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Research Paper

A key role for EZH2 in epigenetic silencing of HOX genes in mantle cell lymphoma

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Pages 1280-1288 | Received 26 Jun 2013, Accepted 19 Sep 2013, Published online: 09 Oct 2013

Abstract

The chromatin modifier EZH2 is overexpressed and associated with inferior outcome in mantle cell lymphoma (MCL). Recently, we demonstrated preferential DNA methylation of HOX genes in MCL compared with chronic lymphocytic leukemia (CLL), despite these genes not being expressed in either entity. Since EZH2 has been shown to regulate HOX gene expression, to gain further insight into its possible role in differential silencing of HOX genes in MCL vs. CLL, we performed detailed epigenetic characterization using representative cell lines and primary samples. We observed significant overexpression of EZH2 in MCL vs. CLL. Chromatin immune precipitation (ChIP) assays revealed that EZH2 catalyzed repressive H3 lysine 27 trimethylation (H3K27me3), which was sufficient to silence HOX genes in CLL, whereas in MCL H3K27me3 is accompanied by DNA methylation for a more stable repression. More importantly, hypermethylation of the HOX genes in MCL resulted from EZH2 overexpression and subsequent recruitment of the DNA methylation machinery onto HOX gene promoters. The importance of EZH2 upregulation in this process was further underscored by siRNA transfection and EZH2 inhibitor experiments. Altogether, these observations implicate EZH2 in the long-term silencing of HOX genes in MCL, and allude to its potential as a therapeutic target with clinical impact.

Introduction

Mantle cell lymphoma (MCL) is a clinically aggressive B-cell malignancy with a poor prognosis. The genetic hallmark of MCL is the chromosomal rearrangement caused by the t(11;14)(q13;q32), which results in overexpression of cyclin D1 and deregulated cell cycle control, an essential part of MCL pathobiology.Citation1 Limited knowledge exists regarding the role of epigenetic modifications and their potential impact on MCL pathogenesis. In MCL, the chromatin modifier EZH2 is overexpressed in proliferating cells and associated with poor outcome,Citation2,Citation3 similar to other malignancies.Citation4,Citation5 EZH2 is a core member of polycomb repressive complex (PRC) 2, mediating repressive H3 histone K27 lysine tri methyltransferase activity (H3K27me3) of the chromatin.Citation6 On the other hand, along with histone methyltransferase activity, EZH2 has also been reported to directly control DNA methylation through its association with and regulation of the activity of DNA methyltransferases.Citation7

Using methylation microarrays, we recently reported differential methylation of HOX genes (n = 13) in MCL compared with the more indolent chronic lymphocytic leukemia (CLL).Citation8 Notably, despite their differential methylation status in MCL and CLL, HOX genes were not expressed in either entity, thus indicating that both DNA methylation-dependent and independent mechanisms may operate to silence HOX genes. HOX genes are a highly conserved group of genes which encode homeodomain containing transcriptional factors that are essential during early embryonic development and regulate cell differentiation and hematopoiesis in adult cells.Citation9,Citation10 Inappropriate or deregulated expression of HOX genes has been implicated in the development of several cancers, including hematologic malignancies.Citation11,Citation12 However, HOX genes have both tumor suppressor and oncogenic activity and these contrasting actions occur in a tissue-dependent fashion.Citation13,Citation14

Epigenetic mechanisms, such as DNA methylation and the activity of the polycomb and trithorax group of proteins, including EZH2, have been implicated in the deregulation of HOX genes in human cancers.Citation15,Citation16 For instance, hypermethylation and transcriptional silencing of the complete HOXA cluster has been linked to tumor progression in breast cancer.Citation13 Methylation changes in HOXA have also been proposed as biomarkers for grading gliomas.Citation17 Furthermore, hypermethylation of HOXA cluster genes has been shown to correlate with disease progression in leukemia;Citation18 however, it is not clear whether methylation is a primary determinant of gene silencing or if it occurs as a consequence of silencing mediated by other mechanisms.

