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非霍奇金淋巴瘤的染色体研究:14;18易位的作用

Chromosome studies in the non-Hodgkin's lymphomas: the role of the 14;18 translocation.

作者信息

Rowley J D

机构信息

Department of Medicine, University of Chicago, IL.

出版信息

J Clin Oncol. 1988 May;6(5):919-25. doi: 10.1200/JCO.1988.6.5.919.

Abstract

The 14;18 translocation [t(14;18)] is the most common chromosome abnormality noted in the non-Hodgkin's lymphomas (NHL). Although the translocation is seen in various histologic subtypes, it is most commonly associated with the follicular lymphomas, especially the small-cleaved cell (FSC) and mixed-cell (FM) subtypes. The translocation breakpoint has been cloned and DNA probes from the junction on chromosome 18 can now be used to detect the genetic consequences of the translocation in tumors with few dividing cells. This will allow a more precise classification of this subset of lymphomas and should lead to better understanding of the biology of this category of lymphomas. Finally, these insights will help in the development of more effective and possibly less toxic therapy.

摘要

14;18易位[t(14;18)]是非霍奇金淋巴瘤(NHL)中最常见的染色体异常。尽管这种易位可见于多种组织学亚型,但它最常与滤泡性淋巴瘤相关,尤其是小裂细胞(FSC)和混合细胞(FM)亚型。易位断点已被克隆,来自18号染色体连接处的DNA探针现在可用于检测几乎没有分裂细胞的肿瘤中易位的遗传后果。这将使这类淋巴瘤的分类更加精确,并有助于更好地理解这类淋巴瘤的生物学特性。最后,这些见解将有助于开发更有效且可能毒性更小的治疗方法。

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