Sargent Jennifer L, Milano Ausra, Connolly M K, Whitfield Michael L
Department of Genetics, Dartmouth Medical School, 7400 Remsen, Hanover, NH 03755, USA.
Curr Rheumatol Rep. 2008 Jul;10(3):205-11. doi: 10.1007/s11926-008-0034-5.
Gene expression studies in scleroderma have shown large and consistent changes in the gene expression of end-target tissues. These changes reflect the lymphocyte infiltration and pathway deregulation potentially linked to disease pathogenesis. Gene expression in scleroderma also reflects the clinical heterogeneity in the disease and can be used to categorize patients. Contained within these gene expression signatures are groups of genes that could serve as biomarkers for clinical end points and disease activity. The use of mechanism-derived gene expression signatures in scleroderma will provide a better understanding of the deregulated pathways contributing to disease pathogenesis.
硬皮病的基因表达研究表明,终末靶组织的基因表达发生了巨大且一致的变化。这些变化反映了可能与疾病发病机制相关的淋巴细胞浸润和信号通路失调。硬皮病中的基因表达也反映了该疾病的临床异质性,可用于对患者进行分类。这些基因表达特征中包含的基因群组可作为临床终点和疾病活动的生物标志物。在硬皮病中使用源自机制的基因表达特征将有助于更好地理解导致疾病发病机制的失调信号通路。