Since EZH2 has been shown to regulate HOX gene expression,Citation15,Citation16 one possible scenario is that HOXA genes could be targets of EZH2 in MCL. To gain insight into the mechanisms involved in silencing of HOXA genes in MCL and CLL, we investigated the functional roles of repressive chromatin modifications, such as H3K27me3, as well as EZH2 in the recruitment of the DNA methylation machinery. Importantly, while HOX genes were silenced by H3K27me3 histone trimethylation in CLL, EZH2 overexpression with subsequent recruitment of methyltransferases to the HOXA promoter was critical for long-term silencing of these genes by DNA methylation in MCL. The central role for EZH2 in gene silencing was further evidenced by EZH2 siRNA experiments and by applying an EZH2 inhibitor, ultimately highlighting EZH2 as a target of potential therapeutic interest in MCL.

Results and Discussion

Overexpression of EZH2 in MCL compared with CLL

In line with previous studies in MCL,Citation2,Citation3 we observed a significantly higher EZH2 expression level in MCL (n = 20) compared with CLL (n = 116) using RQ-PCR (fold difference (FD) 1.97 and P < 0.0001). When EZH2 expression levels were compared separately with favorable-prognostic IGHV-mutated CLL samples (n = 61), the FD was even more pronounced (FD 2.77, P < 0.0001), whereas the comparison against poor-prognostic IGHV-unmutated CLL samples (n = 55) rendered a slightly lower FD (FD 1.35, P < 0.02). These results are also in agreement with previous reports in diffuse large B cell lymphoma (DLBCL) and follicular lymphoma, thus indicating that EZH2 overexpression in B-cell lymphomas might be considered as a sign of clinical aggressiveness.Citation4

The entire HOXA gene cluster is differentially methylated in MCL vs. CLL

An important finding in our previous genome-wide methylation array study of MCL and CLL concerned the identification of 13 differentially methylated HOX genes. While these genes were hypermethylated in MCL and predominantly hypomethylated in CLL, none were expressed in either entity.Citation8 In order to gain insight into the epigenetic mechanisms involved in HOX gene silencing in each disease, we selected for further analysis genes from the HOXA cluster located on chromosome 7, i.e., HOXA2, HOXA9, and HOXA13 ().Citation8 Similar to our recent finding that the methylation status of the HOXA13 gene differed between MCL and CLL,Citation8 by analyzing 9 MCL and 12 CLL samples using pyrosequencing we also observed differential methylation between MCL vs. CLL for the HOXA9 gene (). Hence, using a more quantitative methodology such as pyrosequencing, significantly higher methylation levels of HOXA genes were validated in MCL vs. CLL.

Figure 1. Physical map showing the location of the HOXA and miR196B genes on chromosome 7.

Figure 1. Physical map showing the location of the HOXA and miR196B genes on chromosome 7.

Figure 2.HOXA9 and HOXA13 genes were differentially methylated in CLL and MCL primary samples. Box plots showing DNA methylation levels of the HOXA9/HOXA13 genes in CLL and MCL primary samples, as quantified by pyrosequencing.

Figure 2.HOXA9 and HOXA13 genes were differentially methylated in CLL and MCL primary samples. Box plots showing DNA methylation levels of the HOXA9/HOXA13 genes in CLL and MCL primary samples, as quantified by pyrosequencing.

In addition to HOX genes, a CpG island flanking the miR196B is located in the HOXA cluster between the HOXA9 and HOXA10 genes (). Previous studies have indicated that methylation of CpG islands regulates not only the expression of HOX genes but also the nearby microRNA miR196b promoter.Citation19 Using pyrosequencing to measure the methylation level at the miR196B promoter site, as for the HOXA genes, a significant difference in the level of methylation was observed between disease entities, i.e., hypermethylation in MCL (n = 8) and hypomethylation in CLL (n = 10) (P = 0.0004, Fig. S1A), in line with earlier studies in other malignancies.Citation19,Citation20 However, similar to HOXA genes, the expression levels of miR196b were extremely low in both MCL and CLL samples/cell lines as compared with normal human fibroblasts (~100 fold lower expression; Fig. S1B).

Therefore, we conclude that the entire HOXA cluster, including miR196B, is silenced in both MCL and CLL, however this is accomplished via different mechanisms, with DNA methylation likely playing a more prominent role in MCL. That said, since the methylation level of HOXA cluster genes was < 50% in MCL samples (), we cannot exclude that this could either be due to differential methylation of the HOXA alleles or due to other cell types present in the samples (although all MCL samples contained >70% tumor cells).

