The faculty of two institutions, Weill Cornell Medical College (WCMC) and Memorial Sloan-Kettering Cancer Center (MSKCC), are requesting funds to support a collaborative training program in research in the area of cancer pharmacology. The collaboration consists of an integrated set of training activities for Ph.D. students and postdoctoral fellows. The strength and diversity of the 16 faculty provide opportunities for research in a variety of different areas, such as the development of new cancer therapeutic agents (e.g. through organic synthesis, monoclonal antibody technology, differentiation therapy, and the screening of new compounds), and the analysis of molecular mechanisms by which drugs act on cancer cells. Additionally, research concerning the mechanisms by which dioxin and environmental pollutants cause cancer is a part of the training program. Training program faculty research includes basic, mechanistic studies of the molecular actions of drugs used in cancer treatment and prevention, and research leading to more clinical endpoints. The graduate Ph.D. program consists of course work and three laboratory rotations, followed by an admission to candidacy exam and thesis research. A graduate course in Cancer Pharmacology is part of this program and represents a commitment of the faculty to the training of students in this area. Students and fellows present their research at the annual two-day Pharmacology Program retreat. Postdoctoral fellows attend a weekly journal club, take courses in cancer pharmacology, and present a formal seminar in the cancer pharmacology seminar series. It is expected that this training program will provide students and fellows with a broader understanding of the interrelationships between research on the basic mechanisms of drug action and drug development and clinical issues so that both clinicians and basic scientists will be better prepared to carry out research to prevent or treat cancer. Our request for continued NIH support of a training program in Cancer Pharmacology builds on major commitments of the participating institutions to the enhancement of research in this area. The faculty of this training program are members of the joint WCMC/SKI graduate program, with a total of 31 Pharmacology Ph.D. Program faculty. Thus, this faculty represents a cohesive, interactive group with a common interest in research and training in the area of cancer pharmacology.

Public Health Relevance

This Training program is unusual in several respects. First, this is one of the few training programs focused specifically on cancer pharmacology. Second, this training program features cancer research training in molecular pharmacology, animal models of cancer, and human clinical trials research. Many of the faculty are physician-scientists who treat patients as well as perform research. Third, this group of faculty is very collaborative. All of these features make this program extremely relevant and useful for training the next generation of cancer pharmacology researchers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA062948-18
Application #
8282708
Study Section
Subcommittee G - Education (NCI)
Program Officer
Lim, Susan E
Project Start
1994-09-01
Project End
2015-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
18
Fiscal Year
2012
Total Cost
$491,720
Indirect Cost
$40,602
Name
Weill Medical College of Cornell University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Guney, Tezcan; Wenderski, Todd A; Boudreau, Matthew W et al. (2018) Synthesis of Benzannulated Medium-ring Lactams via a Tandem Oxidative Dearomatization-Ring Expansion Reaction. Chemistry 24:13150-13157
Trasino, Steven E; Tang, Xiao-Han; Shevchuk, Maria M et al. (2018) Amelioration of Diabetic Nephropathy Using a Retinoic Acid Receptor ?2 Agonist. J Pharmacol Exp Ther 367:82-94
Patil, Deepak P; Pickering, Brian F; Jaffrey, Samie R (2018) Reading m6A in the Transcriptome: m6A-Binding Proteins. Trends Cell Biol 28:113-127
Quintero, Cynthia M; Laursen, Kristian B; Mongan, Nigel P et al. (2018) CARM1 (PRMT4) Acts as a Transcriptional Coactivator during Retinoic Acid-Induced Embryonic Stem Cell Differentiation. J Mol Biol 430:4168-4182
Jena, Prakrit V; Safaee, Mohammad M; Heller, Daniel A et al. (2017) DNA-Carbon Nanotube Complexation Affinity and Photoluminescence Modulation Are Independent. ACS Appl Mater Interfaces 9:21397-21405
Vu, Ly P; Pickering, Brian F; Cheng, Yuanming et al. (2017) The N6-methyladenosine (m6A)-forming enzyme METTL3 controls myeloid differentiation of normal hematopoietic and leukemia cells. Nat Med 23:1369-1376
Verano, Alyssa L; Tan, Derek S (2017) Family-level stereoselective synthesis and biological evaluation of pyrrolomorpholine spiroketal natural product antioxidants. Chem Sci 8:3687-3693
Olarerin-George, Anthony O; Jaffrey, Samie R (2017) MetaPlotR: a Perl/R pipeline for plotting metagenes of nucleotide modifications and other transcriptomic sites. Bioinformatics 33:1563-1564
Galassi, Thomas V; Jena, Prakrit V; Roxbury, Daniel et al. (2017) Single Nanotube Spectral Imaging To Determine Molar Concentrations of Isolated Carbon Nanotube Species. Anal Chem 89:1073-1077
Dao, Tao; Korontsvit, Tatyana; Zakhaleva, Victoria et al. (2017) An immunogenic WT1-derived peptide that induces T cell response in the context of HLA-A*02:01 and HLA-A*24:02 molecules. Oncoimmunology 6:e1252895

Showing the most recent 10 out of 148 publications