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与胃腺瘤相关的差异基因表达谱

Differential gene-expression profiles associated with gastric adenoma.

作者信息

Takenawa H, Kurosaki M, Enomoto N, Miyasaka Y, Kanazawa N, Sakamoto N, Ikeda T, Izumi N, Sato C, Watanabe M

机构信息

Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Br J Cancer. 2004 Jan 12;90(1):216-23. doi: 10.1038/sj.bjc.6601399.

Abstract

Gastric adenomas may eventually progress to adenocarcinomas at varying rates. The purpose of the present study was to identify gene-expression profiles linked to the heterogeneous nature of gastric adenoma as compared to adenocarcinoma. Suppression subtractive hybridisation analysis was performed to extract relevant genes from two cases of low- and high-grade gastric adenomas. The identified genes were quantified by RT-PCR in 14 low-grade adenoma, nine high-grade adenoma and nine adenocarcinoma samples, followed by hierarchical clustering analysis to separate tumours into groups according to their gene-expression profiles. Nine genes previously implicated in carcinogenesis in a variety of organs, including three genes related to gastric adenocarcinoma, were identified. The overexpression of these genes in gastric adenoma has not been reported previously. The clustering analysis of these nine genes across 32 cases identified three groups, one of which consisted primarily of adenocarcinomas, whereas the other two groups consisted of adenomas. One group of adenomas, characterised by larger tumour size, exhibited gene-expression profiles of an intestinal cell lineage implicated in the pathogenesis of an intestinal-type gastric adenocarcinoma. Another adenoma group consisting of low-grade adenomas with smaller tumour size exhibited a unique expression profile. In conclusion, clustering analysis of expression profiles using a limited number of genes may serve as molecular markers for gastric adenoma with different biological properties. Although the prognostic values of these gene-expression profiles need to be evaluated in further follow-up study of adenoma cases, these findings add new insights to (a) our understanding of the pathogenesis of gastric tumours, (b) the development of specific tumour markers for clinical practice, and (c) the design of novel therapeutic targets.

摘要

胃腺瘤可能最终以不同速率进展为腺癌。本研究的目的是确定与腺癌相比,与胃腺瘤异质性相关的基因表达谱。进行抑制性消减杂交分析以从两例低级别和高级别胃腺瘤中提取相关基因。通过逆转录聚合酶链反应(RT-PCR)对14例低级别腺瘤、9例高级别腺瘤和9例腺癌样本中鉴定出的基因进行定量,随后进行层次聚类分析,根据基因表达谱将肿瘤分为不同组。鉴定出9个先前与多种器官致癌作用相关的基因,其中包括3个与胃腺癌相关的基因。这些基因在胃腺瘤中的过表达此前未见报道。对这9个基因在32例样本中的聚类分析确定了3组,其中一组主要由腺癌组成,而另外两组由腺瘤组成。一组以肿瘤体积较大为特征的腺瘤表现出与肠型胃腺癌发病机制相关的肠细胞谱系的基因表达谱。另一组由肿瘤体积较小的低级别腺瘤组成的腺瘤组表现出独特的表达谱。总之,使用有限数量的基因进行表达谱聚类分析可作为具有不同生物学特性的胃腺瘤的分子标志物。尽管这些基因表达谱的预后价值需要在腺瘤病例的进一步随访研究中进行评估,但这些发现为(a)我们对胃肿瘤发病机制的理解、(b)临床实践中特异性肿瘤标志物的开发以及(c)新型治疗靶点的设计提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5399/2395343/3eb682ade10e/90-6601399f1.jpg

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