Skip to main content

CD146 promotes metastasis and predicts poor prognosis of hepatocellular carcinoma

Abstract

Background

Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related mortality worldwide. Recurrence and metastasis after curative resection remain critical obstacles in HCC treatment. CD146 predicted poor prognosis of a variety of cancers including melanoma, breast tumors, prostate cancer, and gastric cancer. However, the role of CD146 in HCC has not yet been systematically explored.

Methods

To investigate the role of CD146 in HCC, we evaluated its expression in HCC tissues and HCC cell lines using real-time PCR and western blotting (WB). Second, we established HCC cell lines that stably overexpressed and interfered CD146 and explored the function of CD146 in HCC in vitro and in vivo. Third, we conducted microarray analysis to investigate the potential mechanism by identifying differentially expressed genes. Last, follow ups were conducted to help uncover the connection of CD146 expression and the prognosis of HCC patients.

Results

We found that CD146 was overexpressed in HCC tissues and that high CD146 expression predicted poor overall survival time and shorter recurrence period in HCC patients. In vitro and in vivo experiments indicated that CD146 promoted migration and invasion of HCC cell lines. Further study indicated that CD146 promoted epithelial mesenchymal transition (EMT), IL-8 upregulation, and STAT1 downregulation. CD146 was upregulated in HCC tissues and cell lines.

Conclusions

CD146 promoted metastasis of HCC cells and predicted poor prognosis of HCC patients. CD146 induced EMT, and IL-8 upregulation and STAT1 downregulation may be the potential underlying mechanism. The exact mechanism still needs further investigation.

Background

Hepatocellular carcinoma (HCC) is the fifth most common malignant cancer and the third leading cause of cancer-related mortality in China [1]. Recurrence and metastasis after curative resection are the most challenging burdens for HCC treatment [2]. However, the underlying mechanism of HCC metastasis is largely unknown.

CD146 was first reported in malignant melanomas [3]. CD146 is a 113-kD membrane glycoprotein that contains five immunoglobulin-like domains, a transmembrane region, and a short cytoplasmic tail [4]. Early research indicated that CD146 expressed in normal tissues is restricted to the blood vessels and smooth muscle cells [5]. Whereas, subsequent research indicated CD146 is a multifunctional molecule that participates in several physiological and pathological processes involving in development, immunity, and angiogenesis [6]. CD146 mediates development of the nervous system, kidney, and retina [7–9]. Knockdown of CD146 protein expression hinders vascular development whereas overexpression of CD146 in zebrafish induces sprouting angiogenesis [10]. CD146 was also found to play a critical role in cancer progression. In most cancers, CD146 was found to promote cancer progression, enhanced migration and invasion was observed in melanoma, gallbladder adenocarcinoma, breast cancer and prostate cancer [11–14]. In gastric cancer, lung adenocarcinoma, malignant pleural mesothelioma, and non-small-cell lung cancer, CD146 has been identified as an indicator of poor prognosis [15–18]. However, in oral mucoepidermoid carcinoma, CD146 expression was greater in intermediate/high grade tumors, was weaker in patients that presented local recurrence, regional and distant metastasis [19]. Most researches above focused on relationship between CD146 expression and clinical outcomes, the underlying mechanism of CD146 induced migration and invasion has not yet been systemically explored. the mechanism besides CD146 induced angiogenesis was rarely explored. In HCC research, CD146 was reported to be used as endothelial marker in selective targeting of liver cancer treatment [20]. The role of CD146 in HCC cells has not yet been explored.

In this study, we set out to investigate the role of CD146 in HCC. We mainly focused on the CD146 on tumor cells whereas the role of CD146 in endothelial cells was not addressed. Firstly, the expression of CD146 in HCC tissues and HCC cell lines was detected using RT-PCR and WB, the location of CD146 was confirmed using IHC; Secondly, we established in vitro and in vivo models to investigate the biologic function of CD146 in HCC cells; Thirdly, we conducted a mRNA microarray to systemically explore the mechanism of CD146 induced biologic behavior variation of HCC cells; lastly, CD146 expression and clinical prognosis of HCC patients was concerned.

Methods

Cell lines and cell culture

Cell lines used in this study include eight human HCC cell lines, MHCC-97H, MHCC-97 L, HepG2, SMMC-7721, Focus, YY-8103, LM3, and HLF, and one human noncancerous hepatic cell line, L02. All these cell lines were provided and identified by our key laboratory of living donor liver transplantation. All cells were cultured in Dulbecco’s Modified Eagle medium (Gibco, Grand Island, NY, USA) containing 10 % FBS (Hyclone, Logan, UT, USA), 100 U/mL penicillin and 100 μg/mL streptomycin (Invitrogen, Carlsbad, CA, USA) at 37 °C in 5 % CO2.

