期刊文献+

TOP2A基因表达对膀胱癌的预后价值分析 被引量:10

Prognostic value analysis of TOP2A gene expression for bladder cancer
原文传递
导出
摘要 目的探讨DNA拓扑异构酶Ⅱα(TOP2A)基因表达与膀胱癌患者临床病理特征的关系及其对预后评价的意义。方法收集膀胱癌基因表达谱数据集GSE13507(n=165)和GSE31189(n=52),对膀胱癌患者样本表达谱资料及其对应的临床信息进行病理指标的回顾性分析和生存期分析;利用基因集富集分析(GSEA)方法预测受TOP2A调控的相关通路。结果TOP2A基因在膀胱癌组织中的表达水平明显高于其在正常膀胱组织中的表达(5.823±1.079∶4.820±1.129),差异有统计学意义(t=4.336,P<0.001)。TOP2A基因在膀胱癌中的表达与患者年龄(χ2=5.926,P=0.015)、性别(χ2=6.046,P=0.014)、T分期(χ2=19.484,P<0.001)、N分期(χ2=9.178,P=0.002)、M分期(χ2=21.142,P<0.001)、疾病分级(χ2=47.005,P<0.001)、病情进展(χ2=11.735,P=0.001)有关,而与肿瘤是否复发(χ2=0.808,P=0.369)无明显相关性。生存分析结果显示,TOP2A基因高表达组患者第100个月时的肿瘤特异性生存率明显低于TOP2A低表达组患者(66.59%∶87.95%),差异有统计学意义(χ2=15.820,P<0.001);TOP2A高表达组和低表达组患者的中位总生存期分别为51.77个月和134.97个月,差异有统计学意义(χ2=11.280,P=0.008)。GSEA结果提示TOP2A可能调节了MYCV1信号通路(P=0.035,FDR=0.132)、MYCV2信号通路(P=0.012,FDR=0.058)、E2F信号通路(P<0.001,FDR=0.006)和G2M检查点(P=0.006,FDR=0.044)相关的基因集。结论TOP2A基因表达与膀胱癌患者的临床病理特征密切相关,TOP2A可作为潜在的判断膀胱癌患者预后的标志物。 ObjectiveTo investigate the relationship between DNA topoisomerase Ⅱα (TOP2A) gene expression and clinicopathological characteristics and its significance of prognostic evaluation for patients with bladder cancer. MethodsBladder cancer gene expression profile GSE13507 (n=165) and GSE31189 (n=52) were obtained. The expression profile and clinical information of patients with bladder cancer were retrospectively analyzed, and the survival analysis was made. Gene set enrichment analysis (GSEA) was conducted to explore the related pathways which were regulated by TOP2A. ResultsCompared with normal bladder tissues, TOP2A was upregulated in bladder cancer tissues (5.823±1.079 vs. 4.820±1.129), with a statistically significant difference (t=4.336, P〈0.001). The TOP2A gene expression in patients with bladder cancer was correlated with the age of patients (χ2=5.926, P=0.015), sex (χ2=6.046, P=0.014), T staging (χ2=19.484, P〈0.001), N staging (χ2=9.178, P=0.002), M staging (χ2=21.142, P〈0.001), tumor grade (χ2=47.005, P〈0.001), and progression (χ2=11.735, P=0.001), but it was not correlated with recurrence (χ2=0.808, P=0.369). Survival analysis showed that the specific survival rate in the 100 months of TOP2A gene high expression group and low expression group had a statistically significant difference (66.59% vs. 87.95%, χ2=15.820, P〈0.001). The median overall survival time of TOP2A gene high expression group and low expression group were 51.77 months and 134.97 months respectively, with a statistically significant difference (χ2=11.280, P=0.008). The results of GSEA indicated that TOP2A could regulate gene sets related with several pathways like MYCV1 signaling (P=0.035, FDR=0.132), MYCV2 signaling (P=0.012, FDR=0.058), E2F signaling (P〈0.001, FDR=0.006) and G2M checkpoint (P=0.006, FDR=0.044). ConclusionThe TOP2A gene expression is closely related with clinicopathological characteristics of patients with bladder cancer. TOP2A may function as a potential marker of prognosis for patients with bladder cancer.
作者 袁佳仪 何恒晶 毕娅琼 郭梓鑫 肖宇 李胜 Yuan Jiayi , He Hengiing, Bi Yaqiong, Guo Zixin, Xiao Yu, Li Sheng.(Department of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan 430071, Chin)
出处 《国际肿瘤学杂志》 CAS 2018年第1期22-26,共5页 Journal of International Oncology
基金 国家自然科学基金(81772730) 珞珈青年学者科研基金(武汉大学“351人才计划”)
关键词 DNA拓扑异构酶类 Ⅱ型 膀胱肿瘤 基因表达 预后 DNA topoisomerases, type Ⅱ Urinary bladder neoplasms Gene expression Prognosis
  • 相关文献

参考文献5

二级参考文献37

  • 1李向阳,张伟宏.乳癌组织中PTEN的表达[J].郑州大学学报(医学版),2005,40(6):1112-1114. 被引量:1
  • 2谢庆祥,林吓聪,韩聪祥.膀胱癌分子病理学与预后之间关系的研究[J].中国现代医学杂志,2005,15(24):3727-3729. 被引量:1
  • 3渠武帅,段建敏,秦大山,岳中谨,王志平,王青兵,史庭楷.c-FLIP/BCL-2/Ki-67在膀胱移行细胞癌中的表达与临床病理学特征及对预后影响的研究[J].中国现代医学杂志,2006,16(9):1353-1357. 被引量:3
  • 4廖之君,马文丽,梁爽,郑文岭.GeneSifter在基因表达谱芯片数据挖掘中的应用[J].医学信息(西安上半月),2007,20(11):1882-1887. 被引量:5
  • 5李莉.膀胱肿瘤的超声诊断[J].医药前沿,2011,1(24):175-175.
  • 6Vazquez A, Bond EE, Levine A J, et al. The genetics of the p53 pathway, apoptosis and cancer therapy [ J ]. Nat Rev Drug Discov, 2008,7(12) :979 -987.
  • 7Mattioni M, Soddu S, Porrello A, et al. Serum anti - p53 antibodies as a useful marker for prognosis of gastric carcinoma [J]. Int J Biol Markers,2007,22(4) :302 -306.
  • 8Chien WP, Wong RH, Wu TC, et al. Potential increase in the prognostic value of p53 mutation by Pro72 allele in stage I non- small-cell lung cancer. [ J]. Ann Surg Oneol, 2009, 16 ( 7 ) : 1918 - 1924.
  • 9Huo Q ,Yang Q. P53-binding protein 1 : a new player for tumori- genesis and a new target for breast cancer treatment. [ J ] .Med Hypotheses ,2011,77 ( 3 ) :359 - 363.
  • 10Mitra AP,Datar RH, Cote RJ. Molecular pathways in invasive blad- der cancer: new insights into mechanisms, progression, and target i- dentification[J]. J Clin Oncol,2006,24(35) :5552 -5564.

共引文献47

同被引文献77

引证文献10

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