Huang Hervé, Okamoto Yoshikazu, Yokoo Hideaki, Heppner Frank L, Vital Anne, Fevre-Montange Michelle, Jouvet Anne, Yonekawa Yasuhiro, Lazaridis Emmanuel N, Kleihues Paul, Ohgaki Hiroko
International Agency for Research on Cancer (IARC), 150 Cours Albert-Thomas, F-69372 Lyon Cedex 08, France.
Oncogene. 2004 Aug 5;23(35):6012-22. doi: 10.1038/sj.onc.1207781.
The histological diagnosis of low-grade astrocytomas and oligodendrogliomas (WHO grade II) is often challenging, particularly in cases that show both astrocytic and oligodendroglial differentiation. We carried out gene expression profiling on 17 oligodendrogliomas (93% with LOH 1p and/or 19q) and 15 low-grade astrocytomas (71% with a TP53 mutation), using a cDNA array containing 1176 cancer-related genes. In oligodendrogliomas, 40 genes showed on average higher expression (at least a two-fold increase) than in astrocytomas, including DES, TDGF1, TGF-beta, GABA-BR1A, Histone H4, CDKN1A, PCDH43, Rho7 and Jun-D, while 39 genes were expressed at lower levels (at least a two-fold decrease), including JNK2, ITGB4, JNK3A2, RhoC, IFI-56K, AAD14 and EGFR. Immunohistochemistry revealed nuclear staining of Jun-D in oligodendrogliomas, in contrast to the immunoreactivity of cytoplasm and cell processes in low-grade astrocytomas. Partial least-squares analysis of the 79 genes at least two-fold differentially expressed between oligodendrogliomas and low-grade astrocytomas demonstrated perfect separation of oligodendrogliomas from low-grade astrocytomas and normal cerebral white matter. Clustering analysis based on the entire gene set divided the 17 subjects with oligodendrogliomas into two subgroups with significantly different survival (log-rank test, P=0.0305; survival to 5-years, 80 vs 0%, P=0.048). These results demonstrate that oligodendrogliomas and low-grade astrocytomas differ in their gene expression profiles, and that there are subgroups of oligodendroglioma with distinct expression profiles related to clinical outcome.
低级别星形细胞瘤和少突胶质细胞瘤(世界卫生组织二级)的组织学诊断通常具有挑战性,尤其是在那些显示星形细胞和少突胶质细胞分化的病例中。我们使用包含1176个癌症相关基因的cDNA阵列,对17例少突胶质细胞瘤(93%伴有1p和/或19q杂合性缺失)和15例低级别星形细胞瘤(71%伴有TP53突变)进行了基因表达谱分析。在少突胶质细胞瘤中,40个基因平均表达水平比星形细胞瘤高(至少增加两倍),包括结蛋白(DES)、畸胎瘤衍生生长因子1(TDGF1)、转化生长因子-β(TGF-beta)、γ-氨基丁酸B受体1A(GABA-BR1A)、组蛋白H4、细胞周期蛋白依赖性激酶抑制剂1A(CDKN1A)、原钙黏蛋白43(PCDH43)、Rho7和Jun-D,而39个基因表达水平较低(至少降低两倍),包括应激活化蛋白激酶2(JNK2)、整合素β4(ITGB4)、JNK3A2、RhoC、干扰素诱导蛋白56K(IFI-56K)、醛脱氢酶家族1成员4(AAD14)和表皮生长因子受体(EGFR)。免疫组织化学显示,Jun-D在少突胶质细胞瘤中呈核染色,而在低级别星形细胞瘤中呈细胞质和细胞突起免疫反应。对少突胶质细胞瘤和低级别星形细胞瘤之间至少两倍差异表达的79个基因进行偏最小二乘法分析,结果显示少突胶质细胞瘤与低级别星形细胞瘤以及正常脑白质完全分离。基于整个基因集的聚类分析将17例少突胶质细胞瘤患者分为两个亚组,其生存率有显著差异(对数秩检验,P = 0.0305;5年生存率,80%对0%,P = 0.048)。这些结果表明,少突胶质细胞瘤和低级别星形细胞瘤在基因表达谱上存在差异,并且少突胶质细胞瘤存在与临床结局相关的具有不同表达谱的亚组。