|Year : 2019 | Volume
| Issue : 2 | Page : 329-335
The effects of microRNA-1224-5p on hepatocellular carcinoma tumor endothelial cells
Chao Hu1, Xi Cheng1, Qi MingYu1, Xin Bao Wang1, Shi Qiang Shen2
1 Department of Abdominal Surgical Oncology, Zhejiang Cancer Hospital, Hangzhou, China
2 Department of General Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China
|Date of Web Publication||1-Apr-2019|
Dr. Shi Qiang Shen
Department of General Surgery, Renmin Hospital of Wuhan University, No. 99, Zhang Zhidong Road, Wuchang District, Wuhan 430060, Hubei Province
Source of Support: None, Conflict of Interest: None
Aim: The aim of this study was to investigate the effect of microRNA-1224-5p (miR-1224-5p) on tumor endothelial cells (TECs) of human hepatocellular carcinoma (HCC).
Subjects and Methods: Oligonucleotides were chemically synthesized and transfected into TECs using Lipofectamine 2000. TECs were divided into three groups, namely a control (CON) group without transfection, a negative control (NC) group transfected with negative control oligonucleotides and green fluorescent protein (GFP), and a micro-up (MU) group transfected with miR-1224-5p mimic and GFP. The expression of miR-1224-5p was quantified via quantitative reverse-transcription polymerase chain reaction (qRT-PCR). The proliferation of TECs was detected using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and the optical density value at 490 nm was measured after every 24 h. Apoptosis was detected via flow cytometry using a 7-aminoactinomycin/APC Annexin V kit. The migration and invasion of TECs were detected using transwell assay. The tube formation ability was evaluated using the tube formation assay.
Results: Oligonucleotides were successfully transduced into TECs, and the expression of miR-1224-5p was specifically upregulated. The results of qRT-PCR analysis showed that the expression of miR-1224-5p was significantly upregulated in the MU group (2–ΔΔCt = 3.27 ± 0.15) than in the CON group (2–ΔΔCt = 1) and NC group (2–ΔΔCt = 1.08 ± 0.11) (P < 0.01). The results of MTT assay showed that the cell proliferation was significantly inhibited in the MU group at four time points than in the CON and NC groups (P < 0.01). Flow cytometry analysis revealed the significant increase in apoptosis of cells from the MU group (19.29% ± 0.95%) than those from the CON (8.73% ± 0.64%) and NC (9.51% ± 0.56%) (P < 0.01) groups. The migration ability was significantly inhibited in MU group (51.0 ± 3.6) as compared with CON (77.7 ± 2.5) and NC (79.2 ± 3.5) groups (P < 0.01). The invasion ability of TECs was significantly inhibited in MU group (9.8 ± 1.3) than in CON (15.8 ± 0.8) and NC (15.4 ± 0.9) groups (P < 0.01). The ability of tube formation of TECs was completely inhibited in MU group but remained unaffected in CON and NC groups.
Conclusions: miR-1224-5p may serve as a potential tumor suppressor in HCC. Upregulation in miR-1224-5p expression may decrease proliferation, induce apoptosis, inhibit migration and invasion, and suppress tube formation in TECs of human HCC.
Keywords: Hepatocellular carcinoma, microRNA-1224-5p, tumor endothelial cell
|How to cite this article:|
Hu C, Cheng X, MingYu Q, Wang XB, Shen SQ. The effects of microRNA-1224-5p on hepatocellular carcinoma tumor endothelial cells. J Can Res Ther 2019;15:329-35
|How to cite this URL:|
Hu C, Cheng X, MingYu Q, Wang XB, Shen SQ. The effects of microRNA-1224-5p on hepatocellular carcinoma tumor endothelial cells. J Can Res Ther [serial online] 2019 [cited 2019 Apr 21];15:329-35. Available from: http://www.cancerjournal.net/text.asp?2019/15/2/329/255093
| > Introduction|| |
Hepatocellular carcinoma (HCC) is a common cancer worldwide. In particular, the occurrence of liver cancer is much common in men than in women. HCC is the second most common cause of cancer-related deaths in men and the sixth leading cause of cancer-related deaths in women. The only treatment that may cure patients with HCC is surgical resection or liver transplantation. However, only about 20% of patients may receive surgical treatment, owing to limitations such as the stage of the carcinoma, liver function, and function of other organs. Furthermore, no effective treatment strategy is yet available after the failure of surgical treatment, especially for patients with advanced HCC. Therefore, identification of novel therapeutic strategies for HCC is desirable.
