Usefulness of [18F]-DA and [18F]-DOPA for PET imaging in a mouse model of pheochromocytoma

被引:9
作者
Martiniova, Lucia [1 ,11 ]
Cleary, Susannah [2 ]
Lai, Edwin W. [1 ]
Kiesewetter, Dale O. [3 ]
Seidel, Jurgen [4 ]
Dawson, Linda F. [5 ]
Phillips, Jacqueline K. [5 ,6 ]
Thomasson, David [7 ]
Chen, Xiaoyuan [3 ]
Eisenhofer, Graeme [8 ,9 ]
Powers, James F. [10 ]
Kvetnansky, Richard [11 ]
Pacak, Karel [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Reprod & Adult Endocrinol, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Neurol Disorders & Stroke, Clin Neurocardiol Sect, NIH, Bethesda, MD 20892 USA
[3] Natl Inst Biomed Imaging & Bioengn, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
[4] NCI, Mol Imaging Program, NIH, Bethesda, MD 20892 USA
[5] Murdoch Univ, Fac Hlth Sci, Perth, WA 6150, Australia
[6] Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia
[7] NIH, Lab Diagnost Radiol, Warren Grant Magnuson Clin Ctr, Bethesda, MD 20892 USA
[8] Univ Dresden, Dept Med, D-01307 Dresden, Germany
[9] Univ Dresden, Inst Clin Chem & Lab Med, D-01307 Dresden, Germany
[10] Tufts Med Ctr, Dept Pathol, Boston, MA 02111 USA
[11] Slovak Acad Sci, Inst Expt Endocrinol, SK-83306 Bratislava, Slovakia
关键词
Pheochromocytoma; PET; MicroCT; MRI; Metastatic mice model; Fluorodopamine; Fluorodopa; Norepinephrine transporter; Vesicular monoamine transporter; POSITRON-EMISSION-TOMOGRAPHY; METASTATIC PHEOCHROMOCYTOMA; NORADRENALINE TRANSPORTER; ENDOCRINE-CELLS; EXPRESSION; LOCALIZATION; PLASMA; TUMORS; 6-FLUORODOPAMINE; INHIBITION;
D O I
10.1016/j.nucmedbio.2011.07.007
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
Purpose: To evaluate the usefulness of [F-18]-6-fluorodopamine ([F-18]-DA) and [F-18]-L-6-fluoro-3,4-dihydroxyphenylalanine ([F-18-DOPA) positron emission tomography (PET) in the detection of subcutaneous (s.c.) and metastatic pheochromocytoma in mice; to assess the expression of the norepinephrine transporter (NET) and vesicular monoamine transporters I and 2 (VMAT1 and VMAT2), all important for [F-18]-DA and [F-18]-DOPA uptake. Furthermore, to compare tumor detection by micro-computed tomography (microCT) to magnetic resonance imaging (MRI) in individual mouse. Methods: SUVmax values were calculated from [F-18]-DA and [F-18]-DOPA PET, tumor-to-liver ratios (TLR) were obtained and expression of NET, VMAT1 and VMAT2 was evaluated. Results: [F-18]-DA detected less metastatic lesions compared to [F-18]-DOPA. TLR values for liver metastases were 2.26-2.71 for [F-18]-DOPA and 1.83-2.83 for [F-18]-DA. A limited uptake of [F-18]-DA was found in s.c. tumors (TLR=0.22-0.27) compared to [F-18]-DOPA (TLR=1.56-2.24). Overall, NET and VMAT2 were expressed in all organ and s.c. tumors. However, s.c. tumors lacked expression of VMAT1. We confirmed [F-18]-DA's high affinity for the NET for its uptake and VMAT1 and VMAT2 for its storage and retention in pheochromocytoma cell vesicles. In contrast, [F-18]-DOPA was found to utilize only VMAT2. Conclusion: MRI was superior in the detection of all organ tumors compared to microCT and PET. [F-18]-DOPA had overall better sensitivity than [F-18]-DA for the detection of metastases. Subcutaneous tumors were localized only with [F-18]-DOPA, a finding that may reflect differences in expression of VMAT1 and VMAT2, perhaps similar to some patients with pheochromocytoma where [F-18]-DOPA provides better visualization of lesions than [F-18]-DA. (C) 2012 Elsevier Inc. All rights reserved.
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收藏
页码:215 / 226
页数:12
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