Gastric cancer (GC) is one of the most lethal cancers with tremendous cancer-related mortality (Van Cutsem et al., 2016). For the last few decades, GC has generally been divided into histological subtypes according to the Lauren classification (Lauren, 1965). As medicine becomes more precise, there has been an urgent need for the use of molecular biology to more prominently guide the therapeutic strategies and target agents in GC. The Cancer Genome Atlas (TCGA) project had raised the molecular classification of four subtypes with distinct genetic signatures in GC (The Cancer Genome Atlas Research Network, 2014). Meanwhile, recent research has also proposed four GC subtypes on the basis of distinct molecular signatures (Cristescu et al., 2015).
The urokinase-type plasminogen activator (uPA) system plays a crucial role in tumorigenesis. By mediating proteolysis and the degradation of the extracellular matrix (ECM), the uPA system regulates tumor angiogenesis and locomotion via the activation of matrix metalloproteinases (MMPs) and latent growth factors (Santibanez et al., 2018). Plasminogen activator inhibitor-1 (PAI-1), encoded by the Serpin E1 (SERPINE1) gene, is a key regulator of the uPA system. PAI-1 is supposed to restrain the activation of uPA, whereas, paradoxical data implies that SERPINE1 may exert its role of promoting carcinogenesis in various cancers (Li et al., 2018). Emerging evidence indicates that SERPINE1 is upregulated in GC tissues compared with normal tissues. Elevated levels of SERPINE1 are significantly correlated with unfavorable clinical features and a poor prognosis in GC patients (Liao et al., 2018; Liu et al., 2018), suggesting a pro-tumor effect of SERPINE1 in gastric tumorigenesis.
The epithelial-to-mesenchymal transition (EMT), a shift from the epithelial to mesenchymal state with highly plastic and dynamic features, enables the cells to possess a greater ability for migration and invasion (Nieto et al., 2016). Previous reports demonstrated that the upregulation of SERPINE1 in TGFβ induced EMT in triple-negative breast cancer (Xu et al., 2018). The administration of exogenous recombinant PAI-1 promoted cell locomotion and increased the expression of EMT markers (Kang et al., 2016). However, it still remains unclear whether SERPINE1 is involved in EMT in gastric tumorigenesis.
In this study, we screened the differentially expressed genes (DEGs) associated with gastric tumorigenesis from the Gene Expression Omnibus (GEO) datasets. Through integrative analysis, we identified that SERPINE1 was correlated with EMT in GC and confirmed this with experimental validation. Further investigations revealed that key regulators of the EMT process cooperated with SERPINE1 in GC.
Materials and Methods
Extraction of oligonucleotide microarrays and RNA sequencing data of gastric cancer
Three transcriptional profiling datasets of GC were downloaded and extracted from the GEO database. The GSE54129 dataset was composed of 111 GC and 21 normal tissues and was performed on the Affymetrix Human Genome U133 Plus 2.0 Array platform. The GSE63089 dataset contained 45 paired GC and normal tissues and was performed on the Affymetrix Human Exon 1.0 Array platform (Zhang et al., 2015). The GSE65801 dataset contained 32 paired GC and noncancerous tissues and was performed on the Agilent Human GE 8x60K Microarray platform (Li et al., 2015). Gene symbols were mapped to the probes according to the annotation profile of each platform. Data of the expression matrix, genetic alterations, and the clinical features of patients in TCGA STAD were downloaded from the cBioPortal database (https://www.cbioportal.org). All above-mentioned profiling datasets were accessible online without any conflicts or limitations.
