首页> 美国卫生研究院文献>Journal of Cancer >High Expression of Human AugminComplex Submit 3 Indicates Poor Prognosis and Associates with Tumor Progression in Hepatocellular Carcinoma
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High Expression of Human AugminComplex Submit 3 Indicates Poor Prognosis and Associates with Tumor Progression in Hepatocellular Carcinoma

机译:人类AugminComplex提交3的高表达表明肝细胞癌的不良预后并与肿瘤进展相关。

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摘要

The function of human augmin complex unit 3(Haus3), a component of the HAU augmin-like complex, in various cancers is not clear. This study aims to elucidate the clinical significance and the role of Haus3 in tumor progression of hepatocellular carcinoma (HCC). We analyzed the expression of Haus3 in 50 HCC patients from The Cancer Genome Atlas and 137 HCC patients in our hospital. Compared with adjacent normal tissue, Haus3 expression assessed by immunohistochemical staining was dramatically increased in tumor tissues. A high level of Haus3 expression was significantly correlated with large tumor size (p=0.025) and tumor multiplicity (p=0.004). Univariate and multivariate survival analysis showed thatexpression of Haus3 was an independent prognostic factor for overall survival ofHCCpatients. Western blot analysis showed that Haus3 regulated the phosphorylation of PLK1-T210 and activity of the Cdk1/cyclin B1 complex, indicating that Haus3 disrupted G2/M phase arrest. In immunofluorescence studies, expression of Haus3 correlated with the level ofα-tubulin and γ-tubulin. In summary, Haus3 plays a vital role in regulatingtheactivityof PLK2-T210 and Cdk1/cyclin B1 complex in G2/M phasetransition and the expression of tubulins to ensure normal mitotic progression. Our data suggest that Haus3 might be a promising prognostic biomarker and molecular target of HCC.
机译:尚不清楚人类Augmin复合物单元3(Haus3)是HAU Augmin样复合物的组成部分,在各种癌症中的功能尚不清楚。本研究旨在阐明Haus3在肝细胞癌(HCC)肿瘤进展中的临床意义和作用。我们分析了Haus3在癌症基因组图谱的50例HCC患者和我院的137例HCC患者中的表达。与邻近的正常组织相比,通过免疫组织化学染色评估的Haus3表达在肿瘤组织中显着增加。 Haus3表达的高水平与大肿瘤大小(p = 0.025)和肿瘤多重性(p = 0.004)显着相关。单因素和多因素生存分析表明,Haus3的表达是HCC患者总体生存的独立预后因素。蛋白质印迹分析表明,Haus3调节了PLK1-T210的磷酸化和Cdk1 / cyclin B1复合物的活性,表明Haus3破坏了G2 / M期停滞。在免疫荧光研究中,Haus3的表达与α-微管蛋白和γ-微管蛋白的水平相关。总之,Haus3在调节PLK2-T210和Cdk1 / cyclin B1复合体在G2 / M相变中的活性以及微管蛋白的表达以确保正常的有丝分裂进程中起着至关重要的作用。我们的数据表明,Haus3可能是有希望的肝癌预后标志物和分子靶标。

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