Back to Journals » International Journal of Chronic Obstructive Pulmonary Disease » Volume 17
Identification of Hub Genes Associated with COPD Through Integrated Bioinformatics Analysis
Authors Chen L, Zhu D, Huang J, Zhang H, Zhou G, Zhong X
Received 13 December 2021
Accepted for publication 20 February 2022
Published 3 March 2022 Volume 2022:17 Pages 439—456
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Professor Min Zhang
Lin Chen,1,2 Donglan Zhu,1 Jinfu Huang,1 Hui Zhang,1 Guang Zhou,1 Xiaoning Zhong1
1Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, People’s Republic of China; 2Department of Respiratory and Critical Care Medicine, Liuzhou People’s Hospital, LiuZhou, Guangxi, People’s Republic of China
Correspondence: Xiaoning Zhong, Tel +86 13607881203, Fax +86 771-5356702, Email [email protected]
Purpose: Smoking is recognized as a risk factor for Chronic Obstructive Pulmonary Disease (COPD), yet only 20– 25% of smokers eventually develop COPD. Since its molecular pathogenesis remains unclear, there is an important need to further understand genetic differences between smokers with COPD and healthy smokers, screen out high-risk and susceptible groups among smokers, and find effective therapeutic targets.
Methods: Bioinformatics tools were used to screen biomarkers that were significantly associated with COPD smokers and healthy smokers. qRT-PCR and Western blotting analysis were used to detect hub gene expression in CSE-treated BEAS-2B cells and lung tissue of COPD mouse models.
Results: Our study identified 132 DEGs. The GO and KEGG analyses suggested that the ECM-receptor interaction, MAPK signaling pathway, Chemokine signaling pathway, PI3K-Akt signaling pathway, extracellular matrix organization and collagen fibril organization were associated with the occurrence and development of COPD. In addition, WGCNA analysis of GSE1650 showed that the brown module was most correlated with COPD. The intersection between the brown module and DEGs was used to identify 9 HUB genes (COL14A1, SULF1, MOXD1, CXCL12, CHRNA1, COMP, POU2AF1, MMP11, THBS2) that showed consistent expression and upregulation. Both the mRNA and protein expression levels of the Hub genes (except that of MMP11) were significantly upregulated in tobacco smoke exposed mouse emphysema models and CSE treated BEAS-2B cells.
Conclusion: Our results suggest that COL14A1, SULF1, MOXD1, CXCL12, CHRNA1, COMP, POU2AF1, and THBS2 may be potentially useful biomarkers for identifying smokers with a risk of developing COPD. The GO and KEGG functional enrichment analyses further confirmed the significant role played by ECM in the pathogenesis of COPD. The results of this study may provide further insights into the pathogenetic mechanisms involved in COPD.
Keywords: COPD, GEO, WGCNA, cigarette, bioinformatics
Chronic obstructive pulmonary disease (COPD) will become the third leading cause of death worldwide.1,2 The incidence of COPD worldwide is 13.1%3 and is 13.7% in the Chinese population over 40 years of age.4 Emphysema is one of the most common phenotypes.1 Over the past few decades, we have conducted much research has been conducted on COPD, but due to a low level of understanding of the pathogenesis of COPD, the lack of special treatment means, disease prevention and control is a problem worldwide. Smoking is a recognized cause of disease, but only 20–25% of smokers eventually develop COPD,5 while up to 25% of COPD patients have never smoked.1 This suggests that there are differences in individual susceptibility (eg genetic factors, genetic polymorphisms) for the pathogenesis of COPD.6 Therefore, it is crucial to further understand the genetic differences between smokers with COPD and healthy smokers, screen out high-risk and susceptible groups among smokers, and identify effective therapeutic targets.
In recent decades, high-throughput sequencing has been widely used in various fields of life science and clinical diseases, including COPD. Combined with bioinformatics analysis, it can help explore disease-related genes and mechanisms and predict molecular targets for precision therapy.7,8
In this study, we performed an integrated analysis on gene expression profiling data obtained from two microarray datasets (GSE1650 and GSE76925) containing lung tissues of smokers with severe COPD and smokers with normal lung function, with the aim of identifying potential molecular mechanisms and biomarkers for COPD. R software was used to identify DEGs and were subsequently analyzed using bioinformatic methods. The screened key genes were validated using a COPD mouse model and BEAS-2B cells.
