Taubert H, Meye A, Bache M, Hinze R, Holzhausen H J, Schmidt H, Rath F W, Dunst J, Würl P
Institute of Pathology, Martin Luther University of Halle-Wittenberg, Germany.
Strahlenther Onkol. 1998 Aug;174(8):427-30. doi: 10.1007/BF03038565.
Following therapeutic irradiation after a latency period of many years radiation-induced tumors, often sarcomas, can arise. Results of radiation-induced DNA damage can be 1. p53 over-expression, inducing growth arrest or apoptosis, and 2. occurrence of mutations, frequently including the p53 gene, as one molecular promotor for carcinogenesis. We were interested whether radiation-induced sarcomas are associated with alterations of the p53 status.
Samples from 11 radiation-induced soft-tissue sarcomas (STS) were studied by a non-radioactive PCR-SSCP sequencing analysis and by immunohistochemistry with five antibodies for their p53 status.
A tumor of one patient possessed a G->A transition in codon 280 (exon 8). Of 11 tumors, 9 showed nuclear p53 positivity, detected by monoclonal antibody DO-1. Of these 9 patients, 7 died during the observation period, whereas the 2 patients with DO-1 negative tumor samples are still alive.
p53 over-expression and p53 mutation occur in radiation-induced STS. p53 status is expected to have prognostic impact for radiation-induced STS.
在经过多年潜伏期后接受放射治疗,可能会引发辐射诱导的肿瘤,通常为肉瘤。辐射诱导的DNA损伤结果可能为:1. p53过度表达,诱导生长停滞或凋亡;2. 发生突变,常包括p53基因,作为致癌作用的一种分子促进因素。我们感兴趣的是辐射诱导的肉瘤是否与p53状态的改变有关。
通过非放射性PCR-SSCP测序分析和使用五种抗体进行免疫组织化学检测,研究了11例辐射诱导的软组织肉瘤(STS)样本的p53状态。
一名患者的肿瘤在密码子280(外显子8)处发生了G->A转变。在11例肿瘤中,9例通过单克隆抗体DO-1检测显示核p53阳性。在这9例患者中,7例在观察期内死亡,而2例DO-1阴性肿瘤样本的患者仍然存活。
p53过度表达和p53突变发生在辐射诱导的STS中。预计p53状态对辐射诱导的STS具有预后影响。