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Oligonucleotide Microarray and QRT-PCR Study of Adhesion Protein Gene Expression in Acute Coronary Syndrome Patients

机译:寡核苷酸芯片和QRT-PCR研究急性冠脉综合征患者黏附蛋白基因的表达

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摘要

Cardiovascular diseases, including acute coronary syndrome (ACS), are the leading cause of death among humans. Adhesion proteins, owing to their involvement in the initiation and progression of atherosclerotic lesions, contribute to the progression of coronary disease and ACS occurrence. Considering ambiguosity of results reported to date, we decided to conduct a preliminary investigation of adhesion protein gene expression in ACS patients as well as in healthy subjects by making use of oligonucleotide microarray technology. Analysis of eight microarrays revealed ten upregulated genes differentiating between the two groups: intercellular adhesion molecule-2, platelet/endothelial cell adhesion molecule-1, zyxin, integrin-linked kinase, calcium and integrin binding protein-1 (calmyrin), integrin beta 2, integrin beta 3 (ITGB3), integrin beta 7, integrin alpha 2b, and selectin P ligand. The expression of ITGB3 was found to have been downregulated.
机译:包括急性冠脉综合征(ACS)在内的心血管疾病是人类死亡的主要原因。粘附蛋白由于其参与动脉粥样硬化病变的发生和发展而参与了冠状动脉疾病的发展和ACS的发生。考虑到迄今为止报道的结果存在歧义,我们决定通过使用寡核苷酸微阵列技术对ACS患者以及健康受试者中的粘附蛋白基因表达进行初步研究。对八个微阵列的分析揭示了两组之间有差异的十个上调基因:细胞间粘附分子2,血小板/内皮细胞粘附分子-1,zyxin,整联蛋白连接激酶,钙和整联蛋白结合蛋白1(钙粘蛋白),整联蛋白beta 2 ,整合素beta 3(ITGB3),整合素beta 7,整合素alpha 2b和选择素P配体。发现ITGB3的表达下调。

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