Patients and follow-up

A total of 120 HCC samples and homologous noncancerous tissue samples were randomly obtained from the samples that were removed from the patients and stored in the department of pathology between June 2008 and May 2010, snap frozen in liquid nitrogen, and stored at −80 °C until use. All samples were subjected to routine pathological examination at the First Affiliated Hospital of Nanjing Medical University. All patients underwent curative resection of HCC at the First Affiliated Hospital of Nanjing Medical University (Nanjing, China). The patients’ age ranged from 31 to 83 years. Detailed clinicopathological characteristics of the 120 HCC patients are listed in Table 1. Written informed consent was obtained from each patient before surgery. The patients were followed up after surgical treatment until August 2014. This study was approved by the Ethics Committee of the First Affiliated Hospital of Nanjing Medical University.

Table 1 Clinical characteristics of HCC patients and correlation with CD146 level

RNA extraction and quantitative RT-PCR

Total RNA was extracted from tissue samples and cell lines using Trizol Reagent (Takara, Dalian, China). RNA concentrations and quality were determined with a NanoDrop ND-2000 spectrophotometer (NanoDrop Technologies, IL, USA) and gel analysis. Reverse transcription was performed using PrimeScript® RT Reagent Kit (Takara). Real-time polymerase chain reaction (RT-PCR) amplifications were carried out on ABI stepone RT-PCR Detection System (ABI, Carlsbad, CA, USA) using the SYBR Green PCR detection kit (Takara) according to the manufacturer’s introductions. Primers are summarized in Table S1 (Additional file 1). The cycle time (Ct) values of the selected genes were first normalized with the value of beta actin of the same sample, and then the relative expression of each gene was analyzed using the 2-ΔΔCt method.

Western blotting

Western blotting was performed using standard techniques as previously described [11]. Briefly, total protein was extracted using RIPA lysis buffer (50 mM Tris-Cl pH 7.4, 150 mM NaCl, 0.5 % sodium deoxycholate, 1 % NP-40, 0.1 % SDS, 1 mM EDTA, 100 mM NaF, 1 mM Na3VO4, 1 mM PMSF, and 2 μg/mL aprotinin) on ice. Protein samples (50 μg) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred to polyvinylidene difluoride membranes. Membranes were blocked with 5 % nonfat milk in TBST (10 mM Tris, pH 7.4, 150 mM NaCl, and 0.1 % Tween-20) at room temperature for 1 h and incubated with indicated primary antibodies at 4 °C overnight with gentle rocking. After washing with TBST, the membrane was incubated with the appropriate HRP-conjugated secondary antibodies for 1 h at 37 °C. After extensive washing with TBST, proteins were visualized by the enhanced chemiluminescence detection kit in accordance with the manufacturer’s recommendations (Thermo Fisher scientific, MA , USA). Antibodies used in this study are summarized in Table S2 (Additional file 2).

Immunohistochemistry

Immunohistochemical staining was performed using the diaminobenzidine detection kit (Maixin-Bio, Fuzhou, China) following the manufacturer’s instructions. Briefly, human hepatocellular carcinoma tissues with matched peritumor tissues were processed by standard histological techniques. Tissue sections were deparaffinized and rehydrated. Then, sections were heated in a pressure cooker for 2 min to repair antigenicity and were treated with 3 % H2O2 for 10 min to inactivate endogenous peroxidase activity and incubated with goat serum for 10 min to block nonspecific antibody binding. Sections were incubated with a primary antibody at 37 °C for 1 h, a biotin-labeled secondary antibody for 10 min, and streptavidin-peroxidase conjugate for 10 min. A solution of 0.02 % iaminobenzidine was used as chromogen to visualize peroxidase activity. The sections were lightly counterstained with hematoxylin, mounted with Permount, and examined by light microscopy.

Establishment of stable cell clones

Lentiviruses overexpressing CD146 (Lv-CD146) or silencing CD146 (Lv-shCD146) were purchased from Genechem (Shanghai, China). The sequence of interfere chain was listed in Table S3 (Additional file 3). Lentivirus was infected into HCC cells with a multiplicity of infection (MOI) ranging from 5 to 20 in the presence of polybrene (10 μg/mL). Low CD146 expressing cell lines MHCC-97 L and HLF were infected with Lv-CD146, defined as 97 L-CD146 and HLF-CD146. High CD146 expressing cell lines MHCC-97H and SMMC-7721 were infected with Lv-shCD146, defined as 97H-shCD146 and 7721-sh-CD146. At 72 h after infection, cells were selected for 1 week using puromycin (5 μg/mL). The selected cell lines were prepared for subsequent experiments.

Transwell cell migration and invasion assays

Transwell chambers with an 8-μm pore size were used to measure migration and invasion ability of HCC cells. For migration assays, 5 × 104 cells in 250 μL DMEM containing 0.2 % FBS were seeded into the upper chamber and 500 μL DMEM containing 10 % FBS was added to the lower chamber. For invasion assays, the upper chamber was pre-coated with 50 μL 1:1 mixture of Matrigel (BD Biosciences, USA) and DMEM overnight before 1 × 105 cells were seeded. Cells were incubated in 5 % CO2 at 37 °C for 24 h (migration) or 72 h (invasion), Then, cells on the upper side of well were removed, the wells were fixed in methanol for 20 min, and crystal violet was used to stain cells. Photographs of five random fields were captured for quantification analysis. Three identical replicates were performed.

