Department of Biomedicine & Health Sciences, Department of Medical Lifescience, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea
In Epstein-Barr virus (EBV)-infected epithelial cancers, BamHI A rightward transcript (BART) miRNAs are highly expressed. However, only a few target genes of BART miRNAs have been investigated. Our mRNA microarray data showed that DKK1 was markedly down-regulated in EBV-associated gastric carcinoma (EBVaGC) cells. Using luciferase reporter assay we tested whether miR-BART10-3p regulates DKK1 by directly targeting the 3'-UTR of DKK1 mRNA. We observed that miR-BART10-3p transfection decreased DKK1 expression, while an LNA inhibitor of miR-BART10-3p (LNA-miR-BART10-3p(i)) increased DKK1 expression. Furthermore, miR-BART10-3p and siDKK1 promoted cell proliferation and migration. In contrast, transfecting GC cells with LNA-miR-BART10-3p(i) or DKK1 over expression vector suppressed cell proliferation and migration. Our results suggest that miR-BART10-3p may be involved in the tumor progression of EBVaGC by targeting DKK1.
Keywords: Epstein-Barr virus, BART miRNA, DKK1, cell proliferation, cell migration
Gastric carcinoma (GC) is the third leading cause of cancer mortality worldwide . Most GC cases are diagnosed at an advanced stage, and the clinical outcomes remain unpredictable. Recently, the Cancer Genome Atlas (TCGA) classified GC into four subtypes based on molecular characteristics: microsatellite-unstable, genomically stable, chromosomally unstable, and Epstein-Barr virus (EBV)-associated . As GC subtypes have distinct features, investigating potential targets in each subtype may provide guidelines for treating different GC patient populations.
EBV is a gamma herpesvirus harboring oncogenic DNA that infects more than 90% of the world's adult population. EBV is closely associated with several lymphoid and epithelial malignancies. EBV-associated GC (EBVaGC) accounts for almost 10% of GC cases, which is considerable because of the high incidence of GC. EBVaGC cells express restricted EBV latent genes, such as EBNA1, EBERs, BART microRNAs (miRNAs), and latent membrane protein 2A (LMP2A) [3-5].
MiRNAs are short, single-stranded RNAs about 22 nucleotides in length. They modulate gene expression by forming complementary duplexes with their target mRNAs, leading to translational inhibition and degradation of the target mRNAs. Single miRNA can regulate many targets, and more than one miRNA may target an individual mRNA [6-8]. Because miRNAs have the ability to inhibit gene expression, they play important roles in human cancers. For example, they regulate potential oncogenes or tumor suppressor genes [9, 10]. EBVaGC cells express high levels of BART miRNAs, which are encoded in the BamHI fragment A rightward transcript (BART) region [4, 11, 12]. By targeting cellular or viral genes, these miRNAs are involved in the regulation of multiple cellular responses such as host cell proliferation, apoptosis [12-15], and immune escape [16, 17]. Thus, EBV miRNAs are thought to contribute to the carcinogenesis of EBVaGC. Further studies are needed to elucidate the functions of most EBV-encoded miRNAs.
The Dickkopf (DKK) protein family consists of four members (DKK1~4) and a unique DKK3-related gene, Soggy (DKKL1). DKK1, the most studied member, is a soluble secreted protein involved in embryonic development. DKK1 is known as an antagonist of canonical Wnt signaling. DKK1 competitively interacts with a Wnt co-receptor (LDL receptor-related protein (LRP) 5 or LRP6), leading to the degradation of β-catenin [18-20]. DKK1 is also involved in various tumor processes such as cell proliferation, survival, migration, and invasion [21, 22]. However, the way in which DKK1 functions in EBVaGC cells has not been revealed.
In this study, we founded that DKK1 was markedly decreased in EBVaGC cell lines, and then investigated whether DKK1 was regulated by EBV BART miRNAs or not.
AGS is an EBV-negative gastric carcinoma cell line, while SNU-719 and AGS-EBV are EBV-positive gastric carcinoma cell lines [23, 24]. All gastric carcinoma cells were cultured in RPMI-1640 containing 10% fetal bovine serum, 100 U/ml penicillin, and 100 µg/ml streptomycin. AGS-EBV cells were AGS infected with a recombinant Akata virus . To culture AGS-EBV cells, 400 µg/ml of G418 (Gibco, Carlsbad, CA, USA) was added to the medium. The human embryonic kidney cell line HEK293T was cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% FBS, 100 U/ml penicillin, and 100 µg/ml streptomycin. All cells were incubated at 37°C and supplemented with 5% CO2.
