Howard R B, Mullen J B, Pagura M E, Johnston M R
Department of Surgery, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Clin Exp Metastasis. 1999 Mar;17(2):157-62. doi: 10.1023/a:1006637712294.
The prevailing subcutaneous nude rodent tumor xenograft models used for biological and preclinical studies do not optimally reflect some important biological properties of cancer, especially invasion and metastasis. Orthotopic models have been developed to address this need. However, for lung cancer none of the available models are optimal, in that none originate from an orthotopic (bronchial) primary site and exhibit extensive extrathoracic metastasis. Our goal was to develop a consistent rodent model of non-small cell lung cancer with both of these properties. Groups of male Rowett nude rats were given 500 rads of gamma radiation and then endobronchially implanted in the right caudal lobe airway with 50 mg of small NCI-H460 tumor fragments taken from an orthotopic donor tumor. They were then sacrificed at selected post-implantation times and evaluated grossly and histologically for animal weight, primary tumor take and size, and metastatic tumor incidence at multiple sites. At a late time point (32-35 days), consistency of primary tumor size and metastasis was estimated by comparing results from four groups of rats implanted on different occasions. The results showed that the primary tumors grew steadily, reaching four grams by days 32-35. Rats gained weight until days 14 to 21, but then began to show cachexia. High metastatic rates (>60%) were seen for mediastinal lymph nodes (by 21 days), and kidney, bone and brain (by 28 days). Mean primary tumor size and the incidences of both regional and systemic metastasis were consistent at 32-35 days in four different groups of six animals. In conclusion, this orthotopic lung cancer model is highly metastatic and consistent in terms of both primary tumor growth and metastatic behavior. It is the only available rodent model of human lung cancer emanating from an endobronchial site and metastasizing to multiple extrapulmonary sites, and should be very useful for both biological and preclinical studies of lung cancer, particularly where studies of antimetastatic activity are of interest, and/or where survival studies are desired.
用于生物学和临床前研究的主流皮下裸鼠肿瘤异种移植模型并不能最佳地反映癌症的一些重要生物学特性,尤其是侵袭和转移。为此已开发出原位模型。然而,对于肺癌来说,现有的模型都不理想,因为没有一个模型起源于原位(支气管)原发部位,也没有表现出广泛的胸外转移。我们的目标是开发一种具有这两种特性的非小细胞肺癌一致啮齿动物模型。将雄性罗威特裸鼠分组,给予500拉德的γ射线辐射,然后经支气管在右尾叶气道内植入从原位供体肿瘤获取的50毫克小的NCI-H460肿瘤碎片。然后在选定的植入后时间点将它们处死,并对动物体重、原发肿瘤形成和大小以及多个部位的转移瘤发生率进行大体和组织学评估。在一个较晚的时间点(32 - 35天),通过比较在不同时间植入的四组大鼠的结果来评估原发肿瘤大小和转移的一致性。结果显示,原发肿瘤稳定生长,到32 - 35天时达到4克。大鼠在14至21天体重增加,但随后开始出现恶病质。纵隔淋巴结(到21天)以及肾脏、骨骼和大脑(到28天)出现高转移率(>60%)。在32 - 35天,四组每组六只动物的平均原发肿瘤大小以及局部和全身转移的发生率是一致的。总之,这种原位肺癌模型具有高转移性,在原发肿瘤生长和转移行为方面都具有一致性。它是唯一一种从支气管部位起源并转移到多个肺外部位的人肺癌可用啮齿动物模型,对于肺癌的生物学和临床前研究应该非常有用,特别是在对抗转移活性的研究感兴趣和/或需要进行生存研究的情况下。