Hepatocellular carcinomas (HCC) exhibit distinct promoter hypermethylation patterns, but the epigenetic regulation and function of transcriptional enhancers remain unclear. Here, our affinity- and bisulfite-based whole-genome sequencing analyses reveal global enhancer hypomethylation in human HCCs. Integrative epigenomic characterization further pinpoints a recurrent hypomethylated enhancer of CCAAT/enhancer-binding protein-beta (C/EBPβ) which correlates with C/EBPβ over-expression and poorer prognosis of patients. Demethylation of C/EBPβ enhancer reactivates a self-reinforcing enhancer-target loop via direct transcriptional up-regulation of enhancer RNA. Conversely, deletion of this enhancer via CRISPR/Cas9 reduces C/EBPβ expression and its genome-wide co-occupancy with BRD4 at H3K27ac-marked enhancers and super-enhancers, leading to drastic suppression of driver oncogenes and HCC tumorigenicity. Hepatitis B X protein transgenic mouse model of HCC recapitulates this paradigm, as C/ebpβ enhancer hypomethylation associates with oncogenic activation in early tumorigenesis. These results support a causal link between aberrant enhancer hypomethylation and C/EBPβ over-expression, thereby contributing to hepatocarcinogenesis through global transcriptional reprogramming.
Hepatocellular carcinoma (HCC) is the third leading cause of global cancer-related deaths with an annual incidence rate of approximately 850,000 cases1,2. Major risk factors for HCC include chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections, alcohol abuse, and non-alcoholic fatty liver disease (NAFLD) associated with obesity and diabetes1,2. Genetic and epigenetic alterations that progressively accumulate in the chronic inflammatory milieu lead to the initiation and progression of HCC, but the precise molecular events are only partially understood3. Although much effort has been devoted to elucidating the genetic defects underlying malignant transformation of hepatocytes, only few druggable driver mutations have been revealed for a fraction of HCC patients due to tumor heterogeneity2,3. Given the marginal benefit of the small-molecule agent sorafenib and failure of multiple molecular drugs in phase III trials for HCC patients2, HCC methylome profiling would uncover the epigenetic vulnerabilities for the development of new intervention strategies.
Epigenome disruption has emerged as a major hallmark in HCC as revealed by the discoveries of somatic mutations in chromatin regulators and numerous epigenetic abnormalities4,5. Chronic hepatitis infection and NAFLD have been shown to induce aberrant DNA methylation that may contribute to the development of HCC6,7,8. Genome-scale DNA methylation profiles of nearly two-hundred HCC cases via an array-based platform further revealed distinct cancer-specific DNA hypermethylation clusters9. Most of these studies, however, focused on altered methylation at gene promoters and CpG islands/shores. Apart from the classical promoter hypermethylation-mediated gene silencing, the epigenetic regulation and function of distal cis-regulatory regions have yet to be elucidated.
Transcriptional enhancers are distal non-coding regions crucial for cell identify specification. These key regulatory elements are driven by combinatorial assembly of lineage-determining transcription factors, coactivators and bromodomain and extraterminal domain (BET) family proteins including BRD4, which recruits transcriptional complexes to acetylated lysine 27 of histone H3 (H3K27ac) for enhancer RNA (eRNA) synthesis10,11. Accumulating evidence has shown the importance of enhancers and super-enhancers, i.e., clusters of aberrantly active enhancers that are strongly enriched by BRD4 and H3K27ac, in dysregulated expression of oncogenes12,13. In addition, gene dysregulation is more correlated with altered methylation at their enhancers than promoters in many transformed cell types, including those of hepatocyte origin14,15,16.
We have recently developed a new method for inferring enhancer-target interactions by integrating epigenomic and transcriptomic data from hundreds of primary cells and tissues, which enabled the identification of target genes that are specifically controlled by differentially methylated enhancers (DMEs) in HCC cells17. Utilizing affinity- and bisulfite-based whole-genome sequencing, here we show a genome-wide enhancer hypomethylation pattern in primary human HCCs. Our integrative epigenomic analysis highlights a recurrent hypomethylated enhancer of CCAAT/enhancer-binding protein-beta (C/EBPβ), which exhibits clinical and biological significance in promoting HCC tumorigenicity through global transcriptional reprogramming.
Integrative epigenomic analysis of human HCCs
We performed methyl-binding DNA capture sequencing (MBDCap-seq)18 on 33 pairs of HCC tumors and matched non-tumor tissues from the same patients. From each sample, we obtained on average 51,855,400 sequencing tags that were aligned to the human reference genome hg19. Globally, a clear hypomethylation pattern in the tumor group was observed when compared with the non-tumor group (Fig. 1a). At a Bonferroni-adjusted P-value cutoff of 0.1, we obtained 7182 genomic regions with significant differential methylation between the tumor and non-tumor samples, with nearly two-third of those regions showing hypomethylation in the tumors. As expected, the differentially methylated regions (DMRs) were enriched in various genomic elements19 (Fig. 1b). Notably, we found that 369 FANTOM5 enhancers20 were differentially methylated, leading to a clear enrichment of the DMRs in enhancers (Fig. 1b).
