Utilisation of the Innovative [18F]-Labelled Radiotracer [18F]-BIBD-071 Within HR+ Breast Cancer Xenograft Mouse Models.

IF 4.8 3区 医学 Q2 CHEMISTRY, MEDICINAL Pharmaceuticals Pub Date : 2025-01-09 DOI:10.3390/ph18010066
Di Fan, Xin Wang, Xueyuan Ling, Hongbin Li, Lu Zhang, Wei Zheng, Zehui Wu, Lin Ai
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Abstract

Background/Objectives: Aromatase plays a crucial role in the conversion of androgens to oestrogens and is often overexpressed in hormone-dependent tumours, particularly breast cancer. [18F]BIBD-071, which has excellent binding affinity for aromatase and good pharmacokinetics, has potential for the diagnosis and treatment of aromatase-related diseases. The MCF-7 cell line, which is hormone receptor-positive (HR+), was used in the assessment of the novel [18F]-labelled radiotracer [18F]BIBD-071 via positron emission tomography (PET) imaging of an HR+ breast cancer xenograft model. Methods: [18F]BIBD-071 was synthesised, radiolabelled, and then subjected to in vitro stability testing. MCF-7 cells were cultured and implanted into BALB/c nude mice to establish subcutaneous tumour models. MicroPET/CT imaging was conducted after injection of the tracer at 1 and 2 h, and a blocking study was also conducted using the aromatase inhibitor letrozole. A block experiment was used to prove the specificity of the probe. Biodistribution studies were performed at 0.5, 1, and 2 h post injection (p.i.). Immunofluorescence was used to assess aromatase expression in MCF-7 cells. Results: [18F]BIBD-071 showed excellent in vitro stability and specific uptake in an MCF-7 xenograft tumour model. MicroPET/CT imaging at 1 and 2 h p.i. revealed excellent tumour visualisation with a favourable tumour-to-background ratio. Biodistribution data revealed high tracer uptake in the liver, small intestine, and stomach, with significant washout from the bloodstream and tumour over time. The tumour uptakes at 0.5 h, 1 h, and 2 h were 3.84 ± 0.13, 2.5 ± 0.17, and 2.54 ± 0.32, respectively. The tumour uptake significantly decreased between 0.5 h and 1 h (p < 0.0001), whereas there was no significant difference between 1 and 2 h. The tumour/background ratios at 0.5 h, 1 h, and 2 h were 1.19 ± 0.03, 1.12 ± 0.17, and 1.42 ± 0.11, respectively. Immunofluorescence confirmed robust aromatase expression in MCF-7 cells, which was correlated with [18F]BIBD-071 tumour uptake. Conclusions: [18F]BIBD-071 is a promising PET tracer for diagnosing and monitoring HR+ breast cancer, warranting further research into hormone-dependent cancers.

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创新的[18F]-标记放射性示踪剂[18F]-BIBD-071在HR+乳腺癌异种移植小鼠模型中的应用
背景/目的:芳香化酶在雄激素向雌激素的转化中起着至关重要的作用,在激素依赖性肿瘤,特别是乳腺癌中经常过度表达。[18F]BIBD-071对芳香化酶具有优异的结合亲和力和良好的药代动力学,具有诊断和治疗芳香化酶相关疾病的潜力。采用激素受体阳性(HR+)的MCF-7细胞系,通过对HR+乳腺癌异种移植模型的正电子发射断层扫描(PET)成像,对新型[18F]标记的放射性示踪剂[18F]BIBD-071进行评估。方法:合成BIBD-071 [18F],进行放射性标记,进行体外稳定性试验。培养MCF-7细胞,植入BALB/c裸鼠皮下建立肿瘤模型。在注射示踪剂1和2 h后进行MicroPET/CT成像,并使用芳香化酶抑制剂来曲唑进行阻断研究。用块实验证明了探针的特异性。在注射后0.5、1和2小时(p.i.)进行生物分布研究。免疫荧光法检测MCF-7细胞中芳香化酶的表达。结果:[18F]BIBD-071在MCF-7异种移植肿瘤模型中表现出良好的体外稳定性和特异性摄取。p.i 1和2h时的显微pet /CT成像显示良好的肿瘤显像,肿瘤与背景比良好。生物分布数据显示,示踪剂在肝脏、小肠和胃中有较高的摄取,随着时间的推移,血液和肿瘤中有明显的冲洗。肿瘤在0.5 h、1 h和2 h的摄取分别为3.84±0.13、2.5±0.17和2.54±0.32。肿瘤摄取在0.5 h和1 h之间显著降低(p < 0.0001),而在1和2 h之间无显著差异。0.5 h、1 h和2 h的肿瘤/背景比分别为1.19±0.03、1.12±0.17和1.42±0.11。免疫荧光证实MCF-7细胞中芳香化酶表达强劲,这与[18F]BIBD-071肿瘤摄取相关。结论:[18F]BIBD-071是一种很有前景的诊断和监测HR+乳腺癌的PET示踪剂,值得进一步研究激素依赖性癌症。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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