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Oncology Letters logoLink to Oncology Letters
. 2017 Sep 15;14(5):6210–6216. doi: 10.3892/ol.2017.6979

The expression and significance of histone lysine methylation in endometrial cancer

Qing Li 1, Nan Jia 1, Xiang Tao 2, Keqin Hua 1,3, Weiwei Feng 1,3,✉
PMCID: PMC5661412  PMID: 29113269

Abstract

Histone modifications of lysine residues have been implicated as having diagnostic and/or prognostic significance in numerous types of cancer. In the present study, the significance of the histone H3 methylation of lysine 4 (H3K4) and lysine 27 (H3K27) were investigated in endometrial cancer. Specifically, immunohistochemical analysis was used to detect the cellular expression levels of H3K27 trimethylation (H3K27me3), H3K4 trimethylation (H3K4me3) and H3K4 dimethylation (H3K4me2) in glandular epithelial tissues and stromal tissues. The association between the methylation levels of histone markers and clinicopathological parameters were analyzed. The results demonstrated that in epithelial cells, H3K4me2 and H3K4me3 exhibited the highest levels in endometrial cancer, followed by precancerous lesions and a normal endometrium. Low expression levels of H3K4me2 in glandular epithelium of endometrial cancer were significantly associated with a clinical early International Federation of Gynecology and Obstetrics stage (P=0.006). For stromal tissues, the expression level of H3K27me3 in Type 1 endometrial cancer was significantly lower compared with that in the normal endometrium (P=0.043) and precancerous lesions (P<0.001). The expression level of H3K4me2 was significantly lower in the stroma of Type 1 and 2 cancer compared within the normal endometrium (P=0.005). A low H3K4me3 expression level in the stroma of endometrial cancer tissues was associated with P53-negativity (P=0.032). In conclusion, the cellular expression levels of histone H3 methylation were differentially presented in glandular epithelial and stromal elements in endometrial tissues. A low expression level of activation marker H3K4me2 in glandular epithelium defined a subset of patients with early-stage endometrial adenocarcinoma and may have potential prognostic value.

Keywords: endometrial cancer, histone modifications, histone 3 lysine methylation

Introduction

Endometrial cancer poses a threat for the health of females, with ~320,000 newly diagnosed cases each year worldwide (1). A total of 76,000 patients eventually succumb to this malignancy per year, making it the sixth most common type of cancer in females (2). In view of the increasing incidence, understanding how this malignancy is initiated and progresses is of great importance, and this knowledge is required. It is now well established that in addition to genetic changes, epigenetic alterations, including DNA methylation and post-translational histone modifications, which control chromatin accessibility and gene activity, are associated with the aberrant expression level of oncogenic or tumor-suppressor genes. Chromatin-modifying enzymes can catalyze reversible modifications of histones, in which lysine methylation serve an important role.

A repression marker, histone H3 lysine 27 trimethylation (H3K27me3), and two activating markers, histone H3 lysine 4 dimethylation (H3K4me2) and histone H3 lysine 4 trimethylation (H3K4me3), were selected as they have been revealed to possess associations with cancer (3–5). These, and other modifications, generate a combinatorial histone code that demarcates chromatin regions for transcription activation or repression. Recently, cellular patterns of histone modifications have been demonstrated to be prognostic indicators for numerous types of tumors, including prostate (6), kidney (7), lung (8), gastric (9), ovarian (10) and breast cancer (11); however, little is known about the global alteration of histone status during tumorigenesis, and cancer progression in endometrial cancer. The present study therefore aimed to assess the clinical significance of selected histone modifications in endometrial tissues, including the normal endometrium, precancerous lesions and endometrial cancer. The association between histone modifications and the clinicopathological data was analyzed in the present study.

