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. 2020 Oct 7;13:9957–9966. doi: 10.2147/OTT.S257951

miR-525-5p Modulates Proliferation and Epithelial–Mesenchymal Transition of Glioma by Targeting Stat-1

Peng Xie 1,*, Qiu Han 2,*, Dachao Liu 3,*, Dan Yao 4, Xiaoqing Lu 5, Ziyu Wang 6,✉, Xiaohua Zuo 7,✉
PMCID: PMC7548333  PMID: 33116581

Abstract

Background

Glioma is the most aggressive human brain tumor. Recent studies revealed that microRNAs play vital roles in glioma. However, the function of microRNA-525-5p (miR-525-5p) in glioma remains unclear.

Methods

qRT-PCR and Western blotting were used to evaluate mRNA and protein levels in glioma tissues and cells. Colony formation, CCK-8, and Edu assays evaluated the growth of glioma cells. Wound-healing, transwell, and 3D invasion assays examined the migration and invasion activities of glioma cells. Luciferase reporter assays assessed the regulatory relationship interaction between miR-525-5p and Stat-1. A mouse xenograft model was used to examine the effect of miR-525-5p on glioma in vivo.

Results

miR-525-5p expression was downregulated in glioma tissues and cells. Overexpressing miR-525-5p decreased the growth of glioma cells and reduced the migration, invasion, and epithelial–mesenchymal transition of glioma cells. Bioinformatics analysis identified Stat-1 as a potential target of miR-525-5p, and dual luciferase reporter assays revealed that miR-525-5p negatively regulates Stat-1. Decreased Stat-1 led to the inhibition of FOXM1, affecting NF-κB signaling activity. Overexpressing miR-525-5p reduced tumor development in vivo.

Conclusion

miR-525-5p negatively regulates cell proliferation, migration, invasion, and epithelial–mesenchymal transition in glioma, and Stat 1 is a target of miR-525-5p. miR-525-5p may be a potential target for glioma treatment.

Keywords: miR-525-5p, glioma, Stat 1, proliferation, EMT

Introduction

Glioma is the most aggressive human brain tumor, with high morbidity and mortality rates.1,2 Despite advances in the treatments for glioma, the prognosis is still poor.3 Therefore, it is vital to understand the mechanisms of the development of glioma, and to develop more effective therapeutic strategies.

MicroRNAs (miRNAs) are small noncoding RNAs 18 to 24 nucleotides in length that specifically bind to the 3′-untranslated region (3′- UTR) of target mRNAs.4–6 miRNAs regulate gene expression through post-transcriptional degradation of mRNA to degradation or by otherwise leading mRNA to degradation.7,8 Aberrant expression of miRNAs is associated with different kinds of tumors, including glioma.9,10

Stat-1 promotes growth of tumor cells.11 Activation of Stat family can promote tumor invasion, angiogenesis, survival and proliferation.12–14 A previous study reported that Stat-1 induced poor survival in glioblastoma.15 Furthermore, inhibition of Stat-1 induced a mesenchymal phenotype and angiogenic factors above basal levels.16

Here, we showed that microRNA-525-5p (miR-525-5p) expression was decreased in glioma cells and tissues. We found that miR-525-5p plays a vital role in regulating the proliferation, migration, invasion, and EMT of glioma cells via targeting Stat-1. Furthermore, decreasing Stat-1 led to the inhibition of FOXM1, thus affecting NF-κB signaling activity. These findings indicate that miR-525-5p could be a promising therapeutic target for glioma.

Materials and Methods

Glioma Cells and Tissues

Glioma cell lines (U87, A172, U251 and T98) were purchased from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). Normal human astrocytes (NHAs) were purchased from Lonza (Walkersville, MD, USA). Cells were maintained in Dulbecco’s Modified Eagle Medium (DMEM) or 1640 medium supplemented with 10% FBS (Invitrogen) in a humidified 37 °C incubator with 5% CO2.

