The goal of the Cancer Imaging Program is to advance cancer research, diagnosis, and management by carrying out novel research in multimodality anatomical and molecular imaging (MI). The ultimate goal is to introduce new multimodality imaging strategies into studies of molecular mechanisms, diagnosis, and treatments of cancer. The program is comprised of investigators whose work stems from seven specialty areas: imaging instrumentation/engineering, modeling/biostatistics, chemistry, molecular imaging assay development, cancer biology/proteomics, mouse models/small animal imaging/in vivo MI/therapeutic applications in cancer therapy, and clinical oncology. Research by program members has resulted in a number of exciting findings, including new methods to image cancer gene therapy, methods to study cell trafficking, new imaging probes for apoptosis, and novel breast cancer imaging instrumentation. The Program adds value to the center by bringing biologists, chemists, engineers, radiologists, computational scientists, and clinical and translational researchers together to participate in developing innovative imaging tools and approaches. The 36 program members come from 11 School of Medicine, School of Engineering, and School of Humanities &Sciences departments. Members are major participants in one P50 program project, one R24 project, two U54 projects (one is an award in progress), two program project grants and three training grants. Direct cost funding in 2005 was $15.9 million including $9 million in NCI research funding and $6.9 million in other peer reviewed funding. Members generated 594 publications over the past six years, of which ~16% and ~11% were intra- and interprogrammatic collaborations, respectively. Dr. Sam Gambhir, the Program leader, is a distinguished physician-scientist with an international reputation in molecular imaging and a laboratory program in multimodality molecular imaging. Dr. Christopher Contag, Program co-leader, is an accomplished scientist with major scientific contributions in the areas of stem cell biology, cancer imaging and tissue response to insult and is co-director of MIPS, and Faculty Advisor of the Cancer Imaging Shared Resource. The leadership is united in its goals for program development to advance cancer imaging.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA124435-03
Application #
7826891
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
3
Fiscal Year
2009
Total Cost
$20,909
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Thorsson, Vésteinn; Gibbs, David L; Brown, Scott D et al. (2018) The Immune Landscape of Cancer. Immunity 48:812-830.e14
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Nair, Viswam S; Sundaram, Vandana; Desai, Manisha et al. (2018) Accuracy of Models to Identify Lung Nodule Cancer Risk in the National Lung Screening Trial. Am J Respir Crit Care Med 197:1220-1223
She, Richard; Jarosz, Daniel F (2018) Mapping Causal Variants with Single-Nucleotide Resolution Reveals Biochemical Drivers of Phenotypic Change. Cell 172:478-490.e15
Champion, Magali; Brennan, Kevin; Croonenborghs, Tom et al. (2018) Module Analysis Captures Pancancer Genetically and Epigenetically Deregulated Cancer Driver Genes for Smoking and Antiviral Response. EBioMedicine 27:156-166
Zhou, Mu; Leung, Ann; Echegaray, Sebastian et al. (2018) Non-Small Cell Lung Cancer Radiogenomics Map Identifies Relationships between Molecular and Imaging Phenotypes with Prognostic Implications. Radiology 286:307-315
Pollom, Erqi L; Fujimoto, Dylann K; Han, Summer S et al. (2018) Newly diagnosed glioblastoma: adverse socioeconomic factors correlate with delay in radiotherapy initiation and worse overall survival. J Radiat Res 59:i11-i18
Nørgaard, Caroline Holm; Jakobsen, Lasse Hjort; Gentles, Andrew J et al. (2018) Subtype assignment of CLL based on B-cell subset associated gene signatures from normal bone marrow - A proof of concept study. PLoS One 13:e0193249
Im, Hogune; Rao, Varsha; Sridhar, Kunju et al. (2018) Distinct transcriptomic and exomic abnormalities within myelodysplastic syndrome marrow cells. Leuk Lymphoma 59:2952-2962
Huang, Min; Zhu, Li; Garcia, Jacqueline S et al. (2018) Brd4 regulates the expression of essential autophagy genes and Keap1 in AML cells. Oncotarget 9:11665-11676

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