As our HCC MBDCap-seq data, which provide resolution up to the length of each sequenced DNA fragment, suggest potential dysregulation of enhancers, we performed single-base resolution whole-genome bisulfite sequencing (WGBS) on three HCC tumors in order to identify enhancers with strong differential methylation at their core regions. After standard processing, we obtained an average of 17.6 aligned reads per CpG site, which concurred with the recommended coverage of WGBS21. Using normal liver from public WGBS data as a comparator, we identified enhancers with the strongest changes (average beta value change ≥0.1 across ≥10 CpG sites) in tumors (Fig. 1c), which exhibited highly significant hypomethylation (P < 2.2e-16; Fig. 1d). Among these DMEs, 854 were hypomethylated while only 40 were hypermethylated in tumors (Fig. 1e). Using the FANTOM5 database, we also identified the potential target genes of these DMEs and further integrated RNA-seq data of the same paired HCC samples. Consistent with the previous observations that enhancer hypo- and hypermethylation could lead to target gene up- and downregulation, respectively14,15, we identified a list of 27 DMEs whose DNA methylation levels had strong inverse correlations with target gene expressions (Supplementary Table 1).
Based on the number of enhancers that target a particular gene and its potential functional significance, we selected a FANTOM5 enhancer region that is ~90-kb downstream to its target gene C/EBPβ (Fig. 1f), a key hepatocyte transcription factor for liver regeneration22,23, for in-depth analysis. With multiple enhancers (3 out of 27) targeted C/EBPβ and a high eRNA-mRNA correlation of 0.863 across 808 FANTOM5 samples, the selected highly confident enhancer-target pair exhibited significant hypomethylation-associated gene upregulation in HCC tumors (Supplementary Table 1). To verify this potential enhancer, we performed nanoscale chromatin profiling24 of the same HCC tissues used for WGBS. Analysis of the chromatin profiles at the central 1-kb region of the hypomethylated C/EBPβ enhancer revealed substantial enrichment of H3K27ac, a high H3K4me1 to H3K4me3 ratio but low H3K27me3 (Fig. 1f), representing an active enhancer in human HCCs11,25.
Hypomethylation of C/EBPβ enhancer relates to poor prognosis
We next validated the WGBS findings by bisulfite pyrosequencing using 48 pairs of human HCC tumor/non-tumor tissues, which exhibited the methylation levels of the 13 CpG sites within the C/EBPβ enhancer (Fig. 1g, h). Consistent with the WGBS findings, the average C/EBPβ enhancer methylation levels of the tumors (~40%) were lower than the non-tumor tissues (~55%, P < 0.005; Fig. 1i). To investigate the relationship between C/EBPβ methylation and expression, quantitative RT-PCR (qRT-PCR) was performed using 33 pairs of the HCC cases of which high quality RNA samples were available. Compared to the non-tumor tissues, we demonstrated significantly higher C/EBPβ mRNA expression in tumors (P < 0.005; Fig. 1j), which was negatively and significantly correlated with the C/EBPβ enhancer methylation (P < 0.01; Fig. 1k). In contrast, the C/EBPβ promoter methylation levels were invariable among the tumor and non-tumor tissues, exhibiting low methylation levels ( < 2%) at the 26 CpGs encompassing the C/EBPβ transcription start site (TSS, −561 to + 458-bp; Supplementary Fig. 1a). We further examined our in-house and published whole-genome sequencing datasets26,27. C/EBPβ promoter mutations were observed in ~1% (4/363) of HCC patients, whereas no mutation could be found in C/EBPβ enhancer. Taken together, these data suggest that enhancer hypomethylation is one of the major mechanisms for C/EBPβ over-expression in human HCC.
Based on the widespread tumorous C/EBPβ enhancer methylation levels (Fig. 1i), we further investigated whether enhancer methylation associates with the survival of HCC patients. Notably, Kaplan–Meier analysis revealed that HCC patients with strong tumorous hypomethylation (compared to the corresponding non-tumor) significantly correlated with shorter overall (hazard ratio = 4.404, P < 0.005; Fig. 1l) and disease-free survival rates (hazard ratio = 3.809, P < 0.01; Fig. 1m). These results demonstrate that C/EBPβ enhancer hypomethylation was correlated with poorer prognosis of HCC patients.
