Huang Hervé, Hara Akira, Homma Taku, Yonekawa Yasuhiro, Ohgaki Hiroko
International Agency for Research on Cancer, Lyon, France, and Department of Neurosurgery, University of Zurich, Zurich, Switzerland.
J Neuropathol Exp Neurol. 2005 Oct;64(10):891-901. doi: 10.1097/01.jnen.0000183345.19447.8e.
Pilocytic astrocytoma (WHO grade I) is a circumscribed, slowly growing, benign astrocytoma that most frequently develops in the cerebellar hemispheres and in midline structures and occurs predominantly in childhood and adolescence. In contrast to diffusely infiltrating gliomas in adults (e.g. grade II astrocytomas, oligodendrogliomas), survival of patients with pilocytic astrocytoma is excellent after surgical intervention. To search for potential molecular mechanisms underlying its benign biologic behavior, we compared gene expression profiles of pilocytic astrocytomas (8 cases) with those of normal cerebellum (4 cases), low-grade astrocytomas (WHO grade II; 15 cases), and oligodendrogliomas (WHO grade II; 17 cases) by cDNA array analysis. A number of immune system-related genes such as HLA-DRalpha, HLA-DPB1, HLA-DQB1, IgG3, IgGK, FCER1G, A2M, FCRN, IFI-56K, and DAP12 were upregulated in pilocytic astrocytomas relative to normal cerebellum, grade II astrocytomas, and oligodendrogliomas. Genes expressed at higher levels in pilocytic astrocytomas than in grade II astrocytomas and oligodendrogliomas include HLA-DRalpha, HLA-DPA1, HLA-DPB1, HLA-DQB1, A2M, TIMP1, TIMP2, CDKN1A, and SOCS3 and those expressed at lower levels include EGFR and PDGFRA. Hierarchical clustering analysis using the entire set of 1176 genes distinguished pilocytic astrocytomas from grade II astrocytomas and oligodendrogliomas. Clustering analysis using selected subgroups of genes based on their molecular functions revealed that immune system-related genes (75 genes) or cell adhesion, migration, and angiogenesis-related genes (69 genes) showed similar power to the entire gene set for separation of pilocytic astrocytomas from diffusely infiltrating low-grade gliomas. Immunohistochemistry revealed that HLA-DRalpha is expressed diffusely in neoplastic cells in pilocytic astrocytomas, whereas in oligodendrogliomas, expression was limited to scattered reactive astrocytes. These results suggest that gene expression profiles of pilocytic astrocytomas differ significantly from those of diffusely infiltrating low-grade gliomas and that their benign biologic behavior may be related to upregulation of immune defense-associated genes.
毛细胞型星形细胞瘤(世界卫生组织一级)是一种边界清晰、生长缓慢的良性星形细胞瘤,最常发生于小脑半球和中线结构,主要见于儿童和青少年。与成人弥漫性浸润性胶质瘤(如二级星形细胞瘤、少突胶质细胞瘤)不同,毛细胞型星形细胞瘤患者手术干预后的生存率很高。为了探寻其良性生物学行为潜在的分子机制,我们通过cDNA阵列分析比较了毛细胞型星形细胞瘤(8例)与正常小脑(4例)、低级别星形细胞瘤(世界卫生组织二级;15例)及少突胶质细胞瘤(世界卫生组织二级;17例)的基因表达谱。相对于正常小脑、二级星形细胞瘤和少突胶质细胞瘤,毛细胞型星形细胞瘤中一些与免疫系统相关的基因如HLA - DRα、HLA - DPB1、HLA - DQB1、IgG3、IgGK、FCER1G、A2M、FCRN、IFI - 56K和DAP12上调。在毛细胞型星形细胞瘤中表达水平高于二级星形细胞瘤和少突胶质细胞瘤的基因包括HLA - DRα、HLA - DPA1、HLA - DPB1、HLA - DQB1、A2M、TIMP1、TIMP2、CDKN1A和SOCS3,而表达水平较低的基因包括EGFR和PDGFRA。使用全部1176个基因进行层次聚类分析可将毛细胞型星形细胞瘤与二级星形细胞瘤和少突胶质细胞瘤区分开来。基于分子功能使用选定基因亚组进行聚类分析显示,与免疫系统相关的基因(75个基因)或与细胞黏附、迁移及血管生成相关的基因(69个基因)在将毛细胞型星形细胞瘤与弥漫性浸润性低级别胶质瘤区分开来方面与整个基因集具有相似的能力。免疫组织化学显示,HLA - DRα在毛细胞型星形细胞瘤的肿瘤细胞中弥漫性表达,而在少突胶质细胞瘤中,表达仅限于散在的反应性星形胶质细胞。这些结果表明,毛细胞型星形细胞瘤的基因表达谱与弥漫性浸润性低级别胶质瘤有显著差异,其良性生物学行为可能与免疫防御相关基因的上调有关。