Bosga-Bouwer Anneke G, van Imhoff Gustaaf W, Boonstra Ronald, van der Veen Anneke, Haralambieva Eugenia, van den Berg Anke, de Jong Bauke, Krause Vanessa, Palmer Martin C, Coupland Robert, Kluin Philip M, van den Berg Eva, Poppema Sibrand
Department of Genetics, University Medical Center Groningen, The Netherlands.
Blood. 2003 Feb 1;101(3):1149-54. doi: 10.1182/blood.V101.3.1149.
Chromosomal translocations involving t(14;18)(q32;q21) and the chromosome 3q27 region are common in B-cell non-Hodgkin lymphoma of germinal center cell origin. Grade 3B follicular lymphoma (FL), consisting almost exclusively of centroblasts, is a distinct subgroup of follicular lymphomas that has more in common clinically with the aggressive diffuse large B-cell lymphomas than with their indolent FL grade 1 and 2 counterparts. We studied the cytogenetic and molecular genetic aberrations by classic cytogenetics, polymerase chain reaction, Southern blot hybridization, and fluorescence in situ hybridization, with special emphasis on t(14;18), affecting bcl-2, and 3q27 rearrangement, affecting bcl-6, in 32 cases of FL grade 3B. Three distinctive subgroups were identified based upon the existence of breakpoint 3q27, a translocation t(14;18), or the absence of both. Group I involved a t(14;18) and no 3q27 aberrations (n = 13); group II was without a t(14;18) and without 3q27 aberrations (n = 9), but had other cytogenetic aberrations; and group III was without a t(14;18) but with aberrations involving 3q27 (n = 10). None of the FL grade 3B cases harbored both a t(14;18) and 3q27 aberration. These results, in particular the finding of a mutual exclusiveness of bcl-2 and bcl-6 rearrangement, indicate at least 3 different pathways of oncogenesis in FL grade 3B. FL grade 3B with bcl-2 rearrangement probably is part of the same entity as the other follicular lymphomas (1, 2, 3A), whereas the cases with 3q27 abnormalities or other unrelated translocations are more closely related to the majority of diffuse large-cell lymphomas of germinal center cell origin.
涉及t(14;18)(q32;q21)和染色体3q27区域的染色体易位在生发中心细胞起源的B细胞非霍奇金淋巴瘤中很常见。3B级滤泡性淋巴瘤(FL)几乎完全由中心母细胞组成,是滤泡性淋巴瘤的一个独特亚组,在临床上与侵袭性弥漫性大B细胞淋巴瘤的共同点比与其惰性的1级和2级FL更多。我们通过经典细胞遗传学、聚合酶链反应、Southern印迹杂交和荧光原位杂交研究了细胞遗传学和分子遗传学异常,特别关注影响bcl-2的t(14;18)和影响bcl-6的3q27重排,研究对象为32例3B级FL。根据3q27断点的存在、t(14;18)易位或两者均不存在,确定了三个不同的亚组。第一组涉及t(14;18)且无3q27异常(n = 13);第二组无t(14;18)且无3q27异常(n = 9),但有其他细胞遗传学异常;第三组无t(14;18)但有涉及3q27的异常(n = 10)。没有一例3B级FL同时存在t(14;18)和3q27异常。这些结果,特别是bcl-2和bcl-6重排相互排斥的发现,表明3B级FL至少有3种不同的肿瘤发生途径。伴有bcl-2重排的3B级FL可能与其他滤泡性淋巴瘤(1、2、3A)属于同一实体,而伴有3q27异常或其他不相关易位的病例与大多数生发中心细胞起源的弥漫性大细胞淋巴瘤关系更密切。