GC miRNA and mRNA expression data were acquired from The Cancer Genome Atlas (TCGA) database (https://portal.gdc.cancer.gov/). The “edgeR” package was used to obtain the differentially expressed miRNAs and mRNAs and a boxplot was constructed and confirmed as the research object. Two databases (TargetScan and miRDB) were employed to predict the downstream target mRNAs of miR-145-5p. A Venn diagram was created to find the potential target mRNA.

The human GC cell lines (BGC-823, MGC-803, HGC-27, and SGC-7901) and the immortalized normal gastric mucosal cell line (GES-1) were purchased from the Cell Bank of the Chinese Academy of Sciences (CAS, China). All cell lines were cultured in RPMI-1640 medium (MACGENE, China) supplemented with 10% fetal bovine serum (EXcell Bio, China), 100 μg/mL streptomycin, and 100 U/mL Penicillin and incubated at 37 °C and 5% CO₂. When the cells reached a confluency of 80%-90%, they were passaged and reseeded at an appropriate density.

For functional assays, miR-145-5p mimic (mimic), miR-145-5p inhibitor (inhibitor), NC for miR-145-5p mimic (mimic-NC), and NC for miR-145-5p inhibitor (inhibitor-NC) were synthesized and purified by Ribobio (China). Transfections were performed using Lipofectamine2000 (Invitrogen, United States) following the provided guidelines: When the cells reached the logarithmic growth phase, trypLE was used to digest the cells. The cells were then centrifuged, resuspended, and counted on a 6-well plate (with a fusion degree of about 80% during cell transfection. The mixed siRNA (100 nM) and an appropriate amount of Lipofectamine2000 dissolved in serum free Opti MEM I was added to the plate. After transfection, the culture medium was replaced after culturing the cells in a CO₂ incubator at 37 °C for 4-6 h. The cells were incubated for 48 h before proceeding with additional experiments.

To verify the role of SERPINE1 in GC, the SGC-7901 and HGC-27 cells were transfected with lentivirus (sourced from Genomedicech), China. The cells were classified into two groups: Overexpressed SERPINE1 (OE) and control (OE-NC). Both the HGC27 and SGC7901 cells were cultivated overnight in 6-well plates. After reaching 40%-50% confluency, lentiviral infection was introduced. Stable transfectants were subsequently selected using 2 ug/mL puromycin screening. The expression of SERPINE1 in stably transfected cell lines was assessed using western blotting and q-PCR.

For the rescue experiment, HGC27 and SGC7901 cells were stably transfected with miR-145-5p-mimic (mimic) and miR-145-5p-mimic-NC (mimic-NC) and divided into four groups: Mimic-NC + OE-NC, mimic + OE-NC, mimic-NC + OE, and mimic + OE.

TRNzol reagent (Tiangen Biotech, China) was used for total RNA extraction and then reverse-transcribed into cDNA using a miRNA 1^st Strand cDNA Synthesis Kit (Vazyme Biotech Co., Ltd, China). The real-time quantitative PCR (qRT-PCR) process was carried out using SYBR Green (Tiangen Biotech Co, Ltd, China) according to a specific thermal cycling protocol. U6 and actin served as endogenous controls, and the target miRNA and mRNA relative expression levels were calculated using the 2^-ΔΔCt method. The primers used in this study were synthesized by Beijing Dingguo Changsheng Biotech. Co., Ltd (Table 1).

Total protein was isolated from the cells using 1 × sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) Sample Loading Buffer (Beyotime Biotechnology, China). A BCA Protein Assay Kit (Beyotime Biotechnology, China) was used to determine the concentration of the protein samples, and the samples were quantified at different concentrations. The proteins were then boiled at 100°C for 10 min with 100 μL of loading buffer (Beyotime Biotechnology, China) and separated by SDS-PAGE at 120 V. After electrophoresis, the proteins were transferred onto PVDF membranes and blocked using 5% BSA/TBST for 60 min. the primary rabbit polyclonal antibodies, SERPINE1 (Proteintech, United States), α-smooth muscle actin (α-SMA) (Proteintech, United States), β-catenin (Proteintech, United States), vimentin (HuaBio, China), ERK1/2 (HuaBio, China), phosphorylation extracellular signal-regulated kinase1/2 (p-ERK1/2) (HuaBio, China) and actin (ZSGB-BIO, China), and the mouse monoclonal antibody E-cad (HuaBio, China), were added to the membranes and incubated overnight at 4 °C. Secondary goat anti-rabbit IgG or goat anti-mouse IgG (ZSGB-BIO, China) antibodies were then added and the membrane was incubated at room temperature for 1 h and then washed three times with TBST buffer for 10 min. The Immobilon Western Chemilum HRP Substrate (WBKLS0500, Millipore, United States) was used to visualize the protein bands, and Image Pro Plus 6.0 (Media Cybernetics, United States) software was employed to analyze the relative protein levels.

