miR-25 enhances cell migration and invasion in non-small-cell lung cancer cells via ERK signaling pathway by inhibiting KLF4

Introduction

Primary lung cancer is the leading cause of global cancer morbidity and cancer-associated mortality, accounting for ~1.59 million cases of mortality annually (1,2). Among lung cancer types, >85% of cases are presently identified as non-small cell lung cancer (NSCLC) (3). The treatment of patients diagnosed with lung cancer has significantly improved due to medical advances; however, the prognosis for NSCLC is remains poor and the 5-year overall survival rate is only 15% (4). The poor prognosis of patients with NSCLC is closely associated with distant metastasis. Consequently, further investigation is required to understand the potential mechanisms of metastasis in NSCLC.

Krüppel-like factors (KLFs) belong to the evolutionary conserved family of zinc finger transcription factors in mammals (5). KLF4, one of the earliest identified genes in the KLF family, is widely detected in a variety of human tissues and is reported to be crucial for diverse physiological processes, including development, differentiation and apoptosis, and stemness in embryonic stem cells (6). KLF4 is a bifunctional molecule displaying dual functions in different human cancers depending on the intracellular environment or the cell type. KLF4 can act as an oncogene, and it was previously reported that the expression levels of KLF4 were elevated in breast cancer and squamous cell carcinoma (7,8); whereas, in esophageal, human colon and gastric cancer, KLF4 served as a tumor suppressor (9–11). Research focusing on the effect of KLF4 in tumorigenesis has increased in recent years; however, the underlying mechanism of KLF4 in tumorigenesis is not clear. MicroRNAs (miRNAs) are single-stranded, non-coding RNA molecules of 18–22 nucleotides that can cause translational inhibition and/or mRNA degradation by binding to the 3′ untranslated region (UTR) of target mRNAs (12). It has been estimated that miRNAs regulate the expression of a third of human genes (13). miRNAs are involved in the regulation of diverse biological processes, including invasion, migration, proliferation and cell apoptosis (14–16). Abnormal expression of miRNAs, including the upregulation of miR-429 (17), miR-19a (18) and miR-146a (19), and downregulation of miR-143 (20), miR-3666 (21) and miR-29b (22) have been detected in lung cancer. Thus, miRNAs have potential as biomarker for diagnosis, targeted therapy and prognosis.

miR-25 is one of the miR-106b-25 cluster (miR-93, miR-25 and miR-106b) (23,24). Evidence has highlighted the key regulatory roles of miR-25 in tumor progression. For instance, Su et al (25) reported that upregulated miR-25 in liver cancer tissues led to a shorter survival time. Li et al (26) also reported that overexpressed miR-25 increased the proliferation, invasion and migration of gastric cancer cells by inducing the degradation of transducer of ERBB2 1 and also demonstrated that serum concentrations of miR-25 were positively associated with poor prognosis in patients with gastric cancer. However, in certain diseases, miR-25 was downregulated. For instance, diminished expression of miR-25 in colorectal cancer induced an increase in expression of angiopoietin like 2 and resulted in reduced cell clones, inhibited invasion and migration (27). Furthermore, Wu et al (28) studied miR-25, which was reported to promote cell growth and inhibit apoptosis in NSCLC by reducing modulator of apoptosis 1 expression. Xiang et al (29) revealed that miR-25 was overexpressed in NSCLC cells and tissues, and promoted the motility and proliferation of NSCLC cells, in part by diminishing F-box and WD repeat domain containing 7 expression levels. The majority of studies have investigated the biological function of miR-25 in lung cancer, however the underlying mechanism is remains unknown. The aim of the present study was to research the function of miR-25 in NSCLC and to improve the understanding of the underlying mechanism of miR-25 in NSCLC.

