GNA13是生发中心源性B细胞淋巴瘤的新标志物

Xiaokang Ke , Qingping Zhang , Pengcheng Zhu , Huihua He , Jingping Yuan , Qilin Ao
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引用次数: 0

摘要

目的评估GNA13在生发中心(GC)源性B细胞淋巴瘤中的表达,以评估其作为诊断标志物的潜力。方法与结果采用免疫组化方法检测129例b细胞非霍奇金淋巴瘤(b - nhl)和8例血管免疫母细胞t细胞淋巴瘤(AITL)中GNA13的表达。此外,通过外显子组测序检测了114例b - nhl患者的GNA13基因突变。50例弥漫性大b细胞淋巴瘤(DLBCL)中,GNA13阳性11例,阳性病例均为生发中心b细胞样(GCB)亚型。42例滤泡性淋巴瘤(FL)中,gna13阳性率为1级100%,2级100%,3a级80.0%,3B级63.2%。6例伯基特淋巴瘤中,3例GNA13阳性。而在小淋巴细胞淋巴瘤、套细胞淋巴瘤和边缘带淋巴瘤中,GNA13阴性或仅在GC中表达。此外,AITL中gna13阳性检出率为100%。GNA13基因在GCB-DLBCL中突变率为27.8%(5/18),在FL中突变率为10.3%(3/29),在GNA13蛋白弱阳性或阴性表达的病例中均发生突变。结论ongna13可作为GC源性b细胞淋巴瘤可靠的新标志物。它的缺乏或低表达可能与gc源性b细胞淋巴瘤的侵袭程度有关,也可能由基因突变引起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GNA13 is a new marker for germinal center-derived B cell lymphomas

Aims

We aim to evaluate the expression of GNA13 in germinal center (GC)-derived B cell lymphomas to evaluate its potential use as marker for diagnosis.

Methods and Results

In this study, GNA13 expression was detected by immunohistochemistry in 129 cases of B-cell non-Hodgkin lymphomas (B-NHLs) and 8 cases of angioimmunoblastic T-cell lymphoma (AITL). Furthermore, mutations in the GNA13 gene in 114 cases of B-NHLs were detected by exome sequencing. In 50 cases of diffuse large B-cell lymphoma (DLBCL), 11 cases were positive for GNA13, and all GNA13-positive cases were of the germinal center B-cell-like (GCB) subtype. In 42 cases of follicular lymphoma (FL), the GNA13-positive rate was 100% in FL grade 1, 100% in FL grade 2, 80.0% in FL grade 3 A, and 63.2% in FL grade 3B. In 6 cases of Burkitt lymphoma, 3 cases were positive for GNA13. However, in small lymphocytic lymphoma, mantle cell lymphoma and marginal zone lymphoma, GNA13 was negative or only expressed in the GC. In addition, the GNA13-positive rate was 100% in AITL. The mutation of the GNA13 gene was 27.8% (5/18) in GCB-DLBCL and 10.3% (3/29) in FL, respectively, and mutation of GNA13 occurred in cases with weak positive or negative expression of the GNA13 protein.

Conclusion

GNA13 may be a reliable new marker for GC cells applied in the diagnosis of GC-derived B-cell lymphomas. Its deficiency or low expression may be related to the degree of invasion of GC-derived B-cell lymphomas, and may result from genetic mutations.

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