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Protein profile of human hepatocarcinoma cell line SMMC-7721: Identification and functional analysis

机译:人肝癌细胞系SMMC-7721的蛋白质谱:鉴定和功能分析

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AIM: To investigate the protein profile of human hepatocarcinoma cell line SMMC-7721, to analyze the specific functions of abundant expressed proteins in the processes of hepatocarcinoma genesis, growth and metastasis, to identify the hepatocarcinoma-specific biomarkers for the early prediction in diagnosis, and to explore the new drug targets for liver cancer therapy. METHODS: Total proteins from human hepatocarcinoma cell line SMMC-7721 were separated by two-dimensional electrophoresis (2DE). The silver-stained gel was analyzed by 2DE software Image Master 2D Elite. Interesting protein spots were identified by peptide mass fingerprinting based on matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and database searching. RESULTS: We obtained protein profile of human hepatocarcinoma cell line SMMC-7721. Among the twenty-one successfully identified proteins, mitofilin, endoplasmic reticulum protein ERp29, ubiquinol-cytochrome C reductase complex core protein Ⅰ, peroxisomal enoyl CoA hydratase, peroxiredoxin-4 and probable 3-oxoacid CoA transferase 1 precursor were the six novel proteins identified in human hepatocarcinoma cells or tissues. Specific functions of the identified heat-shock proteins were analyzed in detail, and the results suggested that these proteins might promote tumorigenesis via inhibiting cell death induced by several cancer-related stresses or via inhibiting apoptosis at multiple points in the apoptotic signal pathway. Other identified chaperones and cancer-related proteins were also analyzed. CONCLUSION: Based on the protein profile of SMMC-7721 cells, functional analysis suggests that the identified chaperones and cancer-related proteins have their own pathways to contribute to the tumorigenesis, tumor growth and metastasis of liver cancer. Furthermore, proteomic analysis is indicated to be feasible in the cancer study.
机译:目的:研究人肝癌细胞系SMMC-7721的蛋白谱,分析大量表达蛋白在肝癌发生,生长和转移过程中的特定功能,鉴定肝癌特有的生物标志物,以进行早期诊断诊断,并探索用于肝癌治疗的新药物靶标。方法:采用二维电泳(2DE)分离人肝癌细胞SMMC-7721中的总蛋白。银染的凝胶通过2DE软件Image Master 2D Elite分析。通过基于基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)和数据库搜索的肽质量指纹识别,可以识别出有趣的蛋白质斑点。结果:我们获得了人肝癌细胞SMMC-7721的蛋白质谱。在21种成功鉴定出的蛋白质中,米特菲林,内质网蛋白ERp29,泛醇-细胞色素C还原酶复合核心蛋白Ⅰ,过氧化物酶体烯酰CoA水合酶,过氧化物酶4和可能的3-氧代酸CoA转移酶1前体是在该蛋白中鉴定出的六个新蛋白。人肝癌细胞或组织。详细分析了鉴定出的热休克蛋白的特定功能,结果表明这些蛋白可能通过抑制几种与癌症相关的应激诱导的细胞死亡或通过抑制凋亡信号通路中多个点的凋亡来促进肿瘤发生。还分析了其他鉴定出的伴侣蛋白和癌症相关蛋白。结论:基于SMMC-7721细胞的蛋白质谱,功能分析表明,鉴定出的分子伴侣和与癌症相关的蛋白质具有自己的途径,有助于肝癌的发生,发展和转移。此外,蛋白质组学分析表明在癌症研究中是可行的。

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