Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, 02115, USA.
Sci Rep. 2019 Jan 24;9(1):622. doi: 10.1038/s41598-018-36874-3.
Breast cancer brain metastasis (BCBM) remains a major clinical problem. Approximately 10-16% of patients with breast cancer develop brain metastases (BCBM). However, no systemic therapy has gained regulatory approval for the specific treatment of BCBM and this remains an area of persistent, unmet medical need. Rapid, predictive and clinically-relevant animal models are critical to study the biology of brain metastases and to identify effective therapeutic approaches for patients with BCBM. Here, we describe a method for efficient establishment of orthotopic mouse models of patient-derived brain metastases via an improved intracarotid injection protocol that permits tumor cell growth in the unique brain microenvironment without compromising the blood-brain barrier (BBB). We demonstrate that our newly improved models of patient-derived brain metastases recapitulate the histologic, molecular, and genetic characteristics of their matched patient tumor specimens and thus represent a potentially powerful tool for pre-clinical and translational research.
乳腺癌脑转移(BCBM)仍然是一个主要的临床问题。约 10-16%的乳腺癌患者会发展为脑转移(BCBM)。然而,目前还没有获得监管部门批准的系统性治疗方法专门用于治疗 BCBM,这仍然是一个持续存在的、未满足的医疗需求领域。快速、预测性和临床相关的动物模型对于研究脑转移的生物学特性以及为 BCBM 患者确定有效的治疗方法至关重要。在这里,我们描述了一种通过改良的颈动脉内注射方案,高效建立源自患者的脑转移的原位小鼠模型的方法,该方案允许肿瘤细胞在独特的脑微环境中生长,而不会破坏血脑屏障(BBB)。我们证明,我们新改进的源自患者的脑转移模型再现了其匹配的患者肿瘤标本的组织学、分子和遗传特征,因此代表了一种用于临床前和转化研究的潜在强大工具。