Differential enrichment of H3K27me3, EZH2, and DMNT1/3b at HOXA promoters in MCL vs. CLL

Since HOX genes are regulated by EZH2, we wanted to investigate if HOXA genes are targets for silencing in MCL and CLL. First, we investigated if the HOXA2, HOXA9, and HOXA13 genes carry other epigenetic modifications in their upstream regulatory regions. For this reason, we performed ChIP assays on MCL and CLL cell lines (Granta 519 and HG3) using antibodies for the repressive histone mark H3K27me3 and EZH2, respectively. Normal human fibroblast cells were used as a negative control for histone methylation, since HOXA13 is highly expressed in these cells.Citation8 Overall, results from the ChIP assays indicate clear differences in H3K27me3 modification between MCL vs. CLL cell lines, with the Granta 519 cell line showing several-fold higher enrichment of H3K27me3 for all three HOXA genes (i.e., HOXA2, HOXA9, and HOXA13) compared with the HG3 cell line (). Furthermore, the degree of H3K27me3 enrichment correlated well with EZH2 binding, i.e., high in MCL and low in CLL ().

Figure 3. Differential EZH2 levels correlated with DNMT1 recruitment in CLL vs. MCL cell lines. Enrichment of H3K27me3, EZH2, DNMT1, and DNMT3b levels at the HOXA gene promoters in the Granta 519 and HG3 cell lines was measured using ChIP with the respective antibody. The data represents values from triplicates plotted over IgG. A human fibroblast cell line was used as a positive control.

Figure 3. Differential EZH2 levels correlated with DNMT1 recruitment in CLL vs. MCL cell lines. Enrichment of H3K27me3, EZH2, DNMT1, and DNMT3b levels at the HOXA gene promoters in the Granta 519 and HG3 cell lines was measured using ChIP with the respective antibody. The data represents values from triplicates plotted over IgG. A human fibroblast cell line was used as a positive control.

Next, we investigated if the differential methylation status of HOXA genes could be related to differences in recruitment of DNA methyltransferases (DNMTs) to the HOXA promoters. To this end, we performed ChIP assays with DNMT1 and DNMT3b antibodies and showed that both DNMT1 and DNMT3b binding levels at the HOX gene promoters were associated with the DNA methylation levels, i.e., higher in the MCL cell line compared with the CLL cell line (). Nevertheless, the HOX genes also showed some background levels of H3K27me3, EZH2, and DNMTs in the control human fibroblast cell line. When extending these ChIP analyses to primary patient material (3 MCL and 3 CLL samples), similar results were obtained for DNMT1, DNMT3b, and EZH2, although the differences in fold enrichment were less pronounced as compared with the more homogeneous cell line data (Fig. S2).

Hence, a higher EZH2 occupancy at the HOXA promoters in MCL may lead to increased enrichment of H3K27me3 and recruitment of DNMT1/3b that in turn execute DNA methylation. Yet, what could be the reasons behind higher EZH2 binding in MCL?

Regulation of EZH2 expression by the cyclin D1/p16-pRB-E2F pathway in MCL

The frequent loss of the p16INKCitation4 tumor suppressor gene (which is an inhibitor of cyclin D1) by genomic deletion or promoter hypermethylation has been shown to be associated with high proliferation and shorter survival in MCL.Citation21,Citation22 Interestingly, in a human mammary breast cancer cell line, it was demonstrated that downregulation of the p16INK4 gene resulted in overexpression of the E2F transcriptional factor and polycomb PcG complex proteins, such as EZH2, leading to DNA hypermethylation of the HOXA9 gene promoter.Citation23 In order to investigate the p16INK4 expression levels, we analyzed 12 MCL and 12 CLL patient samples by RQ-PCR and observed considerably higher expression levels in CLL compared with MCL (P = 0.002) (). Furthermore, we analyzed protein levels of p16, E2F, and EZH2 in the CLL and MCL cell lines using western blotting. p16 protein expression was low and E2F and EZH2 proteins were high in the MCL (Granta 519) cell line as compared with the CLL cell line (HG3) (). The lower expression of p16 in the Granta MCL cell line was expected since this cell line has been shown to carry a homozygous deletion of p16.Citation24 Also, due to the presence of both a mutation in ATM and del(17p), this cell line is more likely to represent aggressive MCL. Hence, reduced p16 expression may lead to increased EZH2 expression in MCL.

