Yang Shao1,2†Jing Kong1†Hanzi Xu3Xiaoli Wu1YuePeng Cao1Weijian Li1
Jing Han4Dake Li1
Kaipeng Xie1*
Jiangping Wu1*- 1Nanjing Maternity and Child Health Care Institute, Nanjing Maternity and Child Health Care Hospital, Women's Hospital of Nanjing Medical University, Nanjing, China
- 2The First People's Hospital of Zhangjiagang City, The Zhangjiagang Affiliated Hospital of Soochow University, Suzhou, China
- 3Department of Radiotherapy, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China
- 4Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China
Background: The association of opioid binding protein cell adhesion molecule-like (OPCML) gene methylation with ovarian cancer risk remains unclear.
Methods: We identified eligible studies by searching the PubMed, Web of Science, ScienceDirect, and Wanfang databases. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were used to determine the association of OPCML methylation with ovarian cancer risk. Meta-regression and subgroup analysis were used to assess the sources of heterogeneity. Additionally, we analyzed the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) datasets to validate our findings.
Results: Our study included 476 ovarian cancer patients and 385 controls from eight eligible studies. The pooled OR was 33.47 (95% CI = 12.43–90.16) in the cancer group vs. the control group under the random-effects model. The association was still significant in subgroups according to sample type, control type, methods, and sample sizes (all P < 0.05). Sensitivity analysis showed that the finding was robust. No publication bias was observed in Begg's (P = 0.458) and Egger's tests (P = 0.261). We further found that OPCML methylation was related to III/IV (OR = 4.20, 95% CI = 1.59–11.14) and poorly differentiated grade (OR = 4.37; 95% CI = 1.14–16.78). Based on GSE146552 and GSE155760, we validated that three CpG sites (cg16639665, cg23236270, cg15964611) in OPCML promoter region were significantly higher in cancer tissues compared to normal tissues. However, we did not observe the associations of OPCML methylation with clinicopathological parameters and overall survival based on TCGA ovarian cancer data.
Conclusion: Our findings support that OPCML methylation is associated with an increased risk of ovarian cancer.
Introduction
Ovarian cancer is the most frequent cause of death in women with gynecological malignancies. In 2020, 313,959 new ovarian cancer cases were diagnosed and 207,252 new deaths occurred from ovarian cancer in the world (Sung et al., 2021). Most patients are diagnosed at an advanced or incurable stage because of asymptomatic development (Lheureux et al., 2019). Therefore, identifying novel biomarkers for early diagnosis and research on treatment strategies could reduce the incidence of ovarian cancer and improve the survival rate in advanced ovarian cancer patients.
Aberrant gene expression, including the activation of oncogenes and inactivation of tumor suppressor genes (TSGs), plays a vital role in tumorigenesis (Ehrlich, 2002). Emerging studies have shown that DNA methylation is a key mechanism of epigenetic variability in gene expression (Wilson et al., 2007). Compared with normal cells, cancer cells exhibit extensive changes in DNA methylation patterns (Vidal et al., 2017). Cancer cells undergo alterations in 5-methylcytosine distribution including global DNA hypomethylation and hypermethylation of CpG islands (Jones, 2012). Notably, aberrant DNA methylation is not only a well-known mechanism of TSG inactivation but also one of the earliest events in carcinogenesis (Rauscher et al., 2015; Widschwendter et al., 2017). DNA methylation is considered a promising biomarker for cancer diagnosis and the prediction of treatment and prognosis (Szyf, 2012; Widschwendter et al., 2017). Intriguingly, the Food and Drug Administration (FDA) has approved the first methylation-based assay in colorectal cancer screening and early detection (Song et al., 2017; Widschwendter et al., 2018). Therefore, evaluating the alteration of DNA methylation in ovarian cancer is urgent.
