Mesenchymal stem cells promote tumor angiogenesis via the action of transforming growth factor β1
- Authors:
- Published online on: December 3, 2015 https://doi.org/10.3892/ol.2015.3997
- Pages: 1089-1094
Abstract
Introduction
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-associated mortality worldwide (1,2). The poor prognosis of HCC is primarily due to the high rate of tumor recurrence following surgery, or the occurrence of intrahepatic metastasis (3,4). Accumulating evidence indicates that the occurrence of liver disease may be strongly associated with bone marrow cells (5–7). Bone marrow mesenchymal stem cells (BM-MSCs) have an inhibitory role in HCC metastasis (8).
Angiogenesis is a process that leads to the formation of novel blood vessels from preexisting vascular networks. Angiogenesis is a necessary process for tumor growth, invasion and metastasis (9). Intratumor microvessel density (MVD) and vascular endothelial growth factor (VEGF) are significant biomarkers for the assessment of angiogenesis (10). Due to the hypervascular nature of HCC tumors, angiogenesis has a significant role in the progression of HCC (11). VEGF and MVD have been demonstrated to be potential predictors for clinical outcomes and HCC metastatic recurrence (12).
It has been reported that BM-MSCs may contribute to tumor vascularization (13). BM-MSCs are a progenitor for angioblasts, which subsequently differentiate into cells that express endothelial markers, which are capable of functioning in vitro as mature endothelial cells, as well as contributing to neoangiogenesis in vivo (14). MSCs are additionally capable of releasing various cytokines, including VEGF and transforming growth factor (TGF)β1 (8,15). These cytokines are able to influence angiogenesis in tumors (16–18). However, the potential role of MSCs in the angiogenesis of HCC tumors remains to be elucidated.
In a previous study conducted by the authors of the present study, it was identified that MSCs are able to home to the sites of HCC tumors, and affect tumor growth and progression via the action of TGFβ1 (8). However, the role of MSCs in the angiogenesis of HCC tumors remains to be elucidated. Therefore, in the present study, the aim was to investigate the potential role of MSCs in the angiogenesis of HCC tumors.
Materials and methods
Cell lines
Human BM-derived MSCs were purchased from Sciencell Research Laboratories (Carlsbad, CA, USA). These cells were isolated from human bone marrow, and characterized by immunofluorescent methods, using cluster of differentiation (CD)44 and CD90 antibodies and lipid staining following differentiation. Following 5 passages of subculture, the cells were re-evaluated by immunocytochemical staining in order to assure that the normal phenotype of MSCs had been retained. The 5th passage MSCs did not express the surface marker CD34, expressed low levels of fetal liver kinase (Flk)-1 and increased levels of CD29 and CD105. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) revealed that the MSCs expressed octamer-binding transcription factor-4 and Flk-1, which was concordant with previously published data concerning MSC cell surface markers (19). Cells were cultured in α-modified minimum essential medium (Gibco; Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific) and 100 U/ml penicillin/streptomycin solution (Sciencell Research Laboratories). The medium was replaced when the cell density reached 5,000 cells/cm2 and the culture reached 50% confluence. Cells were subcultured when 90% confluence was reached. Cells that had undergone between 5 and 8 passages were utilized for the following experiments.
MHCC97-H human HCC cell line was purchased from the Liver Cancer Institute of Fudan University (Shanghai, China). These cells exhibit a high metastatic potential, are positive for α-fetoprotein, albumin and cytokeratin 8 expression, and negative for hepatitis B (HBV) surface antigen. Fluorescence PCR has revealed the occurrence of HBV DNA integration in the cellular genome (20,21). The cells were cultured in high glucose Dulbecco's modified Eagle's medium (Gibco; Thermo Fisher Scientific), supplemented with 10% FBS at 37°C in a humidified incubator with an atmosphere of 5% CO2.
Animal models
In total, 8 female mice and 9 male mice were randomly assigned into two groups, an experimental group and a control group. All mice were fed under specific-pathogen free conditions, food and water were treated by high pressure steam sterilization, and the feeding temperature was 28°C. A total of 6×106 MHCC97-H cells were subcutaneously implanted into nude mice. A total of 30 days subsequent to implantation, subcutaneous tumor tissue was removed and cut into 1×1×1 mm3 tissue sections. These sections were subsequently orthotopically implanted into the livers of 17 nude mice.
The experiments were performed following the approval of Xijing Medical Ethics Committee (Xi'an, China), and were also in compliance with the Helsinki Declaration and Animal Research: Reporting in vivo experiments guidelines (22).
MSC injection
In order to evaluate the potential effects of MSCs on pulmonary metastasis of HCC, 8 of the mice were treated with 5×105 human MSCs via tail vein injection 3 times in one week. The remaining 9 mice were treated with phosphate-buffered saline (PBS; 0.2 ml), 3 times a week, as a control. A total of 35 days following injection, the mice were sacrificed and tumors were removed, weighed and subsequently cryopreserved at −80°C, with a 1:4 dilution of optimal cutting temperature compound (Sakura Finetek, Inc., Torrance, CA, USA) in PBS. Liver and lung tissues were fixed in paraformalin (Sigma-Aldrich, St. Louis, MO, USA) and embedded in paraffin.