C/EBPβ enhancer hypomethylation activates C/EBPβ expression
Given the causal role of eRNAs in transcriptional activation as suggested in some studies11,28,29,30, we speculated that the methylation status of C/EBPβ enhancer controls eRNA expression for C/EBPβ gene regulation. First, we determined the presence of C/EBPβ enhancer-templated eRNAs by northern blot and qRT-PCR analyses. In both HepG2 liver cancer cells and immortalized LO2 liver cells, our data revealed production of a 3-kb polyadenylated RNA transcript from the sense strand, but not the antisense strand, of the C/EBPβ enhancer (Fig. 2a and Supplementary Fig. 2), which is consistent with the features of unidirectional eRNA11. Using a panel of eight HCC and liver cell lines, we next investigated whether C/EBPβ enhancer methylation controls eRNA expression by pyrosequencing and qRT-PCR. We found a significantly negative correlation between C/EBPβ enhancer methylation and eRNA expression (P < 0.005; Fig. 2b), while the C/EBPβ promoter methylation levels were invariably low (~10%; Supplementary Fig. 1b), similar to those observed in the primary HCC tissues. To test for the causative role, we treated PLC5 and SK-Hep1 liver cell lines that harbor high enhancer methylation levels ( > 50%) with 5-aza-2’-deoxycytidine (5-aza-dC). DNA demethylation was observed in C/EBPβ enhancer, but not promoter (Fig. 2c), which resulted in significant reactivation of C/EBPβ eRNA and mRNA in both lines (P < 0.05; Fig. 2d). To exclude potential influences by other hypomethylated sites upon 5-aza-dC treatment, we performed targeted DNA demethylation by a modified dCas9-TET1 hydroxylase fusion construct31 and demonstrated that targeted demethylation of C/EBPβ enhancer increased C/EBPβ eRNA and mRNA expressions (P < 0.001; Supplementary Fig. 3a, b).
To further examine whether DNA methylation-regulated C/EBPβ eRNA is involved in transcriptional upregulation of C/EBPβ, we transfected two independent small interfering RNAs that target C/EBPβ eRNA (sieRNA) or a control sequence (siCtrl) into HepG2 and LO2 cells that highly express the eRNA (Fig. 2a, b). Intriguingly, knockdown of C/EBPβ eRNA in both lines reduced mRNA levels of C/EBPβ (Fig. 2e, f). We observed no change in the expression of the neighboring genes SMIM-25 and DPM1 located upstream and downstream of the C/EBPβ enhancer (Supplementary Figs. 2 and 3c), implying no off-target effect. In a complementary experiment, we treated PLC5 and SK-Hep1 cells with 5-aza-dC or DMSO vehicle, followed by transfection with siCtrl or sieRNA. Notably, we found that C/EBPβ mRNA upregulation by DNA demethylation could be partially abrogated by knockdown of C/EBPβ eRNA (Fig. 2g, h). These results demonstrate that C/EBPβ enhancer hypomethylation is required for efficient C/EBPβ transcription via induction of eRNA. Furthermore, we found an elevation of C/EBPβ eRNA level in HCC tumor compared to non-tumor tissues, which exhibited significantly negative and positive correlations with C/EBPβ enhancer methylation (P < 0.05; Fig. 2i) and C/EBPβ mRNA levels (P < 0.01; Fig. 2j), respectively, thus verifying the clinical relevance of our findings.
C/EBPβ feedback regulates its own enhancer activity
We next speculated that C/EBPβ enhancer hypomethylation facilitates eRNA synthesis via enhanced co-occupancy of the transcriptional complex10,32,33. Indeed, DNA demethylation of C/EBPβ enhancer increased the occupancies of C/EBPβ, BRD4, H3K27ac, and RNA polymerase II (RNPII) at C/EBPβ enhancer in both PLC5 and SK-Hep1 cells (P < 0.05; Fig. 3a). Concordant with the enhancer co-regulatory function of C/EBPβ and BRD434, either siRNA-mediated downregulation of C/EBPβ (Fig. 3b) or treatment with the BET-bromodomain inhibitor JQ1 significantly reduced the C/EBPβ eRNA levels in HepG2 and LO2 cells (P < 0.01; Fig. 3c, d). These observations indicate that C/EBPβ co-localizes with BRD4 at its hypomethylated enhancer to promote eRNA production.
