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Clinicopathological significance of fascin-1 expression in patients with non-small cell lung cancer

机译:Fascin-1在非小细胞肺癌患者中的表达及其临床病理意义

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Purpose: Fascin-1 promotes the formation of filopodia, lamellipodia, and microspikes of cell membrane after its cross-linking with F-actin, thereby enhancing the cell movement and metastasis and invasion of tumor cells. This study explored the fascin-1 protein’s expression in non-small cell lung cancer (NSCLC) tissues and its relationship with clinical pathology and prognostic indicators.Methods: Immunohistochemical analysis was used to determine the expression of fascin-1 in NSCLC tissues. We used quantitative real-time polymerase chain reaction and western blot analysis to further verify the results. The fascin-1 expression and statistical method for clinical pathological parameters are examined by χ2. Kaplan–Meier method is used for survival analysis. Cox’s Proportional Hazard Model was used to conduct a combined-effect analysis for each covariate.Results: In 73 of the 128 cases, NSCLC cancer tissues (57.0%) were found with high expression of fascin-1, which was significantly higher than the adjacent tissues (35/128, 27.3%). The results suggested that the high expression of fascin-1 was significantly correlated with lymph node metastasis (P=0.022) and TNM stage (P=0.042). The high fascin-1 expression patients survived shorter than those NSCLC patients with low fascin-1 expression (P<0.05). Univariate analysis revealed that lymph node metastasis, TNM stage, and fascin-1 expression status were correlated with the overall survival. Similarly, lymph node metastasis, TNM stage, and fascin-1 expression status were significantly associated with the overall survival in multivariate analyses by using the Cox regression model.Conclusion: The fascin-1 protein may be a useful prognostic indicator and hopeful new target for NSCLC patients.
机译:目的:Fascin-1与F-actin交联后,可促进丝状伪足,片状脂蛋白增多和细胞膜微穗的形成,从而增强细胞的移动以及肿瘤细胞的转移和侵袭。本研究探讨了fascin-1蛋白在非小细胞肺癌(NSCLC)组织中的表达及其与临床病理和预后指标的关系。方法:采用免疫组织化学分析法确定fascin-1在非小细胞肺癌组织中的表达。我们使用定量实时聚合酶链反应和蛋白质印迹分析来进一步验证结果。用χ2检验fascin-1的表达和临床病理参数的统计方法。 Kaplan–Meier方法用于生存分析。结果:在128例病例中有73例中,NSCLC癌组织(57.0%)中有高表达fascin-1的组织,明显高于邻近组织,其比例为57.7%。组织(35/128,27.3%)。结果提示fascin-1的高表达与淋巴结转移(P = 0.022)和TNM分期(P = 0.042)显着相关。 fascin-1高表达患者的生存期短于fascin-1低表达的NSCLC患者(P <0.05)。单因素分析显示,淋巴结转移,TNM分期和fascin-1表达状态与总生存率相关。同样,在使用Cox回归模型进行多变量分析时,淋巴结转移,TNM分期和fascin-1表达状态与总生存率显着相关。结论:fascin-1蛋白可能是有用的预后指标,并有望成为新的靶标NSCLC患者。

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