Tumor tissue from human or nude mice was fixed with 4% formaldehyde, dehydrated, embedded in paraffin, and cut into 4 μm thick tissue sections. After heating at 60 °C for 1 h, the slices were dewaxed and rehydrated with a concentration gradient of alcohol (100, 95, 90, 80, and 70%). The tissue sections were boiled in 10 mmol/L sodium citrate buffer (pH 6.0) at a high temperature to recover the antigens, and incubated for 20 min with 3% hydrogen peroxide to block endogenous peroxidase activity. BSA (5%) was added to the sections and sealed for 30 min. The slices were incubated overnight with primary anti-SERPINE1 (Proteintech, United States, 1:500) and anti-Ki67 (Proteintech, United States, 1:10000) antibodies at 4 °C. The tissue was then incubated with a secondary antibody and observed under a microscope. After the slices were slightly dried, the freshly prepared DAB chromogenic solution (TIANGEN, PA140212) was dripped onto the circle. The coloration time was controlled under the microscope, with brown color representing positive staining. The slices were then washed with tap water to stop the coloration. Harris hematoxylin (BOSTER, AR1108) was used to restain the samples for 5 min (the time was controlled by the degree of staining). The samples were then washed in tap water, differentiated with 1% hydrochloric acid alcohol for a few seconds, and rinsed in tap water. When the ammonia water was blue, the samples were rinsed in running water, dehydrated, and sealed. The images were observed and captured using a fluorescence microscope.

A Dual-Luciferase Reporter Gene Assay was conducted to predict the binding site of miR-145-5p and SERPINE1 3'-UTR. Wild-type and mutant SERPINE1 3'-UTR fragments were synthesized and cloned into the pmirGLO plasmid. The amplified sequences of the wild type 3'UTR of SERPINE1 (WT-3'UTR) were cloned into the pmirGLO vectors (Promega Corp., WI, United States) for the construction of luciferase Wt-SERPINE1 vectors and mutant vectors (luciferase Mut-SERPINE1) were synthesized by Sangon Biotech (China). MiR-145-5p mimic and NC were co-transfected into 293T cells with Wt-SERPINE1 or Mut-SERPINE1 (SCSP-502, National Collection of Authenticated Cell Cultures, China), respectively. After 48 h, Firefly and Renilla luciferase activities were measured using the Varioskan LUX Multi-function enzyme labeling instrument (Thermo Scientific, United States).

GC cell proliferation was measured using a cell counting kit-8 (CCK-8), Meilunbio, China. GC cells at a density of 5 × 10³ cells/well were suspended in 100 μL and incubated in 96-well plates at 5% CO₂ and 37 °C for 48 h. CCK-8 reagent (10 μL) was introduced into each well for a 4-h incubation. Absorbance values were recorded at 450 nm.

Cells were dispensed into 6-well plates at a density of 1000 cells/well to assess colony formation. After 10 d, the colonies were preserved using methanol and stained with 0.1% crystal violet alcohol solvent (G1014-50ML, Servicebio, China) for 15 min. Images of the stained colonies were obtained and their numbers were determined.

Flow cytometry was performed according to the Annexin V-FITC/PI apoptosis kit (Multi Sciences, China) instructions. To test the samples, 5 × 10⁵ cells, including those in the culture supernatant, were collected by centrifuging with pre-cooled phosphate-buffered saline (PBS) at 4 °C and 1500 rpm for 5 min. Annexin V-FITC (5 μL) and 10 μL PI were added to each tube, mixed gently, and incubated in the dark at room temperature for 5 min. A CytoFLEX (BECKMAN, United States) was used to analyze the proportion of apoptotic cells in each sample. Annexin V-FITC was detected using the FITC detection channel (Ex = 488 nm; Em = 530 nm), and PI was detected using the PI detection channel (Ex = 535 nm; Em = 615 nm).

