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. 2019 Jun 26;18(3):2523–2529. doi: 10.3892/ol.2019.10530

MicroRNA-744 promotes carcinogenesis in osteosarcoma through targeting LATS2

Liangzhi Sun 1, Ming Liu 2, Suxian Luan 3,✉, Yulin Shi 1, Qiang Wang 2
PMCID: PMC6676671  PMID: 31452740

Abstract

Osteosarcoma (OS) mortality rate is increasing. Various microRNAs (miRNAs) have been investigated in the pathological process of OS except for miR-744. Hence, this research was designed to explore miR-744 function in OS. RT-qPCR and western blot analysis were used to quantify miR-744 and large tumor suppressor kinase 2 (LATS2) expression levels. The function of miR-744 was investigated using MTT and Transwell assays. Target gene of miR-744 was verified by dual-luciferase reporter assay. miR-744 expression was increased in OS, which was associated with worse clinical features and prognosis of OS patients. Importantly, miR-744 promoted cell viability and metastasis in OS. Furthermore, miR-744 induced Wnt/β-catenin pathway and epithelial-mesenchymal transition (EMT) in OS. In addition, miR-744 directly targeted LATS2 and blocked its expression in OS. Moreover, upregulation of LATS2 weakened the promotion of cell viability and metastasis induced by miR-744 in OS. In conclusion, miR-744 accelerated OS progression through restraining LATS2 and activating Wnt/β-catenin pathway and EMT.

Keywords: cell viability, metastasis, miR-744, osteosarcoma, LATS2

Introduction

With the increasing incidence, osteosarcoma (OS) has become a major threat of human health. OS occurs mostly in childhood and adolescence. Approximately 80% of OS affect the growth of the femur and tibia (1). Previous studies have indicated that malignant transformation of OS cells is associated with genetic and environmental factors. The physiological dysfunction of OS cells is mainly caused by changes in oncogene and tumor suppressor activity (2). Moreover, OS cells are highly metastatic, including blood flow and lung metastasis. This high degree of metastasis also leads to worse cure rate and prognosis in patients with OS (3). Despite the rapid development of modern diagnostic techniques, the complex pathological mechanisms of OS remain obstacles to patient survival (4). Therefore, further exploration of the pathogenesis of OS and the development of new treatments are of great significance for patients with OS.

MicroRNAs (miRNAs) are a class of evolutionarily conserved non-coding small RNAs that function to regulate gene expression at the translational level. The diversity and breadth of miRNAs have been revealed in many diseases and cancers in recent years, including OS. Zhou et al found the diagnostic effect of miR-139-5p as an indicator in OS (5). Additionally, miR-199b-5p was upregulated and promoted malignant progression of OS (6). Inversely, downregulation of miR-144 was found in OS. miR-144 overexpression inhibited tumor growth and metastasis in OS (7). Although many miRNAs have been found in OS, the dysregulation of miR-744 has not been investigated in OS. Moreover, the regulatory mechanism of miR-744 varies depending on the type of cancer. For instance, miR-744 was downregulated in glioblastoma and inhibited its aggressive behavior (8). On the contrary, miR-744 expression was increased in pancreatic cancer, which increased its tumorigenicity (9). Furthermore, miR-744 was a potential prognostic marker in patients with hepatocellular carcinoma (10). However, the molecular mechanism of miR-744 remains largely unknown in the pathological process of OS.

As a member of LATS tumor suppressor family, large tumor suppressor kinase 2 (LATS2) has been widely investigated in human cancers. For example, LATS2 was overexpressed in nasopharyngeal carcinoma and predicted poor prognosis (11). Functionally, LATS2, a putative tumor suppressor, inhibited G1/S transition (12). Furthermore, LATS2 was found to induce apoptosis by suppressing Bcl-2 expression (13). Dai et al found that LATS1/2 could inhibit f-actin binding, cell migration, and angiogenesis (14). The interaction between miRNAs and LATS2 had been investigated in some cancers. Lee et al reported that miR-373 post-transcriptionally regulated LATS2 and stimulated proliferation in human esophageal cancer (15). Moreover, miR-103 promoted metastasis and epithelial-mesenchymal transition (EMT) of hepatocellular carcinoma by inhibiting LATS2 (16). However, to the best of our knowledge, the relationship between miR-744 and LATS2 has not been previously investigated.