In the present study, the expression levels of miR-25 were examined in NSCLC tissues via reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Subsequently, in vitro assays, including cell migration and invasion assays, were conducted to understand the biological functions of miR-25 in NSCLC. Additionally, KLF4 was demonstrated to be a novel target gene of miR-25, and to be involved in the invasion and migration in NSCLC cells. Finally, the phosphorylation of extracellular signal-regulated kinase (ERK1/2; p44/42 mitogen-activated protein kinase) demonstrated that the ERK signaling pathway was downstream of miR-25. Collectively, the results of the present study revealed that miR-25 promoted the migration and invasion of NSCLC cells via regulation of the ERK1/2 signaling pathway by targeting KLF4.

Materials and methods

Tissue samples and cell lines

Pairs of normal and NSCLC tissue specimens (n=31; 21 male and 10 female; age, 41–77) were obtained from patients that received surgery at the Cardiovascular Surgery of First Affiliated Hospital of Gannan Medical University (Ganzhou, China) between January 2014 and March 2016. Specimens were placed immediately into liquid nitrogen following collection and were then stored at −80°C until use. Written informed consent was obtained from the patients involved in the present study, which was approved by the Ethics Committee of Gannan Medical University. Human A549 and Calu1 NSCLC cell lines, GES-1 and 293T cells used in the present study were obtained from the Institute of Biochemistry and Cell Biology of the Chinese Academy of Sciences (Shanghai, China), A549, GES-1 and 293T cells were cultured in Dulbecco's modified Eagle's medium (DMEM), Calu1 cells were cultured in McCOYs 5A (HyClone; GE Healthcare Life Sciences, Logan, UT, USA). The culture medium was supplemented with 1% penicillin and streptomycin (HyClone; GE Healthcare Life Sciences), and 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA). The cells were cultivated in a humidified environment at 37°C with 5% CO2.


RT-qPCR

Total RNA was extracted from the cultured cells and NSCLC tissues with TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's protocols. RNA was dissolved in diethylpyrocarbonate water. RT of mRNA and miRNA was conducted using ReverTra Ace® qPCR RT kit (Toyobo Life Science, Osaka, Japan) and miRNA reverse transcription kit (Promega Corporation, Madison, WI, USA). cDNA was subsequently harvested and qPCR was conducted with SYBR® Fast qPCR Mix (Takara Biotechnology Co., Ltd., Dalian, China) using a 7500 Fast Real-Time PCR detection system (Thermo Fisher Scientific, Inc.). qPCR reaction conditions were as follows: 95°C pre-denaturation for 3 min, followed by 40 cycles of denaturing at 95°C for 3 sec, annealing and synthesis at 60°C for 30 sec; the Cq value was then determined. The primers for RT-qPCR was as follows: miR-25 forward, 5′-GCAGCATTGCACTTGTCTCG-3′ and reverse, 5′-AGTGCAGGGTCCGAGGTATTC-3′; and KLF4 forward, 5′-AAGCCAAAGAGGGGAAGACG-3′ and reverse, 5′-GTGCCTGGTCAGTTCATCTGAG-3′. The 18S and U6 were taken as internal control for KLF4 and miR-25 respectively. To calculate the expression levels of miR-25 and KLF4, the 2−ΔΔCq method was used (30). Overexpression was defined as a ≥1.5-fold change and underexpression as a ≤0.67-fold change, based on a previous study (31). All experiments were repeated three times independently.

Bioinformatics analysis

To identify the targets of miR-25 that may regulate the migration and invasion of NSCLC, the target prediction tool TargetScan version 7.1 (http://www.targetscan.org/mmu_71/) was used for target prediction of miR-25. The Database for Annotation, Visualization and Integrated Discovery (version 6.7; https://david.ncifcrf.gov) is a functional annotation tool that provides a comprehensive set of biological annotations to understand the meaning underlying a large list of target genes. The Gene Ontology (GO) (version 4.0; http://www.geneontology.org/) and Kyoto Encyclopedia of Genes and Genomes (KEGG; http://www.genome.jp/kegg/pathway.html) databases were used for functional clustering analysis and pathway location.

