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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >p21WAF1 protein expression determined by quantitative immunoassay in relation to non-small-cell lung cancer aggressiveness.
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p21WAF1 protein expression determined by quantitative immunoassay in relation to non-small-cell lung cancer aggressiveness.

机译:通过定量免疫测定确定的p21WAF1蛋白表达与非小细胞肺癌侵袭性相关。

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PURPOSE: p21WAF1, a cyclin-dependent kinase inhibitor, is an important mediator of the cell-cycle arrest and tumor suppression induced by the protein p53. Although alterations of the p53 gene and its overexpression are frequent in most malignancies, including non-small-cell lung cancer (NSCLC), and may be associated with poor patient prognosis, the clinical utility of p21WAF1 expression in NSCLC has not been established. METHODS: We have used a commercial enzyme-linked immunosorbent assay (ELISA) kit for p21WAF1 to test soluble extracts of 54 NSCLC specimens with known clinicopathological properties. RESULTS: There was no correlation between p21WAF1 and p53 concentrations, the latter being determined by a time-resolved immunofluorometric assay developed in-house. Furthermore, p21WAF1 levels were not associated with patient age, tumorode/metastasis (TNM) stage, lymph node metastasis, histological grade or type, or smoking history, in Mann-Whitney analysis. chi2-tests, based on cutoffs equal to the 25th, 50th, or 75th percentiles of the p21WAF1 distribution, similarly did not reveal any statistically significant associations between p21WAF1 and other clinicopathological variables. Because of the small number of patients and the median follow-up of only 18 months, a meaningful survival analysis could not be performed. CONCLUSION: In summary, this preliminary study suggests that ELISA-quantified p21WAF1 levels in NSCLC extracts are weaker than p53 in terms of prognostic value and do not contribute to the further subclassification of patients.
机译:目的:细胞周期蛋白依赖性激酶抑制剂p21WAF1是由蛋白p53诱导的细胞周期停滞和肿瘤抑制的重要介体。尽管p53基因的改变及其过表达在包括非小细胞肺癌(NSCLC)在内的大多数恶性肿瘤中都很常见,并且可能与患者预后不良相关,但尚未确定p21WAF1在NSCLC中的临床应用。方法:我们使用了用于p21WAF1的商业酶联免疫吸附测定(ELISA)试剂盒来测试54例具有已知临床病理特性的NSCLC标本的可溶性提取物。结果:p21WAF1和p53浓度之间没有相关性,后者是通过内部开发的时间分辨免疫荧光测定法确定的。此外,在Mann-Whitney分析中,p21WAF1水平与患者年龄,肿瘤/淋巴结转移(TNM)阶段,淋巴结转移,组织学等级或类型或吸烟史无关。 chi2-test(基于等于p21WAF1分布的第25、50或75个百分位数的临界值)相似地没有揭示p21WAF1与其他临床病理变量之间的任何统计学显着关联。由于患者人数少且中位随访期仅为18个月,因此无法进行有意义的生存分析。结论:总的来说,这项初步研究表明,ELISA定量的NSCLC提取物中的p21WAF1水平在预后价值方面较p53弱,并且无助于进一步分类患者。

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