To further investigate the C/EBPβ-dependency of the enhancer activity, we cloned the 1-kb enhancer fragment, which contains a 10-bp consensus sequence (ATTGCACAAT) for C/EBP family members35, downstream of the C/EBPβ promoter-driven luciferase gene (Fig. 3e). In both HepG2 and LO2 cells, C/EBPβ enhancer generated significantly higher luciferase activity compared to the C/EBPβ promoter alone (P < 0.01; Fig. 3f). Notably, deletion of C/EBPβ motif by site-directed mutagenesis partially abrogated the transcriptional activity of the enhancer (P < 0.05; Fig. 3e, f), which was consistent with the effect of C/EBPβ knockdown (P < 0.05; Fig. 3g). Enhancers control expression of genes over distance by DNA looping, which brings the distal regulatory elements into close proximity of their target gene promoters36. In concordance, the C/EBPβ enhancer has been shown to physically interact with the C/EBPβ promoter by previously generated Hi-C chromosome conformation capture data from two human cell lines (HeLa and K562)37 (Supplementary Fig. 4), thus supporting long-range transcriptional regulation by C/EBPβ enhancer. Overall, these findings suggest that C/EBPβ feedback trans-activates its own enhancer via direct chromatin regulation.
C/EBPβ enhancer deletion abrogates HCC tumorigenicity
To elucidate the biological and functional significance of C/EBPβ enhancer in tumor development, we generated monoallelic (C/EBPβ enh+/−) and biallelic (C/EBPβ enh−/−) deletion of C/EBPβ enhancer via CRISPR/Cas9 in HepG2 and LO2 cells (Fig. 4a and Supplementary Fig. 5). Compared to the C/EBPβ enh+/+ wild-type (WT) cells, C/EBPβ enh+/− and C/EBPβ enh−/− cells showed significantly reduced C/EBPβ eRNA and mRNA expressions in an allele-dependent manner (P < 0.01; Fig. 4b, c). Functionally, monoallelic and biallelic deletion of C/EBPβ enhancer caused a progressive reduction in cell growth (P < 0.05; Fig. 4d, e) and invasiveness (P < 0.05; Fig. 4f, g). Notably, C/EBPβ enh+/− and C/EBPβ enh−/− cells exhibited remarkable inhibition of tumor growth in xenograft models when compared with WT cells (P < 0.005; Fig. 4h, i). Indeed, C/EBPβ enh−/− HepG2 cells formed either no tumor (3 of 4) or very small tumor (1 of 4) within 4 weeks (Fig. 4h). We next investigated whether C/EBPβ eRNA exhibits similar pro-tumorigenic property. We found that downregulation of C/EBPβ eRNA in HepG2 and LO2 cells significantly reduced cell growth and invasiveness (P < 0.01; Supplementary Fig. 6a, b), and the extents of reduction appeared to be more than those in PLC5 and SK-Hep1 cells whose C/EBPβ enhancer was hypermethylated (Supplementary Fig. 6c, d). As expected, stable C/EBPβ knockdown phenocopied the effects of eRNA knockdown (Supplementary Fig. 6e, f). Taken together, these data suggest that C/EBPβ enhancer methylation may regulate cancer cell phenotypes via C/EBPβ eRNA/mRNA expression.
To examine the C/EBPβ methylation and expression changes leading to HCC, we took advantage of an HBV X protein (HBx) transgenic (TG) mouse model that spontaneously develops HCC tumors at old age38,39,40. Although highly conserved enhancers are much less common than promoters in mammalian species41, high mouse-human conservation was observed in C/ebpβ enhancer, showing similar eRNA expression patterns and occupancy profiles for orthologous C/EBPβ and H3K27ac (Fig. 5a). For the two CpG sites located within the C/ebpβ enhancer, both were significantly hypomethylated in the livers of TG mice at the early stage of tumor development (4-month-old) when compared to the WT counterparts (P < 0.05; Fig. 5b). In contrast, no difference of methylation was observed in C/ebpβ promoter (−645 to + 312-bp relative to TSS; Supplementary Fig. 7a). Moreover, the C/ebpβ eRNA (P < 0.05; Fig. 5c) and mRNA (P < 0.05; Fig. 5d) expressions were concordantly upregulated in TG compared to WT mice, and significantly correlated with each other at early and late (10-month-old) stages (P < 0.05; Supplementary Fig. 7b, c). In parallel, the C/EBPβ protein expressions were also significantly elevated (P < 0.005; Fig. 5e). These data suggest that C/EBPβ dysregulation by enhancer hypomethylation is a molecular event preceding the onset of HCC development in HBx TG mice.
