Devkumar Mustafi1,
Jesse Ward2, Urszula Dougherty3, Erica Markiewicz1,
Marc Bissonnette3, Stefan Vogt2, Gregory S. Karczmar1
1Radiology,
The University of Chicago, Chicago, IL, United States; 2Advanced Photon
Source - Sector 2, Argonne National Laboratory, Lemont, IL, United States; 3Medicine,
The University of Chicago, Chicago, IL, United States
Targeted contrast agents that specifically enhance early cancers could significantly improve diagnostic accuracy. Here we compare a new vanadium-based (VC) MRI contrast agent that is sensitive to glycolysis to a conventional Gd-based agent in a mouse model of colorectal cancer. A novel method is developed for co-registrations of in vivo MR images with ex vivo histological images using agar-based phantoms. X-ray fluorescence microscopy (XFM) imaging was used to quantify contrast uptake directly and to determine cellular and sub-cellular distributions in situ. Results revealed that VC-based agents preferentially accumulate in cancer cells, offering an advantage over less selective Gd-based agents.
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