A total of 26 nontumorous brain tissues (NBTs, obtained from the cortex of decompressive surgery patients with brain trauma or hypertensive intracerebral hemorrhage) and glioma tissues were obtained from the Department of Neurosurgery, Huai’an Hospital Affiliated to Xuzhou Medical University, Second People’s Hospital of Huai’an City. Of the 26 samples, 5 were NBTs, 9 were low-grade glioma (LGG) samples (grade II) and 12 were high-grade glioma (HGG) samples (grade III and IV). All patients were informed of the purpose of this study and signed written informed consent. This study was approved by the Ethics Committee of Xuzhou Medical University. miRNA expression data were obtained from the CGGA database (http://www.cgga.org.cn/portal.php), and gene expression data were obtained from the TCGA database (http://tcga-data.nci.nih.gov).

qRT-PCR

qRT-PCR was performed as previously described.17

Lentivirus and Cell Transfection

T98 and U251 cells were infected with lentiviruses carrying miR-525-5p or control, which were obtained from Genepharma (Shanghai, China). To overexpress Stat-1, T98 and U251 cells were transfected with Stat 1 over-expressing recombinant vector (GenePharma). After 48 h, cells were used for functional and mechanism assays.

Cell Growth Assays

Colony formation, CCK-8, and 5-ethynyl-2′-deoxyuridine (Edu) assays were performed as described previously.18

Flow Cytometry

Glioma cells were harvested, fixed with 70% alcohol and stored at −20 °C for several days. Cells were washed with PBS, treated with 50 mg/mL of propidium iodide and analyzed by flow cytometry.

Migration and Invasion Assays

For migration assays, infected cells were seeded in 6-well plates. A linear scratch was created in the cell monolayer using a pipette tip and then plates were cultured in an incubator. The cells were photographed under a microscope at 0 h and 48 h.

For invasion assays, cells were seeded in the upper chambers of Transwell plates pre-coated with 10 μg of Matrigel diluted with serum-free DMEM medium; medium with 10% FBS was added to the lower chambers. After incubation for 36 h, cells were fixed with 4% formaldehyde, stained with 1% crystal violet and photographed using a microscope (200×).

3D invasion assay was performed as described previously.19

Luciferase Reporter Assay

The regulatory effects of miR-525-5p on Stat-1 were investigated by luciferase reporter assays. Wild-type and mutant 3′-UTR sequences of Stat-1 were cloned into the pGL-3M recombinant plasmid. U251 and T98 cells overexpressing miR-525-5p or control were transfected with the luciferase reporters using Lipofectamine 3000. A plasmid expressing Renilla luciferase was co-transfected for normalization.

Subcutaneous Xenografts Models

Male nude mice were purchased from Beijing Vital River Laboratory Animal Technology. Fourteen mice were randomly assigned into two groups. U251 cells overexpressing miR-525-5p or control were harvested and resuspended in PBS. Cells (1×106) were then inoculated into nude mice. Tumor growth was monitored and tumor volume was calculated using the formula: V = 0.5×length×width2. At 30 days after injection, the mice were sacrificed and the tumors were harvested. The study has been approved by the Ethics Committee of Huai’an Hospital Affiliated to Xuzhou Medical University, Second People’s Hospital of Huai’an City, and is based on the National Institutes of Health’s Guide to the Care and Use of Laboratory Animals.

Western Blotting Assay

Western blot analysis was performed as described previously. Primary antibodies against cyclin D1 (ab40754), CDK2 (ab32147), CDK2 (ab108357), Stat1 (ab30645), Fibronectin (ab2413, Abcam); p65 (#8242), p-p65 (#3033), E-cadherin (#3195), FOXM1 (#5436), N-cadherin (#13116), Vimentin (#5741, Cell Signaling Technology), and actin (Bethyl Laboratories) were used for Western blotting analysis.

Statistical Analysis

All experiments were performed at least three times. Statistical analyses were performed with GraphPad Prism 5. The results are expressed as mean ± SD. Statistical differences were analyzed by Student’s t-test or χ2 test. P<0.05 was considered to indicate statistical significance.

