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CD43 的表达与弥漫性大 B 细胞淋巴瘤非生发中心 B 细胞亚组的不良生存相关。

CD43 expression is associated with inferior survival in the non-germinal centre B-cell subgroup of diffuse large B-cell lymphoma.

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Br J Haematol. 2013 Jul;162(1):87-92. doi: 10.1111/bjh.12356. Epub 2013 Apr 25.

Abstract

We evaluated the prognostic significance of CD43 (SPN), a membrane glycoprotein, in 140 patients with diffuse large B-cell lymphoma (DLBCL) by tissue microarray (TMA) immunostaining, and gene expression profiling (GEP) in 43 patients. CD43 protein was expressed in 19% of the cases and was strongly related to the non-germinal centre B-cell (non-GCB) subgroup by both TMA and GEP. Patients with CD43(+) DLBCL had an inferior 3-year overall survival (OS) compared to those with CD43(-) DLBCL (50% vs. 76%, P = 0·01). Within the non-GCB subgroup, patients with CD43(+) DLBCL had a particularly poor 3-year OS (32% vs. 71%, P < 0·001). Gene set enrichment analysis within the activated B-cell subgroup revealed significant enrichment in the stromal-1 signature in CD43(-) cases. We conclude that CD43 is an adverse prognostic marker in DLBCL, and is preferentially expressed in the non-GCB subgroup. The dismal outcome of CD43(+) cases in the non-GCB subgroup may be explained, at least in part, by a less favourable microenvironment.

摘要

我们通过组织微阵列(TMA)免疫染色评估了 140 例弥漫性大 B 细胞淋巴瘤(DLBCL)患者中膜糖蛋白 CD43(SPN)的预后意义,并对 43 例患者进行了基因表达谱(GEP)分析。CD43 蛋白在 19%的病例中表达,并通过 TMA 和 GEP 均与非生发中心 B 细胞(non-GCB)亚组强烈相关。与 CD43(-)DLBCL 患者相比,CD43(+)DLBCL 患者的 3 年总生存率(OS)较低(50% vs. 76%,P=0.01)。在 non-GCB 亚组中,CD43(+)DLBCL 患者的 3 年 OS 尤其差(32% vs. 71%,P<0.001)。在激活 B 细胞亚组内进行的基因集富集分析显示,CD43(-)病例中基质-1 特征明显富集。我们得出结论,CD43 是 DLBCL 的不良预后标志物,并且在 non-GCB 亚组中优先表达。CD43(+)病例在 non-GCB 亚组中的不良预后至少部分可以通过不太有利的微环境来解释。

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