Vector construction

The primers on the flanks of the coding sequences of KLF4 were: Forward, ATACTCGAGATGAGGCAGCCACCTGGC (Xhol) and reverse, CCACTAGTTTAAAAATGCCTCTTCATGTGTAAG (SpeI). Primers were designed using Primer3 (version 4.1.0; http://primer3.ut.ee) according to the reference sequence in the University of California Santa Cruz Genome Browser (https://genome.ucsc.edu). The KLF4 cDNA reverse transcribed from mRNA of GES-1 was used as a template. For the KLF4 vector, KLF4 cDNA was cloned into the pCMV-N-Flag plasmid (Beyotime Institute of Biotechnology, Shanghai, China) between XhoI and SpeI restriction sites to construct the KLF4 overexpression plasmid. For the 3′-UTR of the KLF4 vector, the primers for the 3′-UTR of KLF4 containing the putative binding site of miR-25 was amplified by PCR. The primers for the 3′-UTR of KLF4 sequence were: Forward, 5′-GGTCTCGAGGGATATGACCCACACTGCC-3′ (Xho1I) and reverse, 3′-TTAAGCGGCCGCCCTTGAGTATGCAAAATACAAACTCC-5′ (NOTI). and cloned into the psi-CHECK2 vector (Promega Corporation) using the restriction endonucleases Xho1I and NotI. The insertion regions were sequenced by Biosune (Platinum Shang Biotechnology, Shanghai, China) to ensure the accuracy of each base.

Cell transfection

miR-25 mimics/inhibitors and its negative control (NC) miRNAs (mimic-NC/inhibitor-NC, respectively), siRNA and its negative control (si-NC) were purchased from Guangzhou RiboBio Co., Ltd. (Guangzhou, China). NC miRNAs of 20–30 base pairs served as the negative control and exhibited minimal effect on cells in the present study. miR-25 mimics are chemically synthesized, double-stranded RNAs which mimic mature endogenous miR-25 following transfection into cells. miR-25 inhibitors are chemically synthesized, single-stranded modified RNAs that specifically inhibit endogenous miRNA function following transfection into cells. Cells were transfected with 50 nM miR-25 mimic (sense, 5′-CAUUGCACUUGUCUCGGUCUGA-3′ and antisense, 3′-GUAACGUGAACAGAGCCAGACU-5′), inhibitor (5′-UCAGACCGAGACAAGUGCAAUG-3′), mimic-NC (sequence unavailable), inhibitor-NC (sequence unavailable), small interfering (si)RNA (hs-KLF4-si forward, 5′-GAGUCAUCUUGUGAGUGGAdTdT-3′ and reverse, 5′-UCCACUCACAAGAUGACUCdTdT-3′) targeting KLF, or si-NC (sequence unavailable) with 3 µl Lipofectamine® 2000 transfection reagent (Invitrogen; Thermo Fisher Scientific, Inc.). Plasmid transfection was conducted using 2 µg KLF4 overexpression plasmid or KLF4-3′UTR plasmid with 4 µl Lipofectamine® 2000 according to the manufacturer's protocols.

Luciferase reporter assay

293T cells transfected with miR-25/miR-NC mimics and wild type (WT)/mutated (MUT) psi-CHECK2-KLF4-3′UTR were transferred into 24-well plates and cultured until 90% confluence was reached. Luciferase activity was detected using the Dual-Luciferase® Reporter Assay System kit (cat. no. E1910; Promega Corporation). After 48 h post-transfection, cells were collected, centrifuged at 56,669 × g for 1 min at 4°C and lysed with passive lysis buffer (Promega Corporation). Culture plates were placed on a rocking platform for 15 min to ensure complete and even coverage of the cell monolayer with PLB. Cell lysates were transferred to a tube, and lysate samples were centrifuged for 30 sec at 56,669 × g at 4°C. Cell lysate (20 µl) was transferred into the luminometer tube containing Luciferase Assay Reagent II and was mixed by pipetting two or three times. Stop & Glo® (100 µl) Reagent was added to the tube which was vortexed briefly to mix. The relative luciferase activity was subsequently detected with a microplate reader (Synergy 2; BioTek China, Beijing, China). The ratio of the Renilla fluorescence value to the firefly fluorescence value was calculated.