Results

MiR-525-5p Expression is Decreased in Glioma Cells and Tissues

We first analyzed the expression of miR-525-5p in the CGGA database. We found that miR-525-5p expression level was higher in LGGs compared with that in HGGs (Figure 1A). We next detected miR-525-5p expression in 26 samples (5 NBTs, 9 LGGs, and 12 HGGs) via qRT-PCR. miR-525-5p level was decreased in LGGs and HGGs compared with NBTs (Figure 1B). The level of miR-525-5p was markedly decreased to 56.6% in LGGs and 18.9% in HGGs compared with levels in NBTs. We then investigated miR-525-5p expression in glioma cell lines (U87, A172, U251, and T98) and NHAs. miR-525-5p expression was decreased in glioma cells compared with NHAs: miR-525-5p level was decreased to 60.6% in U87 cells, 59.0% in A172 cells, 37.3% in U251 cells, and 32.0% in T98 cells (Figure 1C).

Figure 1.

Figure 1

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miR-525-5p is downregulated in glioma tissues and cells. (A) CGGA database showing reduced miR-525-5p expression in LGGs and HGGs. (B) The expression of miR-525-5p in clinical samples (NBTs: 5, LGGs: 9, and HGGs: 12). *P < 0.05. (C) qRT-PCR analysis of miR-525-5p expression in NHAs and glioma cell lines U87, A172, U251, and T98. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05.

Overexpressing miR-525-5p Decreases the Growth of Glioma Cells

We transfected miR-525-5p or the negative control into U251 and T98 glioma cells and confirmed miR-525-5p expression in the cell lines by qRT-PCR (Figure 2A). To determine the effect of miR-525-5p on the growth of glioma cells, we performed colony formation, CCK8, and Edu assays. Colony formation assays indicated that overexpressing miR-525-5p decreased the proliferation of U251 and T98 cells compared with controls (Figure 2B and C). CCK8 assay showed that overexpressing miR-525-5p inhibited the growth of both U251 and T98 cells (Figure 2D). EdU revealed similar results (Figure 2E).

Figure 2.

Figure 2

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Overexpressing miR-525-5p inhibits glioma cell proliferation and induces cell cycle arrest. (A) The mRNA expression level of miR-525-5p in U251 and T98 cells was analyzed by qRT-PCR after transfection. *P < 0.05. (B and C) Cell viability of miR-525-5p was evaluated using the colony formation assay. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (D) Overexpressing miR-525-5p inhibited cell proliferation detected by CCK8 assay. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (E) Overexpressing miR-525-5p on the growth of U251 and T98 cells was examined by EdU assay (original magnification 200 X). Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (F and G) Effect of miR-525-5p on cell cycle distribution in U251 and T98 cells. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (H) Western blot analysis of CDK2, CDK4, and cyclin D1 protein levels in U251 and T98 cells after overexpressing miR-525-5p and miR-NC. β-Actin was used as control.

We further found that overexpressing miR-525-5p induced cell cycle arrest in glioma cells at G1 (Figure 2F and G). The altered expressions of cell cycle-related proteins CDK2, CDK4 and cyclin D1 were consistent with this result (Figure 2H). These results indicate that overexpression of miR-525-5p decreases the proliferation of glioma cells and inducing a G1 cell cycle arrest.

Overexpressing miR-525-5p Reduces EMT in Glioma Cells

We next examined the effects of miR-525-5p on EMT. The levels of mesenchymal markers vimentin, fibronectin, and N-cadherin were downregulated, while E-cadherin levels were upregulated in U251 and T98 cells overexpressing miR-525-5p (Figure 3A). Wound healing assays demonstrated that overexpressing miR-525-5p reduced the migration ability of glioma cells (Figure 3B–D). Furthermore, transwell and 3D-invasion assays showed that overexpressing miR-525-5p reduced the invasion ability of glioma cells (Figure 3E–G). Together these results indicate that overexpression of miR-525-5p reduces EMT, migration, and invasion in glioma cells.

Figure 3.

Figure 3

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miR-525-5p decreased glioma migration, invasion, and EMT. (A) EMT-associated proteins in indicated glioma cells were determined by Western blotting. β-Actin was used as the loading control. (B–D) Wound-healing assay of the migration ability of overexpressing miR-525-5p or miR-NC glioma cells. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (E and F) Transwell invasion assay of the invasive ability of the of overexpressing miR-525-5p or miR-NC glioma cells. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (G) 3D invasion assay of the invasion ability of overexpressing miR-525-5p or miR-NC glioma cells.

