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Introduction

Hepatocellular carcinoma (HCC) is one of the most common human cancers worldwide and ranks third in cancer-related death (1). Although remarkable achievements have been made (2), the long-term prognosis of HCC patients remains poor, particularly for those in advanced stages, with the 5-year survival rate lower than 5% (3). Local and systemic metastasis are the critical reasons for the unsatisfactory survival of HCC patients in advanced stages (4). Elucidating the molecular mechanism of the metastasis of HCC is critical for identifying novel therapeutic targets and may significantly improve the prognosis of HCC patients.

MicroRNAs (miRNAs) are a group of short non-conding RNAs and serve as important post-transcriptional modulator of gene expression by binding to 3′ untranslated region (3′-UTR) of targeted mRNAs and resulting in the suppression of protein translation or the degradation of the target mRNAs (5,6). Numerous studies have demonstrated that miRNAs are involved in various cellular activities (7–9) including proliferation, apoptosis, differentiation and movement. Aberrant expression and function of miRNAs has been found to play fundamental roles in human malignancies (7,10–12). In addition, miRNAs have become promising diagnostic and prognostic biomarkers and attractive therapeutic targets of human cancers (13,14).

Among numerous miRNAs, microRNA-616 (miR-616) has been found to be a novel cancer-associated miRNA. miRNA profiling of human gastric cancer showed that miR-616 was overexpressed in gastric cancer tissues (15). In addition, studies of lung (16) and prostate cancer (17) demonstrated that the level of miR-616 was significantly elevated in the serum of patients. Furthermore, miR-616 was found to play an important role in the development and maintenance of androgen-independent prostate cancer by regulating the expression of TFPI-2 (17). However, the expression and clinical significance of miR-616 in HCC tissues, and its functional role and the underlying mechanisms in HCC cells, are still undefined.

In the present study, we demonstrated that miR-616 was significantly upregulated in HCC tissues. Elevated expression of miR-616 was observed in patients with metastasis and recurrence. Additionally, elevated miR-616 expression was associated with adverse clinicopathological features and poor prognosis of HCC patients. In vitro studies showed that miR-616 promoted the invasive behavior and epithelial-mesenchymal transition (EMT) of HCC cells. Moreover, phosphatase and tensin homolog (PTEN) was identified to be the direct downstream target of miR-616 in HCC. miR-616 contributed to the metastasis and EMT of HCC by inhibiting the expression of PTEN.

Materials and methods

Human tissue specimens and cell lines

The paired HCC and adjacent non-tumor tissues were collected from 80 HCC patients who received surgical resection of primary HCC in the Department of General Surgery at the Second Affiliated Hospital of Xi'an Jiaotong University from January 2006 to December 2009. No local or systemic treatments had been performed before the surgical resection. Informed consent was obtained from each patient before collecting the clinical samples. The demographic and clinicopathological data are presented in Table I. All protocols in the present study were approved by the Xi'an Jiaotong University Ethics Committee according to the Declaration of Helsinki (as revised in Tokyo, 2004).

Table I The association between the clinicopathological features and miR-616 expression in HCC.

Table I

The association between the clinicopathological features and miR-616 expression in HCC.

Clinicopathological features	Total no. of pts.	No. of patients		P-value
		miR-616High	miR-616Low
Gender
Male	59	31	28	0.446
Female	21	9	12
Age (years)
<50	34	18	16	0.651
≥50	46	22	24
HBV infection
Absent	28	15	13	0.639
Present	52	25	27
Cirrhosis
Absent	33	18	15	0.496
Present	47	22	25
Diameter of tumor (cm)
<5	34	19	15	0.366
≥5	46	21	25
No. of tumor nodules
1	44	24	20	0.369
>1	36	16	20
Venous infiltration
Absent	57	24	33	0.026a
Present	23	16	7
Edmondson-Steiner grading
I+II	60	25	35	0.001a
III+IV	20	15	5
TNM stage
I+II	58	22	36	<0.001a
III+IV	22	18	4

a Statistically significant. pts., patients.

Six HCC cell lines, Hep3B, HepG2, Huh7, MHCC97L HCCLM3 and MHCC97H, and the human immortalized normal hepatocyte cell line, LO2 (The Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China) were maintained in complete Dulbecco's modified Eagle's medium (DMEM; HyClone, Logan, UT, USA) supplemented with 10% fetal bovine serum (FBS, HyClone, Thermo Fisher Scientific, Australia) with 100 U/ml penicillin and 100 µg/ml streptomycin (Sigma, USA) in a humidified incubator containing of 5% CO2 at 37°C.

Quantitative real-time PCR (qPCR) analysis

Total RNA from tissues or cells was extracted using TRIzol (Life Technologies) according to the manufacturer's instructions. The PCR amplification for the quantification of the miR-616 was performed using the TaqMan microRNA assay kit (Applied Biosystems, Foster City, CA, USA). U6 was used as endogenous controls. The relative expression of miR-616 was normalized to that of U6.

Cell transfection

miR-616 expression vector (HmiR0186-MR04), the control vector for miR-616 (CmiR0001-MR04), miR-616 inhibitor (HmiR-AN0721-AM03) and the negative control for the miR-616 inhibitor (CmiR-AN0001-AM03), were purchased from GeneCopoeia (Guangzhou, China). Plasmids carrying wt SMAD7 (pCMV5-SMAD7) were obtained from Addgene (Cambridge, MA, USA). The vectors mentioned above were transfected into the HCC cells using Lipofectamine 2000 (Invitrogen, USA) following the manufacturer's protocol.

