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[人肝癌裸鼠系统性位点特异性转移模型的建立]

[The establishment of a systematic site-specific metastasis model of human hepatocellular carcinoma in nude mouse].

作者信息

Tao Zhong-Hua, Wu Wei-Zhong, Wang Xi-Long, Wan Jin-Liang, Sun Hui-Chuan, Wang Lu, Xia Jing-Lin, Fan Jia

机构信息

Liver Cancer Institute and Zhongshan Hospital, Fudan Unviersity, Shanghai 200032, China.

出版信息

Zhonghua Gan Zang Bing Za Zhi. 2011 Feb;19(2):110-3. doi: 10.3760/cma.j.issn.1007-3418.2011.02.009.

Abstract

To establish a systematic site-specific metastatsis model of human hepatocellular carcinoma (HCC) in nude mouse. HCCLM3-R cells were seeded into mice liver to establish xenograft mouse models. With the help of RFP, metastasis foci in lungs and lymph nodes in mice were detected using fluorescent stereomicroscopy and were removed. Cells derived from the metastasis foci were named HCCLM3-R-LM1 and HCCLM3-R-LnM1 respectively. HCCLM3-R-LM1 and HCCLM3-R-LnM1 cells were seeded into mice livers to analyze the lung and lymph node metastasis. Lungs of all tested mice were collected, examined by pathological evaluation and counted lung metastasis. Both lung and lymph node metastasis were found in HCCLM3-R-LM1, HCCLM3-R and HCCLM3-R-LnM1 cells and a significant difference was found between the lung and the lymph node metastasis levels in the three cells. The fluorescent areas (pixels) of lung and lymph node metastasis were 8687.00+/-1844.63 versus 2570.00+/-318.20 (P = 0.0031) in HCCLM3-R-LM1 cells, 6457.67+/-832.62 versus 10 994.33+/-2 212.31 (P = 0.0036) in HCCLM3-R cells, and 2968.67+/-2571.00 versus 24 416.00+/-7 186.13 (P = 0.0094) in HCCLM3-R-LnM1 cells, respectively. The middle numbers of microscopic lung metastatic foci were 775, 430 and 310 in HCCLM3-R-LM1, HCCLM3-R and HCCLM3-R-LnM1 cells (P less than 0.001), respectively, consist with the results quantified by RFP. We established the systematic site-specific metastasis models which demonstrates lung- and lymph node-specific metastasis potential in nude mice and can be used as a model for researches on site-specific metastasis of HCC.

摘要

建立人肝细胞癌(HCC)在裸鼠体内的系统性位点特异性转移模型。将HCCLM3-R细胞接种到小鼠肝脏中以建立异种移植小鼠模型。借助红色荧光蛋白(RFP),使用荧光立体显微镜检测小鼠肺部和淋巴结中的转移灶并将其切除。分别将源自转移灶的细胞命名为HCCLM3-R-LM1和HCCLM3-R-LnM1。将HCCLM3-R-LM1和HCCLM3-R-LnM1细胞接种到小鼠肝脏中以分析肺部和淋巴结转移情况。收集所有受试小鼠的肺部,通过病理评估进行检查并计数肺转移情况。在HCCLM3-R-LM1、HCCLM3-R和HCCLM3-R-LnM1细胞中均发现了肺部和淋巴结转移,且这三种细胞的肺部和淋巴结转移水平存在显著差异。HCCLM3-R-LM1细胞中肺部和淋巴结转移的荧光面积(像素)分别为8687.00±1844.63和2570.00±318.20(P = 0.0031),HCCLM3-R细胞中为6457.67±832.62和10994.33±2212.31(P = 0.0036),HCCLM3-R-LnM1细胞中为2968.67±2571.00和24416.00±7186.13(P = 0.0094)。HCCLM3-R-LM1、HCCLM3-R和HCCLM3-R-LnM1细胞中显微镜下肺转移灶的中位数分别为775、430和310(P<0.001),与通过RFP定量的结果一致。我们建立了系统性位点特异性转移模型,该模型在裸鼠中显示出肺部和淋巴结特异性转移潜能,可作为HCC位点特异性转移研究的模型。

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