Opioid binding protein cell adhesion molecule-like (OPCML) gene at 11q25 is a glycosyl-phosphatidylinositol (GPI)-anchored cell adhesion-like molecule and belongs to the IgLON family (Wu and Sood, 2012). OPCML demonstrates tumor-suppressor function in epithelial ovarian cancer both in vitro and in vivo (Sellar et al., 2003). Subsequently, the same team described the mechanism underlying the phenotype of OPCML. It negatively regulates a specific receptor tyrosine kinase (RTK) repertoire comprising erythropoietin-producing hepatocellular receptor-2 (EPHA2), fibroblast growth factor receptor-1 (FGFR1), fibroblast growth factor receptor-3 (FGFR3), human epidermal growth factor receptor-2 (HER2), and human epidermal growth factor receptor-4 (HER4) receptors by binding to the extracellular domains of RTKs, thus promoting their degradation via a polyubiquitination-associated proteasomal mechanism and leading to growth inhibition (McKie et al., 2012). Additionally, they revealed that a recombinant protein based on OPCML is an active anticancer agent preclinical in vivo. Another study showed that OPCML restoration interfered with HER2-EGFR heterodimer formation and potentiated lapatinib and erlotinib therapy in ovarian and breast cancer cell lines overexpressing HER2 (Zanini et al., 2017). Recent researches on OPCML protein reveal that OPCML is a potential anti-cancer therapy (Birtley et al., 2019; Simovic et al., 2019). Considering the biological and clinical effects of OPCML, research on the mechanism of aberrant expression patterns may benefit ovarian cancer patients from OPCML-based therapy.
Many studies have indicated that OPCML DNA hypermethylation frequently occurs in ovarian cancers. However, the findings remain unclear regarding the small population and different methods in previous studies (Czekierdowski et al., 2006; Zhang et al., 2006, 2014; Chen et al., 2007; Liu et al., 2008; Zhou et al., 2011, 2014a,b; Wang et al., 2015, 2017; Xing et al., 2015). Therefore, we performed a meta-analysis to identify the association of OPCML methylation with ovarian cancer risk. We further assessed whether OPCML methylation was associated with other clinicopathological parameters in eligible studies, such as age, stage, histological type, and tumor differentiation. Additionally, we validated our results based on the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) ovarian cancer datasets.
Materials and Methods
Literature Search Strategy
A systematic literature search was performed in the PubMed, Web of Science, ScienceDirect, and Wanfang databases using the following keywords and search items: (ovarian OR ovary) AND (cancer OR carcinoma OR tumor) AND (OPCML methylation). The search was updated until November 17, 2020.
Study Selection
The inclusion criteria were as follows: (1) studies primarily evaluating the association between OPCML methylation and ovarian cancer, (2) studies including case and control populations, (3) the incidence of OPCML methylation in case and control groups, and (4) studies using human tissues or blood. Based on the inclusion criteria, the titles and abstracts from the preliminary search were evaluated. Subsequently, all related studies were evaluated as full-text papers. Exclusion criteria were (1) book section, conference abstracts, and reviews, (2) studies with insufficient data to provide the methylation frequencies in cancer and control groups, and (3) studies without human samples. In the case of duplicated publications from the shared cohort, we selected the most complete information to be included in the meta-analysis.
Data Extraction and Quality Assessment
The following information was extracted for each eligible study: the first author's name, publication year, country, age, number of methylated and unmethylated samples in cancer and control groups, sample type, control type, methylation detection methods, and other clinicopathological parameters. In our study, controls included adjacent non-cancerous ovarian tissues (AT), tissue and blood samples from benign ovarian tumor (BOT) and other cancer-free patients (NT). Additionally, we used the Newcastle-Ottawa Scale (NOS) to assess the quality. The NOS includes the selection of the research groups (four stars), comparison of the groups (two stars), and ascertainment of the outcome (three stars).