Therefore, the regulatory mechanism of miR-744/LATS2 axis was elucidated in our study. Furthermore, the effect of miR-744 on Wnt/β-catenin pathway and EMT was also investigated in OS. This investigation will help us understand the pathogenesis of OS.

Materials and methods

Experimental sample

Forty-one OS patients in Weifang People's Hospital (Weifang, China) took part in this study. Informed consents of all OS patients were acquired before the experiment. OS tissues and normal tissues were acquired from these patients, who had not received any treatment except for surgery. Permission for this research was acquired from the Institutional Ethics Committee of Weifang People's Hospital.

Cell culture and transfection

Human normal osteoblast hFOB1.19 cells (ATCC® CRL-11372™) and MG-63 OS cell line (ATCC® CRL-1427™) were selected in this study. The growth conditions included 5% CO2, 37°C and culture solution (90% RPMI-1640 + 10% FBS). Next, miR-744 mimics, inhibitor, LATS2 siRNA and vector (RiboBio) were transfected into MG-63 cells, respectively, using Lipofectamine 2000.

RT-qPCR

Total RNA extraction was performed by TRIzol reagent (Sigma-Aldrich; Merck KGaA). The cDNA solution was synthesized using First-Strand cDNA Synthesis kit (cat no. K1611; Promega Corporation). The temperature conditions of the reverse transcription were as follows: 37°C for 15 min and 85°C for 5 sec. We performed RT-qPCR assay using miScript SYBR®-Green PCR kit (cat. no. /ID: 218073; Qiagen, Inc.) based on the manufacturer's instructions. The thermocycling parameters were as follows: 95°C for 3 min and 40 cycles of 95°C for 15 sec followed by 58°C for 30 sec. The 2−∆∆Cq method (17) was applied to measure miR-744 or LATS2 expression levels using internal reference U6 or GAPDH. The following primers were used: miR-744 forward, 5′-ACACTCCAGCTGGGTGCGGGGCTAGGGCTAAC-3′ and reverse, 5′-CTCAACTGGTGTCGTGGA-3′; LATS2 forward, 5′-ATGAGCTCCACTCTGCTCAATGTCACGG-3′ and reverse, 5′-GCAAGCTTCTCTACCAAGAATGAAAGAGCAT-3′; U6 forward, 5′-CTCGCTTCGGCAGCACA-3′ and reverse, 5′-AACGCTTCACGAATTTGCGT-3′; GAPDH forward, 5′-GAAGGTGAAGGTCGGAGTC-3′ and reverse, 5′-GAGATGGTGATGGGATTTC-3′.

Western blot analysis

Transfected MG-63 cells were dissociated using RIPA lysis buffer. Next, 10% SDS-PAGE was used to separate 25 µg protein. Protein concentration was calculated using bicinchoninic acid (BCA). Protein samples were transferred into a polyvinylidene difluoride (PVDF) membrane (Thermo Fisher Scientifc, Inc.). Then, the membranes were blocked with 5% non-fat milk for 1 h at room temperature. Protein samples were incubated with vimentin (rabbit polyclonal antibody; dilution, 1:1,000; cat. no. ab137321; Abcam), N-cadherin (rabbit polyclonal antibody; dilution, 1:1,000; cat. no. ab18203; Abcam), E-cadherin (rabbit monoclonal antibody; dilution, 1:1,000; cat. no. ab1416; Abcam), LATS2 (rabbit polyclonal antibody; dilution, 1:1,000; cat. no. ab110780; Abcam), β-catenin (rabbit polyclonal antibody; dilution, 1:1,000; cat. no. ab6302; Abcam) and GAPDH (rabbit monoclonal primary antibody; dilution, 1:1,000; cat. no. ab181602; Abcam) overnight at 4°C. Secondary mouse anti-rabbit (cat. no. 3678) or goat anti-mouse (cat. no. 58802) antibodies (dilution, 1:2,000) conjugated with horseradish peroxidase (Cell Signaling Technologies, Inc.) were added to incubate protein samples for 1 h at room temperature. Finally, ECL (ECL, Pierce) was used to measure protein expression levels.