The DKK1 sequence used for miRNA target prediction was extracted from the National Center for Biotechnology Information database (NM_012242.3). To examine whether the 3′-UTR of DKK1 could be targeted by BART miRNAs, we used a publicly available RNA hybrid program (http://bibiserv.techfak.uni-bielefeld.de/rnahybrid/). This tool finds the minimum free energy of hybridization needed for miRNAs to specific RNAs.
All BART miRNA mimics and the scrambled control were purchased from Genolution Pharmaceuticals (Seoul, South Korea). The locked nucleic acid (LNA) inhibitor of miR-BART10-3p (LNA-miR-BART10-3p(i)) and the negative control LNA-miRNA inhibitor (control-LNA) were purchased from Exiqon (Vedbaek, Denmark). All transfection experiments were performed using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's protocol. Protein and RNA were extracted 48 h after transfection.
The full-length 3'-UTR of DKK1 was amplified from the cDNA of AGS cells. The 3'-UTR of DKK1 was then cloned into XhoI/NotI sites located between the Renilla luciferase-coding sequence and the poly (A) site of the psiCHECK-2 plasmid (Promega, Madison, WI, USA) to produce psiC_DKK1. The primers used to amplify DKK1 were 5'-TCTAGGCGATCGCTCGAGACCAGCTATCCAAATGCAGT-3' and 5'-TTATTGCGGCCAGCGGCCGCAGGTATTATTAATTTATTGGAAACTATTTTTGA-3'. Mutations were introduced into the seed match sequence of psiC_DKK1 to produce psiC_DKK1m using an EZchange site-directed mutagenesis kit (Enzynomics, Daejeon, South Korea). The primers used for this purpose were 5'-ACAAAATTTTTGTACACATTGATTGTTATCTTGACTGA-3' and 5'-TATCAAGAGGAAAAATAGGCAGTGCAG-3'. The DKK1 coding sequences (DKK1- CDS) were amplified by using cDNA prepared from AGS cells. The primers used were 5'-TGCTAGCGGCCGCTCGAGATGATGGCTCTGGGCGCAGC-3' and 5'-CTTATCATGTCTGGATCCTTAGTGTCTCTGACAAGTGTG-3'. The amplicons were cloned into the XhoI/BamHI sites of the pCEP4 vector (Invitrogen) by using an EZ-Fusion cloning kit (Enzynomics, Daejeon, South Korea). The constructed DKK1 expression vector (pCEP4DKK1) contained a hygromycin selection marker for enrichment of transfected cells.
In order to establish stable cell lines, AGS-EBV cells were seeded into 100 mm cell culture dishes. After 24 h, the cells were transfected with 20 µg of empty vector (pCEP4) or pCEP4DKK1. After selection of transfected cells following 15 days of treatment with 200 µg/ml hygromycin, the cells were harvested to assess DKK1 expression.
To investigate the effect of BART miRNAs on the expression of DKK1, HEK293T cells or AGS cells were seeded in 96-well plates (5103 cells/well). After 24 h, the cells were co-transfected with 20 ng of psiC_DKK1 and 20 nM of indicated BART miRNA. To confirm sequence specific binding of miR-BART20-5p, a seed- sequence-mutated miR-BART10-3p (miR-BART10- 3pm) was also transfected. Luciferase activity was measured 48 h post-transfection using the Dual-Glo luciferase reporter assay system (Promega). For each sample, Renilla luciferase activity was normalized using firefly luciferase activity.
