Hartmann Christian, Bartels Gesine, Gehlhaar Claire, Holtkamp Nikola, von Deimling Andreas
Department of Neuropathology, Charité, Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.
Acta Neuropathol. 2005 Jun;109(6):639-42. doi: 10.1007/s00401-005-1000-1. Epub 2005 May 28.
Glioblastoma multiforme WHO grade IV is the most common and malignant variant of astrocytic tumors. Loss of heterozygosity of chromosome 10 and mutations in the tumor suppressor gene PTEN on 10q are molecular hallmarks of glioblastomas. Recently, mutations were identified in PIK3CA, encoding a protein that antagonizes the function of PTEN protein in the PI3K/Akt pathway. To address the question whether an exclusive mutation pattern can be observed in PIK3CA and PTEN, we determined the frequency of mutations in both genes. All coding exons were examined by single strand confirmation polymorphism and direct sequencing. Additionally, we analyzed chromosome 10 for loss of heterozygosity and evaluated the mutational status of TP53. In 70 glioblastomas, 5 (7%) PIK3CA mutations and 10 (14%) PTEN mutations were found. All mutations in PIK3CA located to exons 1, 9 and 20, thereby supporting the concept of mutational hot spot regions. In all but one glioblastoma, mutations were seen either in PIK3CA or in PTEN. In conclusion, the frequency of PIK3CA mutations in glioblastomas appears to be much lower than initially reported.
世界卫生组织IV级多形性胶质母细胞瘤是星形细胞瘤中最常见且恶性程度最高的变异类型。10号染色体杂合性缺失以及10q上肿瘤抑制基因PTEN的突变是胶质母细胞瘤的分子特征。最近,在编码一种在PI3K/Akt信号通路中拮抗PTEN蛋白功能的蛋白质的PIK3CA基因中发现了突变。为了探讨PIK3CA和PTEN基因中是否能观察到独特的突变模式,我们测定了这两个基因的突变频率。通过单链构象多态性和直接测序对所有编码外显子进行检测。此外,我们分析了10号染色体的杂合性缺失情况,并评估了TP53的突变状态。在70例胶质母细胞瘤中,发现5例(7%)PIK3CA突变和10例(14%)PTEN突变。PIK3CA的所有突变均位于外显子1、9和20,从而支持了突变热点区域的概念。除1例胶质母细胞瘤外,所有病例中PIK3CA或PTEN均有突变。总之,胶质母细胞瘤中PIK3CA突变的频率似乎比最初报道的要低得多。