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Clinical significance of altered nm23-H1, EGFR, RB and p53 expression in bilharzial bladder cancer

机译:nm23-H1,EGFR,RB和p53表达在胆管癌中的临床意义

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Background Clinical characterization of bladder carcinomas is still inadequate using the standard clinico-pathological prognostic markers. We assessed the correlation between nm23-H1 , Rb, EGFR and p53 in relation to the clinical outcome of patients with muscle invasive bilharzial bladder cancer (MI-BBC). Methods nm23-H1 , Rb, EGFR and p53 expression was assessed in 59 MI-BBC patients using immunohistochemistry and reverse transcription (RT-PCR) and was correlated to the standard clinico-pathological prognostic factors, patient's outcome and the overall survival (OS) rate. Results Overexpression of EGFR and p53 proteins was detected in 66.1% and 35.6%; respectively. Loss of nm23-H1 and Rb proteins was detected in 42.4% and 57.6%; respectively. Increased EGFR and loss of nm23-H1 RNA were detected in 61.5% and 36.5%; respectively. There was a statistically significant correlation between p53 and EGFR overexpression ( p Conclusion nm23-H1, EGFR and p53 could be used as prognostic biomarkers in MI-BBC patients. In addition to the standard pathological prognostic factors, a combination of these markers (≥ 2) has synergistic effects in stratifying patients into variable risk groups. The higher is the number of altered biomarkers, the higher will be the risk of disease progression and death.
机译:背景技术使用标准的临床病理预后标志物仍不足以对膀胱癌进行临床表征。我们评估了nm23-H1,Rb,EGFR和p53与肌肉浸润性胆道膀胱癌(MI-BBC)患者的临床结局之间的相关性。方法采用免疫组织化学和逆转录(RT-PCR)技术对59例MI-BBC患者的nm23-H1,Rb,EGFR和p53表达进行评估,并将其与标准的临床病理预后因素,患者预后和总生存期(OS)相关联率。结果EGFR和p53蛋白过表达的比例分别为66.1%和35.6%;分别。检测到nm23-H1和Rb蛋白的丢失率为42.4%和57.6%;分别。表皮生长因子受体升高和nm23-H1 RNA丢失的比例分别为61.5%和36.5%;分别。 p53和EGFR过表达之间存在统计学上的显着相关性(p结论nm23-H1,EGFR和p53可用作MI-BBC患者的预后生物标志物。除标准病理预后因素外,这些标志物的组合(≥2 )在将患者分为不同的风险组中具有协同作用,改变的生物标志物数量越多,疾病进展和死亡的风险就越高。

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