MTT assay

The MG-63 cell suspension was cultured in RPMI-1640 medium containing 10% FBS. Then, 96-well plates were seeded at a density of 4,000 cells per well. After 24, 48, 72 and 96 h of incubation at 37°C, 20 µl of MTT solution (5 mg/ml in PBS) was added to each well. Incubation was continued for 4 h at 37°C and the culture was terminated. The supernatant was discarded, 150 µl of DMSO was added to each well. The mixture was shaken for 10 min to allow the crystals to fully melt. Then, they were dissolved in 100 µl of dimethyl sulfoxide [CAS: (67-68-5), Sangon Biotech]. Finally, at a wavelength of 490 nm the light absorption value of each well was measured on a microplate reader (ELx800; Bio-Tek Instruments) to plot a cell growth curve.

Transwell assay

First, 60 µl of diluted Matrigel (3.9 µg/µl) was added to the upper chamber for cell invasion. Cell migration assay was performed without Matrigel. After 30 min, MG-63 cell suspension (5×103 cells/well) was added to the Transwell upper chamber, and 500 µl of RPMI-1640 medium (10% FBS) was added to the 24-well plate in the lower chamber. After routine incubation for 24 h, the cells on the lower surface of the membrane were fixed with 4% paraformaldehyde [CAS: (30525-89-4), Sangon Biotech] and stained with 1% crystal violet (Solarbio) for 5 min. Observation and photographing were performed using a light microscope (Olympus Corporation).

Luciferase reporter assay

Luciferase vector pcDNA3.1 (Promega Corporation) with Wt-LATS2-3′UTR or Mut-LATS2-3′UTR and miR-744 mimics were transfected into MG-63 OS cell line (ATCC). Next, the transfected cells were incubated in RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc.) at room temperature for 20 min. After 48 h, the medium was discarded and washed with PBS. Finally, luciferase activity was assessed using dual luciferase assay system (Promega Corporation). This experiment was repeated 3 times.

Statistical analysis

Data were analyzed by SPSS 18.0 (SPSS, Inc.) or GraphPad Prism 6 (GraphPad Software, Inc.), and shown as mean ± SD. Chi-square test, one-way ANOVA with Tukey's multiple comparison tests and univariate Kaplan-Meier method with log-rank test were used to analyze differences between the groups. P<0.05 was considered to indicate a statistically significant difference.

Results

miR-744 expression is increased in OS

The alteration of miR-744 expression was assessed in OS by RT-qPCR. We found that miR-744 expression was higher in OS tissues than in normal tissues (P<0.01, Fig. 1A). Moreover, miR-744 was also upregulated in MG-63 cells compared to hFOB1.19 cells (P<0.01, Fig. 1B). In addition, dysregulation of miR-744 affected the prognosis of OS patients. Upregulation of miR-744 was closely associated with worse prognosis in OS patients (P<0.05, Fig. 1C). Besides, abnormal miR-744 expression was associated with distant metastasis and clinical stage (P<0.05, Table I). These findings implied that miR-744 might influence OS progression.

Figure 1.

Figure 1.

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(A) Upregulation of miR-744 in OS. miR-744 expression levels in OS tissues. (B) miR-744 expression levels in MG-63 cells and hFOB1.19 cells. (C) High miR-744 expression was associated with unfavorable prognosis in OS patients. *P<0.05, **P<0.01.

Table I.