AGS, AGS-EBV, or SNU-719 cells were harvested, and total RNA was extracted using the RNAiso Plus reagent (TaKaRa, Tokyo, Japan) according to the manufacturer's instructions. cDNA was synthesized using 3 μg total RNA, oligo(dT) primers (Macrogen, Seoul, South Korea), and Moloney murine leukemia virus reverse transcriptase (Invitrogen). Real-time PCR for the indicated genes was carried out using TOPrealTM Qpcr 2x Pre-MIX SYBR-Green (Enzynomics, Daejeon, Korea) with a real-time PCR system (CFX96, BioRad, Hercules, CA, USA). The sequences of the primers were 5'-AGCACCTTGGATGGGTATTC-3' and 5'-CACAATCCTGAGGCACAGTC-3' for DKK1, and 5'-ATGGGGAAGGTGAAGGTCG-3' and 5'-GGGGTCATTGATGGCAACAATA-3' for GAPDH. PCR conditions were 95°C for 10 min, followed by 35 cycles of 95°C for 10 s, 60°C for 30 s, and 72°C for 30 s. To confirm specific amplification of the PCR product, dissociation curves were checked routinely. For this, reaction mixtures were incubated at 95°C for 60 s, and then ramped from 60°C to 95°C at a heating rate of 0.1°C/s, with fluorescence measured continuously. Relative gene expression was calculated using quantification cycle (Cq) values, with GAPDH as an internal standard.
miRNA cDNA was synthesized using the Mir-X miRNA first-strand synthesis kit (Clontech, Mountain View, CA, USA) according to the manufacturer's instructions. Real-time quantitative PCR was performed using TOPrealTM Qpcr 2x Pre-MIX SYBR-Green (Enzynomics, Daejeon, Korea). The forward primer used for miR-BART10-3p was 5'-TACATAACCATGGAGTTGGCTGT-3'. All amplifications were performed in triplicate, and values were normalized to the value for an endogenous control, U6. The U6 RT primer was supplied in the kit.
Cell proliferation was analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay (Amresco, Shanghai, China). AGS-EBV, SNU-719, or DKK1 over-expressing AGS-EBV cells ( cells/well) were seeded into 96-well plates. After the indicated periods following transfection, 20 µl of MTT solution (5 mg/ml) was added to each well. The absorbance at 595 nm was measured with a SoftMax apparatus (Molecular Devices, Sunnyvale, CA, USA) 4 h after adding MTT solution.
Small interfering RNAs (siRNAs) specific for DKK1 (siDKK1), and a control siRNA lacking any known target, were synthesized by Bioneer (Daejon, South Korea). The sequence of the siDKK1 was 5'-CACUAAACCAGCUAUCCAA-3'. AGS-EBV cells (1 106 cells/dish) were transfected with 30 nM siRNA using Lipofectamine 2000 (Invitrogen) in 100 mm dishes. Cells were harvested to analyze DKK1 expression 48 h after transfection.
Cell lysates in radioimmunoprecipitation assay (RIPA) buffer containing protease inhibitors (1 mM phenylmethylsulfonyl fluoride, 10 µg/ml leupeptin, 10 µg/ml pepstatin A, and 10 µg/ml aprotinin) were mixed with 5loading buffer (Fermentas, Waltham, MA, USA) and heated at 95°C for 5 min. Samples were separated electrophoretically on 8% sodium dodecyl sulfate (SDS)-polyacrylamide gels, and the separated proteins were transferred to a polyvinylidene fluoride (PVDF) membrane (Millipore, Billerica, MA, USA). Membranes were blocked and probed with the following antibodies: rabbit anti-DKK1 (1:500; Cell Signaling Technology, Danvers, MA, USA), mouse anti-β-catenin (1:500; Santa Cruz Biotechnology), and rabbit anti-β-actin (1:3,000; Cell Signaling Technology). Bound antibodies were detected with horseradish peroxidase (HRP)-conjugated anti-mouse or anti-rabbit secondary antibodies (Santa Cruz Biotechnology) at a dilution of 1:3,000 for 45 min at room temperature. Protein bands were visualized using an enhanced chemiluminescence detection system (Amersham Bioscience, GE Healthcare, Piscataway, NJ, USA), and the membrane was exposed to X-ray film (Agfa, Mortsel, Belgium). Anti-β-actin antibody was used to confirm that loading was comparable between gel lanes. The density of each protein band was read and quantified using ImageJ software.
