Effects of miR-330-3p on Invasion, Migration and EMT of Gastric Cancer Cells by Targeting PRRX1-Mediated Wnt/β-Catenin Signaling Pathway
Authors Ma B, Ma J, Yang Y, He X, Pan X, Wang Z, Qian Y
Received 14 November 2019
Accepted for publication 5 March 2020
Published 22 April 2020 Volume 2020:13 Pages 3411—3423
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Geoffrey Pietersz
Bingqiang Ma,* Jianxun Ma,* Yili Yang, Xueyuan He, Xinmin Pan, Zhan Wang, Yaowen Qian
Department of General Surgery, Cancer Center, Key Laboratory for Diagnosis and Treatment of Gastrointestinal Cancer, Gansu Provincial Hospital, Lanzhou, Gansu Province, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Yaowen Qian
General Surgery, Cancer Center, Key Laboratory for Diagnosis and Treatment of Gastrointestinal Cancer, Gansu Provincial Hospital, 204 Donggangxi Road, Chengguan District, Lanzhou, Gansu Province 730000, People’s Republic of China
Tel +86 15293110056
Email [email protected]
Background: miRNA, as a biological marker, had more and more attention in recent years due to the important role it plays in cancer. Currently, there are extensive studies on miRNAs, among which miR-330-3p is reported to be implicated in the pathophysiological processes of various cancers. However, little progress has been made in the mechanism of miR-330-3p in gastric cancer.
Objective: To explore the expression and relevant mechanism of miR-330-3p and PRRX1 in gastric cancer (GC).
Methods: Forty-five GC patients (study group), from whom paired GC and paracancerous tissues were collected, and another 45 healthy subjects (control group) who underwent physical examination during the same period were enrolled. In addition, GC cells and human gastric mucosa cells were purchased, and miR-330-3p-mimics, miR-330-3p-inhibitor, miR-NC, si-PRRX1, and sh-PRRX1 were transfected into MKN45, SGC7901 cell. QRT-PCR was employed to assess the miR-330-3p and PRRX1 expressions in the samples, and the cell expressions of PRRX1, GSK-3β, p-GSK-3β, β-catenin, p-β-catenin, cyclin D1, N-cadherin, E-cadherin and vimentin were evaluated by Western blot (WB). MTT, Transwell and wound-healing experiments were adopted to detect cell proliferation, invasion and migration.
Results: MiR-330-3p was under-expressed, while PRRX1 was highly expressed in the serum of patients, both of which had an area under the curve (AUC) of more than 0.9. MiR-330-3p and PRRX1 were associated with tumor diameter, TNM staging, lymph node metastasis and differentiation of GC patients. Overexpression of miR-330-3p and inhibition of PRRX1 expression could suppress epithelial–mesenchymal transition (EMT), proliferation, invasion and apoptosis of cells. What is more, WB assay showed that overexpressed miR-330-3p and inhibited PRRX1 could inhibit the expression levels of p-GSK-3β, β-catenin, cyclin D1, N-cadherin and vimentin proteins, while elevating GSK-3β, p-β-catenin and E-cadherin protein expressions. Dual-luciferase reporter assay confirmed that there was a targeting relation between miR-330-3p and PRRX1. Furthermore, rescue experiments revealed that the cell proliferation, invasion, migration did not differ significantly between co-transfected miR-330-3p-mimics+sh-PRRX1, miR-330-3p-inhibitor+si-PRRX1 groups of MKN45 and SGC7901 and the miR-NC group (without transfected sequences).
Conclusion: Overexpressed miR-330-3p can promote cell EMT, proliferation, invasion and apoptosis through inhibiting PRRX1-mediated Wnt/β-catenin signaling pathway, which is expected to be a potential therapeutic target for GC.
