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Establishment of a dual-color fluorescence tracing orthotopic transplantation model of hepatocellular carcinoma

机译:肝细胞癌双色荧光示踪原位移植模型的建立

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摘要

Different experimental models of hepatocellular carcinoma (HCC) have been used to investigate the biological mechanisms of hepatocarcinogenesis and its progression. However, previous studies have highlighted the difficulty of distinguishing between the tumor cells and stroma in experimental models of HCC. Therefore the aim of the present study was to establish a red-green dual-color fluorescence tracing orthotopic transplantation model of HCC, and investigate its practical values. Stable high red fluorescent protein (RFP)-expressing HepG2 human hepatoma cells and Hepa1-6 mice hepatoma cells were injected into the right liver lobe of green fluorescent protein-expressing nude mice. The growth and metastasis of the tumors were visualized using a whole-body in vivo fluorescence imaging system in real time. HCC tissues were extracted from tumor-bearing mice, and cut into 5-µm serial frozen slices. The organizational structure of the transplanted tumors was observed under a microscope. A dual-color fluorescence tracing orthotopic transplantation tumor model of HCC was successfully established with a success rate of 100%. The growth and metastasis of the tumors were visualized at each stage of development in the tumor-bearing mice. Tumor cells with red fluorescence and host cells with green fluorescence were identified to merge in the reconstruction region of tumor tissue. The invasion, migration, and cell fusion between tumor and host cells was observed clearly. The dual-color fluorescence tracing ortho-topic transplantation model of HCC was determined to be a stable and reliable method for tracking tumor progression. Mutual interactions between hepatoma cells and host tissues may be observed directly using this model, further elucidating the development of the tumor microenvironment.
机译:肝细胞癌(HCC)的不同实验模型已用于研究肝癌发生及其发展的生物学机制。但是,先前的研究强调了在HCC实验模型中区分肿瘤细胞和基质的困难。因此,本研究的目的是建立红绿双色荧光示踪肝癌原位移植模型,并探讨其实用价值。将表达稳定的高红色荧光蛋白(RFP)的HepG2人肝癌细胞和Hepa1-6小鼠肝癌细胞注入表达绿色荧光蛋白的裸鼠的右肝叶中。使用全身体内荧光成像系统实时可视化肿瘤的生长和转移。从荷瘤小鼠中提取HCC组织,并切成5 µm连续冷冻切片。在显微镜下观察移植肿瘤的组织结构。成功建立了肝癌双色荧光示踪原位移植肿瘤模型,成功率为100%。在荷瘤小鼠的每个发育阶段都可以看到肿瘤的生长和转移。鉴定出具有红色荧光的肿瘤细胞和具有绿色荧光的宿主细胞在肿瘤组织的重建区域中融合。清楚地观察到肿瘤与宿主细胞之间的侵袭,迁移和细胞融合。肝癌的双色荧光示踪原位移植模型被确定为跟踪肿瘤进展的一种稳定可靠的方法。使用该模型可以直接观察到肝癌细胞与宿主组织之间的相互作用,从而进一步阐明了肿瘤微环境的发展。

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