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丝裂原活化蛋白激酶在胶质增生和毛细胞型星形细胞瘤中的作用

Mitogen-activated protein kinase in gliosis and pilocytic astrocytoma.

作者信息

Takeuchi Hiroaki, Neishi Hiroyuki, Higashino Yoshifumi, Kitai Ryuhei, Kikuta Ken-Ichiro, Imamura Yoshiyuki

出版信息

Clin Neuropathol. 2018 Jan/Feb;37(1):36-41. doi: 10.5414/NP301061.

Abstract

Pilocytic astrocytoma (PA), featuring activation of the mitogen-activated protein kinase (MAPK) pathway, is the most common tumor of the pediatric central nervous system. However, it remains unknown whether MAPK activation is present in the reactive gliosis of non-neoplastic lesions. Therefore, we investigated the expression of MAPK in reactive gliosis associated with cavernous angiomas. Immunohistochemical expression and the extent of BRAF, ERK, p38, and JNK were investigated in 10 patients with gliosis surrounding cavernous angiomas (GS group) and 10 patients with PA (PA group). Evaluation of these parameters was scored as 0, none; 1, scarce; 2, moderate; 3, global. In the GS group, histopathologic features of PA (piloid cells, Rosenthal fibers, microcysts with eosinophilic granular bodies) were identified. Expression of ERK, and p38 was shown in all patients in the GS and PA group. Expression of BRAF was identified in 5 patients (50%) in the GS group and in 8 (80%) in the PA group. The mean score of BRAF expression in the PA group was significantly higher than that in the GS group (p = 0.019). Reactive gliosis may resemble PA in histological findings and MAPK activation. Therefore, PA could be indistinguishable from reactive gliosis with classic histopathologic and/or immunohistochemical methods.
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摘要

毛细胞型星形细胞瘤(PA)以丝裂原活化蛋白激酶(MAPK)通路激活为特征,是小儿中枢神经系统最常见的肿瘤。然而,非肿瘤性病变的反应性胶质增生中是否存在MAPK激活仍不清楚。因此,我们研究了与海绵状血管瘤相关的反应性胶质增生中MAPK的表达。对10例海绵状血管瘤周围胶质增生患者(GS组)和10例PA患者(PA组)的BRAF、ERK、p38和JNK进行免疫组化表达及表达程度研究。这些参数的评估分为0分(无)、1分(稀少)、2分(中等)、3分(全部)。在GS组中,发现了PA的组织病理学特征(毛发样细胞、Rosenthal纤维、含嗜酸性颗粒体的微囊肿)。GS组和PA组所有患者均显示ERK和p38的表达。GS组5例(50%)患者和PA组8例(80%)患者检测到BRAF表达。PA组BRAF表达的平均评分显著高于GS组(p = 0.019)。反应性胶质增生在组织学表现和MAPK激活方面可能类似于PA。因此,用经典的组织病理学和/或免疫组化方法可能无法区分PA和反应性胶质增生。

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