Wound healing assay

Cells were transfected with miR-25 inhibitor, mimic, KLF4 siRNA, KLF4 overexpression plasmid, miR-25 inhibitor NC (in-NC), miR-25 mimic NC (miR-NC), si-NC or empty vector. The ability of cell migration was evaluated via a wound healing assay. Calu1 and A549 cells were seeded into a 6-well plate (Corning Incorporated, Corning, NY, USA) at a density of 1.8×105 cells/ml and cultured, then transferred to 12-well plate 24 h post-transfection and permitted to grow to a density of 90%. Cells were scratched with a sterile yellow pipette tip and then washed several times with PBS to remove non-adherent cells. Leica Image Analysis (Leica Microsystem, Inc., Buffalo Grove, IL, USA) was used to capture images; gaps were measured using ImageJ software (version 1.51t; National Institutes of Health, Bethesda, MD, USA) to calculate healing percentages.

Transwell assay

Matrigel was pre-cooled and diluted 1:3 in medium without FBS, 50 µl was added to the upper chamber and placed in the incubator for 1 h. The cells were suspended with the culture medium containing 0.1% bovine serum albumin (BSA; Beyotime Institute of Biotechnology) at a density of 5×105/ml, and 200 µl was added in the upper chamber. A total of ٥٠٠ µl DMEM or McCOYs 5A medium containing 15% FBS was added to the lower chamber. The culture plates were removed from the incubator following incubation for 24 or 48 h at 5% CO2 and 37°C. The cells from the upper layer of the chamber's filter membrane were cleared, and the chamber was washed with PBS, then placed into 95% ethanol to fix the cells adhering on the undersurface of filter membrane at room temperature for 10 min, cells were then stained with 0.5% crystal violet (2 mg/ml; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) at room temperature for 30 min. The number of cells was counted in five fields that were randomly selected under a light microscope, the average number of cells was recorded and analyzed.

Western blotting

Total proteins were harvested from transfected cells at 48 h after transfection and lysed using a mixture of radioimmunoprecipitation assay buffer (Beyotime Institute of Biotechnology), phenylmethane sulfonyl fluoride (Beyotime Institute of Biotechnology) and protease inhibitor cocktail (Roche Applied Science, Penzberg, Germany). The protein amount was determined using a bicinchoninic acid assay kit (Beyotime Institute of Biotechnology); 30 µg total protein was used for western blotting. Different sized proteins were separated by the 10% SDS gel, then electrotransferred to polyvinylidene fluoride membranes (Merck KGaA). BSA (2–5%) was applied to the membranes, which were incubated at room temperature for 1 h to remove nonspecific binding. Subsequently, the membranes were incubated with the following primary antibodies overnight at 4°C (1:1,000): Matrix metalloproteinase 11 (MMP11; cat. no. ab201757; Abcam, Cambridge, UK); E-cadherin (cat. no. ab1416; Abcam); KLF4 (cat. no. 043474; CST Biological Reagents Co., Ltd., Shanghai, China); phosphorylated (p)-ERK1/2 (cat. no. 4370S; CST Biological Reagents Co., Ltd.); ERK1/2 (cat. no. 4695P; CST Biological Reagents Co., Ltd.); N-cadherin (cat. no. 4061p; CST Biological Reagents Co., Ltd.); vimentin (cat. no. 12826; Cell Signaling Technology, Inc., Danvers, MA, USA); anti-β-actin antibody (1:5,000; cat. no. sc-47778; Santa Cruz Biotechnology, Inc., Dallas, TX, USA) and the membrane was incubated. The membranes was washed three times with PBS with Tween-20 to remove the unbound primary antibody, then incubated with the secondary antibodies of corresponding species for 1 h [1:5,000, anti-rabbit (cat. no. BS13278; Biogot Technology Co., Ltd., Nanjing, China) or anti-mouse (cat. no. BS10043; Biogot Technology Co., Ltd.)] at 37°C for 1 h. Protein bands were scanned and visualized under automated chemiluminescence image analysis system (Tanon 5200; Tanon Science and Technology Co., Ltd., Shanghai, China) following incubation with an enhanced chemiluminescent substrate (Thermo Fisher Scientific, Inc.) for 2 min. β-actin served as the internal control.