Relationship between miR-744 expression and the clinicopathological characteristics of OS patients.

miR-744
Characteristics Cases High Low P-value
Age (years) 0.75
  ≥60 25 18 7
  <60 16 14 2
Sex 0.52
  Male 24 19 5
  Female 17 13 4
Tumor size 0.12
  <5 cm 20 13 7
  ≥5 cm 21 19 2
Clinical stage 0.02a
  I–II 32 25 7
  III–IV   9   7 2
Distant metastasis 0.03a
  No 35 29 6
  Yes   6   3 3
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Statistical analyses were performed by the χ2 test.

a

P<0.05 was considered statistically significant.

miR-744 promotes cell viability and metastasis in OS

In order to confirm whether miR-744 was involved in OS development, gain-loss experiment of miR-744 was performed in MG-63 cells. After transfection, miR-744 expression was enhanced by its mimics and reduced by its inhibitor (P<0.01, Fig. 2A). Next, miR-744 mimic overexpression was found to promote cell proliferation in OS. Correspondingly, knockdown of miR-744 inhibitor restrained MG-63 cell proliferation (P<0.05 or 0.01, Fig. 2B). Consistently, cell migration was also promoted by miR-744 mimic overexpression and inhibited by downregulation of miR-744 inhibitor (P<0.01, Fig. 2C). Similarly, miR-744 mimics promoted MG-63 cell invasion. miR-744 inhibitor restrained cell invasion in OS cells (P<0.01, Fig. 2D). Hence, miR-744 played a carcinogenic role in OS development.

Figure 2.

Figure 2.

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miR-744 promotes cell viability and metastasis in OS. (A) miR-744 expression in MG-63 cells with its mimics or inhibitor; (B-D) cell proliferation, migration and invasion were regulated by miR-744 in MG-63 cells. *P<0.05, **P<0.01.

miR-744 induces Wnt/β-catenin pathway and EMT in OS

Next, how miR-744 regulated Wnt/β-catenin pathway and EMT was explored to confirm its effect on OS cell viability and metastasis. The expression levels of EMT makers (E-cadherin, N-cadherin and vimentin) were measured in MG-63 cells with miR-744 mimics or inhibitor. We found that miR-744 mimics promoted N-cadherin and vimentin expression levels and restrained E-cadherin expression in MG-63 cell (Fig. 3). Correspondingly, miR-744 inhibitor enhanced E-cadherin expression and blocked N-cadherin and vimentin expression levels in OS cells (Fig. 3). In addition, we examined β-catenin expression as a regulator in Wnt/β-catenin pathway in MG-63 cells with miR-744 mimics or inhibitor. The expression of β-catenin was promoted by miR-744 mimics and suppressed by miR-744 inhibitor (Fig. 3). These findings indicated that miR-744 promoted OS development through activating Wnt/β-catenin pathway and EMT.

Figure 3.

Figure 3.

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miR-744 induces EMT and Wnt/β-catenin pathway in OS. EMT markers, LATS2 and β-catenin were regulated by miR-744 mimics or inhibitor in MG-63 cells.

miR-744 negatively regulates LATS2 expression in OS

TargetScan database (http://www.targetscan.org/, Fig. 4A) showed that there were binding sites between LATS2 and miR-744 and the prediction was confirmed by luciferase reporter assay. miR-744 mimics lessened luciferase activities of wild LATS2, but had no effect on mutant LATS2 (P<0.01, Fig. 4B). LATS2 expression affected by miR-744 mimics or inhibitor was detected in MG-63 cells. LATS2 expression was found to be blocked by miR-744 mimics and increased by miR-744 inhibitor (P<0.01, Fig. 4C). Downregulation of LATS2 was found in OS tissues compared to normal tissues (P<0.01, Fig. 4D). Furthermore, miR-744 was found to have a negative association with LATS2 expression levels in OS tissues (P<0.0001, R2=0.4971; Fig. 4E). Based on these results, miR-744 directly targeted LATS2 and blocked its expression in OS.

Figure 4.

Figure 4.

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miR-744 negatively regulates LATS2 expression in OS. (A) The binding sites between miR-744 and LATS2. (B) Luciferase reporter assay. (C) LATS2 expression in MG-63 cells with miR-744 mimics or inhibitor. (D) LATS2 expression in OS tissues. (E) Negative association between miR-744 and LATS2. **P<0.01.

miR-744 accelerates OS progression through targeting LATS2

Finally, MG-63 cells with miR-744 mimics were transfected with LATS2 vector to explore their interaction in OS. We found that miR-744 mimics mediated reduction of LATS2 expression which was recovered by LATS2 vector (Fig. 5A). Functionally, promotion of cell proliferation induced by miR-744 overexpression was impaired by upregulation of LATS2 (P<0.01, Fig. 5B). Similarly, promotion of cell migration and invasion regulated by miR-744 was also weakened by LATS2 upregulation (P<0.01, Fig. 5C and D). Combining these results, miR-744 was considered to accelerate OS progression through targeting LATS2.