Bioinformatics Analysis
Two DNA methylation data were downloaded from the Gene Expression Omnibus (GEO) database: GSE146552 (20 high grade serous ovarian cancers, 16 epithelial layer by mechanical scraping of resected fimbriae fallopian tubes and ovaries) and GSE155760 (23 high-grade serous ovarian carcinoma, 11 fallopian tube mucosa from cancer-free normal control). The GEO2R online analysis tool (https://www.ncbi.nlm.nih.gov/geo/geo2r/) was used to identify the differential DNA methylated sites (P < 0.05) between cancer tissues and normal tissues. For the cancer genome atlas (TCGA) ovarian serous cystadenocarcinoma (OV) data, we downloaded the OPCML expression data (log2-transformed RSEM normalized count) based on RNA sequencing (RNA-Seq), OPCML-associated DNA methylation data (cg03923934, cg25853078) based on HumanMethylation27 and the clinical data including age, stage, grade, and overall survival from the website (https://xena.ucsc.edu/).
Statistical Analysis
We calculated the pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) to evaluate the association between OPCML methylation and ovarian cancer risk. The heterogeneity of studies was evaluated by the χ2-based Q-test. When the P > 0.05, the fixed-effects model was used to combine the effect size; otherwise, the random-effects model was adopted. We conducted meta-regression to explore sources of heterogeneity and further performed a subgroup analysis to evaluate the source of the heterogeneity. The contribution of each study to our findings was examined according to sensitivity analysis. We used the Begg's rank correlation method (Begg and Mazumdar, 1994) and a funnel plot for Egger's test (Egger et al., 1997) to evaluate publication bias.
The correlation between OPCML methylation and its expression in TCGA was calculated by Spearman's rank correlation. Kruskal-Wallis and Wilcoxon-Mann-Whitney U tests were applied for comparisons, as appropriate. Survival analysis was performed using the log-rank test and a Cox regression model. Hazard ratios (HRs) and corresponding 95% CIs were calculated to assess the associations of factors with overall survival. All statistical tests were two-sided and performed using the R software (version 3.6). P-value < 0.05 were considered statistically significant.
Results
Study Characteristics
The detailed information of how we selected relevant articles is shown in Figure 1. We initially identified 126 articles from PubMed, Web of Science, ScienceDirect, and Wanfang databases and excluded 34 duplicated articles. After reviewing 92 articles based on titles and abstracts, 75 articles did not meet the selection criteria, leaving 17 studies for detailed full-text evaluation. Seven articles were excluded because they did not report the methylation frequencies in cancers or controls. Three articles were excluded because of overlapping cohorts (Zhou et al., 2011; Zhang et al., 2014; Wang et al., 2017). The study performed by Zhou et al. (2014a) included two sample types, tissue and serum. Thus, we considered this paper as two separate studies. Therefore, seven eligible articles with eight studies including 476 ovarian cancer patients and 385 controls were included in the meta-analysis.
Figure 1. Flowchart of study selection in the meta-analysis.
The characteristics of the eight studies are summarized in Table 1. Seven studies were performed in China and one study was performed in Poland. The cases comprised of cancer tissues and blood from ovarian cancer patients. Among the eight included studies, six studies clearly described that the cases were primary tumor patients whereas two studies (Wang et al., 2015; Xing et al., 2015) did not. In the study performed by Liu et al. (2008), there are 41 metastatic tissues of pelvic and abdomen cavity. We provided this in Table 1. However, we did not include these samples when we calculated the pooled OR. The controls in these studies were not matched to cases for any features. OPCML promoter methylation was detected in all eligible articles. There are four studies that used methylation-specific polymerase chain reaction (MSP), three used restriction enzyme-related analysis [methylation-sensitive restriction enzyme-polymerase chain reaction (MSRE-PCR) and restriction enzyme cut analysis], and one study used cationic conjugated polymer (CCP)-based fluorescence resonance energy transfer (FRET) to detect OPCML methylation in ovarian cancer and controls. According to the NOS criteria, the quality of these studies was six, indicating a relatively high quality. Detailed features are shown in Supplementary Table 1.
Table 1. Characteristics of included studies.
Relationship Between OPCML Methylation and Ovarian Cancer Risk
Because of significant heterogeneity among the included studies, a random-effects model was used to evaluate the effect size (P < 0.01; I2 = 65%; Figure 2). In the overall meta-analysis, the OPCML methylation frequency was significantly associated with an increased risk of ovarian cancer (summary OR: 33.47; 95% CI = 12.43–90.16; P < 0.001; Figure 2).
