EXCEED THE SPACE PROVIDED. This long-standing training program, currently in its 29th year of NRSA support, is centered on the educationaland advanced research functions of the program of Molecular Pharmacology and Cancer Therapeutics (MPCT) in the State Universityof New York at Buffalo (SUNYAB), Roswell Park Graduate Division.The MPCT Program and the NRSA supporting it have traditionally focused on the training of predoctoral students. It reflects the activities of 27 senior faculty of the Grace Cancer Drug Center (GCDC), 1emeritus faculty member, and 2 faculty members who belong to other research units. Program faculty have diverse backgrounds and research interests with a ;ommon focus on exploiting recent advances in the molecularcharacterization of cancer for the development of new approaches to treatment and prevention. Research activities of the program can be broadly classified into molecular target discovery, mechanisms of drug action and resistance, prevention, and therapeutic development. The MPCT program is unique because it provides trainees with a broad perspective on cancer related issues ncluding cancer incidence and survival, the spectrum of scientific approaches to cancer, the importance of nteractions between basic and clinical researchers, and the realities of patient care. Further, trainees are exposed to cutting edge research at each stage of the cancer drug development process, from the laboratory bench to the lospital bedside. This is accomplished by integrating an academic program comprised of a diverse faculty within the setting of a world-renowned, NCI-designated, Comprehensive Cancer Center. The training opportunities offered are supplemented by integration with collaborative studies carried out by Program faculty and colleagues at Roswell Park Cancer Institute (RPCI) and the SUNYAB. Predoctoral students in the MPCT program (average 5.2/entering per yr; 30 currently enrolled; 18 of the 30 have or will receive support from the currently active NRSA) are drawn from excellent national and international institutions. These graduate students have Bachelor's or Master's degrees in the physical or biological sciences, or have M.D. degrees. This application proposes support br 5 predoctoral trainees (6 currently supported with CURE supplement). The labs of the GCDC occupy a six story building (49,655 ft2 net lab space) on the campus of RPCI. The labs, half of which are newly remodeled, are equipped with modem instrumentation appropriate to the training proposed. In addition to the GCDC, trainees lave access to research programs in the areas of immunology, cancer genetics, molecular and cellular biology, ;ancer prevention, molecular and cellular biophysics as well as RPCI clinical units. TraJnee research is facilitated iy RPCI core facilities supported by the Comprehensive Cancer Center Grant and the facilities of SUNYAB. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
3T32CA009072-30S1
Application #
7118860
Study Section
Subcommittee G - Education (NCI)
Program Officer
Aguila, H Nelson
Project Start
1978-07-01
Project End
2010-02-28
Budget Start
2005-09-20
Budget End
2006-02-28
Support Year
30
Fiscal Year
2005
Total Cost
$33,001
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
824771034
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Griffiths, Elizabeth A; Srivastava, Pragya; Matsuzaki, Junko et al. (2018) NY-ESO-1 Vaccination in Combination with Decitabine Induces Antigen-Specific T-lymphocyte Responses in Patients with Myelodysplastic Syndrome. Clin Cancer Res 24:1019-1029
Long, Mark D; Smiraglia, Dominic J; Campbell, Moray J (2017) The Genomic Impact of DNA CpG Methylation on Gene Expression; Relationships in Prostate Cancer. Biomolecules 7:
Singh, Prashant K; van den Berg, Patrick R; Long, Mark D et al. (2017) Integration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-?B binding that is linked to immune phenotypes. BMC Genomics 18:132
Long, Mark D; Campbell, Moray J (2017) Integrative genomic approaches to dissect clinically-significant relationships between the VDR cistrome and gene expression in primary colon cancer. J Steroid Biochem Mol Biol 173:130-138
Mu, Ping; Zhang, Zeda; Benelli, Matteo et al. (2017) SOX2 promotes lineage plasticity and antiandrogen resistance in TP53- and RB1-deficient prostate cancer. Science 355:84-88
Srivastava, Pragya; Paluch, Benjamin E; Matsuzaki, Junko et al. (2016) Induction of cancer testis antigen expression in circulating acute myeloid leukemia blasts following hypomethylating agent monotherapy. Oncotarget 7:12840-56
Swetzig, Wendy M; Wang, Jianmin; Das, Gokul M (2016) Estrogen receptor alpha (ER?/ESR1) mediates the p53-independent overexpression of MDM4/MDMX and MDM2 in human breast cancer. Oncotarget 7:16049-69
Paluch, Benjamin E; Naqash, Abdul R; Brumberger, Zachary et al. (2016) Epigenetics: A primer for clinicians. Blood Rev 30:285-95
Verone-Boyle, Alissa R; Shoemaker, Suzanne; Attwood, Kristopher et al. (2016) Diet-derived 25-hydroxyvitamin D3 activates vitamin D receptor target gene expression and suppresses EGFR mutant non-small cell lung cancer growth in vitro and in vivo. Oncotarget 7:995-1013
Marlowe, Timothy A; Lenzo, Felicia L; Figel, Sheila A et al. (2016) Oncogenic Receptor Tyrosine Kinases Directly Phosphorylate Focal Adhesion Kinase (FAK) as a Resistance Mechanism to FAK-Kinase Inhibitors. Mol Cancer Ther 15:3028-3039

Showing the most recent 10 out of 54 publications