A 24-well Transwell BD Matrigel system (FN, Corning, Costar, China) with an 8 μm pore size was used to measure cellular invasion. Approximately 7.5 × 10⁴ cells were added to the upper chamber pre-coated with a Matrigel matrix (Yes Service Biotech, China), while the lower chamber was filled with RPMI-1640 medium containing 10% FBS to act as an attractant. After 24 h of incubation at 37 °C, non-invading cells on the Matrigel membrane surface were removed. The invading cells were fixed and stained using 4% methanol and 0.1% crystal violet, and two random fields were used to conduct the cell counts under a microscope.

A wound-healing assay was performed to evaluate cellular migration. First, horizontal lines were drawn on the back of a 6-well plate using a marker pen and ruler, with each well crossed by at least five evenly spaced lines. Cells were resuscitated in RPMI-1640 medium containing 10% FBS, seeded on six-well plates at a density of 3 × 10⁵ cells/well density, and incubated overnight. After cell reached 100% confluence, scratched cells with a 200 μL pipette tip and changed previous medium to serum-free medium. Following a 48-h culture, the cells were washed with PBS, and images of the scratch area in each well were taken at various time points. ImageJ software was used to measure the width of the scratch area and cell mobility was calculated to compare differences in tumor cell migration.

Fifteen male nude BALB/c mice, aged 4-6 wk and weighing 18-22 g, were purchased from the Experimental Animal Center of Shandong University. After 1 wk of adaptive feeding, 15 nude mice were randomly divided into three groups: the SERPINE1-NC group (NC) (n = 5), the SERPINE1-overexpression group (OE) (n = 5), and the SERPINE1-OE + PD98059 group (OE + PD98059) (n = 5). The logarithmic growth phase cells in each group were resuspended at 5 × 10⁷/mL, mixed with matrix glue at 1:1, and 0.20 mL of the cell solution was subcutaneously injected into nude mice (0.5 × 10⁷ cells/mouse) to establish a tumor implantation model, with the axillary site used as the injection site. After 18 d, the mice were sacrificed for analysis. The tumor was completely extracted, its mass and volume were calculated, and its length and width were determined to assess growth. Tumor volume was calculated using the formula ½ × length × width². The average volume of the tumors in each group was used to create a growth curve.

All human and animal experiments were approved by the Clinical Research Ethics Committee of Liaocheng People's Hospital (Liaocheng, China) and following the ethical standards of the institutional and national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Written informed consent was obtained from all individual participants included in this study.

IBM SPSS Statistics 26 and GraphPad Prism 5 were used for all statistical analyses. Comparisons between two different groups across three independent experiments were performed using the student’s t-test. A one-way analysis of variance (ANOVA) was used for multiple group comparisons. The data are presented as the means ± SD. P < 0.05 was considered statistically significant.

This study used the “edgeR” package to identify DEmiRNAs in TCGA-CESC data. The findings revealed that miR-145-5p was significantly downregulated in tumor tissues (Figure 1A). RT-PCR was then used to evaluate miR-145-5p expression in 30 paired samples of fresh GC tissues and their corresponding non-tumor tissues (P < 0.001). MiR-145-5p was expressed at much lower levels in GC tissues than their non-tumor counterparts (Figure 1B). Moreover, when compared with the immortalized normal gastric mucosal cell line, miR-145-5p expression was markedly lower in MGC803 (P < 0.05), HGC27 (P < 0.001), BGC823 (P < 0.01), and SGC7901 (P < 0.001) cell lines (Figure 1C). Since miR-145-5p expression was lowest in SGC7901 cells and highest in HGC27 cells, these cell lines were selected for the gain-of-function and loss-of-function assays, respectively.

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Figure 1 MicroRNA-145-5p is poorly expressed in gastric cancer tissues and cells. A: Box diagram showing the differential expression of microRNA-145-5p (miR-145-5p) in normal and tumor data from The Cancer Genome Atlas-STAD; B: Differentially expressed miR-145-5p in the normal and tumor groups; C: MiR-145-5p expression in four gastric cancer (GC) cell lines, MGC803, HGC27, BGC823, SGC7901, and the normal GC line, GES-1. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001.

MiR-145-5p downregulation in GC cells suggested that it may play an inhibitory role in this disease. Thus, its mimics and inhibitors were introduced into GC cells (Figure 2A). As expected, miR-145-5p expression was higher in the mimic group (P < 0.01) and lower in the inhibitor group (P < 0.01) (Figure 2A). CCK-8 and colony formation experiments were used to determine if miR-145-5p could regulate GC proliferation. Cell viability was higher in the miR-145-5p inhibition group than in the inhibitor-NC group (P < 0.001) (Figure 2B), and the number of clones formed was also higher (P < 0.001) (Figure 2C). The miR145-5p-mimic group had less cell proliferation than the mimic group (P < 0.001) (Figure 2B), and a fewer number of clones formed (P < 0.01) (Figure 2C).

