期刊文献+

肝内转移和多中心发生的多结节肝癌蛋白质表达谱的差异分析 被引量:1

Protein profiles of multinodular hepatoceHular carcinoma with multicentric occurrence or with intrahepatic metastasis
原文传递
导出
摘要 目的比较分析多结节肝癌的肝内转移癌灶和多中心发生癌灶的蛋白质表达谱,为更加准确的分子分型方法提供实验依据。方法对5例肝内转移(IM)和6例多中心发生(MO)的多结节肝癌按照结节大小分为IM1、IM2、MO1、MO2四组,联合双向凝胶电泳与质谱技术分析多结节肝癌的蛋白质表达谱;并用Western blot验证质谱结果。结果双向凝胶电泳联合质谱技术鉴定IM1、IM2、MO1、MO2四组共30个差异蛋白质点,确认为25种差异表达的蛋白质;GeneOntology分类显示其与细胞运动、信号转导、氧化还原、脂类代谢、氨基酸代谢等有关。结论多结节肝癌肝内转移和多中心发生的蛋白质表达不同;双向凝胶电泳联合质谱技术可作为二者分子分型的方法,有利于临床医师对肝癌患者实施治疗和判断预后。 Objective To analyze the protein expression profiles of multinodular hepatocellular carcinoma (HCC) with multicentric occurrence (MO) or with intrahepatic metastasis (IM). Methods 5 IM and 6 MO patients were divided into groups of IM1, IM2, MO1 and MO2 according to the size of node of HCC. Two dimensional gel electrophoresis (2-DE) and mass spectrum were Used to analyze the protein expression profiles. Western blot was used to confirm the results obtained by mass spectrum. Results 2-DE of IM1, IM2, MO1 and MO2 indicated that 30 protein dots were differentially expressed in these tumors. By mass spectrum, 25 proteins were identified. Gene ontology classification indicated that these proteins are associated to cell movement, signal transduction, oxidoreduction, lipid metabolism, and amino acid metabolism. Conclusion The protein expression profiles of IM is different from that of MO, 2-DE and mass spectrum can be used to identify the molecular markers of IM and MO of HCC.
出处 《中华肝脏病杂志》 CAS CSCD 北大核心 2009年第5期354-358,共5页 Chinese Journal of Hepatology
基金 国家高技术研究发展计划(863计划,2006AA02A308) 国家自然科学基金(30760243) 广西自然科学基金(桂科自0640092、0640107) 广西卫生厅重点课题(桂卫重200627)
关键词 肝细胞 肿瘤转移 蛋白质组 Carcinoma, hepatocellular Neoplasm metastasis Proteome
  • 相关文献

参考文献7

  • 1Yasui M, Harada A, Nonami T, et al. Potentially multicentric hepatocellular carcinoma: clinicopathologic characteristics and postoperative prognosis. World J Surg, 1997, 21: 860-865.
  • 2Yang M, Zhou H, Kong RY, et al. Mutations at codon 249 of p53 gene in human hepatocellular carcinomas from Tongan, China. Mutat Res, 1997, 381: 25-29.
  • 3Lee HC, Li SH, Lin JC, et al. Somatic mutations in the D-loop and decrease in the copy number of mitochondrial DNA in human hepatocellular carcinoma. Mutat Res, 2004, 547: 71-78.
  • 4Pontisso P, Belluco C, Bertorelle R, et al. Hepatitis C virus infection associated with human hepatocellular carcinoma: lack of correlation with p53 abnormalities in Caucasian patients. Cancer, 1998, 83: 1489-1494.
  • 5Teramoto T, Satonaka K, Kitazawa S, et al. p53 gene abnormalities are closely related to hepatoviral infections and occur at a late stage of hepatocarcinogenesis. Cancer Res, 1994, 54:231-235.
  • 6郭坤,刘银坤,周海君,代智,陈洁,孙瑞霞,孙强玲,卢雯静,康晓楠.热休克蛋白27在转移潜能不同人肝癌细胞系中的表达及机制研究[J].生物化学与生物物理进展,2007,34(7):738-745. 被引量:9
  • 7Adachi E, Maehara S, Tsujita E, et al. Clinicopathologic risk factors for recurrence after a curative hepatic resection for hepatocellular carcinoma. Surgery, 2002, 131(1 Suppl): S148-152.

二级参考文献1

共引文献8

同被引文献10

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部