Department of Nuclear Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Shanghai Institute of Medical Imaging, Shanghai 200032, China.
Sci Rep. 2016 Sep 21;6:33511. doi: 10.1038/srep33511.
SP94 (SFSIIHTPILPL), a novel peptide, has shown specific binding to hepatocellular carcinoma (HCC) cells. We aimed to investigate the capability of SP94 as a targeting probe for HCC imaging and therapy following labeling with technetium-99m ((99m)Tc) and rhenium-188 ((188)Re). HYNIC-SP94 was prepared by solid phase synthesis and then labeled with (99m)Tc. Cell competitive binding, internalization assay, in vitro and in vivo stability, biodistribution and micro-single photon emission computed tomography /computed tomography (SPECT/CT) imaging studies were performed to investigate the capability of (99m)Tc tricine-EDDA/HYNIC-SP94 as a specific HCC imaging probe. Initial promising targeting results inspired evaluation of its therapeutic effect when labeled by (188)Re. HYNIC-SP94 was then labeled again with (188)Re to perform cell apoptosis, microSPECT/CT imaging evaluation and immunohistochemistry. Huh-7 cells exhibited typical apoptotic changes after (188)Re irradiation. According to (99m)Tc tricine-EDDA/HYNIC-SP94 microSPECT/CT imaging, tumor uptake was significantly decreased compared with that of pre-treatment with (188)Re-HYNIC-SP94. The immunohistochemistry also displayed obvious necrosis and apoptosis as well as inhibition of proliferation in the (188)Re-HYNIC-SP94 treatment group. The results supported that (99m)Tc tricine-EDDA/HYNIC-SP94 is able to target HCC cells and (188)Re-HYNIC- SP94 holds potential as a therapeutic agent for HCC, making (99m)Tc/(188)Re-HYNIC-SP94 a promising targeting probe for HCC imaging and therapy.
SP94(SFSIIHTPILPL)是一种新型肽,已显示出对肝细胞癌(HCC)细胞的特异性结合。我们旨在研究 SP94 作为 HCC 成像和治疗的靶向探针的能力,方法是用锝-99m((99m)Tc)和铼-188((188)Re)标记。通过固相合成制备 HYNIC-SP94,然后用(99m)Tc 标记。进行细胞竞争性结合、内化试验、体外和体内稳定性、生物分布和微单光子发射计算机断层扫描/计算机断层扫描(SPECT/CT)成像研究,以研究(99m)Tc 三羧酸/EDDA/HYNIC-SP94 作为特异性 HCC 成像探针的能力。(99m)Tc 三羧酸/EDDA/HYNIC-SP94 的初步有希望的靶向结果激发了对其标记为(188)Re 的治疗效果的评估。然后再次用(188)Re 标记 HYNIC-SP94,以进行细胞凋亡、微 SPECT/CT 成像评估和免疫组织化学分析。(188)Re 照射后,Huh-7 细胞表现出典型的凋亡变化。根据(99m)Tc 三羧酸/EDDA/HYNIC-SP94 的微 SPECT/CT 成像,与(188)Re-HYNIC-SP94 预处理相比,肿瘤摄取明显降低。免疫组织化学也显示出明显的坏死和凋亡以及增殖抑制。(188)Re-HYNIC-SP94 治疗组。结果支持(99m)Tc 三羧酸/EDDA/HYNIC-SP94 能够靶向 HCC 细胞,(188)Re-HYNIC-SP94 具有作为 HCC 治疗剂的潜力,使(99m)Tc/(188)Re-HYNIC-SP94 成为 HCC 成像和治疗的有前途的靶向探针。