The Oncologic Imaging Program (OIP) develops novel imaging agents and innovative methods for radionuclide, MR, ultrasound, optical, and hybrid imaging technologies, including photoacoustic imaging and theranostics. Application of artificial intelligence and informatics platforms to solve advanced oncologic imaging challenges demonstrates the evolving nature of OIP. OIP?s major goals are to facilitate new research initiatives, expand ongoing collaborations, mentor junior faculty, train students and fellows, and develop new methods to solve fundamental and clinical cancer imaging needs. These goals will be achieved through intra- and inter- programmatic activities and external partnerships. OIP?s highest priorities include developing imaging agents and technologies for detecting, diagnosing, and treating cancer, and expanding our knowledge of animal models used for basic cancer research. OIP activities will pursue four specific aims. (1) Develop innovative imaging instruments and methods for diagnostic and theranostic applications and image-guided cancer therapies. (2) Develop new molecular imaging agents and theranostics for accurate detection and, assessment of tumor- specific properties as well as for monitoring therapeutic response to improve treatment outcomes. (3) Advance applications of quantitative imaging (QI) to elucidate the molecular mechanisms driving cancer progression and treatment responses via deep learning and radiomics. (4) Educate, train, and mentor students, fellows, and junior faculty in cancer imaging research. OIP will continue to develop strong intra- and inter-programmatic collaborations, industry partnerships, and integrated trainee support to champion collective innovation in cancer imaging research and clinical translation. The program currently includes 36 members from seven departments and three schools. The extensive collaborative network of OIP members has resulted in more than $10.1 million in current grant awards, of which $5.4 million is NCI funding and $2.5 million is other peer-reviewed funding, and an additional $5 million in NIH S10 large instrument grant funding. OIP research is anchored by one NCI-funded research center (Center for Multiple Myeloma Nanotherapy [U54 CA199092]), the institutionally supported Molecular Imaging Center (continuation of previous NCI-supported ICMIC [CA094056]), three NIH-supported Resource Centers (Gropler P41 EB025815, Marcus U24 CA204854, Shoghi U24 CA209837), two imaging training grants (Culver T32 EB014855, Woodard T32 EB021955), and more than 1,104 publications in the current project period of which 28% are inter-programmatic, 26% are intra-programmatic and 10% with impact factor >10. OIP research has been accelerated by recent installation of several new instruments, including PET/CT scanner (Siemens Vision), micro PET/CT, microPET/MR, GE SPINlab hyperpolarization unit, Oxford Instruments PulsarTM benchtop permanent-magnet-based 1.5-T NMR spectrometer, fluorescence molecular tomography system, multispectral optoacoustic tomography system, and IVIS-CT multimodal imaging system. Clinical translation of new discoveries will remain the cornerstone of OIP.
Cruchaga, Carlos; Del-Aguila, Jorge L; Saef, Benjamin et al. (2018) Polygenic risk score of sporadic late-onset Alzheimer's disease reveals a shared architecture with the familial and early-onset forms. Alzheimers Dement 14:205-214 |
Song, Wilbur M; Joshita, Satoru; Zhou, Yingyue et al. (2018) Humanized TREM2 mice reveal microglia-intrinsic and -extrinsic effects of R47H polymorphism. J Exp Med 215:745-760 |
Gauvain, Karen; Ponisio, Maria Rosana; Barone, Amy et al. (2018) 18F-FDOPA PET/MRI for monitoring early response to bevacizumab in children with recurrent brain tumors. Neurooncol Pract 5:28-36 |
Yang, Ruimeng; Duan, Chong; Yuan, Liya et al. (2018) Inhibitors of HIF-1? and CXCR4 Mitigate the Development of Radiation Necrosis in Mouse Brain. Int J Radiat Oncol Biol Phys 100:1016-1025 |
Willet, Spencer G; Lewis, Mark A; Miao, Zhi-Feng et al. (2018) Regenerative proliferation of differentiated cells by mTORC1-dependent paligenosis. EMBO J 37: |
Staples, Robert; London, Daniel A; Dardas, Agnes Z et al. (2018) Comparative Morbidity of Cubital Tunnel Surgeries: A Prospective Cohort Study. J Hand Surg Am 43:207-213 |
Savage, Jeanne E; Salvatore, Jessica E; Aliev, Fazil et al. (2018) Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples. Alcohol Clin Exp Res 42:520-530 |
Waqar, Saiama N; Boehmer, Leigh; Morgensztern, Daniel et al. (2018) Immunogenicity of Influenza Vaccination in Patients With Cancer. Am J Clin Oncol 41:248-253 |
Duncavage, Eric J; Jacoby, Meagan A; Chang, Gue Su et al. (2018) Mutation Clearance after Transplantation for Myelodysplastic Syndrome. N Engl J Med 379:1028-1041 |
Eberth, Jan M; Josey, Michele J; Mobley, Lee R et al. (2018) Who Performs Colonoscopy? Workforce Trends Over Space and Time. J Rural Health 34:138-147 |
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