Circ_0003356 suppresses gastric cancer growth through targeting the miR-668-3p/SOCS3 axis

Wei-Dong Li,Hai-Tao Wang,Yue-Ming Huang,Bo-Hao Cheng,Li-Jun Xiang,Xin-Hao Zhou,Qing-Yan Deng,Zhi-Gang Guo,Zhi-Feng Yang,Zhi-Fen Guan,Yao Wang

Wei-Dong Li,Hai-Tao Wang,Yue-Ming Huang,Bo-Hao Cheng,Li-Jun Xiang,Xin-Hao Zhou,Qing-Yan Deng,Zhi-Gang Guo,Zhi-Feng Yang,Zhi-Fen Guan,Yao Wang,Department of Gastrointestinal Surgery,Zhongshan City People’s Hospital,Zhongshan 528403,Guangdong Province,China

Abstract BACKGROUND Circular RNAs(circRNAs)have attracted extensive attention as therapeutic targets in gastric cancer(GC).Circ_0003356 is known to be downregulated in GC tissues,but its cellular function and mechanisms remain undefined.AIM To investigate the role of circ_0003356 in GC at the molecular and cellular level.METHODS Circ_0003356,miR-668-3p,and SOCS3 expression were assessed via quantitative real time-polymerase chain reaction(qRT-PCR).Wound healing,EdU,CCK-8,flow cytometry and transwell assays were used to analyze the migration,proliferation,viability,apoptosis and invasion of GC cells.The subcellular localization of circ_0003356 was monitored using fluorescence in situ hybridization.The interaction of circ_0003356 with miR-668-3p was confirmed using RIP-qRT-PCR,RNA pull-down,and dual luciferase reporter assays.We observed protein levels of genes via western blot.We injected AGS cells into the upper back of mice and performed immunohistochemistry staining for examining E-cadherin,N-cadherin,Ki67,and SOCS3 expressions.TUNEL staining was performed for the assessment of apoptosis in mouse tumor tissues.RESULTS Circ_0003356 and SOCS3 expression was downregulated in GC cells,whilst miR-668-3p was upregulated.Exogenous circ_0003356 expression and miR-668-3p silencing suppressed the migration,viability,proliferation,epithelial to mesenchy-mal transition(EMT)and invasion of GC cells and enhanced apoptosis.Circ_0003356 overexpression impaired tumor growth in xenograft mice.Targeting of miR-668-3p by circ_0003356 was confirmed through binding assays and SOCS3 was identified as a downstream target of miR-668-3p.The impacts of circ_0003356 on cell proliferation,apoptosis,migration,invasion and EMT were reversed by miR-668-3p up-regulation or SOCS3 downregulation in GC cells.CONCLUSION Circ_0003356 impaired GC development through its interaction with the miR-668-3p/SOCS3 axis.

Key Words:Epithelial-mesenchymal transition;Circ_0003356;Gastric cancer;Invasion;Proliferation;Migration

INTRODUCTION

Gastric cancer(GC)encompasses a range of gastrointestinal malignancies[1,2],and ranks as the 2ndmain cause of global cancer-associated deaths[3,4].Chemotherapy,radiotherapy,and surgical resection have progressed GC treatment[5,6],but five-year survival rates remain low[7,8].Personalized therapy has shown promise for GC treatment[9],but more effective anti-GC targets are required.Circular RNAs(circRNAs)regulate GC occurrence and development.The downregulation of circ_SKA3 inhibits the colony formation,proliferation,migration,and invasion of GC cellsin vitroand suppresses tumorigenesisin vivo[10].Circ_0005758 up-regulation can inhibit GC cell proliferation,migration and invasion,and suppress tumor growth in xenograft mice[11].Up-regulation of circ_0021087 impairs proliferation,epithelial to mesenchy-mal transition(EMT),and invasion of GC cells and overpowers tumor development in xenograft mice[12].CircRNA analysis in GSE184882 indicates that circ_0003356 is lowly expressed in GC tissues,but the molecular effects governing its role in GC suppression have not been investigated at the molecular level.

MicroRNAs(miRNAs)regulate the post-transcriptional expression of a number of genes[13,14]and play a key role in GC progression.The overexpression of miR-548 promotes proliferation,migration and invasion of GC cellsin vitro[15].Silencing of miR-762 reduces GC cell viability and facilitates apoptosis[16].Inhibition of miR-4742-5p suppresses the proliferation,migration and invasion of GC cells[17].Especially,miR-668-3p is oncogenic in hepatocellular carcinoma(HCC)[18]and colorectal cancer(CRC)cells[19].

SOCS3 is a negative regulator of hormone and cytokine signaling and plays a key role in cancer development[20,21].Available studies have highlighted the importance of SOCS3 in the manipulation of cancer development.A study from Yuet al[22]have revealed that the downregulation of SOCS3 can reverse the suppressive effects of miR-3173-5p inhibitor on colony formation,cell proliferation,migration,invasion and EMT in prostate cancer cells.Another study from Liet al[23]have reported that SOCS3 overexpression also suppresses spheroid formation and CRC cell proliferation.In particular,SOCS3 is proven to exert an important role against tumor in GC.For instance,inhibition of miR-340 suppresses cell cycle progression through enhancing the expression of SOCS3 in GC cells[24].MiR-665 also serves as an oncogene in GC through the downregulation of SOCS3[25].The regulatory effects of miR-668-3p on SOCS3 in GC cells has not been investigated.Here,we show for the first time that circ_0003356 is downregulated in GC cells and tumor tissues and reveal its association with GC progression.

