Song Ho-Taek, Jordan Elaine K, Lewis Bobbi K, Liu Wei, Ganjei Justin, Klaunberg Brenda, Despres Daryl, Palmieri Diane, Frank Joseph A
Frank Laboratory, Radiology and Imaging Sciences Clinical Center, National Institute of Health, Bethesda, MD, USA.
J Transl Med. 2009 Oct 20;7:88. doi: 10.1186/1479-5876-7-88.
Establishing a large rodent model of brain metastasis that can be monitored using clinically relevant magnetic resonance imaging (MRI) techniques is challenging. Non-invasive imaging of brain metastasis in mice usually requires high field strength MR units and long imaging acquisition times. Using the brain seeking MDA-MB-231BR transfected with luciferase gene, a metastatic breast cancer brain tumor model was investigated in the nude rat. Serial MRI and bioluminescence imaging (BLI) was performed and findings were correlated with histology. Results demonstrated the utility of multimodality imaging in identifying unexpected sights of metastasis and monitoring the progression of disease in the nude rat.
Brain seeking breast cancer cells MDA-MB-231BR transfected with firefly luciferase (231BRL) were labeled with ferumoxides-protamine sulfate (FEPro) and 1-3 x 106 cells were intracardiac (IC) injected. MRI and BLI were performed up to 4 weeks to monitor the early breast cancer cell infiltration into the brain and formation of metastases. Rats were euthanized at different time points and the imaging findings were correlated with histological analysis to validate the presence of metastases in tissues.
Early metastasis of the FEPro labeled 231BRL were demonstrated on T2*-weighted MRI and BLI within 1 week post IC injection of cells. Micro-metastatic tumors were detected in the brain on T2-weighted MRI as early as 2 weeks post-injection in greater than 85% of rats. Unexpected skeletal metastases from the 231BRL cells were demonstrated and validated by multimodal imaging. Brain metastases were clearly visible on T2 weighted MRI by 3-4 weeks post infusion of 231BRL cells, however BLI did not demonstrate photon flux activity originating from the brain in all animals due to scattering of the photons from tumors.
A model of metastatic breast cancer in the nude rat was successfully developed and evaluated using multimodal imaging including MRI and BLI providing the ability to study the temporal and spatial distribution of metastases in the brain and skeleton.
建立一种能够使用临床相关磁共振成像(MRI)技术进行监测的大型脑转移瘤啮齿动物模型具有挑战性。小鼠脑转移瘤的非侵入性成像通常需要高场强MR设备和较长的成像采集时间。利用转染了荧光素酶基因的趋脑MDA-MB-231BR细胞,在裸大鼠中研究了转移性乳腺癌脑肿瘤模型。进行了系列MRI和生物发光成像(BLI),并将结果与组织学进行了关联。结果证明了多模态成像在识别意外转移部位和监测裸大鼠疾病进展方面的实用性。
用硫酸鱼精蛋白-超顺磁性氧化铁(FEPro)标记转染了萤火虫荧光素酶的趋脑乳腺癌细胞MDA-MB-231BR(231BRL),并心内注射1-3×10⁶个细胞。进行长达4周的MRI和BLI,以监测早期乳腺癌细胞浸润入脑和转移瘤的形成。在不同时间点对大鼠实施安乐死,并将成像结果与组织学分析相关联,以验证组织中转移瘤的存在。
在细胞心内注射后1周内,通过T2*加权MRI和BLI显示了FEPro标记的231BRL的早期转移。在注射后2周,在T2加权MRI上最早在超过85%的大鼠脑中检测到微转移瘤。通过多模态成像证实并验证了231BRL细胞的意外骨转移。在输注231BRL细胞后3-4周,T2加权MRI上脑转移瘤清晰可见,然而由于肿瘤光子的散射,并非所有动物的BLI都显示出来自脑的光子通量活性。
成功建立了裸大鼠转移性乳腺癌模型,并使用包括MRI和BLI在内的多模态成像进行了评估,从而能够研究脑和骨骼中转移瘤的时间和空间分布。