Taromi Sanaz, Kayser Gian, von Elverfeldt Dominik, Reichardt Wilfried, Braun Friederike, Weber Wolfgang A, Zeiser Robert, Burger Meike
Department of Hematology/Oncology and Stem Cell Transplantation, University Medical Center, Hugstetter Str. 55, 70106, Freiburg, Germany.
Department of Pathology, University Medical Center, Freiburg, Germany.
Clin Exp Metastasis. 2016 Oct;33(7):651-60. doi: 10.1007/s10585-016-9808-8. Epub 2016 Jul 6.
Small cell lung cancer (SCLC) is a highly aggressive subtype of lung cancer with very poor prognosis due to early metastatic spread and development of chemoresistance. In the last 30 years the study of SCLC has been constrained by a lack of primary human tumor specimen thus highlighting the need of a suitable mouse model. In this article we present the establishment of an orthotopic xenograft mouse model which accurately reproduced the clinical course of SCLC. Orthotopic implantation enabled engraftment of primary lung tumors in all injected mice. Furthermore, immunodeficiency of mice allowed formation of spontaneous metastases in characteristic organs. Bioluminescence Imaging, Magnetic Resonance Imaging and Positron emission tomography were applied to monitor engraftment, metabolism and the exact growth of tumors over time. In order to mimic the extensive disease stage, mice were injected with aggressive human chemoresistant cells leading to development of chemoresistant tumors and early metastatic spread. As a proof of concept treatment of tumor-bearing mice with conventional chemotherapeutics reduced tumor volumes, but a complete regression of tumors was not achieved. By mimicking the extensive disease stage our mouse model can facilitate the study of mechanisms contributing to chemoresistance and metastasis formation, as well as drug screening and evaluation of new treatment strategies for SCLC patients.
小细胞肺癌(SCLC)是一种侵袭性很强的肺癌亚型,由于早期发生转移扩散和产生化疗耐药性,其预后非常差。在过去30年里,小细胞肺癌的研究因缺乏原发性人类肿瘤标本而受到限制,因此凸显了建立合适小鼠模型的必要性。在本文中,我们展示了一种原位异种移植小鼠模型的建立,该模型准确再现了小细胞肺癌的临床病程。原位植入使原发性肺肿瘤在所有注射小鼠中得以植入。此外,小鼠的免疫缺陷使得在特征性器官中形成自发性转移灶。应用生物发光成像、磁共振成像和正电子发射断层扫描来监测肿瘤的植入、代谢以及随时间的精确生长情况。为了模拟广泛期疾病阶段,给小鼠注射具有侵袭性的人类化疗耐药细胞,导致化疗耐药肿瘤的形成和早期转移扩散。作为概念验证,用传统化疗药物治疗荷瘤小鼠可减小肿瘤体积,但未实现肿瘤的完全消退。通过模拟广泛期疾病阶段,我们的小鼠模型可以促进对化疗耐药和转移形成机制的研究,以及小细胞肺癌患者的药物筛选和新治疗策略的评估。