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具有间变特征的毛细胞型星形细胞瘤中,ATRX蛋白缺失和PI3K/AKT信号通路失调较为常见。

ATRX protein loss and deregulation of PI3K/AKT pathway is frequent in pilocytic astrocytoma with anaplastic features.

作者信息

Olar Adriana, Tran Diep, Mehta Vidya P, Reinhardt Annekathrin, Manekia Jawad H, Garnovskaya Maria, Ellezam Benjamin, Luthra Rajyalakshmi, Sulman Erik P, Mohila Carrie A, Campbell Gerald A, Powell Suzanne Z, Fuller Gregory N, Aldape Kenneth D, Adesina Adekunle M

出版信息

Clin Neuropathol. 2019 Mar/Apr;38(2):59-73. doi: 10.5414/NP301105.

Abstract

INTRODUCTION

Pilocytic astrocytoma (PA) with anaplastic features (PAAF) is a rare entity associated with decreased survival. It is characterized by hypercellularity, atypia, brisk mitotic activity, variable necrosis, and association with a classic PA component or anaplastic transformation in a recurrent tumor with a previously-documented classic PA.

MATERIALS AND METHODS

We present 5 PAAF cases with clinical, radiological, pathological, and molecular correlation. We interrogated , IDH, , , , , 6q23, p16(Ink4a) by sequencing, FISH, and immunohistochemistry.

RESULTS

Four tumors were located in the cerebellum, and 1 was supratentorial. All showed ATRX protein loss by immunohistochemistry, loss of heterozygosity for , and had no IDH/ mutations, nor amplification. Two of 5 tumors showed duplication by pyrosequencing. All showed loss of PTEN nuclear expression in subsets of tumor cells, which was associated with variable cytoplasmic positivity for pS6. There was a relative correlation between loss of PTEN expression and pS6 cytoplasmic expression. p53 was expressed in ~ 50% of tumor cells in all tumors. P16 was variably lost in all cases. One tumor showed /6q23 deletion.

CONCLUSION: We confirm ATRX protein loss suggestive of alteration as well as dysregulation of the PI3K/AKT pathway and, less often, of the MAPK/ERK pathway in PAAF.
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摘要

引言

具有间变特征的毛细胞型星形细胞瘤(PAAF)是一种罕见的实体瘤,与生存率降低相关。其特征为细胞增多、异型性、活跃的有丝分裂活性、不同程度的坏死,以及与经典的PA成分相关,或在先前记录有经典PA的复发性肿瘤中发生间变转化。

材料与方法

我们报告5例PAAF病例,包括临床、放射学、病理学及分子相关性分析。我们通过测序、荧光原位杂交(FISH)和免疫组化检测了ATRX、IDH、TERT启动子、BRAF、H3K27me3、6q23、p16(Ink4a)。

结果

4例肿瘤位于小脑,1例位于幕上。免疫组化显示所有肿瘤均有ATRX蛋白缺失,TERT启动子杂合性缺失,且无IDH/TERT突变及BRAF扩增。5例肿瘤中有2例经焦磷酸测序显示TERT重复。所有肿瘤在部分肿瘤细胞中均显示PTEN核表达缺失,这与pS6的不同程度胞质阳性相关。PTEN表达缺失与pS6胞质表达之间存在相对相关性。所有肿瘤中约50%的肿瘤细胞表达p53。所有病例中p16均不同程度缺失。1例肿瘤显示TERT/6q23缺失。

结论

我们证实PAAF中存在提示TERT改变的ATRX蛋白缺失,以及PI3K/AKT通路失调,较少见的是MAPK/ERK通路失调。

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