Recent evidence show that tumor microenvironment plays an important role in the progression of cancer. In cancer, tumor cells are very aggressive, and a variety of associated elements from the tumor microenvironment such as tumor stroma, blood vessels, and infiltrating inflammatory cells play the role of supporting players to aid in the progression of malignancy. The nontumor cells in the tumor microenvironment may be modified by the cancerous cells to produce a variety of materials that enhance the proliferation and invasion of the tumor, such as growth factors, chemokines, and matrix-degrading enzymes. Recent studies have suggested various approaches to target different cell types in the tumor microenvironment such as the tumor stroma, tumor vasculature, and immune cells. Hence, treatment regimens that target the tumor microenvironment are thought to offer promising effects.
Hepatocellular cancer is a solid tumor with rich blood supply. HCC growth, invasion, and metastasis are all closely associated with angiogenesis. Therefore, regulation of tumor angiogenesis may control the growth of tumor. The process of tumor development may be divided into two stages, namely the avascular stage and the vascular stage. The volume of tumor may be only 1–2 mm during the avascular stage owing to hypoxia. Disturbance in the balance between the angiogenic growth factors and their inhibitors may induce angiogenesis and progression to the vascular stage. During this stage, the growth of tumor is accelerated. Recent studies have mainly focused on stimulatory factors or inhibitory factors of tumor angiogenesis such as vascular endothelial growth factor, hepatocyte growth factor, and vascular endothelial growth factor inhibitor. Very few studies have been directed toward tumor vascular endothelial cells. Therefore, identification of specific molecular markers of tumor vascular endothelial cells may provide a new basis for antiangiogenic therapy in HCC.
MicroRNAs (miRNAs) are a class of noncoding small RNA molecules comprising 20–22 nucleotides that regulate gene expression at the posttranscriptional level. In cellular pathways, miRNAs play important roles by regulating the expression of downstream target genes at protein level. Many recent studies have suggested that the abnormal expression of miRNA is associated with cell proliferation, apoptosis, invasion, and metastasis in many cancers.,,,, Abnormal expression of microRNA-1224-5p (miR-1224-5p) was recently shown to be associated with several human cancers.,, miR-1224-5p is known as a tumor suppressor in malignant gliomas. However, little is known about the expression and function of miR-1224-5p in tumor endothelial cells (TECs) of human HCC. Our previous studies revealed the downregulation of miR-1224-5p expression in TECs of human HCC. The normalized intensity of hepatic sinusoidal endothelial cells (HSECs) and TECs was 320.137967 and 213.236189, respectively, whereas the log2 (TEC/HSEC) was −0.586241, P = 0.000285 (selection criteria to identify differentially expressed genes were established at log2 |Fold change| ≥0.585 and P < 0.05). Therefore, miR-1224-5p may be a tumor suppressor in TECs of human HCC. To confirm this hypothesis, we designed the present study.
In this study, we demonstrate that the exogenous expression of miR-1224-5p in TECs of human HCC may inhibit the proliferation, migration, invasion, and angiogenesis capability and promote apoptosis of TECs. Our findings provide the first evidence of the role of miR-1224-5p as a tumor suppressor in TECs of human HCC. Based on these findings, miR-1224-5p may serve as a novel therapeutic target for human HCC.
| > Subjects and Methods|| |
We obtained TECs of human HCC and human HSECs from Shanghai Xinran Biotechnology (Shanghai, China). Cells were cultured in Dulbecco's Modified Eagle's Medium (DMEM) with high glucose supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin, and 100 mg/mL streptomycin under 5% CO2 in a humidified incubator at 37°C.
Oligonucleotides and cell transfection
The experimental cells were divided into three groups as follows: a control (CON) group without transfection, negative control (NC) group transfected with negative control oligonucleotides and green fluorescent protein (GFP), and a micro-up (MU) group transfected with miR-1224-5p mimic and GFP. Oligonucleotides were chemically synthesized by Gene Pharma Co., Ltd. (Shanghai, China) based on the following sequences: hsa-miR-1224-5p mimic (MU group), 5'-GUGAGGACUCGGGAGGUGG-3'; scrambled miRNA (NC group), 5'-UUCUCCGAACGUGUCACGUTT-3'. Oligonucleotides were transfected into TECs using Lipofectamine 2000 (Invitrogen) for 6 h.