Materials and methods

Research subject

After obtaining approval from the Obstetrics and Gynecology Hospital of Fudan University (Shanghai, China) Ethics Committee, 99 endometrial tissues (including 24 normal endometrial samples, 18 precancerous lesions, and 44 Type 1 and 13 Type 2 endometrial cancer samples) were obtained from patients treated in the Obstetrics and Gynecology Hospital of Fudan University between June 2008 and December 2012. The mean age of all patients enrolled was 51.7±10.2 years. The mean ages of the normal group, precancerous group, and type 1 and type 2 cancer groups were 47.5±7.2, 44.3±7.7, 56.4±8.8, and 55.15±12.4 years, respectively. Written informed consent was obtained from all patients prior to enrollment in the present study. Normal tissues, including 12 proliferative, 9 secretory and 3 atrophic endometrial tissues, were obtained from patients who had benign disease, including adenomyosis or myoma, and 18 precancerous lesions, including 9 simple hyperplasia, 2 complex hyperplasia and 7 atypical hyperplasia tissues from patients who had irregular bleeding. Hematoxylin and eosin (H&E) (hematoxylin for 5 min and eosin for 10 sec at temperature between 20–24°C) stained tissue sections adjacent to the tissue sections obtained for immunohistochemical staining of all specimens were reviewed by an experienced pathologist to confirm the diagnosis. For patients with endometrial cancer, the clinicopathological parameters, including International Federation of Gynecology and Obstetrics (FIGO) stage, tumor grade, depth of myometrial invasion and p53, as well as estrogen receptor (ER), progesterone receptor (PR) and lymph-vascular space invasion (LVSI) evaluations, were collected. The surgical pathology stage was determined in accordance with the 2009 FIGO guidelines (12).

Immunohistochemistry

Antigen retrieval and antibody dilutions were optimized prior to the initiation of the study (Mingrui Biotech, Shanghai, China). Diagnosis of each case was made by two experienced pathologists without discrepancy. To ensure uniformity, all tissue sections were processed synchronically. The H&E tissue sections (4 µm) adjacent to the sections used for immunohistochemistry assessment were used for pathological diagnosis. The working dilutions of anti-H3K27me3 antibodies (cat. no. CST 9733s; Cell Signaling Technology, Inc., Danvers, MA, USA), anti-H3K4me2 antibodies (cat. no. Ab32356; Abcam, Cambridge, UK) and anti-H3K4me3 antibodies (cat. no. Ab8580; Abcam) were 1:100. Endogenous peroxidase activity was blocked using 0.3% H2O2. Slides were washed and incubated with the biotinylated secondary antibody (polyclonal goat anti-rabbit; Histostain-Plus IHC kit; Mingrui Biotech, Shanghai, China) for 45 min at 37°C and washed with PBS.

Procedures were performed using an immunohistochemistry kit (MR Biotech Ltd., Shanghai, China), according to the manufacturer's protocol. Tissue staining intensities were assessed using double-blinded quantitative scoring. For the semi-quantitative analysis, 5 fields of each slide were randomly selected under magnification, ×10 and further read under magnification, ×40 using light microscope. Positive staining refers to dark brown granules within the nuclear region, with or without brown granules in the cytoplasm. The percentages of positive cells were assessed independently by two observers and the mean values of their results was used for evaluation.

Statistical analysis

All data were statistically analyzed by an independent-sample t-test (Students' t-test) or one-way analysis of variance (ANOVA, Bonferroni used as post-hoc test) using SPSS version 20.0 (IBM Corp., Armonk, NY, USA). The data were presented as mean ± standard deviation. P<0.05 was considered to indicate a statistically significant difference.

Results

Samples from 24 normal endometrial tissues, 18 precancerous lesions, and 44 type 1 and 17 type 2 endometrial cancer tissues were retrieved. The present study observed the methylation expression level of three markers, H3K27me3, H3K4me2 and H3K4me3, by immunohistochemistry in the epithelial, and stromal compartments of tissues. Fig. 1 Presents the representative images.

Figure 1.

Figure 1.

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Representative images of immunohistochemistry staining. (A) Normal endometrium, (B) precancerous lesions, (C) Type 1 endometrial cancer and (D) Type 2 endometrial cancer tissues stained for H3K27me3. (E) Normal endometrium, (F) precancerous lesions, (G) Type 1 endometrial cancer and (H) Type 2 endometrial cancer tissues stained for H3K4me2. (I) Normal endometrium, (J) precancerous lesions, (K) Type 1 endometrial cancer and (L) Type 2 endometrial cancer tissues stained for H3K4me3. All images were captured at magnification ×200 using light microscopy. H3K27me3, histone H3 lysine 27 trimethylation; H3K4me2, histone H3 lysine 4 dimethylation; H3K4me3, histone H3 lysine 4 trimethylation.

