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用于上皮性卵巢癌(EOC)研究的三维体外模型的分子描述。

Molecular description of a 3D in vitro model for the study of epithelial ovarian cancer (EOC).

作者信息

Zietarska Magdalena, Maugard Christine M, Filali-Mouhim Abdelali, Alam-Fahmy Mona, Tonin Patricia N, Provencher Diane M, Mes-Masson Anne-Marie

机构信息

Centre de Recherche du Centre Hospitalier de l'Université de Montréal /Institut du Cancer de Montréal, Québec, Canada.

出版信息

Mol Carcinog. 2007 Oct;46(10):872-85. doi: 10.1002/mc.20315.

Abstract

Epithelial ovarian cancer (EOC) cell lines are useful tools for the molecular and biological characterization of ovarian cancer. The use of an in vitro multidimensional (3-D) culture model recapitulates some of the growth conditions encountered by tumor cells in vivo. Here we describe a molecular comparison of spheroid based 3D EOC models versus monolayer cultures and xenografts using cell lines from malignant ovarian tumors (TOV-21G and TOV-112D) and ascites (OV-90) previously established and characterized in our laboratory. Gene expression analyses of the three models were performed using the Affymetrix HG-U133A high density DNA array. Cluster analysis identified a set of genes that stratified expression profiles from the EOC cell lines grown as spheroids and xenografts from that of monolayer cultures. The gene expression analysis results were validated by Q-PCR analyses on an independent set of RNAs. Differential expression observed for the S100A6 gene between the monolayer, spheroid cultures and xenografts was confirmed at the protein level by immunohistochemistry. The analysis was extended to various ovarian tumor tissues using an EOC tissue array. This result represents an example of a gene that, if studied in vitro, is more representative of the in vivo disease in a 3D model rather than the monolayer culture. Identification of genes in spheroid models that mimic the in vivo tumor gene expression patterns may allow a better understanding of the community effect observed in human disease that is determined by direct or indirect interactions of cells with their environment or other surrounding cells.

摘要

上皮性卵巢癌(EOC)细胞系是用于卵巢癌分子和生物学特征研究的有用工具。使用体外多维(3-D)培养模型可重现肿瘤细胞在体内所遇到的一些生长条件。在此,我们描述了基于球体的3D EOC模型与单层培养和异种移植之间的分子比较,使用的是先前在我们实验室建立并表征的来自恶性卵巢肿瘤(TOV-21G和TOV-112D)和腹水(OV-90)的细胞系。使用Affymetrix HG-U133A高密度DNA阵列对这三种模型进行基因表达分析。聚类分析确定了一组基因,这些基因将作为球体生长的EOC细胞系和异种移植的表达谱与单层培养的表达谱区分开来。基因表达分析结果通过对独立RNA集进行Q-PCR分析得到验证。通过免疫组织化学在蛋白质水平证实了单层、球体培养和异种移植之间S100A6基因的差异表达。使用EOC组织阵列将分析扩展到各种卵巢肿瘤组织。这一结果代表了一个基因的例子,即如果在体外进行研究,在3D模型中比在单层培养中更能代表体内疾病。鉴定出在球体模型中模拟体内肿瘤基因表达模式的基因,可能有助于更好地理解在人类疾病中观察到的由细胞与其环境或其他周围细胞的直接或间接相互作用所决定的群体效应。

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