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Evaluation of malignant and benign gastric biopsy specimens by mRNA expression profile and multivariate statistical methods

机译:通过mRNA表达谱和多元统计方法评估恶性和良性胃活检标本

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Background: mRNA expression array and multivariate statistical analysis of gastric biopsies can yield insight into the molecular biology basis of local alterations, supporting expression-based identification of morphological alterations. Methods: From 11 patients with erosive gastritis(EG), 5 with adenocarcinoma (GC), 11 with atrophic gastritis (AG) gastric biopsies were collected, total RNA isolated, T7 amplification and expression analysis of 1047 mRNAs was performed using commercial glass arrays (Clontech, USA). After microarray quality control, applicable data were available from 7 EG, 4 GC, and 5 AG. Multivariate statistical and cell functional analysis were performed. Real-time RT-PCR and immunohistochemistry were used for validation. Results: GC was characterized by overregulated v-raf, v-erb-a, BCL2-associated- athanogene, immediate-early-response-3, Polo-like kinase, CDK-2, cyclin-C, Pin1 genes, and downregulated ADP-ribosyltransferase, sialophorin and DCC. AG cases had increased PDGF-receptor, TGF-beta-receptor-3, and decreased death-associated-protein-3, beta-1-catenin, topoisomerase-1 levels. In EG upregulation of IGF-receptor-1, CD9, tiransferrin receptor, integrins, and underexpression of keratin-5, caspase-4 was found. Discriminant analysis could reclassify all samples correctly using four parameters. Conclusions: mRNA expression array analysis of gastric biopsies yields previously known and new data in the evaluation of local gastric alterations. (c) 2007 Clinical Cytometry Society.
机译:背景:mRNA表达阵列和胃活检的多变量统计分析可以深入了解局部改变的分子生物学基础,支持基于表达的形态学改变识别。方法:收集11例糜烂性胃炎(EG),5例腺癌(GC),11例萎缩性胃炎(AG)胃活检患者,使用商业化的玻璃阵列进行总RNA分离,T7扩增和1047 mRNA的表达分析(美国Clontech)。在微阵列质量控制后,可从7 EG,4 GC和5 AG获得适用的数据。进行多元统计和细胞功能分析。实时RT-PCR和免疫组织化学用于验证。结果:GC的特征是过度调节v-raf,v-erb-a,BCL2相关的硫基因,立即早期反应3,Polo样激酶,CDK-2,cyclin-C,Pin1基因和ADP下调-核糖基转移酶,唾液蛋白和DCC。 AG患者的PDGF受体,TGF-β-受体3增加,而死亡相关蛋白3,β-1-连环蛋白,拓扑异构酶-1水平降低。在IGF-受体-1,CD9,替铁铁蛋白受体,整联蛋白和角蛋白-5表达不足的EG上调中,发现了胱天蛋白酶-4。判别分析可以使用四个参数正确地对所有样本进行重新分类。结论:胃活检的mRNA表达阵列分析产生了先前已知的和新的数据,用于评估局部胃部改变。 (c)2007临床细胞计数学会。

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