首页> 外文期刊>Journal of clinical and experimental hematopathology : >Cytogenetic Study and Analysis of Protein Expression in Plasma Cell Myeloma with t(11;14)(q13;q32): Absence of BCL6 and SOX11, and Infrequent Expression of CD20 and PAX5
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Cytogenetic Study and Analysis of Protein Expression in Plasma Cell Myeloma with t(11;14)(q13;q32): Absence of BCL6 and SOX11, and Infrequent Expression of CD20 and PAX5

机译:t(11; 14)(q13; q32)浆细胞性骨髓瘤蛋白表达的细胞遗传学研究和分析:缺乏BCL6和SOX11,CD20和PAX5的表达很少

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The t(11;14)(q13;q32) translocation is the most common chromosomal translocation in plasma cell myeloma (PCM), but the cytogenetic and immunophenotypic features of PCM with t(11;14)(q13;q32) remain to be fully elucidated. To address the issue, we retrospectively analyzed 21 newly diagnosed PCM patients with the t(11;14)(q13;q32) translocation in our institute. CD20 is a B-cell-specific transmembrane protein that is the topic of much focus as a potential target in immunotherapy. We observed a low incidence of CD20 expression (2 of 21 patients, 11%), although the expression of CD20 was previously reported to be associated with t(11;14)(q13;q32). PAX5 is an essential transcriptional factor involved in B-cell development and commitment, and is down-regulated upon plasma cell differentiation. We observed one patient (6%) with expression of PAX5. The expression of CD19, CD56, and CD138 was detected in one (0.7%), nine (60%), and 13 patients (87%), respectively. Cyclin D1, CD38, and BCL2 were detected in all patients; on the other hand, neither BCL6 nor SOX11 was detected in any of the evaluated patients. Abnormalities of chromosome 13 were detected in six patients (38%), but deletion of TP53 was not observed in any of the evaluated patients. Our results suggest the absence of BCL6 and SOX11 expression, and infrequent expression of CD20, PAX5, and CD56 in PCM with t(11;14)(q13;q32), in contrast to the findings of earlier reports. [ J Clin Exp Hematop 55(3) : 137-143, 2015 ]
机译:t(11; 14)(q13; q32)易位是浆细胞骨髓瘤(PCM)中最常见的染色体易位,但t(11; 14)(q13; q32)的PCM的细胞遗传学和免疫表型特征仍有待进一步研究。充分阐明。为了解决这个问题,我们回顾性分析了21例新诊断为t(11; 14)(q13; q32)易位的PCM患者。 CD20是B细胞特异的跨膜蛋白,是免疫治疗中潜在的靶标,是许多研究的热点。我们观察到CD20表达的发生率较低(21例患者中有2例,占11%),尽管以前据报道CD20的表达与t(11; 14)(q13; q32)相关。 PAX5是参与B细胞发育和定型的重要转录因子,在浆细胞分化时被下调。我们观察到一名患者(6%)表达PAX5。分别在一名(0.7%),九名(60%)和13名患者(87%)中检测到CD19,CD56和CD138的表达。在所有患者中均检测到细胞周期蛋白D1,CD38和BCL2。另一方面,在所有评估患者中均未检测到BCL6和SOX11。在六名患者(38%)中检测到13号染色体异常,但在所有评估患者中均未观察到TP53的缺失。我们的结果表明,与早期报道相比,t(11; 14)(q13; q32)的PCM中不存在BCL6和SOX11表达,而CD20,PAX5和CD56的表达很少。 [J Clin Exp Hematop 55(3):137-143,2015]

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