脾边缘区淋巴瘤的CD79B和MYD88突变。

ISRN oncology Pub Date : 2013-01-01 Epub Date: 2013-01-10 DOI:10.1155/2013/252318
Gunhild Trøen, Abdirashid Warsame, Jan Delabie
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引用次数: 31

摘要

探讨脾边缘区淋巴瘤中NF-κB信号通路相关基因的突变情况。对通过BCR信号或toll样和白细胞介素信号激活的四个基因CD79A、CD79B、CARD11和MYD88进行DNA序列分析。在10例SMZL病例中检测到CD79B基因(Y196H)的单点突变。此外,在另一个SMZL病例中,在MYD88基因(L265P)中发现了一个点突变。在这些SMZL病例中未发现CD79A或CARD11基因突变。在13份对照MZL样品中均未检测到这4个基因的突变。有趣的是,两例CD79B和MYD88突变的病例显示,在较小的典型边缘带淋巴瘤细胞中扩散的免疫母细胞数量增加。虽然SMZL显示NF-κB信号基因的少量突变,但我们的研究结果表明,这些突变的存在与更高的组织学分级有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CD79B and MYD88 Mutations in Splenic Marginal Zone Lymphoma.

CD79B and MYD88 Mutations in Splenic Marginal Zone Lymphoma.

CD79B and MYD88 Mutations in Splenic Marginal Zone Lymphoma.

CD79B and MYD88 Mutations in Splenic Marginal Zone Lymphoma.

The mutation status of genes involved in the NF-κB signaling pathway in splenic marginal zone lymphoma was examined. DNA sequence analysis of four genes was performed: CD79A, CD79B, CARD11, and MYD88 that are activated through BCR signaling or Toll-like and interleukin signaling. A single point mutation was detected in the CD79B gene (Y196H) in one of ten SMZL cases. Additionally, one point mutation was identified in the MYD88 gene (L265P) in another SMZL case. No mutations were revealed in CD79A or CARD11 genes in these SMZL cases. Neither were mutations detected in these four genes studied in 13 control MZL samples. Interestingly, the two cases with mutations of CD79B and MYD88 showed increased numbers of immunoblasts spread among the smaller and typical marginal zone lymphoma cells. Although SMZL shows few mutations of NF-κB signaling genes, our results indicate that the presence of these mutations is associated with a higher histological grade.

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