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Elevated expression of ΔNp63 in advanced esophageal squamous cell carcinoma

机译:ΔNp63在晚期食管鳞癌中的表达升高

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摘要

This study aims to explore the expression level of ΔNp63 in esophageal squamous cell carcinoma (ESCC). To investigate the association between ΔNp63 (p40) expression and ESCC biology, we compared the levels of ΔNp63 expression in normal and tumor tissues, with a specific focus on the diagnostic value of ΔNp63 in ESCC. We analyzed 160 consecutive patients with ESCC who underwent surgical resection without neoadjuvant chemotherapy at Gunma University Hospital (Maebashi, Japan) between September 2000 and January 2010. The clinicopathological characteristics and survival of patients were subclassified based on the expression of ΔNp63 as determined by immunohistochemistry, indicating that ΔNp63 was highly expressed in 75.6% (121/160) of ESCC patients. Clinicopathological analysis of ΔNp63 expression showed that ΔNp63‐positive tumors significantly correlated with two important clinical parameters: T factor (P = 0.0316) and venous invasion (P = 0.0195). The 5‐year overall survival rates of advanced ESCC patients with positive and negative expression of ΔNp63 were 35.6% and 71.7%, respectively. Multivariate analysis revealed that the expression of ΔNp63 was identified as an independent prognostic factor (P = 0.0049) in advanced ESCC. In line with this, ΔNp63α‐transduced ESCC cell lines increased tumor growth in a soft agar colony formation assay. We report here for the first time that ΔNp63 expression increases the oncogenic potential of ESCC and is an independent marker for predicting poor outcome in advanced ESCC. Our findings suggest that ΔNp63 could serve as a new diagnostic marker for ESCC and might be a relevant therapeutic target for the treatment of patients with this disease.
机译:本研究旨在探讨ΔNp63在食管鳞状细胞癌(ESCC)中的表达水平。为了研究ΔNp63(p40)表达与ESCC生物学之间的关系,我们比较了正常组织和肿瘤组织中ΔNp63表达的水平,特别关注了ΔNp63在ESCC中的诊断价值。我们分析了2000年9月至2010年1月间在群马大学医院(日本前桥市)接受无新辅助化疗手术切除的ESCCC连续患者160例。根据免疫组织化学方法确定的ΔNp63的表达将患者的临床病理特征和生存分为亚类,表明ΔNp63在73.6%(121/160)的ESCC患者中高表达。对ΔNp63表达的临床病理分析表明,ΔNp63阳性肿瘤与两个重要的临床参数显着相关:T因子(P = 0.0316)和静脉浸润(P = 0.0195)。 ΔNp63阳性和阴性的晚期ESCC患者的5年总生存率分别为35.6%和71.7%。多变量分析显示,ΔNp63的表达被确定为晚期ESCC的独立预后因素(P = 0.0049)。与此相符,在软琼脂菌落形成试验中,ΔNp63α转导的ESCC细胞系增加了肿瘤的生长。我们在这里首次报道ΔNp63表达增加了ESCC的致癌潜力,并且是预测晚期ESCC不良预后的独立标志物。我们的发现表明,ΔNp63可以作为ESCC的新诊断标记,并且可能是治疗该病患者的相关治疗靶标。

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