Molecular Biology Laboratory, Istituto Auxologico Italiano, Milano, Italy.
Hum Reprod. 2011 Nov;26(11):3109-17. doi: 10.1093/humrep/der270. Epub 2011 Aug 16.
Pelvic inflammatory phenomena have been suggested as critical players in the natural history of endometriosis. However, to what extent these events could affect the systemic immunologic status remains to be clarified. Here, we compared the gene expression profile in peripheral blood mononuclear cells from endometriosis patients in the severe diseased stage with the profile after a conventional surgical treatment for removal of endometriotic lesions and adhesions.
Microarray analysis included four patients suffering from severe endometriosis in which blood samples were obtained few days before the surgical intervention and again 6 months later. Real-time quantitative PCR analyses on a larger population were performed for some genes up-regulated in the diseased stage in a case-control approach.
Among the 17,665 probe signals detected in the microarray, n = 26 genes resulted up-regulated and n = 15 were down-regulated in the diseased stage. Five genes up-regulated in diseased stage (FBJ Murine osteosarcoma viral oncogene homolog gene, dual specificity phosphatase 1, pre-B-cell colony enhancing factor 1, adrenomedullin and S100 calcium binding protein P) were exactly those shown as up-regulated in peripheral leukocytes of psoriasis patients in a very similar study design (diseased versus 'cured' stage), with a 5.2 × 10(-11) hypergeometric probability that this event could occur by chance.
Endometriosis induces the expression of genes in peripheral leukocytes already identified in non-gynaecologic chronic inflammatory diseases, thus revealing the disease as a local affliction with relevant consequences at the systemic level. Although the commonality of gene expression with other inflammatory diseases prevents the use of these genes as non-invasive diagnostic markers, from a clinical standpoint, the idea that the surgical intervention may reduce the expression of peripheral leukocyte genes represents a novel finding.
盆腔炎被认为是子宫内膜异位症自然史中的关键因素。然而,这些事件在多大程度上可能影响全身免疫状态仍有待阐明。在这里,我们比较了处于严重疾病阶段的子宫内膜异位症患者外周血单个核细胞的基因表达谱与子宫内膜异位症病变和粘连切除后的常规手术治疗后的基因表达谱。
微阵列分析包括 4 名患有严重子宫内膜异位症的患者,在手术干预前几天和 6 个月后分别采集血液样本。采用病例对照方法,对一些在疾病阶段上调的基因进行了更大人群的实时定量 PCR 分析。
在微阵列中检测到的 17665 个探针信号中,n = 26 个基因在疾病阶段上调,n = 15 个基因下调。在疾病阶段上调的 5 个基因(FBJ 鼠骨肉瘤病毒癌基因同源物基因、双重特异性磷酸酶 1、前 B 细胞集落增强因子 1、肾上腺髓质素和 S100 钙结合蛋白 P)与在非常相似的研究设计中(疾病与“治愈”阶段)的银屑病患者外周白细胞中上调的基因完全相同,出现这种情况的超几何概率为 5.2×10(-11)。
子宫内膜异位症诱导外周白细胞中已经在非妇科慢性炎症性疾病中鉴定出的基因表达,从而揭示了疾病作为一种局部疾病,在全身水平上具有相关后果。尽管与其他炎症性疾病的基因表达具有共性,从而阻止了这些基因作为非侵入性诊断标志物的使用,但从临床角度来看,手术干预可能降低外周白细胞基因表达的观点代表了一个新的发现。