Statistical analysis

The data of the present study are presented as the mean ± standard deviation from three independent experiments and analyzed with version 21.0 of SPSS (IBM Corp., Armonk, NY, USA). The difference between two groups was analyzed by Student's t-test. One-way analysis of variance was to compare multiple groups followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

miR-25 is overexpressed in NSCLC tissues

miR-25 expression levels were analyzed in NSCLC tissues and matched normal tissue by RT-qPCR. Overexpression was defined as a >1.5 fold increase and underexpression a <0.67 fold decrease. Analysis demonstrated that 25 of the 31 tissues exhibited miR-25 overexpression compared with in corresponding normal tissues (P<0.05; Fig. 1).

Figure 1. miR-25 is overexpressed in NSCLC tissues. (A) Relative expression levels of miR-25 in tumor and normal tissues were measured by RT-qPCR in 31 pairs of human NSCLC samples and their corresponding normal tissues (n=31 pairs). The relative expression of miR-25 in each tissue was calculated using the 2-∆∆Cq method and U6 acted as the endogenous reference gene. In each pair of clinical samples, the expression of miR-25 in the tumor tissues were referenced to corresponding normal tissues. The settings presented in the figure was as follows: The graph was divided into high expression and low expression sections by black solid lines of T/N=1.5. The expression of miR-25 in 25 pairs cancerous tissue samples was ≥1.5 fold higher than that in adjacent tissues (left side of the black dashed line); the remaining 6 pairs of samples (right side of black dashed line) had T/N <1.5-fold. (B) Distribution of miR-25 expression in 31 pairs clinical specimens, which was divided into three sections by using T/N ≥1.5 and T/N ≤0.67 in the pie chart. (C) Relative expression levels of miR-25 were measured by RT-qPCR in 31 pairs non-small-cell lung cancer tissues and adjacent normal tissues samples. Data are presented as the mean ± standard deviation from three independent experiments. *P<0.05. miR, microRNA; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; T/N, tumor/normal.

miR-25 regulates invasion and migration of NSCLC cells

To research the function of miR-25 in migration and invasion in NSCLC cells, A549 and Calu1 cells were transfected with miR-25 mimics, inhibitor or the negative controls. The transfection efficiency was detected by RT-qPCR (Fig. 2). Results of wound healing assays showed that miR-25 inhibition reduced cell migration compared with control cells, leading to larger scratch areas than control cells (Fig. 3A and B). Cell motility was then assessed via Transwell migration and invasion assays, which indicated that miR-25 inhibition effectively repressed the invasion and migration of NSCLC cells (Fig. 3C and D). By contrast, the scratch gap in the miR-25 overexpression group was smaller than the NC group (Fig. 4A and B), and in the Transwell assays, the number of cells crossing through the membrane was increased by miR-25 mimics compared the NC group (Fig. 4C and D). These results indicated that the inhibition of miR-25 weakened NSCLC cell motility, while overexpression of miR-25 exhibited opposite effects.

Figure 2. miR-25 regulates invasion and migration of pairs non-small-cell lung cancer cells. Transfection efficiencies of inhibitor in (A) Calu1 and (B) A549 cells. Transfection efficiencies of mimics in (C) Calu1 and (D) A549 cells. ***P<0.001. miR, microRNA; in-NC, inhibitor negative control; NC, mimic negative control.

Figure 3. MicroRNA-25 inhibition reduces invasion and migration of non-small-cell lung cancer cells. (A) Calu1 and (B) A549 cells in culture for migration assay were monitored at various time points. The image of the wound gap was captured at 0, 24, 36 and 48 h (magnification, ×50). Quantitative wound confluence data of cell lines. Transwell migration and invasion assays in (C) Calu1 and (D) A549 cells were employed to analyze cell migration and invasive abilities (magnification, ×200; crystal violet staining). *P<0.05, **P<0.01, ***P<0.001 vs. in-NC. in-NC, inhibitor negative control.

