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套细胞淋巴瘤中的bcl-1重排与细胞周期蛋白D1蛋白表达

bcl-1 rearrangement and cyclin D1 protein expression in mantle cell lymphoma.

作者信息

Ott M M, Helbing A, Ott G, Bartek J, Fischer L, Dürr A, Kreipe H, Müller-Hermelink H K

机构信息

Institute of Pathology, University of Würzburg, Germany.

出版信息

J Pathol. 1996 Jul;179(3):238-42. doi: 10.1002/(SICI)1096-9896(199607)179:3<238::AID-PATH566>3.0.CO;2-W.

Abstract

Centrocytic lymphoma, or mantle cell lymphoma (MCL), is characterized by a chromosomal translocation t(11;14) (q13;q32) involving the bcl-1 locus on chromosome 11. Cyclin D1 is a cell-cycle regulatory protein essential for G1-S transition and has been identified as a potential transforming gene affected by the translocation. In this study, 32 cases of MCL were analysed for the bcl-1 rearrangement and cyclin D1 protein expression. In 17 cases, a rearrangement at the major translocation cluster of bcl-1 could be detected. Twenty-four cases exhibited nuclear cyclin D1 expression that was not detectable in other B-cell lymphomas (n = 40) or in normal B-cells. In nine MCL samples, cyclin D1 was expressed without a detectable bcl-1 rearrangement. The detection of a t(11;14) by means of classical cytogenetics in one of these cases, however, may suggest that this discrepancy could be due to chromosomal breakages outside the typical translocation cluster region. In two cases, a bcl-1 rearrangement was not accompanied by cyclin D1 expression. This study provides further evidence that cyclin D1 is involved in the pathogenesis of MCL and can be exploited as a diagnostic marker in the differential diagnosis of B-cell lymphomas and in the identification of MCL.

摘要

中心细胞淋巴瘤,即套细胞淋巴瘤(MCL),其特征是存在涉及11号染色体上bcl-1位点的染色体易位t(11;14) (q13;q32)。细胞周期蛋白D1是一种对G1-S期转换至关重要的细胞周期调节蛋白,已被确定为受该易位影响的潜在转化基因。在本研究中,对32例MCL病例进行了bcl-1重排和细胞周期蛋白D1蛋白表达分析。在17例病例中,可检测到bcl-1主要易位簇处的重排。24例病例表现出核细胞周期蛋白D1表达,而在其他B细胞淋巴瘤(n = 40)或正常B细胞中未检测到。在9例MCL样本中,细胞周期蛋白D1表达但未检测到bcl-1重排。然而,在其中1例病例中通过经典细胞遗传学检测到t(11;14),这可能表明这种差异可能是由于典型易位簇区域外的染色体断裂所致。在2例病例中,bcl-1重排未伴有细胞周期蛋白D1表达。本研究提供了进一步的证据,表明细胞周期蛋白D1参与了MCL的发病机制,可作为B细胞淋巴瘤鉴别诊断和MCL识别中的诊断标志物。

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