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Murine models of breast cancer bone metastasis

机译:乳腺癌骨转移的小鼠模型

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摘要

Bone metastases cause significant morbidity and mortality in late-stage breast cancer patients and are currently considered incurable. Investigators rely on translational models to better understand the pathogenesis of skeletal complications of malignancy in order to identify therapeutic targets that may ultimately prevent and treat solid tumor metastasis to bone. Many experimental models of breast cancer bone metastases are in use today, each with its own caveats. In this methods review, we characterize the bone phenotype of commonly utilized human- and murine-derived breast cell lines that elicit osteoblastic and/or osteolytic destruction of bone in mice and report methods for optimizing tumor-take in murine models of bone metastasis. We then provide protocols for four of the most common xenograft and syngeneic inoculation routes for modeling breast cancer metastasis to the skeleton in mice, including the intra-cardiac, intra-arterial, orthotopic and intra-tibial methods of tumor cell injection. Recommendations for in vivo and ex vivo assessment of tumor progression and bone destruction are provided, followed by discussion of the strengths and limitations of the available tools and translational models that aid investigators in the study of breast cancer metastasis to bone.
机译:骨转移在晚期乳腺癌患者中引起显着的发病率和死亡率,目前被认为是无法治愈的。研究人员依靠转化模型更好地了解恶性骨骼并发症的发病机理,从而确定可最终预防和治疗实体瘤向骨转移的治疗靶标。如今,许多实验性的乳腺癌骨转移实验模型正在使用中,每种模型都有其自己的警告。在此方法审查中,我们表征了在小鼠中引起骨的成骨和/或溶骨性破坏的常用人类和鼠源性乳腺细胞系的骨表型,并报告了在骨转移鼠模型中优化肿瘤吸收的方法。然后,我们提供四种最常见的异种移植和同种接种途径的方案,以模拟乳腺癌在小鼠骨骼中的转移,包括心脏内,动脉内,原位和胫内肿瘤细胞注射方法。提供了有关肿瘤进展和骨破坏的体内和离体评估的建议,然后讨论了可用于协助研究人员研究乳腺癌向骨转移的现有工具和转化模型的优缺点。

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