MATERIALS AND METHODS

Sample collection

GC and normal tissues(n= 80 pairs)were collected from surgical specimens of patients with GC at Zhongshan City People’s Hospital.Patients were diagnosed with GCviahistopathology.No patients had received prior immunotherapy,adjuvant chemotherapy,or radiation therapy before surgery.GC patients were allocated into circ_0003356 low or high-expression groups based on the median expression value in tumor tissues.The Ethics Committee of Zhongshan City People’s Hospital provided approval(K2017-182).All participants agreed to the study and provided informed written consent.

Cell culture

AGS and HGC-27 cell lines(human)and GES-1(non-GC)were cultured in Roswell Park Memorial Institute 1640 medium + 10% fetal bovine serum(FBS)+ 1% streptomycin-penicillin.Cells were maintained at 37 °C 5% CO2.

Quantitative real time-polymerase chain reaction:Cells were lysed in Trizol and total RNA was quantitated on a NanoDrop 2000c spectrophotometer.For circ_0003356 and SOCS3,PrimeScript? RT reagent kits were used for complementary DNA(cDNA)synthesis.For miR-668-3p,a TaqMan miRNA Assay kit was used for cDNA synthesis.cDNA was amplified using BeyoFast? SYBR Green qPCR Mix.Primer sequences as shown in Table 1 were bought from TaKaRa.Relative mRNA expression of circ_0003356 and SOCS3 were normalised to GAPDH and calculated using the 2-ΔΔCtmethod.miR-668-3p was normalised to U6.

Table 1 Primer sequences for quantitative real time-polymerase chain reaction analysis used in this study

Cell transfection

The empty pcDNA3.1 vector,circ_0003356 overexpression vector(pcDNA3.1-circ_0003356),miR-668-3p inhibitor,negative control(NC)inhibitor,miR-668-3p mimic,NC mimic,small interfering RNA(siRNA)against SOCS3(si-SOCS3)and si-NC were bought from GenePharma(Shanghai,China).Above factors were then transfected into AGS and HGC-27 cells using Lipofectamine 3000(Invitrogen,Carlsbad,California,United States)for 48 h.

CCK-8 assay:The proliferation of HGC-27 and AGS cells was evaluatedviaa cell counting kit-8(Dojindo,Osaka,Japan).HGC-27 and AGS cells(1 × 104cells/well)were plated in 96-well plates for incubating 24 h,48 h,72 h and 96 h.After that,each well was treated with CCK-8 reagent(10 μL)for another 1 h.Ultimately,a microplate reader(Bio-Rad,CA,United States)was used for measurement of optical density at 450 nm.

EdU assays:A Cell-Light EdU DNA Cell Proliferation Kit(RiboBio,Guangzhou,China)was used to perform EdU assay.Cells were labeled with 50 μM EdU for 2 h and fixed with 4 % paraformaldehyde(PFA)(4%).Cells were washed in phosphate buffered saline(PBS)containing glycine(2 mg/mL)for 10 min to remove artefacts and permeabilized.Cells were stained with Apollo dye liquor in the dark followed by DAPI.Cells were imaged on a fluorescence microscope.

Flow cytometry analysis:Apoptotic rates were measured by flow cytometry(FACSCalibur,BD,United States).Cells were resuspended in 300 μL binding buffer and incubated with + Annexin V-FITC(5 μL)for 10 min.Cells were labeled with propidium iodide(5 μL)in the dark for 5 min.Apoptotic cells were quantified using FlowJo V10 software.

Wound healing assay:HGC-27 and AGS cells(5 × 104cells/well)were put to 6-well plates coated with extracellular matrix molecule,which were cultured in RPMI1640 including 10% FBS.When the cell monolayer was formed,a sterile pipette tip was utilized for scratching the monolayer and scratch width was recorded under an inverted microscope(TE2000;Nikon,Tokyo,Japan).After being washedviaPBS,FBS-free medium was added to culture cells for 24 h,followed by record of scratch wound.At last,the migration rate was calculated according to the following formula:(1 - 24 h scratch width/0 h scratch width)× 100.

Transwell assay:Matrigel-coated transwell chambers(8 μm;BD Biosciences,Franklin Lakes,NJ,United States)were utilized for evaluating invasion of HGC-27 and AGS cells.In detail,3 × 103cells were resuspended in FBS-free RPMI1640 medium(200 μL),which were appended to the upper chamber.In contrast,RPMI1640 medium containing 10% FBS was appended to bottom chambers.Following 24 h of incubation,cells in upper chambers were removedviaa cotton swab.Cells in bottom chambers were fixedvia4% PFA and stainedvia0.1% crystal violet.At last,the number of these cells was counted through inverted fluorescence microscopy(Leica Microsystems GmbH,Wetzlar,Germany).