C/EBPβ enhancer deletion remodels global enhancer activity
Given the importance of C/EBPβ on global enhancer regulation42, we speculated that C/EBPβ enhancer may influence genome-wide enhancer activity through its regulation of C/EBPβ. Indeed, deletion of C/EBPβ enhancer not only decreased the protein expression of C/EBPβ, but also the global level of H3K27ac in HepG2 cells (Fig. 6a). We next performed ChIP-seq analysis of C/EBPβ, BRD4 and H3K27ac in WT and C/EBPβ enh−/− HepG2 cells. A majority of C/EBPβ binding sites (84.2%) in WT cells showed reduced C/EBPβ and BRD4 co-occupancy in C/EBPβ enh−/− cells (Fig. 6b), consistent with the role of C/EBPβ in chromatin targeting of BRD434. Moreover, we identified reduction in H3K27ac levels at > 30% enhancers (1800/5891) in C/EBPβ enh−/− cells, whereas promoters showed significantly fewer changes (P < 0.0001; Fig. 6c). Notably, H3K27ac signals were diminished in C/EBPβ enh−/− cells at the majority of super-enhancer regions that lost C/EBPβ/BRD4 co-occupancy (Fig. 6d). Similarly, the H3K27ac levels of most C/EBPβ/BRD4-codepleted enhancers were also reduced in C/EBPβ enh−/− cells (Fig. 6e). As H3K27ac distinguishes active enhancers from inactive/poised enhancers25, we investigated whether H3K27ac reduction affects target gene expressions in C/EBPβ enh−/− cells. Indeed, additional loss of H3K27ac at both C/EBPβ/BRD4-codepleted enhancers and super-enhancers correlated with reduced mRNA expressions of the nearest genes, as quantified by RNA-seq (P < 0.0001; Fig. 6f). Altogether, these findings indicate that C/EBPβ enhancer deletion impairs global enhancer activity via C/EBPβ/BRD4 dysregulation.
Gene ontology (GO) analyses43 of the 805 super-enhancer- and 1817 enhancer-target genes whose activities were co-regulated by C/EBPβ and BRD4 (Fig. 6f) uncovered regulators of cancer pathways such as small GTPase-mediated signal transduction, and effectors of cell migration, proliferation, and vasculature development (Fig. 6g, h), consistent with the drastic inhibition of tumorigenicity in C/EBPβ enh−/− cells (Fig. 4). For example, Ras like proto-oncogene B (RALB)44, a key mediator of metabolic and mitogenic pathways in HCC, was markedly downregulated in C/EBPβ enh−/− cells, which were associated with a notable decrease in the co-occupancy of C/EBPβ, BRD4, and H3K27ac at its super-enhancer region (Fig. 6i). Similarly, a pro-metastatic and pro-angiogenic factor over-expressed in human HCCs, namely fibroblast growth factor receptor 2 (FGFR2)45,46, was also deregulated (Fig. 6j). Notably, these HCC driver genes were not only suppressed in C/EBPβ enh−/− cells (P < 0.05; Fig. 6i, j), but also upregulated and correlated with C/ebpβ expression in the pre-malignant liver tissues of the HBx TG HCC model (P < 0.05; Supplementary Fig. 7d, e). Thus, our integrative genome-wide analysis implicates broad control of enhancer activity as the C/EBPβ enhancer function in the establishment and maintenance of HCC phenotypes.
Accumulating evidence has underscored aberrant enhancer-driven transcriptional programs as fundamental drivers of tumor formation and maintenance13,47,48,49. However, the mechanisms underlying enhancer dysregulation, especially from a DNA methylation viewpoint, remain unclear. Through comprehensive profiling of DNA methylation in primary tumors, matched non-tumor and normal liver tissues, we revealed global hypomethylation of transcriptional enhancers in human HCCs. Our study pinpointed an aberrantly-methylated enhancer with prognostic significance, forming a positive circuitry with its target gene to impart HCC hallmarks including proliferation, angiogenesis and invasion. C/EBPβ, over-expressed via its hypomethylated enhancer, has emerged as a crucial regulator of HCC tumorigenicity through genome-wide enhancer and super-enhancer remodeling. Given the well-established inheritance mechanism of DNA methylation, this study provides evidence for the heritability and causality of enhancer alterations in cancer development.
Our work has advanced the understanding of HCC methylome. To our knowledge, this is the first sequencing-based unbiased analysis that reveals a genome-wide enhancer hypomethylation pattern in human HCCs. While promoter hyper- and hypomethylation have been demonstrated in the development of HCC6,7,8,9, we found extensive reduction in methylation at the vast majority of DMEs identified by WGBS. Using nanoscale chromatin profiling in the same HCC tissues, we minimized ambiguity in enhancer localization and confirmed specific enhancer hypomethylation-associated C/EBPβ over-expression using bisulfite pyrosequencing and qRT-PCR in ~100 HCC tumor/non-tumor tissues. Emerging data from leukemias50, breast carcinomas51, metastatic melanoma16, and colorectal cancers14 further support the notion that global enhancer hypomethylation is a common epigenetic feature of cancer development and progression. We and others have previously shown that the similarity of enhancer networks closely follows their cell and tissue lineages17,52. Whether distinct enhancer methylation patterns can specify primary tumors according to their origins and stages remain to be elucidated in future studies.
