Analysis of a single nucleotide polymorphism in codon 388 of the FGFR4 gene in malignant gliomas

被引:17
|
作者
Mawrin, Christian
Kirches, Elmar
Diete, Sabine
Wiedemann, Falk R.
Schneider, Thomas
Firsching, Raimund
Kropf, Siegfried
Bogerts, Bernhard
Vorwerk, Christian K.
Kruger, Sabine
Dietzmann, Knut
机构
[1] Otto Von Guericke Univ, Dept Neuropathol, Inst Neuropathol, D-39120 Magdeburg, Germany
[2] Otto Von Guericke Univ, Dept Neurol, D-39120 Magdeburg, Germany
[3] Otto Von Guericke Univ, Dept Neurosurg, D-39120 Magdeburg, Germany
[4] Otto Von Guericke Univ, Dept Biometr, D-39120 Magdeburg, Germany
[5] Otto Von Guericke Univ, Dept Psychiat, D-39120 Magdeburg, Germany
[6] Otto Von Guericke Univ, Dept Ophthalmol, D-39120 Magdeburg, Germany
[7] Otto Von Guericke Univ, Dept Pathol, D-39120 Magdeburg, Germany
关键词
glioblastoma multiforme; FGFR4; survival;
D O I
10.1016/j.canlet.2005.08.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The FGFR4 codon 388 polymorphism (Arg(388), Arg/Gly(388) or Gly(388)) was determined in glioblastoma multiforme (GBM), anaplastic astrocytomas (AA), diffuse astrocytomas (DA), and control muscles. Arg(388) was rare in AA, GBM, muscles, and was absent in DA. The Arg/Gly(388) and the Gly(388) frequency was equal among GBM and controls. FGFR4 expression was not related to codon 388 in GBM, and no survival differences between Arg/Gly(388) and Gly(388) tumors were found. U87 cells (Arg/Gly(388)) did not show higher invasion than U138 cells (Gly(388)). This suggests that the FGFR4 codon 388 status does not play a major role in malignant gliomas. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:239 / 245
页数:7
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