Abstract
Lung cancer exhibits sex-biased molecular characteristics and epidemiological trends, suggesting a need for sex-specific approaches to understanding its etiology and treatment. DNA methylation alterations play critical roles in lung carcinogenesis and may serve as valuable biomarkers for precision medicine strategies. We employed the Infinium MethylationEPIC array to identify autosomal sex-related differentially methylated CpG sites (DM-CpGs) in lung epithelium of healthy individuals (32 females and 37 males) while controlling for age, BMI, and tobacco use. We correlated DM-CpGs with gene expression in lung epithelium and immune responses in bronchoalveolar lavage. We validated these DM-CpGs in lung tumors and adjacent normal tissue from The Cancer Genome Atlas (TCGA). Among 522 identified DM-CpGs, 61% were hypermethylated in females, predominantly located in promoter regions. These DM genes were implicated in cell-to-cell signaling, cellular function, transport, and lipid metabolism. Correlation analysis revealed sex-specific patterns between DM-CpGs and gene expression. Additionally, several DM-CpGs were correlated significantly with cytokines (IL-1β, IL-4, IL-12p70, and IFN-γ), macrophage, and lymphocyte counts. Also, some DM-CpGs were observed in TCGA lung adenocarcinoma, squamous cell carcinoma, and adjacent normal tissues. Our findings highlight sex-specific DNA methylation patterns in healthy lung epithelium and their associations with lung gene expression and lung immune biomarkers. These findings underscore the potential role of lung sex-related CpGs as epigenetic predispositions influencing sex disparities in lung cancer risk and outcomes, warranting further investigation for personalized lung cancer management strategies.
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Introduction
Sex-based differences in lung health, respiratory diseases, and lung cancer are increasingly recognized, suggesting a complex interplay of biological factors influencing disease susceptibility, progression, and treatment response1,2,3,4. While disparities in smoking rates contribute partially to these differences5,6,7,8, independent of smoking, there may be a sex-related susceptibility for lung cancer development9,10.
Altered DNA methylation signatures have been indicated as biomarkers for diagnosis and prognosis in lung cancer11,12,13,14. This is because altered DNA methylation is involved in several key biological regulatory pathways such as apoptosis, proliferation, cell cycle, DNA repair, tumor invasion, and metastasis15. Thus, sex-specific DNA methylation patterns may elucidate distinct molecular pathways underlying lung cancer development in males and females.
Despite the importance of sex-related DNA methylation in lung disease, genome-wide studies often overlook sex-specific methylation patterns by often controlling for sex in analysis, potentially missing critical insights into sex-related disparities16. While blood-based studies have shown sex-related differential methylation16,17,18,19,20, the lung-specific methylation landscape remains poorly understood. Since DNA methylation is highly tissue-type specific21,22 and regulates tissue-specific gene expression13, investigating sex-related methylation patterns in lung tissue is crucial for understanding sex-based differences in lung health.8.
Moreover, exploring sex-related DNA methylation in healthy individuals can uncover epigenetic biomarkers predisposing individuals to lung cancer, shedding light on potential targets for personalized treatments23. Despite higher lung cancer incidence and mortality rates in males, disparities in treatment response, particularly in immunotherapy, persist24,25,26. Sex-specific immune processes and mutation burdens partially explain these differences24,27,28. However, the contribution of DNA methylation to sex disparities in lung cancer remains largely unexplored. It is postulated that sex-related DNA methylation in lungs explains underlying molecular mechanisms of sex-related dimorphism in lung cancer that can be further utilized as new epigenetic targets unique to males or females. Moreover, the reversible nature of DNA methylation can serve as a guide to monitor cancer treatment response and further identify methylation patterns aimed to help reduce tumor load.
Here, we aim to study sex-related autosomal CpG methylation patterns in the lungs of healthy young adults and further investigate their associations with other lung biomarkers, including inflammation and gene expression. We validated the sex-related CpGs in lung tissues from The Cancer Genome Atlas (TCGA) to find persistent CpG methylation signatures from healthy to a disease state.
Materials and methods
Participants and recruitment
All methods were performed in accordance with relevant guidelines and regulations that were approved by the institutional review board at The Ohio State University. Young adults aged 20 to 30 were recruited from 2015 to 2019 in the central Ohio (Supplementary Table 1)29,30,31,32,33. All participants provided informed consent after receiving study information and an explanation, before undergoing bronchoscopy, bronchial brushing for DNA methylation and gene expression, and bronchoalveolar lavage (BAL) for immune cells and cytokines. Specifically, during the bronchoscopy procedure, sterile salt water was placed into the lung and immediately suctioned back, washing off immune cells and materials lining the area. Fluid was injected approximately 5–7 times, recovering samples at each lavage. Following the washing, a cytology brush was inserted to obtain brushes of grossly normal airway epithelium from the main bronchus of the lung.
