microRNA‑196b promotes cell migration and invasion by targeting FOXP2 in hepatocellular carcinoma

Introduction

According to data of the Global Cancer Statistics, hepatocellular carcinoma (HCC) is the fifth most common malignancy and the second leading cause of cancer-related death worldwide (1). Unfortunately, even though surgery, radiofrequency ablation and chemoembolization are widely applied, HCC with invasive and metastatic characteristics is a lethal disease (2), which highlights the urgent need for new biomarkers for the clinical diagnosis and therapy of HCC.

MicroRNAs (miRNAs) regulate gene expression via the degradation of mRNAs or inhibition of translation. The miR-196 family consists of miR-196a and miR-196b with shared regulatory capacity (3). Studies have shown that miR-196a and miR-196b exert various functions in cancer carcinogenesis and development (4–7). miR-196a-2 polymorphism is associated with susceptibility to HCC and recurrence after liver transplantation (4,8). A recent study found that upregulation of miR-196b is indicative of liver metastasis in patients with colorectal cancer (9). miR-196a and miR-196b overexpression were found to promote migration and invasion without affecting the growth of oral cancer cells (10). Shen et al previously reported that miR-196b was notably upregulated in HCC compared with adjacent non-cancerous tissues (11). Furthermore, upregulation of miR-196b was found to be associated with HCV infection, suggesting a promoting role in HCC development (12). Yet, the clinical significance of miR-196b and its role as well as the underlying mechanisms remain largely unknown in HCC.

In the present study, we found that miR-196b overexpression was associated with poor prognostic features and reduced survival of HCC patients. We present evidence that miR-196b functions as an oncomiR and promotes the migration and invasion of HCC cells by targeting forkhead box P2 (FOXP2). Our results revealed a novel molecular mechanism; the miR-196b/FOXP2 axis may be valuable clinical marker and therapeutical target for HCC patients.

Materials and methods

Clinical samples

Patients (84 HCC tissues and pair-matched adjacent normal liver tissues) who had not undergone radiofrequency ablation or chemoembolization in the present study were enrolled at The First Affiliated Hospital of Xi'an Medical University. Samples were pathologically confirmed and rapidly put into liquid nitrogen after surgical operation. Informed consent was signed by each patient before the clinical specimens were collected and used. Details of the clinicopathological data are shown in Table I. The protocols involved in the use of the clinical specimens in the present study were according to the Research Ethics Committee of Xi'an Medical University.

Table I. Correlation between the clinicopathological features and miR-196b expression in the hepatocellular carcinoma cases (n=84).

Table I.

Correlation between the clinicopathological features and miR-196b expression in the hepatocellular carcinoma cases (n=84).

		miR-196b expression
Characteristics	Total no. of patients	High level (n=42)	Low level (n=42)	P-value
Age (years)
<50	33	19	14	0.264
≥50	51	23	28
Sex
Male	66	30	36	0.111
Female	18	12	6
HBV
Absent	24	9	15	0.147
Present	60	33	27
Serum AFP level (ng/ml)
<400	30	12	18	0.172
≥400	54	30	24
Tumor size (cm)
<5	31	14	17	0.498
≥5	53	28	25
No. of tumor nodules
1	70	32	38	0.079
≥2	14	10	4
Cirrhosis
Absent	34	14	20	0.182
Present	50	28	22
Venous infiltration
Absent	63	27	36	0.023a
Present	21	15	6
Edmondson-Steiner grading
I+II	59	27	32	0.233
III+IV	25	15	10
TNM tumor stage
I+II	61	24	37	0.001a
III+IV	23	18	5

{ label (or @symbol) needed for fn[@id='tfn1-or-39-02-0731'] } HBV, hepatitis B virus; AFP, α-fetoprotein; TNM, tumor-node-metastasis.

a Statistically significant.

Cell culture and transfection

Human HCC cell lines including Hep3B, Huh7, MHCC97H and HCCLM3, and the human immortalized normal hepatocyte cell line (LO2) (Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China) were cultured under standard conditions. hsa-miR-196b mimics (HmiR0103-MR04), inhibitors (HmiR-AN0286-AM04) and their control fragments (NC, CmiR0001-MR04 and CmiR-AN0001-AM04) were produced by GeneCopoeia (Guangzhou, China). FOXP2 siRNA and FOXP2 expression plasmid (pcDNA3.1-FOXP2) were designed and synthesized by GenePharma (Shanghai, China). All vectors were then transfected into HCC cells with Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturers protocol.

