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首页> 外文期刊>Analytical and quantitative cytology and histology >Validation of a multicolor interphase fluorescence in situ hybridization assay for detection of transitional cell carcinoma on fresh and archival thin-layer, liquid-based cytology slides.
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Validation of a multicolor interphase fluorescence in situ hybridization assay for detection of transitional cell carcinoma on fresh and archival thin-layer, liquid-based cytology slides.

机译:验证多色相间荧光原位杂交测定法在新鲜和档案薄层,基于液体的细胞学载玻片上检测过渡细胞癌的能力。

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摘要

OBJECTIVE: To evaluate the feasibility of performing multicolor interphase fluorescence in situ hybridization (FISH) on ThinPrep slides of transitional cell carcinoma (TCC). STUDY DESIGN: Slides from 20 voided urine specimens were prepared by the ThinPrep technique (Cytyc, Boxborough, Massachusetts, U.S.A.), pretreated using a pretreatment kit and subjected to hybridization with the multicolor FISH probe UroVysion (Vysis, Downers Grove, Illinois, U.S.A.). Archival slides were placed in xylene, destained in alcohol and washed prior to pretreatment. Urines from patients with cytology-positive, biopsy-proven grade 1 (n = 5), 2 (n = 7) and 3 (n = 5) TCC and negative cytology and biopsy (n = 3) were selected. Freshly prepared (n = 10) and archival (n = 10) slides were used. RESULTS: All carcinoma cases were FISH positive (> 5 cells with complex abnormalities of > or = 2 studied chromosomes per slide). None of the normal samples were aneusomic. Gain of chromosomes 3, 7 and 17 constituted the majority of positive cases. Proper destaining and slight decrease in stringency wash conditions enabled reliable detection of signals in archival cases. CONCLUSION: Routine ThinPrep slides can be used for multicolor interphase FISH analysis of urine cytology specimens. Archival slides provide the opportunity to analyze by FISH the nature of atypical cells identified by cytology. This revised method allows FISH technology more accessibility for routine use in cytology laboratories.
机译:目的:评估在过渡细胞癌(TCC)的ThinPrep玻片上进行多色相间荧光原位杂交(FISH)的可行性。研究设计:通过ThinPrep技术(Cytyc,美国马萨诸塞州Boxborough,Cytyc)制备了20个排空尿液样本的载玻片,使用预处理试剂盒进行了预处理,并与多色FISH探针UroVysion(Vysis,Downers Grove,伊利诺伊州,美国)进行了杂交。 。将档案载玻片置于二甲苯中,用乙醇脱色并在进行预处理之前洗涤。选择来自细胞学阳性,活检证实为1级(n = 5),2(n = 7)和3(n = 5)TCC且细胞学和活检阴性的患者的尿液(n = 3)。使用新鲜制备的(n = 10)和存档(n = 10)的幻灯片。结果:所有癌症病例均为FISH阳性(每张载玻片中有5个以上的细胞,异常异常≥2个研究染色体)。正常样品均无气雾。阳性病例中,染色体3、7和17的获得占多数。适当的脱色和严格洗涤条件的轻微降低使得在归档情况下能够可靠地检测信号。结论:常规ThinPrep载玻片可用于尿细胞学标本的多色相间FISH分析。存档幻灯片提供了通过FISH分析通过细胞学鉴定的非典型细胞的性质的机会。这种修改后的方法使FISH技术在细胞学实验室常规使用中具有更大的可及性。

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