The long-term goal of the Prostate Cancer (PC) Program is to elucidate the pathogenesis of prostate cancer and implement novel approaches to its prevention, early diagnosis, and individualized treatment. To achieve these ends, the following Specific Goals will be pursued: 1) The molecular oncology of prostate cancer will be elucidated by defining the molecular lesions of proto-oncogenes and tumor suppressor genes that are responsible for tumor formation;2) Experimental models of prostate cancer will be developed and characterized to elucidate critical regulatory networks, enhance preclinical studies, and define new biological endpoints, including the mechanisms of resistance to certain treatments; 3) The experimental therapeutics of prostate cancer will be refined by using molecular determinants to optimize clinical trials and thereby generate novel decision-making tools for disease management. The PC Program replaces the former Urologic Malignancies Program. It now consists of 19 members (12 full members, 4 clinical members, and 3 associate members) from 6 departments within the College of Physicians &Surgeons at Columbia University (CD). Compared to the Urologic Malignancies Program, the new PC Program has fewer members and their interests are more sharply focused on prostate cancer. New leadership has been brought into the Program, with Carlos Cordon-Cardo serving as Program Leader and Daniel Petrylak as Co-Leader. In the past ten months, major investments by the HICCC led to the recruitment of Dr. Cordon-Cardo, as well a several other outstanding basic and translational investigators, including Edward Gelmann, Cory Abate-Shen, and Michael Shen. The comprehensive nature of the restructured PC Program now ranges from chemoprevention to novel chemotherapy, surgical oncology including minimal invasive procedures, radiation therapy, and quality of care programs. The number of trials and the number of patients accrued to such trials have increased. Approximately 78% of clinical trial accruals are of African American or Hispanic ethnicity. Several investigators lead local and multi-center clinical trials. For the last budget year of the grant (July 1, 2006 - June 30, 2007), the PC Program received a total of $7.4M (direct costs) in cancer-relevant grant support, including $1.9M (direct costs) in NCI funding, $1.7M (direct costs) in other cancer-related peer-reviewed funding, and $3.8M (direct costs) in cancer-related non-peer-reviewed funding. The total number of publications since the previous submission was 172, of which 23% were intra-programmatic and 12% interprogrammatic.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013696-36
Application #
7862536
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
36
Fiscal Year
2009
Total Cost
$68,511
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Jauregui, Ruben; Park, Karen Sophia; Duong, Jimmy K et al. (2018) Quantitative progression of retinitis pigmentosa by optical coherence tomography angiography. Sci Rep 8:13130
O'Neil, Daniel S; Prigerson, Holly G; Mmoledi, Keletso et al. (2018) Informal Caregiver Challenges for Advanced Cancer Patients During End-of-Life Care in Johannesburg, South Africa and Distinctions Based on Place of Death. J Pain Symptom Manage 56:98-106
Liu, Katherine Y; Sengillo, Jesse D; Velez, Gabriel et al. (2018) Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity. Orphanet J Rare Dis 13:138
Koch, Susanne F; Tsang, Stephen H (2018) Success of Gene Therapy in Late-Stage Treatment. Adv Exp Med Biol 1074:101-107
DiCarlo, James E; Mahajan, Vinit B; Tsang, Stephen H (2018) Gene therapy and genome surgery in the retina. J Clin Invest 128:2177-2188
Wert, Katherine J; Velez, Gabriel; Cross, Madeline R et al. (2018) Extracellular superoxide dismutase (SOD3) regulates oxidative stress at the vitreoretinal interface. Free Radic Biol Med 124:408-419
Lee, Andreia; CingĂ–z, Oya; Sabo, Yosef et al. (2018) Characterization of interaction between Trim28 and YY1 in silencing proviral DNA of Moloney murine leukemia virus. Virology 516:165-175
Schrank, Benjamin R; Aparicio, Tomas; Li, Yinyin et al. (2018) Nuclear ARP2/3 drives DNA break clustering for homology-directed repair. Nature 559:61-66
Proto, Jonathan D; Doran, Amanda C; Gusarova, Galina et al. (2018) Regulatory T Cells Promote Macrophage Efferocytosis during Inflammation Resolution. Immunity 49:666-677.e6
Hernandez, Celine; Huebener, Peter; Pradere, Jean-Philippe et al. (2018) HMGB1 links chronic liver injury to progenitor responses and hepatocarcinogenesis. J Clin Invest 128:2436-2451

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