Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Cancer Res. 2010 Jun 15;70(12):4859-67. doi: 10.1158/0008-5472.CAN-09-4177. Epub 2010 May 25.
Most cancer deaths are a result of metastasis. To extend our understanding of the factors that influence the process, we aimed to develop a mouse model of pulmonary metastasis that can be assayed in multiple inbred mouse strains for further use in identification of host genetic variants that influence metastasis. We used i.v. injection of Sarcoma 180 (S180) cells, which can be tracked and quantified by bioluminescence imaging. We observed growth of S180 cells solely in the lung and observed a wide range of pulmonary metastasis among inbred mouse strains. Interestingly, we noted that the BTBRT+tf/J strain exhibited complete clearance and provide evidence that the mechanism of resistance may involve immune factors, as strains subjected to whole-body irradiation are significantly more susceptible to tumor growth. One possible mechanism of resistance to pulmonary metastasis in BTBRT+tf/J mice may require T-cell function. Our experiments present a new mouse model for further characterization of the genetics and mechanisms of pulmonary metastasis.
大多数癌症死亡都是转移的结果。为了更深入地了解影响转移过程的因素,我们旨在开发一种可在多种近交系小鼠中进行评估的肺转移小鼠模型,以便进一步鉴定影响转移的宿主遗传变异。我们使用静脉注射肉瘤 180(S180)细胞,该细胞可以通过生物发光成像进行跟踪和定量。我们观察到 S180 细胞仅在肺部生长,并观察到近交系小鼠之间存在广泛的肺转移。有趣的是,我们注意到 BTBRT+tf/J 品系表现出完全清除,这提供了证据表明抵抗机制可能涉及免疫因素,因为接受全身照射的品系对肿瘤生长的敏感性显著增加。BTBRT+tf/J 小鼠对肺转移的一种可能的抵抗机制可能需要 T 细胞功能。我们的实验提供了一种新的小鼠模型,可进一步研究肺转移的遗传学和机制。