Screening and bioinformatic annotations of DEGs in gastric cancer
The web-accessible analysis tool GEO2R was utilized on its default settings to screen the DEGs of each dataset. The cut-off value for the filtration criteria was set at adjusted p < 0.05, logFC ≥ 1. The DEGs for subsequent GO and KEGG analysis were obtained by the overlap of filtered genes in each dataset via an online Venn diagram tool (http://bioinformatics.psb.ugent.be/webtools/Venn/). The DAVID database (https://david.ncifcrf.gov/tools.jsp) was used for GO and KEGG analysis (Huang, Sherman & Lempicki, 2009a, 2009b). Enriched GO and KEGG terms with p-value < 0.05 were considered as statistical significance. Histograms of enriched GO terms and bubble plots of KEGG pathway enrichment were implemented with the ggplot2 package (https://ggplot2.tidyverse.org/) in an R language environment.
Gene set enrichment analysis
Gene set enrichment analysis was carried out as previously described (Subramanian et al., 2005). Defined gene sets, including angiogenesis (HALLMARK_ANGIOGENESIS, M5944), EMT (HALL_EPITHELIAL_MESENCHYMAL_TRANSITION, M5930/JECHLINGER_EPITHELIAL_TO_MESENCHYMAL_TRANSITION_UP, M1406/GOTZMANN_EPITHELIAL_TO_MESENCHYMAL_TRANSITION_UP, M1373), uPA and uPAR induced pathways (PID_UPA_UPAR_PATHWAY, M174), and TGFβ signaling pathway (KEGG_TGF_BETA_SIGNALING_PATHWAY, M2642 / TGFB_UP.V1_UP, M2839), were obtained from the molecular signatures database (http://software.broadinstitute.org/gsea/msigdb) of Broad Institute. Analysis was performed with default settings and a false discovery rate (FDR) < 0.25 was considered as statistical significance.
Cell culture and reagents
The MGC803 and AGS GC cell lines were purchased from the Cell Center of Peking Union Medical College. PCR and cell culturing verified that the cell lines were free of mycoplasma contamination. Authentication of the cell lines was confirmed by STR profiling. All of the results can be viewed on the National Infrastructure of Cell Line Resource website (http://cellresource.cn). Cells were cultured in DMEM or RPMI-1640 medium (Gibco, Carlsbad, CA, USA) with 10% fetal bovine serum (Gibco, Carlsbad, CA, USA). Cells were cultured with 5% CO2 at 37 °C. Tiplaxtinin (PAI-039) was purchased from Selleck (Houston, TX, USA).
Total RNA extraction and qRT-PCR validation
Cells were digested and planted in six-well plates (1 × 106 cells per well). The culture medium was replaced with the administration of different concentrations of Tiplaxtinin after cell adherence. Cells were incubated for 12 h. Total RNA was extracted by the TRIzol (Invitrogen, Carlsbad, CA, USA) reagent and the cDNA was synthesized using the iScript™ Synthesis Kit (BioRad, Hercules, CA, USA) following the manual’s instructions. The PCR procedure was performed by PowerUp™ SYBR™ Green Master Mix Kit (Applied Biosystems™, Foster City, CA, USA). GAPDH was used as an endogenous control. The 2−ΔΔCt method was used to calculate the relative expression of each gene. Each sample per reaction was performed in triplicate. The sequence of primers is listed in Table 1. The primer of GAPDH was purchased from Sangon Biotech (Shanghai, China).
Construction of protein-protein interaction network involved in EMT
To further investigate the sub-clusters of DEGs involved in EMT, overlapped genes between DEGs of GC and a hallmark gene set of EMT were selected to construct the protein-protein interaction (PPI) network by utilizing the STRING database (https://string-db.org) (Szklarczyk et al., 2017). To enhance the dependability of the PPI network, the highest confidence (>0.900) was chosen as the required interaction score. The visualization of the interaction network was implemented via Cytoscape software v3.5.
Validation of prognostic values of EMT-related genes in GEO datasets
The web-based Kaplan–Meier (KM) plotter database is capable of assessing specific genes of survival using the data of 1,065 GC patients from the GEO database (Szasz et al., 2016). Overall survival (OS) and first progression (FP) were selected as the main indicators of prognostic assessment. Mean expression of all probes of the same gene was calculated as the expression of each gene. The log-rank p < 0.05 was considered as statistical significance.
