Bohn Olga, Maeda Takahiro, Filatov Alexander, Lunardi Andrea, Pandolfi Pier Paolo, Teruya-Feldstein Julie
1Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Int J Surg Pathol. 2014 Feb;22(1):6-11. doi: 10.1177/1066896913513833. Epub 2013 Dec 10.
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.
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。