Cytoplasmic and nuclear fractions:AGS and HGC-27 cells were lysed on ice in lysis buffer + protease inhibitors and centrifuged for 3 min.The subsequent pellets and supernatants were harvested as nuclear and cytoplasmic fractions.RNA was extracted from each fraction using Buffer SK.Quantitative realtime polymerase chain reaction(qRT-PCR)analysis was performed for the detection of circ_0003356expression.U6 and 18S rRNA were used as controls of cytoplasmic and nuclear transcripts,respectively.

Fluorescence in situ hybridization(FISH):Fluorescencein situhybridization(FISH)was performed using specific probes against circ_0003356 and miR-668-3p.Briefly,cells were fixed in 4% PFA for 15 min and washed with a 70%,95%,and 100% gradient of ethanol.Cell hybridization was performed at 37 °C in a dark incubator.Cells were blocked in 3% normal goat serum and 1% bovine serum albumin for 1 h.Cells were cultured with HRP-conjugated anti-biotin antibodies at 4 °C for 1 d.Cells were imaged on a fluorescence microscope.

Dual luciferase reporter assay:The online database circinteractome and StarBase v2.0 were used to identify predicted targets of circ_0003356 and miR-668-3p.The interaction of circ_0003356 and miR-668-3p or SOCS3 and miR-668-3p were verifiedviadual luciferase reporter(DLR)assays.Briefly,the 3’-UTR sequences of WT circ_0003356 or SOCS3 comprising the miR-668-3p binding sites were cloned into pRLCMV.3’-UTR sequences of circ_0003356 or SOCS3 containing mutant sites for miR-668-3p were also generated.MiR-668-3p mimic or NC mimic were transfected into HGC-27 and AGS cells and luciferase activity was measured 2 d post-transfection.

RNA binding protein immunoprecipitation assay:Cells were lysed in RNA binding protein immunoprecipitation(RIP)buffer and magnetic beads conjugated with anti-Ago2 and anti-immunoglobulin G(IgG)were added to cell lysates.MiR-668-3p and circ_0003356 levels in the beads were analyzed.

RNA pull-down assays:RNA pull-downs were performed using commercial Magnetic RNA-Protein Pull-Down Kits(Pierce).Cells were transfected with 3’-biotinylated miR-668-3p(Bio-miR-668-3p)or Bio-NC mimics.After 2 d,cells were lysed cells and streptavidin-coupled beads added to pull-down biotincoupled RNA complexes.Circ_0003356 enrichment in the bound fractions was subsequently assayed.

Western blot analysis:Cells were lysed in RIPA buffer and protein content assessedviaBCA assays.A total of 20 μg of protein was resolved on 10% sodium dodecyl sulphate-polyacrylamide gel electrophoresis(SDS-PAGE)gels and transferred to on polyvinylidene difluoride membranes.Membranes were blocked in non-fat milk for 1 h and probed with anti-N-cadherin(1:6000,ab76011),anti-E-cadherin(1:10000,ab40772),anti-SOCS3(1:1000,ab280884)and β-actin(1:1000,ab8224)primary antibodies at 4 °C for 24 h.Cells were subsequently labeled with anti-rabbit secondary antibodies(1:2000,ab205718)and proteins were visualized using chemiluminescence.

Establishment of xenograft tumor models:Mice(4-5 wk-old;BALB/c nude;male)were housed at room temperature with 50% humidity and 12 h light/dark cycle.All experiments were approved by the Animal Care and Use Committee of Zhongshan City People’s Hospital(K2017-182).

Mice were injected into the upper back with 1 × 107AGS cells transfected with circ_0003356 or control vector[26].Mice were assigned into 2 groups(n= 6 mice/group):Thecirc_0003356 group and the vector group.After injection for five weeks,mice were anesthetized with pentobarbital sodium and sacrificedviadislocation of cervical vertebrae.Tumors were dissected and tumor volumes calculated(length × width2)/2.

Immunohistochemistry staining:Mice tumor tissues were fixed in formalin and paraffinized.Tumors were cut into 4 μm sections,dewaxed with xylene,and hydrated in ethanol.Sections were boiled in citrate buffer(10 mmol/L)and cultured using H2O2solution(3%)to inhibit endogenous peroxidase activity.Sections were probed with anti-Ki67(1:200,ab16667),anti-SOCS3(1:1000,ab280884),anti-Ncadherin(1:500,ab76011),and anti-E-cadherin(1:500,ab40772)primary antibodies at 4 °C overnight and labeled with HRP-conjugated secondary antibodies(1:500,ab6112)30 min.Cells were stained using DAB substrate and counterstained using hematoxylin.Cells were imaged on a light microscope.

TUNEL staining:TUNEL assay was performed using the commercially availablein situCell Death Detection Kit as per the manufactures recommendations.