Analysis of the receiver operator characteristic (ROC) curves was performed to explore the efficacy of SERPINE1 in discriminating different molecular subtypes (EMT and non-EMT subtype) and OS prognosis (good OS ≥2 years, living and poor OS <1 year, deceased) in GC. The KM curves were carried out to compare the survival distributions between patients with high and low mRNA levels of SERPINE1 in the TCGA STAD dataset. Univariate and multivariate Cox regressions were implemented to investigate the prognostic impact of SERPINE1 in GC patients of TCGA STAD dataset. Pearson correlation tests were used to assess the relationship between SERPINE1 and EMT-related genes in the TCGA STAD dataset via the GEPIA database (Tang et al., 2017). An independent sample t-test and one-way ANOVA was used to compare the statistical significance between two or more samples, respectively. Two-tailed p-values < 0.05 were considered as statistically significance. Statistical analysis was performed using the SPSS 19.0 (Chicago, IL, USA) and Graphpad Prism 5.0 software (Graphpad Software, Inc., San Diego, CA, USA).
Screening and bioinformatic analysis of DEGs in GEO datasets
To identify DEGs associated with gastric tumorigenesis, we applied the GEO2R tool to screen for DEGs between normal and tumor tissues. To enhance the dependability of our data, we overlapped DEGs from each GEO dataset to obtain commonly upregulated and downregulated DEGs. A total of 104 overlapped upregulated and 61 downregulated DEGs were identified among multiple datasets (Figs. 1A and 1B). To further investigate the functions of filtered DEGs, we employed GO and KEGG enrichment analysis to annotate dysregulated genes and signaling pathways. The results of the GO analysis showed that biological processes such as collagen catabolic process, ECM organization, and collagen fibril organization, and molecular functions like ECM structural constituent, heparin binding, and platelet-derived growth factor binding were found to be significantly enriched among DEGs (Figs. 1C and 1D). Analysis of the cellular components indicated that proteins encoded by DEGs were mainly located in the extracellular space and regions (Fig. 1E). KEGG enrichment analysis showed that ECM-receptor interaction, protein digestion and absorption, PI3K-AKT signaling pathway, gastric acid secretion, and focal adhesion were significantly enriched in DEGs (Fig. 1F), suggesting that alterations of the ECM might be responsible for the malignant progress of GC.
Overexpression of SERPINE1 in gastric cancer is identified by integrative approach
During tumorigenesis, the angiogenic regulators remain activated to support tumor growth (Ferrara, 2009). As a critical part of fibrinolytic system, the uPA system is well known in regulating tissue remodeling, angiogenesis, and cell mobility (Su et al., 2016). We checked if angiogenesis and uPA pathways were activated in GC. As we expected, GSEA analysis showed that gene sets of hallmark angiogenesis and the uPA pathway were significantly enriched in GC compared with normal tissues (Figs. 2A–2D). To further identify key regulators in the above-mentioned processes, we screened overlapped genes between filtered DEGs and genes involved with the positive regulation of angiogenesis and plasminogen activation. Interestingly, SERPINE1 remained to be the only overlapped gene among three gene lists (Fig. 2E). To exclude the impact of genetic variations on the mRNA level of SERPINE1, we checked the genetic alterations of SERPINE1 in the TCGA STAD dataset. Results indicated that only 5% of GC patients showed genetic alterations, including missense mutation, amplification, and deep deletion (Fig. 2F), which suggested the minimal influence of genetic variations on SERPINE1 expression. Levels of SERPINE1 were significantly increased in GC tissues compared with normal issues (Figs. 2G–2I). Altogether, we confirmed that SERPINE1, a key regulator of angiogenesis and the uPA system, was remarkably overexpressed in GC.