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Figure 2 MicroRNA-145-5p inhibits gastric cancer cell proliferation and promotes apoptosis. A: MicroRNA-145-5p expression in transfected gastric cancer cells; B: HGC27 and SGC7901 cell proliferation was evaluated using a cell counting kit-8; C: Colony formation assay; D: HGC27 and SGC7901 cell apoptosis. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001.

Flow cytometry was used to measure HGC27 and SGC7901 cell apoptosis after transfection. The number of apoptotic cells was higher in the miR-145-5p mimic group than in the mimic-NC group (P < 0.05). Furthermore, the number of apoptotic cells was lower in the miR-145-5p inhibitor group than in the inhibitor-NC group (P < 0.01) (Figure 2D).

The wound healing assay results indicated that the up-regulation of miR-145-5p suppressed SGC7901 cell migration (P < 0.01). Conversely, the down-regulation of miR-145-5p expression significantly enhanced HGC27 cell migration (P < 0.001) (Figure 3A). The transwell assays showed similar results, with a significantly lower number of invasive cells in the miR-145-5p mimic group than in the mimic-NC group (P < 0.05). Moreover, the number of invasive cells in the miR-145-5p inhibitor group was higher than in the inhibitor-NC group (P < 0.01) (Figure 3B).

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Figure 3 MicroRNA-145-5p inhibits gastric cancer cell migration, invasion, and epithelial-mesenchymal transition. A: HGC27 and SGC7901 cell migration; scale bar = 100 μm; B: HGC27 and SGC7901 cell invasion; scale bar = 100 μm; C: Epithelial-mesenchymal transition-related marker protein (E-cadherin, β-catenin, vimentin, and α-smooth muscle actin) expression in HGC27 and SGC7901 cells. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001.

To explore whether miR-145-5p could reverse the epithelial-mesenchymal transition (EMT) phenotype, the expression of EMT-related marker proteins (E-cadherin, β-catenin, Vimentin, and α-SMA) was assessed in HGC27 and SGC7901 cells. The upregulation of miR-145-5p significantly increased the expression of E-cadherin and decreased the expression of β-catenin, Vimentin, and α-SMA. Meanwhile, reducing the expression of miR-145-5p had the opposite effect (Figure 3C).

These findings suggest that miR-145-5p acts as a tumor suppressor and can reverse the EMT phenotype, which in turn inhibits GC cell proliferation, invasion, and metastasis.

The bioinformatics tool, TargetScan, was used to predict the binding sites of miR-145-5p and SERPINE1 3'- UTR and better understand the molecular mechanism of miR-145-5p action (Figure 4A). Furthermore, to determine whether miR-145-5p directly regulates SERPINE1, SERPINE1 3'-UTR fragments (both wild-type, WT-LZTS1 3'-UTR, and mutated, Mut-LZTS1 3'-UTR) were cloned into a dual luciferase reporter vector (pmirGLO plasmid) and a luciferase reporter assay was conducted (Figure 4B). Co-transfection of 293T cells with miR-145-5p mimic and a vector carrying WT-SERPINE1 3'-UTR led to a significant reduction in luciferase activity (P < 0.001) (Figure 4C). These results suggest that miR-145-5p negatively regulates SERPINE1 expression by directly targeting its 3'-UTR, confirming the predictive findings of TargetScan.

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Figure 4 Serpin family E member 1 is a target of microRNA-145-5p. A: miRNA-145-5p and serpin family E member 1 (SERPINE1) 3'- UTR binding sites were predicted using TargetScan; B: WT-SERPINE1 and MUT-SERPINE1 sequences; C: Relative luciferase activity of 293T cells transfected with either WT-SERPINE1 or MUT-SERPINE1. ^cP < 0.001.

TargetScan and miRDB bioinformatics tools were used to predict the miR-145-5p target gene and better characterize how this miRNA regulates the biological behavior of GC. A Venn diagram was created to visualize the results (Figure 5A). SERPINE1 was identified as a potential target gene of miR-145-5p. This gene is associated with malignant biological behaviors including tumor cell proliferation, invasion, metastasis, and apoptosis, as well as poor clinical prognosis[26-28]. Assessment of TCGA data confirmed that SERPINE1 expression was significantly higher in tumor tissues than in normal tissues (Figure 5B).

