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Cellular (FLICE) like inhibitory protein (cFLIP) expression in diffuse large B-cell lymphoma identifies a poor prognostic subset, but fails to predict the molecular subtype

机译:弥漫性大B细胞淋巴瘤中的细胞(FLICE)样抑制蛋白(cFLIP)表达可识别预后不良的亚型,但无法预测分子亚型

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摘要

Immunohistochemistry can sub-classify diffuse large B-cell lymphoma (DLBCL) into germinal centre B-cell like (GCB) and non-GCB subtypes. The latter consists predominately of the activated B-cell like subgroup in which nuclear factor kappa-B activation is its characteristic. Expression of cellular caspase 8 (FLICE)-like inhibitory protein (cFLIP), a caspase 8 homologue, is regulated by nuclear factor kappa-B signalling, and it is the main inhibitor of Fas ligand activated apoptosis. To determine if cFLIP expression was confined to non-GCB subtype, we studied 66 cases of DLBCL. cFLIP expression showed no significant correlation to DLBCL subtypes (GCB or non-GCB) but was associated with a worse clinical outcome. For cFLIP positive and negative patients, the five-year event free survival was 20 and 31%, respectively (p=0.049), and the five-year overall survival was 20 and 57%, respectively (p=0.041).
机译:免疫组织化学可以将弥漫性大B细胞淋巴瘤(DLBCL)细分为生发中心B细胞样(GCB)和非GCB亚型。后者主要由活化的B细胞样亚组组成,其中核因子κB活化是其特征。细胞半胱天冬酶8(FLICE)样抑制蛋白(cFLIP)的表达是一种半胱天冬酶8的同源物,受核因子κB信号传导调节,是Fas配体激活细胞凋亡的主要抑制剂。为了确定cFLIP表达是否仅限于非GCB亚型,我们研究了66例DLBCL病例。 cFLIP表达与DLBCL亚型(GCB或非GCB)无显着相关性,但与较差的临床结果相关。对于cFLIP阳性和阴性患者,五年无事件生存率分别为20%和31%(p = 0.049),五年总生存率分别为20%和57%(p = 0.041)。

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