Evaluation of lung metastasis of HCC
The incidence and tumor foci number of the lung metastases were evaluated using hematoxylin and eosin (Beyotime Institute of Biotechnology, Inc., Shanghai, China) staining in 10 consecutive sections, with an interval of 50 µm, and were additionally assessed by two independent pathologists.
MVD counting
Fresh-frozen 8-µm sections of tumor were fixed in acetone sections (Spectrum Chemical Manufacturing Corporation, New Brunswick, NJ, USA), and stained using monoclonal mouse anti-CD31 (CBL1337; dilution, 1:200; EMD Millipore, Billerica, MA); and subsequently donkey anti-mouse Immunoglobulin G-horseradish peroxidase (AP189; dilution, 1:500; EMD Millipore, Billerica, MA) was used as a secondary antibody. Following 3,3-diaminobenzidine (ZSGB-BIO, Beijing, China) staining, the maximum density of positive staining was selected as microscope field (magnification, ×20) and microvessels were counted.
RNA extraction and RT-qPCR
Total RNA of tumor tissues was extracted using TRIzol® reagent (Invitrogen; Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer's protocols. SYBR Green Realtime PCR Master Mix (Toyobo Co., Ltd., Osaka, Japan) was used to perform RT-qPCR analysis, in order to identify the expression levels of TGFβ1, Smad2 and Smad7. The primers were designed using Primer Premier software version 5.0 (PREMIER Biosoft, Palo Alto, CA, USA), and the sequences used are listed in Table I. Amplification conditions were as follows: 95°C for 9 min, followed by 45 cycles at 95°C for 30 sec, 57°C for 30 sec and 72°C for 15 sec, followed by a final extension step at 72°C for 5 min. β-actin served as a control for detection of the presence of amplifiable complementary DNA. The mRNA expression levels were quantified using the 2−∆∆Cq method. In brief, the Cq value for the target gene was subtracted from the Cq value of β-actin in order to give a ∆Cq value. The average ∆Cq value was calculated for the control group, and this value was subsequently subtracted from the ∆Cq value of all other samples (including the control group). This resulted in the production of a ∆∆Cq value for all samples, which was subsequently used in order to calculate the fold-induction of mRNA expression of the target genes using the formula 2−∆∆Cq, as recommended by the manufacturer's protocols (Bio-Rad Laboratories, Inc., Hercules, CA, USA). In the present study, MHCC97-H model samples served as the control group.
Protein extraction and ELISA
Tumor samples were lysed in radioimmunoprecipitation assay buffer (50 mM Tris-HCl, pH 7.5; 150 mM NaCl; 0.5% sodium deoxycholate; 1% NP-40; 0.1% sodium dodecyl sulfate) plus serine protease inhibitors. Protein was extracted by microcentrifugation for 30 min at 13,000 × g. Protein concentration was determined using Bradford Reagent (Beyotime Institute of Biotechnology, Inc.). The VEGF and TGFβ1 concentration in the protein extracts was determined using the Human VEGF Quantikine ELISA assay kit (DVE00; R&D Systems, Inc., Minneapolis, MN, USA) and Human TGF-beta 1 Quantikine ELISA kit (R&D Systems, Inc.)according to the manufacturer's protocol. The optical density values were measured using a Spectramax M5 microplate reader (Molecular Devices, LLC., Sunnyvale, CA, USA) at 450 nm wavelength.
Statistical analysis
Data was analyzed using SPSS version 11.5 (SPSS, Inc., Chicago, IL, USA). Student's t test was utilized for analysis of the significance of differences between tumor weight and volume, and mRNA expression levels of target genes for independent samples. Fishers' exact test was performed for the comparison of ratio involved. All statistical tests performed were two-sided, and P<0.05 was considered to indicate a statistically significant difference.
Results
MSC treatment reduces the rate of pulmonary metastasis of HCC
No difference in tumor weight was observed between the group treated with MSCs and the untreated control group; the ratios of tumor to body weight were 0.14±0.05 vs. 0.13±0.04, respectively (P=0.75). Compared with the control group, the pulmonary metastasis rate of the MSC-treated mice (100 vs. 50%, for the control and MSC-treated mice, respectively) was statistically reduced (100%; P=0.029; Table II).
MSC treatment exerts differential effects on the expression of mRNA of TGFβ1 and Smads in HCC tumors
Levels of TGFβ1 mRNA in the MSC-treated group were 2.15-fold higher compared with the untreated controls (1.27±0.61 vs. 0.59±0.39; P=0.033), however, the levels of Smad7 mRNA were downregulated compared with untreated controls (0.76±0.29 vs. 1.41±0.50; P=0.006; Table III).
MSC treatment exerts differential effects on MVD and VEGF expression in HCC
The expression of VEGF in the MSC-treated group did not significantly differ compared with the untreated control group (0.29±0.05 vs. 0.31±0.13; P=0.631). However, MVD was significantly increased in the MSC-treated group compared with the untreated control group (28.00±9.19 vs. 18.11±3.30; P=0.006; Fig. 1; Table III).