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Figure 5 Serpin family E member 1 is a potential target gene of microRNA-145-5p and is highly expressed in gastric cancer tissues and cells. A: A Venn diagram of overlapping mRNAs from the differentially expressed mRNAs in The Cancer Genome Atlas (TCGA)-STAD data and miRNA-145-5p (miR-145-5p) target genes predicted from the two bioinformatics databases; B: Box diagram showing the differential expression of serpin family E member 1 (SERPINE1) in the normal and tumor data in TCGA-STAD; C: Overall survival curves of patients in the high (red) and low (blue) SERPINE1 expression groups; D: Differential expression of SERPINE1 mRNA (left panel) and protein (middle panel) in gastric cancer (GC) tissue and SERPINE1 mRNA (right panel) in the HGC27 and SGC7901 GC cell lines; scale bar = 20 μm; E: SERPINE1 mRNA and protein expression in the miR-145-5p mimic group in SGC7901 cells and the inhibitor group in HGC27 cells. ^bP < 0.01; ^cP < 0.001; ^dP < 0.0001.

Kaplan-Meier plot analysis revealed that patients with high SERPINE1 expression had a shorter survival rate than those with the low SERPINE1 expression (Figure 5C). Both SERPINE1 mRNA and protein expression were also significantly higher in GC tissue (P < 0.0001) as well as the HGC27 (P < 0.01) and SGC7901 (P < 0.01) cell lines (Figure 5D). Furthermore, SERPINE1 expression was significantly lower in cells in the mimic group (P < 0.01) and increased in cells in the inhibitor group (P < 0.01) (Figure 5E). These findings suggest that there is a negative correlation between miR-145-5p and SERPINE1 in GC.

The SGC7901 cell line was used to stably OE and OE-NC-SERPINE1 (OE-NC) for subsequent experiments. The transfection efficiency of SERPINE1 was assessed using qRT-PCR (P < 0.01) and Western blotting (Figure 6A). The CCK-8 (P < 0.001) (Figure 6B) and colony formation assay (P < 0.01) data (Figure 6C) corroborated that the overexpression of SERPINE1 enhances SGC7901 cell proliferation. Meanwhile, transwell invasion (P < 0.01) (Figure 6D) and wound healing assays (P < 0.05) (Figure 6E) performed on the stably transfected cells indicated that SERPINE1 overexpression stimulates GC cell invasion and metastasis. Flow cytometric analysis revealed that SERPINE1 overexpression inhibits SGC7901 cell apoptosis (P < 0.001) (Figure 6F). These findings suggest that SERPINE1 functions as an oncogene in GC cells.

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Figure 6 Effects of serpin family E member 1 overexpression on gastric cancer cell proliferation, invasion, migration, and apoptosis. A: Serpin family E member 1 (SERPINE1) mRNA and protein expression in lentivirus transfected SGC7901 cells; B: SERPINE1 overexpression promotes SGC7901 cell proliferation; C: SERPINE1 overexpression promotes SGC7901 cell colony formation; D: SERPINE1 promotes SGC7901 cell invasion; scale bar = 100 μm; E: SERPINE1 promotes SGC7901 cell migration; scale bar = 100 μm; F: SERPINE1 overexpression reduces SGC7901 cell apoposis. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001.

Rescue experiments were conducted to further elucidate the effects of SERPINE1 on miR-145-5p-mediated cell proliferation, apoptosis, invasion, metastasis, and EMT. SGC7901 cells were cotransfected with OE-SERPINE1/OE-NC and miR-145-5p mimic/miR-145-5p mimic NC. Western blotting revealed that the miR-145-5p mimic and OE-SERPINE1+ miR-145-5p mimic groups had lower SERPINE1 protein expression than the miR-145-5p mimic NC and OE-NC+ miR-145-5p mimic groups, respectively (Figure 7A). Overexpression of SERPINE1 in SGC7901 cells partially counteracted the inhibitory effect of miR-145-5p on cell proliferation (P < 0.001) (Figure 7B and C), migration (Figure 7D), invasion (Figure 7E), and EMT (Figure 7F). SERPINE1 also partially reversed miR145-5p-induced apoptosis (Figure 7G). These findings suggest that miR145-5p negatively regulates SERPINE1 in GC, thereby facilitating cell apoptosis, inhibiting cell proliferation, invasion, and metastasis, and reversing EMT.

