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EYA4 serves as a prognostic biomarker in hepatocellular carcinoma and suppresses tumour angiogenesis and metastasis

机译:EYA4可作为肝细胞癌的预后生物标志物并抑制肿瘤血管生成和转移

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摘要

Eye absent homolog 4 (EYA4) has been demonstrated to be down‐regulated in hepatocellular carcinoma (HCC), but its biological function and the mechanism in HCC angiogenesis and metastasis remain largely unknown. Herein, we showed that EYA4 expression was frequently low in HCC tissue samples compared with matched adjacent non‐tumourous tissues. In the analysis of 302 HCC specimens, we revealed that decreased expression of EYA4 correlated with tumour differentiation status. Univariate and multivariate analyses identified EYA4 as an independent risk factor for recurrence‐free survival (RFS) and overall survival (OS) among the 302 patients. Functional assays showed that forced expression of EYA4 suppressed HCC cell migration, invasion and capillary tube formation of endothelial cells in vitro, as well as in vivo tumour angiogenesis and metastasis in a mouse model. Furthermore, mechanism study exhibited that EYA4 could inhibit HCC angiogenesis and metastasis by inhibiting c‐JUN/VEGFA pathway. Together, we provide proof that EYA4 is a novel tumour suppressor in HCC and a new prognostic biomarker and therapeutic target in HCC.
机译:眼缺失同源物4(EYA4)已被证明在肝细胞癌(HCC)中被下调,但其生物学功能以及在HCC血管生成和转移中的机制仍然未知。在此,我们显示,与匹配的相邻非肿瘤组织相比,HCC组织样品中的EYA4表达通常较低。在对302例HCC标本的分析中,我们发现EYA4的表达减少与肿瘤分化状态有关。单因素和多因素分析确定302例患者中EYA4是无复发生存(RFS)和总体生存(OS)的独立危险因素。功能测定表明,在小鼠模型中,EYA4的强制表达抑制了HCC细胞的迁移,内皮细胞的侵袭和毛细管形成,以及体内肿瘤血管生成和转移。此外,机理研究表明,EYA4可以通过抑制c-JUN / VEGFA途径来抑制HCC血管生成和转移。在一起,我们提供的证据表明,EYA4是HCC中的新型肿瘤抑制因子,并且是HCC中新的预后生物标志物和治疗靶标。

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