting-retention signal directs nascent Gag polypeptides to a pericentriolar region of the cell. Traffic 4:660-70
de Guzman, Cristina G; Johnson, Amanda; Klug, Christopher A (2003) The ETO domain is necessary for the developmental abnormalities associated with AML1-ETO expression in the hematopoietic stem cell compartment in vivo. Blood Cells Mol Dis 30:201-6
Lanman, Jason; Lam, TuKiet T; Barnes, Stephen et al. (2003) Identification of novel interactions in HIV-1 capsid protein assembly by high-resolution mass spectrometry. J Mol Biol 325:759-72
Sfakianos, Jeffrey N; Hunter, Eric (2003) M-PMV capsid transport is mediated by Env/Gag interactions at the pericentriolar recycling endosome. Traffic 4:671-80

Showing the most recent 10 out of 34 publications