Animals

Male nude mice (4–6 weeks old) were purchased from Yangzhou University and housed in Nanjing Agricultural University under specific pathogen-free conditions and cared for according to the institutional guidelines for animal care. All animal experiments met the National Institutes of Health guidelines and were approved by the Committee on the Ethics of Animal Experiments of Nanjing Medical University.

In vivo metastasis assays

A total of 5 × 106 tumor cells were suspended in 100 μL DMEM and then injected subcutaneously into the upper right flank region of nude mice. When the subcutaneous tumor reached approximately 1 cm in length (approximately 2–4 weeks after injection), it was removed, minced into small pieces of equal volume (1 mm3), and implanted into the livers of nude mice (10 per group). All mice were monitored once every 3 days, and six mice of each group were sacrificed 6 weeks later. The liver and lung tissues were dissected, fixed with 4 % phosphate-buffered neutral formalin, and prepared for histological examination. All metastatic foci in the lung were calculated microscopically to evaluate the development of pulmonary metastasis.

Microarray processing and analysis

Total RNA was isolated from HLF-vec (n = 3) and HLF-CD146 (n = 3) cell lines. RNA samples were analyzed by microarray expression profiling using the Affymetrix Human GeneChip primeview (Affymetrix) according to the manufacturer’s instructions. Briefly, cDNA target preparation and in vitro transcription were conducted using the GeneChip 3′IVT PLUS Kit. Arrays were washed, stained, and processed using the GeneChip Hybridization Wash and Stain Kit, after which they were imaged using the Affymetrix GeneChip Scanner 3000 for subsequent generation of raw data. Genes significantly differentially expressed between HLF-vec and HLF-CD146 cells were selected based on fold change >1.5 and P < 0.05. Functional pathway analysis was conducted using KEGG pathway enrichment analysis and gene ontology analysis according to the manufacturer’s instructions.

Statistical analysis

Statistical analyses were performed using SPSS 18.0 (SPSS, Chicago, IL, USA) or Prism 5.0 (GraphPad Software, La Jolla, CA, USA) software. The results were presented as the mean ± standard error of mean. Quantitative data were performed by the two-tailed Student’s t-test. Categorical data were analyzed by χ2 test. Kaplan–Meier and log-rank analysis was used to assess the survival between subgroups. P < 0.05 was considered statistically significant.

Results

The expression of CD146 is upregulated in HCC

To investigate the role of CD146 in HCC, we first explored the expression of CD146 in HCC tissues and HCC cell lines. We examined CD146 mRNA levels in 120 paired HCC and peritumoral samples using RT-PCR and found that the average expression level of CD146 was significantly higher in HCC than that in peritumoral tissues (Fig. 1a). The upregulation of CD146 was confirmed in 20 paired samples randomly obtained from the 120 paired HCC samples using WB (Fig. 1b (3 pairs) and d, and Additional file 4: Figure S1 (17 pairs)). Immunohistochemical assays revealed that CD146 was located on the membrane of HCC cells (Fig. 1c). CD146 expression was also observed in vascular endothelial cells with much lower intensity, no expression was observed in normal liver cells or other cirrhotic tissue. We then performed RT-PCR and WB to investigate the expression of CD146 in HCC cell lines and noncancerous liver cell lines. We found that the expression of CD146 was markedly upregulated in several HCC cell lines compared with noncancerous cell lines (Fig. 2a and d). Taken together, these data indicated that CD146 is expressed in HCC cells, the expression of CD146 is upregulated in HCC.

Fig. 1
figure 1

CD146 up-regulated in HCC Patients. a RT-PCR of 120 paired HCC and peritumor tissues (***P < 0.001). b Western Blotting of 3 paired HCC and peritumor tissues. c IHC of the location of CD146 is expressed on the membrane of HCC cells (black arrow). d Gray scale analysis of averaged CD146/GAPDH in b (n = 3,**P < 0.01)

Fig. 2
figure 2

Construction of HCC cell lines stably overexpress or interfere CD146 expression. a Western Blot analysis of CD146 in HCC cell lines. b Construction of high CD146 expression cell lines. c Construction of low CD146 expression cell lines. d Gray scale analysis of CD146/GAPDH in a (n = 3). e Gray scale analysis of CD146/GAPDH in B (n = 3, ***P < 0.001). f Gray scale analysis of CD146/GAPDH in c (n = 3, ***P < 0.001)

CD146 promotes migration and invasion of HCC cell lines

To determine the biological function of CD146 in HCC, we first established HCC cell lines that stably overexpress or repress CD146 expression using lentivirus as a vehicle. We overexpressed CD146 in 97 L and HLF cells, which are low CD146-expressing cell lines, by lentiviral particles that overexpresses CD146 and renamed these cell lines as 97 L-CD146 and HLF-CD146 (Fig. 2b and e). We also knocked down CD146 in 97H and SMMC7721 cells, which are high CD146-expressing cell lines, using lentiviral particles that expresses CD146 shRNA, and renamed these cells as 97H-shCD146 and SMMC7721-shCD146 (Fig. 2c and f). We then assessed the effects of CD146 on cell growth, migration, invasion, apoptosis and cell cycle. No obvious differences were observed in cell growth (Additional file 5: Figure S2), apoptosis, or cell cycle (Additional file 6: Figure S3) among all the experimental cells. However, transwell assays demonstrated that upregulation of CD146 expression significantly enhanced the migration and invasion capacities of 97 L-CD146 (Fig. 3a) and HLF-CD146 cells (Fig. 3b). Consistent with these data, CD146 repression in 97H-shCD146 (Fig. 3c) and SMMC7721-shCD146 cells (Fig. 3d) significantly reduced cell migration and invasion. These results indicated that CD146 promotes migration and invasion of HCC cells in vitro.