Figure 4. MicroRNA-25 mimics increase invasion and migration of non-small-cell lung cancer cells. (A) Calu1 and (B) A549 cells in culture for migration assay were monitored at various time points. The image of the wound gap was captured at 0, 24, 36 and 48 h (magnification, ×50). Quantitative wound confluence data of cell lines. Transwell migration and invasion assays in (C) Calu1 and (D) A549 cells were employed to analyze cell migration and invasive abilities (magnification, ×200; crystal violet staining). *P<0.05, **P<0.01, ***P<0.001 vs. NC. NC, mimic negative control.

Identification of KLF4 as an endogenous target gene of miR-25 in NSCLC cells

GO analysis of miR-25 targets demonstrated that the molecular function of the target genes was predominantly concentrated in ‘protein binding’ (Fig. 5A). In addition, KEGG functional annotation of the target genes in cancer pathways is presented in Fig. 5B. In comprehensive consideration of functional targets and literature reports, KLF4 was eventually identified as a potential target gene of miR-25 (Fig. 6A) and further verified by a dual luciferase assay and western blotting. It was observed that overexpression of miR-25 significantly inhibited the relative luciferase value of psi-CHECK2-KLF4-3′UTR-WT; however, it did not alter psi-CHECK2-KLF4-3′UTR-MUT (Fig. 6B). Western blot analysis demonstrated that the miR-25 inhibition promoted KLF4 protein expression, whereas the miR-25 mimics reduced KLF4 protein expression levels (Fig. 6C and D). In addition, RT-qPCR revealed that 28 of 31 pairs of lung cancer tissues exhibited a decrease in KLF4 expression levels (Fig. 6E and F), indicating that KLF4 expression was decreased in NSCLC tissues compared with adjacent control tissues. These data suggested that KLF4 may be a target gene of miR-25.

Figure 5. Functional annotation of the target genes of microRNA-25. (A) Gene Ontology function of the target genes. (B) Kyoto Encyclopedia of Genes and Genomes functional annotation of the target genes. ECM, extracellular matrix.

Figure 6. Identification of KLF4 as an endogenous target gene of miR-25 in NSCLC cells. (A) Wild-type or mutant psi-CHECK2-KLF4-3′-UTR vector sequence and the binding site (blue sequence) between wild-type KLF4-3′-UTR and miR-25 and wild-type mutation location (red sequence) were presented. (B) 293T cells transfected with luciferase vectors containing wide type or mutant KLF4-3′-UTR and NC or miR-25, respectively were used for the luciferase assay. Luciferase activity was normalized to firefly luciferase activity. *P<0.05 vs. NC. Western blotting analysis demonstrated expression KLF4 post-transfection with (C) miR-25 mimic/inhibitor or (D) co-transfection of miR-25 and KLF4. (E) Relative expression alterations of KLF4 (T/N) were measured by RT-qPCR in 31 pairs of human NSCLC samples and their corresponding control tissues. The relative expression levels of KLF4 in each tissue were calculated using the 2−ΔΔCq method using 18S as the endogenous reference gene. In each pair of clinical samples, the expression of KLF4 in the tumor tissues (T) was referenced to corresponding normal tissues (N). The settings presented in the figure were as follows: The graph is divided into high expression and low expression sections by black solid lines of T/N=0.67. The expression of KLF4 in 28 pairs cancerous tissues samples 0.67-fold lower than in adjacent tissues (right of the black dashed line, T/N <0.67-fold), and the remaining 3 pairs of samples (left of black dashed lines) with T/N >0.67-fold. (F) Relative expression levels of KLF4 in 31 pairs NSCLC tissues and adjacent normal tissues samples measured by RT-qPCR and using 18S as reference genes. *P<0.05 vs. normal. RT-qPCR, reverse transcription-quantitative polymerase chain reaction; NSCLC, non-small-cell lung cancer; KLF4, Krüppel-like factor 4; UTR, untranslated region; MUT, mutated; NC, negative control; miR, microRNA; in-NC, inhibitor negative control; T/N, tumor/normal.