Keywords: miR-330-3p, PRRX1, Wnt/β-catenin signaling pathway, biological function, GC
Characterized by early metastasis and poor prognosis in the late stage, gastric cancer, as a common malign tumor of the digestive system, presents an increased morbidity and mortality along with the changes of the social environment and dietary habits.1–3 Currently, surgery and chemotherapy remain the primary treatment approaches for patients with GC, however, with poor and unsatisfactory outcomes. For your consideration, the five-year survival rate accounts less than 30%.4 In view of the unfavorable situation, finding a biomarker with high sensitivity to the diagnosing and treating of gastric cancer has important clinical significance for patients with gastric cancer.
In recent years, the molecular mechanism of miRNA in tumor has been a research hotspot in cancer-related fields. miRNA, as a small non-coding RNA, can adjust and control target genes’ expression by binding to the 3ʹUTR of its target genes.5,6 Among which, miR-330-3p refers to a miRNA with abnormal expression in varying tumor cells. For example, studies7 showed that it could accelerate the cell metastasis of breast cancer by targeting CCBE1. Others8 supported that miR-330-3p was able to inhibit the migration of liver cancer cells by targeting MAP2K1. Although such research demonstrated that miR-330-3p was extensively involved in various tumors, the specific mechanism of its action in GC had not been elaborated. PRRX1 is a homeobox protein and an inducer of epithelial–mesenchymal transition (EMT).9 Previous findings displayed that PRRX1 could promote the EMT process of GC cells by mediating the transmission of Wnt/β-catenin signal pathway.10 As regard to Wnt/β-catenin, it also belongs to a classical signaling pathway in the pathological process of tumor, which is over-expressed in tumor cells and has some certain effects on their proliferation and apoptosis.11
PRRX1 was supposed to be a potential target site for miR-330-3p through online biological prediction software (http://www.targetscan.org/vert_72/). Based on previous research, we speculated that miR-330-3p could affect the biological function of GC cells by targeting Wnt/β-catenin signaling pathway mediated by PRRX1, and thus the following research was conducted.
Data and Methods
Totally 45 patients with GC treated in our hospital from March 2015 to June 2018 were selected as the study group, including 25 male and 20 female, averagely aged (57.4±3.1) years. Forty-five paired cases of gastric cancer tissues and paracancerous tissues were obtained as research specimens during the resection of gastric cancer with the consent of the patients. Another 45 healthy subjects who had a physical examination in our hospital during the same period were assigned into the control group, including 24 males and 21 females, averagely aged (57.5±3.3) years. Though comparable, it was obvious that no significant difference existed in terms of gender and age between the two groups (P>0.05). The inclusion criteria were as follows: All patients enrolled in the study group were diagnosed as GC by pathological diagnosis with an expected survival of more than 3 months. The exclusion criteria were as follows: Patients with severe liver and kidney dysfunction. Patients with other malignant tumors. Patients who had received any treatment before the experiment. Patients with infection or immunity and patients with systemic disorders. All patients and their families agreed to participate in the experiment and written informed consents were obtained. This experiment has got the approval of the Medical Ethics Committee of Gansu Provincial Hospital and Committee on the Ethics of Animal Experiments of Gansu Provincial Hospital, and this study is in line with the Declaration of Helsinki.
