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动态检测尿Livin mRNA表达对膀胱癌早期诊断的临床价值

Clinical value of dynamic detection of urinary Livin mRNA expression in early diagnosis of bladder cancer
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摘要 目的动态检测膀胱癌患者手术前、后尿Livin mRNA表达情况,探讨其对膀胱癌早期诊断的临床价值。方法采用实时荧光定量PCR方法检测30例膀胱移行细胞癌患者术前、术后1周、1个月、3个月、6个月至18个月及30例非泌尿系统肿瘤患者及30例健康志愿者尿Livin mRNA表达情况,并结合临床资料进行分析。结果 Livin mRNA在30例病例组术前尿液中出现高表达,相对拷贝数为(96.33±35.79)/ul,且随着肿瘤临床分期、分级由低到高,其表达水平亦有随之增加的趋势;30例对照组中有2例出现较高表达,相对拷贝数分别为43.17和47.52,其余为低表达,相对拷贝数为(16.25±7.81)/ul;30例正常组为低表达,相对拷贝数为13.74±1.57。病例组术前尿Livin mRNA表达水平明显高于对照组和正常组,其差异有统计学意义(P <0.05);术后1周(27.35±2.21)/ul较术前显著下降(P <0.05);术后1个月(16.72±2.45)/ul、3个月(15.54±2.14)/ul、6个月(14.33±1.71)/ul与对照组和正常组相比差异无统计学意义(P> 0.05)。随访至术后18个月,5例复发者再次手术前(98.27±26.55)/ul与初次术后6个月相比差异有统计学意义(P <0.05)。结论动态检测尿Livin mRNA表达的高特异性、高敏感性,可作为膀胱癌早期诊断的一个无创性指标。 Objective Dynamic detection of urinary Livin mRNA expression in patients with bladder cancer before and after operation and its clinical value in early diagnosis of bladder cancer.Methods Urine of 30 patients with initially diagnosed BTCC was collected before operation and one week,one month,three months,six months and 18 months after operation.Urine of 30 healthy volunteers and 30 Non-urological cancer patients was collected.Expression of survivin mRNA in urine exfoliated cells was detected by real-time PCR.Results Livin mRNA was highly expressed in the urine of 30 patients before operation,and the relative copy number was(96.33±35.79),and the expression level increased with the clinical stage and grade of the tumor from low to high;2 of 30 patients in the control group showed high expression,the relative copy number was 43.17 and 47.52,the other was low expression,and the expression level was low.The copy number was(16.25±7.81);30 cases in normal group were low expression,and the relative copy number was(13.74±1.57).The expression of Livin mRNA in urine of the case group was significantly higher than that of the control group and the normal group(P<0.05);the expression of Livin mRNA in urine of the case group was significantly lower than that of the control group(P<0.05);the expression of Livin mRNA in urine of the case group was significantly lower than that of the normal group(P<0.05);there was no significant difference between the control group and the normal group(P >0.05).Follow-up to 18 months after surgery,5 patients with recurrence before reoperation(98.27±26.55)and 6 months after the initial operation were significantly different(P<0.05).Conclusion Dynamic detection of urinary Livin mRNA expression with high specificity and sensitivity can be used as an important noninvasive marker for early diagnosis of bladder cancer.
作者 江龙来 李彩红 谢梅茂 王晓荣 JIANG Long-lai;LI Cai-hong;XIE Mei-mao;WANG Xiao-rong(Department of Urology,General Hospital of China Aviation,Beijing 100012,China;Department of Urology,The First AffiliatedHospital of Nanchang University,Nanchang 330003,Jiangxi,China)
出处 《肿瘤代谢与营养电子杂志》 2018年第4期395-398,共4页 Electronic Journal of Metabolism and Nutrition of Cancer
基金 江西省卫生厅科技计划项目(20073121)
关键词 膀胱移行细胞癌 实时荧光定量PCR LivinmRNA表达 Bladder transitional cell carcinoma Real-time fluorescent quantitative PCR Livin mRNA
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  • 1宋希双,张志伟,车翔宇,姜涛,李先承,殷积斌.凋亡抑制基因Livin在膀胱癌中的表达及意义[J].中华泌尿外科杂志,2006,27(S1):37-39. 被引量:23
  • 2Kasof GM, Gomes BC. Livin, a novel inhibitor of apoptosis protein family member[J]. J Biol Chem, 2001, 276(5) : 3238-3246.
  • 3Vucic D, Stennicke HR, Pisabarro MT, et al. ML-IAP, a novel inhibitor of apoptosis that is preferentially expressed in human melanomas[J]. Curt Biol, 2000, 10(21) : 1359-1366.
  • 4Lin JH, Deng G, Huang Q, et al. KIAP, a novel member of the inhibitor of apoptosls protein family[ J]. Biochem Biophys Res Commun, 2000, 279(3) : 820-831.
  • 5Ashhab Y, Alian A, Polliack A, et al. Two splicing variants of a new inhibitor of spoptosis gene with different biological properties and tissue distribution pattern[ J]. FEBS Lett, 2001,495 (1) : 56- 60.
  • 6Gazzaniga P, Gradilone A, Giuliani L, et al. Expression and prognostic significance of Livin, surviving and other apoptosis-related genes in the progression of superficial bladder cancer [ J]. Ann Oncol, 2003, 14( 1 ) : 85-90.
  • 7Lin JH, Deng G, Huang Q, et al. KIAP, a novel member of the inhibitor of apoptosis protein family [J]. Biochem Biophys Res Commun, 2000, 279 (3): 820- 831.
  • 8DU C, Fang M, Li Y. et al. Smac, a mitochondrial protein that promotes eytochrome c-depentent caspase activation by eliminating IAP inhibition [J]. Cell, 2000, 102(1): 33-42.
  • 9Verhagen AM , Ekert Identification of DIABLO, PG, Pakusch M, et al. a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins [J].Cell, 2000, 102(1): 43-53.
  • 10Gazzaniga P, Gradilone A, Giuliani L, et al. Expression and prognostic significance of Livin, Survivin and other apoptosis-related genes in the progression of superficial bladder cancer [J]. Ann Oncol, 2003, 14(1): 85-90.

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