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曲妥珠单抗在乳腺癌脑转移的[具体内容缺失]模型中的分布情况。 (注:原文中“an and model”表述不完整,可能影响准确理解)

Trastuzumab distribution in an and model of brain metastases of breast cancer.

作者信息

Terrell-Hall Tori B, Nounou Mohamed Ismail, El-Amrawy Fatema, Griffith Jessica I G, Lockman Paul R

机构信息

Department of Basic Pharmaceutical Sciences, School of Pharmacy, West Virginia University HSC, Morgantown, West Virginia 26506, USA.

Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.

出版信息

Oncotarget. 2017 Jul 26;8(48):83734-83744. doi: 10.18632/oncotarget.19634. eCollection 2017 Oct 13.

Abstract

BACKGROUND

Drug and antibody delivery to brain metastases has been highly debated in the literature. The blood-tumor barrier (BTB) is more permeable than the blood-brain barrier (BBB), and has shown to have highly functioning efflux transporters and barrier properties, which limits delivery of targeted therapies.

METHODS

We characterized the permeability of I-trastuzumab in an , and fluorescent trastuzumab-Rhodamine123 (t-Rho123) in a novel microfluidic , BBB and BTB brain metastases of breast cancer model. : Human MDA-MB-231-HER2+ metastatic breast cancer cells were grown and maintained under static conditions. Cells were harvested at 80% confluency and prepped for intra-cardiac injection into 20 homozygous female Nu/Nu mice. : In a microfluidic device (SynVivo), human umbilical vein endothelial cells were grown and maintained under shear stress conditions in the outer compartment and co-cultured with CTX-TNA2 rat brain astrocytes (BBB) or Met-1 metastatic HER2+ murine breast cancer cells (BTB), which were maintained in the central compartment under static conditions.

RESULTS

Tissue distribution of I-trastuzumab revealed only ~3% of injected dose reached normal brain, with ~5% of injected dose reaching brain tumors. No clear correlation was observed between size of metastases and the amount of I-trastuzumab localized . This heterogeneity was paralleled , where the distribution of t-Rho123 from the outer chamber to the central chamber of the microfluidic device was qualitatively and quantitatively analyzed over time. The rate of t-Rho123 linear uptake in the BBB (0.27 ± 0.33 × 10) and BTB (1.29 ± 0.93 × 10) showed to be significantly greater than 0 (p < 0.05). The BTB devices showed significant heterogenetic tendencies, as seen in .

CONCLUSIONS

This study is one of the first studies to measure antibody movement across the blood-brain and blood-tumor barriers, and demonstrates that, though in small and most likely not efficacious quantities, trastuzumab does cross the blood-brain and blood-tumor barriers.

摘要

背景

药物和抗体向脑转移瘤的递送在文献中一直备受争议。血肿瘤屏障(BTB)比血脑屏障(BBB)更具渗透性,并且已显示具有高效的外排转运蛋白和屏障特性,这限制了靶向治疗的递送。

方法

我们在一种新型微流控乳腺癌脑转移的BBB和BTB模型中,对碘曲妥珠单抗的渗透性以及荧光曲妥珠单抗-罗丹明123(t-Rho123)进行了表征。步骤:人MDA-MB-231-HER2+转移性乳腺癌细胞在静态条件下培养和维持。当细胞达到80%汇合度时收获,并准备好进行心内注射到20只纯合雌性Nu/Nu小鼠体内。步骤:在一个微流控装置(SynVivo)中,人脐静脉内皮细胞在外腔室的剪切应力条件下培养和维持,并与CTX-TNA2大鼠脑星形胶质细胞(BBB)或Met-1转移性HER2+小鼠乳腺癌细胞(BTB)共培养,这些细胞在静态条件下维持在中央腔室。

结果

碘曲妥珠单抗的组织分布显示,仅约3%的注射剂量到达正常脑,约5%的注射剂量到达脑肿瘤。转移瘤大小与局部碘曲妥珠单抗的量之间未观察到明显的相关性。这种异质性在对微流控装置从外腔室到中央腔室的t-Rho123分布随时间进行定性和定量分析时也有体现。t-Rho123在BBB(0.27±0.33×10)和BTB(1.29±0.93×10)中的线性摄取速率显示显著大于0(p<0.05)。如在……中所见,BTB装置显示出明显的异质性倾向。

结论

本研究是首批测量抗体穿过血脑屏障和血肿瘤屏障运动的研究之一,并证明尽管曲妥珠单抗的量很少且很可能无效,但它确实能穿过血脑屏障和血肿瘤屏障。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfea/5663550/074b4f4cc676/oncotarget-08-83734-g001.jpg

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