Our enhancer methylation profile contains a wellspring of both well-validated and uncharacterized targets that may contribute to HCC tumorigenesis. Even though C/EBPβ has been previously reported to orchestrate liver regenerative23 and glucose metabolic programs53, our study is the first to uncover its pro-tumorigenic properties in HCC. Other HCC-related genes such as the SRC tyrosine kinase54 and the autophagy-related pro-survival gene ATG755 have been identified (Supplementary Table 1). New enhancer-hypomethylated and over-expressed targets revealed in this study include IFNGR2 and SLC45A4, which could play important roles in HCC given their functions in regulating HBV viraemia56 and redox homeostasis57. Whereas the distinct DNA hypermethylation profile in human HCCs is disproportionately enriched with the gain-of-function IDH1/2 mutations9, the causes of enhancer hypomethylation warrant further investigation. One potential causative factor may be the HBx oncoprotein, which has been shown to induce demethylation of distal regulatory regions to facilitate HCC tumorigenesis58. Indeed the C/ebpβ enhancer regulatory network is recapitulated in an HBx TG HCC model, highlighting the importance of HCC risk factors in enhancer dysregulation during carcinogenesis.
Our data suggest that, mechanistically, reactivation of eRNA by C/EBPβ enhancer hypomethylation enables C/EBPβ transcription, which in turn binds to and trans-activates its own enhancer to form a self-reinforcing loop. Using Northern blot and strand-specific qRT-PCR analyses, we identified an approximately 3-kb eRNA that is unidirectionally transcribed for specific C/EBPβ gene regulation. Knockdown of this eRNA not only attenuates DNA demethylation-mediated C/EBPβ gene reactivation, but also inhibits HCC cell proliferation and invasion. As we also showed its upregulation and correlations with both C/EBPβ enhancer hypomethylation and mRNA expression in human HCCs, our findings concur with the functional significance of other tumor-specific eRNAs, such as androgen- and estrogen-dependent eRNAs in prostate28 and breast cancers29 that play indispensable roles in gene transcription programs11.
One notable finding from this epigenomic study is the tumorigenic requirement of C/EBPβ enhancer in HCC. Deletion of this enhancer resulted in drastic abrogation in HCC tumorigenicity, which was associated with genome-wide codepletion of C/EBPβ and BRD4 occupancy and extensive dysregulation of gene expressions. Although C/EBPβ function is described at both promoters and enhancers23,42, our findings implicate enhancers as the principal sites at which C/EBPβ/BRD4 complexes target to regulate gene activation in HCC cells. When C/EBPβ enhancer is absent, C/EBPβ/BRD4 is lost from thousands of enhancers that subsequently lose activity—showing reduced H3K27ac levels and expression of nearest genes. Notably, the activities of some super-enhancers, whose target genes are enriched in crucial HCC pathways, namely Ras, PI3K-Akt and MAPK signaling cascades, are also suppressed. For example, RALB is a small GTPase effector of RAS signaling that plays important roles in the proliferation, survival, and metastasis of a variety of human cancers59. C/EBPβ enhancer loss also impairs C/EBPβ/BRD4’s enhancer control of signaling molecules (FGFR2, EGFR, ITGB1, SMAD3, TGFB2) and transcription regulators (HIF1A, RARA, FOXP1, YAP1, ZEB2) critical for angiogenesis and invasion. Given the concordant upregulation of the oncogene orthologs (Fgfr2, Hif1a, Ralb, Rara) in HBx TG mouse model, which is correlated with C/EBPβ, our results suggest a paradigm of enhancer regulation of oncogenic cell signaling for further investigation. On the other hand, the differences in C/EBPβ enhancer methylation levels in clinical specimens and mouse tissues suggest that a fraction of the total HCC cells harbors C/EBPβ enhancer hypomethylation, which may reflect heterogeneity of the epigenome60. In concordance, modest methylation changes were also observed in the hypomethylated super-enhancers regulating the MYC and other oncogenes in the primary colon tumors in comparison with the matched normal colon mucosa14. It is thus conceivable that epigenetic heterogeneity can drive variable tumor-propagating potential, which could be fully delineated by single-cell epigenomic profiling60.
The enhancer landscapes profiled in this study have implications beyond HCC. The oncogenic role of C/EBPβ, a liver-enriched transcription factor required for hepatocyte proliferation22,23, is consistent with the other lineage-survival oncogenes, namely AR in prostate cancer61, MITF in melanoma62, GATA6 in lung adenocarcinoma63 and OCA-B in diffuse large B cell lymphoma48. It is, therefore, conceivable that the lineage dependency or addiction64 can be originated by genetic and/or epigenetic alterations such as enhancer hypomethylation. Targeting C/EBPβ by small-molecule inhibitors65 may be therapeutically relevant to HCC and other human malignancies driven by alterations in C/EBPβ66,67. Like other cancers, HCC is characterized by global DNA hypomethylation, promoter hypermethylation, and more recently, hypomethylation associated with tumor-promoting gene upregulation6,68. Altogether with our discovery of aberrant enhancer hypomethylation that drives vicious positive feedback circuitry, cautions should be taken for the use of DNA hypomethylating agents as cancer therapeutics. The recent advancement in CRISPR/Cas9-mediated epigenome editing31,69 may offer more specific treatment strategies via enhancer reprogramming.
