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A Versatile Orthotopic Nude Mouse Model for Study of Esophageal Squamous Cell Carcinoma

机译:食管鳞状细胞癌研究的多功能原位裸鼠模型

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Increasing evidence indicates tumor-stromal interactions play a crucial role in cancer. An in vivo esophageal squamous cell carcinoma (ESCC) orthotopic animal model was developed with bioluminescence imaging established with a real-time monitoring platform for functional and signaling investigation of tumor-stromal interactions. The model was produced by injection of luciferase-labelled ESCC cells into the intraesophageal wall of nude mice. Histological examination indicates this orthotopic model is highly reproducible with 100% tumorigenesis among the four ESCC cell lines tested. This new model recapitulates many clinical and pathological properties of human ESCC, including esophageal luminal stricture by squamous cell carcinoma with nodular tumor growth, adventitia invasion, lymphovascular invasion, and perineural infiltration. It was tested using an AKT shRNA knockdown of ESCC cell lines and the in vivo tumor suppressive effects of AKT knockdown were observed. In conclusion, this ESCC orthotopic mouse model allows investigation of gene functions of cancer cells in a more natural tumor microenvironment and has advantages over previous established models. It provides a versatile platform with potential application for metastasis and therapeutic regimen testing.
机译:越来越多的证据表明肿瘤 - 基质相互作用在癌症中发挥着至关重要的作用。在体内食管鳞状细胞癌(ESCC)原位动物模型与生物发光成像开发,具有实时监测平台,用于肿瘤 - 基质相互作用的功能和信号调查。该模型是通过将荧光素酶标记的ESCC细胞注射到裸鼠的肿瘤壁中产生的模型。组织学检查表明,这种原位模型在测试的四种ESCC细胞系中具有100%肿瘤性的高度可再现。这种新模型概括了人体ESCC的许多临床和病理特性,包括鳞状细胞癌,鳞状细胞癌,具有结节性肿瘤生长,外膜侵袭,淋巴血管侵袭和麻省危渗透。使用AKT ShRNA敲除ESCC细胞系的敲低测试,观察到Akt敲低的体内肿瘤抑制作用。总之,该ESCC原位小鼠模型允许在更自然的肿瘤微环境中调查癌细胞的基因功能,并优于以前的建立模型。它提供了一个多功能平台,具有转移和治疗方案测试的潜在应用。

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