Synthesis of 2′-deoxy-2′-[18F]fluoro-5-bromo-1-β-D-arabinofuranosyluracil ([18F]-FBAU) and 2′-deoxy-2′-[18F]fluoro-5-chloro-1-β-D-arabinofuranosyl-uracil ([18F]-FCAU), and their biological evaluation as markers for gene expression

被引:31
作者
Alauddin, MM [1 ]
Shahinian, A [1 ]
Park, R [1 ]
Tohme, M [1 ]
Fissekis, JD [1 ]
Conti, PS [1 ]
机构
[1] Univ So Calif, Dept Radiol, PET Imaging Sci Ctr, Los Angeles, CA 90033 USA
关键词
FBAU; FCAU; FMAU; HSV-tk; PET; gene expression;
D O I
10.1016/j.nucmedbio.2003.12.008
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
[F-18]-FBAU and [F-18]-FCAU have been synthesized and evaluated in vivo as markers for HSV1-tk gene expression. At 2 hours, uptake of [F-18]-FBAU and [F-18]-FCAU in HSV1-tk-positive tumors was 7.9-fold and 6.0-fold higher than the control tumors, respectively. Micro-PET images also showed very high uptake in HSV-tk tumors. Compared to [C-14]-FMAU, total uptake of [F-18]-FBAU and [F-18]-FCAU was similar in tk-positive cells, but the uptake ratio (tk+/wild) was higher. [F-18]-FCAU and [F-18]-FCAU appear to be potential PET imaging agents for gene expression. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:399 / 405
页数:7
相关论文
共 35 条
[21]   Synthesis of 2′-deoxy-2′-[18F]fluoro-β-D-arabinofuranosyl nucleosides, [18F]FAU, [18F]FMAU, [18F]FBAU and [18F]FIAU, as potential PET agents for imaging cellular proliferation -: Synthesis of [18F]labeled FAU, FMAU, FBAU, FIAU [J].
Mangner, TJ ;
Klecker, RW ;
Anderson, L ;
Shields, AF .
NUCLEAR MEDICINE AND BIOLOGY, 2003, 30 (03) :215-224
[22]   LYMPHOMA REGRESSION INDUCED BY GANCICLOVIR IN MICE BEARING A HERPES THYMIDINE KINASE TRANSGENE [J].
MOOLTEN, FL ;
WELLS, JM ;
HEYMAN, RA ;
EVANS, RM .
HUMAN GENE THERAPY, 1990, 1 (02) :125-134
[23]   Synthesis of 8-[18F]fluoroguanine derivatives:: In vivo probes for imaging gene expression with positron emission tomography [J].
Namavari, M ;
Barrio, JR ;
Toyokuni, T ;
Gambhir, SS ;
Cherry, SR ;
Herschman, HR ;
Phelps, ME ;
Satyamurthy, N .
NUCLEAR MEDICINE AND BIOLOGY, 2000, 27 (02) :157-162
[24]   GENE-THERAPY FOR THE TREATMENT OF BRAIN-TUMORS USING INTRA-TUMORAL TRANSDUCTION WITH THE THYMIDINE KINASE GENE AND INTRAVENOUS GANCICLOVIR [J].
OLDFIELD, EH ;
RAM, Z ;
CULVER, KW ;
BLAESE, RM ;
DEVROOM, HL .
HUMAN GENE THERAPY, 1993, 4 (01) :39-69
[25]  
RAM Z, 1997, NAT MED, V3, P1353
[26]   L-THYMIDINE IS PHOSPHORYLATED BY HERPES-SIMPLEX VIRUS TYPE-1 THYMIDINE KINASE AND INHIBITS VIRAL GROWTH [J].
SPADARI, S ;
MAGA, G ;
FOCHER, F ;
CIARROCCHI, G ;
MANSERVIGI, R ;
ARCAMONE, F ;
CAPOBIANCO, M ;
CARCURO, A ;
COLONNA, F ;
IOTTI, S ;
GARBESI, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (22) :4214-4220
[27]  
TJUVAJEV JG, 1995, CANCER RES, V55, P6126
[28]  
Tjuvajev JG, 2002, J NUCL MED, V43, P1072
[29]  
Tjuvajev JG, 1998, CANCER RES, V58, P4333
[30]  
Tjuvajev JG, 1999, CANCER RES, V59, P5186