Stat 1 is a Direct Target of miR-525-5p

To search for the molecular mechanism underlying the inhibitory effect of miR-525-5p on proliferation, migration, invasion, and EMT in glioma, we used TargetScan and miRanda algorithms to identify potential targets of miR-525-5p.20,21 Bioinformatics analysis identified binding sites for miR-525-5p in Stat 1 mRNA (Figure 4A). Luciferase reporter assay was used to examine the effect of miR-525-5p on Stat-1. Decreased luciferase activity of reporter vector containing the wild-type 3′-UTR of Stat-1 was observed after transfection with miR-525-5p, whereas no effects were observed with the mutant 3′-UTR reporter vector in which the putative miR-525-5p binding sites were mutated (Figure 4B). We further found that miR-525-5p downregulated the mRNA and protein levels of Stat-1 (Figure 4C and D). Reduction of Stat-1 led to the inhibition of FOXM1, affecting NF-κB signaling activity (Figure 4D). Pearson’s correlation analysis showed a negative correlation between miR-525-5p and Stat-1 in glioma (Figure 4E).

Figure 4.

Figure 4

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Stat-1 is direct target of miR-525-5p in glioma. (A) The miR-525- 5p binding sites in the 3ʹUTR of Stat-1 with the wild type (WT) and mutated (Mut) sequences. (B) Overexpressing miR-525-5p or miR-NC U251 and T98 cells were transfected with luciferase reporter constructs containing either pGL3- Stat-1-3ʹ-UTR-WT or pGL3- Stat 1–3ʹ-UTR-Mut. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (C) Stat-1 mRNA levels in Overexpressing miR-525-5p or miR-NC U251 and T98 cells. Data were expressed as the mean ± SEM from three independent experiments. *P < 0.05. (D) Stat-1, FOXM1, p65, and p-p65 protein levels in overexpressing miR-525-5p or miR-NC U251 and T98 cells. (E) Pearson’s correlation analysis of the relative expression levels of miR-525-5p and the relative Stat-1 mRNA levels in glioma.

Stat 1 Attenuates the Effects of miR-525-5p on Glioma Cell Proliferation, Migration, Invasion, and EMT

We co-overexpressed Stat-1 together with miR-525-5p in U251 and T98 cells and confirmed that co-overexpressing Stat-1 restored the miR-525-5p-mediated effects on Stat-1 protein levels in U251 and T98 cells (Figure 5A). Cell proliferation, migration, and invasion assays showed that co-overexpressing Stat-1 attenuated the inhibitory effects of miR-525-5p on glioma proliferation, migration, and invasion (Figure 5B–H). These results indicated that Stat-1 is a functional target of miR-525-5p in glioma.

Figure 5.

Figure 5

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Stat-1 reintroduction reverses the inhibitory effect of miR-525-5p. (A) Western blot analysis of Stat-1, FOXM1, and p-p65 protein levels in overexpressing miR-525-5p or miR-NC U251 and T98 cells. (B and C) Effect of Stat-1 reintroduction on overexpressing miR-525-5p or miR-NC U251 and T98 cells growth rates as measured by CCK-8 assay. Data were expressed as the mean ± SEM from three independent experiments. *, #P < 0.05. (D–H) Effect of Stat 1 reintroduction on overexpressing miR-525-5p or miR-NC U251 and T98 cells invasion and migration ability as determined by wound-healing transwell assays. Data were expressed as the mean ± SEM from three independent experiments. *, #P < 0.05.

miR-525-5p Exhibits a Tumor Suppressor Role in vivo

We next explored the function of miR-525-5p in glioma development in vivo using subcutaneous xenografts. Nude mice were inoculated with U251 cells overexpressing control miRNA or miR-525-5p. Mice injected with cells overexpressing miR-525-5p showed inhibited tumor growth in vivo compared with controls (Figure 6A–C). We also observed downregulated protein levels of Stat-1, FOXM1, and p-p65 in tumors derived from miR-525-5p-overexpressing cells (Figure 6D), which is consistent with the in vitro results. Taken together, our results suggest that miR-525-5p inhibits the development of glioma both in vitro and in vivo.

