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跨物种染色体显带技术(RxFISH)在T-原淋巴细胞白血病研究中的应用

Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia.

作者信息

Espinet B, Solé F, Salido M, Lloveras E, Abella E, Besses C, Serrano S, Woessner S, Florensa L

机构信息

Laboratori de Citologia Hematològica, Laboratori de Referència de Catalunya, Unitat d'Hematologia 1973, Barcelona, Spain.

出版信息

Haematologica. 2000 Jun;85(6):607-12.

Abstract

BACKGROUND AND OBJECTIVE

Cross-species color banding (RxFISH) is a new FISH technology based on the use of differentially labeled gibbon chromosome probes to obtain a specific color banding pattern for each human chromosome. The aim of the study was to test the RxFISH technique for better characterization of complex karyotypes in patients with T-prolymphocytic leukemia (T-PLL).

DESIGN AND METHODS

The study evaluated the cross-species color banding technique in four patients affected with T-PLL previously studied by conventional cytogenetics.

RESULTS

All patients showed an abnormal karyotype and three of them had a complex karyotype. The involvement of 14q11 in all four cases, the gain of 8q in three cases and a loss of chromosome 10, 15 and 17 and a gain of chromosome 21 in two cases were noted. The RxFISH technique identified from 2 to 7 not previously recognized aberrations per case and confirmed the inv(14)(q11q32).

INTERPRETATION AND CONCLUSIONS

To our knowledge, this is the first application of RxFISH to characterize chromosomal rearrangements in T-cell neoplasms. RxFISH gave rapid and easy identification of chromosome rearrangements that were difficult to recognize by conventional cytogenetics. Using this new technology we identified 15 rearrangements not detected by conventional cytogenetics.

摘要

背景与目的

跨物种染色体显带技术(RxFISH)是一种新的荧光原位杂交(FISH)技术,该技术基于使用差异标记的长臂猿染色体探针,从而为每条人类染色体获得特定的染色体显带模式。本研究的目的是测试RxFISH技术,以便更好地表征T-原淋巴细胞白血病(T-PLL)患者的复杂核型。

设计与方法

本研究评估了跨物种染色体显带技术在4例先前已通过传统细胞遗传学研究的T-PLL患者中的应用。

结果

所有患者均显示核型异常,其中3例具有复杂核型。注意到所有4例均有14q11受累,3例有8q增益,2例有10号、15号和17号染色体缺失以及21号染色体增益。RxFISH技术在每例中鉴定出2至7个先前未识别的畸变,并证实了inv(14)(q11q32)。

解读与结论

据我们所知,这是RxFISH首次应用于表征T细胞肿瘤中的染色体重排。RxFISH能够快速、轻松地识别传统细胞遗传学难以识别的染色体重排。使用这项新技术,我们鉴定出15个传统细胞遗传学未检测到的重排。

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