Materials and Methods
Shared lung tissue chip data on COPD patients were obtained from the GEO database (https://www.ncbi.nlm.nih.gov/gds/?). Microarrays with accession no. GSE1650 and no. GSE76925 were used in this study. GSE1650 assessed gene expression (GPL96 [HG-U133A] Affymetrix Human Genome U133A Array) in 18 patients with severe emphysema and compared it to data on 12 matched phenotypically normal smokers.9 GSE76925 (GPL10558Illumina HumanHT-12 V4.0 expression beadchip) assessed gene expression data on 111 patients with severe emphysema and compared it to data on 40 phenotypically normal smokers.10
Data Pretreatment and Screening of Differentially Expressed Genes (DEGs)
First, the quality of the raw data in GSE1650 and GSE76925 and the grouping of samples were analyzed using PCA and a sample correlation graph. After quality control, the differential expression analysis on mRNA was performed using the Limma and AFFy package in R 4.0.5 software (https://www.r-project.org/). The DEGs between smokers with severe COPD and smokers with normal lung function were identified using a P-value of <0.05 and |fold change|≥1.5 as the cutoff for screening. The volcano map and heatmap of the DEGs were respectively generated using the ggplot2 and pheatmap packages in R software.
Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathway Enrichment Analyses of the DEGs
GO functional annotation includes biological processes (BPs), cellular components (CCs), and molecular functions (MFs), which can be used to clarify the potential biological functions of the target genes. Pathway enrichment analysis can be used to identify the main biochemical metabolic pathways and signal transduction pathways involved in target genes. GO and KEGG enrichment analysis of the DEGs were performed using the ClusterProfiler R package (http://bioconductor.org/packages/release/bioc/html/clusterProfiler.html). A P-value of ≤ 0.05 was used as the cutoff for screening.
Construction of Protein–Protein Interaction (PPI) Network
The STRING database (https://string-db.org/cgi/input.pl) was used to identify interactions between the DEGs. Subsequently, Hub DEGs in the PPI regulatory network were identified using the cytoHubba plugin in CYTOSCAPE (version 3.8.2; http://cytoscape.org/, all filters use default parameters). The role of the gene is greater in the PPI network the darker the color it is.11
Weighted Gene Co-Expression Analysis (WGCNA)
WGCNA can be used to identify highly correlated gene clusters and to determine the association between module and sample traits.12 First, the expression matrix was normalized using the Limma package, and then the clinical or grouping information was sorted. All genes with a P<0.05 in GSE1650 were used for subsequent WGCNA, and discrete samples were evaluated. The WGCNA R package (https://cran.r-project.org/web/packages/WGCNA/index.html) was used to identify coexpression modules. The soft threshold power (β= 6) was selected so that the resulting adjacency matrix approximated a scale-free topology criterion. The adjacency matrix was transformed into a topological overlap matrix (TOM)13 and modules were defined as branches of a hierarchical clustering tree using a dissimilarity measure, and color was assigned to each module.
Screening Hub Genes
Correlation coefficient and P-values were used to analyze the correlation between each module and COPD phenotype, and the gene module with the highest degree of correlation were selected and the intersection between these module genes and the DEGs were defined as key genes. The brown module contained 150 genes, intersected with 132 DEGs and identified 13 key genes. Then, genes with consistent expression and up-regulation in the two datasets were defined as HUB genes and selected for further verification.
C57BL/6 mice (6–8 week old, male, 20–25 g) were purchased from the Guangxi Medical University Laboratory Animal Center (Nanning, China) and were exposed to air or cigarette smoke (CS) (zhenlong unfiltered cigarettes) for 24 weeks (n=6 per group), as previously described.7,14 All animal studies were reviewed and approved by the Laboratory Animal Ethics Committee of Guangxi Medical University (NO.2017-KY-NSFC-111) and in line with the Laboratory animal—Guideline for ethical review of animal welfare (GB/T 35892-2018).