Immunohistochemistry (IHC)

Paraffin sections from HCC tissues underwent deparaffination and then rehydration. Antigen retrieval, suppression of endogenous peroxidase activity and 10% skim milk blocking were performed before primary antibody incubation. FOXP2 primary antibody (; ab16046; Abcam, Cambridge, MA, USA) was used for incubation overnight at 4°C. The slides were subsequently incubated with peroxidase conjugated secondary antibody (ZSGB BIO, Beijing, China) for 90 min, and a peroxidase-labeled polymer, DAB solution was used for signal development for 5 min. The sections were counterstained with hematoxylin followed by dehydrating and mounting. Staining intensity was scored as no staining, 0; weak staining, 1; moderate staining, 2; and strong staining, 3. Staining quantity was graded as <25%, 1; 25–75%, 2; and >75%, 3. IHC score was manually confirmed by two independent experienced pathologists using the formula: IHC score = staining intensity × staining quantity.

Quantitative real-time polymerase chain reaction (qRT-PCR)

RNA was extracted and prepared for qRT-PCR as previously described (13). Total RNA was reverse-transcribed to cDNA with PrimeScript Reverse Transcriptase kit (Takara, Dalian, China) according to the manufacturer's protocol. By using SYBR Green chemistry, qRT-PCR was implemented with the ABI 7900HT sequence detection machine (Bio-Rad, Hercules, CA, USA). The target and reference genes (U6 and GAPDH) were amplified in separate wells in triplicate. Gene expression was calculated with the comparative threshold cycle (2−ΔΔCt) approach. The primers used for miR-196b, U6, FOXP2 and GAPDH were synthesized and purchased from Sangon Biotech (Shanghai, China).

Migration and invasion assays

Transwell chambers (Corning Costar, Cambridge, MA, USA) were employed to evaluate the migratory and invasive abilities of HCC cells. HCC cells were resuspended in serum-free DMEM and subsequently seeded in the upper chambers. To induce the migration and invasion of HCC cells, the lower chambers were filled with 600 µl DMEM supplemented with 20% FBS. Forty-eight hours after cell seeding, HCC cells that migrated or invaded through the membranes (the membranes were covered with 70 µl Matrigel) were stained with crystal violet for cell counting under a microscope.

Western blotting

Total cell lysates were prepared in a 1X sodium dodecyl sulfate buffer and quantified with a BCA protein assay kit (Pierce, Bonn, Germany). Identical quantities of proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred onto PVDF membranes (Bio-Rad, USA). After incubation with the antibody specific for FOXP2 (ab16046, Abcam) overnight, the blots were incubated with secondary antibodies (#7074 and #7076; Cell Signaling Technology, Beverly, MA, USA) and detected using a chemiluminescent detection system (Bio-Rad). GAPDH (sc-47724; Santa Cruz Biotechnology, Santa Cruz, CA, USA) was used as a loading control for western blots. The immunoreactive bands were quantified by the densitometry with ImageJ software (NIH, USA).

Experimental mouse model

BALB/c nude mice aged 4 weeks were subjected to a pulmonary metastasis model. HCCLM3 cells that were transfected with the miR-196b inhibitor or NC inhibitor were injected through the tail vein of nude mice and cultivated for 9 weeks. After euthanasia, the lungs were harvested and fixed, paraffin-embedded, sectioned and stained for hematoxylin and eosin (H&E) (14), and the metastatic nodules were counted. All animal experiments were approved by the Ethics Committee of Xi'an Medical University.

Dual-Luciferase reporter assay

The sequences of FOXP2-3′UTR were cloned into the pmiR-RB-Report™ vector (RiboBio, Guangzhou, China), and its corresponding mutant (mt) 3′UTR sequences were subsequently generated using overlap extension PCR and cloned into the pmiR-RB-Report™ vector. Pmir-RB-FOXP2 or pmir-RB-FOXP2-mt was transfected into Hep3B cells with miR-196b mimic or NC mimic by Lipofectamine-mediated gene transfer. The relative luciferase activity was normalized to Renilla luciferase activity 48 h after transfection.

Statistical analysis

Data are presented as mean ± SD and analyzed by GraphPad Prism 5 software (GraphPad Software, Inc., San Diego, CA, USA). Chi-squared test, Student's t-test, ANOVA, Spearman correlation analysis, Kaplan-Meier method and log-rank test were performed for statistical analysis. A P-value <0.05 was considered statistically significant. *P<0.05.