Figure 2. The summary estimates for OPCML methylation frequency associated with ovarian cancer in the meta-analysis.
Meta-Regression and Subgroup Analysis
To explore the potential sources of heterogeneity, we performed multiple regression model using six variables (publication year, country, sample type, control type, methods, and sample size). However, the source of heterogeneity was not observed among these factors (all P > 0.05; Table 2). We also conducted subgroup analysis to assess the source of the heterogeneity according to country, sample type, sample size, control type, and method (Table 3). In the subgroup analysis of country, the OR was 38.17 (95% CI = 13.21–110.28) in China under the random-effects model. The OR was 102.86 (95% CI = 39.37–268.74) under the fixed-effects model in the serum subgroup, and 18.22 (95% CI = 10.93–30.36) under the fixed-effects model in the tissues subgroup. In the subgroup analysis based on the control type, the OR was 52.77 (95% CI = 16.92–164.55) in the NT group under the fixed-effects model and 35.50 (95% CI = 6.83–197.47) in the NT and BOT groups under the random-effects model. In the subgroup analysis of methods, the OR was 21.78 (95% CI = 6.10–77.79) in the MSP group under the random-effects model and 139.45 (95% CI = 24.06–808.26) in the restriction enzyme-related analysis group under the fixed-effects model. The OR for the sample size subgroup was 34.19 (95% CI = 14.11–82.86) in the <100 subgroup under the fixed-effects model and 35.50 (95% CI = 6.38–197.47) in the ≥100 subgroup under the random-effects model.
Table 2. Meta-regression analysis.
Table 3. Subgroup analysis of associations between OPCML methylation and ovarian cancer risk.
Sensitivity Analysis
As shown in Figure 3, leave-one-out sensitivity analysis was performed by removing a single study at a time under the random-effects model to assess the stability of the results. Our results showed that the ORs ranged from 24.04 (95% CI = 9.22–62.72) to 44.47 (95% CI = 16.61–119.08).
Figure 3. The sensitivity analysis of pooled OR for OPCML methylation and ovarian cancer risk under the random-effects model.
Publication Bias
Begg's and Egger's tests were performed to estimate the publication bias of the included studies. The funnel plot was approximately symmetric (Figure 4), indicating no publication bias in Begg's (P = 0.458) or Egger's tests (P = 0.261).
Figure 4. The funnel plot for assessment of publication bias in the meta-analysis.
Relationship Between OPCML Methylation and Clinicopathological Features
We divided the ovarian cancer patients into groups based on clinical features including stage, histological type, tumor differentiation, and age, and then further valuated the associations between other variables and OPCML methylation (Figure 5). The findings suggested that methylation was related to III/IV (OR = 4.20; 95% CI = 1.59–11.14) and poorly differentiated tumor (OR = 4.37; 95% CI = 1.14–16.78), while methylation was not related to serous histology (OR = 1.46; 95% CI = 0.88–2.41) or older age (OR = 1.42; 95% CI = 0.61–3.30).
Figure 5. Forest plots for OPCML methylation and clinicopathological features of ovarian cancer patients. (A) Forest plot for the relationship between OPCML methylation and III/IV stage. (B) Forest plot for the relationship between OPCML methylation and serous ovarian cancer. (C) Forest plot for the relationship between OPCML methylation and poorly differentiated tumor. (D) Forest plot for the relationship between OPCML methylation and older age.
Validation of the Results in Multiple Public Databases
Based on GSE146552 and GSE155760 datasets, we evaluated the DNA methylation profiling in ovarian cancer tissues and normal tissues (Figure 6A). We firstly analyzed the differential methylated sites between cancer tissues and normal tissues (Figure 6B). Then, we found that methylation levels of 55 differential methylated CpG sites were consistent in two datasets (Table 4). Among them, three CpG sites (cg16639665, cg23236270, cg15964611) were located in OPCML promoter regions (Figures 6C,D, all P < 0.05). In consistent with the results of meta-analysis, the methylation levels of three CpG sites were significantly higher in cancer tissues compared to normal tissues. Based on the TCGA ovarian cancer datasets, two OPCML-associated CpG sites (cg03923934, cg25853078, Figures 7A,B) were significantly associated with OPCML expression (rho = 0.261, P = 5.97 × 10−6; rho = 0.211, P = 2.75 × 10−4). However, we did not observe the significant associations for the clinicopathological parameters and overall survival time (Figures 7C–F).
