A novel rodent model of spinal metastasis and spinal cord compression

被引:6
|
作者
Zibly, Zion [1 ,2 ]
Schlaff, Cody D. [1 ]
Gordon, Ira [1 ]
Munasinghe, Jeeva [3 ]
Camphausen, Kevin A. [1 ]
机构
[1] NCI, Radiat Oncol Branch, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Neurol Disorders & Stroke, Surg Neurol Branch, NIH, Bethesda, MD 20892 USA
[3] Natl Inst Neurol Disorders & Stroke, Cell & Canc Biol Branch, NCI, NIH, Bethesda, MD 20892 USA
来源
BMC NEUROSCIENCE | 2012年 / 13卷
基金
美国国家卫生研究院;
关键词
Spinal metastasis; Spinal cord compression; Animal model; Rat; BONE; NEOPLASMS; CANCER;
D O I
10.1186/1471-2202-13-137
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Spinal cord metastatic lesions affect a high number of cancer patients usually resulting in spinal cord compression syndrome. A major obstacle in the research of spinal metastatic disease is the lack of a simple reproducible animal model that mimics the natural course of the disease. In this study, we present a highly reproducible rodent model that can be used for different types of cancers while mimicking the natural course of human metastatic spinal cord compression syndrome. Results: All sixteen Fisher 344 rats survived the dorsal approach intraosseous implantation of CRL-1666 adenocarcinoma cells and both rats survived the sham control surgery. By Day 13 functional analysis via the modified Basso-Beattie-Bresnahan (BBB) locomotor rating scale showed significant decrease in motor function; median functional score was 3 for the tumor group (p = 0.0011). Median time to paresis was 8.7 days post-operatively. MR imaging illustrated repeated and consistent tumor formation, furthermore, onset of neurological sequale was the result of tumor formation and cord compression as confirmed by histological examination. Conclusions: Analysis of these findings demonstrates a repeatable and consistent tumor growth model for cancer spinal metastases in rats. This novel rat model requires a less intricate surgical procedure, and as a result minimizes procedure time while subsequently increasing consistency. Therefore, this model allows for the preclinical evaluation of therapeutics for spinal metastases that more closely replicates physiological findings.
引用
收藏
页数:7
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