The patients with type 2 cancer were postmenopausal; therefore, the present study compared the methylation levels of the markers in two sessions: Type 1 cancer with a normal endometrium and hyperplasia tissue; and type 2 cancer with an atrophic endometrium. For normal endometrium, the present study used one-way ANOVA to determine whether there were significant differences among the proliferative, secretory and atrophic endometrium tissues. As presented in Fig. 2A, in glandular epithelium, H3K27me3 demonstrated no difference in cancerous tissues and noncancerous tissues; however, in stromal tissue, the expression level of H3K27me3 was lowest in the stroma of Type 1 endometrial cancer compared with in the normal endometrium (P=0.002) and precancerous lesions (P=0.001; Fig. 2B).

Figure 2.

Figure 2.

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Semi-quantified IHC results of H3K27me3, H3K4me2 and H3K4me3 markers. The expression levels of three histone methylation markers in endometrial tissue that were semi-quantified according to the IHC results and compared between various groups. The X axis represents different tissue groups and the Y axis represents positive rates of the three markers. The expression level of H3K27me3 in (A) in the epithlium and (B) stroma. The expression level of H3K4me2 in (C) in the epithelium and (D) stroma. The expression level of H3K4me3 in (E) in the epithlium and (F) stroma. ***P<0.0001, ***P<0.001, **P<0.01, *P<0.05. IHC, immunohistochemistry; H3K27me3, histone H3 lysine 27 trimethylation; H3K4me2, histone H3 lysine 4 dimethylation; H3K4me3, histone H3 lysine 4 trimethylation.

H3K4me2 was highly expressed in the glandular epithelium of Type 1 endometrial cancer compared with in the normal endometrium (P=0.007) and precancerous lesions (P<0.001; Fig. 2C). Conversely, in the stroma, a lower expression level of H3K4me2 was identified in Type 1 endometrial cancer compared with precancerous lesions (P=0.012; Fig. 2D). Similarly, a lower expression level of H3K4me2 in the stroma was demonstrated in Type 2 endometrial cancer compared with intheatrophic endometrium (P=0.009).

In glandular epithelium (Fig. 2E), the expression level of H3K4me3 was higher in Type 1 endometrial cancer compared within the normal endometrium (P=0.02) and precancerous lesions (P<0.001), which was similar to the expression level of H3K4me2. The H3K4me3 expression levels were also higher in epithelial cells of Type 2 endometrial cancer compared within the atrophic endometrium (P=0.002). Lower expression levels of H3K4me3 in the stroma were revealed in Type 1 endometrial cancer compared with in the normal endometrium (P=0.03; Fig. 2F).

Subsequently, the present study investigated the association between the expression levels of histone modification markers and clinicopathological features in endometrial cancer.

As presented in Tables I and II, there were no significant differences between the H3K27me3 expression levels and clinical characteristics, including FIGO stage, tumor grade, depth of myometrial invasion, P53, ER, PR, and LVSI. In the epithelial elements of Type 1 endometrial cancer, a low expression level of H3K4me2 was associated with an early FIGO stage (P=0.006). In the stroma of Type 2 endometrial cancer, a low expression level of H3K4me3 was associated with P53 negativity (P=0.032).

Table I.

Association between the expression levels of histone modification markers and clinicopathological features in glandular epithelium of endometrial cancer.