To study the effect of miR-BART10-3p on cell migration, cells (3 x 105 cells/well) were seeded into 12-well plates and allowed to reach 90-95% confluence. Cells were scratched with a sterile 200 µl pipette tip through the confluent monolayer and subsequently washed with phosphate buffered saline to remove cell debris. Four hours later, the cells were transfected with miR-BART10-3p, LNA-miR-BART10-3p(i), siDKK1, or pCEP4DKK1. The cells were then cultured in RPMI-1640 medium containing 3% FBS at 37˚C in a humidified chamber supplied with 5% CO2. The scratched wounds were observed by an Axiovert 200 (Carl Zeiss, Thornwood, NY, USA) microscope just after transfection (time 0) and 48 h after transfection. Photographs were taken to assess the level of migration in each group of transfected cells, and wound areas were measured by ImageJ software. The experiments were performed in triplicate.
The data were analyzed using the Student's t-test, two-way repeated-measure analysis of variance (ANOVA), or curve fit. Analyses were performed using GraphPad Prism software (GraphPad Software, San Diego, CA, USA). P-values <0.05 were considered statistically significant. All results were expressed as the mean standard deviation (SD).
To analyze the effect of EBV infection on DKK1 expression, we compared microarray data  between AGS and AGS-EBV cells. Noticeably, DKK1 showed reduced expression in EBV-infected cells (Fig. 1A). To validate these data, DKK1 expressions in AGS and AGS-EBV cell lines were determined by real-time RT-PCR and Western blot. We found that DKK1 mRNA and protein levels decreased in AGS-EBV cells by 71% and 47%, respectively, compared to those in AGS cells (Fig. 1B-D). We also analyzed β-catenin expression to assess the possible relationship between DKK1 and β-catenin. The results showed that β-catenin protein levels are elevated in AGS-EBV cells than in AGS cells (Fig. 1D).
Reduction of DKK1 expression in EBV-infected GC cells. (A) Microarray analyses of AGS and AGS-EBV cells (n=5). (B) DKK1 mRNA expression was measured by real-time RT-PCR using a SYBR green qPCR kit. (C) DKK1 and β-catenin protein levels were assessed by Western blot analysis. Anti-β-actin antibody was used as a loading control. (D) Western blots were performed on two additional sets of independently cultured cells. Results were normalized using β-actin and expressed as ratios relative to values obtained from AGS cells. Error bars indicate the SD (n=3).
To test whether EBV miRNAs down-regulate DKK1 expression in EBV-positive cells, EBV miRNAs showing a seed match to DKK1 were identified using an RNA hybrid program (http://bibiserv.techfak.uni-bielefeld.de/rnahybrid/). Four BART miRNAs (miR-BART5-5p, miR-BART8-3p, miR-BART10-3p, and miR-BART17-5p) were selected to further analyze their possible interaction with the 3'-UTR of DKK1 (Fig. 2A).
To investigate whether these miRNAs directly targeted DKK1, we constructed a luciferase reporter vector containing the entire 3'-UTR region of DKK1 (psiC_DKK1). The psiC_DKK1 reporter vector and each of the four BART miRNA mimics were co-transfected into HEK293T cells. Only the miR-BART10-3p mimic significantly reduced Luciferase activity when compared to the scrambled control in HEK293T cells (Fig. 2B). Because the other mimics did not inhibit luciferase activity, miR-BART10-3p was selected for further studies.
To identify whether miR-BART10-3p specifically targets DKK1, miR-BART10-3pm, which contains a mutation at sites 1-3 of the seed sequence of miR-BART10-3p, was used for a luciferase assay (Fig. 2C). Unlike miR-BART10-3p, the mutant mimic (miR-BART10-3pm) failed to suppress luciferase activity in HEK293T cells (Fig. 2D). We also substituted sites 2, 3, 4, and 7 of the seed match sequence for miR-BART10-3p in psiC_DKK1 to prepare psiC_DKK1m (Fig. 2C). When psiC_DKK1m was transfected into HEK293T (Fig. 2D) or AGS (Fig. 2E), luciferase activity was not reduced with co-transfected miR-BART10-3p. These results suggest that miR-BART10-3p inhibits DKK1 expression through a sequence-specific interaction with the 3'-UTR of DKK1 mRNA.
We next tested the effect of endogenously expressed miR-BART10-3p on DKK1 expression in EBV-infected GC cells using an LNA-inhibitor (LNA-miR-BART10-3p(i)). When co-transfected into ASG-EBV or SNU-719 cells, LNA-miR-BART10-3p(i) increased the luciferase activity of psiC_DKK1, but not that of psiC_DKK1m (Fig. 2F). These results suggest that the endogenously expressed level of miR-BART10-3p in ASG-EBV and SNU-719 cells was sufficient to suppress DKK1 expression by specifically targeting the 3'-UTR of DKK1. Collectively, these results support the hypothesis that miR-BART10-3p binds to the 3'-UTR of DKK1 sequence specifically.
