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首页> 外文期刊>Journal of Cancer Therapy >No Association between p53 Immunohistochemical Staining and RASSF1 or DAPK1 Hypermethylation in Non-Small Cell Lung Cancer
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No Association between p53 Immunohistochemical Staining and RASSF1 or DAPK1 Hypermethylation in Non-Small Cell Lung Cancer

机译:在非小细胞肺癌中,p53免疫组织化学染色与RASSF1或DAPK1甲基化程度之间无关联

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p53 mutations have been linked with shortened survival rates in non-small cell lung cancer (NSCLC). Hypermethylation of RASSF1 and DAPK1 genes, which are downstream targets of p53, has also been linked to a poor prognosis in lung cancer patients. We investigated whether p53 mutations, assessed as p53 stabilization by immunohistochemistry (IHC), were independent of DAPK1 and RASSF1 promoter hypermethylation. We examined 103 resected NSCLC tumors for which we had p53 IHC and RASSF1 and DAPK1 methylation data. p53 protein expression was determined by IHC and graded using a semi-quantitative scoring method. DAPK1 and RASSF1 methylations were determined on tumor blocks by MethyLight real-time PCR assays represented as the percent of methylated reference DNA (PMR). Our primary results found no evidence for an association between the p53 IHC score and RASSF1 and DAPK1 PMR values, P = 0.46 and P = 0.68, respectively.
机译:在非小细胞肺癌(NSCLC)中,p53突变与存活率降低有关。 RASSF1和DAPK1基因的高甲基化是p53的下游靶标,也与肺癌患者的不良预后有关。我们调查了p53突变(通过免疫组织化学(IHC)评估为p53稳定化)是否独立于DAPK1和RASSF1启动子超甲基化。我们检查了103例切除的NSCLC肿瘤,这些肿瘤具有p53 IHC和RASSF1和DAPK1甲基化数据。通过IHC确定p53蛋白表达,并使用半定量评分方法对其进行分级。通过MethyLight实时PCR测定法在肿瘤块上确定了DAPK1和RASSF1甲基化,以甲基化参考DNA(PMR)的百分比表示。我们的主要结果没有发现p53 IHC评分与RASSF1和DAPK1 PMR值相关的证据,分别为P = 0.46和P = 0.68。

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