Array-based DNA methylation profiling of primary lymphomas of the central nervous system
BMC Cancer volume 9, Article number: 455 (2009)
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.
Primary lymphomas of the central nervous system (PCNSL) are highly malignant B-cell lymphomas confined to the central nervous system (CNS) with a poor prognosis . They are considered as separate entity within the updated WHO classification , although they cannot be distinguished histologically and immunophenotypically from extracerebral diffuse large B-cell lymphoma (DLBCL). However, based on the remarkably worse clinical course and prognosis it is still a matter of debate whether PCNSL differ from systemic DLBCL with respect to their molecular features and pathogenesis. Interphase cytogenetic and molecular genetic studies have shown that PCNSL share a variety of features with systemic DLBCL. These include rearranged immunoglobulin (IG) gene segments with evidence for ongoing somatic hypermutation, aberrant somatic hypermutation of non-IG genes, translocations affecting the IG and BCL6 genes, gains in chromosome band 18q21, and mutations of the PRDM1 gene . With respect to their gene expression profile PCNSL segregate along the spectrum of systemic DLBCL including the ABC- and GCB-types of DLBCL [3, 4].
Epigenetic silencing of functionally important genes by DNA methylation may also contribute to PCNSL development [5–10]. By studying DNA methylation of 14 tumor suppressor genes in 25 PCNSL using methylation-specific PCR, Chu et al.  demonstrated that all PCNSL had methylated at least two of the genes studied. Although these findings suggest DNA methylation of tumor suppressor genes to be a common event in PCNSL, previous studies on DNA methylation have been limited to a rather small number of a few selected genes. The recent availability of array-based techniques offers the opportunity for a more comprehensive DNA methylation profiling [11, 12]. Here, a series of PCNSL was studied for DNA methylation of 1,505 CpG sites from 807 selected genes including a significant number of genes relevant for tumorigenesis. By comparing DNA methylation profiles of PCNSL to those recently obtained for normal hematopoietic controls and 49 systemic DLBCL , we identified 194 genes to be differentially methylated between PCNSL and normal controls. Four genes were putatively differentially methylated between PCNSL and systemic DLBCL. Based on the DNA methylation pattern these lymphoma entities did not segregate suggesting DNA methylation pattern of PCNSL and systemic DLBCL to be highly comparable.
DNA extraction and samples
DNA samples from five tumors diagnosed as PCNSL (two of ABC- and three of GCB-subtype, all from female patients) as described recently  and classified according to the WHO classification 2008  were subjected to array-based DNA methylation profiling. Systemic lymphoma manifestation was excluded by extensive staging. All studies were approved by local ethics committees. Informed consent was provided according to the Declaration of Helsinki. DNA extraction was performed as described previously . The DNA samples of 49 systemic DLBCL and of 10 normal controls have been described in detail recently [12, 14]. The tumor cell content of DLBCL samples was >70% as verified by a panel of experienced pathologists.
DNA methylation profiling using universal BeadArrays
DNA methylation analyses were performed using the GoldenGate Methylation Cancer Panel I (Illumina Inc., San Diego, CA) as described previously . The array allows assaying 1,505 CpG sites from 807 selected genes, which include numerous genes relevant for tumorigenesis including oncogenes, tumor suppressor genes, and genes involved in metastasis, differentiation, cell cycle control, and apoptosis. The complete dataset is provided as supplementary information (Additional file 1). The reproducibility and accuracy of the GoldenGate Cancer Panel I based DNA methylation analysis has been demonstrated extensively [11, 12].