Figure 6.

Figure 6

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Overexpressing miR-525-5p suppresses glioma growth in vivo. (A–C) Animals with U251 xenografts were separated into miR-NC or miR-525-5p groups. Overexpressing miR-525-5p inhibited the glioma progression in vivo, as revealed by measuring the tumors volume and tumors weight. (D) Stat-1, FOXM1, and p-p65 protein levels in tumor of miR-NC and miR-525-5p group. *P < 0.05.

Discussion

miRNAs play important roles in the development of cancers, including glioma, and can function as tumor suppressors or oncogenes by regulating the target genes.22,23 Therefore, miRNAs may be potential diagnostic and therapeutic targets in glioma.24

Dysregulated miRNAs are important for the pathology of glioma.25,26 Here, we found that miR-525-5p was downregulated in both glioma tissues and human glioma cells. We observed a significant decrease of glioma cell growth when miR-525-5p was overexpressed, and overexpressing miR-525-5p induced cell cycle arrest in G1. We further showed that miR-525-5p promoted EMT, migration, and invasion of glioma cells. Additionally, we confirmed a tumor inhibitory role of miR-525-5p in a xenograft tumor model.

Stat-1 closely involved in several biological functions, including cell proliferation, differentiation, migration, invasion, and apoptosis.27 Previous studies have reported that Stat-1 is upregulated in different types of tumors, including glioma.28–30 Stat-1 is regulated by IGFBP-3 and is a predictor for poor survival in glioblastoma.31 Moreover, Stat-1 is downregulated in gastric cancer tissue and involved in cell metastasis.32 We investigated the mechanisms underlying the inhibitory effect of miR-525-5p on glioma cell proliferation and EMT using bioinformatics analysis, and the results identified Stat-1 as a predicted target molecule of miR-525-5p. Overexpressing miR-525-5p reduced the protein and mRNA levels of Stat-1. Stat-1 inhibited NF-κB signaling through FOXM1.28 Additionally, restoration of Stat-1 expression could rescue the inhibition of cell proliferation and EMT that resulted from miR-525-5p overexpression. Together these data indicate that Stat-1 is a direct target gene of miR-525-5p and that Stat-1 attenuates the effects of miR-525-5p on the proliferation and EMT of glioma cells.

Conclusions

In this study, we investigated the effects of miR-525-5p on glioma. miR-525-5p was downregulated in glioma cells and tissues. Functional experiments indicated that miR-525-5p inhibits the proliferation, migration, invasion, and EMT of glioma and targets Stat-1. These findings suggest that miR-525-5p may be a potential target for glioma.

Acknowledgments

We thank Gabrielle White Wolf, PhD, from Liwen Bianji, Edanz Editing China, for editing the English text of a draft of this manuscript.

Funding Statement

This study was supported by the Research Program of Science and Technology Support Program of Huai’an (HAB201931) and Open Project of Key Laboratory of Universities of Jiangsu Province (XZSYSKF2019002).

Data Sharing Statement

The datasets used and analyzed during the current study are available from the corresponding author (Xiaohua Zuo) on reasonable request.

Ethics Approval and Consent to Participate

The study protocol was designed and approved by the ethical committee of the Affiliated Huai’an Hospital of Xuzhou Medical University, the Second People’s Hospital of Huai’an. All animal experiments were conducted under the approval of the Affiliated Huai’an Hospital of Xuzhou Medical University, the Second People’s Hospital of Huai’an, and is based on the National Institutes of Health’s Guide to the Care and Use of Laboratory Animals.

Consent for Publication

All authors agree on publication of the results of the present manuscript.

Author Contributions

XHZ, ZYW and PX designed the experiments; PX, QH, and DCL performed the experiments; DY and XQL analysis the results; PX wrote the paper. All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Disclosure

The authors declare that they have no competing interests.

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