Figure 6. The OPCML methylation status in ovarian cancer tissues and normal tissues. (A) The workflow of differential methylated sites in GSE146552 and GSE155760. (B) Volcano plots of differential methylated sites based on GSE146552 and GSE155760. (C) There are seven CpG sites in OPCML promoter regions. (D) The methylation status of seven CpG sites in GSE146552 and GSE155760. Among them, three differential methylated sites (cg16639665, cg23236270, cg15964611) were observed in both GSE146552 and GSE155760.
Table 4. Consistently differential DNA methylated sites (P < 0.05 and the same direction of logFC in both datasets) between ovarian cancer tissues and normal tissues based on GEO DNA methylation datasets.
Figure 7. The methylation status of OPCML-associated CpG sites in the TCGA dataset. (A) There are only two CpG sites from HumanMethylation27k, and the location of two CpG sites in OPCML. (B) There are significantly positive associations between two CpG sites and OPCML expression. (C) The methylation levels were not significantly associated with clinical stage. (D) The methylation levels were not significantly associated with clinical grade. (E) No significant associations were observed in patient with different methylation levels using log-rank analysis. (F) No significant associations were observed in patient with different methylation levels using cox analysis.
Discussion
In the present study, we pooled eight studies together and compared the frequency of OPCML methylation in 476 ovarian cancers with 385 non-malignant tissues or blood samples. The results indicated that OPCML methylation was associated with ovarian cancer risk. The association was still significant in subgroups according to sample type, control type, methods, and sample size. Additionally, we observed significant associations between OPCML methylation and clinical stages and the grade of differentiation in ovarian cancer based on meta-analysis.
OPCML widely downregulated in many tumor types including brain tumors (Reed et al., 2007), non-small cell lung carcinoma (Tsou et al., 2007), bladder cancer (Duarte-Pereira et al., 2011), cholangiocarcinoma (Sriraksa et al., 2011), nasopharyngeal, esophageal, gastric, hepatocellular, colorectal, breast, cervical cancers, and ovarian cancer (Cui et al., 2008). Zanini et al. (2017) found that OPCML expression is associated with better progression free survival in HER2-positive ovarian cancer patients. Notably, exogenous recombinant OPCML protein inhibited ovarian cancer cell growth in vitro and in vivo (McKie et al., 2012; Wu and Sood, 2012). Recently, the advances in structure-function relationships of OPCML give rise to its potential as an anti-cancer therapy (Birtley et al., 2019). DNA methylation is the most common epigenetic modification and is widely reported for the transcriptional silencing of tumor suppressor genes in ovarian cancer. Previous studies have indicated that OPCML methylation is associated with the inactivation of OPCML, which has a tumor suppressor function in ovarian cancer (Simovic et al., 2019). However, studies with small sample sizes and different control types and methylation methods might produce inconsistent results. For example, in the study performed by Czekierdowski et al. (2006) OPCML methylation was observed in 20 out of 43 cases of ovarian cancer, but no methylation was found in four normal ovaries. No significant association was observed in this study. The control sample size in this study was small. Additionally, most previous studies reported the methylation frequency of OPCML in tumor and non-tumor tissues or serum, but the precise estimates for the associations were unclear. In the present study, we attempted to consolidate the available data and found that OPCML methylation was associated with an increased risk of ovarian cancer. The findings from the sensitivity analysis showed that our results are reliable and stable. Overall, given the TSG role and frequent methylation inactivation of OPCML in ovarian cancer, the restoration of OPCML expression could be a promising approach for ovarian cancer treatment.
