Current clinical measurements for tumor treatment efficiency rely often on changes in tumor volume measured as shrinkage by CT or MRI, which become apparent after multiple lines of treatment and pose a physical and psychological burden on the patient. Detection of therapy-induced cell death in the tumor can be a fast measure for treatment efficiency. However, there are no reliable clinical tools for detection of tumor necrosis. Previously, we studied the necrosis avidity of cyanine-based fluorescent dyes, which suffered long circulation times before tumor necrosis could be imaged due to low hydrophilicity. We now present the application of radiolabeled 800CW, a commercially available cyanine with high hydrophilicity, to image tumor necrosis in a mouse model.
We conjugated 800CW to DOTA via a PEG linker, for labeling with single-photon emission-computed tomography isotope indium-111, yielding [ ¹¹¹ In]In-DOTA-PEG ₄ -800CW. We then investigated specific [ ¹¹¹ In]In-DOTA-PEG ₄ -800CW uptake by dead cells in vitro, using both fluorescence and radioactivity as detection modalities. Finally, we investigated [ ¹¹¹ In]In-DOTA-PEG ₄ -800CW uptake into necrotic tumor regions of a 4T1 breast tumor model in mice.
We successfully prepared a precursor and developed a reliable procedure for labeling 800CW with indium-111. We detected specific [ ¹¹¹ In]In-DOTA-PEG ₄ -800CW uptake by dead cells, using both fluorescence and radioactivity. Albeit with a tumor uptake of only 0.37%ID/g at 6 h post injection, we were able to image tumor necrosis with a tumor to background ratio of 7:4. Fluorescence and radioactivity in cryosections from the dissected tumors were colocalized with tumor necrosis, confirmed by TUNEL staining.
[ ¹¹¹ In]In-DOTA-PEG ₄ -800CW can be used to image tumor necrosis in vitro and in vivo. Further research will elucidate the application of [ ¹¹¹ In]In-DOTA-PEG ₄ -800CW or other radiolabeled hydrophilic cyanines for the detection of necrosis caused by chemotherapy or other anti-cancer therapies. This can provide valuable prognostic information in treatment of solid tumors.