Statistical analysis

GraphPad Prism 8.0 was used for data analysis.Experiments were performed on a minimum of 3 occasions and are shown as the mean ± SD.Survival curves were plotted using the Kaplan-Meier method.Data were compared using a student’st-test.

RESULTS

Circ_0003356 expression is down-regulated in GC tissues

Published GEO and GSE184882 datasets were analyzed[27,28].Five circRNAs with significant expression differences in GC tissues were identified and selected for heat map analysis(Figure 1A).Then their expression was further determinedviaqRT-PCR.Five circRNAs with low relative expression in tumor tissues compared to normal tissues were identified(n= 20),amongst which circ_0003356 expression(0.2 ± 0.06532)was the lowest(P= 0.0002,Figure 1B).Circ_0003356 was selected for further analysis.

Circ_0003356 expression was validated in GC normal and tumor tissues(n= 80).As expected,circ_0003356 expression was markedly downregulated in tumor tissues(0.4908 ± 0.02457)compared to normal adjacent tissues(0.99 ± 0.0243;P＜ 0.0001,Figure 1C).Patients with low circ_0003356 expression correlated with a short survival time(P＜ 0.0001,Figure 1D).Moreover,circ_0003356 displayed lower expression in AGS(0.3833 ± 0.06012)and HGC-27 cells(0.4967 ± 0.06012)than GES-1 cells(P= 0.0004,P= 0.0001,Figure 1E).

Circ_0003356 overexpression promotes cell apoptosis and impairs invasion,proliferation,migration and EMT of AGS and HGC-27 cells

Circ_0003356 was overexpressed in AGS and HGC-27 cells to further explore its influence on GC cell proliferation,apoptosis,migration,invasion,and EMT.Circ_0003356 expression in AGS cells(2.613 ± 0.05207)and HGC-27 cells(2.5 ± 0.05774)was dramatically increased following transfection of pcDNA3.1-circ_0003356(P＜ 0.0001,P＜ 0.0001,Figure 2A).Functional analyses showed that the viability of AGS(1.183 ± 0.06155)and HGC-27 cells(1.247 ± 0.0636)at 96 h were attenuated after circ_0003356 overexpression(P= 0.0002,P= 0.0002,Figure 2B).EdU assays also revealed that the proliferative ability of AGS(22.33 ± 1.764)and HGC-27 cells(20 ± 1.732)was attenuated by circ_0003356 overexpression(P= 0.0025,P= 0.0043,Figure 2C).Apoptotic rates in AGS(22.68 ± 0.2887)and HGC-27 cells’(18.38 ± 0.2887)were increased by circ_0003356 overexpression(P＜ 0.0001,P＜ 0.0001,Figure 2D).In terms of the migration and invasion of AGS(24.33 ± 2.728)and HGC-27 cells(20.33 ± 1.764),decreased numbers of invading AGS(168 ± 11.27)and HGC-27 cells(161.7 ± 12.35)were observed in response to circ_0003356 overexpression(P= 0.0001,P= 0.0031,P= 0.0002,P= 0.0016,Figures 2E and F).Circ_0003356 overexpression also attenuated the EMT of AGS(1.07 ± 0.6531,0.57 ± 0.5168)and HGC-27(0.93 ± 0.06533,0.39 ± 0.06137)cells evidenced by reduced N-cadherin expression and the enhanced expression of E-cadherin(P= 0.0006,P= 0.0023,P= 0.0021,P= 0.0007,Figure 2G).

Circ_0003356 directly binds to miR-668-3p

The subvocalization of circ_0003356 in AGS and HGC-27 cells was confirmed through FISH,which showed that circ_0003356 located in AGS and HGC-27 cells’ cytoplasm(Figure 3A).The findings were confirmed by qRT-PCR,showing that the circ_0003356 level was in AGS and HGC-27 cells markedly higher in the cytoplasm(85%)than the nuclear(15%)(Figure 3B).

Target predictions were performed using circinteractome,indentifing binding sites between miR-668-3p and circ_0003356(Figure 3C).We verified this relationshipviaRIP-qRT-PCR,RNA pull-down,and DLR assays.The Ago2 group showed enrichment for circ_0003356 and miR-668-3p in AGS(12.3 ± 0.7024,15.33 ± 0.3801)and HGC-27 cells(11.3 ± 0.6272,14.33 ± 0.6912)compared to the IgG group(P= 0.000087,P= 0.0000029,P= 0.00008,P= 0.00004,Figure 3D).The biotinylated miR-668-3p probe enriched more circ_0003356 than the biotinylated NC probe in AGS(0.9033 ± 0.03756)and HGC-27 cells(0.9167 ± 0.0491)(P= 0.0002,P= 0.0004,Figure 3E).Relative luciferase activity in AGS(0.35 ± 0.06532)and HGC-27(0.31 ± 0.06478)were reduced in cells co-transfected with miR-668-3p mimic and circ_0003356 WT relative to miR-668-3p mimic and circ_0003356 MUT(P= 0.00057,P= 0.00041,Figure 3F).High expression of miR-668-3p was observed in tumor tissues(2.006 ± 0.02872)compared to healthy tissues(0.9984 ± 0.02829)(P＜ 0.0001,Figure 3G).An inverse relationship between the expression of miR-668-3p and circ_0003356 in tumor tissues was also observed(r= -0.8783,P= 0.0007,Figure 3H).

