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CCL14 serves as a novel prognostic factor and tumor suppressor of HCC by modulating cell cycle and promoting apoptosis

机译:CCL14通过调节细胞周期并促进细胞凋亡,用作HCC的新型预后因子和肿瘤抑制剂

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摘要

CCL14 is a member of CC chemokines and its role in hepatocellular carcinoma (HCC) is still unknown. In this study, CCL14 expression were analyzed by tissue microarray (TMA) including 171 paired tumor and peritumor tissues of patients from Zhongshan Hospital of Fudan University. We found for the first time that CCL14 was downregulated in HCC tumor tissues compared with peritumor tissues (P?=?0.01). Meanwhile, CCL14 low expression in HCC tumor tissues is associated with a poor prognosis (P?=?0.035). CCL14 also displayed its predictive value in high differentiation (P?=?0.026), liver cirrhosis (P?=?0.003), and no tumor capsule (P?=?0.024) subgroups. The underlying mechanisms were further investigated in HCC cell lines by CCL14 overexpression and knock-down in vitro. We found overexpression of CCL14 suppressed proliferation and promoted apoptosis of HCC cells. Finally, the effect was confirmed by animal xenograft tumor models in vivo. The results shown overexpression of CCL14 lead to inhibiting the growth of tumor in nude mice. Interestingly, our data also implied that CCL14 played these effects by inhibiting the activation of Wnt/β-catenin pathway. These findings suggest CCL14 is a novel prognostic factor of HCC and serve as a tumor suppressor.
机译:CCL14是CC趋化因子的成员,其在肝细胞癌(HCC)中的作用仍然未知。在该研究中,通过组织微阵列(TMA)分析CCL14表达,其中包括来自中山医院的患者的171个成对的肿瘤和蠕虫组织。与腹膜组织相比,我们首次发现CCL14在HCC肿瘤组织中下调(P?= 0.01)。同时,HCC肿瘤组织中的CCL14低表达与预后差有关(P?= 0.035)。 CCL14还在高分化(P?= 0.026)中显示其预测值(P?= 0.026),肝硬化(P?= 0.003),没有肿瘤胶囊(P?= 0.024)个子组。通过CCL14过表达和倒闭在体外,在HCC细胞系中进一步研究潜在的机制。我们发现CCl14的过表达抑制了抑制了HCC细胞的增殖和促进凋亡。最后,体内动物异种移植肿瘤模型证实了该效果。结果表明CCL14的过表达导致抑制裸鼠肿瘤的生长。有趣的是,我们的数据还暗示CCL14通过抑制Wnt /β-catenin途径的激活来发挥这些效果。这些发现表明CCL14是HCC的新预后因子,并用作肿瘤抑制剂。

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