首页> 外文期刊>European review for medical and pharmacological sciences. >Reduced EBP50 expression or mis-localization of the EBP50 protein is associated with the malignant progression of esophageal squamous cell carcinoma
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Reduced EBP50 expression or mis-localization of the EBP50 protein is associated with the malignant progression of esophageal squamous cell carcinoma

机译:EBP50表达降低或EBP50蛋白错误定位与食管鳞状细胞癌的恶性进展有关

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PURPOSE: The aim of this study was to examine the significance of EBP50 (ezrin-radixin-moesin binding phosphoprotein 50) expression in esophageal squamous cell carcinoma (ESCC). MATERIALS AND METHODS: Real-time PCR (qRT-PCR), western blotting, and immunohistochemical staining were performed to detect EBP50 expression in pairs of ESCCs and matched non-tumor tissues, and the relationships between EBP50 expression and other clinical factors in ESCC were analyzed. An iRNA targeting EBP50 was transfected into EC9706 cells. MTT and plate colony assays were performed to assess the effects of EBP50 down-regulation on cell growth, and flow cytometry was used to evaluate the influence of inhibiting EBP50 on cell cycle progression. RESULTS: The real-time PCR (qRT-PCR), western blotting, and immunohistochemical staining results showed that EBP50 expression was significantly lower in ESCCs compared to matched non-tumor tissues. In addition, decreased EBP50 expression correlated with differentiation, T stage, lymph node (LN) metastasis, and poor prognosis in patients with ESCC. The down-regulation of EBP50 may significantly promote the growth and proliferation of EC9706 cells while accelerating cell cycle progression from the G1to S phase. CONCLUSIONS: EBP50 expression was decreased in ESCC, indicating that EBP50 might play a significant role in the malignant progression of ESCC and be a prognostic marker for patients with ESCC.
机译:目的:本研究的目的是检查在食管鳞状细胞癌(ESCC)中EBP50(ezrin-radixin-moesin结合磷酸蛋白50)表达的意义。材料与方法:采用实时荧光定量PCR(qRT-PCR),蛋白质印迹法和免疫组织化学染色法检测成对的ESCCs和匹配的非肿瘤组织中的EBP50表达,EBP50表达与ESCC中其他临床因素之间的关系为分析。将靶向EBP50的iRNA转染到EC9706细胞中。进行MTT和平板菌落分析以评估EBP50下调对细胞生长的影响,并且使用流式细胞术评估抑制EBP50对细胞周期进程的影响。结果:实时荧光定量PCR(qRT-PCR),免疫印迹和免疫组织化学染色结果表明,与匹配的非肿瘤组织相比,ESCCs中的EBP50表达明显更低。此外,ESCP患者中EBP50表达降低与分化,T期,淋巴结转移和预后不良有关。 EBP50的下调可能会显着促进EC9706细胞的生长和增殖,同时加速从G1期到S期的细胞周期进程。结论:ESCC中EBP50表达降低,提示EBP50可能在ESCC的恶性进展中起重要作用,并可能成为ESCC患者的预后指标。

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