Suppr超能文献

人类肿瘤在实验动物中的转移

Metastases of human tumors in experimental animals.

作者信息

Doré J F, Bailly M, Bertrand S

机构信息

INSERM U 218, Centre Léon Bérard, Lyon, France.

出版信息

Anticancer Res. 1987 Sep-Oct;7(5B):997-1003.

PMID:3324940
Abstract

A large variety of models of both artificial and spontaneous metastases have been developed in experimental animals. These models have enabled the characterization of metastatic cancer cells and have helped in understanding the metastatic process. Studies of experimental metastases of human tumors have so far been rather limited; these have been developed by xenografting human tumors in immuno-compromised animals, especially athymic nude mice. Although nude mice only seldom develop metastases when grafted with human tumor cells, the selection of human cancer cells with increased metastatic abilities could be obtained in a number of cases. Human melanoma variants and clones with increased metastatic abilities were obtained from melanoma cell lines in nude mice and in immunosuppressed newborn rats. Subcutaneous transplantation in a nude mouse of a human melanoma metastatic nodule resulted in a subcutaneous tumor (NTT) and in spontaneous lung (NTP) and lymph node (NTG) metastases which were first maintained in vivo by subcutaneous passages in nude mice and then cultured in vitro as cell lines. Cytogenetic studies showed that all three tumor lines have a common origin and that metastases resulted from a population selection. After 15 in vitro passages, NTP cells were reinjected s.c. in nude mice: serial transplantation was accompanied by an increase in metastatic abilities of tumor cells. Melanoma cell lines, tumorigenic but non metastatic in nude mice were xenografted to ATS-treated newborn rats. 3 weeks after s.c. injection of 10(6) cells, nearly all rats developed tumors and a proportion of them lung and lymph node metastases. Agar cloning of M4Beu line showed that it is heterogeneous and contains poorly tumorigenic but highly metastatic cells. In addition, serial in vivo passages resulted in the selection of highly tumorigenic but poorly metastatic cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在实验动物中已开发出多种人工和自发性转移模型。这些模型有助于对转移性癌细胞进行表征,并有助于理解转移过程。迄今为止,对人类肿瘤实验性转移的研究相当有限;这些研究是通过将人类肿瘤异种移植到免疫受损动物,尤其是无胸腺裸鼠中开展的。尽管裸鼠接种人类肿瘤细胞后很少发生转移,但在许多情况下可以筛选出具有更高转移能力的人类癌细胞。从裸鼠和免疫抑制新生大鼠的黑色素瘤细胞系中获得了具有更高转移能力的人类黑色素瘤变体和克隆。将人类黑色素瘤转移结节皮下移植到裸鼠中,会形成皮下肿瘤(NTT)以及自发性肺转移(NTP)和淋巴结转移(NTG),这些转移首先通过在裸鼠中的皮下传代在体内维持下来,然后作为细胞系进行体外培养。细胞遗传学研究表明,所有这三种肿瘤系都有共同的起源,转移是由群体选择导致的。在体外传代15次后,将NTP细胞再次皮下注射到裸鼠中:连续移植伴随着肿瘤细胞转移能力的增强。将在裸鼠中具有致瘤性但无转移性的黑色素瘤细胞系异种移植到经ATS处理的新生大鼠中。皮下注射10(6)个细胞3周后,几乎所有大鼠都出现了肿瘤,其中一部分发生了肺和淋巴结转移。M4Beu系的琼脂克隆显示它是异质性的,包含致瘤性差但转移性高的细胞。此外,连续的体内传代导致筛选出了致瘤性高但转移性差的细胞。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验