Clinicopathological characteristic H3K27me3 P-valuea H3K4me2 P-valueb H3K4me3 P-valuec
FIGO stage 0.325 0.006 0.814
  I 0.58±0.22 0.42±0.18 0.47±0.27
  II–IV 0.49±0.31 0.60±0.20 0.49±0.30
Tumor grade NS NS NS
  G1 0.56±0.27 0.47±0.14 0.47±0.29
  G2 0.63±0.16 0.61±0.26 0.48±0.21
  G3 0.43±0.33 0.54±0.17 0.43±0.33
  Type 2 0.63±0.34 0.55±0.23 0.46±0.08
Endometrial infiltration NS NS NS
  Limited to endometrium 0.58±0.39 0.33±0.15 0.29±0.30
  <1/2 0.58±0.19 0.44±0.17 0.44±0.29
  ≥1/2 0.47±0.34 0.60±0.20 0.32±0.33
P53 0.105 0.339 0.631
  Negative 0.57±0.23 0.48±0.19 0.39±0.30
  Positive 0.76±0.13 0.58±0.21 0.46±0.40
ER 0.193 0.078 0.723
  Negative 0.40±0.33 0.61±0.20 0.37±0.34
  Positive 0.61±0.20 0.46±0.19 0.42±0.30
PR 0.773 0.653 0.460
  Negative 0.53±0.39 0.60±0.43 0.30±0.32
  Positive 0.49±0.29 0.47±0.17 0.42±0.31
LVSI 0.182 0.682 0.234
  No 0.60±0.24 0.51±0.17 0.42±0.28
  Yes 0.48±0.26 0.48±0.21 0.28±0.28
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Data were presented as the mean ± standard deviation.

a

Comparison between the level of H3K27me3 in glandular epithelium of endometrial cancer in different indexes, such as FIGO stage I and FIGO stage II–IV.

b

Comparison between the level of H3K4me2 in glandular epithelium of endometrial cancer in different indexes.

c

Comparison between the level of H3K4me3 in glandular epithelium of endometrial cancer in different indexes. NS, not significant; FIGO, International Federation of Gynecology and Obstetrics; ER, estrogen receptor; PR, progesterone receptor; LVSI, lymph-vascular space invasion; H3K27me3, histone H3 lysine 27 trimethylation; H3K4me2, histone H3 lysine 4 dimethylation; H3K4me3, histone H3 lysine 4 trimethylation.

Table II.

Association between the expression levels of histone modification markers and clinicopathological features in the stroma of endometrial cancer.

Clinicopathological characteristic H3K27me3 P-valuea H3K4me2 P-valueb H3K4me3 P-valuec
FIGO stage 0.514 0.910 0.437
  I 0.18±0.16 0.20±0.15 0.27±0.17
  II–IV 0.15±0.13 0.20±0.07 0.22±0.17
Tumor grade NS NS NS
  G1 0.16±0.12 0.22±0.19 0.22±0.15
  G2 0.08±0.03 0.17±0.05 0.26±0.18
  G3 0.18±0.15 0.27±0.12 0.15±0.15
  Type 2 0.19±0.28 0.12±0.08 0.41±0.30
Endometrial infiltration NS NS NS
  Limited to endometrium 0.15±0.18 0.08±0.06 0.34±0.27
  <1/2 0.15±0.14 0.18±0.15 0.22±0.17
  ≥1/2 0.10±0.10 0.19±0.09 0.13±0.15
P53 0.394 0.112 0.032
  Negative 0.16±0.15 0.19±0.14 0.20±0.15
  Positive 0.10±0.07 0.09±0.08 0.36±0.25
ER 0.217 0.818 0.395
  Negative 0.09±0.11 0.18±0.09 0.16±0.16
  Positive 0.16±0.15 0.19±0.15 0.23±0.19
PR 0.096 0.877 0.163
  Negative 0.03±0.04 0.20±0.13 0.10±0.14
  Positive 0.16±0.15 0.19±0.14 0.23±0.19
LVSI 0.853 0.731 0.203
  No 0.14±0.15 0.17±0.14 0.22±0.18
  Yes 0.15±0.09 0.19±0.11 0.13±0.16
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Data were presented as the mean ± standard deviation.

a

Comparison between the level of H3K27me3 in the stroma of endometrial cancer in different indexes, such as FIGO stage I and FIGO stage II–IV.

b

Comparison between the level of H3K4me2 in the stroma of endometrial cancer in different indexes.

c

Comparison between the level of H3K4me3 in the stroma of endometrial cancer in different indexes. NS, no statistic difference; FIGO, International Federation of Gynecology and Obstetrics; ER, estrogen receptor; PR, progesterone receptor; LVSI, lymph-vascular space invasion; H3K27me3, histone H3 lysine 27 trimethylation; H3K4me2, histone H3 lysine 4 dimethylation; H3K4me3, histone H3 lysine 4 trimethylation.

