首页> 外文期刊>Japanese Journal of Cancer Research >Establishment of an in vivo highly metastatic rat hepatocellular carcinoma model.
【24h】

Establishment of an in vivo highly metastatic rat hepatocellular carcinoma model.

机译:建立体内高转移大鼠肝细胞癌模型。

获取原文
获取原文并翻译 | 示例
           

摘要

We previously found by chance that N-nitrosomorpholine (NMOR) given after a multi-carcinogenic treatment induces liver carcinomas with 56% lung metastasis, and it was confirmed that hepatocellular carcinoma (HCC) with 100% lung metastasis was produced by 24-week treatment with NMOR and additional treatment with diethylnitrosamine (DEN). In the present study, we modified the duration of NMOR to establish an animal model with a simple experimental protocol and an appropriate experimental duration which would facilitate further study of the mechanisms of metastasis and antimetastatic agents. The results revealed DEN exposure followed by a 16-week treatment with NMOR to be a most efficient method for the induction of HCC metastasizing to the lung. Loss of cadherin, demonstrated immunohistochemically, occurred in an early stage of carcinogenesis, and this was reflected in malignant conversion of primary lesions. This model, with its essential similarities to malignant tumor behavior in man, should find application not only for elucidation of the mechanisms underlying metastasis, but also in the development of anti-metastatic agents.
机译:我们先前偶然发现,经过多致癌性治疗后给予的N-亚硝基吗啉(NMOR)诱导了肺癌转移率为56%的肝癌,并且证实经过24周的治疗会产生100%肺转移的肝细胞癌(HCC)。用NMOR进行处理,并用二乙基亚硝胺(DEN)进行进一步处理。在本研究中,我们修改了NMOR的持续时间,以建立具有简单实验方案和适当实验持续时间的动物模型,这将有助于进一步研究转移和抗转移药物的机制。结果表明,DEN暴露后再用NMOR治疗16周是诱导HCC转移到肺部的最有效方法。免疫组织化学证明,钙黏着蛋白的丢失发生在癌变的早期阶段,这反映在原发灶的恶性转化中。该模型与人类恶性肿瘤的行为具有本质相似性,不仅应用于阐明转移的机制,而且还应用于抗转移药物的开发。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号