Knockdown of KLF4 increases invasion and migration of NSCLC cells

In order to investigate the biological function of KLF4, KLF4 expression was inhibited by transfection with siRNA (Fig. 7A-C). A wound healing assay demonstrated that knockdown of KLF4 accelerated the migration of cells compared with the control groups (Fig. 7D and E). The results of the migration and invasion assays were consistent with those of the wound healing assay (Fig. 7F and G), which suggested that the effects of KLF4 knockdown were similar to those of miR-25 overexpression.

Figure 7. Knockdown of KLF4 increases non-small-cell lung cancer cells invasion and migration ability. KLF4 mRNA levels were measured in (A) Calu1 and (B) A549 cells transiently transfected with si-KLF4 or si-NC, and (C) protein expression levels of KLF4 are were determined by western blotting. Wound healing assays in (D) Calu1 and (E) A549 cells transfected with si and NC (magnification, ×50). Quantitative data of gap closure was measured. (F) Calu1 and (G) A549 cells were transfected with si or si-NC, and migratory and invasive cells were detected in Transwell assays (magnification, ×200; crystal violet staining). *P<0.05, **P<0.01, ***P<0.001. KLF4, Krüppel-like factor 4; si, KLF4 small interfering RNA; si-NC, siRNA negative control.

Migration and invasion-promoting effects of miR-25 are partially attenuated by KLF4 overexpression

To further investigate whether KLF4 upregulation may attenuate the oncogenic effects of miR-25 on NCSLC cells, the pCMV-N-flag-KLF4 plasmid was transfected into miR-25-overexpressing A549 and Calu1 cells (Fig. 8A and B). Wound healing assays (Fig. 8C and D) and Transwell invasion and migration assays (Fig. 8E and F) demonstrated that the exogenous supplementation of KLF4 may weaken the oncogenic function of miR-25 in NSCLC cells. The results of the present study suggested that miR-25 promoted NSCLC cell migration and invasion by inhibiting KLF4 expression.

Figure 8. Migration and invasion promoting-effects of miR-25 are attenuated partially by KLF4 overexpression. Transfection efficiency was verified in (A) Calu1 and (B) A549 cells by reverse transcription-quantitative polymerase chain reaction analysis in cells transfected with vector + NC, vector+ miR-25 and KLF4 + miR-25. Transfected (C) Calu1 and (D) A549 cells were used in would healing assays. Transfected (E) Calu1 and (F) A549 cells were used in migration and invasion assays. *P<0.05, **P<0.01 and ***P<0.001. NC, mimic negative control; miR, microRNA; KLF4, Krüppel-like factor 4.

miR-25 promotes cells invasion and migration via the ERK signaling pathway

To clarify the mechanism of miR-25 in regulating cell motility, the downstream signaling pathways of miR-25 were investigated. Considering that KLF4 inhibited the role of miR-25 in suppressing NSCLC cell invasion and migration, and KLF4 is involved in the ERK signaling pathway, this suggests that miR-25 may regulate the ERK1/2 pathway by inhibiting the expression of KLF4. As presented in Fig. 9, the level of p-ERK1/2 and the markers of invasion and metastasis (vimentin, N-cadherin and MMP11) were reduced, and expression of E-cadherin was increased by miR-25 inhibition. Consistent with these findings, the overexpression of miR-25 in NSCLC cells activated the ERK1/2 signaling pathway, which was reversed by overexpression of KLF4 via co-transfection with pCMV-N-flag-KLF4. The findings of the present study demonstrated that miR-25, which inhibited KLF4 expression, promoted cell invasion and migration by activating the ERK signaling pathway.

