? COMPARATIVE PATHOLOGY & DIGITAL IMAGING SHARED RESOURCE (CPDISR) The CPDISR provides expert, readily available and affordable experimental pathology support to investigators conducting research for understanding the development and treatment of cancer using preclinical animal models and/or human tissues procured for translational research. During the current funding period, a recent major development was the inclusion of complete histology services optimized for human tissues, as well as expanded slide digitization and quantitative image analysis services for stained human and animal tissue slides. As a result, Dr. Anil Parwani (MCC) has been named co-Director with Dr. Krista La Perle (CB), the name of the shared resource (SR) has been changed to the Comparative Pathology & Digital Imaging Shared Resource, and the Specific Aims have been modified accordingly.
The Specific Aims are to: 1) provide consultative services to OSUCCC investigators for optimal experimental design, sample submission and data analysis, and interactions with other SRs; 2) provide support for preclinical efficacy and toxicity animal studies as well as translational studies that utilize human tissues; and 3) perform digitization and quantitative image analysis of stained slides from animal and human tissues. During the current 5-year grant cycle, a third board certified veterinary pathologist and seven additional technical staff have been added to anticipate usage in conjunction with the robust OSUCCC recruitment and strategic priorities. The CPDISR also acquired a Leica PELORIS 3 dual retort tissue processor after successful peer-reviewed funding through the OSUCCC Intramural Research Program. During this grant cycle, the CPDISR contributed to 84 publications (12 > 10 impact factor), 537 investigators, and 57 NCI grants, including 1 K12, 1 K22, 1 K24, 5 P01s, 1 P50, 35 R01s, 7 R21s, 2 R35s, 1 T32, and 3 U01s involving members of all five OSUCCC research programs. For the next grant cycle, the CPDISR will be a regular member of the Immune Monitoring and Discovery Platform, an overarching shared resource initiative fostering complex immuno-oncology projects. In addition, a major emphasis will be to continue to expand our available menu of antibodies optimized for immunohistochemistry, immunofluorescence and in situ hybridization in tissues of animal and human origin by various staining platforms, including multiplexing, according to the specific needs of OSUCCC members. We will also increase our support of image analysis projects allowing machine learning approaches to be developed with the center for cancer engineering; and continue to evaluate available open source and commercial image analysis software platforms/modules to complement our Aperio and Visiopharm software in order to quantify biomarkers in animal and human tissues. The annual budget of the CPDISR is $1,863,254, yet the CCSG request is $107,366. As such, the CPDIR seeks only 5.8% budgetary support from CCSG funds.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016058-45
Application #
10090009
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
Siegel, Marni B; He, Xiaping; Hoadley, Katherine A et al. (2018) Integrated RNA and DNA sequencing reveals early drivers of metastatic breast cancer. J Clin Invest 128:1371-1383
White, Brian S; Lanc, Irena; O'Neal, Julie et al. (2018) A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5. Blood Cancer J 8:35
Owen, Dwight; Chaft, Jamie E (2018) Immunotherapy in surgically resectable non-small cell lung cancer. J Thorac Dis 10:S404-S411
O'Brien, Susan M; Jaglowski, Samantha; Byrd, John C et al. (2018) Prognostic Factors for Complete Response to Ibrutinib in Patients With Chronic Lymphocytic Leukemia: A Pooled Analysis of 2 Clinical Trials. JAMA Oncol 4:712-716
Guo, Sijin; Piao, Xijun; Li, Hui et al. (2018) Methods for construction and characterization of simple or special multifunctional RNA nanoparticles based on the 3WJ of phi29 DNA packaging motor. Methods 143:121-133
Sadowski, Abbey R; Gardner, Heather L; Borgatti, Antonella et al. (2018) Phase II study of the oral selective inhibitor of nuclear export (SINE) KPT-335 (verdinexor) in dogs with lymphoma. BMC Vet Res 14:250
Barredo, Julio C; Hastings, Caroline; Lu, Xiamin et al. (2018) Isolated late testicular relapse of B-cell acute lymphoblastic leukemia treated with intensive systemic chemotherapy and response-based testicular radiation: A Children's Oncology Group study. Pediatr Blood Cancer 65:e26928
Kim, So-Youn; Nair, Devi M; Romero, Megan et al. (2018) Transient inhibition of p53 homologs protects ovarian function from two distinct apoptotic pathways triggered by anticancer therapies. Cell Death Differ :
Yadav, Marshleen; Song, Feifei; Huang, Jason et al. (2018) Ocimum flavone Orientin as a countermeasure for thrombocytopenia. Sci Rep 8:5075
Farquhar, Neil; Thornton, Sophie; Coupland, Sarah E et al. (2018) Patterns of BAP1 protein expression provide insights into prognostic significance and the biology of uveal melanoma. J Pathol Clin Res 4:26-38

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