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DNA双链断裂修复蛋白RAD51在喉癌中的表达及意义 被引量:4

Expression of RAD51 in carcinomas of cancer of larynx and its clinical significance
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摘要 目的:探讨DNA双链断裂修复蛋白RAD51在喉癌细胞中的表达及其临床意义。方法:应用免疫组织化学SP法检测喉癌和声带息肉组织中RAD51的表达情况,并结合肿瘤的临床TNM分期、淋巴结转移及其病理分化程度等分析它在肿瘤发生发展中的作用。结果:①RAD51在喉癌组中的表达明显强于声带息肉组,差异有统计学意义(P〈0.01);②RAD51在喉癌组3~4期中的表达强于1~2期喉癌,差异有统计学意义(P〈0.01);③RAD51在低、中分化喉癌中的表达强于高分化喉癌(P〈0.05),差异有统计学意义;④RAD51在有淋巴结转移喉癌中的表达强于无淋巴结转移喉癌,差异有统计学意义(P〈0.05)。结论:RAD51在喉癌的发生、发展中可能起重要作用,它可能成为临床诊断和治疗喉癌的一个潜在靶点,对预测肿瘤的预后有一定的意义。 Objective:To investigate the expression and clinical significance of RAD51 in laryngocarcinoma, Method:The expression of RAD51 in laryngocarcinoma and polyp of vocal cord tissues were determined by immunohistochemical staining. The results were analyzed and compared with the clinical stage, lymph node metastasis and pathologic grade. Result:①The expression of RAD51 in laryngocarcinoma group was extremely stronger than that in polyp of vocal cord group( P〈0. 01) .②There was significant difference for RAD51 expression in cancer cells between earlier clinical stage group and advanced clinical stage group( P 〈0.01). ③There was significant difference for RAD51 expression in different pathologic grades( P〈0.05), OThere was also significant difference for RAD51 expression between groups with and without lymph node metastasis. Conclusion: RAD51 may play a critical role in tumorigenesis of laryngocarcinoma. RAD51 may be a potential marker for clinical diagnosis and treatment of Laryngocarcinoma, It may be significant in predicting clinical stage, pathologic grade and metastasis.
出处 《临床耳鼻咽喉头颈外科杂志》 CAS CSCD 北大核心 2007年第12期540-542,共3页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
关键词 喉肿瘤 DNA修复酶类 RAD51 Laryngeal neoplasms DNA repair enzymes RAD51
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  • 1TEBBS R S,ZHAO Y,TUCKER J D,et al.Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene[J].Proc Natl Acad Sci USA,1995,92:6354-6358.
  • 2WANG Z M,CHEN Z P,XU Z Y,et al.In vitro evidence for homologous recombinational repair in resistance to melphalan[J].J Natl Cancer Inst,2001,93:1473-1478.
  • 3XIA S J,SHAMMAS M A,Shmookler Reis R J.Elevated recombination in immortal human cells is mediated by HsRAD51 recombinase[J].Mol Cell Biol,1997,17:7151-7158.
  • 4HANSEN L T,LUNDIN C,SPANG-THOMSEN M,et al.The role of RAD51 in etoposide (VP16) resistance in small cell lung cancer[J].Int J Cancer,2003,105:472-479.
  • 5MAACKE H,HUNDERTMARK C,MISKA S,et al.Autoantibodies in sera of pancreatic cancer patients identify recombination factor Rad51 as a tumourassociated antigen[J].J Cancer Res Clin Oncol,2002,128:219-222.
  • 6MAACKE H,OPITZ S,JOST K,et al.Over-expression of wild-type Rad51 correlates with histological grading of invasive ductal breast cancer[J].Int J Cancer,2000,88:907-913.
  • 7SHARAN S K,MORIMATSU M,ALBRECHT U,et al.Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2[J].Nature,1997,386:804-810.
  • 8CONNELL P P,JAYATHILAKA K,HARAF D J,et al.Pilot study examining tumor expression of RAD51 and clinical outcomes in human head cancers[J].Int J Oncol,2006,28:1113-1119.
  • 9RICHARDSON C.RAD51,genomic stability,and tumorigenesis[J].Cancer Lett,2005,218:127-139.

同被引文献74

  • 1Liu Y,Masson J Y,Shah R,et al.RAD51C is required for Holliday junction processing in mammalian cells[J].Science,2004,303:243-6.
  • 2Richardson C,Stark J M,Ommundsen M,et al.Rad51 overexpression promotes alternative double-strand break repair pathways and genome instability[J].Oncogene,2004,23:546-53.
  • 3Lee SA,Roques C,Magwood A C,et al.Recovery of deficient homologous recombination in Brca2-depleted mouse cells by wild-type Rad51 expression[J].DNA Repair(Amst),2009,8(2):170-81.
  • 4Klein H L.The consequences of Rad51 overexpression for normal and tumor cells[J].DNA Repair(Amst),2008,7,686-93.
  • 5Lazaro-Trueba I,Arias C,Silva A.Double bolt regulation of Rad51 by p53:a role for transcriptional repression[J].Cell Cycle,2006,5:1062-5.
  • 6Martin R W,Orelli B J,Yamazoe M,et al.RAD51 up-regulation bypasses BRCA1 function and is a common feature of BRCA1-deficient breast tumors[J].Cancer Res,2007,67:9658-65.
  • 7Martin R W,Connell P P,Bishop D K.The Yin and Yang of treating BRCA-deficient tumors[J].Cell,2008,132:919-20.
  • 8Hasselbach L,Haase S,Fischer D,et al.Characterisation of the promoter region of the human DNA-repair gene Rad51[J].Eur J Gynaecol Oncol,2005,26:589-98.
  • 9Wang Z,Dong H,Fu Y,et al.RAD51 135G》C polymorphism contributes to breast cancer susceptibility:a meta-analysis involving 26,444 subjects[J].Breast Cancer Res Treat,2010,124(3):765-9.
  • 10Romanowicz-Makowska H,Smolarz B,Zadrozny M,et al.Analysis of RAD51 polymorphism and BRCA1 mutations in Polish women with breast cancer[J].Exp Oncol,2006,28(2):156-9.

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