Institute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.
BMC Cancer. 2009 Dec 21;9:455. doi: 10.1186/1471-2407-9-455.
Although primary lymphomas of the central nervous system (PCNSL) and extracerebral diffuse large B-cell lymphoma (DLBCL) cannot be distinguished histologically, it is still a matter of debate whether PCNSL differ from systemic DLBCL with respect to their molecular features and pathogenesis. Analysis of the DNA methylation pattern might provide further data distinguishing these entities at a molecular level.
Using an array-based technology we have assessed the DNA methylation status of 1,505 individual CpG loci in five PCNSL and compared the results to DNA methylation profiles of 49 DLBCL and ten hematopoietic controls.
We identified 194 genes differentially methylated between PCNSL and normal controls. Interestingly, Polycomb target genes and genes with promoters showing a high CpG content were significantly enriched in the group of genes hypermethylated in PCNSL. However, PCNSL and systemic DLBCL did not differ in their methylation pattern.
Based on the data presented here, PCNSL and DLBCL do not differ in their DNA methylation pattern. Thus, DNA methylation analysis does not support a separation of PCNSL and DLBCL into individual entities. However, PCNSL and DLBCL differ in their DNA methylation pattern from non- malignant controls.
尽管中枢神经系统原发性淋巴瘤(PCNSL)和脑外弥漫性大 B 细胞淋巴瘤(DLBCL)在组织学上无法区分,但 PCNSL 是否在分子特征和发病机制方面与系统性 DLBCL 存在差异仍存在争议。DNA 甲基化模式的分析可能会提供进一步的分子水平上区分这些实体的数据。
我们使用基于阵列的技术评估了五个 PCNSL 中 1505 个单个 CpG 位点的 DNA 甲基化状态,并将结果与 49 个 DLBCL 和 10 个造血对照的 DNA 甲基化图谱进行了比较。
我们鉴定了 PCNSL 与正常对照之间存在 194 个差异甲基化基因。有趣的是,多梳靶基因和启动子中具有高 CpG 含量的基因在 PCNSL 中高度甲基化的基因群中显著富集。然而,PCNSL 和系统性 DLBCL 在其甲基化模式上没有差异。
根据这里提出的数据,PCNSL 和 DLBCL 在其 DNA 甲基化模式上没有差异。因此,DNA 甲基化分析不支持将 PCNSL 和 DLBCL 分离成单独的实体。然而,PCNSL 和 DLBCL 与非恶性对照在 DNA 甲基化模式上存在差异。