Molecular Imaging Program at Stanford (MIPS), Department of Radiology and Bio-X Program, Canary Center at Stanford for Cancer Early Detection, Stanford University, Stanford, California, 94305-5344, USA.
Bioconjug Chem. 2010 Dec 15;21(12):2355-60. doi: 10.1021/bc100391a. Epub 2010 Nov 12.
In order to accomplish in vivo molecular imaging of melanoma biomarker melanocortin 1 receptor (MC1R), several α-melanocyte-stimulating hormone (α-MSH) analogues have been labeled with N-succinimidyl-4-¹⁸F-fluorobenzoate (¹⁸)F-SFB) and studied as positron emission tomography (PET) probes in our recent studies. To further pursue a radiofluorinated α-MSH peptide with high clinical translation potential, we utilized 4-nitrophenyl 2-¹⁸F-fluoropropionate (¹⁸F-NFP) to radiofluorinate the transition metal rhenium cyclized α-MSH metallopeptides for PET imaging of MC1R positive malignant melanoma. Metallopeptides Ac-d,Lys-ReCCMSH(Arg¹¹) (two isomers, namely RMSH-1 and RMSH-2) were synthesized using conventional solid phase peptide synthesis chemistry and rhenium cyclization reaction. The two isomers were then conjugated with ¹⁹F-NFP or ¹⁸F-NFP. The resulting cold or radiofluorinated metallopeptides, (¹⁸/¹⁹)F-FP-RMSH-1 and (¹⁸/¹⁹)F-FP-RMSH-2, were further evaluated for their in vitro receptor binding affinities, in vivo biodistribution, and small-animal PET imaging properties. The binding affinities of ¹⁹F-FP-RMSH-1 and ¹⁹F-FP-RMSH-2 were determined to be within low nanomolar range. In vivo studies revealed that both F-labeled metallopeptides possessed good tumor uptake in the B16F10 murine model with high MC1R expression, while possessing much lower uptake in A375M human melanoma xenografts. Moreover, ¹⁸F-FP-RMSH-1 displayed more favorable in vivo performance in terms of higher tumor uptake and much lower accumulation in the kidney and liver, when compared to that of ¹⁸F-FP-RMSH-2 at 2 h postinjection (p.i.). ¹⁸F-FP-RMSH-1 also displayed lower liver and lung uptake when compared with that of the same peptide labeled with ¹⁸F-SFB (named as ¹⁸F-FB-RMSH-1). Small animal PET imaging of ¹⁸F-FP-RMSH-1 in mice bearing B16F10 tumors at 1 and 2 h showed good tumor imaging quality. As expected, much lower tumor uptake and poorer tumor/normal organ contrast were observed for A375M model compared to those of the B16F10 model. ¹⁸F-FP-RMSH-1 also exhibited higher tumor uptake and better tumor retention when compared with ¹⁸F-FB-RMSH-1. ¹⁸F-FP-RMSH-1 demonstrates significant advantages over ¹⁸F-FB-RMSH-1 and ¹⁸F-FP-RMSH-2. It is a promising PET probe for imaging MC1R positive melanoma and MC1R expression in vivo.
为了实现黑色素瘤生物标志物黑色素皮质素 1 受体 (MC1R) 的体内分子成像,我们最近的研究中使用 N-琥珀酰亚胺基-4-¹⁸F-氟苯甲酸酯(¹⁸F-SFB)标记了几种 α-促黑素细胞激素(α-MSH)类似物,并将其作为正电子发射断层扫描(PET)探针进行了研究。为了进一步研究具有高临床转化潜力的放射性标记 α-MSH 肽,我们利用 4-硝基苯基 2-¹⁸F-氟丙酸盐(¹⁸F-NFP)对过渡金属铼环化的 α-MSH 金属肽进行放射性标记,用于 MC1R 阳性恶性黑色素瘤的 PET 成像。使用传统的固相肽合成化学和铼环化反应合成了 Ac-d,Lys-ReCCMSH(Arg¹¹)(两种异构体,即 RMSH-1 和 RMSH-2)的金属肽。然后将这两种异构体与 ¹⁹F-NFP 或 ¹⁸F-NFP 缀合。所得冷或放射性标记的金属肽(¹⁸/¹⁹)F-FP-RMSH-1 和(¹⁸/¹⁹)F-FP-RMSH-2 进一步评估了它们的体外受体结合亲和力、体内生物分布和小动物 PET 成像特性。¹⁹F-FP-RMSH-1 和 ¹⁹F-FP-RMSH-2 的结合亲和力被确定为纳摩尔范围内。体内研究表明,在高 MC1R 表达的 B16F10 小鼠模型中,两种 F 标记的金属肽均具有良好的肿瘤摄取,而在 A375M 人黑色素瘤异种移植瘤中摄取较低。此外,与 ¹⁸F-FP-RMSH-2 相比,¹⁸F-FP-RMSH-1 在注射后 2 小时(p.i.)时具有更高的肿瘤摄取和更低的肾脏和肝脏蓄积,表现出更有利的体内性能。¹⁸F-FP-RMSH-1 在肝脏和肺部的摄取也低于用¹⁸F-SFB 标记的相同肽(称为¹⁸F-FB-RMSH-1)。在携带 B16F10 肿瘤的小鼠中,¹⁸F-FP-RMSH-1 的小动物 PET 成像在 1 和 2 小时均显示出良好的肿瘤成像质量。如预期的那样,与 B16F10 模型相比,A375M 模型的肿瘤摄取和肿瘤/正常器官对比度较低。与¹⁸F-FB-RMSH-1 相比,¹⁸F-FP-RMSH-1 也具有更高的肿瘤摄取和更好的肿瘤保留。¹⁸F-FP-RMSH-1 与¹⁸F-FB-RMSH-1 和 ¹⁸F-FP-RMSH-2 相比具有显著优势。它是一种有前途的用于成像 MC1R 阳性黑色素瘤和体内 MC1R 表达的 PET 探针。