Fig. 3
figure 3

In vitro migration and invasion assays. a Overexpression of CD146 in 97 L enhanced cell migration and invasion in transwell assays (n = 3, *P < 0.05, **P < 0.01). b Overexpression of CD146 in HLF enhanced cell migration and invasion in transwell assays (n = 3, **P < 0.01, ***P < 0.001). c Inhibition of CD146 in 97H decreased cell migration and invasion in transwell assays (n = 3, **P < 0.01, ***P < 0.001). d Inhibition of CD146 in SMMC-7721 decreased cell migration and invasion in transwell assays (n = 3, *P < 0.05, **P < 0.01)

We further examined the role of CD146 in HCC metastasis by establishing an orthotropic tumor metastasis model in nude mice, which closely mimics the process of human HCC metastasis after the formation of the primary foci. Histological analysis of liver tissues revealed a significant effect of CD146 in local invasion of the HCC tumors in the livers. The tumors of the high-CD146 expressing HCC groups (97H-vec and 7721-CD146) had more frequent invasive growth fronts with irregular tumor borders, whereas those of the low-CD146 expressing HCC groups (7721-vec and 97H-shCD146) showed less invasive foci and regular tumor borders. Histological analysis of lung tissue showed that the incidence of lung metastasis in the high CD146-expressing HCC groups was significantly higher than that in the low CD146-expressing HCC groups (Fig. 4). Taken together, these data confirmed that CD146 promotes migration and invasion of HCC cell lines.

Fig. 4
figure 4

In vivo metastasis assays using orthotropic tumor metastasis model. a HCC cell lines with high CD146 indicated more frequent metastasis nodules in liver (40X vs 200X). b HCC cell lines with high CD146 indicated more frequent metastasis nodules in lung (40X vs 200X). c statistical analysis of liver and lung metastasis

CD146 promotes EMT and IL-8 upregulation and STAT1 downregulation

To uncover the mechanism underlying CD146-induced migration and invasion, we conducted a microarray analysis to identify genes whose expression was modified by CD146 upregulation using HLF-vec and HLF-CD146 cell lines (Fig. 5a). A total of 131 genes were upregulated and 365 genes were downregulated after CD146 overexpression (P < 0.05 and fold change >1.5). Supervised analysis was conducted following KEGG and the Gene Ontology technical route. We focused on cancer-related pathways and found that 16 genes showed modified expression upon CD146 overexpression (Additional file 7: Table S4). A network diagram was drawn to show the potential connection between each gene (Fig. 5b).

Fig. 5
figure 5

Mechanism analysis of CD146 induced metastasis. a A 3 × 3 DNA microarray of HLF-vec and HLF-CD146. A total of 496 genes were found modified after CD146 overexpression (P < 0.05 and fold change >1.5). b GO analysis of potential regulatory mechanisms of CD146

Further verification was conducted using western blotting. Interlukin-8 (IL-8) was upregulated whereas signal transducer and activator of transcription 1 (STAT1) was downregulated after CD146 overexpression (Fig. 6a) and the opposite effects were observed upon CD146 downregulation (Fig. 6b). Pathway analysis indicated that mitogen activated protein kinase 1 (MAPK1) may be the potential pathway by which CD146 induced IL-8 and STAT1 modification. We confirmed that phosphorylation of MAPK1 [Alternative Name: extracellular signal regulated kinase 1 and 2 (ERK1/2)] was markedly increased after CD146 overexpression (Fig. 6a) and decreased after CD146 downregulation (Fig. 6b).

Fig. 6
figure 6

Western blotting vertification of the mechanism of CD146 induced metastasis. a CD146 induced ERK1/2 phosphorylation, IL-8 upregulation and STAT1 down regulation in HLF and 97 L cell lines (n = 3, **P < 0.01, ***P < 0.001). b Interfere CD146 inhibited ERK1/2 phosphorylation, induced IL-8 downregulation and STAT1 upregulation in 97H and 7721 cell lines (n = 3, **P < 0.01, ***P < 0.001). c CD146 induced EMT (E-cad downregulation, vimentin, slug upregulation ) in HLF and 97 L cell lines (n = 3, **P < 0.01, ***P < 0.001). d Interfere CD146 inhibited EMT in 97H and 7721 cell lines (n = 3, **P < 0.01, ***P < 0.001)

We also tested migration-associated EMT markers and found that E-cadherin was downregulated and vimentin and slug were upregulated in the CD146 overexpressed HCC cells (Fig. 6c). Interfering with CD146 expression showed the opposite results (Fig. 6d).