Evaluation of an Experimental Mouse Model of Emphysema
After cigarette smoke exposure, the mice were anesthetized and sacrificed. The right lungs were fixed in 4% neutral formalin, embedded in paraffin and cut into 5 µm transverse sections and stained with H&E solution to conduct histopathological studies. We quantified the severity of emphysema by determining the mean linear intercept (Lm).7,14 For each animal, three fields on the right lobe of the lung were randomly selected (excluding large airways and vessels) and were examined by two independent observers.
Cigarette Smoke Extract (CSE) Preparation
Cigarette smoke was slowly dissolved in DMEM medium to obtain a concentration of 20% CSE, which was filtered and sterilized using a 0.22 um filter and kept for use in subsequent experiments.15
BEAS-2B Cell Culture and Treatment
Cells of the normal human bronchial and lung epithelial cell line, BEAS-2B (China Center for Type Culture Collection, CCTCC), were cultured in DMEM medium (Gibco, Shanghai, China) containing 10% fetal bovine serum and 1% penicillin/streptomycin (Solarbio, Beijing, China) at 37°C in a 5% CO2 humidified atmosphere. The BEAS-2B cells were seeded into 10 cm petri dishes and were stimulated with 0.15% (final concentration) CSE for 24 h. The cells were collected and proteins were extracted to conduct the Western blotting analysis.
Cell Viability Assay
Cell viability was assessed using the cell counting kit 8 (CCK-8; Vazyme Biotech, Nanjing, China) according to the manufacturer’s instructions. The BEAS-2B cells (1×104/well) were incubated with different concentrations of CSE in 96-well plates for 24 h, and then 10 ul of CCK-8 solution was added to the culture medium. The cells were further incubated for 50 min at 37°C, and the optical density was measured at 450 nm and was considered the indirect index of relative cell viability.
RNA Extraction and Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR)
Total RNA was extracted from the left lung using TRIzol reagent (Sangon Biotech, Shanghai, China) and was reverse-transcribed into complementary DNA, following the manufacturer’s protocol. Then, the samples were evaluated on a RT-PCR system (Thermo Fisher Scientific) using the ChamQ SYBR qPCR Master Mix (Vazyme Biotech, Nanjing, China) kit, following the manufacturer’s instructions. The primers of these mRNAs were obtained from Sangon Biotech (Shanghai, China). The ΔΔCT method was used to evaluate the relative expression level of each target gene after normalization using GAPDH. The primer sequences used for each target gene are listed in Table 1.
Table 1 Primers Used for qPCR in This Study
Western Blotting Analysis
Total protein was extracted from BEAS-2B cells and lung tissue using RIPA lysis buffer containing PMSF (Solarbio, Shanghai, China) and protein concentration was determined using a BCA protein assay kit. Then, the proteins were isolated using 8–15% SDS-PAGE and transferred onto PVDF membranes, which were blocked at room temperature with 5% skim milk for 1 hour. The membranes were incubated overnight at 4°C with primary antibodies, including anti-COL14A1 (1:1000, Invitrogen), anti-SULF1, anti-MOXD1, anti-CXCL12, anti-CHRNA1, anti-MMP11, anti-THBS2, anti-POU2AF1 (1:1000, ABclonal), anti-COMP (1:1000, Proteintech), and GAPDH as the control (1:2500, SAB). The next day the membranes were washed with TBST, and then incubated for 1 h at room temperature with HRP labeled secondary antibodies (goat-anti-rabbit as appropriate, 1:2500, Proteintech), and visualized using the ECL detection system (Beyotime Institute of Biotechnology). Band intensity was analyzed using ImageJ software. Each assay was performed in triplicate.
The two-tailed Student’s t-test was employed to compare the expression at mRNA and protein levels between the two groups. All statistical analyses were performed using GraphPad Prism 8 (Graph-Pad Software, Inc., La Jolla, CA, USA). Differences in a P-value of <0.05 were considered statistically significant.
Identification of DEGs in COPD
After the PCA analysis of sample grouping and quality control were conducted, the DEGs between COPD and the control group in each dataset were analyzed using the Limma and AFFy packages, and were visualized using a heat map and a volcano map, as shown in Figure 1A–D. Then, the intersection between different genes in the two datasets is shown using a Venn diagram (Figure 1E). 132 different genes were shared between the two datasets.