Cell counts and cytokines in bronchoalveolar lavage
BAL was centrifuged at 300g at 4 °C. The cell pellets and supernatant were separated for immune cell counts and cytokines, respectively. Cell counts were performed using Countess Automated Cell Counter (Invitrogen, Waltham, MA), and differential cell count was determined using Diff-Quik stained cytospins and light microscopy through a clinical histopathologist. The supernatant was analyzed for cytokines using Meso Scale Discovery29,30.
Genome-wide DNA methylation and whole transcriptome array in lung epithelium
Allprep DNA/RNA kit (Qiagen, Germantown, MD) was used to extract total DNA from the bronchial brushings for the Infinium MethylationEPIC BeadChip (Illumina, San Diego, CA) and RNA for the GeneChip Human Transcriptome Array 2.0 (HTA 2.0; Affymetrix Inc., Santa Clara, CA) as we previously reported29. Briefly, raw data from the arrays were processed using Partek Genomics Suite 6.6 (Partek, St Louis, Missouri), and potential batch effects were removed using ANOVA (Analysis of Variance). For methylation data, raw data (idat files) were normalized by Subset-quantile Within Array Normalization (SWAN)34,35, and β-values were converted to M-values to control for heteroscedasticity by logit-transformation36,37. GRCh37/hg19 (Human Genome version 19) was used as a reference genome. Prior to statistical analysis, we excluded probes that were in the X or Y chromosomes, SNP-associated, off-target or had a detection P > 0.0538,39. For transcriptome data, raw data (CEL files) were normalized using Robust Multi-Array analysis (RMA)40,41 and log2 transformed in Partek. Analysis of covariance (ANOVA) was used to remove potential batch effects.
Statistical analysis
All statistical analysis was performed through JMP Pro Version 15 (SAS, Cary, NC) and Partek. To identify differentially methylated CpGs, (DM-CpGs), a multivariate linear regression model was used by controlling for age, body mass index (BMI), and smoking status at Benjamini–Hochberg False Discovery Rate (FDR) < 0.1. To characterize the patterns of DM-CpGs, signatures were characterized by functional roles according to the following genomic locations: promoter, within 1500 bps of a transcription start site (TSS) (TSS1500), within 200 bps of a TSS (TSS200), 5ʹ untranslated regions (5ʹUTR), first exon (1stExon), body (non-promoter), 3ʹUTR (non-promoter); and intergenic regions21,29. The location of CpGs relative to the CpG island and surrounding regions were defined according to the Illumina annotation file. Further, downstream analyses were performed to correlate methylation levels of the DM-CpGs with inflammatory markers (cytokines and cells) and gene expression (CpG site within ± 1.5 Kb from transcript TSS using a Spearman correlation within each sex group. In this study, unique genes are referred to as not repeated or duplicated in the findings to avoid double counting results. For the downstream analyses of correlations between identified sex-related DM-CpGs and other lung biomarkers, a statistical significance was defined at FDR < 0.2.
Comparison of DM-CpGs with The Cancer Genome Atlas (TCGA)
We utilized TCGA’s Lung Adenocarcinoma (LUAD, n = 29 for adjacent normal tissue and n = 433 for tumor tissues) and Lung Squamous Cell Carcinoma (LUSC, n = 42 for adjacent normal and n = 358 for tumor tissues (Supplementary Table 2). Of 522 DM-CpGs identified from this study of healthy individuals, we used a targeted approach and matched 275 CpGs that were available on the Illumina 450 K array for TCGA data to our list of sex-related DM-CpGs. To determine the DM-CpGs between females and males, we used one-way ANOVA. A statistically significant correlation for downstream analysis was defined at FDR < 0.2.
Ingenuity pathway analysis
The DM-CpGs genes were classified by ingenuity pathway analysis (IPA; Ingenuity Systems, Qiagen) to investigate the potential biological roles of the signatures. The score [score = − log10(P value)] was used to measure the probability of finding identified genes in a set of biological functions stored in the IPA Knowledge Base (IPKB) by chance alone.
Ethics approval and consent to participate
The study was approved by the institutional review board at The Ohio State University, and all participants signed informed consent.