Taken together, these data indicated that CD146 may regulate IL-8 to activate the MAPK1 signaling pathway, and further regulate STAT1 and EMT to promote migration and invasion of HCC cell lines.

CD146 predicted poor prognosis of HCC patients

We also followed up HCC patients in this study. 120 patients were divided into CD146 high group (n = 58) and CD146 low group (n = 62) according to their relative CD146 mRNA expression, averaged 2^-ΔCT value was used as a cut off point. Patient demographics were listed in Table 1. By the time of analysis, recurrence had occurred in 70 of 120 patients, with a mean follow-up time of 38.0 ± 2.1 months (median, 23.0 months; range, 6.0–73.0 months). Among these 70 patients, 58 had intrahepatic recurrence only, 5 had lung metastasis only, and 7 suffered both intrahepatic recurrence and lung metastasis.

Recurrence was observed in 43 of 70 patients with high CD146, while only 27 of 73 patients with low CD146. Among 12 patients who developed lung metastasis, 9 patients had high CD146. In addition, CD146 high group were more likely to manifest high AFP level (P = 0.009), vascular invasion (P = 0.016), satellite lesions (P = 0.028), no tumor encapsulation (P = 0.019), poor tumor differentiation (P = 0.006), and higher recurrence (P < 0.001, Table 1).

Using a averaged 2^-ΔCT value of CD146 mRNA expression as the cutoff value in univariate analysis, preoperative CD146 mRNA expression showed prognostic significance for TTR (time to recurrence) (P = 0.001, Table 2). Patients in CD146 high group had significantly shorter TTR (median, 9.0 months vs. not reached) and higher recurrence rates (81.0 % vs. 37.1 %) than those in Patients in CD146 low group (P < 0.001, Fig. 7a). Levels of AFP, tumor number, vascular invasion, satellite lesion, tumor encapsulation and Edmondson stage were also unfavorable prognostic variables for recurrence (all P values of <0.05, Table 2). In multivariate analysis, high CD146 mRNA expression was the strongest independent prognostic factor for TTR [hazard ratio (HR) =2.49; 95 % confidence interval (CI), 2.43–4.00, P < 0.001; Table 2].

Table 2 Univariate and multivariate Cox proportional regression analysis of factors associated with recurrence
Fig. 7
figure 7

CD146 predicted poor prognosis of HCC patients. a Patients in comparative CD146 high group (n = 62) had higher recurrence rate than those in comparative CD146 low group (n = 58) (P <0.001). b patients in comparative CD146 high group (n = 62) had lower overall survival time than those in comparative CD146 low group (n = 58) (P < 0.001)

Patients in CD146 high group had obvious higher recurrence probability and shorter overall survival time than those in CD146 low group (Fig. 7a and b). This finding enrolled CD146 with clinical significance. Targeting CD146 may become a potential therapeutic strategy of HCC treatment.

Discussion

In this study, we demonstrate for the first time that CD146 promotes HCC progression. We confirmed this finding by providing the following evidence. First, CD146 was frequently upregulated in human HCC tissues compared with adjacent noncancerous tissues and a high CD146 level predicted high recurrence probability and poor overall survival time. Second, in vitro experiments showed that overexpression of CD146 in low CD146-expressing HCC cell lines markedly promoted cell migration and invasion whereas interfering with CD146 expression in high CD146-expressing HCC cell lines showed opposite results. In vivo experiments using the orthotropic tumor metastasis model confirmed these results; more intraliver invasion nodules and lung metastatic foci were observed with CD146 overexpressing cell lines and the opposite effects were observed with CD146 silenced cell lines.

We further investigated the potential mechanisms of CD146-induced migration and invasion by whole genome DNA microarrays and WB validation. We found that STAT1 was downregulated whereas IL-8 was upregulated after CD146 overexpression. Although a few reports indicated STAT1 promoted cancer progression [21, 22], it has been widely accepted that STAT1 negatively regulates cancer progression. STAT1 negatively regulates angiogenesis, tumorigenicity, and metastasis of tumor cells by inhibiting the expression of bFGF, MMP-2, and MMP-9 [23]. STAT1 also functions as a suppressor of HCC cell proliferation and a regulator of HCC cell apoptosis by regulating p53 and cyclin E expression [24]. IL-8 was first identified as a chemotactic factor for leukocytes and was demonstrated to function in cancer progression over recent decades. Serum IL-8 was found upregulated in HCC patients and was correlated with larger tumor volume and advanced tumor stage. IL-8 promoted HCC invasion and the incidence of microscopic vessel invasion was significantly higher in IL-8-positive than in IL-8-negative HCC tissues. Further investigation indicated that IL-8 may function by promoting EMT [25–27]. In this study, STAT1 was downregulated and IL-8 was upregulated after CD146 overexpression. Because previous studies showed that STAT1 and IL-8 could regulate HCC metastasis, together these data indicate that CD146 could promote HCC metastasis by, or at least partially by, regulating STAT1 and IL-8. However, the precise mechanism of the regulation process still needs further investigation.

