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首页> 外文期刊>American Journal of Cancer Research >Elevated HBXIP expression is associated with aggressive phenotype and poor prognosis in esophageal squamous cell carcinoma
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Elevated HBXIP expression is associated with aggressive phenotype and poor prognosis in esophageal squamous cell carcinoma

机译:食管鳞癌中HBXIP表达升高与侵袭性表型和预后不良有关

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The oncoprotein hepatitis B virus X-interacting protein (HBXIP) has been suggested to play an essential role in several malignancies. However, the clinicopathological significance and prognostic value of HBXIP expression in esophageal squamous cell carcinoma (ESCC) is still unknown. Therefore the aim of this study was to characterize HBXIP expression and its prognostic value in ESCC. Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot were performed to assess the mRNA and protein expression of HBXIP in ESCC tissues and cell lines. Immunohistochemistry (IHC) was conducted to characterize the expression pattern of HBXIP in 152 archived paraffin-embedded ESCC and matched nontumorous tissues. The mRNA and protein expression of HBXIP in ESCC tissues was significantly higher than those in adjacent nontumorous tissues. High HBXIP expression was associated with histological grade (P=0.016), depth of tumor invasion (P=0.012), lymph node metastasis (P<0.001) and TNM stage (P=0.002). Kaplan-Meier analysis indicated that ESCC patients with high HBXIP expression had poor disease-free survival (DFS) and overall survival (OS). Furthermore, multivariate Cox regression analyses demonstrated that HBXIP expression remained an independent prognostic factor for DFS and OS. Collectively, our present study demonstrated that HBXIP may be a candidate molecular prognostic marker for ESCC.
机译:已建议癌蛋白B型肝炎病毒X相互作用蛋白(HBXIP)在几种恶性肿瘤中起重要作用。然而,HBXIP表达在食管鳞状细胞癌(ESCC)中的临床病理学意义和预后价值仍然未知。因此,本研究的目的是表征HBXIP表达及其在ESCC中的预后价值。进行实时定量聚合酶链反应(qRT-PCR)和蛋白质印迹,以评估ESCC组织和细胞系中HBXIP的mRNA和蛋白表达。进行了免疫组织化学(IHC)来表征HBXIP在152个已存档石蜡包埋的ESCC和匹配的非肿瘤组织中的表达模式。食管鳞癌组织中HBXIP的mRNA和蛋白表达显着高于癌旁组织。 HBXIP高表达与组织学分级(P = 0.016),肿瘤浸润深度(P = 0.012),淋巴结转移(P <0.001)和TNM分期(P = 0.002)有关。 Kaplan-Meier分析表明,HBXIP高表达的ESCC患者的无病生存期(DFS)和总体生存期(OS)较差。此外,多变量Cox回归分析表明HBXIP表达仍然是DFS和OS的独立预后因素。总体而言,我们目前的研究表明HBXIP可能是ESCC的分子预后标志物。

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