Analyses of the DNA methylation data obtained by the GoldenGate Methylation Cancer Panel I
DNA methylation profiling data from 10 hematopoietic controls (analysed in replicates) and 49 systemic DLBCL obtained recently with the same platform served for comparison and have been reanalyzed in this study . As detailed in Additional file 2, normal controls contained two samples of tonsillar germinal center B-cells, two normal peripheral blood samples, and six lymphoblastoid cell lines. Systemic DLBCL were classified as non molecular Burkitt lymphoma (non-mBL) by gene expression profiling and included 29 ABC and 20 GCB-type DLBCL [12, 14]. Identification of imprinted CpGs and gender-specifically methylated CpGs on chromosome X has been performed as described recently . Using BeadStudio software (ver.3, Illumina Inc., San Diego, CA) agglomerative hierarchical clustering was performed in PCNSL, systemic DLBCL, and normal hematopoietic controls excluding CpG loci located in imprinted genes and X-chromosomal genes with gender-specific methylation (1,284 CpGs corresponding to 716 genes were included for further analysis). The statistical analyses used to define the different DNA methylation subgroups have been detailed recently . The data obtained from the arrays were not normalized. In addition, differential methylation analysis (DMA) has also been performed using the BeadStudio Software. CpG loci with calculated DiffScores below -30 or above 30 (corresponding to a p-value of p > 0.001, based on a t-statistic) simultaneously showing an absolute DeltaBeta value above 0.3 (corresponding to a difference of 30% in the DNA methylation level) were considered as differentially methylated. The global DNA methylation data per case shows a bimodal distribution in which beta values < 0.25 defines the unmethylated CpGs and beta values> 0.75 the methylated CpGs . Thus, beta values below 0.25 and above 0.75 were selected as threshold-values to define unmethylated and methylated CpG loci for further analysis.
Enrichment for PcG-marks and promoter classes in different DNA methylation groups
Identification of Polycomb target genes and promoter classification into promoters with high (HCP), intermediate (ICP), and low (LCP) CpG content respectively, are based on recent publications [15–17]. Annotation lists of Polycomb group (PcG) marks and promoter classes were compared with the genes analyzed for methylation via gene symbol or locuslink ID. Proportions of genes in the different methylation groups were compared with respect to PcG-marks and promoter classes as described previously .
Principal component analysis (PCA)
PCA has been performed using the Omics Explorer, Version 2.0 Beta (Qlucore AB, Lund, Sweden).
The "Gene Annotation Tool to Help Explain Relationships" (GATHER; http://gather.genome.duke.edu) has been used to determine the enrichment of individual ontology terms in the group of genes differentially methylated in PCNSL and normal controls (with respect to the overall composition of the GoldenGate array). Ontology terms with an at least twofold increase in numbers of genes between the tested group and the array containing at least five individual genes, were tested for significance of enrichment by performing Fisher's exact test.
Fisher's exact test and Mann-Whitney test were performed using GraphPad Prism version 4.02 for Windows, GraphPad Software, San Diego, CA.
Array-based DNA methylation profiling of PCNSL
The BeadArray technology [11, 18] was applied to perform quantitative DNA methylation analyses of 1,505 individual CpGs corresponding to 807 genes relevant for tumorigenesis in five PCNSL. Results were compared to those recently obtained for ten hematopoietic controls and 49 systemic DLBCL . Genes known to be imprinted and X-chromosomal genes with gender-specific methylation were excluded from the analysis, as they are partially methylated under physiological conditions and might represent a confounding variable to classify cases according to their DNA methylation profile. Thus, a total of 1,284 CpGs corresponding to 716 genes entered the analysis.
Identification of genes differentially methylated between PCNSL and hematopoietic controls
PCA based analysis applying most stringent conditions differentiates normal controls from both PCNSL and systemic DLBCL samples in a highly significant fashion (p = 1.2 × 10-12, q = 3.9157 × 10-11; Fig. 1A). 33 CpG loci (corresponding to 30 genes) differentiating between PCNSL and controls performed in replicates were significantly hypermethylated while three CpG loci showed hypomethylation in PCNSL compared to hematopoietic controls (Fig. 1B).
Supervised cluster analysis of the 1,284 CpGs comparing the five PCNSL to ten hematopoietic controls resulted in 296 differentially methylated CpGs corresponding to 194 genes (Additional file 3). Of these 194 genes, 153 genes were hypermethylated while 41 genes were hypomethylated in PCNSL. Unsupervised cluster analysis of the five PCNSL and the 10 hematopoietic controls along with the 49 systemic DLBCL samples for all 1,284 CpGs separated all lymphoma samples from normal controls (Fig. 1C). These findings suggest that the methylation profile of PCNSL strongly differs from that of normal hematopoietic tissues including tonsillar germinal center B-cells and lymphoblastoid cells.