Reagents and Materials
MKN-28, MKN-45, MGC-803, SGC-7901 of Human GC cell lines and GES of human normal gastric mucosal cell lines were acquired from Bena Culture Collection, Beijing, China, Subordinate agent of ATCC, with the item number of 341,748, 337,682, 100,665, 100,114, 337,970, respectively. TransScript Green miRNA Two-Step qRT-PCR SuperMix and TransScript II Green Two-Step qRT-PCR SuperMix kits were purchased from TransGen Biotech Co., Ltd., Beijing, China, with the corresponding item number of AQ202-0 1, AQ301-01. The MTT, dual-luciferase reporter gene assay kit and RIPA was obtained from Biolab Technology Co., Ltd., Beijing, China, with the item number of SY0502, KFS303, JN0190, respectively. The Transwellkit, PBS and FBS were all acquired from Gibco Co., USA, with the item number of 1,142,802, 10,010,049, 10,437,028, respectively. The BCA protein kit was acquired from Thermo Scientific Company, with the item number of A53225, and Trizol kit from Invitrogen with the item number of 10,296,010. The PRRX1, GSK-3β, p-GSK-3β, β-catenin, p-β-catenin, cyclin D1, N-cadherin, E-cadherin, vimentin and β-Actin antibodies were all obtained from Cell Signaling Technology Company. The goat anti-rabbit IgG antibody was purchased from Boster Biological Technology Co., Ltd., Wuhan, China, ECL developer from Thermo Company, and PCR7500 from ABI Company, USA. Sangon Biotech (Shanghai) Co., Ltd. was responsible for the design and synthesis of all primers.
Cell Culture, Passage and Transfection
GC cell lines were cultured in a medium containing 10% PBS DMEM at 37°C with 5% CO2. When the cell adherent growth and fusion reached 85%, 25% trypsin was added for digestion. After that, GC cell lines were placed in the medium for further culture, passage, and finally cell transfection. MiR-330-3p-inhibitor (suppression sequence), miR-330-3p-mimics (overexpression sequence), miR-negative control (miR-NC), PRRX1 RNA (si-PRRX1), PRRX1 RNA (sh-PRRX1), negative control RNA (NC) were transfected by Lipofectamine™ 2000 kit, and the procedures were carried out strictly according to the kit instructions.
Serum and cells were collected and TRIzol kit was used to abstract the total RNA, whose purity and concentration was detected by ultraviolet spectrophotometer. Then, 5μg of the total RNA was taken for cDNA reverse transcription according to the kit instructions, followed by the amplification of the synthesized cDNA (1μg). The miR-330-3p amplification system: cDNA: 1μL, upstream and downstream primers: 0.4 μL, respectively, 2×TransTaq® Tip Green qPCR SuperMix:10 μL, Passive Reference Dye (50X): 0.4 μL, and ddH2O was added to complete to 20μL. The amplification conditions were as follows: The PCR reaction conditions were to pre-denaturate at 94°C for 30 s, then denaturate at 94°C for 5 s, and then annealing at 60°C for 30 s, and the operation was repeated for a total of 40 cycles. The PRRX1 amplification system: cDNA: 1 μL, upstream and downstream primers: 0.4 μL, respectively, 2X TransScript® Tip Green qPCR SuperMix: 10 μL, Passive Reference Dye (50X): 0.4 μL, and added Nuclease-free Water to complete up to 20μL. The amplification conditions were stated as below: Pre-denaturation: 95°C/30 s, denaturation: 95°C/5 s, annealing: 60°C/30 s, totaling 40. Three repeat holes were set for each sample, and the experiment was carried out for a total of 3 times. U6 was represented as the internal reference for miR-330-3p, β-Actin as the internal reference for PRRX1, and 2−ΔΔct was employed to analyze the data.
First, the tissue was embedded in paraffin and sectioned, and then stained according to the experimental procedure. Next, the tissue sections were incubated at room temperature and 3% H2O2 for 20 min to remove endogenous peroxidase activity, and then washed with PBS. Then, the sections were incubated with PRRX1 primary antibody at 4°C overnight. After PBS washing, the sections and horseradish peroxidase-labeled goat anti-rabbit IgG were placed at room temperature for 30 min. Then, the sections were re-rinsed with PBS, and incubated with the solution of streptomycin antibiotic protein peroxidase at 37°C for 10 min. Under the microscope, the sections developed with the freshly prepared diaminobenzidine were observed for 20 s. After re-dyeing with hematoxylin, the sections were rinsed with water for 15 min, dehydrated with ethanol, and then cleared of xylene and sealed with neutral gum. Followed by the observation of staining under the microscope. After re-dyeing with hematoxylin, the sections were rinsed with water for 15 min, dehydrated with ethanol, then cleared of xylene and sealed with neutral gum. Finally, the staining was observed under the microscope.
