The long-term goal of this postdoctoral training grant is to develop independent investigators who will think critically about problems in the field of cancer biology. They will also have gained a high degree of technical competence in specific areas of cancer research and during this training period have acquired a broad and clinically relevant understanding of cancer as a biological and molecular process. A fundamental tenet of the program anticipates that investigators who study cancer related problems from the context of specific traditional disciplines will be better prepared and more likely to develop creative and realistic solutions than if the program was confined to a single discipline or department. Six fellows will be supported per year. Trainees must have advanced degrees, e.g. Ph.D., M.D., D.M.V., or D.D.S., and the training will be for a two year period. The main experimental training will be carried in the laboratory of the Trainer, each being an experienced researcher with extramural federal funding. Breadth of training will be attained through the association with an interactive faculty representing many basic sciences and clinical disciplines, interacting through Cancer Center based laboratory programs, formal lectures, Cancer Center Grand Rounds and Annual Cancer Center Symposium as well as other informal settings. Investigators at the University of Rochester James P. Wilmot Cancer Center are studying cancer from the point of view of biochemistry, biophysics, epidemiology, genetics, immunology and immune therapy, mathematics, microbiology, pathology, pharmacology and toxicology, physics and radiation oncology. Trainees will attend a graduate level course on """"""""Cancer Biology"""""""" which consists of a multi-disciplinary body of knowledge presented in a didactic structure with topics ranging from basic, translational and clinical research topics to cancer epidemiology and is designed specifically to provide the broadest basis for cancer research. Trainees must also enroll in the course entitled """"""""Ethics in Research"""""""" and are expected to attend the weekly Cancer Center Grand Rounds and research program meetings.

Public Health Relevance

By providing outstanding training and preparation for young scientists, this program will facilitate advances in basic, translational, and clinical cancer research and will foster improvements in treatment and prevention of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA009363-28
Application #
8132857
Study Section
Subcommittee G - Education (NCI)
Program Officer
Lim, Susan E
Project Start
1980-07-01
Project End
2014-08-31
Budget Start
2011-09-01
Budget End
2012-08-31
Support Year
28
Fiscal Year
2011
Total Cost
$247,098
Indirect Cost
Name
University of Rochester
Department
Genetics
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Gleghorn, Michael L; Zhao, Jianbo; Turner, Douglas H et al. (2016) Crystal structure of a poly(rA) staggered zipper at acidic pH: evidence that adenine N1 protonation mediates parallel double helix formation. Nucleic Acids Res 44:8417-24
Guy, Michael P; Phizicky, Eric M (2015) Conservation of an intricate circuit for crucial modifications of the tRNAPhe anticodon loop in eukaryotes. RNA 21:61-74
McCall, Matthew N; McMurray, Helene R; Land, Hartmut et al. (2014) On non-detects in qPCR data. Bioinformatics 30:2310-6
Gleghorn, Michael L; Maquat, Lynne E (2014) 'Black sheep' that don't leave the double-stranded RNA-binding domain fold. Trends Biochem Sci 39:328-40
Haider, Baqer A; Baras, Alexander S; McCall, Matthew N et al. (2014) A critical evaluation of microRNA biomarkers in non-neoplastic disease. PLoS One 9:e89565
McCall, Matthew N; Jaffee, Harris A; Zelisko, Susan J et al. (2014) The Gene Expression Barcode 3.0: improved data processing and mining tools. Nucleic Acids Res 42:D938-43
Barone, Maria Cecilia; Bohmann, Dirk (2013) Assessing neurodegenerative phenotypes in Drosophila dopaminergic neurons by climbing assays and whole brain immunostaining. J Vis Exp :e50339
Gleghorn, Michael L; Gong, Chenguang; Kielkopf, Clara L et al. (2013) Staufen1 dimerizes through a conserved motif and a degenerate dsRNA-binding domain to promote mRNA decay. Nat Struct Mol Biol 20:515-24
Park, Eonyoung; Gleghorn, Michael L; Maquat, Lynne E (2013) Staufen2 functions in Staufen1-mediated mRNA decay by binding to itself and its paralog and promoting UPF1 helicase but not ATPase activity. Proc Natl Acad Sci U S A 110:405-12
McCall, Matthew N (2013) Estimation of Gene Regulatory Networks. Postdoc J 1:60-69

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