首页> 外文期刊>Calcified tissue international. >Correlation of high-resolution X-ray micro-computed tomography with bioluminescence imaging of multiple myeloma growth in a xenograft mouse model.
【24h】

Correlation of high-resolution X-ray micro-computed tomography with bioluminescence imaging of multiple myeloma growth in a xenograft mouse model.

机译:高分辨率X射线微计算机断层扫描与异种移植小鼠模型中多发性骨髓瘤生长的生物发光成像的相关性。

获取原文
获取原文并翻译 | 示例
           

摘要

Multiple myeloma (MM) is an incurable B-cell neoplasia in which progressive skeletal lesions are a characteristic feature. Earlier we established an animal model for human MM in the immune-deficient RAG2(-/-)gammac(-/-) mouse, in which the growth of luciferase-transduced MM cells was visualized using noninvasive bioluminescence imaging (BLI). This model appeared well suited to study disease progression and response to therapy by identifying the location of various foci of MM tumor growth scattered throughout the skeleton and at subsequent time points the quantitative assessment of the tumor load by using BLI. We report here on the corresponding high-resolution X-ray micro-computed tomographic (micro-CT) analysis to study skeletal defects in the mice with full-blown MM. Several anatomical derangements were observed, including abnormalities in geometry and morphology, asymmetrical bone structures, decreased overall density in the remaining bone, loss of trabecular bone mass, destruction of the inner microarchitecture, as well as cortical perforations. Using the combination of BLI, micro-CT imaging, and immune-histopathological techniques, we found a high correlation between the micro-CT-identified lesions, exact tumor location, and infiltration leading to structural lesions and local bone deformation. This confirms that this animal model strongly resembles human MM and has the potential for studying the biology of MM growth and for preclinical testing of novel therapies for MM and for repair of MM-induced bone lesions.
机译:多发性骨髓瘤(MM)是一种不可治愈的B细胞瘤,其中进行性骨骼病变是其特征。早先,我们在免疫缺陷的RAG2(-/-)gammac(-/-)小鼠中建立了人类MM的动物模型,其中使用无创生物发光成像(BLI)可视化了荧光素酶转导的MM细胞的生长。通过确定散布在整个骨骼中的MM肿瘤生长的各种病灶的位置,并在随后的时间点使用BLI定量评估肿瘤负荷,该模型似乎非常适合研究疾病的进展和对治疗的反应。我们在这里报告了相应的高分辨率X射线计算机断层扫描(micro-CT)分析,以研究具有成熟MM的小鼠的骨骼缺陷。观察到了几种解剖学上的紊乱,包括几何形状和形态异常,不对称的骨结构,剩余骨中总体密度降低,小梁骨质量减少,内部微结构破坏以及皮层穿孔。通过结合使用BLI,微CT成像和免疫组织病理学技术,我们发现微CT识别的病变,确切的肿瘤位置和导致结构性病变和局部骨变形的浸润之间具有高度相关性。这证实了这种动物模型与人类MM非常相似,并且具有研究MM生长生物学,进行MM新疗法的临床前测试以及修复MM引起的骨病变的潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号