Western Blot Detection
RIPA lysate was added to the cells of each group after culture, and the total protein in the cells was extracted. Then, the protein concentration was detected by BCA assay. The protein concentration was adjusted to 4ug/μL, electrophoretically separated by 12% SDS-PAGE before transferring to PVDF membrane, and then sealed by 5% skim milk powder for 2 h. Next, PRRX1 (1:500), GSK-3β (1:500), p-GSK-3β (1:500), β-catenin (1:500), p-β-catenin (1:500), cyclin D1 (1:500), N-cadherin (1:500), E-cadherin (1:500), vimentin (1:500) and β-Actin I antibody (1:1000) were added and sealed overnight at 4°C. After that, the membrane was washed to remove the primary antibody, followed by the adding of horseradish peroxidase-labeled goat anti-rabbit secondary antibody (1:500), incubated at 37°C for 1 h, and rinsed with PBS for 3 times, 5 min each. Developed in a dark room, dried the extra liquid on the membrane with filter paper, and developed with ECL luminescence. Finally, the protein bands were scanned and analyzed in Quantity One software for grayscale value, where the relative protein expression = grayscale value of the target protein bands/grayscale value of the β-Actin protein bands.
MTT Assay for Cell Viability
After 24-h transfection, cells were collected and adjusted to 5*103cells, inoculated on 96-well plates, and cultured for 24 h, 48 h and 72 h. At each time point, 20μL MTT solution (5μL/mL) was added to each well for 4 h of continuous culture at 37°C, and the 200μL dimethyl sulfoxide was added. At last, OD value of each group was then assessed by a spectrophotometer at 570 mm wavelength.
Cells were collected 24 h after transfection, and its density was adjusted to 3*104 cells/well. Then, the cells were inoculated in 24-well plates, digested with trypsin, and transferred to the upper chamber, where 200μL RPMI1640 culture solution was added, and 500μL RPMI1640 (with 10% FBS) was added into the lower chamber, then cultured at 37°C for 48 h. The stroma and cells failed to cross the membrane surface were wiped and rinsed with PBS for 3 times, followed by a 10-min fixing with paraformaldehyde, and then washed with double-steamed water for 3 times. After drying, they were stained with Crystal Violet Stain Solution with a concentration of 0.5%, and the cell invasion was observed using a microscope.
Wound-Healing Assay for the Observation of Cells’ in vitro Migration Ability
The cells were diluted to 3 x 105 cells/mL and inoculated in 6-well plates. When the cells grew to 85%, the cells were divided into a cell-free area by p200 Pipet tips. Then, the wounded cells were rinsed with PBS and added to the new medium for culture, whose migration ability was measured by the healing of three different wound sites at 0 h (W0) and 24 h (W24) using a microscope.
Dual-Luciferase Reporter Assay
The 3ʹ-UTR of PRRX1 containing the miR-330-3p putative binding site was amplified and subcloned into the pGL3 luciferase promoter vector (Promega Corporation, Fitchburg, WI, USA). Then, the vector combined with miR-330-3p mimics was co-transfected into 293T cells for 48 h. Then, the cells were harvested and tested for relative luciferase activity using the dual-luciferase reporting kit (Promega Corporation) according to the manufacturer’s instructions. Subsequently, miR-330-3p-inhibitor, miR-330-3p-mimics, and control sequences were co-transfected into GC cells by Lipofectamine 3000 (Invitrogen, Thermo Fisher Scientific, USA). The effect of miR-330-3p on PRRX1 protein expression was detected by, Western Blot. All experiments were performed 3 times.
