Author/Authors :
Moghiseh, Mahdieh Department of Radiology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand , Lowe, Chiara Department of Radiology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand , Lewis, John G Canterbury Health Laboratories - 524 Hagley Ave - Christchurch, New Zealand , Kumar, Dhiraj Department of Obstetrics and Gynecology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand , Butler, Anthony Department of Radiology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand , Anderson, Nigel Department of Radiology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand , Raja, Aamir Department of Radiology - University of Otago - Christchurch School of Medicine - 2 Riccarton Avenue - Christchurch, New Zealand
Abstract :
The purpose of the present study was to demonstrate an in vitro proof of principle that spectral photon-counting CT can measure
gold-labelled specific antibodies targeted to specific cancer cells. A crossover study was performed with Raji lymphoma cancer
cells and HER2-positive SKBR3 breast cancer cells using a MARS spectral CT scanner. Raji cells were incubated with monoclonal
antibody-labelled gold, rituximab (specific antibody to Raji cells), and trastuzumab (as a control); HER2-positive SKBR3 breast
cancer cells were incubated with monoclonal antibody-labelled gold, trastuzumab (specific antibody to HER2-positive cancer
cells), and rituximab (as a control). The calibration vials with multiple concentrations of nonfunctionalised gold nanoparticles
were used to calibrate spectral CT. Spectral imaging results showed that the Raji cells-rituximab-gold and HER2-positive cellstrastuzumab-gold had a quantifiable amount of gold, 5.97 mg and 0.78 mg, respectively. In contrast, both cell lines incubated with
control antibody-labelled gold nanoparticles had less gold attached (1.22 mg and 0.15 mg, respectively). These results demonstrate
the proof of principle that spectral molecular CT imaging can identify and quantify specific monoclonal antibody-labelled gold
nanoparticles taken up by Raji cells and HER2-positive SKBR3 breast cancer cells. The present study reports the future potential of
spectral molecular imaging in detecting tumour heterogeneity so that treatment can be tuned accordingly, leading to more
eective personalised medicine.