Second, CD146 was reported to promote metastasis by regulating EMT in other solid tumors such as breast tumor [13, 28]. EMT was believed to endow cancer cells with migratory and invasive properties and induce cancer stem cell properties [29, 30]. However, whether CD146 could induce EMT in HCC has never been explored. We found that CD146 induced E-cadherin loss and vimentin and slug overexpression, and this phenomenon reversed after CD146 inhibition. This indicated that CD146-induced EMT may also count for CD146-induced metastasis of HCC cell lines.

Last, we investigated the potential signaling pathway of CD146-induced metastasis. According to Gene Ontology analysis, a MAPK1-associated signaling pathway was indicated to play a central role. We confirmed that MAPK1 was phosphorylated after CD146 overexpression and the opposite effects were observed after CD146 downregulation. MAPKs are generally expressed in all cell types and transduce stimulations, growth factors, cytokines, and extracellular stress signals into intracellular responses [31]. MAPK1 is one of the subfamilies of MAPKs that functions in various physiological and pathological processes. The role of MAPK1 in cancer development has also been widely explored. MAPK1 phosphorylation was involved in S100p-induced proliferation and metastasis, as well as EMT in colon cancer [32]. The insulin-like growth factor binding protein 5 inhibited MAPK1, resulting in compromised growth and migration ability in melanoma cells [33]. Scribble acts as an oncogene in Eμ-myc-driven lymphoma, and the potential mechanism partially involves the activation of MAPK1 [34]. In HCC development, simultaneous activation of the MAPK1 pathways has been shown to enhance cell-cycle progression [35]. Recently, EDIL3 was identified to promote angiogenesis, metastasis, and recurrence of HCC by MAPK1 and TGF-β signaling pathways [36]. These studies indicate the pivotal role of MAPK1 in cancer progression, especially in cancer metastasis and EMT.

Conclusion

In conclusion, our findings show that CD146 promotes migration and invasion of HCC cell lines by regulating EMT. CD146-induced IL-8 upregulation and further activation of MAPK1 signaling pathways may be its potential regulating methods. However, unraveling the detailed signaling pathways involved in CD146-induced EMT will require further research. In recent years, circulating cancer cell research has Enrich the means to detect tumor cells [37, 38], and the potential of CD146 on circulating tumor cell research still need further investigation.

To our knowledge, this is the first report to identify the striking correlation between high CD146 expression and poor prognosis of HCC patients. Furthermore, we demonstrated that CD146 plays a critical role in HCC progression by MAPK1 signaling dependent EMT activation. Our results indicate that CD146 can be used as a potential HCC marker and may therefore be helpful in developing an effective treatment against cancer.

Abbreviations

EMT:

epithelial mesenchymal transition

ERK1/2:

extracellular signal regulated kinase 1 and 2

HCC:

hepatocellular carcinoma

IL-8:

interleukin-8

MAPK 1:

mitogen activated protein kinase 1

RT-PCR:

real-time polymerase chain reaction

STAT1:

signal transducer and activator of transcription 1

TTR:

time to recurrence

WB:

western blotting

References

  1. Chen W, Zheng R, Baade PD, Zhang S, Zeng H. Cancer statistics in China, 2015. CA Cancer J Clin. 2016. doi:10.3322/caac.21338.

  2. Lau WY, Lai EC. Hepatocellular carcinoma: current management and recent advances. Hepatobiliary Pancreat Dis Int. 2008;7:237–57.

    PubMed  Google Scholar 

  3. Lehmann JM, Riethmüller G, Johnson JP. MUC18, a marker of tumor progression in human melanoma, shows sequence similarity to the neural cell adhesion molecules of the immunoglobulin superfamily. Proc Natl Acad Sci U S A. 1989;86:9891–5.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  4. Sers C, Kirsch K, Rothbächer U, Riethmüller G, Johnson JP. Genomic organization of the melanoma-associated glycoprotein MUC18: implications for the evolution of the immunoglobulin domains. Proc Natl Acad Sci U S A. 1993;90:8514–8.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Sers C, Riethmüller G, Johnson JP. MUC18, a Melanoma-Progression Associated Molecule, and Its Potential Role in Tumor Vascularization and Hematogenous Spread. Cancer Res. 1994;54:5689–94.

    CAS  PubMed  Google Scholar 

  6. Wang Z, Yan X. CD146, a multi-functional molecule beyond adhesion. Cancer Lett. 2013;330:150–62.

    Article  CAS  PubMed  Google Scholar 

  7. Taira E, Kohama K, Tsukamoto Y, Okumura S, Miki N. CD146 is involved in neurite extension of NGF-treated PC12 cells. J Cell Physiol. 2005;204:632–7.

    Article  CAS  PubMed  Google Scholar 

  8. Takaha N, Taira E, Taniura H, Nagino T, Tsukamoto Y, Matsumoto T, et al. Expression of gicerin in development, oncogenesis and regeneration of the chick kidney. Differentiation. 1995;58:313–20.

