International Agency for Research on Cancer, Lyon, France.
Neuropathology. 2011 Dec;31(6):583-8. doi: 10.1111/j.1440-1789.2011.01204.x. Epub 2011 Mar 7.
The aim of this study was to establish the frequency of amplification of tyrosine kinase receptor genes PDGFRA, KIT and KDR (VEGFR2) at 4q12 in glioblastomas at a population level, and to assess whether such alterations have any clinical impact. Screening of 390 glioblastomas from a population-based study by differential PCR revealed amplification of the PDGFRA, KIT and KDR genes in 33 (8.5%), 17 (4.4%) and 13 (3.3%) glioblastomas, respectively. None of these alterations was prognostic for overall survival. Patients with glioblastoma showing KIT amplification were significantly younger than those with glioblastoma showing no amplification (51.7 ± 21.7 years vs. 59.3 ± 13.1 years; P=0.0231). Twelve glioblastomas showed concurrent amplification of the PDGFRA, KIT and KDR genes, whereas 18 glioblastomas showed PDGFRA amplification only. A significant inverse association was observed between KIT amplification and EGFR amplification (P=0.0260), whereas a borderline positive association was found between KIT amplification and TP53 mutation (P=0.0579). No significant difference was observed in the frequency of amplification of these genes in primary and secondary glioblastomas or in glioblastomas with and without IDH1 mutations, suggesting that amplification of PDGFRA, KIT and KDR may be implicated in the pathogenesis of a small fraction of both subtypes of glioblastoma.
本研究旨在确定 PDGFRA、KIT 和 KDR(VEGFR2)酪氨酸激酶受体基因在人群水平上于 4q12 的扩增频率,并评估这些改变是否具有任何临床影响。通过差异 PCR 对基于人群的研究中的 390 例胶质母细胞瘤进行筛选,结果显示 PDGFRA、KIT 和 KDR 基因分别在 33 例(8.5%)、17 例(4.4%)和 13 例(3.3%)胶质母细胞瘤中扩增。这些改变均与总生存期无关。显示 KIT 扩增的胶质母细胞瘤患者明显比未显示 KIT 扩增的患者年轻(51.7±21.7 岁 vs. 59.3±13.1 岁;P=0.0231)。12 例胶质母细胞瘤同时显示 PDGFRA、KIT 和 KDR 基因扩增,而 18 例胶质母细胞瘤仅显示 PDGFRA 扩增。观察到 KIT 扩增与 EGFR 扩增呈显著负相关(P=0.0260),而 KIT 扩增与 TP53 突变呈边缘正相关(P=0.0579)。在原发性和继发性胶质母细胞瘤或 IDH1 突变阳性和阴性的胶质母细胞瘤中,这些基因的扩增频率没有显著差异,这表明 PDGFRA、KIT 和 KDR 的扩增可能与这两种亚型的一小部分胶质母细胞瘤的发病机制有关。