Figure 4. Differential expression of p16 in CLL and MCL. (A) Box plots showing relative p16 expression levels in CLL and MCL primary samples quantified using RQ-PCR. (B) Western blot analysis of p16, EZH2, E2F, and β actin in the HG3 and Granta 519 cell line.

Figure 4. Differential expression of p16 in CLL and MCL. (A) Box plots showing relative p16 expression levels in CLL and MCL primary samples quantified using RQ-PCR. (B) Western blot analysis of p16, EZH2, E2F, and β actin in the HG3 and Granta 519 cell line.

The HOXA DNA methylation status is determined by the EZH2 levels

Since EZH2 can physically interact with DNMT1 and DNMT3b and recruit them to the gene promoters to silence HOX genes,Citation7,Citation16,Citation25 this may be the case for MCL. To corroborate the direct role of EZH2 in orchestrating DNA methylation of HOX genes, EZH2 expression was first abrogated using RNA interference. In this experiment, siRNA knockdown of EZH2 mRNA revealed a significant decrease in EZH2 protein levels in the MCL cell line as determined by western blot analysis. EZH2 knockdown also resulted in an expected decrease in the levels of H3K27me3, and a corresponding increase in the levels of the HOXA9, HOXA2, and HOXA13 proteins (). These results were also validated at the mRNA level using RQ-PCR (Fig. S3A).

Figure 5. Downregulation of EZH2 using siRNA results in loss of DNA methylation and re-expression of HOXA genes in MCL. (A) Western blot analysis of EZH2, all three HOXA proteins (HOXA2, HOXA9, and HOXA13) and H3K27me3 expression after treatment with control siRNA or EZH2 siRNA in the Granta 519 MCL cell line. Histone H3 and GAPDH were used as internal loading controls. (B) Bisulfite sequencing analysis of the HOXA2 and HOXA9 genes in the Grant 519 cell line after treatment with EZH2 siRNA and control siRNA. The methylation status of 10 clones is presented for each sample; each circle represents one CpG site indicating either cytosine (open circles), methyl cytosine (filled circles) or non-CpG site (missing circles). (C) Enrichment of H3K27me3, EZH2, DNMT1, and DNMT3b levels at the HOXA gene promoters in the Granta519 MCL cell line using control siRNA and EZH2 siRNA treated. The data represents values from triplicates plotted over IgG.

Figure 5. Downregulation of EZH2 using siRNA results in loss of DNA methylation and re-expression of HOXA genes in MCL. (A) Western blot analysis of EZH2, all three HOXA proteins (HOXA2, HOXA9, and HOXA13) and H3K27me3 expression after treatment with control siRNA or EZH2 siRNA in the Granta 519 MCL cell line. Histone H3 and GAPDH were used as internal loading controls. (B) Bisulfite sequencing analysis of the HOXA2 and HOXA9 genes in the Grant 519 cell line after treatment with EZH2 siRNA and control siRNA. The methylation status of 10 clones is presented for each sample; each circle represents one CpG site indicating either cytosine (open circles), methyl cytosine (filled circles) or non-CpG site (missing circles). (C) Enrichment of H3K27me3, EZH2, DNMT1, and DNMT3b levels at the HOXA gene promoters in the Granta519 MCL cell line using control siRNA and EZH2 siRNA treated. The data represents values from triplicates plotted over IgG.

To investigate the impact of decreased EZH2 levels on the DNA methylation status of the HOXA genes, bisulfite sequencing was also performed, verifying the loss of DNA methylation at most CpG sites analyzed on both the HOXA2 and HOXA9 genes (). Since the downregulation of EZH2 resulted in re-expression of HOXA genes, we also measured the degree of histone methylation and binding of DNMTs to HOXA gene promoters upon EZH2 depletion using ChIP. As expected, there was a significant loss of H3K27me3 as well as DNMT1 and DNMT3B at the HOXA promoters in response to EZH2 depletion ().

