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LRF/Pokemon与NOTCH1蛋白表达在鉴别结节性淋巴细胞为主型霍奇金淋巴瘤和经典型霍奇金淋巴瘤中的作用

Utility of LRF/Pokemon and NOTCH1 protein expression in the distinction between nodular lymphocyte-predominant Hodgkin lymphoma and classical Hodgkin lymphoma.

作者信息

Bohn Olga, Maeda Takahiro, Filatov Alexander, Lunardi Andrea, Pandolfi Pier Paolo, Teruya-Feldstein Julie

机构信息

1Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

出版信息

Int J Surg Pathol. 2014 Feb;22(1):6-11. doi: 10.1177/1066896913513833. Epub 2013 Dec 10.

Abstract

Classical Hodgkin lymphoma (CHL) and nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) are considered separate entities with different prognosis and treatment. However, morphologic features can be similar and immunohistochemical studies are essential in the distinction; thus, determination of additional biomarkers is of utmost importance. LRF/Pokemon is a proto-oncogene, an interacting partner co-expressed with BCL6 in germinal centers and highly expressed in diffuse large B-cell lymphoma and follicular lymphoma. Conversely, loss of the LRF gene in mouse hematopoietic stem cells results in complete block of early B cell development with concomitant Notch de-repression, indicating its critical role in B versus T cell fate decision at the hematopoietic stem cell stage. For the first time, we show that LRF/Pokemon is predominantly expressed in NLPHL cases as is BCL6 with low to absent NOTCH1 protein expression; while Hodgkin Reed-Sternberg (HRS) cells in CHL show low to absent BCL6 and LRF/Pokemon expression with higher NOTCH1 expression. We illustrate a potential functional interaction between LRF and BCL6 in NLPHL pathogenesis, and differential expression of LRF/Pokemon and NOTCH1 proteins in CHL thus showing differential expression, making for an additional diagnostic marker and therapeutic target.

摘要

经典型霍奇金淋巴瘤(CHL)和结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)被认为是具有不同预后和治疗方式的独立实体。然而,它们的形态学特征可能相似,免疫组化研究对于鉴别至关重要;因此,确定额外的生物标志物至关重要。LRF/Pokemon是一种原癌基因,是在生发中心与BCL6共表达且在弥漫性大B细胞淋巴瘤和滤泡性淋巴瘤中高表达的相互作用伴侣。相反,小鼠造血干细胞中LRF基因的缺失会导致早期B细胞发育完全受阻,并伴随Notch去抑制,表明其在造血干细胞阶段B细胞与T细胞命运决定中起关键作用。我们首次表明,LRF/Pokemon在NLPHL病例中主要表达,BCL6也是如此,而NOTCH1蛋白表达低或缺失;而CHL中的霍奇金-里德-斯腾伯格(HRS)细胞BCL6和LRF/Pokemon表达低或缺失,NOTCH1表达较高。我们阐述了LRF和BCL6在NLPHL发病机制中的潜在功能相互作用,以及LRF/Pokemon和NOTCH1蛋白在CHL中的差异表达,从而显示出差异表达,这使其成为一种额外的诊断标志物和治疗靶点。

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