Figure 1 Circ_0003356 is expressed to low levels in gastric cancer tissues.A:CircRNAs in GSE184882 were analyzed and five with the most significant expression differences in gastric cancer(GC)were used for heat map analysis;B:Relative expression of circRNAs in tumor and normal tissues determined by quantitative real-time polymerase chain reaction(qRT-PCR);C:Relative expression of circ_0003356 in tumor and normal tissues determined by qRT-PCR;D:Kaplan-Meier analysis of the correlation between circ_0003356 expression and overall survival of GC patients;E:Relative expression of circ_0003356 in GES-1,HGC-27,and AGS cells determined by qRT-PCR.aP ＜ 0.05,bP ＜ 0.01,cP ＜ 0.001.NC:Negative control;GC:Gastric cancer.

Suppression of miR-668-3p promotes apoptosis and reduces proliferation,migration,invasion,and EMT in AGS and HGC-27 cells

Accordingly,the influences of miR-668-3p on cell migration,apoptosis,proliferation,invasion,and EMT were explored.Firstly,miR-668-3p expression in HGC-27(2.8 ± 0.05508)and AGS(3 ± 0.1155)cells was found to be remarkably higher than GES-1 cells(1.007 ± 0.05207)(P＜ 0.0001,P＜ 0.0001,Figure 4A).When we determined its specific functions,we found that the viability(1.393 ± 0.06128,1.342 ± 0.0636)and proliferative capacity(12.33 ± 1.453,14 ± 2.082)of AGS and HGC-27 cells were attenuated by miR-668-3p suppression(P= 0.00037,P= 0.00039,P= 0.0033,P= 0.0020,Figures 4B and C).Apototic rates in AGS(21.29 ± 0.8838)and HGC-27 cells’(21.09 ± 0.9074)were raised following miR-668-3p suppression(P＜ 0.0001,P= 0.0001,Figure 4D).The migration(25.67 ± 2.603,41.67 ± 2.906 )and invasion(174.7 ± 9.262,175.7 ± 9.025)of AGS and HGC-27 cells were also repressed following miR-668-3p downregulation(P= 0.0001,P= 0.0019,P= 0.0026,P= 0.0023,Figures 4E and F).The EMT of AGS(1.09 ± 0.06348,0.4 ± 0.06137)and HGC-27 cells(0.9 ± 0.05627,0.31 ± 0.06137)was similarly attenuated by miR-668-3p suppression,evidenced by decreased N-cadherin and increased E-cadherin expression(P= 0.00089,P= 0.00051,P= 0.00066,P= 0.00054,Figure 4G).

Figure 2 Upregulation of circ_0003356 promotes cell apoptosis and suppresses proliferation,migration,invasion,and epithelialmesenchymal transition of AGS and HGC-27 cells.A:Relative expression of circ_0003356 in AGS and HGC-27 cells detected by quantitative real-time polymerase chain reaction;B:Cell viability in AGS and HGC-27 cells assessed by CCK-8 assay;C:Proliferation of AGS and HGC-27 cells assessed by EdU assays.D:Apoptosis of AGS and HGC-27 cells assessed by flow cytometry;E:Migration of AGS and HGC-27 cells detected by wound healing assays;F:Invasion of AGS and HGC-27 cells detected by transwell assay;G:Levels of epithelial-mesenchymal transition-related proteins(E-cadherin and N-cadherin)in AGS and HGC-27 cells determined using western blotting.bP ＜ 0.01,cP ＜ 0.001.

SOCS3 is targeted by miR-668-3p

MiR-668-3p targets were assessed using the starbase2.0 database.SOCS3 contained binding sequences(AGUGAC)of miR-668-3p(Figure 5A).DLR assay was performed to validate this interaction.Relative luciferase activity in AGS(0.37 ± 0.06532)and HGC-27 cells(0.32 ± 0.06532)transfected with SOCS3 WT reporter was reduced in response to transfection of miR-668-3p mimic(P= 0.00041,P= 0.00065,Figure 5B).The SOCS3 MUT reporter showed no such changes following miR-668-3p mimic addition(Figure 5B),suggestive of a direct interaction between miR-668-3p and SOCS3.The regulatory relation between miR-668-3p and SOCS3 was assessed through western blotting.SOCS3 expression in AGS and HGC-27 cells was reduced through the addition of miR-668-3p mimic(0.5833 ± 0.03756,0.6633 ± 0.03528)and boosted by the miR-668-3p inhibitor(1.03 ± 0.04619,0.92 ± 0.03786),implying an inverse regulatory relationship between miR-668-3p and SOCS3(P= 0.0076,P= 0.0036;P= 0.0038,P= 0.0047,Figures 5C and D).Lower expression of SOCS3 in tumor tissues(0.5001 ± 0.02447)compared to normal tissues(0.9979 ± 0.02526)(P＜ 0.0001,Figure 5E)was also observed.Upon correlation analysis between circ_0003356 and SOCS3 expression(P＜ 0.0001,r= 0.9364;Figure 5F),the expression of SOCS3 was negatively associated with miR-668-3p in tumor tissues(P＜ 0.0001,r= -0.8438;Figure 5G).

