Chinese PLA Medical School, Chinese PLA General Hospital, Beijing 100853, China.
Department of Nuclear Medicine, Chinese PLA General Hospital, Beijing 100853, China.
Molecules. 2022 Apr 24;27(9):2736. doi: 10.3390/molecules27092736.
With the increasing detection rate of early prostate cancer (PCa), the proportion of surgical treatment is increasing. Surgery is the most effective treatment for PCa. Precise targeting of tumors during surgery can reduce the incidence of positive surgical margins (PSMs) and preserve the neurovascular bundles (NVBs) as much as possible. The objective of this study was to synthesize a PSMA fluorescent probe (PSMA-Cy5) and verify the targeting specificity of the probe for prostate cancer, thereby providing a theoretical basis for the development of PSMA fluorescent probes for clinical application in the future. In this study, a novel water-soluble 3H-indocyanine-type bioluminescent dye-Cy5-labeled prostate-specific membrane antigen (PSMA) ligand (PSMA-Cy5) was synthesized by liquid phase synthesis. The PSMA ligand was developed based on the glutamine-urea-lysine (Glu-urea-Lys) structure. The new fluorescent probe was evaluated in vitro and in vivo, and its safety was evaluated. Confocal microscopy was used to observe the binding uptake of PSMA-Cy5 with PSMA (+) LNCaP cells, PSMA (-) PC3 cells and blocked LNCaP cells. In in vivo optical imaging studies, the targeting specificity of PSMA (+) 22Rv1 tumors to probe binding was validated by tail vein injection of PSMA-Cy5. The safety of the PSMA-Cy5 probe was evaluated by histopathological analysis of mouse organs by a single high-dose tail vein injection of PSMA-Cy5. In vitro fluorescence cell uptake experiments showed that the binding of PSMA-Cy5 to LNCaP cells has targeting specificity. PC3 cells and blocked LNCaP cells showed almost no uptake. The results of in vivo optical imaging studies showed that the tumor-to-background ratio in the 22Rv1 group was 3.39 ± 0.47; in the 22Rv1 blocking group it was 0.78 ± 0.15, and in the PC3 group it was 0.94 ± 0.09, consistent with the in vitro results. After a high-dose injection of PSMA-Cy5, there were no abnormalities in the tissues or organs of the mice. The probe showed good safety. PSMA-Cy5 is a probe with good targeting specificity and low toxicity that can accurately visualize tumors in vivo. This study has an important reference value for the development of PSMA fluorescent probes. In the future, it can be applied to precise tumor imaging during radical prostatectomy to reduce the incidence of postoperative PSM.
随着早期前列腺癌 (PCa) 检出率的提高,手术治疗的比例也在增加。手术是治疗 PCa 的最有效方法。术中精确靶向肿瘤可以降低阳性手术切缘 (PSM) 的发生率,并尽可能保留神经血管束 (NVB)。本研究旨在合成一种 PSMA 荧光探针 (PSMA-Cy5),并验证该探针对前列腺癌的靶向特异性,为未来临床应用开发 PSMA 荧光探针提供理论依据。
在这项研究中,通过液相合成合成了一种新型水溶性 3H-吲哚菁绿型生物发光染料-Cy5 标记的前列腺特异性膜抗原 (PSMA) 配体 (PSMA-Cy5)。PSMA 配体基于谷氨酰胺-脲-赖氨酸 (Glu-urea-Lys) 结构开发。该新型荧光探针进行了体外和体内评价,并对其安全性进行了评价。共聚焦显微镜观察 PSMA-Cy5 与 PSMA(+)LNCaP 细胞、PSMA(-)PC3 细胞和阻断 LNCaP 细胞的结合摄取情况。在体内光学成像研究中,通过尾静脉注射 PSMA-Cy5 验证了 PSMA(+)22Rv1 肿瘤对探针结合的靶向特异性。通过单次尾静脉注射高剂量 PSMA-Cy5 对小鼠器官进行组织病理学分析,评估 PSMA-Cy5 探针的安全性。
体外荧光细胞摄取实验表明,PSMA-Cy5 与 LNCaP 细胞的结合具有靶向特异性。PC3 细胞和阻断的 LNCaP 细胞几乎没有摄取。体内光学成像研究结果表明,22Rv1 组肿瘤与背景的比值为 3.39±0.47;在 22Rv1 阻断组为 0.78±0.15,在 PC3 组为 0.94±0.09,与体外结果一致。高剂量注射 PSMA-Cy5 后,小鼠组织或器官无异常。探针显示出良好的安全性。
PSMA-Cy5 是一种具有良好靶向特异性和低毒性的探针,可在体内准确可视化肿瘤。本研究对 PSMA 荧光探针的开发具有重要参考价值。将来,它可以应用于根治性前列腺切除术中的精确肿瘤成像,以降低术后 PSM 的发生率。