Boonstra Ronald, Bosga-Bouwer Anneke, Mastik Mirjam, Haralambieva Eugenia, Conradie Jelle, van den Berg Eva, van den Berg Anke, Poppema Sibrand
Department of Pathology and Laboratory Medicine, University Hospital Groningen, The Netherlands.
Hum Pathol. 2003 Sep;34(9):915-23. doi: 10.1016/s0046-8177(03)00350-2.
The histological transformation from a follicular lymphoma (FL) to a diffuse large B-cell lymphoma (DLBL) occurs in 22% to 30% of all cases of FL. The aim of this study was to identify specific chromosomal gains/losses associated with transformation of FL to DLBL, in addition to the well-known mechanisms like p53 mutation and protein expression and c-myc translocation and up-regulation. This is the first study to meet 2 important conditions for such a comparison. First, we demonstrate that the FL and the DLBL were clonally related, based on identical immunoglobulin gene rearrangements in 5 of the 6 cases. Second, we used laser microdissection microscopy to isolate only the neoplastic cells from the initial FL samples. The results indicate that no single chromosomal abnormality seems to be responsible for the transformation of FL to DLBL. P53 protein overexpression was found in 4 and c-myc translocation in 3 of the 6 transformed DLBLs, but not in the initial FL samples. Additional chromosomal abnormalities were detected by comparative genomic hybridization in all 6 cases when the DLBL was compared with the FL. In the 5 cases with transformation of grade 1 or 2 FL to DLBL, gains at chromosomes 7 (5 of 5 cases), 10p1 (3 of 5 cases), 12 (3 of 5 cases), and 20p13 (2 of 5 cases) and loss at 9q (4 of 5 cases) were the most frequently found abnormalities. A gain on chromosome 7p, in combination with a loss on 9q, was found in 4 of the 5 DLBL that transformed from FL grade 1 or 2.
在所有滤泡性淋巴瘤(FL)病例中,有22%至30%会发生组织学转化,转变为弥漫性大B细胞淋巴瘤(DLBL)。本研究的目的是确定除了诸如p53突变和蛋白表达、c-myc易位和上调等已知机制外,与FL向DLBL转化相关的特定染色体增加/缺失情况。这是第一项满足此类比较的两个重要条件的研究。首先,基于6例中的5例具有相同的免疫球蛋白基因重排,我们证明FL和DLBL是克隆相关的。其次,我们使用激光显微切割显微镜仅从初始FL样本中分离肿瘤细胞。结果表明,似乎没有单一的染色体异常可导致FL向DLBL的转化。在6例转化的DLBL中,有4例发现p53蛋白过表达,3例发现c-myc易位,但在初始FL样本中未发现。当将DLBL与FL进行比较时,通过比较基因组杂交在所有6例中均检测到其他染色体异常。在5例1级或2级FL转化为DLBL的病例中,最常发现的异常是7号染色体增加(5例中的5例)、10p1增加(5例中的3例)、12号染色体增加(5例中的3例)和20p13增加(5例中的2例)以及9q缺失(5例中的4例)。在从1级或2级FL转化而来的5例DLBL中,有4例发现7p增加并伴有9q缺失。