The overall objectives of the University of Chicago Medicine Comprehensive Cancer Center (UCCCC) Advanced Imaging (AI) Program are to improve cancer detection and treatment by applying functional and anatomic imaging to noninvasively study cancer initiation, progression, and metastasis. Underpinning this research is the Program?s unique expertise in quantitative image acquisition, analysis and reconstruction, and development of image-based biomarkers. Imaging plays a key role in the UCCCC's efforts to develop precision medicine through the use of non-invasive methods to assess individual risk, find early cancer, guide treatment delivery, assess therapeutic response, and evaluate and prevent adverse health outcomes - particularly for breast, prostate, and lung cancer (cancers with increased incidence and/or mortality in our catchment area). The AI Program is developing more robust predictive biomarkers, imaging strategies, and therapeutic approaches. Noninvasive anatomic, functional, and molecular imaging is used to guide therapy based on specific physiologic, anatomic, metabolic, and molecular characteristics of each tumor. In addition, the AI Program is developing and testing sophisticated image-guided therapies, such as intensity-modulated radiation therapy (IMRT) and MRI-guided high-intensity focused ultrasound (HIFU) that can deliver optimal treatments locally using minimally invasive approaches. The themes around which our research efforts are organized include: 1) Image-based screening; 2) Image-guided therapy; 3) Radiomics; and 4) Molecular imaging. To support and enhance applications of imaging to cancer, the Program continues to foster strong collaborations between imaging scientists, cancer biologists, and physician scientists to share expertise, determine the most relevant research questions, and identify new opportunities for use of imaging and image-guided therapy in both clinical and basic research arenas. UCCCC-supported joint meetings, an interdisciplinary Imaging Working Group, and targeted retreats/symposia facilitate these efforts. The result is a highly collaborative, productive, and well-integrated imaging program, as evidenced by the number of inter- and intraprogrammatic publications (25% and 28%, respectively, 239 publications, 2013-2016), inter-institutional publications (48.5%) and collaborative funding. The AI Program includes 19 members from Radiology and Radiation and Cellular Oncology across a wide range of disciplines, from imaging physics to radiation physics, and radiology to radiation oncology. Research includes studies of patients, volunteers, animal models, tissues, and materials, simulations, data-mining, and development of new devices ? all focused on cancer. Total support for the AI Program is $3.29 million (direct costs), and includes $1,710,047 from the NCI, $1,058,332 from other NIH Institutes, and $521,509 from other sources. Future plans include enhancing each of the four thematic areas, with an emphasis on leveraging the new Cyclotron Facility and expanding the radiochemistry program, as well as conducting clinical trials of screening and risk evaluation.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014599-43
Application #
9489803
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-05-22
Budget End
2019-03-31
Support Year
43
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Trujillo, Jonathan A; Sweis, Randy F; Bao, Riyue et al. (2018) T Cell-Inflamed versus Non-T Cell-Inflamed Tumors: A Conceptual Framework for Cancer Immunotherapy Drug Development and Combination Therapy Selection. Cancer Immunol Res 6:990-1000
Zeng, Zongyue; Huang, Bo; Huang, Shifeng et al. (2018) The development of a sensitive fluorescent protein-based transcript reporter for high throughput screening of negative modulators of lncRNAs. Genes Dis 5:62-74
Lee, Ji-Hye; Park, Beom Seok; Han, Kang R et al. (2018) Insight Into the Interaction Between RNA Polymerase and VPg for Murine Norovirus Replication. Front Microbiol 9:1466
Cheng, Jason X; Chen, Li; Li, Yuan et al. (2018) RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia. Nat Commun 9:1163
Johnson, Marianna B; Hoffmann, Joscelyn N; You, Hannah M et al. (2018) Psychosocial Stress Exposure Disrupts Mammary Gland Development. J Mammary Gland Biol Neoplasia 23:59-73
Sweis, Randy F; Zha, Yuanyuan; Pass, Lomax et al. (2018) Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer. J Immunother Cancer 6:24
Kathayat, Rahul S; Cao, Yang; Elvira, Pablo D et al. (2018) Active and dynamic mitochondrial S-depalmitoylation revealed by targeted fluorescent probes. Nat Commun 9:334
Liu, Jun; Eckert, Mark A; Harada, Bryan T et al. (2018) m6A mRNA methylation regulates AKT activity to promote the proliferation and tumorigenicity of endometrial cancer. Nat Cell Biol 20:1074-1083
Bhanvadia, Raj R; VanOpstall, Calvin; Brechka, Hannah et al. (2018) MEIS1 and MEIS2 Expression and Prostate Cancer Progression: A Role For HOXB13 Binding Partners in Metastatic Disease. Clin Cancer Res 24:3668-3680
Wood, Kevin; Byron, Elizabeth; Janisch, Linda et al. (2018) Capecitabine and Celecoxib as a Promising Therapy for Thymic Neoplasms. Am J Clin Oncol 41:963-966

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