? TRANSLATIONAL THERAPEUTICS (TT) The Translational Therapeutics (TT) Program at The Ohio State University Comprehensive Cancer Center (OSUCCC), co-led by David Carbone, MD, PhD, Blake Peterson, PhD, and Elaine Mardis, PhD, unites an outstanding team of 79 basic, translational and/or clinical researchers from 18 departments within The Ohio State University (OSU) Colleges of Medicine, Pharmacy, and Veterinary Medicine and Nationwide Children?s Hospital (NCH). The goal of the TT program is to translate advances in solid tumor molecular biology and promising preclinical studies into innovative clinical trials to improve the state of the art in the diagnosis and treatment of solid tumors. Solid tumors are by far the major causes of cancer death in our catchment area (the state of Ohio), dominated by diseases of special interest in this program, including lung, breast, colorectal, head and neck, thyroid, and gynecologic cancers. As a result of existing expertise and collaborative scientific efforts, as well as focused recruitments across a spectrum of disciplines, the TT program exhibits strength in basic and translational research in lung cancer, gastrointestinal malignancies, breast cancer, sarcoma, and glioblastoma, as well as newly enhanced capabilities in drug development.
The Specific Aims of the TT program are to: 1) identify and therapeutically target alterations in solid tumor proliferation and survival signaling pathways; 2) identify tumor-host interactions and target them via small molecule and immunotherapeutic approaches; and 3) develop and improve upon approaches for determining prognosis, selecting appropriate therapies, and evaluating the response to treatment. During the current funding cycle, the TT Program successfully recruited 28 solid tumor clinicians, basic scientists, and physician-scientists. In addition, TT investigators produced 1130 peer-reviewed publications; 178 of these were published in high impact (?10) journals, 16% resulted from intra- programmatic collaborations, and 31% from inter-programmatic collaborations; 74% were multi-institutional; a total of 86% were collaborative publications. TT members collaborated on programmatic grant submissions and were awarded one NCI P01, two U01s, and two UG1s, as well as two T32 training grants. The TT Program has $9.2M in current annual direct costs from peer-reviewed grants, $6.6M (71%) of which is from the NCI. The TT Program is well-integrated with the clinical teams via participation in the multidisciplinary Disease Specific Research Groups (DSRG) and organizes Pan-Disease Investigator-Initiated Trial meetings to catalyze interactions between DSRGs. As such, there were 4,070 accruals to interventional clinical trials during the last funding cycle, of which 3,351 (82%) were therapeutic, including 1,144 (28%) investigator-initiated trials. Future directions focused on the OSUCCC research priorities and cancers relevant to our catchment area and growth in cellular and checkpoint inhibitor research (adult and pediatric), immunogenomics, tumor resistance and tumor heterogeneity and small molecule drug development.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016058-45
Application #
10089997
Study Section
Subcommittee H - Clinical Groups (NCI)
Project Start
1997-09-12
Project End
2025-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
45
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Brasky, Theodore M; Hinton, Alice; Doogan, Nathan J et al. (2018) Characteristics of the Tobacco User Adult Cohort in Urban and Rural Ohio. Tob Regul Sci 4:614-630
Saini, Uksha; Suarez, Adrian A; Naidu, Shan et al. (2018) STAT3/PIAS3 Levels Serve as ""Early Signature"" Genes in the Development of High-Grade Serous Carcinoma from the Fallopian Tube. Cancer Res 78:1739-1750
Olaverria Salavaggione, Gonzalo N; Duggan, Megan C; Carson, William E (2018) Analysis of MLN4924 (pevonedistat) as a potential therapeutic agent in malignant melanoma. Melanoma Res 28:390-397
Jones, Caitlin E; Hammer, Anisha M; Cho, YouJin et al. (2018) Stromal PTEN Regulates Extracellular Matrix Organization in the Mammary Gland. Neoplasia 21:132-145
Fenn, J Daniel; Monsma, Paula C; Brown, Anthony (2018) Axonal neurofilaments exhibit frequent and complex folding behaviors. Cytoskeleton (Hoboken) 75:258-280
Zhang, Lingling; Yu, Jianhua; Wei, Wei (2018) Advance in Targeted Immunotherapy for Graft-Versus-Host Disease. Front Immunol 9:1087
Jasinski, Daniel L; Li, Hui; Guo, Peixuan (2018) The Effect of Size and Shape of RNA Nanoparticles on Biodistribution. Mol Ther 26:784-792
Gordillo, Gayle M (2018) Reply: Urinary Excretion of MicroRNA-126 Is a Biomarker for Hemangioma Proliferation. Plast Reconstr Surg 141:320e
Ott, Christopher J; Federation, Alexander J; Schwartz, Logan S et al. (2018) Enhancer Architecture and Essential Core Regulatory Circuitry of Chronic Lymphocytic Leukemia. Cancer Cell 34:982-995.e7
Willis, William L; Wang, Linan; Wada, Takuma Tsuzuki et al. (2018) The proinflammatory protein HMGB1 is a substrate of transglutaminase-2 and forms high-molecular weight complexes with autoantigens. J Biol Chem 293:8394-8409

Showing the most recent 10 out of 2602 publications