Circ_0003356 inhibits malignant behavior of GC cells via sponging miR-668-3p to target SOCS3

SOCS3 was silencedviatransfection of si-SOCS3 and its reduced expression confirmed in AGS(0.7267 ± 0.05044)and HGC-27 cells(0.5933 ± 0.05207)(P= 0.0086,P= 0.0065,Figure 6A).miR-668-3p overexpression(0.6467 ± 0.06394,0.6633 ± 0.04322 )or SOCS3 downregulation(0.6433 ± 0.06394,0.6267 ± 0.04527)reversed the promoting effect of circ_0003356 on SOCS3 expression level in AGS and HGC-27 cells(P= 0.0012,P= 0.0032,P= 0.0030,P= 0.0022,P= 0.0031,P= 0.0031,Figure 6B).The viability and proliferative capacity of AGS and HGC-27 cells were attenuated by circ_0003356 overexpression,whilst miR-668-3p upregulation or SOCS3 downregulation recovered the circ_0003356-mediated decrease in cell viability and proliferative capacity(P= 0.00039,P= 0.0025,P= 0.0037,P= 0.00042,P= 0.0035,P= 0.0051;P＜ 0.0001,P= 0.0002,P＜ 0.0001,P＜ 0.0001,P= 0.0044,P= 0.0012;Figures 6C and D).The effects of circ_0003356 on the apoptotic rates of AGS and HGC-27 cells were similarly reversed by miR-668-3p upregulation or SOCS3 downregulation(P＜ 0.0001,Figure 6E).When it came to circ_0003356-mediated inhibition of migration,invasion,and EMT,miR-668-3p up-regulation or SOCS3 downregulation could partially eliminate them(P＜ 0.0001,P= 0.0017,P= 0.0007,P＜ 0.0001,P= 0.0039,P= 0.0011;P＜ 0.0001,P= 0.0009,P= 0.0004,P＜ 0.0001,P= 0.0006,P= 0.0003;P= 0.0028,P= 0.010,P= 0.0164,P= 0.0029,P= 0.023,P= 0.0278;P= 0.00314,P= 0.0213,P= 0.0144,P= 0.00285,P= 0.0267,P= 0.00914;Figures 6F-H).

Circ_0003356 impedes GC tumorigenesis in vivo

A xenograft mouse model was constructed to confirm the anti-tumor role of circ_0003356 in GC.As depicted in Figures 7A-C,tumor size,volume(110 ± 5.859,P= 0.0001),and weight(0.2833 ± 0.03528,P= 0.0007)were reduced when circ_0003356 was overexpressed.Decreased expressions of Ki67(proliferative marker protein)and N-cadherin were observed following circ_0003356 overexpression,while SOCS3 and E-cadherin expression increased,suggestive of inhibitory effects on cell proliferation and EMT(Figure 7D).TUNEL staining indicated that circ_0003356 upregulation increased apoptosis in tumor tissues of mice(Figure 7E).Circ_0003356 expression was found to be boosted(2.423 ± 0.09135)and expression of miR-668-3p(0.5 ± 0.06531)was diminished after circ_0003356 was overexpressed in mouse tumor tissues(P= 0.000099,P= 0.0016,Figure 7F).

Figure 3 Circ_0003356 directly binds to miR-668-3p.A:Fluorescence in situ hybridization assays were used to detect the sub-cellular localization of circ_0003356 in AGS and HGC-27 cells;B:Quantitative real-time polymerase chain reaction(qRT-PCR)was used to detect the expression of circ_0003356 in the nucleus and cytoplasm;C:Binding sequences between circ_0003356 and miR-668-3p predicted by circinteractome;D:Interaction between circ_0003356 and miR-668-3p in AGS and HGC-27 cells validated by RIP-qRT-PCR;E:interaction between circ_0003356 and miR-668-3p in AGS and HGC-27 cells validated by RNA pulldown assays;F:Interaction between circ_0003356 and miR-668-3p in AGS and HGC-27 cells validated by dual-luciferase reporter assays;G:Relative expression of miR-668-3p detected by qRT-PCR in tumor tissues and normal tissues;H:Correlation between circ_0003356 and miR-668-3p in gastric cancer tissues analyzed by Pearson’s correlation analysis.cP ＜ 0.001.

Figure 4 Suppression of miR-668-3p promotes cell apoptosis and impairs the proliferation,migration,invasion,and epithelialmesenchymal transition of AGS and HGC-27 cells.A:Relative expression of miR-668-3p in GES-1,AGS,and HGC-27 cells detected by quantitative realtime polymerase chain reaction(qRT-PCR);B:Cell viability in AGS and HGC-27 cells assessed by CCK-8 assay;C:Proliferation of AGS and HGC-27 cells assessed by EdU assays;D:Apoptosis of AGS and HGC-27 cells assessed by flow cytometry;E:Relative migration of AGS and HGC-27 cells detected by wound healing assays;F:Invasion of AGS and HGC-27 cells detected by transwell assays;G:Levels of epithelial-mesenchymal transition-related proteins(E-cadherin and Ncadherin)in AGS and HGC-27 cells determined using western blotting.bP ＜ 0.01,cP ＜ 0.001.