CpG loci differentially methylated in PCNSL and systemic DLBCL
The methylation pattern of both PCNSL and systemic DLBCL were very heterogeneous with respect to total DNA methylation (data not shown). To address the question whether the DNA methylation pattern of PCNSL differs from that of systemic DLBCL, we compared DNA methylation values of 1,284 CpG loci from the five PCNSL with those of the 49 systemic DLBCL. Of the 194 genes differentially methylated between normal controls and PCNSL, using the same analysis approach, 157 genes were among the 174 genes differentially methylated between controls and DLBCL (Additional file 4). Neither supervised nor unsupervised cluster analysis separated PCNSL from systemic DLBCL (Fig. 1C, D, and data not shown). A differential methylation analysis (DMA) of PCNSL and systemic DLBCL cases yielded only four CpGs differentially methylated between PCNSL and systemic DLBCL (ESR1, EFNA1, MATK, and PDE1B). However, hierarchical cluster analysis performed on these four CpG loci failed to distinguish PCNSL from systemic DLBCL (Additional file 5). Thus, methylation analysis of these CpG loci does not allow a proper assignment of unknown samples to either PCNSL or systemic DLBCL. Furthermore, PCA failed to differentiate between PCNSL and systemic DLBCL (Fig. 1A, and data not shown). In conclusion, PCNSL did not exhibit a specific DNA methylation signature as compared to systemic DLBCL including more than 700 genes which had entered this study.
Classification of genes based on their DNA methylation pattern in PCNSL as compared to non-neoplastic hematopoietic tissues
To get further insight into DNA hypermethylation in PCNSL, we compared the class of genes methylated in PCNSL but not in controls (meP/umC, n = 138) to the classes of genes unmethylated or methylated in both PCNSL and controls (umP/umC, n = 348 genes and meP/meC, n = 91 genes), respectively. These groups provided the basis for further analysis (Additional file 6).
The group of genes methylated in PCNSL but unmethylated in non-neoplastic hematopoietic controls is enriched for polycomb targets in embryonic stem cells and promoters with high CpG content
The group of genes unmethylated in the hematopoietic controls but methylated in PCNSL was highly significantly enriched for genes repressed by the polycomb (PcG) repressing complexes (PRC2) in embryonic stem cells compared to the genes present on the array (Fig. 2A; RR = 2.55; p < 0.0001, Fisher's exact test). This group was also enriched for the simultaneous presence of all three PRC2 marks as described previously [12, 15, 16]: EED (RR = 2.62), SUZ12 (RR = 2.68) and 3 mK27-H3 (RR = 2.54) (Fig. 2B). However, the targets of a specific PRC2 mark were not preferentially enriched in any group (Fig. 2C). While the percentage of PcG target genes in the group of genes unmethylated (um) in both controls (C) and PCNSL (P) (umP/umC) did not differ significantly from the one of the GoldenGate array (RR = 0.81; p = 0.1675), the percentage of PcG target genes was significantly reduced (RR = 0,30; p = 0.0010) in the group of genes methylated (me) in both PCNSL and normal controls (meP/meC) (Fig. 2A, B).
Since it was reported previously that particular promoters with high CpG content and CpG islands become methylated in tumors [19–22], we have sorted the genes in the groups defined above in genes having promoters with high (HCP), intermediate (ICP), or low (LCP) CpG content , respectively. While the group of genes methylated in both PCNSL and controls (meP/meC) was enriched for genes with low CpG content promoters (LCP; RR = 2.21; p < 0.0001), the remaining two groups were enriched by genes having promoters with high CpG content (umP/umC: RR = 1.17; p = 0.0023; meP/umC: RR = 1.35; p < 0.0001; Fig. 2D). The CpG loci belonging to genes methylated in PCNSL and controls were furthermore significantly enriched for loci located outside of CpG Islands (RR = 2.24; p < 0.0001).
