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High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer

机译:肿瘤基质中高水平的EGFR表达与上皮性卵巢癌的侵袭性临床特征相关

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Purpose: The aim of this study was to investigate the clinical significance and biological function of epidermal growth factor receptor (EGFR) expressed in tumor stroma of epithelial ovarian cancer. Methods: Immunohistological staining of EGFR was evaluated in 242 patients with epithelial ovarian cancer. The correlations of EGFR expression in tumor stroma with clinicopathological features and with the expression level of Ki-67 were analyzed by SPSS software. Kaplan–Meier analysis and the Cox proportional hazard model were used to analyze the effect of EGFR expression in tumor stroma on the prognosis of patients with epithelial ovarian cancer. Meanwhile, the activities of proliferation and migration of tumor cells were detected when EGFR overexpressed in stroma cells. Results: EGFR expression in tumor stroma correlated significantly with clinical stage ( χ 2=7.002, P =0.008) and distant metastases ( χ 2=16.59, P <0.001). Furthermore, there was a significantly positive correlation between the level of EGFR expressed in tumor stroma and the level of Ki-67 expressed in tumor cells ( χ 2=6.120, P =0.013). Patients with high EGFR expression level in tumor stroma showed poor survival ( P =0.002). Multivariate analysis showed that high expression of EGFR in tumor stroma was an independent predictor for epithelial ovarian cancer patients (hazard ratio =1.703; 95% confidence interval 1.125–2.578, P =0.012). Furthermore, stroma cells overexpressing EGFR could promote the proliferation and migration of adjacent tumor cells. Conclusion: High expression of EGFR in tumor stroma correlates with aggressive clinical features in epithelial ovarian cancer, and is an independent prognostic factor.
机译:目的:本研究的目的是研究表皮生长因子受体(EGFR)在上皮性卵巢癌肿瘤基质中表达的临床意义和生物学功能。方法:对242例上皮性卵巢癌患者进行EGFR的免疫组织学评价。用SPSS软件分析EGFR在肿瘤基质中的表达与临床病理特征及Ki-67表达水平的相关性。使用Kaplan–Meier分析和Cox比例风险模型分析了肿瘤基质中EGFR表达对上皮性卵巢癌患者预后的影响。同时,当EGFR在基质细胞中过表达时,检测到肿瘤细胞的增殖和迁移活性。结果:EGFR在肿瘤基质中的表达与临床分期(χ2 = 7.002,P = 0.008)和远处转移(χ2= 16.59,P <0.001)显着相关。此外,在肿瘤基质中表达的EGFR水平与在肿瘤细胞中表达的Ki-67水平之间存在显着正相关(χ2 = 6.120,P = 0.013)。肿瘤基质中EGFR表达水平高的患者生存期较差(P = 0.002)。多变量分析表明,EGFR的高表达是卵巢上皮癌患者的独立预测因子(危险比= 1.703; 95%置信区间1.125-2.578,P = 0.012)。此外,过度表达EGFR的基质细胞可以促进邻近肿瘤细胞的增殖和迁移。结论:EGFR在肿瘤基质中的高表达与上皮性卵巢癌的侵袭性临床特征有关,是独立的预后因素。

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