Patients and integrative epigenomic analysis
HCC patients who underwent hepatectomy at the Prince of Wales Hospital (Hong Kong) were included in this study (Supplementary Table 2). The specimens were processed immediately after surgery and snap-frozen in liquid nitrogen for DNA and RNA extraction. Informed consent was obtained from all human subjects, and the study protocol was approved by the Joint Chinese University of Hong Kong-New Territories East Cluster Clinical Research Ethics Committee. Our integrative epigenomic analysis is comprised of MBDCap-seq, WGBS, nanoscale chromatin profiling, and RNA-seq. The procedures and data analyses are provided in the Supplementary Information.
DNA samples were bisulfite-converted using EZ DNA Methylation™ Kit (Zymo). Primers targeting the DNA regions were designed by Qiagen PyroMark Assay Design SW 2.0. Taqgold DNA polymerase (ThermoFisher) was used for PCR amplification. A biotin-labeled primer was used for PCR product purification by Sepharose beads according to manufacturer’s protocols. The PCR product was sequenced by PyroMark MD Q96 MD System with sequencing primer. The level of CpG methylation was calculated by the signal to ratio of methylated cytosines to unmethylated cytosines. Non-CpG cytosine within the target regions was used as control to verify complete bisulfite conversion.
Cell culture, 5-aza-dC/JQ1 treatment, and gene knockdown
The eight immortalized human liver cell lines, LO2 (Cellosaurus, CVCL_6926), MIHA (Cellosaurus, CVCL_SA12), BEL7404 (Cellosaurus, CVCL_6568), Hep3B (ATCC, HB-8064), HepG2 (ATCC, HB-8065), Huh7 (JCRB, 0403), PLC5 (ATCC, CRL-8024), and SK-Hep1 (ATCC, HTB-52), were maintained in Dulbecco’s modified Eagle’s medium (Gibco) with 10% fetal bovine serum (HyClone). All cells were cultured at 37 °C in a humidified chamber containing 5% CO2. For pharmacological DNA demethylation and BRD inhibition experiments, liver cells seeded in 6-well plate at 50% confluency overnight were treated with 10 μM of 5-aza-dC (Sigma–Aldrich) for 3 days and 2.5 μM JQ1 (Selleck) for 2 days, respectively. In all, 25 nM siRNA was transfected into cells for 48 h using HiPerfect (Qiagen). Two siRNAs targeting C/EBPβ were purchased from ThermoFisher. Two siRNAs targeting C/EBPβ eRNA were designed based on BLOCK-iT™ RNAi Designer. The sense and antisense sequences of siC/EBPβ−1 are GGAGGUAAUAUAGUGCCUGTT and CAGGCACUAUAUUACCUCCTT. The sense and antisense sequences of siC/EBPβ−2# are GGUAAUAUAGUGCCUGCUCTT and GAGCAGGCACUAUAUUACCTT. The short-hairpin RNA (shRNA) vector targeting C/EBPβ was purchased from GenePharma. C/EBPβ expression vector was purchased from FulenGen. CRISPR/Cas9 blank vector was purchased from Addgene. Construction of CRISPR-C/EBPβ eRNA-sgRNA vectors was performed following the protocol by Addgene.
Targeted DNA demethylation
The pPlatTET-gRNA2 vector for dCas9-GCN4 and scFv-TET1CD-GFP fusion protein expression was obtained from Addgene (#82559)31. A single guide RNA (sgRNA) expression vector was modified from MLM3636 (Addgene #43860), in which 20-bp sgRNAs designed by CRISPR/Cas9 Target Online Predictor (CCTop)70 were cloned. The sgRNA sequences for a control region69 and C/EBPβ enhancer are 5′-CCCCCGGGGGAAAAATTTTT-3′ and 5′-CACACACACAGGGCCACCGA-3′, respectively. The pPlatTET-gRNA2 and sgRNA-expressing vectors were co-transfected into SK-Hep1 cells by jetPRIME from Polyplus Transfection according to the manufacturer’s instructions. After 48 h, transfected cells were flow-sorted to isolate GFP-positive cells, followed by cell expansion for pyrosequencing and qRT-PCR analyses.
Luciferase assay and site-directed mutagenesis
The C/EBPβ promoter and enhancer regions were cloned into pGL3–basic vector (Promega) to generate the luciferase reporters. The C/EBPβ enhancer luciferase plasmid with deletion of C/EBP binding motif (ATTGCACAAT) was generated by the QuikChange II Site-Directed Mutagenesis Kit (Stratagene). All plasmids were verified by DNA sequencing.
