Hurtt M R, Moossy J, Donovan-Peluso M, Locker J
Department of Pathology, University of Pittsburgh School of Medicine, PA 15261.
J Neuropathol Exp Neurol. 1992 Jan;51(1):84-90. doi: 10.1097/00005072-199201000-00010.
In order to evaluate the incidence and prognostic significance of gene amplification in primary brain neoplasms we measured the number of gene copies per cell of three oncogenes (epidermal growth factor receptor [EGFR] gene, N-myc, C-myc) and syntenic control genes in 40 specimens using quantitative DNA dot blots. We observed EGFR gene amplification in astrocytomas and anaplastic astrocytomas with approximately the same incidence as in glioblastoma multiforme (33%), although large amplifications were only seen in glioblastoma multiforme. Fourteen patients had a supratentorial glioblastoma multiforme; six had EGFR gene amplification and eight had either normal EGFR gene copy number or elevated EGFR copy number attributable to extra copies of chromosome 7. Patients with gene amplification had shorter survival than patients without gene amplification (p = 0.01). The observed difference in survival was not likely to be due to group differences in age, sex, treatment, or histopathology.
为了评估原发性脑肿瘤中基因扩增的发生率及其预后意义,我们使用定量DNA斑点印迹法,测定了40份标本中三个癌基因(表皮生长因子受体[EGFR]基因、N - myc、C - myc)以及同线对照基因的每个细胞的基因拷贝数。我们在星形细胞瘤和间变性星形细胞瘤中观察到EGFR基因扩增,其发生率与多形性胶质母细胞瘤中的发生率大致相同(33%),不过只有在多形性胶质母细胞瘤中观察到了大量扩增。14例患者患有幕上多形性胶质母细胞瘤;6例有EGFR基因扩增,8例EGFR基因拷贝数正常或因7号染色体额外拷贝而导致EGFR拷贝数升高。基因扩增的患者比无基因扩增的患者生存期短(p = 0.01)。观察到的生存期差异不太可能归因于年龄、性别、治疗或组织病理学方面的组间差异。