人类肿瘤在胸腺小鼠体内的转移模型:药物开发的有用模型。

D L Fine, R Shoemaker, A Gazdar, J G Mayo, O Fodstad, M R Boyd, B J Abbott, P A Donovan
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引用次数: 0

摘要

尽管人类肿瘤异种移植已被广泛用于抗肿瘤药物的临床前评估,但大多数工作都是基于肿瘤大小变化的皮下或肾下胶囊测定。为了获得更能反映人类临床情况的实验模型,我们开发了几种转移性模型,这些模型基于并补充了用于大规模体外药物筛选的一组细胞株。在BALB/C胸腺裸小鼠皮下、腹腔或脾内接种后60天内,1例黑色素瘤和4例肺肿瘤在肺部产生转移性病变。一些肿瘤也产生肝脏病变,一个肺肿瘤株显示转移到脑部。转移性病变在组织学上类似于在接种部位生长的肿瘤。体外和体内细胞株均来自转移灶。这些系统可为实验性药物和免疫治疗试验提供实用模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metastasis models for human tumors in athymic mice: useful models for drug development.

Although human tumor xenografts have been extensively used for preclinical evaluation of antitumor agents, most of this work has utilized subcutaneous or subrenal capsule assays based on change in tumor size. To obtain experimental models more reflective of the human clinical situations, we have developed several metastatic models that are based on and complement a panel of cell strains used in large-scale in vitro drug screening. One melanoma and four lung tumors produced metastatic lesions in the lung within 60 days following subcutaneous, intraperitoneal, or intrasplenic inoculation of BALB/C athymic nude mice. Several tumors also produced liver lesions, and one lung tumor strain showed metastasis to the brain. The metastatic lesions histologically resembled the tumors that grew at the inoculation site. In vitro and in vivo cell strains were rederived from the metastatic lesions. These systems may provide practical models for experimental drug and immunotherapeutic trials.

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