The group of genes differentially methylated in PCNSL is enriched for genes involved in neurological processes and cellular signaling pathways
As genes studied with the methylation-specific BeadArray were selected for their involvement in tumorigenesis, they will "by definition" be deregulated in various tumors. Even considering this bias, we tested whether genes differentially methylated in PCNSL and normal controls were enriched for specific Gene Ontology (GO) terms. Surprisingly, we observed that terms particularly involved in neurophysiological and perception processes were significantly enriched (Additional file 7). However, the same GO terms were also enriched in systemic DLBCL. Thus, a PCNSL specific enrichment of individual GO terms differing from DLBCL was not identified.
In the present study, we determined DNA methylation patterns in tumor samples of five patients suffering from PCNSL and compared them to the methylation pattern of 49 systemic DLBCL and ten normal hematopoietic controls, which have been characterized in detail before [12, 14]. The GoldenGate Cancer Panel I used in this study offers the possibility to analyze 1,505 single CpG loci corresponding to 807 genes in parallel. To prevent any bias because of gender specific DNA methylation and imprinting effects, X-chromosomal genes and genes known to be imprinted, the methylation extent of which varies under normal physiological conditions, have been excluded from further analyses. The reproducibility and the accuracy of this array based approach have been extensively demonstrated before [12, 18].
Of the 1,284 CpG loci focused on in this study, we identified 296 CpG loci to be differentially methylated between normal hematopoietic controls and PCNSL corresponding to 194 genes. These include numerous genes known to affect tumorigenesis e.g. by influencing cell proliferation (e.g. CCNA1), signal transduction (e.g. JAK3, IGF1, FGF3, FGFR2, EGF, EGFR), differentiation (e.g. SOX1, SOX17, SOX2, MYOD1, PAX6, HOXA9, HOXB13, ETS2) or spread of tumor cells within the brain (e.g. MMP19, MMP2, MMP7) [23–26]. Furthermore, by applying a more stringent PCA based approach, 36 CpG loci sufficient to differentiate between PCNSL and hematopoietic controls in a highly significant fashion have been identified.
Previous studies on DNA methylation in PCNSL were limited by their restriction to a low number of selected genes. Our data are in line with Chu et al. and Gonzales-Gomez et al. [5, 8] analyzing the DNA methylation of CDKN2B, DAPK1, GSTP1, MGMT, MLH1, RARB, THBS1, TIMP2, and TIMP3 in PCNSL by MSP (Additional file 8) further supporting the validity of our analysis. This is of special interest, since our data on PCNSL are based on a minor number of five cases, because of the limited availability of sample material. Our results regarding CDKN2A are somewhat contradictory, however, one should keep in mind that the CpG loci analyzed by the GoldenGate array and by MSP are not identical. In addition, MSP data are not quantitative  and analysis of the CDKN2A locus might be affected by recurrent deletions of this gene in PCNSL .
A further analysis of genes which were unmethylated in hematopoietic controls and methylated in PCNSL (meP/umC) showed a significant enrichment of genes which are repressed by components of the PRC2 in embryonic stem cells. Components of the PRC2 complex are essential for the maintenance of the undifferentiated state of embryonic stem cells by suppressing genes called PcG target genes, the activation of which leads to cellular differentiation [16, 29]. Indeed, hypermethylation of PcG target genes has been described for several tumor entities  including systemic mature aggressive B-cell lymphomas . This enrichment of genes controlled by PRC2 during stem cell maintenance could lead to the hypothesis that the tumor cells of PCNSL cells derive from a stem cell like progenitor cell. Alternatively, dedifferentiation and epigenetic reprogramming of an already differentiated precursor cell could also explain the DNA methylation pattern . The latter model is supported by previous data lending support for the hypothesis that the tumor cells derived from mature GC exit B-cells . Finally, genes anyhow silenced in the hematopoietic lineage could become switched off by DNA methylation in tumor cells .
