The Database Shared Resource (DBSR) is a new core within the Herbert Irving Comprehensive Cancer Center (HICCC), whose central function is to provide oversight and infrastructure for the development and maintenance of cancer-related clinical databases and link them to existing biobanks. Our overall objective is to stimulate multi-disciplinary clinical and translational research utilizing these databases and biobanks. Services provided include: Coordinating clinical database-related services with other shared resources Providing IT support for data storage, clinical data extraction, and quality measures Providing support and resources for questionnaire development for biobanks Disseminating information about the clinical databases and biobanks to the research community Reviewing requests to access the clinical databases and biobanks and tracking utilization There are currently sixteen cancer-related clinical databases and biobanks at Columbia University Medical Center (CUMC). Our goal is to standardize and streamline the management of these clinical databases and biobanks, ensure that they meet IRB, HIPAA, and CUMC IT Security requirements, and develop them into a valuable resource for the HICCC research community. This entails the coordination of efforts with other shared resources to facilitate recruitment and consenting of database participants, administration of epidemiologic questionnaires, collection of biospecimens, and extraction of clinical data from the cancer registry and electronic health record (EHR). Our future plans include integrating these cancer-related clinical database and biobanking efforts with the Personalized Medicine Research Initiative at CUMC and to develop more efficient ways of extracting clinical data from the EHR, including the use of patient portals. Our goal is to merge all of the disease-specific databases into one HICCC clinical database, which will enroll all newly diagnosed cancer patients and healthy at-risk individuals seen at our Cancer Center and link their epidemiologic questionnaire data and clinical information with tumor tissue, blood, DNA, and other biospecimens. The proposed total operating budget for the DBSR is $153,887, ofwhich we are requesting $35,223 from the CCSG.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013696-40
Application #
8753134
Study Section
Subcommittee G - Education (NCI)
Project Start
1997-07-04
Project End
2019-06-30
Budget Start
2014-07-17
Budget End
2015-06-30
Support Year
40
Fiscal Year
2014
Total Cost
$50,233
Indirect Cost
$18,837
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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