RNA extraction and qRT-PCR
RNA was extracted using RNA extraction kit (Fastagen) or Trizol and quantified by NanoDrop ND-2000 (NanoDrop Technologies). For reverse transcription, 2 µg of RNA was first treated with DNAse (Invitrogen). PrimeScript RT Master Mix (Takara) was then used for cDNA generation. For quantitative PCR analysis, SYBR Green PCR Master Mix (Takara) was used. The target genes were amplified in QS7 or 7500 Fast Real-Time PCR machine (Applied Biosystems). The experiments were replicated three times in two independent experiments. The primers are listed in Supplementary Table 3.
The primary antibodies for western blotting are CEBPB (sc-150, Santa Cruz Biotechnology, 1:1000), β-actin (8H10D10, Cell Signaling Technology, 1:10,000), Vinculin (sc-25336, Santa Cruz Biotechnology, 1:1000), H3K27ac (39133, Active Motif, 1:1000), and H3 (4499, Cell Signaling Technology, 1:1000). Cellular proteins were extracted in lysis buffer (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1% NP-40, 0.5% Na-deoxycholate) with protease inhibitors (Roche), and their concentrations were measured by DC Protein Assay (Bio-Rad). Protein samples were loaded into 8–12% sodium dodecyl sulfate polyacrylamide gel for electrophoresis and transferred to nitrocellulose membrane (Bio-Rad). Primary and secondary antibodies were sequentially added, and the target proteins were detected by Enhanced Chemiluminescence (GE Healthcare Life Sciences). β-actin or vinculin served as loading control. Uncropped western blots are shown in Supplementary Fig. 8.
Cell proliferation, colony formation, and cell invasion
For measuring cell proliferation, 103 cells were seeded in individual wells of 96-well plate, and CellTiter Proliferation Assay kit (Promega) was used according to manufacturer’s instructions. For measuring colony formation, cells seeded on a 6-well plate at 50–80% confluency were transiently transfected with plasmids. After 2 days, the cells were cultured in antibiotic-containing medium for 2–3 weeks. The resistant colonies were stained with 0.2% crystal violet and counted in three independent experiments. For cell invasion assay, BD BioCoat Matrigel invasion chambers (BD Biosciences) was used. The cells were fixed and stained with crystal violet, followed by counting. The experiments were replicated three times in two independent experiments.
The experimental use of all mice was approved by the Animal Experimentation Ethics Committee of the Chinese University of Hong Kong. All mice received humane care according to the criteria outlined in the Guide for the Care and Use of Laboratory Animals (NIH). The strain of HBx TG mice was fixed to C57BL/6 by backcrossing with the C57BL/6 strain for more than 20 generations37. Male HBx TG and WT mice were sacrificed at either 4 or 10 months of age, and the liver tissues were excised and snap-frozen. For xenograft assay, 5 × 106 cells were subcutaneously injected into the left and right flanks of nude mice. Tumor size was measured using a caliper, and the tumor volume was calculated as 0.5 × l × w2, with l indicating length and w indicating width. The mice were euthanized at 5–6 weeks, and the tumors were excised and snap-frozen.
GraphPad Prism 5 (GraphPad Software) was used for statistical analysis. The difference between two groups was calculated by independent Student’s t-test or Wilcoxon signed-rank test. The correlation among methylation and eRNA/mRNA expression was analyzed using Pearson correlation test. Chi-square test with Yates correction was used to determine whether distributions of H3K27ac levels differ between promoters and enhancers. Kaplan–Meier survival analysis was used to determine the overall and disease-free survival rates, which were calculated from the date of curative surgery to death, HCC recurrence or the last follow-up; the differences were compared by log-rank Mantel–Cox test.
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
All data supporting the findings of this study are available within the article and Supplementary Information, or from the corresponding author upon request. All ChIP-seq and RNA-seq data generated in this study are deposited in the Gene Expression Omnibus (GEO) database under the accession numbers ‘‘GSE123097’’, ‘‘GSE123098’’, and ‘‘GSE123099.’’ Public sequencing datasets used in this study are: patterns of C/EBPβ eRNA (CAGE reads, ‘FANTOM5 [http://fantom.gsc.riken.jp/5/data]’), and C/EBPβ and H3K27ac binding in the human HepG2 genome (GEO: ‘‘GSM935493’’) and mouse hepatocyte genome (GEO: ‘‘GSM1854433’’). A reporting summary for this article is available as a Supplementary Information file.
Journal peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.
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This project is supported by the University Grants Committee through the Collaborative Research Fund C4017–14G and the Focused Innovations Scheme-Scheme B 1907309 from the Chinese University of Hong Kong (CUHK). Alfred Cheng is supported by funding from the Young Researcher Award, CUHK.