Suppr超能文献

具有t(14;18)染色体易位的肿瘤性B细胞染色体断点的克隆。

Cloning of the chromosome breakpoint of neoplastic B cells with the t(14;18) chromosome translocation.

作者信息

Tsujimoto Y, Finger L R, Yunis J, Nowell P C, Croce C M

出版信息

Science. 1984 Nov 30;226(4678):1097-9. doi: 10.1126/science.6093263.

Abstract

From an acute B-cell leukemia cell line, a DNA probe was obtained that was specific for chromosome 18 and flanked the heavy chain joining region of the immunoglobulin heavy chain locus on chromosome 14. This probe detected rearrangement of the homologous DNA segment in the leukemic cells and in follicular lymphoma cells with the t(14:18) chromosome translocation but not in other neoplastic or normal B or T cells. The probe appears to identify bcl-2, a gene locus on chromosome 18 (band q21) that is unrelated to known oncogenes and may be important in the pathogenesis of B-cell neoplasms with this translocation.

摘要

从一种急性B细胞白血病细胞系中获得了一种DNA探针,该探针特异于18号染色体,且位于14号染色体上免疫球蛋白重链基因座的重链连接区两侧。该探针检测到白血病细胞和伴有t(14:18)染色体易位的滤泡性淋巴瘤细胞中同源DNA片段的重排,但在其他肿瘤性或正常B或T细胞中未检测到。该探针似乎识别出了bcl-2,这是18号染色体(q21带)上的一个基因座,与已知癌基因无关,可能在伴有这种易位的B细胞肿瘤的发病机制中起重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验