Apoptosis and Angiogenesis in Varicose Veins Using Gene Expression Profiling

Mei-Yin Chang , Pai-Tsung Chiang , Yi-Chen Chung , Shiu-Yen Ho , Sin-Daw Lin , Shiu-Ru Lin , Choo-Aun Neoh
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引用次数: 6

Abstract

Little information is known about the genetic mechanisms of the pathophysiology of varicose veins (VVs). The purpose of this study was to systematically explore the biological pathways of genes speculatively participating in VVs by microarray bioinformatics analysis methods. The results showed that 32 genes were upregulated and 74 genes were downregulated in VVs. Gene Ontology and relevant bioinformatics tools indicated that the functional categories in which 106 genes (2.8%; 106/3800) of the most frequent alteration belonged to were apoptosis and angiogenesis. The analysis of 20 VV tissue specimens demonstrated that genes involved in angiogenesis and apoptosis pathways had high rates of overexpression. In addition, we discovered that genes involved in the angiogenesis pathways included HSP90, ILK, and TGFB1, and they played key roles in the development of VVs. This study demonstrated that the angiogenesis and apoptosis pathways may play an important role in the formation of VVs, but their molecular mechanisms need further investigation.

利用基因表达谱研究静脉曲张的细胞凋亡和血管生成
关于静脉曲张(VVs)病理生理的遗传机制知之甚少。本研究的目的是通过微阵列生物信息学分析方法系统地探索推测参与VVs的基因的生物学途径。结果表明,VVs中有32个基因上调,74个基因下调。基因本体论和相关生物信息学工具显示,其中106个基因(2.8%;106/3800)最常见的改变属于细胞凋亡和血管生成。对20个VV组织标本的分析表明,参与血管生成和凋亡途径的基因具有高的过表达率。此外,我们发现参与血管生成途径的基因包括HSP90、ILK和TGFB1,它们在VVs的发展中起着关键作用。本研究表明血管生成和凋亡途径可能在VVs的形成中发挥重要作用,但其分子机制有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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