MS2-RNA Binding Protein Immunoprecipitation (RIP)
MS2-PRRX1-WT vector (containing miR-330-3p binding site) and MS2-PRRX1-MUT vector (without miR-330-3p binding site) with MS2 hairpin structure were constructed. The vectors were then transfected into gastric cancer cells. Forty-eight hours later, immunoprecipitation was performed using Magna RIPTM RNA-binding protein immunoprecipitation kit (Millipore). QPCR was adopted to quantify the expression of miR-330-3p.
Xenograft Model of Tumor in Nude Mice
Female BALB/c nude mice aged 4-weeks old were raised in a sterile environment, and then 3x106 MDN-45 cells of the stable miR-330-3p-mimics and its control plasmid were subcutaneously injected into the left abdomen of the nude mice. The nude mice were grouped with 5 in each, whose tumor growth was detected every 7 days. After 28 days of continuous injection, the mice were executed by cervical dislocation and the size and mass of the tumor in the body were precisely measured. Animal experiments are performed in accordance with the US Guide to Management and Use of Laboratory Animals. This experiment has been declared through animal experiment ethics。
The collected data were statistically analyzed using SPSS20.0 software and plotted by GraphPad 7 in the current study. An independent sample t-test was adopted for intra-group comparison. One-way ANOVA was employed for multi-group comparisons and expressed as F. LSD-t test was used for post-hoc pairwise comparison, and repeated measurement ANOVA was used for multiple time points, represented by F. Bonferroni was used for post-test verification and ROC was adopted to map the diagnostic significance of miR-330-3p and PRRX1 in GC. Pearson test was conducted to analyze the relation between the expression of miR-330-3p and PRRX1 in the serum of patients. K-M survival curve was used to plot the 3-year survival of the patients and Log-rank test for analysis. A statistically significant difference was assumed at P<0.05.
Expression and clinical value of miR-330-3p and PRRX1 in the serum of GC patients
The serum miR-330-3p and PRRX1 expressions of the participants were detected, it was found that the study group had a significantly decreased miR-330-3p expression and a markedly increased PRRX1 expression than those of the control group, which was statistically different (P<0.05). In addition, the expression detection of miR-330-3p and PRRX1 in patients’ tissues showed that, compared with paracancerous tissues, the miR-330-3p expression was noticeably lower while the PRRX1 expression was remarkably higher in the GC tissues. Immunohistochemical detection also revealed that the positive rate of PRRX1 in GC tissues was significantly higher than that in paracancerous tissues. Pearson’s analysis demonstrated that the expression of miR-330-3p and PRRX1 in the serum of GC patients was negatively correlated (P<0.05). According to ROC curve, the AUC of miR-330-3p and PRRX1 was 0.944 and 0.920, respectively. Further analysis of the relationship between these two indicators and the pathological data of patients demonstrated that miR-330-3p and PRRX1 were bound up with tumor diameter, differentiation degree, TNM staging, as well as lymph node metastasis (P<0.05). (Table 1, Figure 1)
Table 1 Correlation Between miR-330-3p, PRRX1 and Pathological Data of GC Patients
Effects of miR-330-3p on Proliferation, Invasion, Migration and EMT of GC Cells
The detection of miR-330-3p expression in GC cells revealed that, in contrast with normal gastric mucosal cells, MKN-28, MKN-45, MGC-803 and SGC-7901 of human GC cell lines presented a markedly reduced miR-330-3p expression (P<0.05). After transfecting miR-330-3p-mimics, miR-330-3p-inhibitor and miR-NC into MKN-45 and MGC-803 cells, the miR-330-3p expression of miR-330-3p-mimics transfected cells was markedly elevated, while that of miR-330-3p-inhibitor-transfected cells substantially decreased in comparison with the cells transfected with miR-CN. In addition, the miR-330-3p-mimics transfected cells displayed significantly reduced, and the miR-330-3p-inhibitor-transfected cells showed the markedly elevated ability of cell proliferation, invasion and migration than miR-CN transfected cells in the biological function detection of the two groups. What is more, the expressions of p-GSK-3β, β-catenin, cyclin D1, N-cadherin, vimentin were significantly reduced, and GSK-3β, p-β-catenin and E-cadherin expressions were markedly enhanced after miR-330-3p-mimics transfection compared to miR-NC transfected cells, while the case was reversed after transfecting with miR-330-3p-inhibitor (Figure 2).