Results

miR-196b expression is upregulated in HCC

A previous study reported that miR-196b expression was upregulated in HCC tissues compared to non-tumor tissues (11). Consistently, the qRT-PCR analysis revealed that miR-196b expression was markedly increased in HCC tissues compared with that noted in the adjacent non-cancerous tissues from 84 patients in the present study (P<0.05, Fig. 1A). In accordance, we found that miR-196b was also significantly upregulated in 4 HCC cell lines compared with that noted in the normal hepatic cell line LO2 (P<0.05, Fig. 1B). These findings provide valid evidence that miR-196b could be implicated in the pathogenesis and development of HCC.

Figure 1. Expression of miR-196b in HCC. (A) Eighty-four paired HCC and tumor-adjacent tissues were subjected to qRT-PCR for miR-196b expression. Quantitative data revealed that miR-196b expression was decreased in HCC tissue compared with that noted in the tumor-adjacent tissues. n=84, *P<0.05 by t-test. (B) The expression of miR-196b in 4 different HCC cells lines (Hep3B, Huh7, MHCC97H and HCCLM3) and the human immortalized normal hepatic cell line (LO2). n=3, *P<0.05 vs. LO2 by ANOVA, respectively.

miR-196b expression correlates with the prognosis of HCC patients

Different subgroups (miR-196b low/high expression) were plotted according to the cut-off values of miR-196b, which were defined as the median of the cohort. Relationship between the clinical characteristics of the HCC patients and miR-196b expression are listed in Table I. High miR-196b expression was associated with venous infiltration (P=0.023) and advanced TNM tumor stage (P=0.001). Furthermore, survival analyses indicated that miR-196b high expressing HCC patients showed a significant reduced 5-year overall survival and disease-free survival (P<0.05, respectively, Fig. 2). Thus, we suggest that miR-196b is a possible prognostic biomarker for HCC patients.

Figure 2. The prognostic significance of miR-196b in HCC. Different subgroups (miR-196b low/high expression) were plotted according to the cut-off values of miR-196b, which were defined as the median of the cohort. Compared with miR-196b low-expressing cases (n=42), miR-196b high-expressing HCC patients (n=42) showed a significantly reduced overall survival and disease-free survival. P<0.05 by log-rank test.

miR-196b enhances the migration and invasion of HCC cells

To detect the effects of miR-196b on migration and invasion of HCC cells, Transwell assays were conducted when miR-196b expression was downregulated or upregulated. HCCLM3 cells showed the highest level of miR-196b, while Hep3B cells showed the lowest level of miR-196b. Thus, HCCLM3 and Hep3B were used for loss- and gain-of-function experiments, respectively. miR-196b was obviously knocked down by miR-196b inhibitor in HCCLM3 cells (P<0.05, Fig. 3A). Transwell assays revealed that miR-196b knockdown significantly weakened the migratory and invasive abilities of HCCLM3 cells (P<0.05, respectively, Fig. 3B). In turn, overexpression of miR-196b was confirmed by qRT-PCR after miR-196b mimic transfection in Hep3B cells (P<0.05, Fig. 3C). Our data showed that upregulation of miR-196b significantly facilitated migration and invasion of Hep3B cells compared with the NC group (P<0.05, respectively, Fig. 3D). Based on the findings in vitro, we further probed the role of miR-196b during HCC progression with xenograft models. A notable decrease in metastatic nodes in the lung was noted in the miR-196b inhibitor group when compared with the NC inhibitor groups (P<0.05, Fig. 4). Thus, miR-196b exerts a pro-metastatic role in HCC.

Figure 3. miR-196b enhances migration and invasion of HCC cells. (A) HCCLM3 cells that were transfected with miR-196b inhibitor or negative control (NC) inhibitor were detected by qRT-PCR for miR-196 expression. n=3, *P<0.05 by t-test. (B) Transwell assays confirmed that miR-196b knockdown restrained migration and invasion of HCCLM3 cells. n=3, *P<0.05 by t-test, respectively. (C) Hep3B cells were transfected with miR-196b mimic or negative control (NC) mimic and measured by qRT-PCR for miR-196 expression. n=3, *P<0.05 by t-test. (D) Upregulation of miR-196 expression enhanced the migratory and invasive abilities of Hep3B cells. n=3, *P<0.05 by t-test, respectively.