Gene Function and Annotation Enrichment Analysis of DEGs
To understand the biological classification and function of the 132 DEGs, the ClusterProfiler R Package was used to conduct the GO and KEGG pathway enrichment analyses. GO functional notes in the BP suggested that the DEGs were enriched in “extracellular matrix organization”, “collagen fibril organization”, and “cellular response to organic substance” (Figure 2A). In the CC category, the DEGs were enriched in “collagen-containing extracellular matrix”, “platelet alpha granule,” and “secretory granule” (Figure 2B). In the MF category, the DEGs were involved in “kinase regulator activity”, “protein kinase regulator activity”, and“Acetylcholine binding” (Figure 2C). The KEGG pathway analysis indicated that the DEGs were associated with the following pathways: ECM-receptor interaction, MAPK signaling pathway, Chemokine signaling pathway, and the PI3K-Akt signaling pathway (Figure 2D). Enrichment analyses identify major biochemical metabolic pathways and signal transduction pathways involved in the DEGs and may reveal new pathways of pathogenesis.
Figure 2 GO and KEGG pathway enrichment analyses of the DEGs.
Notes: The first 15 GO functional notes of the DEGs, including BP (A), CC (B), and MF (C) and the first 15 KEGG enriched pathways (D) of the DEGs are shown in the Figure 2. The x-axis represents the enrichment score, and y-axis represents the annotation function or the name of the corresponding pathway, while the circle size represents the number of genes, and the color represents the significance level of the enriched pathway.
PPI Network Analysis of the DEGs
To further study interactions between the 132 DEGs, we constructed a PPI network using the STRING database using a combined score > 0.4 as the cutoff criterion. The PPI network for the integrated top 50 DEGs is shown in Figure 3. To more accurately locate potential target genes, we performed a WGCNA analysis on the dataset.
Weighted Gene Co-Expression Network Construction
In this study, the WGCNA R package was used to identify coexpression modules for all genes with P-value of <0.05 in the GSE1650 dataset. The clinical or grouping information was sorted and the discrete samples were evaluated, with the results presented in the Figure 4A. In this study, we used β=6 as the soft-threshold to ensure a scale-free network (Figure 4B).
Identification of Modules
After determining the optimal soft-threshold to be used to construct the co-expression network and dividing genes into different modules, we plotted the gene cluster tree. A total of 13 gene modules were obtained through clustering (Figure 4C). To screen for the gene module with the strongest degree of correlation with COPD and to understand the relationship between each module and gene expression, we analyzed the correlation between the module and phenotype using the correlation coefficient and the p-value (Figure 5A and B). We found that the brown module showed the highest degree of correlation with disease development, compared with other disease modules. The brown module was therefore identified as a clinically significant module and was selected for use in further analyses.
Selection of Key Genes
The brown module containing 150 genes was intersected with 132 DEGs to obtain 13 key genes (Figure 5C). We further selected 9 genes (COL14A1, SULF1, MOXD1, CXCL12, CHRNA1, COMP, POU2AF1, MMP11, THBS2) from among the 13 genes, which had an expression level that was consistent with our results and was upregulated in the two datasets, for further verification.
Effect of CSE Concentration on Cell Viability
Cell viability was assessed using the cell counting kit 8 according to the manufacturer’s instructions. The BEAS-2B cells (1×104/well) were incubated with different concentrations of CSE (final concentration 0.05%, 0.1%, 0.15%, 0.2%, 0.25%, 0.3%, 0.35%, 0.4%) in 96-well plates for 24 h. The results showed that 0.15% CSE final concentration had no significant effect on cell viability. The results were presented in the Figure 6.
Figure 6 CCK-8 detected the effect of CSE on BEAS-2B cytotoxicity, and 0.15%CSE had no significant effect on cell viability. *, p<0.05.
