On Target Laboratories Inc., West Lafayette, IN, 47906, USA.
Department of Chemistry and Institute for Drug Discovery, Purdue University, West Lafayette, IN, 47907, USA.
Mol Imaging Biol. 2020 Apr;22(2):377-383. doi: 10.1007/s11307-019-01391-w.
Neuroendocrine tumors (NETs) have reasonably high 5-year survival rates when diagnosed at an early stage but are significantly more lethal when discovered only after metastasis. Although several imaging modalities such as computed tomography (CT), positron emission tomography, and magnetic resonance imaging can detect neuroendocrine tumors, their high false positive rates suggest that more specific diagnostic tests are required. Targeted imaging agents such as Octreoscan® have met some of this need for improved specificity, but their inability to image poorly differentiated NETs suggests that improved NET imaging agents are still needed. Because neurokinin 1 receptors (NK1Rs) are widely over-expressed in neuroendocrine tumors, but show limited expression in healthy tissues, we have undertaken to develop an NK1R-targeted imaging agent for improved diagnosis and staging of neuroendocrine tumors.
A small molecule NK1R antagonist was conjugated via a flexible spacer to a Tc-99m chelating peptide. After complexation with Tc-99m, binding of the conjugate to human embryonic kidney (HEK293) cells transfected with the human NK1R was evaluated as a function of radioimaging agent concentration. In vivo imaging of HEK293-NK1R tumor xenografts in mice was also performed by single-photon emission computed tomography/computed tomography (γ-SPECT/CT), and the distribution of the conjugate in various tissues was quantified by tissue resection and γ-counting.
NK1R-targeted Tc-99m-based radioimaging agent displayed excellent affinity (K = 16.8 nM) and specificity for HEK293-NK1R tumor xenograft. SPECT/CT analysis of tumor-bearing mice demonstrated significant tumor uptake and high tumor to background ratio as early as 2 h post injection.
The excellent tumor contrast afforded by our NK1R-targeted radioimaging agent exhibits properties that could improve early diagnosis and staging of many neuroendocrine tumors.
神经内分泌肿瘤(NETs)在早期诊断时具有相当高的 5 年生存率,但在转移后发现时则明显更为致命。虽然计算机断层扫描(CT)、正电子发射断层扫描和磁共振成像等几种成像方式可以检测神经内分泌肿瘤,但它们的高假阳性率表明需要更具特异性的诊断测试。奥曲肽等靶向成像剂在一定程度上满足了提高特异性的需求,但它们无法对分化不良的 NET 进行成像,这表明仍需要改进的 NET 成像剂。由于神经激肽 1 受体(NK1R)在神经内分泌肿瘤中广泛过表达,但在健康组织中表达有限,我们已着手开发一种用于改善神经内分泌肿瘤诊断和分期的 NK1R 靶向成像剂。
通过柔性间隔物将小分子 NK1R 拮抗剂与 Tc-99m 螯合肽连接。在与 Tc-99m 络合后,评估了配体与转染人 NK1R 的人胚肾(HEK293)细胞的结合情况,作为放射性成像剂浓度的函数。还通过单光子发射计算机断层扫描/计算机断层扫描(γ-SPECT/CT)对小鼠 HEK293-NK1R 肿瘤异种移植进行了体内成像,并通过组织切除和γ计数对配体在各种组织中的分布进行了定量。
基于 Tc-99m 的 NK1R 靶向放射性成像剂对 HEK293-NK1R 肿瘤异种移植显示出优异的亲和力(K=16.8 nM)和特异性。荷瘤小鼠的 SPECT/CT 分析表明,在注射后 2 小时即可获得显著的肿瘤摄取和高肿瘤与背景比。
我们的 NK1R 靶向放射性成像剂提供的优异肿瘤对比度具有改善许多神经内分泌肿瘤早期诊断和分期的特性。