Aberrant expression of CD10 and BCL6 in mantle cell lymphoma

淋巴瘤 套细胞淋巴瘤 免疫组织化学 生物 细胞周期蛋白D1 病理 荧光原位杂交 分子生物学 抗体 基因 医学 免疫学 遗传学 细胞周期 染色体
作者
Marco Pizzi,Claudio Agostinelli,Simona Righi,Anna Gazzola,Claudia Mannu,Francesca Galuppini,Matteo Fassan,Andrea Visentin,Francesco Piazza,Gianpietro Semenzato,Massimo Rugge,Elena Sabattini
出处
期刊:Histopathology [Wiley]
卷期号:71 (5): 769-777 被引量:30
标识
DOI:10.1111/his.13286
摘要

Aims Mantle cell lymphoma ( MCL ) is characterized by distinctive histological and molecular features. Aberrant expression of BCL 6 and CD 10 has been reported occasionally, but the biological features of such cases are largely unknown. This study aimed to define the epidemiological, histological and cytogenetic characteristics of BCL 6 and CD 10‐positive MCL s, also investigating possible biological features. Methods and results A total of 165 cases of cyclin D1 and t(11;14)(q13;q34)‐positive MCL s were studied for CD 10 and BCL 6 immunohistochemical expression, which was documented in 26 of 165 (15.8%) cases ( BCL 6 17 of 165; CD 10 11 of 165; BCL 6 and CD 10 co‐expression two of 165). CD 10‐positivity was significantly more frequent in females (63.3%; P < 0.01). Either expression correlated significantly with higher mean proliferation index and higher prevalence of MUM 1 positivity ( P < 0.05). Fluorescence in‐situ hybridization ( FISH ) for BCL 6 (3q27) gene derangements was performed on the BCL 6‐ and CD 10‐positive cases and 98 matched controls: amplifications were documented more frequently in BCL 6‐positive than ‐negative cases (50.0% versus 19.4% of cases) ( P < 0.05). The mutational status of the variable immunoglobulin heavy chain genes ( IGVH ) was investigated by Sanger sequencing: five of the six successfully tested cases (83.3%) showed no somatic hypermutations. Conclusions Aberrant CD 10 and BCL 6 expression defines a subset of MCL s with higher mean Ki‐67 index and higher prevalence of MUM 1 expression. BCL 6 protein positivity correlates with cytogenetic aberrations involving the BCL 6 gene. Although examined successfully in few cases, the high prevalence of unmutated IGVH genes also points at a pregerminal cell origin for these phenotypically aberrant cases.
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