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Nuclear NHERF1 expression as a prognostic marker in breast cancer

机译:核NHERF1表达作为乳腺癌的预后指标

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Our purpose was to investigate whether Na+/H+ exchanger regulatory factor 1 (NHERF1) expression could be linked to prognosis in invasive breast carcinomas. NHERF1, an ezrin-radixin-moesin (ERM) binding phosphoprotein 50, is involved in the linkage of integral membrane proteins to the cytoskeleton. It is therefore believed to have an important role in cell signaling associated with changes in cell cytoarchitecture. NHERF1 expression is observed in various types of cancer and is related to tumor aggressiveness. To date the most extensive analyses of the influence of NHERF1 in cancer development have been performed on breast cancer. However, the underlying mechanism and its prognostic significance are still undefined. NHERF1 expression was studied by immunohistochemistry (IHC) in a cohort of 222 breast carcinoma patients. Association of cytoplasmic and nuclear NHERF1 expression with survival was analyzed. Disease-free survival (DFS) and overall survival (OS) were determined based on the Kaplan–Meier method. Cytoplasmic NHERF1 expression was associated with negative progesterone receptor (PgR) ( P =0.017) and positive HER2 expression ( P =0.023). NHERF1 also showed a nuclear localization and this correlated with small tumor size ( P =0.026) and positive estrogen receptor (ER) expression ( P =0.010). Multivariate analysis identified large tumor size ( P =0.011) and nuclear NHERF1 expression ( P =0.049) to be independent prognostic variables for DFS. Moreover, the nuclear NHERF1(?)/ER(?) immunophenotype (27%) was statistically associated with large tumor size ( P =0.0276), high histological grade ( P =0.0411), PgR-negative tumors ( P P =0.0027). These patients had worse DFS compared with patients with nuclear NHERF1(+)/ER(+) tumors (75.4% versus 92.6%; P =0.010). These results show that the loss of nuclear NHERF1 expression is associated with reduced survival, and the link between nuclear NHERF1 and ER expression may serve as a prognostic marker for the routine clinical management of breast cancer patients.
机译:我们的目的是研究Na + / H + 交换调节因子1(NHERF1)的表达是否与浸润性乳腺癌的预后相关。 NHERF1是一种结合了ezrin-radixin-moesin(ERM)的磷蛋白50,参与整合膜蛋白与细胞骨架的连接。因此,据信在与细胞细胞结构变化有关的细胞信号传导中起重要作用。 NHERF1表达在各种类型的癌症中观察到,并且与肿瘤侵袭性有关。迄今为止,已经对乳腺癌进行了NHERF1对癌症发展影响的最广泛的分析。但是,其潜在的机制及其预后意义仍然不确定。通过免疫组化(IHC)在222例乳腺癌患者队列中研究了NHERF1表达。分析了细胞质和核NHERF1表达与存活的关系。根据Kaplan-Meier方法确定无病生存期(DFS)和总生存期(OS)。细胞质NHERF1表达与孕激素阴性受体(PgR)(P = 0.017)和HER2表达阳性(P = 0.023)相关。 NHERF1还显示出核定位,这与小肿瘤尺寸(P = 0.026)和雌激素受体(ER)阳性表达(P = 0.010)相关。多变量分析确定大的肿瘤大小(P = 0.011)和核NHERF1表达(P = 0.049)是DFS的独立预后变量。此外,核NHERF1(α)/ ER(β)免疫表型(27%)与肿瘤大(P = 0.0276),组织学等级高(P = 0.0411),PgR阴性肿瘤(P P = 0.0027)有统计学意义。与患有核NHERF1(+)/ ER(+)肿瘤的患者相比,这些患者的DFS较差(75.4%对92.6%; P = 0.010)。这些结果表明核NHERF1表达的丧失与存活率降低相关,并且核NHERF1和ER表达之间的联系可能成为乳腺癌患者常规临床治疗的预后标志物。

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