Figure 5 SOCS3 is targeted by miR-668-3p.A:Binding sites between SOCS3 and miR-668-3p were predicted by Starbase v2.0 software;B:Dual-luciferase reporter assays were used to confirm the targeting relationship between SOCS3 and miR-668-3p in AGS and HGC-27 cells;C:Relative expression of SOCS3 in AGS and HGC-27 cells detected by western blotting following miR-668-3p overexpression;D:Relative protein expression of SOCS3 in AGS and HGC-27 cells detected by western blotting after miR-668-3p inhibition;E:Relative mRNA expression of SOCS3 was detected by quantitative real-time polymerase chain reaction in tumor tissues and normal tissues;F:Correlation between circ_0003356 and SOCS3 in gastric cancer(GC)tissues analyzed by Pearson’s correlation analysis;G:Correlation between miR-668-3p and SOCS3 in GC tissues analyzed by Pearson’s correlation analysis.bP ＜ 0.01,cP ＜ 0.001.

Figure 6 Circ_0003356 overexpression suppresses the malignant behavior of gastric cancer cells via sponging miR-668-3p to target SOCS3.A and B:Protein expression of SOCS3 in AGS and HGC-27 cells detected by western blot;C:Cell viability in AGS and HGC-27 cells detected by CCK-8 assay;D:Proliferation of AGS and HGC-27 cells assessed by EdU assay;E:Apoptosis of AGS and HGC-27 cells assessed by flow cytometry;F:Relative migration of AGS and HGC-27 cells detected by wound healing assay;G:Relative invasion of AGS and HGC-27 cells detected by transwell assay;H:Levels of epithelialmesenchymal transition-related proteins(E-cadherin and N-cadherin)in AGS and HGC-27 cells determined by western blotting.aP ＜ 0.05,bP ＜ 0.01,cP ＜ 0.001.

Figure 7 Circ_0003356 upregulation impedes gastric cancer tumorigenesis in vivo.A:Representative images of tumor in xenograft mice;B:Average volumes of xenograft mice;C:Average tumor weights of xenograft mice;D:Expression of E-cadherin,N-cadherin,Ki67,and SOCS3 in tumor tissues of xenograft mice determined by immunohistochemical staining;E:TUNEL staining to detect cell apoptosis in tumor tissues of mice;F:Expression of circ_0003356 and miR-668-3p determined by quantitative real-time polymerase chain reaction in tumor tissues of mice.bP ＜ 0.01,cP ＜ 0.001.

DISCUSSION

Due to a lack of effective treatment strategies and prognostic indicators,GC remains a threat to human health[29,30].Emerging evidence has implicated circRNAs during GC development[31,32].Thence,great efforts should be made to comprehensively understand circRNAs.To date,many circRNAs show low expression in GC,such as circ_0021087[12],hsa_circ_0005556[33],and circPSMC3[34].Here,we observed low expression levels of circ_0003356 in GC cells and tissues.This is the first report to show an association of circ_0003356 with GC.Moreover,increasing findings have indicated that several circRNAs act as prognostic indicators for GC,including hsa_circ_0005556[33]and circ_0000260[35].Here,based on Kaplan-Meier analysis,patients with low circ_0003356 had poor survival rates.

Accumulating data reveal that circRNAs have an anti-tumor function in GC.For instance,circ_0021087 overexpression suppresses the proliferation,migration,invasion,and EMT of GC cells and impairs tumorigenesis in xenograft mice[12].CircPSMC3 up-regulation prevents GC cells from migrating,proliferating,and invading,thereby suppressing tumorigenesis in xenograft mice[36].Similarly,we found that circ_0003356 overexpression repressed proliferation,migration,invasion,and EMT of GC cells and enhanced GC cell apoptosis.In vivo,circ_0003356 overexpression suppressed tumorigenesis.These results suggest an anti-tumor role for circ_0003356’s in GC,highlighting its potential in the clinical management of GC.

To our knowledge,circRNAs affect gene expressionviasponging downstream miRNAs in cancer cell[37,38].Inspired by this,we predicted downstream miRNAs of circ_0003356 using circinteractome.MiR-668-3p was identified as one such target.We performed RIP-qRT-PCR,RNA pull-downs,and DLR assays to verify our prediction.In previous reports,miR-668-3p has shown high expression and carcinogenesis in HCC and CRC[18,19].Consistent with these studies,we discovered high miR-668-3p expression in GC tissues and cells.The down-regulation of miR-668-3p enhanced cell apoptosis and impaired the proliferation,migration,invasion,and EMT of cells(AGS and HGC-27).These outcomes suggest that miR-668-3p is oncogenic in GC.Several cirRNAs,including circ_0014717 and circTMEM59,target miR-668-3p to suppress tumor development[18,19].Here,an inverse relationship was observed between miR-668-3p and circ_0003356 expression in tumor tissues of GC patients.MiR-668-3p was negatively regulated by circ_0003356 in mouse tumor tissues.In particular,the inhibitory influence of circ_0003356 on the proliferation,migration,invasion.EMT of GC cells were reversed by miR-3619-5p overexpression.We deduced that circ_0003356 prevents GC malignancy through sponging miR-668-3p.