To further investigate the role of EZH2 in the recruitment of DNMTs to HOXA gene promoters, EZH2 was depleted by treating the MCL cell line with the H3K27me3 histone methyl inhibitor 3-Deazaneplanocin A (DZNep), which is a cyclopentenyl analog of 3-deazaadenosine. Previously, this drug has been shown to deplete EZH2 levels and to inhibit H3K27me3 in acute myeloid leukemiaCitation5 and multiple myeloma cells in a dose- and time-dependent manner.Citation26 When the MCL cell line was treated with increasing concentrations of DZNep, ranging from 0 to 10µM, a significant reduction in EZH2 as well as H3K27me3 levels was detected, followed by activation of the HOXA9 gene ().

Figure 6. Re-expression of HOXA proteins after DZNep treatment. Western blot analysis of EZH2, H3K27me3, and HOXA proteins (HOXA2, HOXA9, and HOX13) levels in the Granta 519 cell line treated with increasing concentrations of DZNep ranging from 0–10 µM for 4 d. Beta actin levels are used as internal loading control.

Figure 6. Re-expression of HOXA proteins after DZNep treatment. Western blot analysis of EZH2, H3K27me3, and HOXA proteins (HOXA2, HOXA9, and HOX13) levels in the Granta 519 cell line treated with increasing concentrations of DZNep ranging from 0–10 µM for 4 d. Beta actin levels are used as internal loading control.

EZH2: a potential novel target for epigenetic therapy?

In conclusion, this study for the first time highlights the epigenetic silencing mechanisms underlying differential HOX gene regulation in MCL vs. CLL. In the case of CLL, HOX genes appear to be silenced primarily by H3K27me3 histone methylation, which is catalyzed by EZH2, while in MCL EZH2 also binds to DNMTs thereby recruiting the DNA methylation machinery for efficient silencing of the HOXA genes. More specifically, HOXA gene promoters exhibited greater enrichment with EZH2 in MCL as compared with CLL, which in turn correlated with increased DNMT1 recruitment and CpG methylation, thus indicating that the level of EZH2 indeed determines the level of DNA methylation through DNMTs. This is in contrast to normal B cells which expressed HOXA genes at higher levels comparable to the expression levels in normal fibroblast cells (Fig. S3).Citation8

Given that DNA methylation is a more stable epigenetic mark compared with histone modifications, EZH2-mediated specific methylation of the HOXA promoters could be a critical step in conferring an aggressive phenotype to MCL. This important function of EZH2 has also been reflected in B-cell activation and lymphomagenesis, where EZH2 acts as an epigenetic switch in promoting H3K27me3 toward DNA hypermethylation.Citation27 This transition toward DNA methylation reduces epigenetic plasticity and locks the target genes in a stable repressive state, and hence prevents any major transcriptional changes irrespective of external cues. Accordingly, our current data implies that EZH2-mediated DNA methylation ensures the stable repression of HOXA genes, a step that may be critical in the aggressive phenotype of MCL. Our novel observations also advocate that EZH2 plays a crucial role in HOX gene silencing in MCL, which was also confirmed by our siRNA and EZH2 inhibitor experiments, and that DNA methylation occurs as a secondary event following EZH2 recruitment to the HOX promoter. This is further supported by the fact that most MCL patient samples did not show complete methylation of HOXA cluster genes.

The key role for EZH2 in MCL lymphomagenesis is also underscored by the recent finding that the MYC oncogene upregulates EZH2 in MCL, eventually leading to decreased expression of the tumor suppressor miRNA, miR29.Citation28-Citation30 Furthermore, EZH2 inhibition was very recently pointed out as a potential treatment strategy for the germinal center subtype of DLBCL.Citation4,Citation5,Citation31-Citation33 For all these reasons, as well as the well-established notion that EZH2 overexpression is associated with tumor invasion, tumor progression and poor prognosis in many different cancer types,Citation34-Citation36 our novel observations highlight EZH2 as a potential novel target for epigenetic-based therapy in MCL. Nevertheless, systematic investigations of EZH2 target genes are required before this can be attempted in a clinical setting.