Figure 5.

Figure 5.

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miR-744 accelerates OS progression via regulating LATS2. (A) LATS2 level in MG-63 cells containing miR-744 mimics and LATS2 vector. (B-D) Cell proliferation, migration and invasion in MG-63 cells with miR-744 mimics and LATS2 vector. *P<0.05, **P<0.01.

Discussion

As important regulators, miRNAs have been found to take part in the regulation of OS progress. Similarly to our results, miR-214 expression was increased in OS and promoted its malignant behavior (18). Li et al demonstrated that miR-374a activated Wnt/β-catenin signaling to promote OS development (19). Here, upregulation of miR-744 was also measured in OS. Furthermore, this dysregulation was associated with worse clinical features and prognosis of OS patients. Functionally, promotion of OS cell proliferation, migration and invasion mediated by miR-744 was identified. Moreover, miR-744 activated Wnt/β-catenin pathway and EMT to exhibit carcinogenesis in OS. Besides, we found that miR-744 accelerated OS progression through targeting LATS2. These findings implied that miR-744 acted as an oncogene in OS.

Consistent with our results, high expression of miR-744 was observed in nasopharyngeal carcinoma, which predicts poor prognosis (20). Moreover, similar results were also identified in pancreatic cancer (21). In addition, Li et al showed that miR-744 enhanced motility of SiHa cervical cancer cells (22), which agreed with our findings. At the same time, oncogenic miR-744 was found to promote prostate cancer growth (23). In our study, we also found miR-744 mediated promotion of cell viability in OS. It was reported that miR-744 promoted prostate cancer progression through aberrantly activating Wnt/β-catenin signaling (24). Similarly, Wnt/β-catenin pathway was also activated by miR-744 in OS, but the activation of EMT induced by miR-744 has not been investigated in previous studies. Previous studies have indicated that miR-744 carries out its functions by regulating the expression levels of its targets, such as KLLN and EEF1A2 (25,26). Therefore, we investigated the interaction of LATS2 and miR-744 in this study. miR-744 was found to directly target LATS2 and block its expression in OS.

As a target gene, the expression of LATS2 is affected by other miRNAs in different cancers, such as miR-93 and miR-372 (27,28). As a tumor suppressor, dysregulation of LATS2 has been assessed in many malignant tumors. Downregulation of LATS2 was detected in colorectal cancer and esophageal squamous cell carcinoma (29,30). In the current study, LATS2 was also downregulated in OS. Furthermore, LATS2 had a negative association with miR-744 expression in OS tissues, which was consistent with previous studies. Functionally, miR-25 promoted ovarian cancer proliferation and motility by targeting LATS2 (31). Moreover, miR-650 promoted metastasis and EMT of hepatocellular carcinoma by inhibiting LATS2 expression (32). Here, miR-744 was also considered to facilitate cell proliferation and metastasis in OS through targeting LATS2.

Collectively, miR-744 expression was increased in OS, which predicted poor clinical features and prognosis. Moreover, miR-744 accelerated cell viability and metastasis in OS through downregulating LATS2. Furthermore, miR-744 activated Wnt/β-catenin pathway and EMT to facilitate OS progression. Therefore, our study provides a new therapeutic target for OS patients.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

LS contributed to the study design, data acquisition and analysis and drafted the manuscript. ML performed RT-qPCR and western blot analysis. SL and YS were responsible for MTT, Transwell and dual-luciferase reporter assays. QW contributed to analysis of observation indexes. All the authors read and approved the final manuscript.

Ethics approval and consent to participate

The study was approved by the Institutional Ethics Committee of Weifang People's Hospital (Weifang, China). Patients who participated in this research, had complete clinical data. Signed informed consents were obtained from the patients or the guardians.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

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