RESUMO
FDG-PET is used to measure the metabolic rate of glucose. Transport and phosphorylation determine the amount of hexose analog that is phosphorylated and trapped. Competition occurs for both events, such that extracellular glucose concentration affects the FDG image. This study investigated the effect of glucose concentration on the rate of FDG accumulation in three cell lines. The results show that extracellular glucose concentration has a greater impact on the rate of FDG accumulation than the relative abundance of GLUT transporter subtypes.
Assuntos
Espaço Extracelular/metabolismo , Fibroblastos/metabolismo , Fluordesoxiglucose F18/farmacocinética , Glioma/metabolismo , Glucose/metabolismo , Macrófagos/metabolismo , Animais , Biomarcadores Tumorais , Linhagem Celular , Linhagem Celular Tumoral , Meios de Cultura/metabolismo , Espaço Extracelular/diagnóstico por imagem , Fibroblastos/diagnóstico por imagem , Glioma/diagnóstico por imagem , Humanos , Macrófagos/diagnóstico por imagem , Taxa de Depuração Metabólica , Camundongos , Cintilografia , Compostos Radiofarmacêuticos/farmacocinética , RatosRESUMO
OBJECTIVES: To determine the influence of breast tumor blood flow on MIBI kinetics, we compared MIBI uptake and washout to [O-15]-water PET estimates of blood flow in patients with locally advanced breast cancer. METHODS: Prior to therapy, 37 patients underwent MIBI and [O-15]-water PET imaging; 22/37 also had MIBI washout analysis. Twenty-five patients underwent serial imaging over the course of chemotherapy. RESULTS: MIBI uptake and blood flow had a significant positive correlation pre-therapy. The change in MIBI uptake over the course of therapy also correlated with the change in blood flow. The half-time of MIBI washout inversely correlated with blood flow, indicating faster MIBI washout with higher blood flow. CONCLUSIONS: Blood flow strongly influences early MIBI uptake and can be a factor affecting the rate of MIBI washout in breast tumors. We present a model of MIBI kinetics in tumors which forms a hypothesis for further mechanistic studies of MIBI uptake and washout in breast cancer.