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t(3;14) 或其变体与其他淋巴瘤特异性易位的频繁关联。

Frequent association of t(3;14) or variant with other lymphoma-specific translocations.

作者信息

Horsman D E, McNeil B K, Anderson M, Shenkier T, Gascoyne R D

机构信息

Division of Laboratory Medicine, British Columbia Cancer Agency, Vancouver, Canada.

出版信息

Br J Haematol. 1995 Mar;89(3):569-75. doi: 10.1111/j.1365-2141.1995.tb08365.x.

Abstract

Malignant lymphomas (ML) with t(3;14) or variant t(2;3) and t(3;22) have recently been recognized. These translocations have been shown to associate predominantly with B-cell diffuse large cell lymphoma (DLCL) and less frequently with follicular lymphoma (FL). The molecular alterations associated with these translocations involve one of the immunoglobulin gene (Ig) loci and a recently cloned gene, bcl-6 located at 3q27 which codes for a zinc-finger protein that may function as a transcription factor. We have identified by cytogenetic analysis 22 cases of ML with a 3q27/Ig translocation. The pathologic diagnoses of these cases include DLCL, FL, small non-cleaved non-Burkitt lymphoma and chronic lymphocytic leukaemia. Molecular analysis confirmed a bcl-6 rearrangement in 10/12 cases tested. The karyotype in 5/22 cases revealed the t(3;14) or variant in association with another lymphoma-specific translocation, t(14;18) in three cases and t(8;14) in two cases. ML with dual translocations that implicate Ig genes in the deregulation of proto-oncogenes are being increasingly recognized and may represent distinct subtypes or 'hybrid' forms of malignant lymphoma.

摘要

近期已确认存在伴有t(3;14)或变异型t(2;3)及t(3;22)的恶性淋巴瘤(ML)。这些易位主要与B细胞弥漫性大细胞淋巴瘤(DLCL)相关,较少与滤泡性淋巴瘤(FL)相关。与这些易位相关的分子改变涉及免疫球蛋白基因(Ig)位点之一以及一个最近克隆的基因,位于3q27的bcl - 6,它编码一种可能作为转录因子发挥作用的锌指蛋白。我们通过细胞遗传学分析鉴定出22例伴有3q27/Ig易位的ML病例。这些病例的病理诊断包括DLCL、FL、小无裂非伯基特淋巴瘤和慢性淋巴细胞白血病。分子分析证实,在检测的12例病例中有10例存在bcl - 6重排。22例病例中的5例核型显示t(3;14)或变异型与另一种淋巴瘤特异性易位相关,3例为t(14;18),2例为t(8;14)。涉及Ig基因参与原癌基因失调的双重易位的ML越来越受到认可,可能代表恶性淋巴瘤的不同亚型或“混合”形式。

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