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Figure 7 Serpin family E member 1 reverses microRNA-145-5p-mediated gastric cancer cell proliferation, invasion, metastasis, epithelial-mesenchymal transition, and apoptosis. A: Serpin family E member 1 protein expression in co-transfected cells; B: Co-transfected cell proliferation; C: Co-transfected cell colony formation; D: Co-transfected cell migration; scale bar = 100 μm; E: Co-transfected cell invasion; scale bar = 100 μm; F: Epithelial-mesenchymal transition-related marker protein (E-cadherin, β-catenin, Vimentin, and α-smooth muscle actin) expression in co-transfected cells; G: Apoptosis of co-transfected cells. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001.

The salvage experiment assessed ERK1/2 and p-ERK1/2 protein expression in the four groups. While miR145-5p and SERPINE1 did not affect ERK1/2 protein expression, miR-145-5p overexpression suppressed p-ERK1/2 expression. Meanwhile, elevated SERPINE1 levels partially counteracted the effect of miR-145-5p (Figure 8A).

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Figure 8 Effect of serpin family E member 1 overexpression on gastric cancer cell proliferation and the signal-regulated kinase-1/2 pathway invitro and invivo. A: Expression of signal-regulated kinase-1/2 (ERK1/2) and p-ERK1/2 in SGC7901 co-transfected cells; B: Image of xenograft tumors at day 18 post-inoculation; C: Xenograft tumor growth, volume, and mass at day-18 post-inoculation. n = 5 mice per group; D: Ki67 expression in xenograft tumor tissue; Scale bar = 20 μm; E: E-cadherin, vimentin, serpin family E member 1, ERK1/2, and p-ERK1/2 expression in xenograft tumor tissues. ^aP < 0.05; ^bP < 0.01; ^cP < 0.001. SERPINE1: Serpin family E member 1; ERK1/2: Signal-regulated kinase-1/2.

To further verify this mechanism, a GC tumor model was established in nude mice. All nude mice were evenly distributed into three groups (NC, OE, and OE + PD98059). Tumor tissues in the mice that overexpressed SERPINE1 (OE group) were heavier and larger in volume than those in the NC group. In contrast, nude mice that received PD98059, an ERK1/2 signal inhibitor, via intraperitoneal administration, had reduced tumor weight (P < 0.01) and volume (P < 0.001) (Figures 8B and C). Immunohistochemical analysis of the tumor tissue revealed that Ki67 was highly expressed in the group with SERPINE1 overexpression. However, its expression was diminished in the tissues from the OE+PD98059 group (Figure 8D). Western blot results revealed that while SERPINE1 overexpression inhibited E-cadherin expression, boosted vimentin expression, induced EMT, and increased ERK1/2 phosphorylation, it had no impact on total ERK1/2 expression. In contrast, PD98059-induced blockage of the ERK1/2 pathway increased E-cadherin and reduced vimentin expression (Figure 8E). In summary, these results indicate that miR-145-5p negatively regulates SERPINE1, inhibiting ERK1/2 signaling, and ultimately suppressing GC proliferation and EMT.

Gastric cancer (GC), a common malignancy of the digestive system, has an increasing incidence rate and poses a substantial threat to human health.

MicroRNAs (miRNA) play important roles in gene regulation and modulate many physical and pathological processes. The research motivation of this study was to identify the role of miRNA-145-5p (miR-145-5p) in the development of GC and its underlying mechanisms.

This study sought to compare miR-145-5p expression in GC and adjacent normal tissues, clarify the role of miR-145-5p in GC cell proliferation, invasion, metastasis, epithelial-mesenchymal transition (EMT), and apoptosis, and identify the direct target of miR-145-5p in GC cells.

Real-time polymerase chain reaction was performed to detect miRNA expression. Wound-healing and Transwell assays were performed to evaluate cancer cell migration and invasion, respectively. Cell proliferation was examined using cell counting kit-8 and colony formation assays. Cell apoptosis was assessed using flow cytometry. Western blotting analysis was used to identify EMT-associated proteins. A dual-luciferase reporter system was used to validate the target of miR-145-5p. Tumor formation in nude mice was assessed to further explore the mechanism by which miR-145-5p inhibits the progression of GC.

MiR-145-5p was decreased in GC tissues. Serpin family E member 1 (SERPINE1) was characterized as a direct target of miR-363-3p. MiR-145-5p was shown to target SERPINE1 to regulate extracellular signal-regulated kinase-1/2 (ERK1/2) signaling.

MiR-145-5p inhibits GC progression via the SERPINE1-ERK1/2 axis.

The miR-145-5p/SERPINE1/ERK1/2 axis may serve as a GC treatment target.