Screening of BART miRNAs targeting DKK1. (A) Seed match results between BART miRNAs and the 3'-UTR of DKK1 mRNA. (B) Luciferase activity was measured in HEK293T cells co-transfected with BART miRNA mimics and psiC_DKK1. (C) Sequences of the seed match sequence-mutated (psiC_DKK1m) 3'-UTR of DKK1 mRNA (upper panel) and mutant miR-BART10-3p (miR-BART10-3pm) (lower panel) are shown. (D) Luciferase activity was measured in HEK293T cells co-transfected with the miR-BART10-3p mimic or miR-BART10-3pm, and psiC_DKK1 or psiC_DKK1m. (E) Luciferase activity was measured in AGS cells co-transfected with 30 nM BART miRNA mimics, and wild type or mutant luciferase reporter vector. (F) Luciferase activity was measured in AGS-EBV (left panel) or SNU-719 (right panel) cells co-transfected with the control LNA or LNA-miR-BART10-3p(i), and psiC_DKK1 or psiC_DKK1m. Luciferase activity was measured 48 h after transfection. Luciferase activity was normalized using firefly luciferase activity, and expressed as a ratio to the luciferase activity obtained from the scrambled control-transfected cells. Error bars indicate the SD (n=3).
Unexpectedly, AGS cells co-transfected with the psiCHECK empty vector and miR-BART10-3p showed up-regulated luciferase activity (Fig 2E). Accordingly, both EBV infected GC cell lines (AGS-EBV and SNU-719) showed down-regulated luciferase activity when co-transfected with psiCHECK and LNA-miR-BART10-3p(i) (Fig 2F).
To confirm the regulatory effect of miR-BART10-3p on DKK1, AGS cells were transfected with miR-BART10-3p, and DKK1 mRNA levels were quantified by real-time RT-PCR. Transfected miR-BART10-3p reduced DKK1 mRNA expression by 25% compared to the scrambled control in AGS cells (Fig. 3A). Likewise, a Western blot analysis revealed that DKK1 protein levels decreased approximately 60% following miR-BART10-3p transfection (Fig. 3B, C). These results support the hypothesis that miR-BART10-3p regulates DKK1 expression. We then investigated the effect of miR-BART10-3p on cell proliferation and migration. A cell proliferation assay revealed that miR-BART10-3p had a growth-enhancing effect on transfected AGS cells (Fig. 3D). A wound healing assay showed that AGS cell migration was significantly enhanced following miR-BART10-3p transfection, relative to transfection with a scrambled control (Fig. 3E, F).
We next investigated whether the endogenously expressed level of miR-BART10-3p was sufficient to affect DKK1 and β-catenin expression in EBV-infected GC cells. Real-time RT-PCR and Western blot were performed to compare DKK1 levels after transfection with LNA-miR-BART10-3p(i) or with control LNA. In AGS-EBV cells, DKK1 mRNA and protein levels increased 2.9-fold and 6.5-fold, respectively, following LNA-miR-BART10-3p(i) transfection relative to cells transfected with control LNA. In SNU-719 cells, DKK1 mRNA and protein levels increased 1.3-fold and 2.9-fold, respectively, by LNA-miR-BART10-3p(i) transfection (Fig. 4A-C). These results indicate that endogenously expressed levels of miR-BART10-3p efficiently suppressed DKK1 in EBV-infected GC cells. In contrast, β-catenin protein levels decreased following by LNA-miR-BART10-3p(i) transfection in both AGS-EBV and SNU-719 cells. A cell proliferation assay showed reduced growth by LNA-miR-BART10-3p(i) transfection in both AGS-EBV and SNU-719 (Fig. 4D). Next, we examined the effect of miR-BART10-3p inhibition on cell migration. A wound healing assay showed suppressed cell migration following transfection with LNA-miR-BART10-3p(i) than control LNA (Fig. 4E, F).
