Galamb Orsolya, Sipos Ferenc, Molnar Bela, Szoke Dominika, Spisak Sandor, Tulassay Zsolt
2nd Department of Internal Medicine, University Semmelweis, Faculty of Medicine, Budapest, Hungary.
Cytometry B Clin Cytom. 2007 Sep;72(5):299-309. doi: 10.1002/cyto.b.20189.
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.
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.
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, transferrin receptor, integrins, and underexpression of keratin-5, caspase-4 was found. Discriminant analysis could reclassify all samples correctly using four parameters.
mRNA expression array analysis of gastric biopsies yields previously known and new data in the evaluation of local gastric alterations.
胃活检组织的mRNA表达阵列及多变量统计分析可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。
收集11例糜烂性胃炎(EG)、5例腺癌(GC)、11例萎缩性胃炎(AG)患者的胃活检组织,分离总RNA,使用商用玻璃芯片(美国Clontech公司)对1047种mRNA进行T7扩增及表达分析。经芯片质量控制后,获得了7例EG、4例GC和5例AG的可用数据。进行了多变量统计和细胞功能分析。采用实时RT-PCR和免疫组织化学进行验证。
GC的特征是v-raf、v-erb-a、BCL2相关抗凋亡蛋白、早期快速反应蛋白-3、Polo样激酶、细胞周期蛋白依赖性激酶-2、细胞周期蛋白-C、Pin1基因上调,而ADP-核糖基转移酶、涎酸糖蛋白和结肠癌缺失基因下调。AG病例中血小板衍生生长因子受体、转化生长因子-β受体-3增加,死亡相关蛋白-3、β-连环蛋白、拓扑异构酶-1水平降低。在EG中发现胰岛素样生长因子受体-1、CD9、转铁蛋白受体、整合素上调,角蛋白-5、半胱天冬酶-4表达不足。判别分析使用四个参数可将所有样本正确重新分类。
胃活检组织的mRNA表达阵列分析在评估局部胃改变时可产生已知和新的数据。