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基因表达的微阵列分析反映了卵巢癌模型的生物学特性。

Microarray analysis of gene expression mirrors the biology of an ovarian cancer model.

作者信息

Tonin P N, Hudson T J, Rodier F, Bossolasco M, Lee P D, Novak J, Manderson E N, Provencher D, Mes-Masson A M

机构信息

Department of Medicine, McGill University, Montréal, Québec, Canada H3G 1A4.

出版信息

Oncogene. 2001 Oct 4;20(45):6617-26. doi: 10.1038/sj.onc.1204804.

Abstract

We have previously described an ovarian cancer model based on four independent spontaneously immortalized epithelial ovarian cancer cell lines (TOV-21G, TOV-81D, TOV-112D and OV-90) from patients who were never exposed to chemotherapy or radiation therapy. These cell lines are particularly interesting since they retain characteristics of the original epithelial ovarian cancers (EOC) from which they were derived. Here we report the characterization of this model system using high-density DNA microarrays in order to assess gene expression. Expression profiles were generated from total RNAs extracted from the four EOC cell lines. For comparison, expression profiling is also provided for a primary culture of normal ovarian surface epithelium (NOV-31) and a fresh EOC sample (TOV-578G). Comparison of expression profiles revealed patterns of expression that distinguish NOV-31 from that of all tumor derived samples. The expression pattern of TOV-81D, an EOC cell line that was derived from a patient with indolent disease, most closely resembles NOV-31 while profiles of samples derived from patients with more aggressive disease (TOV-21G, OV-90, TOV-112D and TOV-578G) showed more divergent patterns of expression. The microarray analysis (http://genome.mcgill.ca) results confirm the usefulness of an ovarian cancer model based on the characterization of these EOC cell lines.

摘要

我们之前描述过一种卵巢癌模型,该模型基于来自从未接受过化疗或放疗患者的四种独立的自发永生化上皮性卵巢癌细胞系(TOV - 21G、TOV - 81D、TOV - 112D和OV - 90)。这些细胞系特别有趣,因为它们保留了其来源的原始上皮性卵巢癌(EOC)的特征。在此,我们报告使用高密度DNA微阵列对该模型系统进行的表征,以评估基因表达。表达谱由从这四种EOC细胞系中提取的总RNA生成。为作比较,还提供了正常卵巢表面上皮原代培养物(NOV - 31)和新鲜EOC样本(TOV - 578G)的表达谱分析。表达谱的比较揭示了区分NOV - 31与所有肿瘤来源样本的表达模式。TOV - 81D是一种源自惰性疾病患者的EOC细胞系,其表达模式与NOV - 31最为相似,而源自侵袭性更强疾病患者的样本(TOV - 21G、OV - 90、TOV - 112D和TOV - 578G)的表达谱则显示出更不同的表达模式。微阵列分析(http://genome.mcgill.ca)结果证实了基于这些EOC细胞系表征的卵巢癌模型的实用性。

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