Effect of miR-BART10-3p on DKK1 expression in AGS cells. AGS cells were transfected with 30 nM scrambled control or miR-BART10-3p. After 48 h, cells were harvested for RNA and protein preparation. (A) Real-time RT-PCR analysis was carried out to access DKK1 mRNA expression using a SYBR green qPCR kit. (B) DKK1 and β-catenin protein levels were analyzed by Western blot analysis. Anti-β-actin antibody was used as a loading control. (C) Western blots were performed on two additional sets of independently transfected AGS cells. Results were normalized to β-actin and are expressed as ratios. (D) At the indicated times after transfection, 20 µl of MTT solution was added to each well to assess cell proliferation. (E) A wound healing assay was performed to evaluate the effect of miR-BART10-3p on cell migration using transfected AGS cells. (F) Widths between wound edges were evaluated using ImageJ software. The percentages of wound closure from three independent experiments are shown as bar graphs. Error bars indicate the SD (n=3).
Effect of LNA-miR-BART10-3p(i) in AGS-EBV and SNU-719 cells. AGS-EBV or SNU-719 cells were transfected with 30 nM control LNA or LNA-miR-BART10-3p(i). After 48 h, cells were harvested for RNA and protein preparation. (A) Real-time RT-PCR analysis of DKK1 mRNA expression was carried out using a SYBR green qPCR kit. (B) DKK1 and β-catenin protein levels were analyzed by Western blot analysis. Anti-β-actin antibody was used as a loading control. (C) Western blots were performed on two additional sets of independently transfected AGS-EBV or SNU-719 cells. Results were normalized to β-actin and are expressed as ratios. (D) At the indicated times after transfection, 20 µl of MTT solution was added to each well to assess cell proliferation. (E) A wound healing assay was performed to evaluate the effect of LNA-miR-BART10-3p(i) on cell migration using transfected AGS-EBV cells. Widths between wound edges were evaluated using ImageJ software. The percentages of wound closure from three independent experiments are shown as bar graphs. Error bars indicate the SD (n=3).
To investigate whether siRNA targeting DKK1 (siDKK1) generates a similar phenotype to miR-BART10-3p, siDKK1 was transfected into AGS cells. After 48h, real-time RT-PCR and Western blot analyses were performed to assess DKK1 and β-catenin expression levels. The siDKK1 transfection of AGS cells efficiently knocked down DKK1 mRNA expression (by approximately 76%, Fig. 5A) and protein expression (by approximately 72%, Fig. 5B, C). In addition, β-catenin level was increased by knocking down DKK1. To further explore the role of DKK1 in AGS cells, we analyzed the effect of siDKK1 in controlling cell proliferation and migration. MTT and wound healing assays demonstrated that DKK1 knockdown by siDKK1 transfection promoted cell proliferation (Fig. 5D) and migration (Fig. 5E, F).
The effect of DKK1 knockdown was accessed in AGS-EBV cells, too. After 48 h, real-time RT-PCR and Western blot analyses were performed to assess DKK1 and β-catenin expression levels. The siDKK1 transfection of AGS-EBV cells efficiently knocked down DKK1 mRNA expression (by approximately 65%, Fig. 6A) and protein expression (by approximately 68%, Fig. 6B, C). In addition, β-catenin level was increased by knocking down DKK1.
To further explore the role of DKK1 in AGS-EBV cells, we analyzed the effect of siDKK1 in controlling cell proliferation and migration. MTT and wound healing assays demonstrated that DKK1 knockdown by siDKK1 transfection promoted cell proliferation (Fig. 6D) and migration (Fig. 6E, F).
In order to confirm the function of DKK1 in EBV-positive GC cells, we tested the effect of DKK1 over-expression on cell proliferation and migration. AGS-EBV cells were transfected with a DKK1 over-expression vector (pCEP4DKK1) or an empty control vector (pCEP4). After selecting for 15 days in 200 µg/ml hygromycin-containing media, the transfected cells were used for analyses. Real-time RT-PCR and Western blot analyses showed that DKK1 mRNA and protein levels increased 5.2-fold and 8.2-fold, respectively, in pCEP4DKK1-transfected AGS-EBV cells (Fig. 6A-C). Conversely, β-catenin level was suppressed by DKK1 overexpression. As expected, the over-expression of DKK1 in AGS-EBV cells suppressed cell proliferation and migration (Fig. 6D-F).