Results
Identification and characterization of DM-CpGs
We identified 522 sex-related DM-CpGs after adjusting for age, BMI, and tobacco use at FDR < 0.1. The majority of the DM-CpGs were hypermethylated in females compared to males (61.5% vs. 38.5%), as shown in the hierarchical clustering (Fig. 1A) and volcano plot (Fig. 1B). When compared to the mean β-values (reflecting global methylation) of 522 DM-CpGs, females had a significantly higher mean methylation level compared to males (0.48 vs. 0.46, P < 0.001 Fig. 1C right panel), while no difference was found for the entire set of CpGs analyzed (0.51 vs. 0.51, P = 0.98 Fig. 1C left panel). There was a statistically significantly different distribution of DM-CpGs across functional genomic locations (P = 0.013) and islands (P < 0.0001). Specifically, females had more hypermethylation of DM-CpGs in promoter regions, especially within 5ʹUTR, compared to hypermethylated CpGs in males (13.0% vs 6.0%) (Fig. 1D, Supplementary Table 3). In relation to CpG islands and their surrounding regions, females had more hypermethylation in Opensea (60.7% vs. 40.3%), while males had more hypermethylation in islands (30.3% vs. 19.6%) and shores (24.4% vs. 15.9%) (Fig. 1E, Supplementary Table 3).
Potential biological roles of DM-CpGs genes and sex-related different patterns of correlation with gene expression
Sex-related methylation genes are involved in cell-to-cell signaling (n = 38), cellular function and maintenance (n = 23), molecular transport (n = 25), and lipid metabolism (n = 8) (Fig. 2A, Supplementary Table 4). The top diseases and disorders include cancer (n = 134), organismal injury and abnormalities (n = 135), endocrine system disorders (n = 121), gastrointestinal diseases (n = 124), and reproductive system disease (n = 105) (Fig. 2B, supplementary 4). The gene networks related to DM-CpGs genes are shown in Fig. 2C, and the top gene network is cell morphology, cellular assembly/organization, cellular function, and maintenance, including ARRB2, NOS3, NR3C1, and P2RY2 that are known to play a role in respiratory system development and function.
Of the identified 522 DM-CpGs, there were 412 with corresponding methylation and gene expression at transcription levels data. Females had twice as many unique genes significantly correlated with corresponding DM-CpGs than males. In a separate correlation analysis within males or females, females had 12 significant unique genes to be correlated with corresponding DM-CpGs, including cg09241427 with SHANK2 (r = 0.61), cg24533097 with PCDHB11 (r = − 0.57), cg19935288 with HERC3 (r = − 0.56), cg20811988 with FRG1B (r = − 0.57), cg22363520 with FKBP5 (r = − 0.56), cg21710255 with CRISP2 (r = − 0.61), cg05468028 with RWDD2B (r = − 0.53), cg05114739 with HDAC4 (r = − 0.53), cg23512306 with FMNL2 (r = − 0.51), cg20440093 with MUC4 (r = − 0.50), cg11792815 with HPD (r = 0.49), cg05221720 with COL9A1 (r = 0.48) (Fig. 3, Table 1). In males, 6 unique genes were significantly correlated with corresponding DM− CpGs: cg25304146 with WBP11P1 (r = 0.54), cg14815891 with FRG1B (r = − 0.56), cg02411284 with CLMN (r = 0.53), cg02810012 with LINC00598 (r = − 0.52), cg12607525 with UBTF (r = 0.47), cg24127414 with PCDHB11 (r = − 0.47) (Fig. 3B, Table 1). In both females and males, methylation levels of FRG1B and PCDHB11 were significantly correlated with their corresponding gene expression (Fig. 3B).
Different correlation patterns between DM-CpGs and inflammatory markers in bronchoalveolar lavage between males and females
In females only, one DM-CpG (cg18379042) in SGMS1 was negatively correlated with IFN-γ (r = − 0.60), IL-12p70 (r = − 0.61), and IL-4 (r = − 0.61). One intergenic CpG (cg03258975) was positively correlated with IL-1ß (r = 0.62) (Fig. 4A, Table 2). Also, there were three DM-CpGs (cg18023724 in NAF1, cg12717584 in EPHB2, and cg09119495 in ADGRV1) negatively correlated with lymphocyte counts. In addition, there were two positively correlated DM-CpGs (cg15228509 within an intergenic region and cg26761618 in P2RY2) to macrophage and lymphocyte counts, respectively (Fig. 4B, Table 2). In a separate analysis of males, cg06574436 within an intergenic region was found to be positively correlated with IFN-γ (r = 0.57), while cg07258241 in TMED10 were found to be negatively correlated with macrophages (r = − 0.59) (Fig. 4B, Table 2).
