Positron-emission tomography with [18F]fluorodeoxyglucose Part I.: Biochemical uptake mechanism and its implication for clinical studies

被引:132
作者
Pauwels, EKJ
Sturm, EJC
Bombardieri, E
Cleton, FJ
Stokkel, MPM
机构
[1] Leiden Univ, Med Ctr, Div Nucl Med, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Div Clin Oncol, Leiden, Netherlands
[3] Inst Nazl Studio & Cura Tumori, Milan, Italy
关键词
PET; FDG; uptake mechanism; malignancy;
D O I
10.1007/PL00008465
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the past decades, Positron Emission Tomography has opened a new field of imaging. Nowadays, this technique is being used for diagnosing, staging disease as well as for prognostic stratification and monitoring therapy. In this respect, [F-18]fluorodeoxyglucose (FdGlc) is by far the most commonly used PET agent. Many factors have been identified being responsible for a high uptake of this agent in malignancy. However, additional factors such as tumour treatment may interfere with the uptake mechanism. Knowledge of all these factors is a prerequisite for an optimal interpretation of PET studies and, consequently, for a reliable judgement of tumour status. In this article, a review is given of the factors influencing FdGlc uptake and the implications for clinical studies.
引用
收藏
页码:549 / 559
页数:11
相关论文
共 93 条
[61]   D-19575 - A SUGAR-LINKED ISOPHOSPHORAMIDE MUSTARD DERIVATIVE EXPLOITING TRANSMEMBRANE GLUCOSE-TRANSPORT [J].
POHL, J ;
BERTRAM, B ;
HILGARD, P ;
NOWROUSIAN, MR ;
STUBEN, J ;
WIESSLER, M .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1995, 35 (05) :364-370
[62]  
PRINTZ RL, 1993, ANNU REV NUTR, V13, P463, DOI 10.1146/annurev.nu.13.070193.002335
[63]   Moving GLUT4: The biogenesis and trafficking of GLUT4 storage vesicles [J].
Rea, S ;
James, DE .
DIABETES, 1997, 46 (11) :1667-1677
[64]  
Reisser C, 1999, INT J CANCER, V80, P194
[65]   Glucose catabolism in cancer cells: Regulation of the Type II hexokinase promoter by glucose and cyclic AMP [J].
Rempel, A ;
Mathupala, SP ;
Pedersen, PL .
FEBS LETTERS, 1996, 385 (03) :233-237
[66]   DIFFERENCES IN EXPRESSION AND INTRACELLULAR-DISTRIBUTION OF HEXOKINASE ISOENZYMES IN RAT-LIVER CELLS OF DIFFERENT TRANSFORMATION STAGES [J].
REMPEL, A ;
BANNASCH, P ;
MAYER, D .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1994, 1219 (03) :660-668
[67]   Oncological applications of positron emission tomography with fluorine-18 fluorodeoxyglucose [J].
Rigo, P ;
Paulus, P ;
Kaschten, BJ ;
Hustinx, R ;
Bury, T ;
Jerusalem, G ;
Benoit, T ;
FoidartWillems, J .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1996, 23 (12) :1641-1674
[68]  
Schmidt KC, 1996, J NUCL MED, V37, P394
[69]   GLUCOSE REGULATES GLUT-1 FUNCTION AND EXPRESSION IN FETAL-RAT LUNG AND MUSCLE INVITRO [J].
SIMMONS, RA ;
FLOZAK, AS ;
OGATA, ES .
ENDOCRINOLOGY, 1993, 132 (06) :2312-2318
[70]   ALTERATIONS IN GLUCOSE-METABOLISM IN CHICK-EMBRYO CELLS TRANSFORMED BY ROUS-SARCOMA VIRUS - TRANSFORMATION-SPECIFIC CHANGES IN ACTIVITIES OF KEY ENZYMES OF GLYCOLYTIC AND HEXOSE MONOPHOSPHATE SHUNT PATHWAYS [J].
SINGH, M ;
SINGH, VN ;
AUGUST, JT ;
HORECKER, BL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1974, 165 (01) :240-246