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首页> 外文期刊>Translational research: the journal of laboratory and clinical medicine >Identification of candidate genes in scleroderma-related pulmonary arterial hypertension.
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Identification of candidate genes in scleroderma-related pulmonary arterial hypertension.

机译:硬皮病相关肺动脉高压中候选基因的鉴定。

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We hypothesize that pulmonary arterial hypertension (PAH)-associated genes identified by expression profiling of peripheral blood mononuclear cells (PBMCs) from patients with idiopathic pulmonary arterial hypertension (IPAH) can also be identified in PBMCs from scleroderma patients with PAH (PAH-SSc). Gene expression profiles of PBMCs collected from IPAH (n = 9), PAH-SSc (n = 10) patients, and healthy controls (n = 5) were generated using HG_U133A_2.0 GeneChips and were processed by the RMA/GCOS_1.4/SAM_1.21 data analysis pipeline. Disease severity in consecutive patients was assessed by functional status and hemodynamic measurements. The expression profiles were analyzed using PAH severity-stratification, and identified candidate genes were validated with real-time polymerase chain reaction (PCR). Transcriptomics of PBMCs from IPAH patients was highly comparable with that of PMBCs from PAH-SSc patients. The PBMC gene expression patterns significantly correlate with right atrium pressure (RA) and cardiac index (CI), which are known predictors of survival in PAH. Array stratification by RA and CI identified 364 PAH-associated candidate genes. Gene ontology (GO) analysis revealed significant (Z(score) > 1.96) alterations in angiogenesis genes according to PAH severity: matrix metalloproteinase 9 (MMP9) and vascular endothelial growth factor (VEGF) were significantly upregulated in mild as compared with severe PAH and healthy controls, as confirmed by real-time PCR. These data demonstrate that PBMCs from patients with PAH-SSc carry distinct transcriptional expression. Furthermore, our findings suggest an association between angiogenesis-related gene expression and severity of PAH in PAH-SSc patients. Deciphering the role of genes involved in vascular remodeling and PAH development may reveal new treatment targets for this devastating disorder.
机译:我们假设通过特发性肺动脉高压(IPAH)患者的外周血单个核细胞中也可以鉴定出特发性肺动脉高压(IPAH)患者的外周血单个核细胞(PBMC)表达谱所鉴定的肺动脉高压(PAH)相关基因。使用HG_U133A_2.0 GeneChips生成从IPAH(n = 9),PAH-SSc(n = 10)患者和健康对照(n = 5)收集的PBMC的基因表达谱,并通过RMA / GCOS_1.4 / SAM_1.21数据分析管道。通过功能状态和血液动力学测量评估连续患者的疾病严重程度。使用PAH严重程度分层分析表达谱,并通过实时聚合酶链反应(PCR)验证鉴定的候选基因。来自IPAH患者的PBMC的转录组学与来自PAH-SSc患者的PMBC的转录组学高度可比。 PBMC基因表达模式与右心房压力(RA)和心脏指数(CI)显着相关,后者是PAH存活率的已知预测因子。 RA和CI进行的阵列分层鉴定了364个PAH相关的候选基因。基因本体论(GO)分析显示,根据PAH严重程度,血管生成基因发生显着变化(Z(得分)> 1.96):与轻度PAH和轻度PAH相比,基质金属蛋白酶9(MMP9)和血管内皮生长因子(VEGF)明显上调实时PCR证实健康的对照。这些数据表明,患有PAH-SSc的患者的PBMC具有独特的转录表达。此外,我们的发现提示在PAH-SSc患者中,血管生成相关基因表达与PAH严重程度之间存在关联。破译参与血管重塑和PAH发育的基因的作用可能会揭示这种破坏性疾病的新治疗靶标。

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