Expression of the 9 Key Genes in the Mouse Model of Emphysema and CSE-Induced BEAS-2B Cells
First, the success of the CS-induced emphysema mouse model was confirmed. Second, we discussed whether the 9 key genes were associated with the pathogenesis of emphysema. According to our previous studies,7,14 the Lm of mice exposed to tobacco smoke was significantly higher than that of control mice, indicating that an emphysema model was successfully established (Figure 7A–C).
Figure 7 HE micrographs of lung tissues of mice exposed to AIR (A) and CS (B) at a magnification of ×20. (C) The mean linear intercept (Lm) in the lung of mice exposed to AIR and CS.
Next, as shown in Figure 8, compared with the control mice, the mRNA expression level of the 9 hub genes were found to be higher in the lung tissue of CS-exposed mice. Second, the protein expression level of all these 9 key genes in the lung tissue of COPD mouse model (Figure 9) and BEAS-2B cells stimulated using 0.15% CSE (Figure 10) were measured. Figures 9 and 10 shows that after CSE treatment, the protein expression levels of 8 of these genes, except MMP11, were significantly increased.
Figure 8 The mRNA expression level of the 9 key genes in the lung tissues of CS-exposed and control mice (n=6). *, p<0.05; **, p<0.01; ***, p<0.001.
Figure 9 The protein expression level of the 9 key genes in lung tissues of mouse exposed to AIR and CSE. *, p<0.05; **, p<0.01; ****, p<0.0001.
Abbreviation: ns, No Significance.
Figure 10 The protein expression level of the 9 key genes in control and CSE treated BEAS-2B cells. *, p<0.05; **, p<0.01.
Abbreviation: ns, No Significance.
COPD is a major global health problem due to its high prevalence and ever increasing incidence.2 Chronic bronchiolitis and emphysema are the most notable phenotypes of COPD.15 Over the past few decades, we have conducted many research on COPD, but unfortunately, due to limited understanding of its pathogenesis and a lack of specific methods of treatment, these patients still show an unfavorable prognosis. Smoking is recognized as the most important risk factor for COPD, but only 20–25% of smokers eventually develop COPD.5 Therefore, there is a need to further explore the genetic differences and potential methods of pathogenesis between smokers with COPD and healthy smokers.
After the rapid developments over the past decade, high-throughput sequencing has penetrated into all fields of life science and has managed to not only effectively cause developments in research, but has also gradually been applied in clinical practice. High-throughput sequencing can identify many differentially expressed genes in a short duration. Combined with bioinformatics analysis, it can help to explore disease-related genes and mechanisms to predict molecular targets to develop precision therapies.7,8 WGCNA results are highly reliable as it can comprehensively evaluate the correlation between co-expression modules and clinical features.12,16 Therefore, bioinformatics methods in conjunction with WGCNA were used in our study to screen differential genes.
In this study, we analyzed gene expression profile data on the lung tissues of smokers with severe COPD and smokers with normal lung function to identify potential differential biomarkers. First, 132 differentially expressed genes were identified. Subsequently, the ClusterProfiler R package was used to conduct GO and KEGG analyses. The GO analysis showed that the DEGs were mostly enriched in extracellular matrix organization, collagen fibril organization, and cellular response to organic substance. The KEGG analysis showed that the DEGs were mostly enriched in ECM-receptor interaction, MAPK and PI3K-Akt signaling pathways, and the Chemokine signaling pathway. Next, we used WGCNA to identify the brown modules as the most associated with COPD emphysema phenotypes in the GSE1650 dataset and intersected it with the 132 DEGs. 9 key genes (COL14A1, SULF1, MOXD1, CXCL12, CHRNA1, COMP, POU2AF1, MMP11, THBS2) were found to be strongly associated with the occurrence of COPD. qRT-PCR and Western blotting analysis were used to validate the expression of these genes in a mouse emphysema model and in CSE-induced BEAS-2B cells, respectively. The results indicated that the mRNA expression levels of the 9 hub genes were higher in the lungs of CS-exposed mice compared with AIR-exposed mice (Figure 8). The protein expression levels of the other 8 genes, except MMP11, were also significantly elevated in lung tissue of COPD mouse model and BEAS-2B cells stimulated using 0.15% CSE (Figures 9 and 10). Among these 9 hub genes, except for POU2AF1 and CXCL12, the other 7 genes have not yet been studied in COPD.
