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SP94 肽作为肝细胞癌成像和治疗的特异性探针的研究。

Investigation of SP94 Peptide as a Specific Probe for Hepatocellular Carcinoma Imaging and Therapy.

机构信息

Department of Nuclear Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

Shanghai Institute of Medical Imaging, Shanghai 200032, China.

出版信息

Sci Rep. 2016 Sep 21;6:33511. doi: 10.1038/srep33511.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd2/5030711/99c4bb2651e0/srep33511-f1.jpg

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