The Ohio State University Comprehensive Cancer Center (OSUCCC) is currently in its 24th year as an NCI-designated CCC and is now requesting continued federal support for the next five years. The OSUCCC came under its 3rd Director in August 1997 and has initiated a series of changes aimed at creating new scientific direction and revitalizing existing clinical disciplines. The overall goal remains to reduce cancer morbidity and mortality through continu4ed basic, translational and clinical research. To accomplish this the OSUCCC has, in the last 18 months, 1) created a new Division of Human Cancer Genetics with committed institutional support currently in excess of $50 million; 2) created, eliminated and restructured existing CCC programs to be consistent with existing scientific CCC programs to be consistent with existing scientific and clinical strengths and future direction; 3) recruited 32 programs to be consistent with existing scientific and clinical strengths and future direction; 3) recruited 32 new full time faculty to OSU, all with cancer relevant research and/or clinical care, including 9 physician scientists to medical or surgical oncology; 4) developed a new clinical trials infrastructu7re to better facilitate innovative clinical cancer research; 5) acquired a 64% increase in new space allocated for cancer research. The 201 OSUCCC members are currently served by 8 shared resources and are distributed among 7 programs: Cancer Prevention & Control, Experimental Therapeutics, Hormones and Cancer, Immunology, Molecular Biology & Cancer Genetics, Molecular and Cellular Carcinogenesis, and RNA Oncogenic Virus. These programs are supported by over $29 million in annual direct costs from NCI approved peer-reviewed funding, with $10.6 million of that funding coming from 95 NCI-sponsored projects, representing a 153% increase in NCI funding since last submission. The new OSUCCC director and her recruits have resulted in a substantial increase in University and philanthropic support, NCI-approved grant dollars. OSUCCC laboratory and clinical space, and published evidence of intra- and inter-programmatic collaboration. The changes in OSUCCC leadership, support for new scientific directions, and revitalization of translational and clinical cancer research efforts should greatly strengthen the OSUCCC's ability to achieve its overall goal during the next 5 years.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016058-28
Application #
6624642
Study Section
Subcommittee G - Education (NCI)
Program Officer
Marino, Michael A
Project Start
1977-07-01
Project End
2004-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
28
Fiscal Year
2003
Total Cost
$2,760,556
Indirect Cost
Name
Ohio State University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
071650709
City
Columbus
State
OH
Country
United States
Zip Code
43210
Straus, David J; Jung, Sin-Ho; Pitcher, Brandelyn et al. (2018) CALGB 50604: risk-adapted treatment of nonbulky early-stage Hodgkin lymphoma based on interim PET. Blood 132:1013-1021
Kim, Yangjin; Yoo, Ji Young; Lee, Tae Jin et al. (2018) Complex role of NK cells in regulation of oncolytic virus-bortezomib therapy. Proc Natl Acad Sci U S A 115:4927-4932
Wang, Xinmei; Kwak, Kwang Joo; Yang, Zhaogang et al. (2018) Extracellular mRNA detected by molecular beacons in tethered lipoplex nanoparticles for diagnosis of human hepatocellular carcinoma. PLoS One 13:e0198552
Callahan, Catherine L; Bonner, Matthew R; Nie, Jing et al. (2018) Lifetime exposure to ambient air pollution and methylation of tumor suppressor genes in breast tumors. Environ Res 161:418-424
Gopalakrishnan, Bhavani; Cheney, Carolyn; Mani, Rajeswaran et al. (2018) Polo-like kinase inhibitor volasertib marginally enhances the efficacy of the novel Fc-engineered anti-CD33 antibody BI 836858 in acute myeloid leukemia. Oncotarget 9:9706-9713
Hankey, William; Frankel, Wendy L; Groden, Joanna (2018) Functions of the APC tumor suppressor protein dependent and independent of canonical WNT signaling: implications for therapeutic targeting. Cancer Metastasis Rev 37:159-172
Felix, A S; Brasky, T M; Cohn, D E et al. (2018) Endometrial carcinoma recurrence according to race and ethnicity: An NRG Oncology/Gynecologic Oncology Group 210 Study. Int J Cancer 142:1102-1115
Stover, Daniel G; Parsons, Heather A; Ha, Gavin et al. (2018) Association of Cell-Free DNA Tumor Fraction and Somatic Copy Number Alterations With Survival in Metastatic Triple-Negative Breast Cancer. J Clin Oncol 36:543-553
Kelly, Rachel S; Lasky-Su, Jessica; Yeung, Sai-Ching J et al. (2018) Integrative omics to detect bacteremia in patients with febrile neutropenia. PLoS One 13:e0197049
ElNaggar, Adam C; Hade, Erinn M; O'Malley, David M et al. (2018) Time to chemotherapy in ovarian cancer: Compliance with ovarian cancer quality indicators at a National Cancer Institute-designated Comprehensive Cancer Center. Gynecol Oncol 151:501-505

Showing the most recent 10 out of 2602 publications