Replication of DM-CpGs in TCGA-LUAD and TCGA-LUSC datasets
To replicate DM-CpGs identified in healthy individuals, we utilized TCGA-LUAD and TCGA-LUSC datasets for adjacent normal (n = 29 and n = 42) and tumor tissues (n = 433 and n = 358), respectively. Of the 522 DM-CpGs identified in the healthy individuals, 275 DM-CpGs were also found in the TCGA datasets. In normal adjacent tissue, 112 (with 95% in the expected direction) and 134 (with 96% in the expected direction) were found to be significantly differentially methylated between males and females LUAD and LUSC, respectively (Fig. 5A, Supplementary Table 5). In tumors, 207 DM-CpGs (with 95% in the expected direction) and 146 DM-CpGs (with 98% in the expected direction) were found to be validated in tissues from LUAD and LUSC, respectively (Fig. 5B on the right panel, Supplementary Table 5). There were 44 DM-CpGs that were uniquely identified in the lungs of healthy individuals, while there were 57 DM-CpGs to be validated in normal and tumor tissues from both LUAD and LUSC (Supplementary Fig. 1). Examples of validated DM-CpGs from LUAD and LUSC datasets are shown in Fig. 5C and D, respectively.
Discussion
There is evidence of sex disparities in lung cancer regarding risk and treatment outcomes1,2,3,4. Sex-related biological differences for epigenetics in the lungs may explain this in part, but little is known about DNA methylation differences in healthy lungs before the carcinogenic process occurs. This cross-sectional study sheds light on sex-related DNA methylation differences in healthy lungs, potentially contributing to the understanding of sex disparities observed in lung cancer risk and treatment outcomes. The findings suggest that females exhibit increased gene methylation compared to males, with enrichment in pathways related to cancer and reproductive functions. These pathways, including cell-to-cell signaling, cellular function, transport, lipid metabolism, and cell morphology and maintenance, are crucial for disease progression, possibly implicating them in the observed sex disparities in lung cancer. Furthermore, the study establishes correlations between some DM-CpGs and gene expression in the lungs, providing evidence for the biological impact of sex-related DNA methylation. These results were validated by replicating the findings in adjacent non-tumor lung tissue and tumors of both males and females from the TCGA dataset, further supporting the relevance of these epigenetic differences in lung health and disease.
To our knowledge, this study is the first to identify sex-related DNA methylation in the lungs of healthy young adults, which was also observed in TCGA data. Some of the sex-related methylation genes, including ARRB224, NOS341, NR3C142, and P2RY243, are known to be involved in respiratory system development and function. Many of these findings are consistent with existing literature. For example, 6 separate studies showed sex-related DM-CpGs matched with 80 (98% concordance), 28 (100% concordance), 55 (100% concordance), 65 (100% concordance), 70 (100% concordance), and 145 (100% concordance) in various tissues from healthy individuals, such as in brain tissues44, in myoblasts/myotubes31 in pancreatic islets45, in leukocytes20 in whole blood17 in cord blood35 (Supplementary Table 6). Thus, some DM-CpGs may be used as robust sex-related methylation markers across tissues, but still, many lung DM-CpGs seem to be tissue-specific37.
In this study, we observed more hypermethylation patterns, especially within promoter regions, in females compared to males, consistent with previous findings8,17,18,20,35,46,47. This may indicate that female-biased hypermethylation may result in sex hormones-related gene regulation, given that sex hormones (i.e., estrogen) play an essential role in lung carcinogenesis and prognosis48,49. In this study, we found that there was sex-related differential methylation that correlated with gene expression for SHANK250 and HDAC451 which are known to be regulated by sex hormones. SHANK2 is a scaffold gene that plays an oncogenic role in lung cancer52. HDAC4 is a histone deacetylase that interacts with transcription factors, altering gene expression53. HDAC4 promotes the progression of lung cancer by promoting epithelial–mesenchymal transition progress54. Also, sex-related methylation genes in this study included 105 reproductive system-related genes. Thus, our findings support further investigation of possible interactions between sex hormones and sex-related DNA methylation to address sex-based dimorphism in lung cancer.
