The objective of this proposal is to continue an interdisciplinary program for training predoctoral students at Northwestern University in the area of carcinogenesis which will provide research and training opportunities in this area of distinction at Northwestern University. This program has served as a focus for students, postdoctoral fellows, and faculty interested in studying various aspects of carcinogenesis and providing a stimulating forum for their interaction. In this grant, we have expanded the number of faculty by the addition of individuals who have consistently contributed to the program. The faculty identified in this proposal have active research programs in the areas of: 1) mechanisms of chemical carcinogenesis; 2) DNA damage and repair; 3) tumor viruses; 4) gene expression; 5) differentiation; 6) membrane alterations in transformation; 7) peroxisome proliferators and cancer induction; 8) genetic analysis of the malignant phenotype; and 9) modulation of carcinogenesis utilizing transgenic models. The program during the past 10 years was based on the strong existing graduate programs in Molecular and Cell Biology, Medicine, Microbiology-Immunology, Pathology, Tumor Cell Biology, Biochemistry, Cell Biology and Molecular Biology, and Molecular Pharmacology and Biochemistry. In this application, we add faculty from the departments of Chemistry (Evanston), Urology, and Pediatrics. Thus, graduate students admitted to any of these departments or programs and working with preceptors who are on this training grant, will be considered for support by the training grant. Despite the large number of programs from which trainees were drawn, the training will be coordinated to produce PhDs who are well trained in the study of carcinogenesis. The Integrated Graduate Program in the Life Sciences has markedly increased as the quality and number of excellent students recruited into the carcinogenesis program. Carcinogenesis training consists of one and a half years of course work in the basic life sciences and carcinogenesis followed by three years of thesis research. Integrative aspects of this program include weekly carcinogenesis group meetings and a carcinogenesis seminar program and an annual symposium given by invited speakers. These features collectively have resulted in increased interactions between preceptors and trainees, and to a higher level of collaboration among investigators involved in carcinogenesis research at Northwestern University.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA009560-14
Application #
2894406
Study Section
Cancer Research Manpower and Education Review Committee (CRME)
Program Officer
Gorelic, Lester S
Project Start
1986-08-01
Project End
2001-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
14
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Pathology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Mehta, Manan M; Weinberg, Samuel E; Steinert, Elizabeth M et al. (2018) Hexokinase 2 is dispensable for T cell-dependent immunity. Cancer Metab 6:10
Swaroop, Alok; Oyer, Jon A; Will, Christine M et al. (2018) An activating mutation of the NSD2 histone methyltransferase drives oncogenic reprogramming in acute lymphocytic leukemia. Oncogene :
Kong, Hyewon; Chandel, Navdeep S (2018) Regulation of redox balance in cancer and T cells. J Biol Chem 293:7499-7507
Putzbach, Will; Haluck-Kangas, Ashley; Gao, Quan Q et al. (2018) CD95/Fas ligand mRNA is toxic to cells. Elife 7:
Gao, Quan Q; Putzbach, William E; Murmann, Andrea E et al. (2018) 6mer seed toxicity in tumor suppressive microRNAs. Nat Commun 9:4504
Murmann, Andrea E; Gao, Quan Q; Putzbach, William E et al. (2018) Small interfering RNAs based on huntingtin trinucleotide repeats are highly toxic to cancer cells. EMBO Rep 19:
Bell, Jonathan B; Rink, Jonathan S; Eckerdt, Frank et al. (2018) HDL nanoparticles targeting sonic hedgehog subtype medulloblastoma. Sci Rep 8:1211
Putzbach, William; Gao, Quan Q; Patel, Monal et al. (2018) DISE: A Seed-Dependent RNAi Off-Target Effect That Kills Cancer Cells. Trends Cancer 4:10-19
Reczek, Colleen R; Birsoy, K?vanç; Kong, Hyewon et al. (2017) A CRISPR screen identifies a pathway required for paraquat-induced cell death. Nat Chem Biol 13:1274-1279
Spriggs, Chelsey C; Laimins, Laimonis A (2017) Human Papillomavirus and the DNA Damage Response: Exploiting Host Repair Pathways for Viral Replication. Viruses 9:

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