Puig Oscar, Yuan Jeffrey, Stepaniants Sergey, Zieba Renata, Zycband Emanuel, Morris Mark, Coulter Silvija, Yu Xiang, Menke John, Woods John, Chen Fabian, Ramey Dena R, He Xuanmin, O'Neill Edward A, Hailman Eric, Johns Douglas G, Hubbard Brian K, Yee Lum Pek, Wright Samuel D, Desouza Mary M, Plump Andrew, Reiser Vladimír
Department of Molecular Profiling,, Merck Research Laboratories, Rahway, NJ 07033, USA.
Circ Cardiovasc Genet. 2011 Dec;4(6):595-604. doi: 10.1161/CIRCGENETICS.111.960773. Epub 2011 Oct 18.
Atherosclerosis is a complex disease requiring improvements in diagnostic techniques and therapeutic treatments. Both improvements will be facilitated by greater exploration of the biology of atherosclerotic plaque. To this end, we carried out large-scale gene expression analysis of human atherosclerotic lesions.
Whole genome expression analysis of 101 plaques from patients with peripheral artery disease identified a robust gene signature (1514 genes) that is dominated by processes related to Toll-like receptor signaling, T-cell activation, cholesterol efflux, oxidative stress response, inflammatory cytokine production, vasoconstriction, and lysosomal activity. Further analysis of gene expression in microdissected carotid plaque samples revealed that this signature is differentially expressed in macrophage-rich and smooth muscle cell-containing regions. A quantitative PCR gene expression panel and inflammatory composite score were developed on the basis of the atherosclerotic plaque gene signature. When applied to serial sections of carotid plaque, the inflammatory composite score was observed to correlate with histological and morphological features related to plaque vulnerability.
The robust mRNA expression signature identified in the present report is associated with pathological features of vulnerable atherosclerotic plaque and may be useful as a source of biomarkers and targets of novel antiatherosclerotic therapies.
动脉粥样硬化是一种复杂疾病,需要改进诊断技术和治疗方法。对动脉粥样硬化斑块生物学的深入探索将有助于这两方面的改进。为此,我们对人类动脉粥样硬化病变进行了大规模基因表达分析。
对101例外周动脉疾病患者的斑块进行全基因组表达分析,确定了一个强大的基因特征(1514个基因),该特征主要由与Toll样受体信号传导、T细胞活化、胆固醇外流、氧化应激反应、炎性细胞因子产生、血管收缩和溶酶体活性相关的过程主导。对显微切割的颈动脉斑块样本中的基因表达进行进一步分析发现,该特征在富含巨噬细胞和平滑肌细胞的区域差异表达。基于动脉粥样硬化斑块基因特征开发了定量PCR基因表达面板和炎症综合评分。将其应用于颈动脉斑块连续切片时,观察到炎症综合评分与斑块易损性相关的组织学和形态学特征相关。
本报告中确定的强大mRNA表达特征与易损动脉粥样硬化斑块的病理特征相关,可能作为生物标志物来源和新型抗动脉粥样硬化治疗靶点。