In the subgroup analysis, the OR was 38.17 in China but 7.85 in Poland. The cause may be due to the limited studies in Poland. Therefore, more studies should be performed to confirm these observations in Europeans. In the serum subgroup, the OR value was highest (OR = 102.86) than that in the tissue subgroup (OR = 18.22). The results should be interpreted with caution because of the relatively small number of subjects included in the serum subgroup. Given that serum is a promising biomarker for non-invasive ovarian cancer diagnosis, further well-designed studies are warranted to explore the diagnostic performance of OPCML methylation in serum. Regarding the methods, the OR was 21.78 in the MSP group and 139.45 in the restriction enzyme-related analysis group. Technically, MSP amplify either methylated (M) or unmethylated (U) alleles after bisulfite conversion and evaluate methylation status in CpG regions (Herman et al., 1996). MSRE-PCR can recognize and degrade unmethylated DNA sequences whereas the methylated DNA sequences remain intact (Ramsahoye et al., 1997). Taken together, the results of subgroup analyses showed that OPCML methylation was significantly associated with an increased risk of ovarian cancer, regardless of the sample size, sample type, control type, and methods. Additionally, we found that the methylation status was associated with III/IV stage and poorly differentiated tumors. This finding suggests that OPCML is related to the malignant progression of ovarian cancer.
Based on publicly available datasets, we observed that the DNA methylation levels of cg16639665, cg23236270, and cg15964611 were consistently higher in cancer tissues than that in normal tissues, which validated some results of our meta-analysis. However, we did not confirm the difference of the OPCML methylation levels in different groups of clinical stage, grade, and so on. We found the positive association between DNA methylation level of cg25853078 in OPCML promoter region and OPCML expression. This positive association did not fit the hypothesis that DNA methylation levels in promoter region suppress the expression and contribute to ovarian cancer development. The DNA methylation levels in previous published papers were regions but not one CpG site. There are some CpG sites in OPCML promoter region, but we only assessed one CpG site in the promoter region based on the HumanMethylation27 platform. Therefore, other CpG sites were not calculated based on the TCGA data, which may have significant roles in the regulation of OPCML expression. Our study possessed several limitations. First, the total sample size in our study was relatively small and enrolled studies had low quality. Second, all the eligible studies were case-control designs and we could not explore the causation between OPCML methylation and ovarian cancer risk. Additionally, we used the incidence of OPCML methylation in the case and control groups to evaluate the pooled estimates because the adjusted ORs were not reported in the original studies. Further prospective studies with large samples are warranted to determine the role of OPCML in ovarian cancer risk and progression.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
Author Contributions
YS, KX, and JW: conception and design. YS and JK: acquisition of data. HX, XW, YC, WL, JH, and DL: analysis and interpretation of data. YS, KX, and JW: manuscript drafting or revising. All authors contributed to the article and approved the submitted version.
Funding
This work was financially supported by the Nanjing Medical Science and Technique Development Foundation (JQX18009) and National Natural Science Foundation of China (81702569).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We are thankful to the publicly available datasets (TCGA, GEO).
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcell.2021.570898/full#supplementary-material
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Keywords: OPCML, methylation, ovarian cancer, risk, progression
Citation: Shao Y, Kong J, Xu H, Wu X, Cao Y, Li W, Han J, Li D, Xie K and Wu J (2021) OPCML Methylation and the Risk of Ovarian Cancer: A Meta and Bioinformatics Analysis. Front. Cell Dev. Biol. 9:570898. doi: 10.3389/fcell.2021.570898
Received: 01 July 2020; Accepted: 08 February 2021;
Published: 11 March 2021.
Edited by:
Xiao Zhu, Guangdong Medical University, ChinaReviewed by:
Abhijit Shukla, Memorial Sloan Kettering Cancer Center, United StatesMingzhi Han, University of Bergen, Norway
Copyright © 2021 Shao, Kong, Xu, Wu, Cao, Li, Han, Li, Xie and Wu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jiangping Wu, wujiangping@njmu.edu.cn; Kaipeng Xie, kaipengxie@njmu.edu.cn
†These authors have contributed equally to this work