Effect of DKK1 knockdown using siDKK1 in AGS cells. AGS cells were transfected with 20 nM siDKK1 or control siRNA. (A) A real-time RT-PCR analysis of DKK1 mRNA expression was carried out using a SYBR green qPCR kit. (B) DKK1 and β-catenin protein levels were analyzed by Western blot analysis. Anti-β-actin antibody was used as a loading control. (C) Western blots were performed on two additional sets of independently transfected AGS cells. Results were normalized to β-actin and are expressed as ratios. (D) At the indicated times after transfection, 20 µl of MTT solution was added to each well to assess cell proliferation. (E) Widths between wound edges were evaluated using ImageJ software. The percentages of wound closure from three independent experiments are shown as bar graphs. Error bars indicate the SD (n=3).
Effect of DKK1 knockdown using siDKK1 in AGS-EBV cells. AGS-EBV cells were transfected with 20 nM siDKK1 or control siRNA. (A) A real-time RT-PCR analysis of DKK1 mRNA expression was carried out using a SYBR green qPCR kit. (B) DKK1 and β-catenin protein levels were analyzed by Western blot analysis. Anti-β-actin antibody was used as a loading control. (C) Western blots were performed on two additional sets of independently transfected AGS-EBV cells. Results were normalized to β-actin and are expressed as ratios. (D) At the indicated times after transfection, 20 µl of MTT solution was added to each well to assess cell proliferation. (E) Widths between wound edges were evaluated using ImageJ software. The percentages of wound closure from three independent experiments are shown as bar graphs. Error bars indicate the SD (n=3).
Effect of DKK1 over-expression in AGS-EBV cells. (A) A real-time RT-PCR analysis of DKK1 mRNA expression was carried out using a SYBR green qPCR kit. (B) DKK1 and β-catenin protein levels were analyzed by Western blot. Anti-β-actin antibody was used as a loading control. (C) Western blots were performed on two additional sets of independently transfected AGS-EBV cells. Results were normalized to β-actin and are expressed as ratios. (D) At the indicated times after transfection, 20 µl of MTT solution was added to each well to assess cell proliferation. (E) Widths between wound edges were evaluated using ImageJ software. The percentages of wound closure from three independent experiments are shown as bar graphs. Error bars indicate the SD (n=3).
In this study, we demonstrated a role for miR-BART10-3p and DKK1 in the cell proliferation and migration of EBV-infected cells. Data from microarrays, real-time RT-PCR, and Western blot assays revealed that DKK1 expression was suppressed in EBV-infected cells. We therefore hypothesized that DKK1 may function as a tumor suppressor in EBV-infected GC cells. miR-BART10-3p reduced the expression of DKK1 by directly targeting the 3'-UTR of DKK1. Accordingly, the inhibitor of miR-BART10-3p rescued DKK1 expression in AGS-EBV and SNU-719 cells. In addition, miR-BART10-3p induced cell proliferation and migration, which was mimicked by siDKK1. In contrast, the inhibitor to miR-BART10-3p reduced cell proliferation and migration, as did over-expressed DKK1.
Unexpectedly, the luciferase activity of the psiCHECK control vector was enhanced by co-transfected miR-BART10-3p mimic (Fig. 2D, E) and suppressed by a co-transfected LNA-BART10-3p(i) inhibitor (Fig. 2F). To understand these observations, we have checked coincidental seed match between miR-BART10-3p and psiCHECK control vector, but could not find the possibility. Further investigations are warranted to clarify the underlying mechanisms of these observations.
In AGS and AGS-EBV cells, miR-BART10-3p enhanced cell proliferation and migration suggesting that BART10-3p may contribute to EBVaGC metastasis. Consistent with our findings, Yan et al.  demonstrated that miR-BART10-3p promotes the invasion and migration capabilities of nasopharyngeal carcinoma (NPC) cells. They showed that miR-BART10-3p targeted the beta-transducin repeat-containing E3 ubiquitin protein ligase (BTRC) in NPC. Taken together, miR-BART10-3p may induce metastasis in EBV-associated carcinomas such as NPC and GC by promoting cell growth and migration.