Elevated mRNA level of SERPINE1 predicts poor outcome of gastric cancer patients
To investigate the prognostic value of mRNA levels of SERPINE1 in GC patients, KM curves were plotted in GC patients with high or low expression groups. Results showed that patients with higher mRNA levels of SERPINE1 had a shorter OS and disease-free survival (DFS) in GC (Figs. 3A and 3B), suggesting that the higher expression of SERPINE1 was a risk factor for the prognosis of GC. Univariate and multivariate analysis revealed a higher level of SERPINE1 as an independent predictor for poor prognosis in GC patients (Table 2). To verify our survival analysis, pre-defined poor (<1 year, deceased) and good (>2 years, living) OS groups of GC patients in the TCGA STAD and GSE62254 datasets were selected for further study. Results indicated that the level of SERPINE1 were significantly higher in patients with a poor OS vs. those with a good OS. Similar results were also observed in patients with poor (<1 year, recurred or deceased) and good (>2 years, disease free and living) DFS (Figs. 3D–3F). Moreover, ROC analysis indicated that the mRNA level of SERPINE1 was able to discriminate a poor and good OS in GC patients (Figs. 3G and 3H). Taken together, a higher mRNA level of SERPINE1 was correlated with a poor prognosis in GC patients.
|Variable||Univariate analysis||Multivariate analysis3|
|Overall survival (n = 351)|
|Male (n = 220)||1.325||0.924–1.900||0.125|
|Female (n = 131)|
|>60 (n = 234)||1.731||1.182–2.533||0.005||2.076||1.407–3.062||0.000|
|≤60 (n = 117)|
|T3/T4 (n = 263)||1.715||1.109–2.652||0.015||1.198||0.720–1.994||0.486|
|T1/T2 (n = 88)|
|N1/2/3 (n = 241)||1.906||1.259–2.885||0.002||1.405||0.797–2.478||0.240|
|N0 (n = 110)|
|M1 (n = 24)||1.945||1.074–3.523||0.028||1.993||1.073–3.702||0.029|
|M0 (n = 327)|
|Stage III/IV (n = 193)||1.944||1.359–2.779||0.000||1.325||0.764–2.298||0.316|
|Stage I/II (n = 158)|
|G3 (n = 226)||1.434||1.002–2.052||0.049||1.452||1.006–2.094||0.046|
|G1/G2 (n = 125)|
|High (n = 176)||1.941||1.377–2.737||0.000||1.843||1.305–2.603||0.001|
|Low (n = 175)|
|Disease-free survival (n = 280)|
|Male (n = 178)||2.179||1.357–3.497||0.001||2.021||1.256–3.252||0.004|
|Female (n = 102)|
|>60 (n = 175)||0.999||0.670–1.490||0.996|
|≤60 (n = 105)|
|T3/T4 (n = 204)||1.408||0.882–2.247||0.151|
|T1/T2 (n = 76)|
|N1/2/3 (n = 182)||1.774||1.121–2.807||0.014||1.658||0.925–2.973||0.089|
|N0 (n = 98)|
|M1 (n = 16)||1.482||0.647–3.393||0.352|
|M0 (n = 264)|
|Stage III/IV (n = 142)||1.500||1.007–2.234||0.046||1.030||0.620–1.711||0.908|
|Stage I/II (n = 138)|
|G3 (n = 176)||1.198||0.795–1.805||0.388|
|G1/G2 (n = 104)|
|High (n = 140)||1.800||1.206–2.687||0.004||1.755||1.175–2.621||0.006|
|Low (n = 140)|
Overexpression of SERPINE1 is correlated with EMT in gastric cancer
Previous reports identified four molecular subtypes associated with distinct clinical outcomes in GC (Cristescu et al., 2015). To further investigate the possible mechanisms that SERPINE1 may involve in GC, we compared the mRNA level of SERPINE1 among four subtypes including MSS/TP53 activation, MSS/TP53 loss, microsatellite instability (MSI), and EMT. Interestingly, the mRNA level of SERPINE1 was much higher in the EMT subtype than in other subtypes, indicating a potential correlation between SERPINE1 and EMT in GC (Fig. 4A). ROC analysis showed that the mRNA level of SERPINE1 effectively discriminated between EMT and non-EMT subtypes in the GSE62254 dataset (Fig. 4B). Furthermore, GSEA analysis demonstrated that EMT-related gene sets were significantly enriched in patients with higher SERPINE1 expression in the GSE63089 and TCGA STAD datasets (Figs. 4C–4H). TGFβ exerts as a master inducer of EMT in various cancers. To determine whether SERPINE1 was involved in the TGFβ-induced signaling pathway, we employed TGFβ associated gene sets to perform GSEA analysis in the TCGA dataset. Results showed that a high SERPINE1 expression was significantly correlated with the activation of the TGFβ signaling pathway (Figs. 4I and 4J). Above all, the expression of SERPINE1 was significantly upregulated in the EMT subtype of GC patients and a higher expression of SERPINE1 was positively correlated with TGFβ-induced EMT in GC.