Figure 4. miR-196b knockdown restrains lung metastasis of HCC in mice. HCCLM3 cells that were transfected with miR-196b inhibitor or negative control (NC) inhibitor were intravenously injected into nude mice via the tail vein. Lungs of mice were sectioned and stained by H&E. miR-196b knockdown significantly reduced the number of metastatic nodules in mouse lungs. n=5, *P<0.05 by t-test. Scale bars, 100 µm.

miR-196b directly targets FOXP2 in HCC

In order to explore the molecular mechanisms underlying miR-196b, first, bioinformatic prediction (TargetScan: http://www.targetscan.org and miRanda: http://www.microrna.org/microrna/hpme.do) showed that miR-196b could bind to the 3′UTR of FOXP2 mRNA (Fig. 5A). qRT-PCR and immunoblotting results indicated that miR-196b overexpression reduced the levels of FOXP2 mRNA and protein in Hep3B cells (P<0.05, respectively, Fig. 5B and C). Then, to further confirm the binding of miR-196b and 3′UTR of FOXP2, a dual-luciferase reporter assay was implemented. Co-transfection of Hep3B cells with Pmir-RB-FOXP2 vector and miR-196b mimic significantly reduced luciferase reporter activity compared with the negative control (P<0.05, Fig. 5D). This repressive effect was abolished by directed mutagenesis of the miR-196b-binding seed region in 3′UTR of FOXP2 (Fig. 5D), which initially suggested that the miR-196b and 3′UTR of FOXP2 may combine with each other. A recent study found that FOXP2 was prominently reduced in HCC tissues and inhibited migration and invasion of cancer cells (15). Data from the GEO database (GSE45436) demonstrated that the expression of FOXP2 in HCC tissues was notably downregulated compared to that noted in normal liver tissues (P<0.0001, Fig. 5E). Moreover, IHC data revealed that the expression of FOXP2 in miR-196b low-expressing HCCs was significantly higher than that in high-expressing cases (P<0.05, Fig. 5F). Subsequently, a significant negative correlation between miR-196b and FOXP2 expression was observed in HCC tissues (r=−0.7051, P<0.001, Fig. 5G). Together, these data demonstrated that FOXP2 is a direct target of miR-196b in HCC.

Figure 5. FOXP2 is a direct target of miR-196b in HCC. (A) The sequences of wild-type (wt) or mutant (mt) FOXP2-3′UTR were cloned into the pmiR-RB-Report™ vector. (B) Hep3B cells were transfected with miR-196b mimic or negative control (NC) mimic and measured by qRT-PCR for FOXP2 mRNA. n=3, *P<0.05 by t-test. (C) miR-196b overexpression reduced the level of FOXP2 protein in Hep3B cells. n=3, *P<0.05 by t-test. (D) Co-transfection of Hep3B cells with Pmir-RB-FOXP2 vector and miR-196b mimic significantly reduced luciferase reporter activity compared with the negative control. miR-196 mimic showed no significant effect on luciferase reporter activity of mt FOXP2-3′UTR. n=3, *P<0.05 by t-test. (E) The data from GEO database (GSE45436) confirmed the downregulation of FOXP2 in HCC tissues. P<0.0001 by t-test. (F) Representative IHC staining indicated that strong staining of FOXP2 was observed in miR-196b low-expressing HCC tissues, while miR-196b high-expressing HCC tissue showed a weak signal of FOXP2. Quantitative data revealed that the expression of FOXP2 in miR-196b low-expressing HCCs (n=42) was obviously higher than that in miR-196b high-expressing cases (n=42). *P<0.05 by t-test. Scale bar, 50 µm. (G) A obvious negative correlation between miR-196b and FOXP2 expression was observed in HCC tissues. n=84, P<0.001 by Spearman correlation analysis.

FOXP2 functions in miR-196b-induced migration and invasion of HCC cells

Next, we tested whether FOXP2 was able to mediate the function of miR-196b in HCC cells. Co-transfection of miR-196b inhibitor + FOXP2 siRNA was able to abrogate the miR-196b silencing-induced upregulated expression of FOXP2 (P<0.05, Fig. 6A). Furthermore, FOXP2 knockdown enhanced the migration and invasion of HCCLM3 cells with miR-196b silencing (P<0.05, respectively, Fig. 6B). In accordance, co-transfection of miR-196b + FOXP2 abrogated the miR-196b-induced downregulation of FOXP2 expression and metastasis of Hep3B cells (P<0.05, respectively, Fig. 7). Therefore, these results indicate that FOXP2 may function in miR-196b-induced HCC metastasis.

