(Applicant's Description) The University of Pittsburgh Cancer Institute (UPCI) is a multidisciplinary cancer research center, with programs in basic research, translational research and clinical investigations, prevention and control, early diagnosis and treatment, and behavioral medicine research. In addition, it has responsibility of cancer education and clinical care. The UPCI is comprised of faculty form the University of Pittsburgh and Carnegie Mellon University and utilizes the clinical facilities of the University of Pittsburgh and Medical Center Health System plus two University affiliated hospitals (Children's Hospital of Pittsburgh and Magee Women's Hospital). The UPCI has established programs in: molecular and cellular oncology, molecular therapeutic and drug discovery, immunology, molecular virology, lung cancer, prostate and urologic cancers, head and neck cancer, biological therapeutics, cancer epidemiology, prevention and control, and behavioral medicine and oncology. To assist its research efforts, the UPCI maintains shared facilities including: Biostatistics Facility, Clinical Research Support Services, Immunologic Monitoring Laboratory, Cellular Products Laboratory, Hybridoma Facility, Flow Cytometry Facility, DNA Sequencing Facility, Peptide Synthesis Facility, Animal Facility, Glassware Facility, Oligonucleotide Facility, and Cell and Tissue Imaging Facility. This application requests continued cancer center support grant (CCSG) funding for the University of Pittsburgh Cancer Institute's program for years 12-16.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA047904-14S1
Application #
6400737
Study Section
Special Emphasis Panel (ZCA1-SRRB-Y (M1))
Program Officer
Smith, Wendy B
Project Start
1988-08-01
Project End
2004-07-30
Budget Start
2001-09-26
Budget End
2002-07-31
Support Year
14
Fiscal Year
2001
Total Cost
$196,831
Indirect Cost
Name
University of Pittsburgh
Department
Pathology
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Thakur, Prakash C; Miller-Ocuin, Jennifer L; Nguyen, Khanh et al. (2018) Inhibition of endoplasmic-reticulum-stress-mediated autophagy enhances the effectiveness of chemotherapeutics on pancreatic cancer. J Transl Med 16:190
Posluszny, Donna M; Bovbjerg, Dana H; Agha, Mounzer E et al. (2018) Patient and family caregiver dyadic adherence to the allogeneic hematopoietic cell transplantation medical regimen. Psychooncology 27:354-358
Li, Chunlei; Song, Baobao; Santos, Patricia M et al. (2018) Hepatocellular cancer-derived alpha fetoprotein uptake reduces CD1 molecules on monocyte-derived dendritic cells. Cell Immunol :
Willis, John; Epperly, Michael W; Fisher, Renee et al. (2018) Amelioration of Head and Neck Radiation-Induced Mucositis and Distant Marrow Suppression in Fanca-/- and Fancg-/- Mice by Intraoral Administration of GS-Nitroxide (JP4-039). Radiat Res 189:560-578
Roy, Somak; LaFramboise, William A; Liu, Ta-Chiang et al. (2018) Loss of Chromatin-Remodeling Proteins and/or CDKN2A Associates With Metastasis of Pancreatic Neuroendocrine Tumors and Reduced Patient Survival Times. Gastroenterology 154:2060-2063.e8
Thapa, Dharendra; Wu, Kaiyuan; Stoner, Michael W et al. (2018) The protein acetylase GCN5L1 modulates hepatic fatty acid oxidation activity via acetylation of the mitochondrial ?-oxidation enzyme HADHA. J Biol Chem 293:17676-17684
Jin, Tao; Iordanova, Bistra; Hitchens, T Kevin et al. (2018) Chemical exchange-sensitive spin-lock (CESL) MRI of glucose and analogs in brain tumors. Magn Reson Med 80:488-495
Samal, Jasmine; Kelly, Samantha; Na-Shatal, Ali et al. (2018) Human immunodeficiency virus infection induces lymphoid fibrosis in the BM-liver-thymus-spleen humanized mouse model. JCI Insight 3:
Hartman, Douglas J; Ahmad, Fahad; Ferris, Robert L et al. (2018) Utility of CD8 score by automated quantitative image analysis in head and neck squamous cell carcinoma. Oral Oncol 86:278-287
Leibowitz, Brian J; Yang, Liheng; Wei, Liang et al. (2018) Targeting p53-dependent stem cell loss for intestinal chemoprotection. Sci Transl Med 10:

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