Discussion

Histone is the key component of nucleosomes and serves a significant role in epigenetics. Numerous epigenetic studies have investigated the role of DNA methylation (13–15), but there are few reports regarding histone methylation and its significance in endometrial cancer. To the best of our knowledge, the present study analyzed the expression of H3K4me2, H3K4me3 and H3K27me3 in endometrial tissues by immunohistochemistry for the first time, assessing the potential association between endometrial cancer progression, and the expression levels of these three markers.

The trimethylation of H3K27 is associated with the transcriptional inhibition of genes. Enhancer of zeste 2 polycomb repressive complex 2 subunit, a methyl-transferase for H3K27, is upregulated in a variety of tumors and serves an essential role in tumor promotion (2,16); our previous study reached the same conclusion (17). Certain studies have widely associated H3K27me3 with gene silencing and transcriptional inhibition (6,18); however, these studies have not achieved a consensus on the level of H3K27me3 and the significance of its aberrant expression in human tumorigenesis. Previous studies have suggested that the low expression level of H3K27me3 in tumor tissues may enhance the expression of oncogenes and consequently promote tumor growth (19–22); however, Nakazawa et al (23) revealed no significant differences when comparing the expression levels of H3K4me2 and H3K27me3 in 85 cases of colorectal cancer with the paired normal colorectal tissues. Conversely, high expression levels of H3K27me3 were detected in other neoplasms (24,25). In the present study, the expression level of H3K27me3 in the endometrial stroma was significantly lower in Type 1 endometrial cancer compared within the normal endometrium (P=0.043) and precancerous lesions (P<0.001). A low expression level of H3K27me3 may predict a more aggressive biological behavior in endometrial carcinoma; however, there were no significant differences in glandular epithelium of cancerous tissues and noncancerous tissues, which may be due to insufficient sample sizes. Stroma-tumor communication serves an important role in the genesis of neoplasia (26). The endometrium is composed of epithelium and lamina propria. The epithelium comprises columnar epithelial cells (endometrial epithelial cells) with a secretary function. Lamina propria consists of endometrial stromal cells (ESCs), immune cells, reticular fibers, matrix, blood vessels and nerves, forming the microenvironment of the epithelial cells. Tan et al (27) demonstrated that the epithelial-to-mesenchymal transition of prostate cancer cells was inhibited by adiponectin (ADN), which is also inversely correlated with the risk of endometrial cancer (28), with decreasing expression levels of H3K27me3 at the ADN promoter in 22RV1cells (a human prostate cancer cell line). To date, to the best of our knowledge, no previous study has focused on the association between adiponectin and H3K27me3 in stromal cells of endometrial cancer. Future studies are required to assess its potential role as a prognostic marker.

Presently, there is no definite understanding of H3K4me2 in cancer tissues. Previous studies suggested that it was positively associated with a poor prognosis in tumors (29,30), whereas others held converse opinions (31,32) or revealed no difference between the H3K4me2 expression levels and prognoses (23). In the present study, the H3K4me2 expression levels increased with the malignant degree of endometrial tissues in the epithelium, indicating that H3K4me2 was involved in the oncogenesis of endometrial cancer. Furthermore, low expression levels of H3K4me2 in glandular epithelium of endometrial cancer were significantly associated with a clinical early FIGO stage (P=0.006). This finding indicated that endometrial cancer with high expression levels of H3K4me2 tended to be more invasive. Lei et al (33) and Liu et al (34) demonstrated that LIM-only protein 3 and PR domain containing 16 were associated with a poor prognosis in patients with astrocytoma and glioma. Both were indirectly inhibited by the tumor suppressor microRNA-101 with decreased H3K4me2 expression levels (33,34). Cannuyer et al (35) revealed that MAGE family member A1 demethylation and activation in melanoma cells were associated with decreased expression levels of H3K9me2, and increased expression levels of H3ac and H3K4me2, where they encode tumor-specific antigens. Conversely, the stromal expression level of H3K4me2 was significantly lower in type 1 and type 2 endometrial cancer compared within the normal endometrium (all P=0.005). Different expression levels of H3K4me2 in the epithelium and stroma may indicate diverse mechanisms, and influences. Further studies are required to explore the role of histone modifications in the stroma in order to elucidate the interactive effect between the microenvironment and tumor cells.