Quantitative reverse-transcription polymerase chain reaction for mature microRNA-1224-5p expression
Quantitative reverse-transcription polymerase chain reaction (PCR) was performed to detect the expression of miR-1224-5p in different groups. U6 small nuclear RNA was used as the internal standard control. Total RNA was harvested from cells of different groups using the Trizol reagent (Invitrogen) according to the manufacturer's instructions. For reverse transcription, 5 μg of total RNA was converted to cDNA using a TaqMan MicroRNA Reverse Transcription Kit (Fermentas) according to the manufacturer's protocol. The resulting cDNA was diluted 1:10 and used for PCR with 4 μL of miR-1224-5p or U6 TaqMan primers and SYBR Green/Fluorescein qPCR Master Mix (Fermentas) in the ABI PRISM 7900HT (Applied Biosystems, Foster City, CA, USA). The sequences of the primers were as follows: miR-1224-5p forward, 5'-TGCGCGTGAGGACTCGGGA-3'; miR-1224-5p reverse, 5'-CTCAAGTGTCGTGGAGTCGGCAA-3'; U6 forward, 5'-CGCTTCGGCAGCACATATAC-3'; U6 reverse, 5'-AAATATGGAACGCTTCACGA-3'. PCR amplification from cDNA was performed in a final volume of 25 μL, and the cycling parameters included preheating at 95°C for 10 min, followed by 40 cycles of 95°C for 30 s and 60°C for 1 min and a melting curve analysis. The specificity of the PCR amplification was confirmed via a dissociation curve analysis. All reactions were performed in triplicates. ΔCt data were automatically collected and −ΔΔCt was calculated using the following formula: −ΔΔCt = ΔCt of CON group −ΔCt of the NC or MU group. The relative expression of the target gene was calculated using 2−ΔΔCt.
Detection of tumor endothelial cell proliferation using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay
Cells from each group were seeded at a density of 5000 cells/well in 96-well plates (five replicates per well per condition) and cultured overnight. The cells were transfected with miR-1224-5p mimic or a scrambled control construct. The proliferation of the cells was measured every 24 h after transfection using an MTT Cell Proliferation Assay Kit (Beyotime, China) according to the manufacturer's instructions. The cell viability was determined at 490-nm absorbance using a microplate reader, and the results were statistically analyzed.
Flow cytometry detection of apoptosis in tumor endothelial cells
Apoptosis was determined using a 7-amino-actinomycin (7-AAD)/APC Annexin V kit (eBioscience, San Diego, CA, USA). TECs from each group were plated into six-well plates and transfected with oligonucleotides. The apoptosis ratio was analyzed 48 h after transfection according to the manufacturer's instructions. This assay allows identification of early apoptotic cells (7-AAD negative, APC Annexin V positive) and late apoptosis or already dead cells (both APC Annexin V and 7-AAD positive). Assessment of apoptosis was repeated in triplicates.
Cell migration assay by transwell
A total of 3 × 104 cells were resuspended in serum-free DMEM after transfection and placed in the top portion of a transwell chamber with 8-μm pores (Millipore). The lower portion of the chamber contained 10% FBS as a chemoattractant. The chambers were incubated at 37°C in 5% CO2 for 12 h. Nonmigrating cells on the top of the membrane were removed with cotton swabs. Cells that migrated to the bottom of the insert were fixed with 95% ethanol, stained with 0.2% crystal violet (Beyotime, China), and counted and photographed under ×100 magnification. Five random fields were analyzed in each chamber.
Cell invasion assay by transwell
A total of 3 × 104 cells were resuspended in serum-free DMEM after transfection and placed on the top portion of a transwell chamber with 8-μm pores (Millipore) and coated with 30 mg/cm2 Matrigel extracellular matrix gel (Sigma-Aldrich, USA). The lower portion of the chamber contained 10% FBS as a chemoattractant. The chambers were incubated at 37°C in 5% CO2 for 24 h. Cells on the top of the membrane were removed with cotton swabs. Cells that invaded to the bottom of the insert were fixed with 95% ethanol, stained with 0.2% crystal violet (Beyotime, China), and counted and photographed under ×100 magnification. Five random fields were analyzed in each chamber.
Tube formation assay
A total of 5 × 104 TECs were resuspended in DMEM supplemented with 10% FBS after transfection and seeded in 48-well culture dishes coated with Matrigel. Peak tube formation was observed at 12 h posttreatment, and five random fields were observed under a microscope. This experiment was independently repeated thrice.