Interestingly, genes with three PcG-marks in the promoter region were significantly enriched, while there was no enrichment of a specific mark (neither EED, SUZ12 or 3 meK27-H3) in PCNSL. This is in line with results obtained for systemic mature B-cell lymphomas . Furthermore, also similar to the scenario described for other B-cell lymphomas, in particular genes with high CpG content promoters become methylated in PCNSL. This correlates well with the known phenomenon that CpG islands in promoter regions become methylated during tumorigenesis [31–33].
In a recent study addressing genomic imbalances in PCNSL  several genes hypermethylated in PCNSL, including e.g. ERBB3, PDE1B, ASCL1, and BCAM were located in regions with recurrent genomic gains. However, they were not expressed in the tumor . Since DNA methylation has been associated with gene repression in numerous studies [35–37], our data on DNA methylation might offer a putative explanation why increased gene dosage does not lead to increased gene expression and even transcriptional silencing in PCNSL. However, since a number of recent studies have shown little correlation between tumor specific hypermethylation and changes in gene expression [12, 38, 39], this must be addressed by future studies.
Comparing the DNA methylation state of 1,284 CpG loci in PCNSL, systemic DLBCL, and hematopoietic controls, a DNA methylation pattern exclusively specific for PCNSL was not identified. The methylation data do not allow distinguishing PCNSL from systemic DLBCL on the basis of DNA methylation levels. However, the present study does not exclude the possibility that analysis of a larger number of CpG loci of the genome in a larger series of PCNSL might identify PCNSL specific features.
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW: WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, Fourth Edition. 2008, Geneva: WHO Press
Montesinos-Rongen M, Siebert R, Deckert M: Primary lymphoma of the central nervous system: just DLBCL or not?. Blood. 2009, 113 (1): 7-10. 10.1182/blood-2008-04-149005.
Montesinos-Rongen M, Brunn A, Bentink S, Basso K, Lim WK, Klapper W, Schaller C, Reifenberger G, Rubenstein J, Wiestler OD, et al: Gene expression profiling suggests primary central nervous system lymphomas to be derived from a late germinal center B cell. Leukemia. 2008, 22 (2): 400-405. 10.1038/sj.leu.2405019.
Rubenstein JL, Treseler P, O'Brien JM: Pathology and genetics of primary central nervous system and intraocular lymphoma. Hematol Oncol Clin North Am. 2005, 19 (4): 705-717. 10.1016/j.hoc.2005.05.012.
Chu LC, Eberhart CG, Grossman SA, Herman JG: Epigenetic silencing of multiple genes in primary CNS lymphoma. Int J Cancer. 2006, 119 (10): 2487-2491. 10.1002/ijc.22124.
Cobbers JM, Wolter M, Reifenberger J, Ring GU, Jessen F, An HX, Niederacher D, Schmidt EE, Ichimura K, Floeth F, et al: Frequent inactivation of CDKN2A and rare mutation of TP53 in PCNSL. Brain Pathol. 1998, 8 (2): 263-276.
Ferreri AJ, Dell'Oro S, Capello D, Ponzoni M, Iuzzolino P, Rossi D, Pasini F, Ambrosetti A, Orvieto E, Ferrarese F, et al: Aberrant methylation in the promoter region of the reduced folate carrier gene is a potential mechanism of resistance to methotrexate in primary central nervous system lymphomas. Br J Haematol. 2004, 126 (5): 657-664. 10.1111/j.1365-2141.2004.05109.x.
Gonzalez-Gomez P, Bello MJ, Arjona D, Alonso ME, Lomas J, Aminoso C, de Campos JM, Sarasa JL, Gutierrez M, Rey JA: CpG island methylation of tumor-related genes in three primary central nervous system lymphomas in immunocompetent patients. Cancer Genet Cytogenet. 2003, 142 (1): 21-24. 10.1016/S0165-4608(02)00799-9.
Nakamura M, Ishida E, Shimada K, Nakase H, Sakaki T, Konishi N: Defective expression of HRK is associated with promoter methylation in primary central nervous system lymphomas. Oncology. 2006, 70 (3): 212-221. 10.1159/000094322.
