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运用多色光谱核型分析和微荧光原位杂交技术对一名原发性浆细胞白血病患者的复杂核型进行详细表征。

Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISH.

作者信息

Nordgren A, Farnebo F, Björkholm M, Sahlén S, Porwit-MacDonald A, Osby E, Kytölä S, Larsson C, Nordenskjöld M, Blennow E

机构信息

Department of Molecular Medicine, Karolinska Institutet at Karolinska Hospital, Stockholm, Sweden.

出版信息

Hematol J. 2000;1(2):95-101. doi: 10.1038/sj.thj.6200011.

Abstract

INTRODUCTION

Plasma cell leukaemia is a rare disorder that usually carries an aggressive course with a rapidly fatal outcome. A variety of chromosomal abnormalities have been reported in plasma cell leukaemia but the clinical significance of an abnormal karyotype is still unclear.

MATERIALS AND METHODS

We have applied the molecular cytogenetic techniques multicolour spectral karyotyping and microdissection in combination with fluorescence in situ hybridization on metaphases from a patient with primary plasma cell leukaemia and a fatal outcome.

RESULTS AND CONCLUSION

The chromosome analysis showed severe hypodiploidy and 12 marker chromosomes. Identification of the structural rearrangements was not possible using routine cytogenetic methods. Utilizing the methods above, all marker chromosomes could be identified in detail and the karyotype was shown to be very complex. Forty-three breakpoints were found, and 25 could be identified at the band level, among others 14q32 where the immunoglobulin heavy chain locus is situated. Thus, these techniques provide the opportunity to resolve very complex chromosomal changes in a way that has not been previously possible and will consequently be of great importance in the search for hot spots that may harbour new cancer genes.

摘要

引言

浆细胞白血病是一种罕见的疾病,通常病程进展迅速,预后凶险。已有多种染色体异常在浆细胞白血病中被报道,但异常核型的临床意义仍不明确。

材料与方法

我们应用了分子细胞遗传学技术,即多色光谱核型分析和显微切割技术,并结合荧光原位杂交技术,对一名原发性浆细胞白血病且预后凶险的患者的中期染色体进行分析。

结果与结论

染色体分析显示严重的亚二倍体和12条标记染色体。采用常规细胞遗传学方法无法鉴定结构重排。利用上述方法,可以详细鉴定所有标记染色体,结果表明核型非常复杂。共发现43个断点,其中25个可在带水平上鉴定,包括免疫球蛋白重链基因座所在的14q32。因此,这些技术提供了以一种前所未有的方式解析非常复杂的染色体变化的机会,这对于寻找可能包含新癌症基因的热点区域将具有重要意义。

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