Figure 6. FOXP2 silencing abrogates the effects of miR-196b knockdown on HCCLM3 cells. (A) HCCLM3 cells were transfected with the negative control (NC) inhibitor, miR-196b inhibitor or miR-196b inhibitor + FOXP2 siRNA were subjected to immunoblotting for FOXP2. n=3, *P<0.05 by ANOVA. (B) FOXP2 silencing reversed the anti-metastatic effects of miR-196b knockdown on HCCLM3 cells. n=3, *P<0.05 by ANOVA.

Figure 7. FOXP2 abolishes the effects of miR-196b in Hep3B cells. (A) Hep3B cells were transfected with the negative control (NC) mimic, miR-196b mimic or miR-196b mimic + FOXP2 and subjected to immunoblotting for FOXP2. n=3, *P<0.05 by ANOVA. (B) FOXP2 restoration reversed the pro-metastatic effects of miR-196b on Hep3B cells. n=3, *P<0.05 by ANOVA.

Discussion

Recently, increasing evidence has shown that miRNAs play a crucial role in the tumorigenesis and development of tumors (16–18). Searching a miRNA signature may be of clinical value for the diagnosis, therapy and prognosis of HCC (18). Upregulation of miR-196b has been reported in glioblastoma and may be a biomarker for indicating poor prognosis (19,20). The prognostic significance of miR-196b was also confirmed in pancreatic cancer (21), gastric cancer (5) and osteosarcomas (22). Currently, the clinical significance of miR-196b has been disclosed in HCC. We found that high expression of miR-196b was associated with venous infiltration and advanced TNM tumor stage. More importantly, a high miR-196b level was correlated with a reduced 5-year overall survival and disease-free survival. Therefore, miR-196b potentially serves as a promising biomarker for the prognosis of patients.

Tumor metastasis and recurrence are the root of poor clinical outcome for HCC patients (23). Meanwhile, tumor metastasis and recurrence are inseparable from enhanced cancer cell mobility (24). Thus, investigating the molecular mechanisms involved in the migration and invasion of HCC cells are beneficial to explore anti-metastatic therapy. The expression of miR-196b was found to be increased in liver metastatic tumors compared to that in primary colorectal cancer (9). Increased circulating miR-196a/b levels were markedly associated with the metastatic potential of gastric cancer (5,25). In oral cancer, miR-196 plays a pro-metastatic role by targeting the NME4/JNK/TIMP1/MMP signaling pathway (10). However, miR-196b overexpression abolished the migration and invasion of breast cancer cells, and restrained tumor metastasis in vivo via suppression of HOXC8 (26). Recently, miR-196b underexpression was found in colorectal cancer and resulted in enhanced invasion and metastasis of cancer cells (27). The above studies suggest that the expression status and role of miR-196b is inconsistent in different cancers. Thus, it is worth disclosing the role of miR-196b in HCC. Subsequently, our data showed that miR-196b promoted the migration and invasion of HCC cells, and miR-196b silencing reduced lung metastasis in nude mice. Accordingly, we suggest that miR-196b promotes tumor progression via exerting a pro-metastatic role in HCC. FOXP2 has been recognized as a tumor suppressor and suppresses the metastasis of HCC and breast cancer (15,28). Data from the GEO database further confirmed the underexpression of FOXP2 in HCC. miR-196b inversely regulated FOXP2 abundance in HCC cells. Finally, luciferase reporter assay revealed that miR-196b directly targets FOXP2 in HCC. Rescue experiments indicated that FOXP2 is not only a downstream target but also a functional mediator of miR-196b in HCC.

In summary, we demonstrated that upregulation of miR-196b was correlated with the invasion and metastasis of HCC, indicating the pathological importance of miR-196b in tumor progression according to qRT-PCR and clinical data. A high miR-196b level was indicative of a poor prognosis of HCC patients. Subsequently, the novel molecular mechanism underlying the role of miR-196b in invasion and metastasis was explored. Upregulation of miR-196b functionally exerted an endogenous suppressive effect on the target gene FOXP2. Moreover, we found that the miR-196b/FOXP2 axis stimulated the migration and invasion of HCC cells.

Acknowledgements

The present study was supported by the Scientific Research Project of Shaanxi Provincial Department of Education (2013JK0791).

References