Effects of PRRX1 on Proliferation, Invasion, Migration and EMT of GC Cells
The expression of PRRX1 in human GC cell lines represented by MKN-28, MKN-45, MGC-803 and SGC-7901 was substantially elevated than that of GES in normal gastric mucosa cell lines (P<0.05). While after transfection of MKN-45 and SGC-803 cells with si-PRRX1, sh-PRRX1 and miR-NC, the expression of PRRX1 in the si-PRRX1 transfected cells with MKN-45 and MGC-803 was significantly reduced, and that of the sh-PRRX1 transfected cells with EC109 and EC9706 was significantly increased than NC transfected cells (P<0.05). Additionally, the biological functions detection revealed that compared to the NC transfected cells, the proliferation, invasion and migration of si-PRRX1 transfected cells were substantially abated, while those of the sh-PRRX1 transfected cells significantly increased (P<0.05). Moreover, the expressions of p-G, SK-3β, β-catenin, cyclinD1, N-cadherin vimentin were substantially abated after transfection of si-PRRX1, and the GSK-3β, p-β-catenin and E-cadherin expressions were significantly increased in si-PRRX1 transfected cells in contrast with NC transfected cells, while the case was reversed in cells transfected with sh-PRRX1 (P<0.05). (Figure 3)
Target Gene Identification of miR-330-3p
For further verifying the relationship between miR-330-3p and PRRX1, the target binding site between PRRX1 and miR-330-3p was detected by predicting the downstream target gene of miR-330-3p through Targetscan7.2. What is more, dual-luciferase reporter assay displayed that overexpressed miR-330-3p remarkably downregulated the luciferase activity of pmirGLO-PRRX1-3 ‘UT Wt (P<0.05), but had no effect on that of pmirglo-PRRL1-3ʹ UTR Mut (P>0.05). Furthermore, WB detection revealed that PRRX1 expression was markedly reduced in MKN-45 and MGC-803 cells after transfection with miR-330-3p-mimics, and substantially elevated after transfecting miR-330-3p-inhibitor (P<0.05). (Figure 4)
Further co-transfection of miR-330-3p-mimics+sh-PRRX1 or miR-330-3p-inhibitor+si-PRRX1 into MKN-45, MGC-803 cells revealed no significant difference in proliferation, invasion and migration between the two and when in contrast with the miR-NC group. However, comparing to miR-330-3p-mimics, miR-330-3p-mimics+sh-PRRX1 and miR-330-3p-inhibitor+si-PRRX1 showed significantly increased proliferation, invasion and migration ability (P<0.05), while presented significantly decreased ones compared with miR-330-3p-mimics (P<0.05). EMT-related protein detection revealed that there was no significant difference in the E-cadherin, N-cadherin and vimentin expressions in miR-330-3p-mimics+sh-PRRX1 and miR-330-3p-inhibitor+si-PRRX1 than those of the miR-NC group (P>0.05). When compared with miR-330-3p-mimics, E-cadherin expression of miR-330-3p-mimics + sh-PRRX1 and miR-330-3p-inhibitor+si-PRRX1 was significantly reduced, while N-cadherin and vimentin expression were markedly elevated. While compared with the miR-330-3p-inhibitor, miR-330-3p-mimics+sh-PRRX1 and miR-330-3p-inhibitor + si-PRRX1 presented markedly boosted E-cadherin expression, and significantly reduced expressions of N-cadherin and vimentin (Figure 5).
