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原发性脑恶性淋巴瘤:重排免疫球蛋白重链基因的突变模式

Primary malignant lymphoma of the brain: mutation pattern of rearranged immunoglobulin heavy chain gene.

作者信息

Endo Sumio, Zhang Shu-Jing, Saito Takafumi, Kouno Mitsuo, Kuroiwa Toshihiko, Washiyama Kazuo, Kumanishi Toshiro

机构信息

Molecular Neuropathology, Brain Research Institute, Niigata University, Niigata 951-8585, Japan.

出版信息

Jpn J Cancer Res. 2002 Dec;93(12):1308-16. doi: 10.1111/j.1349-7006.2002.tb01239.x.

Abstract

Using reverse transcription-polymerase chain reaction (RT-PCR), six primary brain lymphomas, pathologically diagnosed as diffuse large B-cell lymphoma, were examined for rearranged VH-D-JH sequences of the immunoglobulin heavy chain gene, focusing on somatic mutations and intraclonal heterogeneity. The reliability of the isolated PCR clones was confirmed by in situ hybridization (ISH) with complementarity-determining region (CDR) 3 oligonucleotide probes. Sequence analysis of the PCR clones revealed a high frequency of somatic mutation, ranging from 8.8 to 27.3% (mean 18.2%) in the VH gene segments in all the lymphomas. A significantly lower frequency of replacement (R) mutations than expected was also seen in their frameworks (FRs) in all cases. These findings suggested that the precursor cells were germinal center (GC)-related cells in these lymphomas. However, despite extensive cloning experiments, intraclonal heterogeneity was not detected in any case except for one in which it could not be ruled out. Thus, it seemed likely that all of our brain lymphomas were derived from GC-related cells and that at least most of them were from post-GC cells.

摘要

使用逆转录聚合酶链反应(RT-PCR),对6例经病理诊断为弥漫性大B细胞淋巴瘤的原发性脑淋巴瘤进行免疫球蛋白重链基因重排的VH-D-JH序列检测,重点关注体细胞突变和克隆内异质性。通过使用互补决定区(CDR)3寡核苷酸探针的原位杂交(ISH)来确认分离的PCR克隆的可靠性。PCR克隆的序列分析显示,所有淋巴瘤的VH基因片段中体细胞突变频率很高,范围为8.8%至27.3%(平均18.2%)。在所有病例中,其框架区(FRs)中的置换(R)突变频率也明显低于预期。这些发现表明,这些淋巴瘤中的前体细胞是生发中心(GC)相关细胞。然而,尽管进行了广泛的克隆实验,但除了1例无法排除克隆内异质性的情况外,在任何病例中均未检测到克隆内异质性。因此,我们所有的脑淋巴瘤似乎都源自GC相关细胞,并且至少其中大多数来自GC后细胞。

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