期刊文献+

肾母细胞瘤中ERCC1、TUBB3、TOP2A mRNA的表达及临床意义 被引量:9

Expression and clinical significance of ERCC1,TUBB3 and TOP2A mRNA in nephroblastoma
下载PDF
导出
摘要 目的探讨核苷酸切除修复交叉互补基因(excision repair cross complementation 1,ERCC1)、3型β微管蛋白编码基因(ClassⅢβ-tubulin,TUBB3)和DNA拓扑异构酶Ⅱα(TopoisomeraseⅡA,TOP2A)mRNA在小儿肾母细胞瘤组织中的表达及临床意义。方法收集18例肾母细胞瘤组织标本及14例癌旁组织标本,通过分支-DNA液相芯片法检测标本中ERCC1、TUBB3、TOP2A mRNA的表达水平,并分析上述基因表达与肾母细胞瘤临床病理的关系。结果肾母细胞瘤组织中ERCC1、TUBB3和TOP2A高表达率分别为44.4%、50.0%和66.7%,均显著高于癌旁组织的7.1%、7.1%和14.3%,差异有统计学意义(P<0.05)。ERCC1高表达率与肾母细胞瘤临床分期和病理类型有关(P<0.05),TOP2A高表达率与肾母细胞瘤临床分期相关(P<0.05)。结论小儿肾母细胞瘤组织中ERCC1、TUBB3和TOP2A mRNA表达高于癌旁组织,可能参与肾母细胞瘤的发生发展过程。 Objective To investigate the expression and clinical significance of excision repair cross complementation 1(ERCC1),Class Ⅲ β-tubulin(TUBB3)and topoisomerase ⅡA(TOP2A)in nephroblastoma.Methods The expression levels of ERCC1,TUBB3 and TOP2 A in 18 cases of nephroblastoma tissue and 14 cases of peritumoral tissue were detected by branch-DNA liquid chip technology.The relationship of the expressions of the above genes with the clinicopathologic characteristics of nephroblastoma was analyzed.Results The high expression rates of ERCC1,TUBB3 and TOP2 A in nephroblastoma tissues(44.4%,50.0%,66.7%) were significantly higher than those in peritumoral tissues(7.1%,7.1% and 14.3%)(P〈0.05).The high expression of ERCC1 was correlated with the clinical stage and histopathologic type(P〈0.05).TOP2 A was correlated with the clinical stage(P〈0.05).Conclusion The expressions of ERCC1,TUBB3 and TOP2 A were higher in nephroblastoma than in normal renal tissue.High expressions of ERCC1,TUBB3 and TOP2 A may play an important role in carcinogenesis and progression of nephroblastoma.
出处 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2016年第5期689-692,共4页 Journal of Xi’an Jiaotong University(Medical Sciences)
基金 国家自然科学基金资助项目(No.81172589)~~
关键词 肾母细胞瘤 ERCC1 TUBB3 TOP2A nephroblastoma ERCC1 TUBB3 TOP2A
  • 相关文献

参考文献17

  • 1DAVIDOFF AM. Wilms' tumor[J]. Curr Opin Pediatr, 2009, 21(3) :357-364.
  • 2PASTORE G, ZNAOR A, SPREAFICO F, et al. Malignant renal tumours incidence and survival in European children (1978-1997) : report from the Automated Childhood Cancer In- formation System project[J]. Eur J Cancer, 2006, 42 (13) : 2103-2114.
  • 3SAEBO M, SKJELBRED CF, NEXO BA,et al. Increased mR- NA expression levels of ERCC1, OGG1 and RAI in colorectal adenomas and carcinomas[J]. BMC Cancer, 2006, 16(6) :208-215.
  • 4OLAUSSEN KA, DUNANT A, FOURET P, et al. DNA re- pair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy[J]. N Engl J Med, 2006, 355 (10) : 983- 991.
  • 5VILMAR A, GARCIA-FONCILLAS J, HUARRIZ M, et al. RT-PCR versus immunohistochemistry for correlation and quantification of ERCC1, BRCA1, TUBB3 and RRM1 in NSCLC[J]. Lung Cancer, 2012, 75(3):306-312.
  • 6PRESS MF, SAUTER G, BUYSE M, et al. Alteration of to- poisomerase II-alpha gene in human breast cancer: association with responsiveness to anthracyclinc-based chemotherapy[J]. J Clin Oncol, 2011, 29(7):859-867.
  • 7NAKAMURA L, RITCHEY M. Current management of Wilms' tumor[J]. Curt Urol Rep, 2010, 11(1):58-65.
  • 8TSODIKOV OV, JVANOV D, ORELLI B, et al. Structural basis for the recruitment of ERCCI-XPF to nucleotide excision repair complexes by XPA[J]. EMBO, 2007, 26 (22) : 4768- 4776.
  • 9FAUTREL A, ANDRIEUX L, MUSSO O, et al. Overexpres- sion of the two nucleotide excision repair genes ERCC1 and XPC in human hepatocellular carcinoma[J]. J Hepatol, 2005, 43(2) : 288-293.
  • 10ZHOU W, LIU G, PARK S, et al. Gene-smoking interaction associations for the ERCC1 polymorphisms in the risk of lung cancer[J]. Cancer Epidemiol Biomarkers Prey, 2005, 14 (2): 491-496.

同被引文献53

引证文献9

二级引证文献23

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