Zhang SJ, Endo S, Saito T, Kouno M, Kuroiwa T, Washiyama K, Kumanishi T: Primary malignant lymphoma of the brain: frequent abnormalities and inactivation of p14 tumor suppressor gene. Cancer Sci. 2005, 96 (1): 38-41.
Bibikova M, Lin Z, Zhou L, Chudin E, Garcia EW, Wu B, Doucet D, Thomas NJ, Wang Y, Vollmer E, et al: High-throughput DNA methylation profiling using universal bead arrays. Genome Res. 2006, 16 (3): 383-393. 10.1101/gr.4410706.
Martin-Subero JI, Kreuz M, Bibikova M, Bentink S, Ammerpohl O, Wickham-Garcia E, Rosolowski M, Richter J, Lopez-Serra L, Ballestar E, et al: New insights into the biology and origin of mature aggressive B-cell lymphomas by combined epigenomic, genomic, and transcriptional profiling. Blood. 2009, 113 (11): 2488-2497. 10.1182/blood-2008-04-152900.
Montesinos-Rongen M, Kuppers R, Schluter D, Spieker T, Van Roost D, Schaller C, Reifenberger G, Wiestler OD, Deckert-Schluter M: Primary central nervous system lymphomas are derived from germinal-center B cells and show a preferential usage of the V4-34 gene segment. Am J Pathol. 1999, 155 (6): 2077-2086.
Hummel M, Bentink S, Berger H, Klapper W, Wessendorf S, Barth TF, Bernd HW, Cogliatti SB, Dierlamm J, Feller AC, et al: A biologic definition of Burkitt's lymphoma from transcriptional and genomic profiling. N Engl J Med. 2006, 354 (23): 2419-2430. 10.1056/NEJMoa055351.
Bracken AP, Dietrich N, Pasini D, Hansen KH, Helin K: Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions. Genes Dev. 2006, 20 (9): 1123-1136. 10.1101/gad.381706.
Lee TI, Jenner RG, Boyer LA, Guenther MG, Levine SS, Kumar RM, Chevalier B, Johnstone SE, Cole MF, Isono K, et al: Control of developmental regulators by Polycomb in human embryonic stem cells. Cell. 2006, 125 (2): 301-313. 10.1016/j.cell.2006.02.043.
Schubeler D, Elgin SC: Defining epigenetic states through chromatin and RNA. Nat Genet. 2005, 37 (9): 917-918. 10.1038/ng0905-917.
Bibikova M, Fan JB: GoldenGate(R) Assay for DNA Methylation Profiling. Methods Mol Biol. 2009, 507: 149-163. full_text.
Antequera F, Bird A: CpG islands. Exs. 1993, 64: 169-185.
Antequera F, Boyes J, Bird A: High levels of de novo methylation and altered chromatin structure at CpG islands in cell lines. Cell. 1990, 62 (3): 503-514. 10.1016/0092-8674(90)90015-7.
Laird PW: Cancer epigenetics. Hum Mol Genet. 2005, 14 (Spec No 1): R65-76. 10.1093/hmg/ddi113.
Weber M, Hellmann I, Stadler MB, Ramos L, Paabo S, Rebhan M, Schubeler D: Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet. 2007, 39 (4): 457-466. 10.1038/ng1990.
De Luca A, Carotenuto A, Rachiglio A, Gallo M, Maiello MR, Aldinucci D, Pinto A, Normanno N: The role of the EGFR signaling in tumor microenvironment. J Cell Physiol. 2008, 214 (3): 559-567. 10.1002/jcp.21260.
Eads CA, Lord RV, Wickramasinghe K, Long TI, Kurumboor SK, Bernstein L, Peters JH, DeMeester SR, DeMeester TR, Skinner KA, et al: Epigenetic patterns in the progression of esophageal adenocarcinoma. Cancer Res. 2001, 61 (8): 3410-3418.
