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
Chakraborty, Mahul; VanKuren, Nicholas W; Zhao, Roy et al. (2018) Hidden genetic variation shapes the structure of functional elements in Drosophila. Nat Genet 50:20-25
Morozko, Eva L; Ochaba, Joseph; Hernandez, Sarah J et al. (2018) Longitudinal Biochemical Assay Analysis of Mutant Huntingtin Exon 1 Protein in R6/2 Mice. J Huntingtons Dis 7:321-335
Carpenter, Philip M; Ziogas, Argyrios; Markham, Emma M et al. (2018) Laminin 332 expression and prognosis in breast cancer. Hum Pathol 82:289-296
Yan, Huaming; Romero-López, Mónica; Benitez, Lesly I et al. (2018) Multiscale modeling of glioblastoma. Transl Cancer Res 7:S96-S98
Yu, James; Landberg, Jenny; Shavarebi, Farbod et al. (2018) Bioengineering triacetic acid lactone production in Yarrowia lipolytica for pogostone synthesis. Biotechnol Bioeng 115:2383-2388
Oliver, Andrew; Kay, Matthew; Cooper, Kerry K (2018) Comparative genomics of cocci-shaped Sporosarcina strains with diverse spatial isolation. BMC Genomics 19:310
Mahlbacher, Grace; Curtis, Louis T; Lowengrub, John et al. (2018) Mathematical modeling of tumor-associated macrophage interactions with the cancer microenvironment. J Immunother Cancer 6:10
Neek, Medea; Tucker, Jo Anne; Kim, Tae Il et al. (2018) Co-delivery of human cancer-testis antigens with adjuvant in protein nanoparticles induces higher cell-mediated immune responses. Biomaterials 156:194-203
McLelland, Bryce T; Lin, Bin; Mathur, Anuradha et al. (2018) Transplanted hESC-Derived Retina Organoid Sheets Differentiate, Integrate, and Improve Visual Function in Retinal Degenerate Rats. Invest Ophthalmol Vis Sci 59:2586-2603
Bota, Daniela A; Chung, Jinah; Dandekar, Manisha et al. (2018) Phase II study of ERC1671 plus bevacizumab versus bevacizumab plus placebo in recurrent glioblastoma: interim results and correlations with CD4+ T-lymphocyte counts. CNS Oncol 7:CNS22

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