首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Expression of pERK and pAKT in pediatric high grade astrocytomas: Correlation with YKL40 and prognostic significance
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Expression of pERK and pAKT in pediatric high grade astrocytomas: Correlation with YKL40 and prognostic significance

机译:小儿高度星形细胞瘤中pERK和pAKT的表达:与YKL40的相关性及预后意义

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摘要

The Ras signaling pathway, consisting of mitogen-activated protein kinase (MAPK) and PI3K/AKT signaling, is a prominent oncogenic pathways in adult diffuse gliomas, but few studies have evaluated such pathways in pediatric malignant gliomas. We investigated by immunohistochemistry MAPK and AKT signaling in a series of 28 pediatric high-grade gliomas (WHO grade III and IV). We sought a possible association of phospho-ERK (p-ERK) and phospho-AKT (p-AKT) with expression of other proteins involved in the Ras pathway, that is, YKL40, epidermal growth factor receptor (EGFR), EGFR vIII and c-Met. Moreover we correlated the expression of p-ERK and p-AKT with prognosis. No cases showed expression for c-Met and EGFR, and only one case was positive for EGFR vIII. YKL-40 protein was expressed in 43% of cases. We detected expression of p-ERK and p-AKT in 61% and 57%, respectively, of pediatric high grade gliomas. Statistical analysis comparing the two groups in term of high and low p-ERK and p-AKT expression showed a trend toward worse overall survival in patients with high expression of p-AKT. The activation of ERK and AKT suggest a possible role of this protein in inducing activation of the Ras signaling pathway in pediatric high-grade gliomas. Moreover high levels of p-AKT are associated with worse overall survival.
机译:由有丝分裂原激活蛋白激酶(MAPK)和PI3K / AKT信号转导组成的Ras信号转导通路是成人弥漫性神经胶质瘤的主要致癌通路,但很少有研究评估这种通路在儿科恶性神经胶质瘤中的作用。我们通过免疫组化MAPK和AKT信号转导了一系列28例儿科高级神经胶质瘤(WHO III和IV级)。我们寻求磷酸化ERK(p-ERK)和磷酸化AKT(p-AKT)与参与Ras途径的其他蛋白质(即YKL40,表皮生长因子受体(EGFR),EGFR vIII和满足。此外,我们将p-ERK和p-AKT的表达与预后相关。没有病例显示c-Met和EGFR表达,只有1例EGFR vIII阳性。 YKL-40蛋白在43%的病例中表达。我们分别在小儿高级别神经胶质瘤中检测到p-ERK和p-AKT的表达分别为61%和57%。统计分析比较了两组中p-ERK和p-AKT的高表达和低表达,表明p-AKT高表达的患者的总生存率趋于恶化。 ERK和AKT的激活表明该蛋白可能在小儿高级神经胶质瘤中诱导Ras信号通路的激活。此外,高水平的p-AKT与较差的总生存期有关。

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