Correlation and validation of EMT markers with SERPINE1 in gastric cancer
To explore the regulatory mechanism between SERPINE1 and EMT in GC, correlations between the expression of SERPINE1 and the EMT markers were analyzed using the GEPIA database. As expected, the expression of SERPINE1 was positively correlated with EMT markers (TWIST1, TWIST2, CDH2, and FN1) in the TCGA STAD dataset (Figs. 5A–5D). To further verify our bioinformatic analysis, Tiplaxtinin, a specific inhibitor of SERPINE1, was selected for biological validation. The mRNA expression of the EMT markers significantly decreased following treatment with Tiplaxtinin in a concentration-dependent manner (Figs. 5E and 5F), indicating that the inhibition of SERPINE1 sufficiently suppressed the expression of EMT markers in GC.
Identification of EMT-related genes associated with SERPINE1 in gastric cancer
To explore the potential molecules and underlying mechanisms linked to SERPINE1, we obtained 38 EMT-related genes among DEGs from the intersection of two gene lists (Fig. 6A). A PPI network of these 38 EMT genes was constructed to reveal the potential interactions using the STRING database. Four gene clusters were identified among 38 EMT-related DEGs according to the highest confidence. Among these clusters, we noticed the genes including SERPINE1, SERPINE2, FN1, SPARC, TIMP1, and MMP2 were closely connected in a common cluster (Fig. 6B), suggesting a potential regulatory network among these molecules. To further validate our data, we performed a Pearson correlation analysis between SERPINE1 and these genes in the TCGA STAD dataset. As we expected, genes including FN1, SPARC, TIMP1, and MMP2 showed high correlation coefficients (R > 0.3) with SERPINE1 in GC (Figs. 6C–6F), suggesting potential regulations between SERPINE1 and these EMT-related genes.
Prognostic values of EMT-related genes correlated with SERPINE1 in gastric cancer patients
To access the prognostic values of genes tightly correlated with SERPINE1, we performed a KM curve for each gene (TIMP1, MMP2, FN1, and SPARC). Similar to those of SERPINE1, the results showed that a higher expression of TIMP1, MMP2, FN1, and SPARC was significantly correlated with shorter OS and FP in GC patients (Fig. 7).
