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Identification and Comparison of Differentiation-Related Proteins in Hepatocellular Carcinoma Tissues by Proteomics

机译:蛋白质组学鉴定和比较肝细胞癌组织中分化相关蛋白

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摘要

Histological differentiation is a major pathological criterion indicating the risk of tumor invasion and metastasis in patients with hepatocellular carcinoma. The degree of tumor differentiation is controlled by a complex interacting network of associated proteins. The principal aim of the present study is to identify the possible differentiation-related proteins which may be used for early diagnosis and more effective therapies. We compared poorly differentiated and well-differentiated hepatocellular carcinoma tissues by using 2-dimensional gel electrophoresis and matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Among the 11 identified protein spots, 6 were found to be upregulated in poorly differentiated hepatocellular carcinoma tissues and 5 were correspondingly downregulated. Immunohistochemistry was performed on 106 hepatocellular carcinoma tissues to confirm the results of the proteomic analysis. By using bioinformatic tools GO and STRING, these proteins were found to be related to catalytic activity, binding, and antioxidant activity. In particular, our data suggest that overexpression of peroxiredoxin-2, annexin A2, and heat shock protein β-1 was correlated with tumor invasion, metastasis, and poor prognosis, and therefore, these proteins may serve as potential diagnostic and therapeutic biomarkers.
机译:组织学分化是指示肝细胞癌患者肿瘤侵袭和转移风险的主要病理学标准。肿瘤分化程度由相关蛋白的复杂相互作用网络控制。本研究的主要目的是鉴定可能与分化相关的蛋白,这些蛋白可用于早期诊断和更有效的治疗。我们通过使用二维凝胶电泳和基质辅助激光解吸电离飞行时间质谱法比较了分化低下和分化良好的肝细胞癌组织。在鉴定出的11个蛋白斑点中,发现6个在低分化肝细胞癌组织中表达上调,而5个被相应下调。对106个肝细胞癌组织进行了免疫组织化学检查,以确认蛋白质组学分析的结果。通过使用生物信息学工具GO和STRING,发现这些蛋白质与催化活性,结合和抗氧化活性有关。特别是,我们的数据表明过氧化物酶2,膜联蛋白A2和热休克蛋白β-1的过表达与肿瘤的侵袭,转移和预后不良有关,因此,这些蛋白可作为潜在的诊断和治疗生物标志物。

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