Onn Amir, Isobe Takeshi, Itasaka Satoshi, Wu Wenjuan, O'Reilly Michael S, Ki Hong Waun, Fidler Isaiah J, Herbst Roy S
Department of Thoracic/Head and Neck Medical Oncology, Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Clin Cancer Res. 2003 Nov 15;9(15):5532-9.
This study was conducted to develop biologically relevant animal models of human lung cancer that are reproducible, inexpensive, and easy to perform.
Human lung adenocarcinoma (PC14PE6), bronchioloalveolar carcinoma (NCI-H358), squamous cell carcinoma (NCI-H226), poorly differentiated non-small cell lung cancer (NCI-H1299 and A549), or small cell lung cancer (NCI-H69) cells in Matrigel were injected percutaneously into the left lungs of nude mice. The growth pattern of the different lung cancer tumors was studied. For PC14PE6 and NCI-H358, the growth pattern in the subcutis and the response to paclitaxel were also studied.
As is observed for human primary lung cancer, tumors formed from a single focus of disease and progressed to a widespread and fatal thoracic process characterized by diffuse dissemination of lung cancer in both lungs and metastasis to intra- and extrathoracic lymph nodes. When the lung cancer cell lines were implanted s.c., systemic therapy with paclitaxel induced tumor regression. However, only a limited therapeutic response to paclitaxel was observed when the same cells were implanted orthotopically into the lung. Immunohistochemical analysis of tumor tissue revealed increased expression of the proangiogenic factors interleukin 8, basic fibroblast growth factor, and vascular endothelial growth factor/vascular permeability factor.
Our orthotopic models of human lung cancer confirm the "seed and soil" concept and likely provide more clinically relevant systems for the study of both non-small cell lung cancer and small cell lung cancer biology, and for characterizing novel therapeutic strategies.
开展人类肺癌的生物学相关动物模型研究,该模型应具有可重复性、成本低且易于操作的特点。
将基质胶中培养的人肺腺癌(PC14PE6)、细支气管肺泡癌(NCI-H358)、鳞状细胞癌(NCI-H226)、低分化非小细胞肺癌(NCI-H1299和A549)或小细胞肺癌(NCI-H69)细胞经皮注射到裸鼠左肺。研究不同肺癌肿瘤的生长模式。对于PC14PE6和NCI-H358,还研究了皮下生长模式及对紫杉醇的反应。
正如在人类原发性肺癌中观察到的那样,肿瘤由单一病灶形成,并发展为广泛且致命的胸部病变,其特征为肺癌在双肺弥漫性播散以及转移至胸内和胸外淋巴结。当肺癌细胞系皮下植入时,紫杉醇全身治疗可诱导肿瘤消退。然而,当将相同细胞原位植入肺时,仅观察到对紫杉醇有限的治疗反应。肿瘤组织的免疫组化分析显示促血管生成因子白细胞介素8、碱性成纤维细胞生长因子和血管内皮生长因子/血管通透性因子的表达增加。
我们的人类肺癌原位模型证实了“种子与土壤”概念,可能为非小细胞肺癌和小细胞肺癌生物学研究以及新型治疗策略的表征提供更具临床相关性的系统。