Liu D, Nakano J, Ishikawa S, Yokomise H, Ueno M, Kadota K, Urushihara M, Huang CL: Overexpression of matrix metalloproteinase-7 (MMP-7) correlates with tumor proliferation, and a poor prognosis in non-small cell lung cancer. Lung Cancer. 2007, 58 (3): 384-391. 10.1016/j.lungcan.2007.07.005.
Tokumaru Y, Yamashita K, Osada M, Nomoto S, Sun DI, Xiao Y, Hoque MO, Westra WH, Califano JA, Sidransky D: Inverse correlation between cyclin A1 hypermethylation and p53 mutation in head and neck cancer identified by reversal of epigenetic silencing. Cancer Res. 2004, 64 (17): 5982-5987. 10.1158/0008-5472.CAN-04-0993.
Ammerpohl O, Martin-Subero JI, Richter J, Vater I, Siebert R: Hunting for the 5th base: Techniques for analyzing DNA-methylation. BBA - General Subjects. 2009, doi:10.1016/j.bbagen.2009.02.001
Stranks G, Height SE, Mitchell P, Jadayel D, Yuille MA, De Lord C, Clutterbuck RD, Treleaven JG, Powles RL, Nacheva E, et al: Deletions and rearrangement of CDKN2 in lymphoid malignancy. Blood. 1995, 85 (4): 893-901.
Tanay A, O'Donnell AH, Damelin M, Bestor TH: Hyperconserved CpG domains underlie Polycomb-binding sites. Proc Natl Acad Sci USA. 2007, 104 (13): 5521-5526. 10.1073/pnas.0609746104.
Ohm JE, McGarvey KM, Yu X, Cheng L, Schuebel KE, Cope L, Mohammad HP, Chen W, Daniel VC, Yu W, et al: A stem cell-like chromatin pattern may predispose tumor suppressor genes to DNA hypermethylation and heritable silencing. Nat Genet. 2007, 39 (2): 237-242. 10.1038/ng1972.
Baylin SB, Ohm JE: Epigenetic gene silencing in cancer - a mechanism for early oncogenic pathway addiction?. Nat Rev Cancer. 2006, 6 (2): 107-116. 10.1038/nrc1799.
Feinberg AP: The epigenetics of cancer etiology. Semin Cancer Biol. 2004, 14 (6): 427-432. 10.1016/j.semcancer.2004.06.005.
Esteller M: Epigenetic gene silencing in cancer: the DNA hypermethylome. Hum Mol Genet. 2007, 16 (Spec No 1): R50-59. 10.1093/hmg/ddm018.
Schwindt H, Vater I, Kreuz M, Montesinos-Rongen M, Brunn A, Richter J, Gesk S, Ammerpohl O, Wiestler OD, Hasenclever D, et al: Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma. Leukemia. 2009
Mueller W, Nutt CL, Ehrich M, Riemenschneider MJ, von Deimling A, Boom van den D, Louis DN: Downregulation of RUNX3 and TES by hypermethylation in glioblastoma. Oncogene. 2007, 26 (4): 583-593. 10.1038/sj.onc.1209805.
Mulero-Navarro S, Esteller M: Chromatin remodeling factor CHD5 is silenced by promoter CpG island hypermethylation in human cancer. Epigenetics. 2008, 3 (4): 210-215.
Strathdee G, Holyoake TL, Sim A, Parker A, Oscier DG, Melo JV, Meyer S, Eden T, Dickinson AM, Mountford JC, et al: Inactivation of HOXA genes by hypermethylation in myeloid and lymphoid malignancy is frequent and associated with poor prognosis. Clin Cancer Res. 2007, 13 (17): 5048-5055. 10.1158/1078-0432.CCR-07-0919.
Killian JK, Bilke S, Davis S, Walker RL, Killian MS, Jaeger EB, Chen Y, Hipp J, Pittaluga S, Raffeld M, et al: Large-scale profiling of archival lymph nodes reveals pervasive remodeling of the follicular lymphoma methylome. Cancer Res. 2009, 69 (3): 758-764. 10.1158/0008-5472.CAN-08-2984.
