al-Sarraj S, Bridges L R, Cawkwell L, Lewis F A, Quirke P
Department of Neuropathology, Institute of Psychiatry, London, UK.
Neuropathol Appl Neurobiol. 1995 Aug;21(4):344-51. doi: 10.1111/j.1365-2990.1995.tb01069.x.
Previous reports have shown that p53 gene alteration plays an important role in tumourigenesis. Allelic loss of 17p in astrocytomas was detected in previous studies by restriction fragment length polymorphisms (RFLP). In this study we have analysed 47 cases of astrocytic tumours (26 glioblastomas [grade IV], 11 anaplastic astrocytomas [grade III], seven fibrillary astrocytomas [grade II] and three pilocytic astrocytomas [grade I]) for the presence of allelic imbalance at the p53 gene locus using intragenic markers. We used an informative method based on microsatellite polymorphisms at the p53 gene locus and fluorescent PCR. The fluorescently-labelled PCR products were then detected and analysed using an automated DNA sequencer with appropriate software. Seven of 47 (14.9%) cases were homozygous (uninformative). Five of the remaining 40 cases (12.5%) showed allelic imbalance at the p53 locus (three anaplastic astrocytomas [grade III] and two glioblastomas [grade IV]). None of the fibrillary astrocytomas (grade II) or pilocytic astrocytomas (grade I) showed allelic imbalance at the p53 locus. These results suggest that allelic imbalance at the p53 locus is not frequent and when it does occur is in high grade tumours.
先前的报道表明,p53基因改变在肿瘤发生中起重要作用。以往的研究通过限制性片段长度多态性(RFLP)检测星形细胞瘤中17号染色体短臂的等位基因缺失。在本研究中,我们使用基因内标记分析了47例星形细胞肿瘤(26例胶质母细胞瘤[IV级]、11例间变性星形细胞瘤[III级]、7例纤维型星形细胞瘤[II级]和3例毛细胞型星形细胞瘤[I级])p53基因位点等位基因失衡的情况。我们采用了一种基于p53基因位点微卫星多态性和荧光PCR的信息性方法。然后使用带有适当软件的自动DNA测序仪检测和分析荧光标记的PCR产物。47例中有7例(14.9%)为纯合子(无信息)。其余40例中有5例(12.5%)在p53位点显示等位基因失衡(3例间变性星形细胞瘤[III级]和2例胶质母细胞瘤[IV级])。纤维型星形细胞瘤(II级)或毛细胞型星形细胞瘤(I级)在p53位点均未显示等位基因失衡。这些结果表明,p53位点的等位基因失衡并不常见,且一旦发生则多见于高级别肿瘤。