Levels of TGFβ1 mRNA are associated with MVD
According to the median levels of TGFβ1 mRNA, Smad2 mRNA, Smad7 mRNA, TGFβ1 protein and VEGF protein, expression levels were divided into two groups, high-level and low-level. MVD was increased in the TGFβ1 mRNA high-level group compared with the low-level group (26.50±9.11 vs. 19.44±6.14; P=0.038), however, the levels of Smad2 mRNA (23.67±7.84 vs. 21.75±9.14; P=0.648), Smad7 mRNA (24.33±8.26 vs. 21.00±8.46; P=0.424), VEGF protein levels (22.12±8.82 vs. 23.33±8.23; P=0.375) and TGFβ1 protein levels (23.66±8.23 vs. 20.63±8.29; P=0.375) demonstrated no significant difference between the two groups (Fig. 2A).
TGFβ1 and VEGF protein levels are associated with metastasis
In the present study, it was identified that TGF protein levels were closely correlated with VEGF protein levels using linear correlation analysis (R2=0.55; P=0.006; Fig. 2B). In addition, TGFβ1 and VEGF protein levels were observed to be associated with the tumor foci number of metastasis (R2=0.28 and P=0.030; and R2=0.30 and P=0.001, respectively; Fig. 2C and D).
MVD was not observed to be associated with tumor growth and metastasis of HCC
According to the median levels of MVD, samples were divided into two groups, dependent on high or low MVD. No statistically significant differences were identified between the two groups, including for tumor weight, pulmonary metastasis rate, tumor foci number of metastasis and cellular number of metastases (Table IV).
Discussion
MVD is a direct reflection of tumor angiogenesis, and may be visualized using immunohistochemical staining with antibodies of anti-CD31, anti-CD34, factor VIII and α-smooth muscle actin (23). In the present study, it was identified that MSC is capable of enhancing the MVD of HCC tumors, as well as inhibiting pulmonary metastasis. The results of the present study provided evidence and indicated that MSC may promote tumor angiogenesis and influence tumor progression.
In HCC, MVD is closely associated with tumor size, recurrence and disease-free survival (24). However, the present study did not identify an association between MVD and metastasis and tumor size. Although intratumor MVD is a marker for angiogenesis, it is not able to provide any functional information concerning the underlying molecular pathways involved in the angiogenic activity of a specific tumor (25). Multivariate analysis has indicated that MVD is not an effective prognostic factor when tumor size is >5 cm (9). In addition, three types of intratumor microvessels may be identified in HCC, including capillary-like, sinusoid-like and mixed-type, which make the prognostic value of MVD uncertain (24).
Cytokines have a significant role in tumor metastasis and angiogenesis (26,27). TGFβ1 may influence the invasiveness and metastasis of carcinoma (28–30), and has been observed to particularly promote angiogenesis (31–34). The present study identified that MSCs were able to significantly enhance the expression of TGFβ1 mRNA, however, inhibited the expression of Smad7 mRNA. Additionally, TGFβ1 mRNA expression levels correlated with MVD. The results of the present study suggested that MSCs may promote angiogenesis via the TGFβ1/Smad signaling pathway, and may have revealed a novel mechanism for the role of MSCs in tumor progression. The present study detected TGFβ1 mRNA and protein levels and demonstrated that MVD was correlated with the levels of TGFβ1 mRNA, however, was not correlated with the levels of TGFβ1 protein. This divergence may be due to the complicated post-transcriptional mechanisms involved in translation of mRNA into proteins (35).
No association was identified between MSC injection and VEGF expression, and VEGF was not observed to enhance MVD in the present study. However, a close association was observed between TGFβ1 and VEGF, and these cytokines were demonstrated to be associated with tumor metastasis, which may indirectly reflect the role of VEGF in tumor angiogenesis. It has been reported that VEGF and TGFβ1 interact with each other during the process of angiogenesis. This interaction complicates their role in angiogenesis, and in some cases may induce an inhibitory effect on cancer proliferation (36–39).
In conclusion, the results of the present study suggested that MSCs may enhance the angiogenesis of HCC through the action of TGFβ1. The TGFβ1/Smad signaling pathway and its interaction with VEGF may partly explain the intricate role of MSCs in tumor progression. Whether the increase in angiogenesis is due to the differentiation of MSCs or caused by alternative vascular regulators secreted by MSCs requires investigation in future studies.
Acknowledgements
The authors would like to thank Dr Qiong Xue, Dr Dongmei Gao and Dr Jun Chen in Liver Cancer Institute of Fudan University (Shanghai, China) for their assistance with the animal experiments, Dr Ruixia Sun and Dr Jie Chen in Zhongshan hospital of Fudan University for their suggestions for cell culture, and Dr Haiying Zeng and Dr Tengfang Zhu in the Pathological Department of Zhongshan Hospital of Fudan University, for their assistance with pathological experiments.
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