Some of the DM-CpGs were correlated with lung immune cells and cytokines. A study of cancers showed a correlation between global DNA methylation and immune evasion in lung cancer, so that DNA methylation alterations may be pathologically related to immune evasion and may be a marker in precision immunotherapy55. Herein, we observed lung cytokines and immune cells to be correlated with some DM-CpG differently between males and females. For example, in females only, cg18379042 in SGMS1 was significantly correlated with type 1 (IL-12p70 and IFN-γ) and type 2 (IL-4) cytokines. SGMS1 is a key enzyme involved in the biosynthesis of sphingomyelins which plays a critical role in proliferation, apoptosis, membrane mobility, and airway smooth muscle functions56. Thus, DM-CpGs may explain sex-related disparities in lung cancer incidence and outcome by mediating different immune responses between males and females. As a follow-up analysis, we examined if there was an enrichment of cancer-related genes in our sex-related CpG genes by comparing our list of significant genes for over-representation of “lung cancer genes” from Ingenuity Pathway Analysis (IPA) (32.8% vs. 26.1%, Fisher’s Exact test P = 0.012) and “cancer genes” from the Catalogue of Somatic Mutations In Cancer (COSMIC) database (5.2% vs. 2.7%, Fisher’s Exact test P = 0.016), also indicating that sex-related methylation may play a role in cancer.
It is important to note that there are a few limitations to this study that should be considered in the interpretation of its findings. Small numbers precluded an analysis by tobacco group use (including no use), so DM-CpGs were identified after controlling for smoking status. Thus, we could not evaluate a possible important effect of lung toxicant exposure. Also, the sample size was too small to assess effects by BMI or age, and other possible intrinsic (i.e., mutations) and extrinsic factors, including environmental and occupational exposure. Moreover, the study only included young, healthy participants, which may limit the generalizability of the findings to broader populations. We utilized bronchial brushing, which is known to be mostly composed of epithelium cells, but we could not pathologically confirm the cellular composition of collected tissues. However, we confirmed that none of the estimated immune cell proportions, using Houseman et al.’s method (a gold standard for adjusting immune cell compositions in the blood), was associated with sex. Lastly, due to the cross-sectional design, causal relationships between differential methylation and other biomarkers could not be established. Despite these limitations, the study also had several strengths. It focused on the lungs as the target organ, providing insights into differential methylation patterns without morphological alterations or significant respiratory diseases. The comprehensive analysis of differential methylation and its biological implications, including inflammation and gene expression, adds depth to our understanding of epigenetic regulation in the lungs. Furthermore, the replication of some findings in independent datasets, including lung cancer datasets, enhances the robustness of the study’s conclusions.
In summary, the study contributes valuable insights into autosomal differential methylation in the lungs between sexes among young and healthy individuals. The correlations between some differential methylation sites and lung immune system biomarkers suggest potential implications for understanding sex-based dimorphism in lung cancer. However, further research addressing the study’s limitations and exploring causal relationships is warranted to fully elucidate the role of epigenetic differences in lung health and disease.
Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author upon reasonable request.
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Acknowledgements
We acknowledge the support of the Recruitment, Intervention and Survey Shared Resource (RISSR). We thank the study participants, the staff and nurses of the OSU Clinical Research Center.
Funding
Research reported in this publication was supported by funding from the National Cancer Institute of the National Institutes of Health (NIH) (P30 CA016058), the Food and Drug Administration Center for Tobacco Products (CTP) (P50CA180908), the National Center For Advancing Translational Sciences (UL1TR001070), Pelotonia Intramural Research Funds, the Prevent Cancer Foundation, research start-up from OSU Comprehensive Cancer Center and OSU College of Public Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or the FDA. None of the funders played a role other than funding.
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MAS and PGS made significant contributions to the conception or design of this study. DP and MAS analyzed data. DP, MAS, and PGS interpreted findings. DP wrote the first draft. DP and MAS were major contributors in the writing. PGS, JPE, DYW, SK, SAR, JLF, and MDW have contributed significantly to the evaluation of the data and findings, review, and manuscript revision. MDW performed bronchoscopies. JPM oversaw the statistical data analysis. DYW contributed to the sample processing, data collection and/or assembly. SK assisted in recruiting participants and managing clinical data. MAS, PGS and DP had full access to all data included in this study, and MAS and PGS had final responsibility for the decision to submit for publication. All authors read, revised, and approved the manuscript.
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Patel, D., McElroy, J.P., Weng, D.Y. et al. Sex-related DNA methylation is associated with inflammation and gene expression in the lungs of healthy individuals. Sci Rep 14, 14280 (2024). https://doi.org/10.1038/s41598-024-65027-y
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DOI: https://doi.org/10.1038/s41598-024-65027-y
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