镓-68标记的正电子发射计算机断层扫描示踪剂靶向Glypican-3的高对比度肝细胞癌成像。

IF 4.9 Q1 CHEMISTRY, MEDICINAL
ACS Pharmacology and Translational Science Pub Date : 2024-11-26 eCollection Date: 2024-12-13 DOI:10.1021/acsptsci.4c00504
Zhongjing Li, Chunwei Mo, Chengzhe Li, Qiong Wang, Size Huang, Yong Huang, Ying Liang
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引用次数: 0

摘要

肝细胞癌(HCC)是原发性肝癌的主要形式,然而早期、精确和无创检测仍然是一个相当大的临床挑战。Glypican-3 (GPC3)是一种膜结合蛋白多糖,在大多数HCC病例中明显过表达,而在正常和肝炎影响的肝组织中表现为低表达。鉴于其在恶性转化和肿瘤进展中的关键作用,GPC3成为一个引人注目的成像靶点。在这项研究中,我们开发并评估了2个68ga标记的gpc3靶向正电子发射断层扫描(PET)探针,每个探针都含有聚乙二醇(PEG)或4-(对甲基苯基)丁酸(白蛋白结合部分)。对比分析显示,与68Ga-PEG2-GBP相比,含有白蛋白结合部分的68Ga-ALB-GBP在皮下HCC小鼠模型中表现出更好的体内稳定性、增强的肿瘤摄取和改善的肿瘤-肝比。68Ga-ALB-GBP原位肝癌微PET/计算机断层扫描显示,注射后3 h肿瘤与肝脏的比值为2.29±0.13,肿瘤与肌肉的比值为13.03±1.63,优于临床使用的18f -氟脱氧葡萄糖PET成像。这些发现表明,68Ga-ALB-GBP是一种很有前景的HCC诊断工具,在诊断和治疗方面都具有潜在的临床翻译潜力。此外,在PET示踪剂中加入白蛋白结合片段可以显著延长血液循环时间,从而提高生物利用度,促进高对比度PET成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gallium-68 Labeled Positron Emission Computed Tomography Tracer Targeting Glypican-3 with High Contrast for Hepatocellular Carcinoma Imaging.

Hepatocellular carcinoma (HCC) represents the predominant form of primary liver cancer, yet early, precise, and noninvasive detection continues to pose a considerable clinical challenge. Glypican-3 (GPC3), a membrane-bound proteoglycan, is markedly overexpressed in most HCC cases, while exhibiting low expression in normal and hepatitis-affected liver tissues. Given its crucial role in malignant transformation and tumor progression, GPC3 emerges as a compelling target for imaging. In this study, we developed and evaluated 2 68Ga-labeled GPC3-targeted positron emission tomography (PET) probes, each incorporating either polyethylene glycol (PEG) or 4-(p-methylphenyl)butanoic acid (an albumin-binding moiety). Comparative analyses revealed that 68Ga-ALB-GBP, which includes the albumin-binding moiety, exhibited superior in vivo stability, enhanced tumor uptake, and an improved tumor-to-liver ratio relative to 68Ga-PEG2-GBP in subcutaneous HCC mouse models. Micro-PET/computed tomography imaging of orthotopic liver cancer with 68Ga-ALB-GBP demonstrated a tumor-to-liver ratio of 2.29 ± 0.13 and a tumor-to-muscle ratio of 13.03 ± 1.63 at 3 h postinjection, outperforming the performance of the clinically used 18F-fluorodeoxyglucose PET imaging. These findings suggest that 68Ga-ALB-GBP is a promising diagnostic tool for HCC and a strong candidate for clinical translation with potential utility in both diagnostic and therapeutic settings. Moreover, the incorporation of an albumin-binding moiety into PET tracers significantly extends blood circulation time, thereby enhancing bioavailability and facilitating high-contrast PET imaging.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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