COL14A1 encodes for the XIV collagen α chain and interacts with decorin to regulate cell growth and survival.17 At present, abnormal methylation of COL14A1 has been found in a variety of diseases, including esophageal squamous cell carcinoma,18 renal cell carcinoma,17 and coronary artery disease.19 MOXD1, a member of the monooxygenase family, is potentially involved in the biosynthesis of norepinephrine.20,21 MOXD1 is widely expressed in the brain, kidney, heart, and lung.21 However, since the substrate of MOXD1 has not been determined, its function is still unknown. MOXD1 is located in the endoplasmic reticulum of cells and cannot be secreted21 but may be involved in the regulation of sex-biased behaviors and physiology22 and is associated with schizophrenia.20 MOXD1 knockdown suppresses the proliferation and xenograft tumor growth in osteosarcoma cells via inducing apoptosis.23 MOXD1 has not yet been studied in COPD. CHRNA1, encode for the α1 subunit of the adult nicotinic acetylcholine receptor, whose mutation is known to cause Congenital myasthenic syndromes,24 as well as multiple pterygium and fetal akinesia syndrome.25 CHRNA1 was also identified to be associated with disuse atrophy of skeletal muscles26 and macrophage inflammation,27 but studies have not been conducted on CHRNA1 in the lung tissue of COPD yet. COMP can interact with multiple extracellular matrix proteins in cartilage and other tissues. COMP plays a role in fibrogenesis, chondrocyte proliferation, and collagen secretion.28 Abnormal COMP expression has been found in many diseases, including cardiomyopathy,29 fibrosis30,31 and many types of cancer.32,33 COMP has been shown to be a biomarker of IPF (idiopathic pulmonary fibrosis), osteoarthritis, rheumatoid arthritis, and a prognostic marker of joint injury.28,30,34 THBS2 is a member of the thrombospondins family and is released from several types of cells, including endothelial cells and immune cells. THBS2 can bind to extracellular matrix (ECM) proteins and cell surface receptors to exert diverse biological effects, such as proliferation, apoptosis, cell adhesion, and migration.35 Thus far, studies conducted on THBS2 have mainly focused on its effect on tumors. In some tumors, THBS2 acts as a negative regulator of tumor aggressiveness, and in others, it may promote tumor growth.36,37 However, COL14A1, MOXD1, CHRNA1, COMP, and THBS2 have not been studied in COPD. Our study found that the mRNA and protein expression levels of these genes were significantly elevated in both the COPD mouse model and CSE treated normal human bronchial epithelial cells, which may indicate its involvement in the pathogenesis of COPD. However, whether these genes can be used as biomarkers to distinguish COPD patients from healthy smokers and their specific roles needs to be studied further.
MMP11 (Matrix metalloproteinase 11) is an extracellular proteolytic enzyme that belongs to the matrix metalloproteinase family. These proteases are involved in extracellular matrix remodeling and recent studies on MMP11 have mainly focused on their effect on tumors. MMP11 has been found to be upregulated in a variety of tumors, accelerates tumor growth, and is associated with poor survival.38,39 However, MMP11 has not been studied in COPD. Our bioinformatics analysis found that MMP11 expression increased in smoking COPD lung tissue samples, but we found no evidence of elevated MMP11 expression in CSE-stimulated human bronchial epithelial cells. Therefore, the expression and role of MMP11 in COPD patient lung tissues needs to be studied further. Sulf1 can regulate the sulfate state of heparin sulfate proteoglycans (HSPGs), one of the main components of ECM. HSPGs play a variety of signal transduction functions by binding to cytokines, matrix proteins, chemokines.40 Therefore, SULF1 is released by a variety of cells and may alter the function of ECM, which plays a significant role in the pathogenesis of COPD, by altering the structure of HSPGs.41 SULF1 gene expression was found to be elevated in various cancers.42,43 These results are inconsistent with the results of previous studies, which considered SULF1 to be a tumor suppressor.44 This effect may be related to the alternative splicing of the Sulf1 gene. The full length SULF1 shows opposite effects with the shorter splicing variant.45 SULF2 levels in the serum of COPD patients has been found to be elevated, but there have not been any recent studies conducted on SULF1 in COPD.43 At present, SULF1 has been confirmed to be significantly elevated in a mouse emphysema model and in vitro in bronchial epithelial cells stimulated by tobacco smoke, but its specific mechanism of action on the pathogenesis of COPD needs to be further elucidated. POU2AF1, previously thought to be expressed specifically in lymphocytes, regulates the expression of immunoglobulin and other host defense genes.46,47 A previous study found that smoking can downregulate the expression of POU2AF1 and host defense-related genes in airway epithelial cells. The upregulation of POU2AF1 can attenuate the downregulation of smoking-related airway epithelial-host defense genes.48 However, our study found that POU2AF1 was upregulated in the cigarette smoke-stimulated mouse emphysema model and in vitro in CES-stimulated human bronchial epithelial cells. Therefore, the role of this gene in COPD needs to be studied further.