All data were expressed as the mean ± standard deviation. SPSS 17.0 software (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. Differences among groups were assessed using an unpaired Student's t-test. P values less than 0.05 were considered statistically significant.
| > Results|| |
Evaluation of the effects of transfection
After 24 h of transfection, the expression of GFP was observed under a fluorescence microscope. [Figure 1]A1, [Figure 1]B1, and [Figure 1]C1 shows the morphology of cells in the CON, NC, and MU groups, respectively, under bright field. [Figure 1]A2, [Figure 1]B2, and [Figure 1]C2 shows the same fields under green fluorescence. The CON group showed no green fluorescence [Figure 1]A2, whereas obvious green fluorescence was reported for the NC group [Figure 1]B2 and MU group [Figure 1]C2. These results indicate that the oligonucleotides were successfully transfected into TECs.
|Figure 1: Evaluation of the effects of transfection. Figure 1 shows the morphology of cells in the three groups under bright field and green fluorescence field (A1: CON ×100 B; B1: NC ×100 B; C1: MU ×100 B; A2: CON ×100 G; B2: NC ×100 G; and C2: MU ×100 G). B and G indicate the bright field and green fluorescence field, respectively. CON=Control, NC=Negative control, MU=Micro-up|
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MicroRNA-1224-5p expression in tumor endothelial cells from the three groups
As seen in [Figure 2], the expression of miR-1224-5p was significantly increased in the MU group (2−ΔΔCt = 3.27 ± 0.15) as compared to the CON group (2−ΔΔCt = 1) and the NC group (2−ΔΔCt = 1.08 ± 0.11) (P < 0.01). No significant difference was observed between the NC and CON groups (P > 0.05).
|Figure 2: MicroRNA-1224-5p expression in tumor endothelial cells from the three groups. The expression of microRNA-1224-5p was significantly upregulated in micro-up group as compared to negative control and control groups (P < 0.01). No significant difference was observed between the negative control and control groups (P > 0.05). #P < 0.01 compared with control and negative control groups|
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Detection of tumor endothelial cell proliferation by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay
As shown in [Figure 3], cell proliferation was significantly inhibited in MU group at four time points (optical density value at the wave length of 490 nm [OD490] from 24 to 96 h was 0.460 ± 0.022, 0.878 ± 0.018, 1.716 ± 0.035, and 2.257 ± 0.054) as compared with the CON group (OD490 from 24 to 96 h was 0.587 ± 0.006, 1.238 ± 0.005, 2.426 ± 0.040, and 3.240 ± 0.048) and the NC group (OD490 from 24 to 96 h was 0.575 ± 0.004, 1.228 ± 0.057, 2.279 ± 0.086, and 3.154 ± 0.038) (P < 0.01). On the other hand, the cell proliferation was unaffected in CON and NC groups (P > 0.05).
|Figure 3: Detection of tumor endothelial cell proliferation by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Cell proliferation was significantly inhibited in micro-up group compared with control and negative control groups (P < 0.01), whereas no significant difference was observed between control and negative control groups (P > 0.05). #P < 0.01 compared with control and negative control groups|
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Flow cytometric detection of apoptosis in each group after transduction
[Figure 4] shows the apoptosis of TECs from three groups. No significant difference was observed between the CON group (8.73% ± 0.64%) and NC group (9.51% ± 0.56%) (P > 0.05). However, the apoptosis percentage was significantly higher in the MU group (19.29% ±0.95%) than in other groups (P < 0.01).
|Figure 4: Flow cytometric detection of apoptosis in each group after transduction. (a) Flow cytometry results of control group. (b) Flow cytometry results of negative control group. (c) Flow cytometry results of micro-up group. Cells positive for APC were considered apoptotic (right upper quadrant and right lower quadrant). P < 0.01 compared with control and negative control groups|
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Cell migration assay by transwell in each group after transduction
As shown in [Figure 5], the number of cells that migrated to the lower portion of the chamber in the CON, NC, and MU groups was 77.7 ± 2.5, 79.2 ± 3.5, and 51.0 ± 3.6, respectively. Thus, the migration ability was significantly inhibited for TECs from the MU group as compared to those from the CON and NC groups (P < 0.01). No significant difference was observed between the CON and NC groups (P > 0.05).
|Figure 5: Cell migration assay by transwell. The number of cells migrated to the lower portion of the chamber was significantly decreased in micro-up group as compared to control and negative control groups (P < 0.01). No significant difference was observed between control and negative control groups (P > 0.05). #P < 0.01 (a: Control group; b: Negative control group; c: Micro-up group, ×100)|
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Cell invasion assay by transwell in each group after transduction
As observed in [Figure 6], the number of cells that invaded the lower portion of the chamber in the CON, NC, and MU groups was 15.8 ± 0.8, 15.4 ± 0.9, and 9.8 ± 1.3, respectively. Thus, the invasion ability was significantly inhibited for TECs from the MU group as compared with those from CON and NC groups (P < 0.01). No significant difference was observed between the CON and NC groups (P > 0.05) [Figure 6].