Overexpressed miR-330-3p Inhibited Tumor Growth in Nude Mice
Tumor formation model was constructed by injecting MKN-45 cells transfected with miR-330-3p-mimics and miR-NC into the abdomen of nude mice. The results showed that there was a markedly lower tumor growth rate in the miR-330-3p-mimics group than that of the miR-NC group, so was the case with the tumor size and mass after the execution of nude mice (P<0.05), suggesting that overexpressed miR-330-3p can inhibit the tumors grow in vivo (Figure 6).
Gastric cancer (GC) is a common malignancy of digestive system, whose poor prognosis largely results from its inconspicuous symptoms and metastasis in early stage.12 In recent years, miRNAs have been proved to act as tumor suppressor genes or pro-oncogene, whose abnormal expression is closely germane to the genesis and progression of tumors, and are thus generally considered as the target direction of cancer diagnosis or treatment.13 Previous research demonstrated that miR-330-3p was abnormally expressed in manifold kinds of tumors and acts as oncogene promoter or suppressor. For example, studies14 indicated that miR-330-3p was elevated and could promote the proliferation of NSCLC cells by targeting EGR2. Others15 revealed that there was a certain relevance between the abnormal expression of serum miR-330-3p of patients with leukemia as well as the clinical outcomes of patients. Additionally, some scholars16 found that miR-330-3p was down-regulated in GC tissues, and that miR-330-3p could inhibit the EMT of GC cells. The specific mechanism, however, has not elucidated yet.
Therefore, the clinical significance and potential molecular mechanism of miR-330-3p have been explored in the current study. Firstly, it was revealed that miR-330-3p was down-regulated in the serum and tissues of GC patients, which was consistent with previous studies. What is more, the decreased expression of miR-330-3p was found to be related to tumor diameter, differentiation degree, TNM staging and lymph node metastasis of GC patients when analyzing the clinical value of miR-330-3p. Moreover, the AUC curve of miR-330-3p was more than 0.9, indicating that miR-330-3p had a high diagnostic value for GC. Based on the above findings, it was suggested that miR-330-3p is strongly linked with the genesis and progression of GC, so cell experiments were further carried out.
To begin with, the expression of miR-330-3p in GC cell lines was determined to be markedly down-regulated by GES in contrast with normal gastric mucosa cells, which validated the results of the current study. Then, the up-regulation and down-regulation of miR-330-3p in MKN-45 and MGC-803 cells showed that the proliferation, invasion and migration ability of MKN-45 and MGC-803 cells transfected with miR-330-3p-mimics were remarkably suppressed, the N-cadherin and vimentin expression of EMT-related proteins were substantially abated, while the expression of E-cadherin was markedly boosted. However, the related expression of MKN-45 and MGC-803 cells after the transfection of miR-330-3p-inhibitor was contrary to that of miR-330-3p-mimics transfected ones, suggesting that miR-330-3p can be functioned as a potential target in GC treatment, and overexpressed miR-330-3p can inhibit cell proliferation, invasion, migration and EMT. In addition, the overexpressed miR-330-3p was found to be able to significantly promote the formation and growth of tumor through in vitro tumorigenesis in nude mice, which further suggested the significance of miR-330-3p in GC. However, how miR-330-3p affects the biological function and EMT of GC cells remains poorly understood.
