Stem Cells and Cancer Laboratory, Vall d'Hebron Institute of Oncology (VHIO).
Preclinical Therapeutics Core, University of California San Francisco.
J Vis Exp. 2023 Feb 10(192). doi: 10.3791/64629.
Over the last decade, more sophisticated preclinical colorectal cancer (CRC) models have been established using patient-derived cancer cells and 3D tumoroids. Since patient derived tumor organoids can retain the characteristics of the original tumor, these reliable preclinical models enable cancer drug screening and the study of drug resistance mechanisms. However, CRC related death in patients is mostly associated with the presence of metastatic disease. It is therefore essential to evaluate the efficacy of anti-cancer therapies in relevant in vivo models that truly recapitulate the key molecular features of human cancer metastasis. We have established an orthotopic model based on the injection of CRC patient-derived cancer cells directly into the cecum wall of mice. These tumor cells develop primary tumors in the cecum that metastasize to the liver and lungs, which is frequently observed in patients with advanced CRC. This CRC mouse model can be used to evaluate drug responses monitored by microcomputed tomography (µCT), a clinically relevant small-scale imaging method that can easily identify primary tumors or metastases in patients. Here, we describe the surgical procedure and the required methodology to implant patient-derived cancer cells in the cecum wall of immunodeficient mice.
在过去的十年中,已经建立了使用患者来源的癌细胞和 3D 肿瘤球体的更复杂的临床前结直肠癌 (CRC) 模型。由于患者来源的肿瘤类器官可以保留原始肿瘤的特征,这些可靠的临床前模型使癌症药物筛选和耐药机制研究成为可能。然而,患者的 CRC 相关死亡主要与转移性疾病的存在有关。因此,评估相关体内模型中抗癌疗法的疗效至关重要,这些模型能够真实再现人类癌症转移的关键分子特征。我们已经建立了一种基于将 CRC 患者来源的癌细胞直接注射到小鼠盲肠壁中的原位模型。这些肿瘤细胞在盲肠中形成原发性肿瘤,然后转移到肝脏和肺部,这在晚期 CRC 患者中经常观察到。这种 CRC 小鼠模型可用于评估通过微计算机断层扫描 (µCT) 监测的药物反应,µCT 是一种临床相关的小型成像方法,可轻松识别患者的原发性肿瘤或转移灶。在这里,我们描述了将患者来源的癌细胞植入免疫缺陷小鼠盲肠壁中的手术过程和所需方法。