首页> 外文期刊>The Journal of Urology >Prospective evaluation of genetic abnormalities and telomerase expression in exfoliated urinary cells for bladder cancer detection.
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Prospective evaluation of genetic abnormalities and telomerase expression in exfoliated urinary cells for bladder cancer detection.

机译:对脱落性泌尿细胞的遗传异常和端粒酶表达进行前瞻性评估以检测膀胱癌。

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PURPOSE: To evaluate alternative procedures to cytoscopic examination we prospectively compared noninvasive procedures for detecting bladder cancer namely cytology, loss of heterozygosity (LOH), microsatellite instability and human telomerase catalytic subunit reverse transcriptase (hTERT) messenger (m) RNA detection. MATERIALS AND METHODS: Specificity and cutoff values were established in the blood and urine sediment of 50 controls. Sensitivity was analyzed in the urine and tissue samples of 50 patients with bladder cancer. The diagnosis was established by cystoscopic and histological examination. Genomic alterations were studied using a panel of 24 microsatellite markers to detect LOH events, while 3 additional mononucleotide repeats were analyzed for microsatellite instability detection. Telomerase expression was detected in urinary cells by nested RT-polymerase chain reaction amplification of hTERT mRNA. All techniques were compared by cytological examination. RESULTS: Sensitivity and specificity were 31% and 100% for cytological testing, 96% and 100% for LOH, and 75% and 69% for RT-polymerase chain reaction of hTERT, respectively. No alteration was detected on microsatellite instability analysis in urine or tumor tissue cells. Using only the 5 markers most strongly associated with bladder cancer selected by logistic regression analysis, namely ABL1, IFNa, D9S12, MJD58 and D18S364, LOH test sensitivity slightly decreased to 90%. CONCLUSIONS: Urinary LOH analysis was the most sensitive and specific method for bladder cancer detection and it appeared less dependent on urine sediment quality. The logistic regression score may be an interesting complement to cystoscopy. The specificity of hTERT mRNA detection was incomplete since false-positives were observed in 31% of cases. Absent microsatellite instability in our cohort showed that these genomic alterations are not present at the early step of bladder cancer.
机译:目的:为了评估细胞镜检查的替代程序,我们前瞻性地比较了用于检测膀胱癌的非侵入性程序,即细胞学,杂合性丧失(LOH),微卫星不稳定性和人类端粒酶催化亚基逆转录酶(hTERT)信使(m)RNA检测。材料与方法:确定了50名对照的血液和尿液沉积物中的特异性和临界值。分析了50例膀胱癌患者尿液和组织样本中的敏感性。通过膀胱镜和组织学检查确定诊断。使用一组24个微卫星标记来研究基因组改变以检测LOH事件,同时分析了3个其他单核苷酸重复序列以检测微卫星不稳定性。通过hTERT mRNA的巢式RT-聚合酶链反应扩增检测尿细胞中的端粒酶表达。通过细胞学检查比较所有技术。结果:细胞学检测的敏感性和特异性分别为31%和100%,LOH的敏感性为96%和100%,hTERT的RT聚合酶链反应的敏感性为75%和69%。在尿液或肿瘤组织细胞中的微卫星不稳定性分析中未检测到改变。仅使用通过逻辑回归分析选择的与膀胱癌最相关的5个标记,即ABL1,IFNa,D9S12,MJD58和D18S364,LOH测试敏感性略降至90%。结论:尿液LOH分析是检测膀胱癌最灵敏,最特异性的方法,对尿沉渣质量的依赖性较小。逻辑回归评分可能是膀胱镜检查的有趣补充。 hTERT mRNA检测的特异性不完全,因为在31%的病例中观察到了假阳性。我们队列中缺乏微卫星不稳定性表明在膀胱癌的早期阶段不存在这些基因组改变。

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