    Article  CAS  PubMed  Google Scholar 

  9. Tsukamoto Y, Taira E, Nakane Y, Tsudzuki M, Kohama K, Amin H, et al. Expression of gicerin, a cell adhesion molecule, in the abnormal retina in silver plumage color mutation of Japanese quail (Coturnix japonica). Neurosci Lett. 1999;266:53–6.

    Article  CAS  PubMed  Google Scholar 

  10. Chan B, Sinha S, Cho D, Ramchandran R, Sukhatme VP. Critical roles of CD146 in zebrafish vascular development. Dev Dyn. 2005;232:232–44.

    Article  CAS  PubMed  Google Scholar 

  11. Lei X, Guan CW, Song Y, Wang H. The multifaceted role of CD146/MCAM in the promotion of melanoma progression. Cancer Cell Int. 2015;15:3.

    Article  PubMed Central  PubMed  Google Scholar 

  12. Wang W, Yang ZL, Liu JQ, Jiang S, Miao XY. Identification of CD146 expression, angiogenesis, and lymphangiogenesis as progression, metastasis and poor-prognosis related markers for gallbladder adenocarcinoma. Tumour Biol. 2012;33:173–82.

    Article  PubMed  Google Scholar 

  13. Zabouo G, Imbert AM, Jacquemier J, Finetti P, Moreau T, Esterni B, et al. CD146 expression is associated with a poor prognosis in human breast tumors and with enhanced motility in breast cancer cell lines. Breast Cancer Res. 2009;11:R1.

    Article  PubMed Central  PubMed  Google Scholar 

  14. Wu GJ, Wu MW, Wang SW, Liu Z, Qu P, Peng Q, et al. Isolation and characterization of the major form of human MUC18 cDNA gene and correlation of MUC18 overexpression in prostate cancer cell lines and tissues with malignant progression. Gene. 2001;279:17–31.

    Article  CAS  PubMed  Google Scholar 

  15. Liu WF, Ji SR, Sun JJ, Zhang Y, Liu ZY, Liang AB, et al. CD146 Expression Correlates with Epithelial-Mesenchymal Transition Markers and a Poor Prognosis in Gastric Cancer. Int J Mol Sci. 2012;13:6399–406.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  16. Oka S, Uramoto H, Chikaishi Y, Tanaka F. The expression of CD146 predicts a poor overall survival in patients with adenocarcinoma of the lung. Anticancer Res. 2012;32:861–4.

    PubMed  Google Scholar 

  17. Sato A1, Torii I, Okamura Y, Yamamoto T, Nishigami T, Kataoka TR, et al. Immunocytochemistry of CD146 is useful to discriminate between malignant pleural mesothelioma and reactive mesothelium. Mod Pathol. 2010;23:1458–66.

    Article  CAS  PubMed  Google Scholar 

  18. Kristiansen G, Yu Y, Schlüns K, Sers C, Dietel M, Petersen I. Expression of the cell adhesion molecule CD146/MCAM in non-small cell lung cancer. Anal Cell Pathol. 2003;25:77–81.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. Pires FR, Shih IM, da Cruz Perez DE, de Almeida OP, Kowalski LP. Mel-CAM (CD146) expression in parotid mucoepidermoid carcinoma. Oral Oncol. 2003;39:277–81.

    Article  CAS  PubMed  Google Scholar 

  20. Thomann S, Longerich T, Bazhin AV, Mier W, Schemmer P, Ryschich E. Selective targeting of liver cancer with the endothelial marker CD146. Oncotarget. 2014;5:8614–24.

    Article  PubMed Central  PubMed  Google Scholar 

  21. Malilas W, Koh SS, Kim S, Srisuttee R, Cho IR, Moon J, et al. Cancer upregulated gene 2, a novel oncogene, enhances migration and drug resistance of colon cancer cells via STAT1 activation. Int J Oncol. 2013;43(4):1111–6.

    CAS  PubMed  Google Scholar 

  22. Khodarev NN, Roach P, Pitroda SP, Golden DW, Bhayani M, Shao MY, et al. STAT1 pathway mediates amplification of metastatic potential and resistance to therapy. PLoS One. 2009;4(6):e5821.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Huang S, Bucana CD, Van Arsdall M, Fidler IJ. Stat1 negatively regulates angiogenesis, tumorigenicity and metastasis of tumor cells. Oncogene. 2002;21:2504–12.

    Article  CAS  PubMed  Google Scholar 

  24. Chen G, Wang H, Xie S, Ma J, Wang G. STAT1 negatively regulates hepatocellular carcinoma cell proliferation. Oncol Rep. 2013;29:2303–10.

    CAS  PubMed  Google Scholar 

  25. Ren Y, Poon RT, Tsui HT, Chen WH, Li Z, Lau C, et al. Interleukin-8 serum levels in patients with hepatocellular carcinoma: correlations with clinicopathological features and prognosis. Clin Cancer Res. 2003;9:5996–6001.

    CAS  PubMed  Google Scholar 

  26. Kubo F, Ueno S, Hiwatashi K, Sakoda M, Kawaida K, Nuruki K. Interleukin 8 in human hepatocellular carcinoma correlates with cancer cell invasion of vessels but not with tumor angiogenesis. Ann Surg Oncol. 2005;12:800–7.