Methods

Patient material

In this present study, we included tumor samples from MCL and CLL patients collected from the biobanks at Uppsala University Hospital and Karolinska University Hospital, Sweden, and G. Papanicolaou Hospital, Thessaloniki, Greece. All MCL cases fulfilled the diagnostic criteria of the World Health Organization Classification.Citation8 All CLL samples (poor-prognostic subset #1 and favorable prognostic subset #4) were diagnosed according to recently revised criteria showing a typical CLL immunophenotype.Citation37 Clinical and molecular data are summarized in Table S1. Sorted CD19+ B cells from healthy control was obtained from 3H Biomedical, Uppsala, Sweden.

Cell lines and cell culture conditions

Two EBV transformed cell lines, one CLL (HG3)Citation38 and one MCL (Granta 519)Citation39 were used for ChIP assays and siRNA transfection assays. The cell lines were cultured in RPMI 1640 (Invitrogen) supplemented with glutamine (4 mM glutamine for Granta 519 and 2 mM Glutamine for HG3), 10% fetal bovine serum (FBS; Invitrogen), and 1× penicillin/streptomycin (Invitrogen, Carlsbad, CA, USA).

Chromatin immunoprecipitation assay

Chromatin immune precipitation was performed using the Shearing module kit and OneDay ChIP Kit™ (Diagenode) according to the manufacturer’s instructions. Antibodies used were: EZH2 polyclonal antibody (Diagenode, pAB-039-050), H3K27me3 polyclonal antibody (Diagenode, pAB-069-050), Dnmt1 monoclonal antibody (Imgenex, IMG-261A), Dnmt3b polyclonal antibody (Diagenode, pAB-076-005), and IgG (negative control, OneDay ChIP Kit™Diagenode). The detailed protocol is listed in the Supplemental Material.

Gene and protein expression analysis

Total RNA was prepared using the TRIzol method (Invitrogen Life Technologies) or the AllPrep DNA/RNA kit (Qiagen) according to the manufacturer’s instructions. The reverse transcription reaction was performed using MMLV-RT or Superscript II reverse transcriptase (Invitrogen) and random hexamers (Fermentas) according to the manufacturer’s protocol. RQ-PCR analysis for the determination of the p16 and EZH2 mRNA levels was performed as described in the Supplementary Material. Results for EZH2 mRNA expression in CLL that were used for comparison to MCL have been reported previously.Citation40

Western blot analysis was performed using total cell lysates and the detailed protocol has been provided in the Supplementary Material.

Pyrosequencing and bisulfite sequencing

Both pyrosequencing and bisulfite sequencing were performed as in our previous publicationsCitation8,Citation41 and detailed protocols are provided in the Supplementary Material.

siRNA transfections and DZNep treatment assay

Granta 519 cells were transfected with predesigned siRNA against EZH2 using Stealth RNAi siRNA, containing a mixture of three oligos (HSS103462; HSS176652, and HSS176653) in equal concentrations (Invitrogen). The siRNA negative control (Invitrogen) was used as control siRNA. Transient transfection was performed on an Amaxa Nucleofection Device (Lonza Cologne AG) according to the manufacturer's instruction. In brief, Granta 519 cells were split at a density of 5 × 105/ml in the medium 48 h before transfection. Thereafter, 4 × 106 cells were collected and resuspended in 100 µl human cell line nucleofector solution C with 100 pmol of EZH2 siRNA mix or control siRNA using the X-01 electroporation program.

The Granta 519 cells were treated with the EZH2 inhibitor, 3-Deazaneplanocin A (DZNep) (Cayman chemicals) for three days using different concentrations ranging from 0‒10 µM.

Supplemental material

Additional material

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10.4161/epi.26546

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Authorship

Kanduri M designed and performed the research, analyzed the data and wrote the paper. Papakonstantinou N, Ntoufa S, and Sutton L performed research. Sander B, Stamatopoulos K, and Kanduri C analyzed data and wrote the paper. Rosenquist R supervised the research and wrote the paper.

Supplemental Materials

Supplemental materials may be found here: http://www.landesbioscience.com/journals/epigenetics/article/26546/

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