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适用于研究转移潜能和抗癌药物效果的人肺癌原位植入SCID小鼠模型。

Orthotopically implanted SCID mouse model of human lung cancer suitable for investigating metastatic potential and anticancer drug effects.

作者信息

Kondo Kazuya, Fujino Haruhiko, Miyoshi Takanori, Ishikura Hisashi, Sakiyama Shoji, Monden Yasumasa

机构信息

Department of Oncological and Regenerative Surgery, Institute of Health Biosciences, University of Tokushima Graduate School, 3-chome, Kuramoto-cho, Tokushima City 770-8503, Japan.

出版信息

Oncol Rep. 2004 Nov;12(5):991-9.

Abstract

To evaluate the effects of drugs in clinical settings, an animal model of lung cancer similar to clinical cancer is necessary. Our previous studies described an SCID mouse model using orthotopic implantation of the human lung cancer cell line which mimicked the lymph node metastasis of patients with lung cancer. In this study, we made animal models that reflected various metastatic forms of lung cancer in humans. We applied our procedure to 6 lung cancer cell lines. Suspensions of 2.0 x 10(4) cancer cells were injected into the left lung of SCID mice. We evaluated the mRNA expressions of 52 proteins related to the metabolism of and resistance to anticancer drugs of each tumor cell line and its orthotopically implanted tumor using a customized cDNA array. Three lung cancer cell lines had the potential of lymphogenous metastasis and 3 cell lines had the potential of hematogenous metastasis in this model system. The A549 line showed multiple metastases, and Ma2 line showed solitary metastasis. The expression of 52 genes in each implanted tumor was closely correlated with that in each cell lines (correlation coefficients: 0.8883-0.9533), and the gradient of the regression line was more than 0.9. This model was similar to the metastatic form in patients with lung cancer. The similar expression of proteins in each tumor cell line in vitro and implanted tumor in vivo gives an advantage in evaluating the effects of molecular-targeted drugs and the relationship between specific genes and tumor potential in preclinical studies.

摘要

为了评估药物在临床环境中的效果,建立一种与临床癌症相似的肺癌动物模型是必要的。我们之前的研究描述了一种SCID小鼠模型,该模型采用人肺癌细胞系原位植入,模拟了肺癌患者的淋巴结转移。在本研究中,我们制作了反映人类肺癌各种转移形式的动物模型。我们将该方法应用于6种肺癌细胞系。将2.0×10(4)个癌细胞悬液注入SCID小鼠的左肺。我们使用定制的cDNA阵列评估了每个肿瘤细胞系及其原位植入肿瘤中与抗癌药物代谢和耐药相关的52种蛋白质的mRNA表达。在该模型系统中,3种肺癌细胞系具有淋巴道转移潜能,3种细胞系具有血道转移潜能。A549细胞系表现为多发转移,Ma2细胞系表现为单发转移。每个植入肿瘤中52个基因的表达与每个细胞系中的表达密切相关(相关系数:0.8883 - 0.9533),回归线的斜率大于0.9。该模型与肺癌患者的转移形式相似。每个肿瘤细胞系在体外和体内植入肿瘤中蛋白质的相似表达,在临床前研究中评估分子靶向药物的效果以及特定基因与肿瘤潜能之间的关系方面具有优势。

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