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采用表达绿色荧光蛋白的癌细胞构建原位移植小鼠模型,以可视化转移和血管生成。

Orthotopic transplant mouse models with green fluorescent protein-expressing cancer cells to visualize metastasis and angiogenesis.

作者信息

Hoffman R M

机构信息

AntiCancer, Inc., San Diego, CA, USA.

出版信息

Cancer Metastasis Rev. 1998;17(3):271-7. doi: 10.1023/a:1006188412324.

Abstract

There have been major efforts in metastasis research in recent years, especially on the role of angiogenesis in the metastatic process. Much of the information in this area has been obtained from model systems that are not representative of clinical cancer. The technique of surgical orthotopic implantation (SOI) has allowed the development of clinically relevant metastatic models of human cancer in immunodeficient rodents such as the nude and SCID mouse. In order to allow direct visualization of the metastatic process, we took advantage of the green fluorescent protein (GFP) of the jellyfish, Aequorea victoria. A series of cancer cell lines have been stably transfected with vectors containing humanized GFP cDNA. To utilize GFP expression for metastasis studies, fragments of subcutaneously growing tumor, which were comprised of GFP-expressing cells, were implanted by SOI in nude mice. Subsequent metastases were visualized in systemic organs by GFP fluorescence in the lung, liver, bones, brain and other organs down to the single-cell level. With this fluorescent tool, we detected and visualized for the first time tumor cells at the microscopic level in fresh viable tissue in their normal host organs even in the live animal. Angiogenesis is readily visualized in the transplanted GFP-expressing tumors in real time in situ in the live animal using simple laparotomy and fluorescent techniques. The results with the GFP-transfected tumor cells, combined with the use of SOI, demonstrate a fundamental advance to visualize and study cancer metastasis and the role of angiogenesis and other factors in the metastatic process.

摘要

近年来,转移研究领域付出了巨大努力,尤其是关于血管生成在转移过程中的作用。该领域的许多信息来自于不代表临床癌症的模型系统。手术原位植入(SOI)技术使得在免疫缺陷啮齿动物(如裸鼠和SCID小鼠)中建立与临床相关的人类癌症转移模型成为可能。为了直接观察转移过程,我们利用了维多利亚多管水母的绿色荧光蛋白(GFP)。一系列癌细胞系已被稳定转染含有人源化GFP cDNA的载体。为了将GFP表达用于转移研究,将由表达GFP的细胞组成的皮下生长肿瘤片段通过SOI植入裸鼠体内。随后,通过肺、肝、骨、脑及其他器官中的GFP荧光在全身器官中观察到转移情况,甚至能观察到单细胞水平。借助这种荧光工具,我们首次在活体动物的正常宿主器官中,在新鲜的活组织中以微观水平检测并观察到肿瘤细胞。使用简单的剖腹术和荧光技术,可在活体动物中原位实时观察移植的表达GFP肿瘤中的血管生成。GFP转染肿瘤细胞的结果,结合SOI的使用,证明了在观察和研究癌症转移以及血管生成和其他因素在转移过程中的作用方面取得了根本性进展。

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