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Diagnosis of bladder cancer from the voided urine specimens using multi-target fluorescence in situ hybridization

机译:多靶点荧光原位杂交技术从排尿样中诊断膀胱癌

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The present study aimed to evaluate the diagnostic value of chromosomal analysis by fluorescence in situ hybridization (FISH) for bladder cancer in light of the histological diagnosis. Several valuable observations using FISH technologies in voided urine cells were also reported. The multi-target FISH-containing probes for the centromeres of chromosomes 3, 7 and 17 and the 9p21 locus were applied to cytospin specimens prepared from voided urine. Urine samples from 53 bladder cancer patients and 30 patients with benign alterations were used for this study. The histological observations of surgical resection specimens showed that the specificity and sensitivity for the technique were 100.0 and 88.0%, respectively. Statistical analyses showed that there was no significant correlation between FISH-positive rate and the tumor stage/grade (P<0.05). However, the proportion of tumor cells with genetic abnormalities positively correlated with the tumor stage (P<0.01). Furthermore, the number of abnormal cells in muscle-invasive pT2 was significantly higher than that in non-muscle-invasive pTa, pT1 (P<0.01). Of 50 patients with bladder cancer, polysomies of chromosomes 3, 7 and 17 were detected in 84.0, 48.0 and 78.0% of cases, respectively, and loss of the 9p21 gene was detected in 80.0% of cases. In addition, the detailed results from different urine specimens showed.
机译:本研究旨在根据组织学诊断评估荧光原位杂交(FISH)技术对膀胱癌的诊断价值。还报告了在排尿细胞中使用FISH技术的一些有价值的观察结果。将用于染色体3、7和17的着丝粒和9p21基因座的含多目标FISH的探针应用于从空尿制备的cytospin标本中。本研究使用了53例膀胱癌患者和30例良性改变患者的尿液样本。手术切除标本的组织学观察表明,该技术的特异性和敏感性分别为100.0%和88.0%。统计分析表明,FISH阳性率与肿瘤分期/分级无显着相关性(P <0.05)。然而,具有遗传异常的肿瘤细胞比例与肿瘤分期呈正相关(P <0.01)。此外,肌肉侵袭性pT2中的异常细胞数量明显高于非肌肉侵袭性pTa,pT1(P <0.01)。在50例膀胱癌患者中,分别在84.0%,48.0%和78.0%的病例中检测到3、7和17号染色​​体的多态性,在80.0%的病例中检测到9p21基因的缺失。此外,还显示了来自不同尿液样本的详细结果。

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