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Establishment of a Fluorescent Implantation Metastasis Model of Bladder Cancer and Real-time Microscopic Detection in Nude Mice

机译:膀胱癌荧光植入转移模型的建立及裸鼠实时显微检测

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Objective: To establish a fluorescent implantation metastasis model of bladder carcinoma with high metastaticpotential in nude mice and observe development and metastasis. Methods: Human bladder cancer EJ cells withhigh invasive ability were screened and transfected with GFP plasmid to screen stable enhanced GFP-expressingclones instilled into the bladders of nude mice. Subsequent growth, invasion, and metastasis of the implantedtumors were observed and evaluated with a whole-body fluorescence optical imaging system. Results: Thetransfected bladder cancer EJ cells stably and efficiently expressed EGFP. The growth, invasion and metastasisof the implant bladder tumor were readily observed and accurately evaluated by fluorescent microscopy. Inthe bladders of nude mice, the rates of EGFP expression detected by flow cytometry at weeks 1-4 were 22.6%,46.7%, 62.3% and 72.7%, respectively, with clear increase over time. Conclusion: GFP-labeled bladder cancerEJ cells display green fluorescence under fluorescent microscopy and show stable GFP expression. The model willprovide a simple and reliable means for studying the mechanism of implantation metastasis of human bladdercancers in vivo.
机译:目的:建立高转移潜能的裸鼠膀胱癌荧光植入转移模型,观察其发展和转移情况。方法:筛选具有高侵袭能力的人膀胱癌EJ细胞,并用GFP质粒转染,以筛选稳定的增强GFP表达的克隆,该克隆被注入裸鼠的膀胱。用全身荧光光学成像系统观察并评估植入的肿瘤的随后生长,侵袭和转移。结果:转染的膀胱癌EJ细胞稳定高效表达EGFP。易于观察并通过荧光显微镜准确评估植入物膀胱肿瘤的生长,侵袭和转移。在裸鼠的膀胱中,在第1-4周通过流式细胞术检测到的EGFP表达率分别为22.6%,46.7%,62.3%和72.7%,并随时间明显增加。结论:GFP标记的膀胱癌EJ细胞在荧光显微镜下显示绿色荧光,并显示稳定的GFP表达。该模型将为研究体内人膀胱癌的植入转移机制提供一种简单可靠的手段。

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