Figure 9. miR-25 promotes cells invasion and migration via the ERK signaling pathway. The expression of E-cadherin, N-cadherin, vimentin, MMP11, p-ERK1/2, t-ERK1/2 and β-actin in A549 and Calu1 post-transfection with miR-25 inhibitor, miR-25 mimic, KLF4 si or KLF4 + miR-25. MMP11, matrix metalloproteinase; p-, phospho-; ERK, extracellular signal-regulated kinase; t-, total-; in-NC, inhibitor negative control; NC, mimic negative control; si-NC, si negative control; si, KLF4 small interfering RNA; miR, microRNA; KLF4, Krüppel-like factor 4.

Discussion

NSCLC, the most common lung cancer type, is studied by researchers worldwide. As invasion and metastasis facilitate NSCLC progression, it is important to further clarify the mechanisms of pathogenesis and metastasis of NSCLC.

The results of the present study indicated that miR-25 promoted the invasion and migration of NSCLC cells via the ERK1/2 signaling pathway by targeting KLF4. In the present study, the detailed experiments revealed that miR-25 was upregulated within NSCLC tumor tissue samples compared with in the corresponding paracancerous tissues by RT-qPCR analysis. Downregulation of miR-25 using miR inhibitor repressed the migration and invasion of NSCLC cells. By contrast, overexpression of miR-25 by transfection with miR-25 mimic accelerated the motility of NSCLC cells in vitro. The results of the present study suggested that miR-25 promoted the invasion and migration of NSCLC cells.

In addition, using the prediction software, TargetScan 7.1, KLF4 was identified as a potential target of miR-25, which was verified by luciferase reporter assay and western blot analysis. Subsequently, the clinical expression of miR-25 and KLF4 was investigated. Previous studies have reported the role of KLF4 on inducible senescence in the process of the generation of induced pluripotent stem cells (32–34). Xu et al (35) clarified that cell senescence may be promoted by KLF4 via the miR-203-survivin-p21 pathway. Studies have indicated that KLF4 may act as an anti-oncogene in lung cancer (36,37). Exogenous KLF4 may reduce the colony formation and viability ability of cells in in vitro assays. Additionally, overexpressing KLF4 in lung cancer cells also inhibits tumor proliferation in vivo (38). The findings of the present study demonstrated that the knockdown of KLF4 promoted cell invasion and migration, similar to the effects of miR-25 overexpression; However, overexpressing KLF4 induced the opposite effects.

Providing that the restoration of KLF4 partly reversed the effect of miR-25 on inhibiting lung cancer cell invasion and migration, the present study aimed to identify the downstream cascade effectors. Based on previous work, particular attention given to ERK1/2, a promoter of cell invasion progression. Zheng et al (39) demonstrated that KLF4 was involved in antiproliferative functions in vascular smooth muscle cells in culture, and knockdown of KLF4 slightly increased p-ERK1/2 levels. Thus, the present study aimed to verify whether miR-25 regulated the ERK signaling pathway by altering the expression of KLF4. Markers of invasion (MMP11, vimentin) and epithelial-to-mesenchymal transition (E- and N-cadherin) were detected at the protein level. The results of the present study demonstrated that the downregulation of KLF4 activated the ERK signaling pathway, increasing the expression of N-cadherin, MMP11 and vimentin, with reduced E-cadherin expression.

Currently, few reports have investigated the downstream signaling pathway of miR-25, or the association between miR-25 and ERK signaling. Additionally, few studies have assessed the expression of miR-25 and KLF4 in clinical samples. The limited number of clinical sample abundance and lack of further research regarding how KLF4 affects the ERK pathway were limitations of the present study.

In summary, miR-25 was significantly overexpressed in NSCLC tissues compared with paracancerous tissue in the present study, and the exogenous addition of miR-25 significantly promoted cell motility of NSCLC cells by reducing the expression of KLF4. In addition, miR-25 was observed to induce migration and invasion of NSCLC cells by regulating the ERK signaling pathway, particularly by affecting the phosphorylation status of molecules upstream of ERK1/2. The results of the present study indicated that miR-25 may be a potential therapeutic target for future NSCLC treatment.

References