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具有少突胶质细胞成分的胶质母细胞瘤:一项病理与分子研究。

Glioblastomas with an oligodendroglial component: a pathological and molecular study.

作者信息

He J, Mokhtari K, Sanson M, Marie Y, Kujas M, Huguet S, Leuraud P, Capelle L, Delattre J Y, Poirier J, Hoang-Xuan K

机构信息

Biologie des Interactions Neurone-Glie, INSERM U495 et Universite P. et M. Curie, Paris, France.

出版信息

J Neuropathol Exp Neurol. 2001 Sep;60(9):863-71. doi: 10.1093/jnen/60.9.863.

Abstract

Glioblastoma (GBM) is considered by the WHO classification to represent the most malignant grade of the astrocytic tumors. However, a subset of GBM includes recognizable areas with oligodendroglial features, suggesting that some GBM may also have an oligodendroglial origin. The aim of this study was to analyze the molecular profile of GBM associated with an oligodendroglial component (GBMO). We analyzed a series of 25 GBMO. Loss of heterozygosity (LOH) on 1p and 19q, known as common markers of oligodendroglial tumors, were observed in 40% and 60% of cases, respectively; 72% of the tumors displayed one or both of these markers. All but 4 tumors (84%) showed alterations known to be preferentially involved in the progression of astrocytic tumors to GBM, such as EGFR amplification (44%), P16 deletion (48%), LOH on 10q (64%), PTEN (20%), and TP53 (24%) mutations. Therefore, GBMO displayed all the genetic aberrations found in "standard" GBM with a comparable incidence, but differed from GBM by having a higher rate of LOH on 1p and 19q. These results suggest that GBMO might represent a subgroup of tumors of oligodendroglial origin that is distinct from the "standard" GBM in terms of tumorigenesis pathway.

摘要

根据世界卫生组织的分类,胶质母细胞瘤(GBM)被认为是星形细胞瘤中最恶性的级别。然而,一部分GBM包含具有少突胶质细胞特征的可识别区域,这表明一些GBM可能也起源于少突胶质细胞。本研究的目的是分析与少突胶质细胞成分相关的GBM(GBMO)的分子特征。我们分析了一系列25例GBMO。分别在40%和60%的病例中观察到1p和19q上的杂合性缺失(LOH),这是少突胶质细胞瘤的常见标志物;72%的肿瘤显示出这两种标志物中的一种或两种。除4例肿瘤外(84%),所有肿瘤均显示出已知优先参与星形细胞瘤向GBM进展的改变,如表皮生长因子受体(EGFR)扩增(44%)、P16缺失(48%)、10q上的LOH(64%)、磷酸酶和张力蛋白同源物(PTEN)(20%)以及TP53(24%)突变。因此,GBMO显示出在“标准”GBM中发现的所有遗传畸变,且发生率相当,但与GBM的不同之处在于1p和19q上的LOH发生率更高。这些结果表明,GBMO可能代表了起源于少突胶质细胞的肿瘤亚组,在肿瘤发生途径方面与“标准”GBM不同。

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