Rehulkova H, Rehulka P, Myslivcova Fucikova A, Stulik J, Pudil R
Department of Molecular Pathology and Biology, Faculty of Military Health Sciences, University of Defence, Hradec Kralove, Czech Republic.
Physiol Res. 2016 Nov 23;65(5):751-762. doi: 10.33549/physiolres.933253. Epub 2016 Jul 15.
In-depth proteome discovery analysis represents new strategy in an effort to identify novel reliable specific protein markers for hypertrophic cardiomyopathy and other life threatening cardiovascular diseases. To systematically identify novel protein biomarkers of cardiovascular diseases with high mortality we employed an isobaric tag for relative and absolute quantitation (iTRAQ) proteome technology to make comparative analysis of plasma samples obtained from patients suffering from non-obstructive hypertrophic cardiomyopathy, stable dilated cardiomyopathy, aortic valve stenosis, chronic stable coronary artery disease and stable arterial hypertension. We found 128 plasma proteins whose abundances were uniquely regulated among the analyzed cardiovascular pathologies. 49 of them have not been described yet. Additionally, application of statistical exploratory analyses of the measured protein profiles indicated the relationship in pathophysiology of the examined cardiovascular pathologies.
深入的蛋白质组发现分析代表了一种新策略,旨在识别肥厚型心肌病和其他危及生命的心血管疾病的新型可靠特异性蛋白质标志物。为了系统地识别具有高死亡率的心血管疾病的新型蛋白质生物标志物,我们采用了等压标签相对和绝对定量(iTRAQ)蛋白质组技术,对来自非梗阻性肥厚型心肌病、稳定型扩张型心肌病、主动脉瓣狭窄、慢性稳定型冠状动脉疾病和稳定型动脉高血压患者的血浆样本进行比较分析。我们发现128种血浆蛋白的丰度在分析的心血管疾病中受到独特调节。其中49种尚未被描述。此外,对测量的蛋白质谱进行统计探索性分析表明,所检查的心血管疾病在病理生理学上存在关联。