In this study, we screened multiple GEO datasets and obtained 104 overlapped upregulated and 61 downregulated DEGs. GO annotations recognized the functional enrichment of DEGs in the collagen catabolic process, ECM organization, and cell adhesion. KEGG analysis showed enrichment of ECM-receptor interaction, protein digestion and absorption, PI3K-Akt signaling pathway and focal adhesion, which indicated that the alteration of ECM was a hallmark of GC. We identified that the angiogenesis related gene SERPINE1, a key regulator of the uPA system, was overexpressed in GC. Further investigations demonstrated that a higher mRNA level of SERPINE1 predicted poor clinical prognosis in GC patients in the TCGA STAD and GEO datasets. Moreover, we verified the strong correlation between the SERPINE1 and EMT process in GC by integrative analysis and dependable validation. The constructed PPI network revealed that EMT-related genes (FN1, MMP2, TIMP1, and SPARC) were closely linked with SERPINE1, which developed a potential regulatory network of SERPINE1 in GC. Pearson correlation analysis showed positive correlations between mRNA levels of SERPINE1 and EMT related genes. KM survival analysis indicated that the four-gene cluster of EMT associated with SERPINE1 was correlated with a poor outcome in GC, which provided a more comprehensive insight into SERPINE1 and might serve as the therapeutic target in reversing EMT of GC.
The uPA system is mainly composed of four molecules including urokinase (encoded by PLAU gene), urokinase receptor (encoded by PLAUR gene), PAI-1 (encoded by SERPINE1 gene) and PAI-2 (encoded by SERPINB2 gene). In cancers, the uPA system catalyzes plasminogen to plasmin and directly induces the degradation of the ECM components, which leads to the activation of metalloproteinases and the release of latent growth factors (Laufs, Schumacher & Allgayer, 2006). PAI-1, which belongs to the family of serine proteinase inhibitors, is the main suppressor of uPA (Kruithof, Baker & Bunn, 1995). Previous reports have revealed that PAI-1 is a key regulator of angiogenesis. The physiological concentration of PAI-1 was necessary for tumor invasion and vascularization, while an excessive or low level of PAI-1 both demonstrated the suppression of tumorigenesis (Bajou et al., 2004; Kwaan, Mazar & McMahon, 2013). HUVECs showed impaired angiogenic potential when cultured with a conditional media from SERPINE1KD cells (Gomes-Giacoia et al., 2013). A higher level of SERPINE1 was correlated with the angiogenic pattern in NSCLC patients (Offersen et al., 2007). An association between SERPINE1 and vessel remodeling was also observed in breast cancer (Fox et al., 2001). In this study, we confirmed the abnormal activation of angiogenesis and the uPA/uPAR pathway in GC by GSEA analysis. Through the overlap of genes involved in angiogenesis and plasminogen activation, we identified that SERPINE1 was the only key regulator of these processes in GC.
The overexpression of SERPINE1 was observed in many tumors, including GC. The higher expression of SERPINE1 was related with an unfavorable prognosis (Pavon et al., 2015). In our study, the overexpression of SERPINE1 was observed in GC tissue, and high mRNA levels of SERPINE1 was correlated with a poor clinical prognosis in GC patients. It was reported that the elevated expression of SERPINE1 was correlated with more aggressive lymph node metastasis based on a DNA microarray and TMA analysis in GC (Suh et al., 2015). A meta-analysis indicated that SERPINE1 expression was significantly associated with advanced T/N stage, and lymphatic and vascular invasion in gastroesophageal cancer (Brungs et al., 2017). Recently, studies based on a public database showed that SERPINE1 was upregulated in GC and correlated with poor outcomes in GC patients (Liao et al., 2018; Liu et al., 2018). Similarly, the authors identified overlapped DEGs and enriched functions among multiple datasets. Then, SERPINE1 was recognized as a potential marker of the prognosis for GC patients by integrative analysis of the constructed PPI network of filtered DEGs. However, whether SERPINE1 potentially participated with or was involved in any biological processes was not reported. At present, we found that the expression of SERPINE1 was much higher in the EMT subtype compared with the non-EMT subtypes, and confirmed the evidence between SERPINE1 and EMT in GC via GSEA analysis. Moreover, the overexpression of SERPINE1 promoted the EMT-mediated metastasis by the activation of STAT3 signaling in NSCLC cells (Lin et al., 2017). The enhanced proliferation and migration of breast cancer cells was induced by recombinant PAI-1 while the administration of Tiplaxtinin significantly reversed the malignant phenotype (Fang et al., 2018). Induced SERPINE1 by TGFβ stimulation increased expression of EMT markers, including N-cadherin, Snail and Twist (Xu et al., 2018). As a target gene of TGFβ signaling, SERPINE1 was correlated with TGFβ activity in multiple cancers (Frei et al., 2015; Sitaram et al., 2016). In our study, Tiplaxtinin significantly repressed the expression of EMT markers, which was consistent with previous reports. Furthermore, we verified the correlation between the SERPINE1 and TGFβ-induced signaling pathway by GSEA analysis. However, we did not validate the regulatory relationship and potential mechanism between SERPINE1 and TGFβ-induced EMT under experimental condition, which was one of the limitations in this study.