The online target gene prediction website indicated that there were binding targets between PRRX1 and miR-330-3p. PRRX1 is a member of the homeostatic family, which exerts a marked effect in transcriptional activation and induction of downstream gene expression.17 It has been reported that PRRX1, as one of the inducers of EMT, plays an essential part in the EMT process of different tumors as well as the invasion and metastasis of tumor cells.18 In the current study, PRRX1 was highly expressed in the serum and tissues of patients with GC. Meanwhile, ROC curve analysis revealed that PRRX1 had a high diagnostic value for GC with the AUC of more than 0.9, and there was a strong connection between PRRX1 and tumor diameter, differentiation degree, TNM staging and lymph node metastasis, suggesting that PRRX1 may also be a potential diagnostic target for GC. Subsequently, the regulation of PRRX1 expression in MKN-45 and MGC-803 cells demonstrated that silencing PRRX1 could inhibit the EMT, proliferation, invasion and migration of GC cells, but the opposite results were observed after the over-expression of PRRX1. EMT has always been a hotspot in the study of tumor discovery mechanism, and the occurrence of EMT can weaken the connection between cells and promote their invasion and migration.19 Therefore, it is speculated that silencing PRRX1 may inhibit the invasion and migration of GC cells by suppressing EMT, which requires further verification. In addition, rescue experiments showed that, compared with miR-330-3p-mimics, the proliferation, the invasion and migration of MKN-45, MGC-803 increased significantly and EMT remarkably enhanced after simultaneous overexpression of miR-330-3p and PRRX1 or simultaneous underexpression of miR-330-3p and PRRX1, suggesting that there were closer ties between miR-330-3p and PRRX1. Therefore, the interrelation between miR-330-3p and PRRX1 was further assessed by dual-luciferase reporter assay, which demonstrated that the overexpression of miR-330-3p notably downregulated the luciferase activity of pmirglo-PRRX1-3 ‘UT Wt, without effect on that of pmirglo-PRRX1-3ʹ UTR Mut. Moreover, PRRX1 expression was markedly reduced in miR-330-3p-mimics transfected cells, while remarkably elevated in miR-330-3p-inhibitor-transfected ones, indicating a targeted regulatory connection between miR-330-3p and PRRX1. Through the experiments mentioned above, it is preliminarily proved that up-regulated miR-330-3p expression can inhibit the PRRX1 expression, thus affecting the biological function of GC cells. The specific pathway through which it is regulated, however, remains unclear.
Previous studies believed that Wnt signaling pathway remained to be one of the primary signaling pathways implicated in EMT, as well as one of the essential pathways involved in cell invasion and migration.20,21 Some others22 found that PRRX1 could promote invasion, migration and EMT of breast cancer cells by stimulating Wnt/β-catenin signaling pathway in breast cancer cells. The Wnt/β-catenin signaling pathway-related proteins in GC cells treated with over-expressed and under-expressed of miR-330-3p and PRRX1 were detected in the present study. It was found that the PRRX1, p-GSK-3β, β-catenin, cyclinD1, N-cadherin and vimentin expressions were markedly abated, while the expression of GSK-3β, p-β-catenin, E-cadherin were significantly boosted in MKN-45 and MGC-803 cells transfected with the over-expressed miR-330-3p or under-expressed PRRX1 and vise vista, suggesting that miR-330-3p could inhibit the phosphorylation of GSK-3β protein by regulating PRRX1 and promote the phosphorylation of β-catenin to suppress the activation of Wnt/β-catenin signal pathway, thus inhibiting the EMT of cells. Previous reports23 also revealed that the activation of Wnt/β-catenin signaling pathway could enhance the proliferation and invasion of GC cells. In addition, studies24 revealed that miR-519d of different sizes could inhibit the activation of Wnt/β-catenin signaling pathway in GC cells by targeting Twist1 to further inhibit the EMT of GC cells, which all validate the findings in the current study. However, this study also has some shortcomings. For example, due to the small number of cases and the limited time of sample collection, the prognosis of patients cannot be further analyzed. Besides, though there have been many reports on the mechanism of miRNA in gastric cancer, its upstream and downstream mechanism remains elusive, which is another end in our future research. In the future experiments, we will further increase the number of cases, expand the inclusion time of cases and carry out more basic experiments, so as to address the shortcomings of our study.
In conclusion, miR-330-3p can affect the invasion, migration and EMT of GC cells by targeting PRRX1-mediated Wnt/β-catenin signaling pathway, which is expected to be a clinical target for the diagnosis and treatment of GC.
This study was financially supported by the Training Program of the Research Plan of the National Foundation of Gansu Provincial Hospital (19SYPYA-5).
The authors report no conflicts of interest in this work.
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