The function of P-gp expressed in Bcap37/MDR1 cells was evaluated using verapamil (VER), a classical inhibitor of P-gp. The accumulation of 99mTc-methoxyisobutylisonitrile ([99mTc]MIBI) in vitro was measured. In vivo imaging of severe combined immune deficiency (SCID) mice implanted with Bcap37 and Bcap37/MDR1 cells was performed by scintigraphy and micro-positron emission tomography (PET).
The uptake of [99mTc]MIBI was 0.62%卤0.05%in the Bcap37/MDR1 cells and 2.02%卤0.28%in the Bcap37 cells. VER significantly increased the uptake of [99mTc]MIBI in the Bcap37/MDR1 cells (1.90%卤0.09%) but not in the Bcap37 cells (2.15%卤0.27%). In vivo, neither the Bcap37 nor Bcap37/MDR1 tumors grown in the SCID mice could be detected by [99mTc]MIBI scintigraphy. Both the Bcap37 and Bcap37/MDR1 tumors were visible by micro-PET. The mean standardized uptake value (SUV) was significantly higher in the Bcap37 tumors (1.00卤0.06) than in the Bcap37/MDR1 (0.67卤0.11) tumors. VER significantly increased the mean SUV in the Bcap37/MDR1 tumors (1.02卤0.16) but not in the Bcap37 tumors (1.09卤0.22).
[18F]FDG combined with VER may be an effective noninvasive method of determining P-gp expression in tumors.