A Radiofluorinated Divalent Cystine Knot Peptide for Tumor PET Imaging

被引:13
作者
Jiang, Lei [1 ,2 ]
Kimura, Richard H. [2 ]
Ma, Xiaowei [2 ]
Tu, Yingfeng [2 ]
Miao, Zheng [2 ]
Shen, Bin [2 ]
Chin, Frederick T. [2 ]
Shi, Hongcheng [1 ]
Gambhir, Sanjiv Sam [2 ]
Cheng, Zhen [2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Nucl Med, Shanghai 200032, Peoples R China
[2] Stanford Univ, Canary Ctr Stanford Canc Early Detect, Dept Radiol & BioX Program, Mol Imaging Program Stanford, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
Cystine-knot peptide; divalent; integrin alpha beta(3); F-18; PET; ALPHA(V)BETA(3) INTEGRIN EXPRESSION; AGOUTI-RELATED PROTEIN; ALPHA-V-BETA-3; EXPRESSION; RGD; ANGIOGENESIS;
D O I
10.1021/mp500018s
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A divalent knottin containing two separate integrin binding epitopes (RGD) in the adjacent loops, 3-4A, was recently developed and reported in our previous publication. In the current study, 3-4A was radiofluorinated with a 4-nitrophenyl 2-F-18-fluoropropinate (F-18-NFP) group and the resulting divalent positron emission tomography (PET) probe, F-18-FP-3-4A, was evaluated as a novel imaging probe to detect integrin av beta 3 positive tumors in living animals. Knottin 3-4A was synthesized by solid phase peptide synthesis, folded, and site-specifically conjugated with F-18/19-NFP to produce the fluorinated peptide F-18/19-fluoropropinate-3-4A (F-18/19-FP-3-4A). The stability of F-18-FP-3-4A was tested in both phosphate buffered saline (PBS) buffer and mouse serum. Cell uptake assays of the radiolabeled peptides were performed using U87MG cells. In addition, small animal PET imaging and biodistribution studies of F-18-FP-3-4A were performed in U87MG tumor-bearing mice. The receptor targeting specificity of the radiolabeled peptide was also verified by coinjecting the probe with a blocking peptide cyclo(RGDyK). Our study showed that F-18-FP-3-4A exhibited excellent stability in PBS buffer (pH 7.4) and mouse serum. Small animal PET imaging and biodistribution data revealed that F-18-FP-3-4A exhibited rapid and good tumor uptake (3.76 +/- 0.59% ID/g and 2.22 +/- 0.62% ID/g at 0.5 and 1 h, respectively). F-18-FP-3-4A was rapidly cleared from the normal tissues, resulting in excellent tumor-to-normal tissue contrasts. For example, liver uptake was only 0.39 +/- 0.07% ID/g and the tumor to liver ratio was 5.69 at 1 h p.i. Furthermore, coinjection of cyclo(RGDyK) with F-18-FP-3-4A significantly inhibited tumor uptake (0.41 +/- 0.12 vs 1.02 +/- 0.19% ID/g at 2.5 h) in U87MG xenograft models, demonstrating specific accumulation of the probe in the tumor. In summary, the divalent probe F-18-FP-3-4A is characterized by rapid and high tumor uptake and excellent tumor-to-normal tissue ratios. F-18-FP-3-4A is a highly promising knottin based PET probe for translating into clinical imaging of tumor angiogenesis.
引用
收藏
页码:3885 / 3892
页数:8
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