It is acknowledged that the miRNA-circRNA-mRNA network is closely related to the regulation of GC progression[39].We therefore predicted target genes of miR-668-3p and found that SOCS3 was targeted by miR-668-3p.SOCS3 has been shown to display low expression in GC tissues and to participate in tumor suppression in GC[24,40].In this study,we observed that the downregulation of SOCS3 expression in GC tissues was regulated by miR-668-3p.An inverse correlation between SOCS3 and miR-668-3p expression levels in tumor tissues of GC patients was observed.Thus,we deduced that miR-668-3p acts as a tumor promoter,targeting SOCS3 in GC.Additionally,we identified a positive relationship between SOCS3 and circ_0003356 and found that the suppressive effects of circ_0003356 on cell proliferation,migration,invasion,and EMT were reversed by SOCS3 upregulation in GC cells.These findings strongly support the notion that circ_0003356 has an anti-tumor role through sponging miR-668-3p to target SOCS3 in GC.

CONCLUSION

In summary,we show that circ_0003356 expression is low in GC tissues and cells and positively related to GC patient prognosis.Circ_0003356 up-regulation or miR-668-3p inhibition facilitated cell apoptosis and suppressed proliferation,migration,invasion and EMT in cells(AGS and HGC-27).Circ_0003356 overexpression also prevented tumor growth in mice.Mechanistically,circ_0003356 was found to interact with the miR-668-3p/SOCS3 axis to impair GC development.Overall,this investigation provides a new perspective on the therapeutic targets of GC.

ARTICLE HIGHLIGHTS

Research background

Gastric cancer(GC)is a common malignant tumor with high prevalence and mortality.Circular RNA(circRNA)analysis in GSE184882 has indicated that circ_0003356 shows abnormal expression in GC tissues,but the function of circ_0003356 remains unclear in GC.

Research motivation

To seek the prognostic biomarker and therapeutic target for GC.

Research objectives

In order to explore the function and mechanism of circ_0003356 in GC.

Research methods

Quantitative real-time polymerase chain reaction was used to detect expression of circ_0003356.The clinical value of circ_0003356 for GC prognosis was evaluated.The role of circ_0003356 in GC was assessedvia in vitroandin vivoexperiments.The molecular mechanism of circ_0003356 on miR-668-3p/SOCS3 axis was validated.

Research results

Circ_0003356 expression was markedly decreased in GC tissues and cells,and it was positively associated with survival time of GC patients.Moreover,functional analyses showed that circ_0003356 overexpression inhibited malignant behaviors of GC cellsviatargeting the miR-668-3p/SOCS3 axis.

Research conclusions

Circ_0003356 is lowly expressed in GC tissues and cells,displaying potential as a prognostic biomarker for GC.Circ_0003356 up-regulation represses the malignancy of GCviatargeting the miR-668-3p/SOCS3 axis.

Research perspectives

Other mechanisms of circ_0003356 in GC may be probed in future researches,and its application in treatment of GC will be extended.

FOOTNOTES

Author contributions:Li WD,Wang HT,and Wang Y designed the study;Huang YM,Cheng BH,Xiang LJ,and Zhou XH collected the data;Deng QY,Guo ZG,Yang ZF,Guan ZF,and Wang Y analyzed the data;Li WD and Wang HT wrote the manuscript;and all authors approved the final manuscript.

Supported byZhongshan Social Public Welfare and Basic Research Project,No.200421093453685.

Institutional review board statement:The Ethics Committee of Zhongshan City People’s Hospital gave the approval(K2017-182).

Institutional animal care and use committee statement:All experiments were approved by the Animal Care and Use Committee of Zhongshan City People’s Hospital(K2017-182).

Informed consent statement:All participants have also agreed to this investigation by offering their written consent.

Conflict-of-interest statement:All the authors report no relevant conflicts of interest for this article.

Data sharing statement:All the data used to support the findings of this study are included within the article.

ARRIVE guidelines statement:The authors have read the ARRIVE guidelines,and the manuscript was prepared and revised according to the ARRIVE guidelines.

Open-Access:This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers.It is distributed in accordance with the Creative Commons Attribution NonCommercial(CC BYNC 4.0)license,which permits others to distribute,remix,adapt,build upon this work non-commercially,and license their derivative works on different terms,provided the original work is properly cited and the use is noncommercial.See:https://creativecommons.org/Licenses/by-nc/4.0/

Country/Territory of origin:China

ORCID number:Wei-Dong Li 0000-0001-5924-7989;Yao Wang 0000-0003-2777-0796.

S-Editor:Wang JJ

L-Editor:A

P-Editor:Zhang XD