Our long range goal is to develop non-invasive multi- modality imaging that yields biological information of human cancers in 3-dimensions (3D). The short-term objectives are to use NMR and PET for imaging tumor biology and hypoxia in rodent tumors and xenografts. In addition, pO2 levels will be directly measured in the same tumors, and tumor sections characterized to provide a biological basis for the NMR and PET images. All the 3D data sets of images and tumor sections will be spatially correlated with a stereotaxic reference system implanted around the rodent tumors and xenografts. There are three areas of investigation. First, microPET (an animal scanner) studies will be performed: (i) in vivo imaging of radiation-induced apoptosis with 124I- Annexin V, (ii) IAZG uptake as a surrogate of pO2 level, (iii) comparing 124IAZG with 18Fmiso as hypoxia markers, and (iv) assessing the effect of hypoxia on FDG uptake. Second, NMR studies will include: (i) mapping """"""""tumor perfusion"""""""" by Gd-DTPA uptake, (ii) assessing lactate level with 1H NMR, and (iii) testing the hypothesis that 1H and 31P NMR spectral changes can predict the susceptibility of individual tumors to hypoxia- modulation. Third, biological features will be measured/analyzed in vivo and in tumor sections for the same tumors: (i) pO2 level with an oxygen probe, (ii) blood perfusion with Hoescht 33342, (iii) histochemical analysis, (iv) comparison of the TUNEL and Annexin V assays, and (v) phosphor plate autoradiography. The above will be spatially-correlated using an implantable stereotaxic marker system that identifies the image coordinates of the multiple data-sets and image registration software adapted from existing algorithms in our radiotherapy treatment planning system. Of significance is the spatial correlation of all the 3D data sets, thus relating biological attributes to image features. We believe that this is the first attempt to directly correlate invasive biological endpoints with image features from non- invasive imaging using spatially registered data-sets. Thus, this project integrates physics, chemistry, biology, engineering and computer sciences to study tumor biology and hypoxia, with considerable significance for cancer diagnosis and treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA084596-02
Application #
6522538
Study Section
Special Emphasis Panel (ZRG1-SRB (03))
Program Officer
Farahani, Keyvan
Project Start
2001-09-30
Project End
2006-08-31
Budget Start
2002-09-01
Budget End
2003-08-31
Support Year
2
Fiscal Year
2002
Total Cost
$902,848
Indirect Cost
Name
Sloan-Kettering Institute for Cancer Research
Department
Type
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10065
Li, Jianbo; Zhang, Guojian; Wang, Xuemei et al. (2015) Is carbonic anhydrase IX a validated target for molecular imaging of cancer and hypoxia? Future Oncol 11:1531-41
Bokacheva, Louisa; Kotedia, Khushali; Reese, Megan et al. (2013) Response of HT29 colorectal xenograft model to cediranib assessed with 18 F-fluoromisonidazole positron emission tomography, dynamic contrast-enhanced and diffusion-weighted MRI. NMR Biomed 26:151-63
McCall, Keisha C; Humm, John L; Bartlett, Rachel et al. (2012) Copper-64-diacetyl-bis(N(4)-methylthiosemicarbazone) pharmacokinetics in FaDu xenograft tumors and correlation with microscopic markers of hypoxia. Int J Radiat Oncol Biol Phys 84:e393-9
Oehler, Christoph; O'Donoghue, Joseph A; Russell, James et al. (2011) 18F-fluromisonidazole PET imaging as a biomarker for the response to 5,6-dimethylxanthenone-4-acetic acid in colorectal xenograft tumors. J Nucl Med 52:437-44
Li, Xiao-Feng; Sun, Xiaorong; Ma, Yuanyuan et al. (2010) Detection of hypoxia in microscopic tumors using 131I-labeled iodo-azomycin galactopyranoside (131I-IAZGP) digital autoradiography. Eur J Nucl Med Mol Imaging 37:339-48
Li, Xiao-Feng; Ma, Yuanyuan; Sun, Xiaorong et al. (2010) High 18F-FDG uptake in microscopic peritoneal tumors requires physiologic hypoxia. J Nucl Med 51:632-8
Carlin, Sean; Pugachev, Andrei; Sun, Xiaorong et al. (2009) In vivo characterization of a reporter gene system for imaging hypoxia-induced gene expression. Nucl Med Biol 36:821-31
Chang, Jenghwa; Wen, Bixiu; Kazanzides, Peter et al. (2009) A robotic system for 18F-FMISO PET-guided intratumoral pO2 measurements. Med Phys 36:5301-9
Wen, Bixiu; Urano, Muneyasu; Humm, John L et al. (2008) Comparison of Helzel and OxyLite systems in the measurements of tumor partial oxygen pressure (pO2). Radiat Res 169:67-75
Li, Xiao-Feng; O'Donoghue, Joseph A (2008) Hypoxia in microscopic tumors. Cancer Lett 264:172-80

Showing the most recent 10 out of 26 publications