The association between H3K4me3 expression level and the prognosis of tumors also remains controversial. In an effort to assess the cellular expression level of H3K4me3 in HCC and its association with clinicopathological variables and outcomes, expression levels of H3K4me3, and histone methyltransferase SET and MYND domain-containing protein 3were investigated using western blotting, and immunohistochemistry in cell lines and tumor tissue microarrays from a well-characterized series of patients with HCC (n=168) (29). The author compared two experimental results, and revealed that patients with maximum tumor diameters of <5 cm, a low tumor-node-metastasis score, no intravascular invasion and no recurrence of hepatocellular carcinoma had a lower expression level of H3K4me3 (P<0.05) (29). It was also demonstrated that as the expression level of H3K4me3 increased, the prognosis of patients suffering from HCC worsened (P<0.0001) (36). However, this conclusion has been disputed by another report (37). In the present study, the expression levels of H3K4me3 increased with the malignant degree of endometrial tissues in the epithelium; however, the specific underlying mechanism remains to be further explored. The factor p53 has a high level of association with tumors in humans. The overexpression of p53 is often observed in malignant tumors and can be a reliable marker for enhanced proliferation (38). In the present study, a low expression level of H3K4me3 in the stroma was associated with p53-negativity (P=0.032), which predicts a benign prognosis in humans with endometrial cancer. Tang et al (39) demonstrated that enhancer/promoter-bound p53, via direct interactions, recruits p300 and SET1 complex (SET1C) to affect associatedH3K4me3 events via additional p300-SET1C interactions at the contiguous enhancer-core promoter region. Mungamuri et al (40) revealed that in response to p53 stabilization, its pro-apoptotic target promoters become enriched with the H3K4me3 epigenetic mark and its readers. Lauberth et al (41) also demonstrated a direct effect of H3K4me3 on p53-dependent transcription. It may serve as a potential therapeutic target for the treatment of endometrial cancer. Future studies are required to further evaluate the biological function of H3K4me3 in endometrial tissue and prospectively assess its potential role as a prognostic marker.

The majority of previous studies have focused on glands; however, few have paid attention to the stroma in endometrial cancer. The pathological diagnosis of endometrial cancer primarily depends on its glandular component in a high state of dysplasia. The stromal components of tumors (vascular, lymphatic interstitial and protein) serve an important role during the tumor growth and development. The roles of the stroma and its properties have not been studied extensively. ESCs and gland cells maybe homologous during embryogenesis for development from the Mullerian duct (42). ESC and gland cells express steroid receptors, meaning that they are regulated by steroid hormones in the peripheral blood (43). Furthermore, the development of cancer of gland cells accompanies the decline of ESCs until they disappear (44). The present study analyzed the expression level of histone methylation in the stroma of endometrial tumors, and proposed that the expression levels of H3K27me3 and H3K4me2 are low in the stroma of endometrial cancerous tumors. Low expression levels of H3K4me3 in the stroma of endometrial cancerous tumors may be associated with poor prognosis.

Acknowledgements

The present study was supported by the National Natural Science Foundation of China (grant nos. 30973185 and 81572836) and by the Shanghai Science and Technology Committee (grant nos. 15140903200 and 16411953500).

Glossary

Abbreviations

H3K27me3

trimethylation of histone 3 lysine 27

H3K4me2

dimethylation of histone 3 lysine 4

H3K4me3

trimethylation of histone 3 lysine 4

LVSI

lymph-vascular space involvement

HCC

hepatocellular carcinoma

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