Cigarette smoke and other irritants may be able to activate innate cells in the lung to release chemokines and damage-associated molecular patterns (DAMPs). Chemokines can interact with endogenous DAMPs. For example, high mobility group box 1 can form a complex with CXCL12 (a chemokine) to enhance CXCL12 activity49 and protect CXCL12 from degradation.50 Therefore, chemokines play a key role in the pathogenesis of COPD patients. Studies have found that CXCL12 is significantly upregulated in the serum of COPD patients compared with that of healthy controls, and is positively correlated with small airway disease and emphysema detected using high-resolution chest CT scans.51 When the Cxcl12/Cxcr4 signaling axis was blocked, the number of neutrophils decreased, and reverse migration increased inflammation levels.52 The CXCL12 antagonist, AMD3100, can ameliorates emphysema-like manifestations in mice induced using cigarette smoke.53 Consistent with the results of previous reports, our study also found that CXCL12 was significantly elevated in the lungs of mouse COPD models, but the specific role of CXCL12 in COPD requires further investigation.
Among the 9 HUB genes identified in our study, MMP11, CXCL12, COMP, SULF1, COL14A1, and THBS2 have all been reported to be associated with ECM, which has been confirmed to play a significant role in the pathogenesis of COPD. KEGG enrichment analysis also showed that the DEGs were mainly enriched in ECM-receptor interactions. This result confirms the reliability of our research study.
However, our study has some limitations. First, due to the lack of prognostic information included with the data, the relationship between these HUB genes and prognosis could not be analyzed. Second, our findings mainly focused on gene expression, and in-depth functional research and mechanism analysis was not conducted. Third, the expression of these genes has not been further verified in human tissues. In future studies, the collection of clinical data (including general conditions, lung function, and prognosis) should be improved as much as possible and verified in human lung tissue or peripheral blood samples as much as possible, while specific functional genes should be further identified and confirmed through mechanism studies.
In conclusion, this study provides a basis for exploring the genetic differences between smokers with severe COPD and smokers with normal lung function. Further, functional enrichment analysis using GO and KEGG analyses further confirmed the significant role of ECM in the pathogenesis of COPD. Therefore, this study provides new insights for identifying biomarkers and therapeutic targets for smokers with severe COPD.
Our results revealed that COL14A1, SULF1, MOXD1, CXCL12, CHRNA1, COMP, POU2AF1, and THBS2 are highly expressed in COPD, and that these genes can be potentially used as biomarkers and even therapeutic targets for COPD. Additionally, the functional enrichment analyses conducted further confirmed the significant role played by ECM in the pathogenesis of COPD. Therefore, this research study may provide insights into the pathogenetic mechanisms involved in COPD.
Lin Chen designed the study, completed the experiment and data analysis, and wrote the manuscript. Xiaoning Zhong proposed the conception and designed the experiment, and reviewed the paper and made the final revision. Donglan Zhu and Jinfu Huang helped complete the experiment and constructed the animal model of COPD. Hui Zhang and Guang Zhou assisted in analyzing the data and gave valuable suggestions for the paper writing. Everyone reviews and agrees to be responsible for the content of the article.
The authors report no conflicts of interest in this work.
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