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本文引用的文献

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In vivo characterization of changing blood-tumor barrier permeability in a mouse model of breast cancer metastasis: a complementary magnetic resonance imaging approach.在乳腺癌转移的小鼠模型中,对血肿瘤屏障通透性变化的体内特征进行鉴定:一种互补的磁共振成像方法。
Invest Radiol. 2011 Nov;46(11):718-25. doi: 10.1097/RLI.0b013e318226c427.
2
In vivo single scan detection of both iron-labeled cells and breast cancer metastases in the mouse brain using balanced steady-state free precession imaging at 1.5 T.在 1.5T 场强下使用平衡稳态自由进动成像技术对小鼠脑内铁标记细胞和乳腺癌转移灶进行单次扫描检测。
J Magn Reson Imaging. 2011 Jul;34(1):231-8. doi: 10.1002/jmri.22593.
3
3D-FIESTA MR images are useful in the evaluation of the endoscopic expanded endonasal approach for midline skull-base lesions.3D-FIESTA MR 图像有助于评估经鼻内镜扩大颅底中线入路治疗中线颅底病变。
Acta Neurochir (Wien). 2011 Jan;153(1):12-8. doi: 10.1007/s00701-010-0852-x. Epub 2010 Nov 8.
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Heterogeneous blood-tumor barrier permeability determines drug efficacy in experimental brain metastases of breast cancer.异质性血脑屏障通透性决定乳腺癌实验性脑转移的药物疗效。
Clin Cancer Res. 2010 Dec 1;16(23):5664-78. doi: 10.1158/1078-0432.CCR-10-1564. Epub 2010 Sep 9.
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The hypoxia-selective cytotoxin NLCQ-1 (NSC 709257) controls metastatic disease when used as an adjuvant to radiotherapy.缺氧选择性细胞毒素 NLCQ-1(NSC 709257)作为放射治疗的辅助药物时,可以控制转移性疾病。
Br J Cancer. 2010 Jul 13;103(2):201-8. doi: 10.1038/sj.bjc.6605753. Epub 2010 Jun 29.
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Brain metastases.脑转移瘤。
Semin Neurol. 2010 Jul;30(3):217-35. doi: 10.1055/s-0030-1255225. Epub 2010 Jun 24.
7
Imaging iron-loaded mouse glioma tumors with bSSFP at 3 T.在 3T 场强下使用 bSSFP 对载铁的小鼠神经胶质瘤肿瘤进行成像。
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Prediction of myocardial signal during CINE balanced SSFP imaging.电影平衡稳态进动快速成像心肌信号预测。
MAGMA. 2010 Apr;23(2):85-91. doi: 10.1007/s10334-010-0202-2. Epub 2010 Mar 13.
9
Rat model of metastatic breast cancer monitored by MRI at 3 tesla and bioluminescence imaging with histological correlation.通过3特斯拉磁共振成像(MRI)和生物发光成像并结合组织学相关性监测的转移性乳腺癌大鼠模型
J Transl Med. 2009 Oct 20;7:88. doi: 10.1186/1479-5876-7-88.
10
Vorinostat inhibits brain metastatic colonization in a model of triple-negative breast cancer and induces DNA double-strand breaks.伏立诺他在三阴性乳腺癌模型中抑制脑转移定植并诱导DNA双链断裂。
Clin Cancer Res. 2009 Oct 1;15(19):6148-57. doi: 10.1158/1078-0432.CCR-09-1039. Epub 2009 Sep 29.

体内磁共振成像用于研究乳腺癌引起的实验性脑转移的发展和分布。

In Vivo Magnetic Resonance Imaging for Investigating the Development and Distribution of Experimental Brain Metastases due to Breast Cancer.

机构信息

Robarts Research Institute, London, Ontario, Canada.

出版信息

Transl Oncol. 2012 Jun;5(3):217-25. doi: 10.1593/tlo.12109. Epub 2012 Jun 1.

DOI:10.1593/tlo.12109
PMID:22741041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3384276/
Abstract

INTRODUCTION

The overall goal of this study was to assess the utility of three-dimensional magnetic resonance imaging (MRI) for monitoring the temporal and spatial development of experimental brain metastasis in mice.

MATERIALS AND METHODS

Brain metastatic human breast cancer cells (231-BR or 231-BR-HER2) were injected intracardially in nude mice for delivery to the brain. Mouse brains were imaged in vivo at different time points using a balanced steady-state-free precession (bSSFP) pulse sequence at 1.5 T. Brains were categorized into four regions: cortex, central brain, olfactory, and posterior. The number of metastases and their volumes were quantified for both cell lines.

RESULTS

There was no difference in the mean number of metastases for either cell line. The volumes of metastases in mice injected with 231-BR-HER2 cells were significantly larger than those for mice injected with 231-BR cells. The growth rate for 231-BR-HER2 metastases was 67.5% compared with 54.4% for the 231-BR metastases. More than 50% of metastases were located in the cortex and 25% to 30% of metastases were identified in the central brain for each time point and for mice injected with either cell line. The volumes of metastases were significantly larger in mice with fewer metastases at end point. SIGNIFICANT CONCLUSIONS: MRI provided a comprehensive accounting of the number and size of experimental brain metastases in the whole mouse brain at multiple time points. This approach has provided new information about the temporal and spatial development of metastases in the brain not possible by other histopathologic or imaging methods.

摘要

简介

本研究的总体目标是评估三维磁共振成像(MRI)在监测实验性脑转移小鼠时空发展中的应用。

材料与方法

通过心内注射脑转移性人乳腺癌细胞(231-BR 或 231-BR-HER2),将其递送至小鼠脑内。使用 1.5T 的平衡稳态自由进动(bSSFP)脉冲序列对不同时间点的小鼠脑进行体内成像。将脑分为四个区域:皮质、中央脑、嗅球和后颅窝。对两种细胞系的转移数量及其体积进行量化。

结果

两种细胞系的平均转移数量无差异。注射 231-BR-HER2 细胞的小鼠转移体积明显大于注射 231-BR 细胞的小鼠。与 231-BR 转移相比,231-BR-HER2 转移的生长速度为 67.5%。对于每个时间点和注射两种细胞系的小鼠,超过 50%的转移位于皮质,25%至 30%的转移位于中央脑。在终点时,转移数量较少的小鼠的转移体积明显更大。

结论

MRI 提供了一种全面的方法,可以在多个时间点对整个小鼠脑内的转移数量和大小进行成像。与其他组织病理学或影像学方法相比,这种方法提供了关于脑转移时空发展的新信息。