首页> 外文会议>Genetically Engineered and Optical Probes for Biomedical Applications IV; Progress in Biomedical Optics and Imaging; vol.8 no.26; Proceedings of SPIE-The International Society for Optical Engineering; vol.6449 >Non-invasive and real-time monitoring of molecular targeting therapy for lymph node and peritoneal metastasis in nude mice bearing xenografts of human colorectal cancer cells tagged with GFP and DsRed
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Non-invasive and real-time monitoring of molecular targeting therapy for lymph node and peritoneal metastasis in nude mice bearing xenografts of human colorectal cancer cells tagged with GFP and DsRed

机译:非侵入性实时监测分子靶向疗法对带有GFP和DsRed标签的人大肠癌细胞异种移植的裸鼠淋巴结和腹膜转移的作用

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We have developed an in vivo imaging system consisting of GFP- and DsRed-tagged human colonic cancer cell line, which has peritoneal and lymph node metastatic potential and show high sensitivity to EGFR targeting drugs, and convenient detection devices for GFP and DsRed. The latter includes a small handy fluorescence detection device for external monitoring of the therapeutic effect of the drug and a convenient stereo fluorescent microscope for internal visualization of micrometastases. We applied this imaging system to investigate anti-metastatic effects of EGFR targeting drugs such as gefitinib (Iressa). This system allowed sensitive detection of the development of peritoneal and lymph node metastases from the micrometastasis stage at the cellular level and also permited noninvasive, non-anesthetic monitoring of anti-metastatic effect of the drug in an animal facility without any pretreatment. Significant decreases in the intraabdominal metastatic tumor growth and prevention of inguinal lymph node metastasis by gefitinib treatment could be clearly monitored. These results suggest that convenient, low-cost, true real-time monitoring of therapeutic effect using such a fluorescence-mediated whole body imaging system seems to enhance the speed of preclinical study for novel anti-cancer agents and will allow us to understand the action mechanism of molecular targeting drugs.
机译:我们已经开发了一种由GFP和DsRed标签的人类结肠癌细胞系组成的体内成像系统,该系统具有腹膜和淋巴结转移潜能,并且对EGFR靶向药物显示出高敏感性,并提供了方便的GFP和DsRed检测装置。后者包括用于外部监测药物治疗效果的小型便捷荧光检测装置,以及用于内部可视化微转移的便捷立体荧光显微镜。我们应用该成像系统研究了EGFR靶向药物如吉非替尼(Iressa)的抗转移作用。该系统允许在细胞水平上从微转移阶段灵敏地检测到腹膜和淋巴结转移的发展,并且还允许在动物设施中进行无创,无麻醉的药物抗转移作用监测,而无需任何预处理。可以清楚地监测吉非替尼治疗的腹腔内转移性肿瘤生长的显着降低和腹股沟淋巴结转移的预防。这些结果表明,使用这种荧光介导的全身成像系统方便,低成本,实时地实时监测治疗效果似乎可以提高新型抗癌药临床前研究的速度,并使我们能够了解其作用。分子靶向药物的作用机理。

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