结直肠癌cdh17特异性免疫pet显像的发展和临床前评估。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Xinbing Pan, Qianyun Wu, You Zhang, Dongsheng Xu, Xinyuan Zhou, Lianghua Li, Cheng Wang, Weijun Wei, Shuxian An*, Gang Huang* and Jianjun Liu*, 
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引用次数: 0

摘要

Cadherin 17 (CDH17)在结直肠癌(CRC)中异常表达,并与预后相关。它在原发性和转移性结直肠癌中的一致存在使其成为一种有前景的生物标志物。本研究旨在开发cdh17靶向免疫正电子发射断层扫描(immunopositron emission tomography, pet)探针,并评估其诊断CRC的潜力。免疫组织化学(IHC)染色CRC组织微阵列分析CDH17的表达。流式细胞术检测结直肠癌细胞(LS174T、HCT116、Caco-2)和胰腺癌细胞(AsPC-1)中CDH17的表达。制备了cdh17特异性纳米体(即CDH1),并用镓-68 (68Ga)和氟-18 (18F)标记以生成成像探针。采用免疫pet显像评价探针对肿瘤模型的诊断能力。CRC组织微阵列的免疫组化染色显示,与邻近正常组织相比,恶性组织中CDH17的表达升高。流式细胞术显示CDH17在Caco-2和AsPC-1细胞表面表达,而在HCT116和LS174T细胞表面不表达。[68Ga]Ga-NOTA-CDH1免疫pet显像成功显示CDH17在ccao -2肿瘤中的表达,而在HCT116肿瘤中未观察到明显的示踪剂摄取。[18F]AlF-RESCA-CDH1免疫pet成像显示CDH17在LS174T和AsPC-1肿瘤中均有表达。IHC证实CDH17在Caco-2和AsPC-1细胞膜上表达,而在HCT116细胞膜上无显著表达。CDH17在LS174T肿瘤囊组织中表达明显。在本研究中,我们开发了三种靶向CDH17的纳米体示踪剂,其中[68Ga]Ga-NOTA-CDH1和[18F]AlF-RESCA-CDH1在临床前模型中无创表达CDH17。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and Preclinical Evaluation of CDH17-Specific ImmunoPET Imaging in Colorectal Cancers

Development and Preclinical Evaluation of CDH17-Specific ImmunoPET Imaging in Colorectal Cancers

Cadherin 17 (CDH17) is found to be abnormally expressed in colorectal cancer (CRC) and linked to a prognosis. Its consistent presence in both primary and metastatic CRC positions it as a promising biomarker. This study aims to develop CDH17-targeted immuno-positron emission tomography (immunoPET) probes and evaluate their potential for diagnosing CRC. Immunohistochemical (IHC) staining was performed on CRC tissue microarrays to analyze CDH17 expression. The CDH17 expression of CRC cells (LS174T, HCT116, and Caco-2) and pancreatic cancer cells (AsPC-1) was detected by flow cytometry. CDH17-specific nanobodies (i.e., CDH1) were produced and labeled with gallium-68 (68Ga) and fluorine-18 (18F) to generate imaging probes. ImmunoPET imaging was conducted to evaluate the probes’ diagnostic abilities in tumor models. IHC staining of CRC tissue microarrays demonstrated an elevated expression of CDH17 in malignant tissues relative to that in adjacent normal tissues. Flow cytometry showed that CDH17 was expressed on the surface of Caco-2 and AsPC-1 cells but not on the surface of HCT116 or LS174T cells. ImmunoPET imaging with [68Ga]Ga-NOTA-CDH1 successfully visualized CDH17 expression in Caco-2 tumors, whereas no significant tracer uptake was observed in HCT116 tumors. [18F]AlF-RESCA-CDH1 immunoPET imaging demonstrated CDH17 expression in both LS174T and AsPC-1 tumors. IHC confirmed CDH17 expression on the membrane of Caco-2 and AsPC-1 cells with no significant expression on HCT116 cells. CDH17 expression was evident in the LS174T tumor capsule tissue. In this study, we developed three nanobody-based tracers targeting CDH17, of which [68Ga]Ga-NOTA-CDH1 and [18F]AlF-RESCA-CDH1 noninvasively demonstrated CDH17 expression in preclinical models.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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