The broad goal of the OIB Program is to develop and assess quantitative systems and technologies thatimprove detection, clinical management, and quality of life for cancer patients. OIB is strongly interdisciplinary,integrating basic scientists with technologists and clinicians and is focused around 3 key themes. Critically,each of the themes includes basic science, technology development, and translational research activitiesspanning from animal models to human subjects in various types of cancers, including breast, skin, GI, oralcavity, prostate, and brain. We also apply emerging technologies in multi-center and cooperative group clinicaltrials in order to standardize and validate methods and endpoints for improved cancer detection and clinicalmanagement. The three themes are: 1) Cancer imaging and treatment using Biophotonics and BiomedicalOptics technologies, including a broad range of non-linear optical microscopies, Laser Microbeams, OpticalCoherence Tomography, Acousto-Optic Imaging and Elastography, Laser Speckle Imaging, Spatial FrequencyDomain Imaging, and Diffuse Optical Spectroscopy and Imaging; 2) Cancer imaging and treatment using MRI,Nuclear, X-Ray/CT, multi-Modality technologies; and 3) Cancer detection and therapy using molecular, cellular,and material technologies, from nano- and microfluidic platforms and integrated ?lab-on-a-chip? and ?body-ona-chip? systems, to advanced cellular and molecular diagnostics for improved cancer detection and therapy.Importantly, the new technologies and methods for engineering cellular systems we are developing areoptimized such that their integration into multi-system platforms allows visualization using many of thetechnologies developed in themes 1 and 2. OIB leadership works to leverage these technologies to improvecancer detection, clinical management and patient quality of life through three Specific Aims: 1) Develop noveltools for cancer detection and treatment; 2) Foster multi-disciplinary collaborations to validate these tools inpreclinical cancer models; and, 3) Validate novel technologies in multi-center and cooperative group clinicaltrials.Membership: 28 Members from 15 DepartmentsFunding: $3,516,292 NCI (Totals); $5,218,874 Other Peer-Reviewed (Totals)Publications: 347 Publications, 11% Inter-programmatic; 22% Intra-programmatic

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA062203-20
Application #
9208766
Study Section
Subcommittee A - Cancer Centers (NCI-A)
Project Start
Project End
Budget Start
2017-02-01
Budget End
2018-01-31
Support Year
20
Fiscal Year
2017
Total Cost
$9,471
Indirect Cost
$3,341
Name
University of California Irvine
Department
Type
Domestic Higher Education
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Koay, Eugene J; Lee, Yeonju; Cristini, Vittorio et al. (2018) A Visually Apparent and Quantifiable CT Imaging Feature Identifies Biophysical Subtypes of Pancreatic Ductal Adenocarcinoma. Clin Cancer Res 24:5883-5894
Wilford, Justin; Osann, Kathryn; Hsieh, Susie et al. (2018) Validation of PROMIS emotional distress short form scales for cervical cancer. Gynecol Oncol 151:111-116
Bagaev, Alexander; Pichugin, Aleksey; Nelson, Edward L et al. (2018) Anticancer Mechanisms in Two Murine Bone Marrow-Derived Dendritic Cell Subsets Activated with TLR4 Agonists. J Immunol 200:2656-2669
Gong, Nian; Park, John; Luo, Z David (2018) Injury-induced maladaptation and dysregulation of calcium channel ?2 ? subunit proteins and its contribution to neuropathic pain development. Br J Pharmacol 175:2231-2243
Qiu, Xiaolong; Huang, Jen-Huang; Westerhof, Trisha M et al. (2018) Microfluidic channel optimization to improve hydrodynamic dissociation of cell aggregates and tissue. Sci Rep 8:2774
Kim, Seong M; Nguyen, Tricia T; Ravi, Archna et al. (2018) PTEN Deficiency and AMPK Activation Promote Nutrient Scavenging and Anabolism in Prostate Cancer Cells. Cancer Discov 8:866-883
Zhu, Yong; Wang, Xiuye; Forouzmand, Elmira et al. (2018) Molecular Mechanisms for CFIm-Mediated Regulation of mRNA Alternative Polyadenylation. Mol Cell 69:62-74.e4
Mishra, Birendra; Lawson, Gregory W; Ripperdan, Ryan et al. (2018) Charged-Iron-Particles Found in Galactic Cosmic Rays are Potent Inducers of Epithelial Ovarian Tumors. Radiat Res 190:142-150
Song, Wan; Zsindely, Nóra; Faragó, Anikó et al. (2018) Systematic genetic interaction studies identify histone demethylase Utx as potential target for ameliorating Huntington's disease. Hum Mol Genet 27:649-666
Lin, Xiaoxiao; Itoga, Christy A; Taha, Sharif et al. (2018) c-Fos mapping of brain regions activated by multi-modal and electric foot shock stress. Neurobiol Stress 8:92-102

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