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Involvement of Hepatopoietin Cn in the development of human hepatocellular carcinoma

机译:肝细胞生成素Cn参与人类肝细胞癌的发展

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摘要

Hepatopoietin Cn (HPPCn) is a novel nuclear protein with the ability to promote liver regeneration. In the present study, we investigated the expression profile of HPPCn and its functional activity in human hepatocellular carcinoma (HCC) cell line and tissue samples. HPPCn expression was detected in HCC cell lines and 54 paired HCC carcinomas by immunochemical staining and Western blotting. The functional activity of HPPCn in cell lines was evaluated by MTT and colony formation assays and with nude mouse model. The correlation of HPPCn expression with clinicopathological characteristics of 54 HCC patients was also analyzed. Our results showed that HPPCn protein was prominently located within the nuclei of hepatocytes and the expression level was evidently increased in HepG2 and Bel7402 cell lines compared with L02 normal hepatocytes. HPPCn silencing by small interfering RNA greatly suppressed HepG2 cell proliferation and colony formation capacity and the inhibitory effect was also observed in a Balb/c-null mouse model. The silencing HPPCn expression effectively enhanced the apoptosis of HepG2 cells. In addition, HPPCn expression was detected in 48 of 54 (89%) human HCC tissues in sharp contrast with the corresponding non-tumor liver tissues. HPPCn protein was mainly accumulated in the tumor nucleus. The elevated expression of HPPCn protein in tumors was significantly associated with poor tumor cellular differentiation and present of vascular invasion. Patients with higher HPPCn expression in tumors had significantly shorter overall survival (OS) of both all of patients and the patients at the early stage. On multivariate Cox analysis, elevated expression of HPPCn in tumors was found to be an independent prognostic factor for OS. Therefore, these data suggest that HPPCn expression might be involved in the development of HCC and could be served as a promising biomarker.
机译:肝细胞生成素Cn(HPPCn)是一种新型核蛋白,具有促进肝脏再生的能力。在本研究中,我们调查了HPPCn在人肝细胞癌(HCC)细胞系和组织样品中的表达谱及其功能活性。通过免疫化学染色和Western印迹法检测到HPC细胞系和54对配对的HCC癌中HPPCn的表达。通过MTT和集落形成测定以及裸鼠模型评估HPPCn在细胞系中的功能活性。还分析了54例HCC患者HPPCn表达与临床病理特征的相关性。我们的结果表明,与L02正常肝细胞相比,HPPCn蛋白显着位于肝细胞核内,并且在HepG2和Bel7402细胞系中的表达水平明显增加。通过小的干扰RNA使HPPCn沉默大大抑制了HepG2细胞增殖和集落形成能力,并且在Balb / c-null小鼠模型中也观察到了抑制作用。沉默的HPPCn表达有效增强了HepG2细胞的凋亡。此外,在54个人类HCC组织中的48个(89%)中检测到HPPCn表达,与相应的非肿瘤肝组织形成鲜明对比。 HPPCn蛋白主要积累在肿瘤核中。 HPPCn蛋白在肿瘤中的表达升高与不良的肿瘤细胞分化和存在的血管浸润显着相关。 HPPCn在肿瘤中表达较高的患者的所有患者和早期患者的总生存期(OS)均明显缩短。在多变量Cox分析中,发现HPPCn在肿瘤中的升高表达是OS的独立预后因素。因此,这些数据表明HPPCn表达可能参与肝癌的发展,并可以作为有前途的生物标志物。

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