CXCR7<'/> CXCR7 and CXCR4 Expressions in Infiltrative Astrocytomas and Their Interactions with HIF1α Expression and IDH1 Mutation
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CXCR7 and CXCR4 Expressions in Infiltrative Astrocytomas and Their Interactions with HIF1α Expression and IDH1 Mutation

机译:CXCR7和CXCR4在浸润性星形细胞瘤中的表达及其与HIF1α表达和IDH1突变的相互作用

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The CXCR7, a new receptor for CXCL12 with higher affinity than CXCR4 has raised key issues on glioma cell migration. The aim of this study is to investigate the CXCR7 mRNA expression in diffuse astrocytomas tissues and to evaluate its interactions with CXCR4 and HIF1α expression and IDH1 mutation. CXCR7, CXCR4 and HIF1α mRNA expression were evaluated in 129 frozen samples of astrocytomas. IDH1 mutation status was analyzed with gene expressions, matched with clinicopathological parameters and overall survival time. Protein expression was analyzed by immunohistochemistry in different grades of astrocytoma and in glioma cell line (U87MG) by confocal microscopy. There was significant difference in the expression levels of the genes studied between astrocytomas and non-neoplasic (NN) controls (p??0.001). AGII showed no significant correlation between CXCR7/HIF1α (p?=?0.548); there was significant correlation between CXCR7/CXCR4 (p?=?0.042) and CXCR7/IDH1 (p?=?0.008). GBM showed significant correlations between CXCR7/CXCR4 (p?=?0.002), CXCR7/IDH1 (p??0.001) and CXCR7/HIF1α (p?=?0.008). HIF1α overexpression was associated with higher expressions of CXCR7 (p?=?0.01) and CXCR4 (p??0.0001), while IDH1 mutation was associated with lower CXCR7 (p?=?0.009) and CXCR4 (p?=?0.0005) mRNA expressions. Protein expression increased with malignancy and in U87MG cell line was mainly localized in the cellular membrane. CXCR7 was overexpressed in astrocytoma and correlates with CXCR4 and IDH1 in AGII and CXCR4, IDH1 and HIF1α in GBM. Overexpression HIF1α was related with higher expressions of CXCR7 and CXCR4, otherwise IDH1 mutation related with lower expression of both genes. No association between CXCR7 and CXCR4 expression and survival data was related.
机译:CXCR7是CXCL12的一种新受体,具有比CXCR4更高的亲和力,已引起神经胶质瘤细胞迁移的关键问题。这项研究的目的是调查弥漫性星形细胞瘤组织中的 CXCR7 mRNA表达,并评估其与 CXCR4 HIF1α表达式和 IDH1 突变。在129个冰冻的冰冻样本中评估了 CXCR7 CXCR4 HIF1α mRNA表达。星形细胞瘤。通过基因表达分析 IDH1 突变状态,并与临床病理参数和总生存时间相匹配。通过共聚焦显微镜,通过免疫组织化学分析了不同等级的星形细胞瘤和神经胶质瘤细胞系(U87MG)中的蛋白表达。在星形细胞瘤和非肿瘤细胞(NN)对照之间,研究基因的表达水平存在显着差异( p ?<?0.001)。 AGII显示 CXCR7 /HIF1α p ?=?0.548)之间没有显着相关性; CXCR7 / CXCR4 p ?=?0.042)和 CXCR7 / IDH1 p?= ?0.008)。 GBM显示 CXCR7 / CXCR4 p ?=?0.002 ), CXCR7 / IDH1 p ?<?0.001)和< em class =“ EmphasisTypeItalic”> CXCR7 / HIF1α p ?=?0.008)。 HIF1α的过度表达与 CXCR7 的较高表达相关( p ?=? 0.01)和 CXCR4 p ?<?0.0001),而 IDH1 突变与较低的 CXCR7 p ?=?0.009)和 CXCR4 相关>( p ?=?0.0005)mRNA表达。蛋白质表达随恶性肿瘤而增加,并且在U87MG细胞系中主要位于细胞膜中。 CXCR7 在星形细胞瘤中过表达,并与AGII和 CXCR4 IDH1 相关GBM中的 CXCR4 IDH1 HIF1α。过分表达HIF1α CXCR7 CXCR4 的更高表达有关,否则< em class =“ EmphasisTypeItalic”> IDH1 突变与两个基因的较低表达有关。 CXCR7 CXCR4 表达与生存数据之间没有关联。

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