    Article  PubMed  Google Scholar 

  27. Fu XT, Dai Z, Song K, Zhang ZJ, Zhou ZJ, Zhou SL, et al. Macrophage-secreted IL-8 induces epithelial-mesenchymal transition in hepatocellular carcinoma cells by activating the JAK2/STAT3/Snail pathway. Int J Oncol. 2015;46:587–96.

    CAS  PubMed  Google Scholar 

  28. Zeng Q, Li W, Lu D, Wu Z, Duan H, Luo Y, et al. CD146, an epithelial-mesenchymal transition inducer, is associated with triple-negative breast cancer. Proc Natl Acad Sci U S A. 2012;109:1127–32.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  29. Thiery JP, Acloque H, Huang RY, Nieto MA. Epithelial-mesenchymal transitions in development and disease. Cell. 2009;139:871–90.

    Article  CAS  PubMed  Google Scholar 

  30. Mani SA, Guo W, Liao MJ, Eaton EN, Ayyanan A, Zhou AY, et al. The epithelial-mesenchymal transition generates cells with properties of stem cells. Cell. 2008;133:704–15.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  31. Pearson G, Robinson F, Beers Gibson T, Xu BE, Karandikar M, Berman K, et al. Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions. Endocr Rev. 2001;22:153–83.

    CAS  PubMed  Google Scholar 

  32. Shen Z, Deng H, Fang Y, Zhu X, Ye GT, Yan L, et al. Identification of the interplay between SOX9 and S100P in the metastasis and invasion of colon carcinoma. Oncotarget. 2015;6:20672–84.

    Article  PubMed Central  PubMed  Google Scholar 

  33. Wang J, Ding N, Li Y, Cheng H, Wang D, Yang Q, et al. Insulin-like growth factor binding protein 5 (IGFBP5) functions as a tumor suppressor in human melanoma cells. Oncotarget. 2015;6:20636–49.

    Article  PubMed Central  PubMed  Google Scholar 

  34. Hawkins ED, Oliaro J, Ramsbottom KM, Newbold A, Humbert PO, Johnstone RW, et al. Scribble acts as an oncogene in Emu-myc-driven lymphoma. Oncogene. 2015. doi:10.1038/onc.2015.167.

  35. Chin R, Earnest-Silveira L, Koeberlein B, Franz S, Zentgraf H, Dong X, et al. Modulation of MAPK pathways and cell cycle by replicating hepatitis B virus:factors contributing to hepatocarcinogenesis. J Hepatol. 2007;47:325–37.

    Article  CAS  PubMed  Google Scholar 

  36. Xia H, Jianxiang C, Shi M, Gao H, Karthik S, Pratap SV, et al. EDIL3 is a novel regulator of epithelial mesenchymal transition controlling early recurrence of hepatocellular carcinoma. J Hepatol. 2015;63:863–673.

    Article  CAS  PubMed  Google Scholar 

  37. Fan ZC, Yan J, Liu GD, Tan XY, Weng XF, Wu WZ, et al. Real-Time Monitoring of Rare Circulating Hepatocellular Carcinoma Cells in an Orthotopic Model by In Vivo Flow Cytometry Assesses Resection on Metastasis. Cancer Res. 2012;72:2683–91.

    Article  CAS  PubMed  Google Scholar 

  38. Yan J, Fan Z, Wu X, Xu M, Jiang J, Tan C, et al. Circulating tumor cells are correlated with disease progression and treatment response in an orthotopic hepatocellular carcinoma model. Cytometry A. 2015;87:1020–8.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by the National Natural Science Foundation of China (Grant No. 81470901 and No. 81270553).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xuehao Wang.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

GJ and LZ contributed equally to this work. GJ, LZ, QZ, DB, CZ and XW carried out all the experiments, prepared figures and drafted the manuscript. GJ, LZ, CZ and XW participated in data analysis and interpretation of results. GJ and XW designed the study, participated in data analysis and interpretation of results. All authors read and approved the manuscript.

Additional files

Additional file 1: Table S1.

Primer pairs used for real-time PCR in this study. (DOCX 12 kb)

Additional file 2: Table S2.

Antibodies used in this study. (DOCX 13 kb)

Additional file 3: Table S3.

CD146 interfere sequence used in this study. (DOCX 12 kb)

Additional file 4: Figure S1.

Western Blotting of 17 paired HCC and peritumor tissues. (TIF 6418 kb)

Additional file 5: Figure S2.

CD146 expression doesn’t impact cell proliferation in 97H or 97 L cell lines. (TIF 5396 kb)

Additional file 6: Figure S3.

CD146 expression doesn’t impact apoptosis and cell cycle in 97H or 97 L cell lines. (TIF 6329 kb)

Additional file 7: Table S4.

Cancer related pathway genes modulated after CD146 upregulation. (DOCX 13 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jiang, G., Zhang, L., Zhu, Q. et al. CD146 promotes metastasis and predicts poor prognosis of hepatocellular carcinoma. J Exp Clin Cancer Res 35, 38 (2016). https://doi.org/10.1186/s13046-016-0313-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13046-016-0313-3

Keywords