It is well known that DKK1 acts as an important negative regulator of Wnt/β-catenin signaling by directly binding to LRP5/6. In the absence of Wnt stimulation, β-catenin is phosphorylated by CK1α and GSK3β, and then degraded by β-TrCP-mediated ubiquitination. On the other hand, Wnt binding to the Frizzled (FZD) receptor and a co-receptor (LRP5/6) leads to the accumulation of β-catenin in the cytoplasm, allowing localization to the nucleus. There, β-catenin interacts with TCF/LEF to transactivate downstream genes including cyclin D1 and c-myc. Wnt target genes are diverse, and cell- and context-dependent [27, 28]. DKK1 has been shown to be regulated by TCF/β-catenin . Accordingly, previous studies showed increase in c-myc, cyclin D1, and β-catenin expression in EBVaGC cells [29-32]. We also observed that AGS-EBV cells expressed increased levels of β-catenin, along with decreased levels of DKK1, relative to AGS cells.
Even though miR-BART10-3p transfected AGS-EBV cells showed decreased DKK1 expression at both mRNA and protein levels, there might be some other EBV factor(s) down regulating DKK1. For example, DKK1 promoter has 5' CpG islands, and aberrant methylation of this region has been implicated in DKK1 silencing observed in GC , colorectal cancer , cervical cancer , and multiple myeloma . Notably, DNA methylation of both host and viral genomes is one of the features of EBVaGC [2, 37, 38].
DKK1 has been reported to be down- or up-regulated in various cancers and the role of DKK1 in cancer is controversial. DKK1 is elevated in multiple myeloma , breast cancer [40, 41], hepatocellular carcinoma , and prostate cancer [43, 44]. DKK1 has been shown to be a tumor suppressor as well. For example, DKK1 over-expression restored the epithelial phenotype and decreased expression of the EMT transcription factor in colon cancer . DKK1 is down-regulated in metastatic LM-MCF-7 breast cancer cells, and involved in cell proliferation and dysregulation of the Wnt/β-catenin signaling pathway .
In GC, increased levels of serum DKK1 have been reported . However, Sato et al.  have demonstrated that DKK family genes are frequent targets of epigenetic silencing in gastrointestinal tumors. Jia et al.  showed that DKK1 is decreased in the serum and tissues of GC patients. The same authors demonstrated that miR-493 promotes GC progression by suppressing DKK1 expression. We observed that DKK1 knockdown by siDKK1 transfection exerted similar effect with miR-BART10-3p. These results indicated that DKK1 play an important role in promoting gastric cancer cell migration and invasion. Furthermore, slightly bigger changes were observed in AGS cells than in AGS-EBV cells following DKK1 depletion. These may be due to the fact that expression of DKK1 is somewhat suppressed in AGS-EBV cells than in AGS by endogenously expressed miR-BART10-3p. Moreover, we showed reduced expression of DKK1 by miR-BART10-3p causing enhanced cell proliferation and migration in EBVaGC cells. Our data support the hypothesis that DKK1 functions as a tumor suppressor in EBV-associated tumors.
β-Catenin is not only a key protein in Wnt/β-catenin signaling, but also interacts with E-cadherin to play an important role in cell junctions. This binding prevents nuclear translocation of β-catenin, while loss of E-cadherin by such as tumor likely promotes β-catenin release from membrane, and promotes epithelial mesenchymal transition . Here we found that DKK1 expression is inversely associated with β-catenin expression in EBVaGC. Our results support that β-catenin is regulated by DKK1.
Taken together, our findings demonstrate that miR-BART10-3p regulates EBVaGC cell proliferation and migration by directly targeting DKK1, which functions as a tumor suppressor. Thus, miR-BART10- 3p may serve as a potential therapeutic target for patients with EBVaGC.
EBV: Epstein-Barr virus; BART: BamHI A rightward transcript; EBVaGC: EBV-associated gastric carcinoma; GC: gastric carcinoma; TCGA: The cancer genome atlas; DKK1: Dickkopf 1; miRNAs: microRNAs; UTR: Untranslated region; RT-PCR: reverse transcription polymerase chain reaction; LNA: locked nucleic acid; siNC: siRNA negative control.
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2018R1D1A1B07041763).
The authors have declared that no competing interest exists.
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Corresponding author: Suk Kyeong Lee, Mailing address: Department of Biomedicine & Health Sciences, Department of Medical Lifescience, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea. Tel: + 82-2-2258-7480; Fax: + 82-2-535-7481; E-mail: sukkleeac.kr