Pike BL, Greiner TC, Wang X, Weisenburger DD, Hsu YH, Renaud G, Wolfsberg TG, Kim M, Weisenberger DJ, Siegmund KD, et al: DNA methylation profiles in diffuse large B-cell lymphoma and their relationship to gene expression status. Leukemia. 2008, 22 (5): 1035-1043. 10.1038/leu.2008.18.
Jonnalagadda S, Srinivasan R: Principal components analysis based methodology to identify differentially expressed genes in time-course microarray data. BMC Bioinformatics. 2008, 9: 267-10.1186/1471-2105-9-267.
Peterson LE: Partitioning large-sample microarray-based gene expression profiles using principal components analysis. Comput Methods Programs Biomed. 2003, 70 (2): 107-119. 10.1016/S0169-2607(02)00009-3.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/9/455/prepub
This study has been supported by the Deutsche Krebshilfe Grants (107733 and 107747). Studies yielding data used as controls (i.e. extracerebral DLBCL, hematopoietic controls) published by Martin-Subero et al.  were supported by the Deutsche Krebshilfe Network Project "Molecular Mechanisms in Malignant Lymphoma" (grant 70 - 3173-Tr3).
MB and EG are employees of Illumina Inc.; JIMS and OA received speaker's honorary from Illumina Inc.; the study was performed in the framework of an R&D contract between Illumina Inc. and the group of RS.
RS, MD, MB, ODW and JIMS designed the study; MMR and MD performed neuropathology and provided DNA; JR, JIMS, MB and EG performed the experiments, OA and JIMS performed data analysis; JR, OA, MD and RS wrote the manuscript, all authors approved the manuscript.
Julia Richter, Ole Ammerpohl contributed equally to this work.
Electronic supplementary material
Additional file 1: Table of DNA-methylation data (beta-values) obtained from the microarray analysis (0: unmethylated; 1: fully methylated). Additionally, this table contains information about the sequence analyzed, the promoter class and whether the gene is a putative PcG target gene. (XLS 2 MB)
Additional file 4: GeneVenn Diagramm of genes differentially methylated between 5 samples of PCNSL and 10 hematopoietic controls (control-PCNSL, red circle), between 49 cases of systemic DLBCL and 10 haematopoietic controls (control-DLBCL, yellow circle) or between 5 cases of PCNSL and 49 cases of systemic DLBCL (PCNSL-DLBCL, green circle), respectively. http://www.bioinformatics.org/gvenn/ There is a significant overlap of genes differentially methylated in both malignancies compared to controls. A detailed list of genes is presented in Additional file 3. (PPT 107 KB)
Additional file 5: Hierarchical cluster analysis of DNA methylation data obtained from 4 differentially methylated CpG loci in 5 cases of PCNSL (orange boxes in the bar blot below the dendrogramm) and 49 cases of systemic DLBCL (yellow boxes). PCNSL and systemic DLBCL samples were not delineated according to their DNA methylation pattern. (PPT 130 KB)
Additional file 6: List of genes unmethylated in normal controls and methylated in PCNSL (meP/umC), unmethylated in normal controls and unmethylated in PCNSL (umP/umC) or methylated in normal controls and methylated in PCNSL (meP/meC).(DOC 30 KB)
Additional file 7: GeneOntology terms of genes differentially methylated in PCNSL (vs. controls) and DLBCL (vs. controls). RR, OR and p-value are shown.(XLS 24 KB)
Additional file 8: Comparision of the methylation frequency [%] of genes previously determined by other authors (Chu et al., 2006; Gonzalez-Gomez et al., 2003) using MSP and this study. To calculate frequency based on the date obtained from the GoldenGate array, AVG-beta values above 0.3 where considered as methylated. (PPT 106 KB)
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Richter, J., Ammerpohl, O., Martín-Subero, J.I. et al. Array-based DNA methylation profiling of primary lymphomas of the central nervous system. BMC Cancer 9, 455 (2009). https://doi.org/10.1186/1471-2407-9-455