|Figure 6: Cell invasion assay by transwell. The number of cells that invaded to the lower portion of the chamber was significantly decreased in micro-up group as compared to control and negative control groups (P < 0.01). No significant difference was reported between control and negative control groups (P > 0.05). #P < 0.01 (a: Control group; b: Negative control group; c: Micro-up group, ×100)|
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Tube formation assay in each group after transduction
As observed in [Figure 7], the ability of tube formation was unaffected in TECs from the CON and NC groups. However, the tube formation ability of cells from the MU group was inhibited.
|Figure 7: Tube formation assay in each group after transduction. Tumor endothelial cells from control and negative control groups could form tubes. Cells from micro-up group lost their ability to form tubes (a: Control group; b: Negative control group; c: Micro-up group, ×100)|
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| > Discussion|| |
Several recent studies have demonstrated the influence of angiogenesis on tumor germination and growth., Therefore, the selective inhibition of TECs of HCC may serve as a more effective and less toxic therapeutic method for the treatment of patients with HCC. miRNAs play an important role in a variety of cellular processes such as proliferation, apoptosis, differentiation, and cellular migration at posttranscriptional level.,,, Many miRNAs have been found as tumor suppressors and their expressions are downregulated in diverse human cancers., Several independent research groups have reported the downregulation of miR-1224-5p in colorectal, rectal, and lung cancers.,, However, the expression and function of miR-1224-5p in HCC remain unclear. In this study, we explored the effects of the upregulation of miRNA-1224-5p expression on the biological behaviors of TECs from HCC and found that miR-1224-5p upregulation dramatically repressed the proliferation, migration, invasion, and tube formation abilities of TECs of HCC and promoted cell apoptosis.
Tumorigenesis is known to be associated with the imbalance between cell proliferation and apoptosis. Therefore, in this study, we observed the effect of miR-1224-5p on the proliferation and apoptosis of TECs. The results of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay indicated that miR-1224-5p upregulation could significantly decrease the proliferation of TECs. The results of apoptosis detection assay also showed that the upregulation of miR-1224-5p could significantly induce apoptosis in TECs. The death-inducing signaling pathway and mitochondrial pathway are the two major pathways of cellular apoptosis. The mechanism underlying the apoptosis-inducing effect of miR-124-5p in TECs is yet unclear and further studies are warranted to reveal the potential mechanism.
Tumor invasion and metastasis are important causes of morbidity and death in patients with liver cancer. During the progression of invasion and metastasis, blood vessels play an important role. Our experiments for the evaluation of the in vitro migration, invasion, and tube formation abilities showed that the upregulation of miR-1224-5p expression could significantly suppress the migration, invasion, and tube formation abilities of TECs of human HCC. However, we failed to study the effects of miR-1224-5p in solid HCC in vivo and may consider this aim as our primary mission in the near future.
In summary, our study demonstrated that miR-1224-5p may serve as a potential tumor suppressor in HCC. Upregulation in the expression of miR-1224-5p may result in the decrease in the proliferation, induction of apoptosis, inhibition of migration and invasion, and suppression of tube formation in TECs of human HCC. These data suggest that miR-1224-5p may play a critical role in the development of HCC as a tumor suppressor miRNA. The mechanism underlying the effects described above still requires further research. We have found some potential target genes of miR-1224-5p, such as origin recognition complex subunit 2 and cAMP-responsive element-binding protein 1 (CREB1), using the software TargetScan. CREB1 is a transcription factor that has a central role in the regulation of the expression of multiple target genes such as B-cell lymphoma 2 (Bcl2 associated with apoptosis) and matrix metalloproteinase-9 (MMP9 associated with invasion)., We suggest that the expression of miR-1224-5p may reduce the expression of CREB1, which modulates the downstream MMP9 and Bcl-2 and therefore regulates cell proliferation, invasion, and apoptosis. Future studies with luciferase activity assay and northern blotting may help us confirm this hypothesis. In addition, we will perform in vivo experiments to observe the effect of miR-1224-5p on the growth, invasion, and metastasis of HCC.
| > Conclusion|| |
The results of our researches show that upregulation in miR-1224-5p expression may decrease proliferation, induce apoptosis, inhibit migration and invasion, and suppress tube formation in TECs of human HCC. MiR-1224-5p may serve as a potential tumor suppressor in HCC.
The cell culture experiments were performed in the laboratory of “Key Laboratory of Hubei Province for Digestive System Disease.” The authors would like to thank Professor Hong Xia from the Institute of Digestive and Liver Diseases, Wuhan University, for his excellent technical support.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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