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CIP2A在膀胱尿路上皮癌组织中的表达及其临床意义
引用本文:伍耿青,薛义军,邹晓峰,张国玺,袁源湖,肖日海,王晓宁,龙大治,吴玉婷. CIP2A在膀胱尿路上皮癌组织中的表达及其临床意义[J]. 肿瘤防治研究, 2013, 40(4): 353-358. DOI: 10.3971/j.issn.1000-8578.2013.04.009
作者姓名:伍耿青  薛义军  邹晓峰  张国玺  袁源湖  肖日海  王晓宁  龙大治  吴玉婷
作者单位:赣南医学院第一附属医院泌尿外科赣南医学院泌尿外科研究所,江西赣州,341000
摘    要:目的 研究蛋白磷酸酶2A癌性抑制因子(cancerous inhibitor of protein phosphatase 2A,CIP2A)在膀胱尿路上皮癌组织中的表达及其与临床病理特征的关系,探讨其成为膀胱尿路上皮癌预后指标的可行性.方法 应用RT-PCR和Western blot检测CIP2A mRNA和蛋白在25例膀胱尿路上皮癌和对应癌旁组织中的表达情况;应用组织芯片技术和免疫组织化学方法,检测CIP2A在117例膀胱尿路上皮癌和30例癌旁组织中的表达情况,分析CIP2A与膀胱尿路上皮癌患者临床病理特征及预后之间的关系.结果 CIP2A mRNA和蛋白在25例配对膀胱尿路上皮癌组织中的表达水平明显高于癌旁组织.免疫组织化学检测发现,膀胱尿路上皮癌组织中CIP2A蛋白的阳性表达率为76.9%(90/117),明显高于癌旁组织的6.7% (2/30),差异有统计学意义(P<0.001).CIP2A表达与肿瘤病理分级(P<0.001)、临床分期(P<0.001)、肿瘤大小(P=0.002)和淋巴结转移(P=0.046)有关,但与年龄、性别及肿瘤数目无关(P>0.05).KaplanMeier单因素分析显示,CIP2A蛋白高表达是总体生存率和无复发生存率的影响因素(P<0.001).Cox多因素风险比例模型显示,与总生存率相关的独立预后因素为临床分期、肿瘤病理分级和CIP2A表达,与无复发生存率相关的独立预后因素亦为临床分期、肿瘤病理分级和CIP2A表达.结论 CIP2A蛋白在膀胱尿路上皮癌组织中高表达,可能与膀胱尿路上皮癌的进展有关,其表达状态是膀胱尿路上皮癌患者独立预后因素.

关 键 词:膀胱肿瘤  免疫组织化学  基因表达  预后  CIP2A
收稿时间:2012-06-12;

Expression and Clinical Significance of CIP2A in Bladder Urothelial Cell Carcinoma
WU Gengqing,XUE Yijun,ZOU Xiaofeng,ZHANG Guoxi,YUAN Yuanhu,XIAO Rihai,WANG Xiaoning,LONG Dazhi,WU Yuting,YANG Jun,LIU Folin,LIU Min,XU Ruiquan,XU Gang. Expression and Clinical Significance of CIP2A in Bladder Urothelial Cell Carcinoma[J]. Cancer Research on Prevention and Treatment, 2013, 40(4): 353-358. DOI: 10.3971/j.issn.1000-8578.2013.04.009
Authors:WU Gengqing  XUE Yijun  ZOU Xiaofeng  ZHANG Guoxi  YUAN Yuanhu  XIAO Rihai  WANG Xiaoning  LONG Dazhi  WU Yuting  YANG Jun  LIU Folin  LIU Min  XU Ruiquan  XU Gang
Affiliation:Department of Urology,First Affiliated Hospital of Gannan Medical University,Institute of Urology,Gannan Medical University,Ganzhou 341000,China
Abstract:Objective
To investigate the expression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in bladder urothelial carcinoma tissues and its relationship with clinical pathologic characteristics,and to discuss the feasibility of CIP2A as prognostic markers.
Methods
RT-PCR and Western blot were used to evaluate the mRNA and protein expression of CIP2A in cancer tissues and corresponding paracancerous tissues from 25 bladder urothelial carcinoma patients.A tissue microarray (TMA) containing specimens from 117 bladder urothelial cell carcinoma tissues and 30 paracancerous tissues was constructed and then immunohistochemistry was used to examine the protein expression of CIP2A.The correlations between CIP2A and clinicopathological characteristics and prognosis were also analyzed.
Results
CIP2A mRNA and protein were undetectable or very low in paracancerous tissues,but were dramatically elevated in cancer samples in 25 patients.The positive expression rate of CIP2A protein in bladder urothelial cell carcinoma tissues [76.9% (90/117)] was significantly higher than that in paracancerous tissues [6.7% (2/30)].Such difference had statistic significance(P<0.001).CIP2A expression correlated with histological grade (P<0.001),tumor stage (P<0.001),tumor diameter (P=0.002) and lymph nodes metastasis (P=0.046);while it was not related with age,gender,tumor number and tumor recurrence (P>0.05).Kaplan-Meier univariate analysis showed that the overall and recurrence-free survival rates were significantly higher in the group with low expression of CIP2A than in the group with high expression of CIP2A (P<0.001).Cox proportional hazards model revealed that tumor stage,histological grade,and CIP2A expression were independent predictors of an unfavorable prognosis for overall survival rate (P<0.001,P=0.001 and P=0.035,respectively ) and recurrence-free survival rates (P<0.001,P<0.001 and P=0.003,respectively ).
Conclusion
The expression of CIP2A protein is significantly increased in bladder urothelial cell carcinoma tissues,which may be involved in the progress of bladder urothelial cell carcinoma.CIP2A may be a valuable biomarker for assessing the prognosis of bladder urothelial cell carcinoma.
Keywords:Bladder urothelial cell carcinoma  Immunohistochemistry  Gene expression  Progno-sis  CIP2A
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