期刊文献+

肝细胞癌组织中DNA损伤修复基因APE1表达意义 被引量:8

Expression of apurinic/apyrimidinic endonuclease 1 in hepatocellular carcinoma
下载PDF
导出
摘要 目的:探讨脱嘌呤/脱嘧啶核酸内切酶(apurinic/apyrimidinic endonuclease,Apel),又称氧化还原因子(redox fac—tor-1,Ref-1)在肝细胞性肝癌(HCC)的表达特点及其与临床病理因素的关系. 方法:应用免疫组化S-P法分别检测正常肝组织10例、结节性肝硬化组织40例和HCC103例组织中Ape1表达情况. 结果:在HCC组织中Ape1在细胞核、细胞质均可表达, 其中细胞核/细胞质联合表达(49.5%)显著高于结节性肝硬化组(20%)和正常对照组(0%)(P<0.01).Apel细胞核和细胞质阳性分度在正常组、肝硬化组、HCC组之间依次增高,并与HCC组织学分级有密切关系(P<0.01或0.05). 结论:癌细胞过度表达Ape1蛋白可作为判断肝癌组织学分级的有用指标之一.Ape1基因在HCC的发生、发展中可能具有重要作用, AIM: To explore the expression and clinicopathological relevance of apurinic/apyrimidinic endonuclease (Ape1) in hepatocellular carcinoma (HCC). METHODS: Ape1 expression was detected by immu-nohistochemical S-P method in tissues of normal liver (n = 10), hepatocirrhosis (n = 40) and HCC (n = 103). RESULTS: Three types of Ape1 positive staining were noticed in HCC: nuclear, cytoplasmic and mixed. There were significant more mixed type of Ape1 expression in HCC than in hepatocirrhosis and normal liver (49.5% vs 20%, 0%, P<0.01). The positive degree of Ape1 expression in both nucleus and cytoplasm was significantly higher in HCC than that in hepatocirrhosis and normal liver, and higher in hepatocirrhosis than that in normal liver (P<0.01). The positive expression of Ape1 was correlated with the histological grade of HCC (P<0.05). CONCLUSION: Overexperssion of Ape 1 in neoplastic cells might be a useful marker in evaluating histoiogicai grade of HCC. Ape1 gene may play an important role in tumori-genesis and progression of HCC.
出处 《世界华人消化杂志》 CAS 北大核心 2005年第4期508-511,共4页 World Chinese Journal of Digestology
关键词 HCC 表达 肝硬化 结节性 肝细胞癌组织 DNA损伤修复 APE 细胞核 细胞质 E1基因 Apurinic/apyrimidinic endonuclease Hepa-tocellular carcinoma Immunohistochemistry
  • 相关文献

参考文献13

  • 1Loeb KR, Loeb RA. Significance of multiple mutations in cancer.Carcinogenesis 2000;21:379-385.
  • 2Evans AR, Limp-Foster M, Kelley MR. Going APE over ref-1.Mutat Res 2000;461:83-108.
  • 3Gaiddon C, Moorthy NC, Prirs C. Ref-1 regulates the transactivation and pro-apoptotic functions of p53 in vivo.EMBO J 1999;18:5609-5621.
  • 4Huang LE, Arany Z, Livingston DM. Activation of hypoxiainducible transcription factor depends primarily upon redox-sensitive stablization of its alpha subunit. J Biol Chem 1996;271:32253-32259.
  • 5Wang D, Luo MH, Kelley M. Human apurinic endonucleasa 1 (APE1)expressiong and prognostic significance in osteosarcoma:Enhanced sensitivity of osteosarcoma to DNA damaging agents using silencing RNA APE1 expression inhibition. Mol Cancer Ther 2004;3:679-686.
  • 6Puglisi F, Barbone F, Tell G. Prognostic role of Ape/Ref-1 subcellar expression in stage Ⅰ-Ⅲ breast carcinomas. Oncol Rep 2002;9:11-17.
  • 7Kakolyris S, Giatromanolaki A, Koukourakis M. Nuclear localization of human AP endonuclease l(HAP1/Ref-1)associates with prognosis in early operable non-small cell lung cancer(NSCLC). J Pathol 1999;189:351-357.
  • 8Kakolyris S, Kaklamanis L, Engels K. Human AP endonu-clease 1(HAP 1)protein expression in breast cancer correlates with lymph node status and angiogenesis. Br J Cancer 1998;77:1169-1173.
  • 9Mol CD, Hosfield DJ, Tainer JA. Abasic site recognition by two apurinic/apyrimidinic endonuclease families in DNA base excision repair:the 3' ends justify the means. Mutat Res 2000;460:211-229.
  • 10Demple B, Harrison L. Repair of oxidative damage to DNA: enzvmology and biology. Rev Biochern 1994;63:915-948.

同被引文献116

引证文献8

二级引证文献27

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