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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Non-invasive imaging correlates with histological and molecular characteristics of an osteosarcoma model: application for early detection and follow-up of MDR phenotype.
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Non-invasive imaging correlates with histological and molecular characteristics of an osteosarcoma model: application for early detection and follow-up of MDR phenotype.

机译:非侵入性成像与骨肉瘤模型的组织学和分子特征相关:早期检测和MDR表型随访的应用。

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摘要

BACKGROUND: In an orthotopic rat osteosarcoma model, histological and molecular findings were compared with the results of non-invasive imaging methods to assess disease progression at the primary site, the pattern of metastatic dissemination and the chemoresistance phenotype. MATERIALS AND METHODS: Primary tumor engraftment, vascularization, growth and metastatic spread were evaluated using 18FDG tomoscintigraphy. Bone neoformation in the primary tumor and metastasis was determined using 18FNa confirmed by classical histological studies. Chemoresistance phenotype was assessed by analysis of MDR1 and MRP1 genes expression compared to 99mTc MIBI imaging. RESULTS: 99mTc MIBI imaging correlated with the overexpression of the MDR1 and MRP1 genes. 18FDG, 18FNa and 99mTc tomoscintigraphies revealed that the pattern of vascularization, bone neoformation and hematogeneous metastatic dissemination in our animal model mimics its human counterpart. CONCLUSION: Multimodality, non-invasive imaging is a valid surrogate marker of histological and molecular characteristics in an orthotopic osteosarcoma model in immunocompetent rats; it allows extensive in vivo follow-up of osteosarcoma, including longitudinal analysis of chemoresistance.
机译:背景:在原位大鼠骨肉瘤模型中,将组织学和分子发现与非侵入性成像方法的结果进行比较,以评估原发性部位的疾病进展,转移性筛选和化学抑制表型。材料和方法:使用18FDG Tomoscintigraphy评估原发性肿瘤植入,血管化,生长和转移扩散。使用经典组织学研究证实的18fna测定原发性肿瘤和转移中的骨新涂膜。通过分析MDR1和MRP1基因表达的分析评估了化学渗透性表达,与99MTC MIBI成像相比。结果:99MTC MIBI成像与MDR1和MRP1基因的过表达相关。 18fdg,18fna和99mtc tomoscintigraphies揭示了我们动物模型中的血管化,骨新涂养和血液转移传播的模式模仿其人的对应物。结论:多模,非侵入性成像是免疫活性大鼠原位骨肉瘤模型中的组织学和分子特征的有效替代标记物;它允许在骨肉瘤的体内随访中广泛进行,包括纵向分析化学化。

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