Cellular processes always require functional associations among various proteins and molecules. For filtered DEGs, specific constructed PPI networks are conducive for better insight into possible interactions and mechanisms. In this study, we identified a gene cluster (SERPINE1, FN1, TIMP1, SPARC, and MMP2) of EMT in GC. A higher expression of fibronectin was observed in multiple cancers and correlated with malignancy and poor outcomes (Gao et al., 2017; Yi et al., 2016). A previous study showed that SERPINE1 promoted fibronectin assembly in a uPA-independent manner (Vial & McKeown-Longo, 2008). Elevated TIMP1 was observed in GC and associated with a more aggressive phenotype (De Mingo et al., 2007; Omar et al., 2018; Seo et al., 2007). SPARC was reported to be involved in tumorigenesis and EMT of multiple cancers (Chang et al., 2017; Fenouille et al., 2012). The upregulation of SPARC was associated with tumor metastasis and poor prognosis in GC (Li et al., 2016; Sato et al., 2013; Wang et al., 2004; Zhao et al., 2010). The level of MMP2 was significantly higher in tumor tissues and correlated with unfavorable clinical features and prognosis in GC (Alakus et al., 2008; Zhang et al., 2011; Zheng et al., 2006). Consistent with a recent report (Yan et al., 2018), we confirmed that the expression of FN1, TIMP1, SPARC, and MMP2 was associated with a poor prognosis in GC. Furthermore, we uncovered the significant correlations and potential interactions between SERPINE1 and these four genes in GC. However, more investigations need to be carried out to validate the function and regulation between SERPINE1 and EMT-related genes in GC.
In this study, we identified that SERPINE1 was overexpressed and associated with EMT in GC using an integrative bioinformatics approach and dependable experimental validation. However, there were a few limitations in our study. First, the suppression of SERPINE1 by a specific inhibitor might differ depending on the manipulation methods like RNA interference, which might lead to different results affecting EMT-related genes in GC cells. Secondly, intricate modifications of biological processes and methodological variations of microarrays and RNA sequencing data might cause deviations and differences of our bioinformatics analysis, which requires more experimental validation in future.
In summary, we identified that SERPINE1, the key regulator of angiogenesis and the uPA system, was involved in gastric tumorigenesis. Consistent with previous reports, we discovered that SERPINE1 was overexpressed in GC tissues and correlated with a poor prognosis in GC. Further study revealed the overexpression of SERPINE1 in the EMT subtype of GC, and GSEA analysis confirmed that gene sets involved in EMT were significantly enriched in GC patients with higher levels of SERPINE1. Correlation analysis and experimental validation identified significant correlations between the SERPINE1 and EMT markers in GC. The PPI network showed that FN1, TIMP1, SPARC, and MMP2 were closely connected with SERPINE1. Further investigations on potential mechanisms of SERPINE1 participating in EMT of GC are required. In conclusion, our study identified the involvement of SERPINE1 in EMT and potent correlations between SERPINE1 and EMT-related genes, which proved to be potential biomarkers and therapeutic targets in GC.