Migration and invasion assays

Cell migration and invasion assays were evaluated in chambers of 8-µm with Transwell inserts (Millipore, USA) according to the manufacturer's instructions. Cells (5×104) were seeded into the top chamber of each insert in serum-free medium and serum-containing medium was used in the lower chamber as the attractant. Specifically for the invasion assay, before seeding the HCC cells, each chamber was coated with mixture of DMEM and Matrigel (Becton-Dickinson Labware, USA) at a ratio of 6:1. After incubated at 37°C for 24 h, the cells adherent to the upper surface of the filter were removed using a cotton swab. The migrated or invaded cells were fixed and stained with 0.1% crystal violet, air-dried and photographed. Three independent experiments were performed.

Western blotting

HCC cells were washed twice with phosphate-buffered saline (PBS) and lysed on the culture dishes using RIPA lysis buffer (BioMed, China). Protein concentration was measured using the BCA kit (Pierce, USA) and 30 µg of each sample were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred to PVDF membrane. Non-specific binding sites were blocked by incubating with TBST containing 5% skimmed milk/TBST for 2 h at room temperature. The blots were then incubated overnight at 4°C with the following primary antibodies: PTEN (1:1,000), AKT (1:1,000) (both from Santa Cruz, USA), p-AKT (1:1,000), E-cadherin (1:1,000), vimentin (1:1,000) and β-actin (1:1500) (all from Cell Signaling, USA). After washing the membranes with TBST, blots were incubated with horseradish peroxidase-conjugated goat anti-mouse or anti-rabbit secondary antibodies (1:10,000; Bio-Rad, USA), and were detected using the Bio-Rad Gel imaging system.

Luciferase reporter assay

The wild-type 3′-UTR sequence of PTEN (wt PTEN-3′-UTR) predicted to interact with miR-616 or the mutated sequence (mt PTEN-3′-UTR) within the predicted target sites was synthesized and inserted into the pGL3 control vector (Promega, USA). For the reporter assay, Hep3B cells were seeded into 24-well plates and were transfected with the above constructs and miR-616 expressing vector, miR-616 inhibitor, control vector or negative control. After 48 h, the cells were harvested and luciferase activity was measured using the Dual-Luciferase Reporter Assay system (Promega) according to the manufacturer's instructions. Results were obtained from three independent experiments performed in duplicate.

Immunohistochemical staining

After being deparaffinized in xylene and rehydrated in a graded alcohol series and distilled water, the paraffin sections were heated for antigen retrieval in sodium citrate buffer for 10 min, and were quenched for endogenous peroxidase activity in 3% hydrogen peroxide for 15 min. They were incubated with PTEN (1:100) or p-AKT (1:50) antibody at 4°C overnight. Then, sections were incubated with biotinylated secondary antibodies from Zhongshan Golden Bridge Biotechnology (Beijing, China) for 2 h. Sections were stained with the avidin-biotin-peroxidase complex (SABC) method and visualized with diaminobenzidine and counter-stained with hematoxylin.

The staining results for PTEN and p-AKT were semi-quantitatively calculated by multiplying the staining intensity and the percentage of positive staining. Staining intensity was assessed as four grades: 0, none; 1, weak; 2, moderate; and 3, strong. The percentage of positive staining was assessed as the following grades: 0, <5%; 1, 6–25%; 2, 26–50%; 3, 51–75%; and 4, >75%. Ten independent high magnification (×400) fields were assayed for each section. Two experienced pathologists independently evaluated the sections, and obtained the average scores of 10 fields.

Statistical analysis

Results are presented as mean ± SEM. The SPSS statistical package for Windows version 13 (SPSS, Inc., Chicago, IL, USA) and GraphPad Prism 5 software (GraphPad Software, Inc., USA) were employed to perform the statistical analysis. The Pearson's Chi-square test, the Spearman's rank correlation coefficient, the two-tailed Student's t-test, the Kaplan-Meier plot, the log-rank test or ANOVA was used in appropriate situation. Difference was considered to indicate a statistically significant result, at P<0.05.

Results

miR-616 is upregulated in HCC and is associated with the metastasis and recurrence of HCC

To determine the level of miR-616 expression in HCC tissues, the quantitative RT-PCR assay was performed in 40 pairs of HCC and adjacent non-tumor tissues. The expression level of miR-616 in HCC tissues was significantly elevated compared with that in the adjacent non-tumor liver tissues (P<0.01, Fig. 1A). Moreover, in the recurrent cases, the level of miR-616 was significantly higher than that in the non-recurrent cases (P<0.01, Fig. 1B). In addition, patients with metastasis had obviously increased level of miR-616 than those without metastasis (P<0.01, Fig. 1C). These results demonstrated that the expression level of miR-616 is significantly upregulated in HCC tissues and is associated with the recurrence and metastasis of HCC.

Figure 1 Expression of miR-616 in HCC tissues and cells. Comparing the differences in the expression levels of miR-616 between (A) HCC and adjacent non-tumor tissues, (B) patients with recurrence and those without recurrence, (C) patients with metastases and those without metastases, and (D) HCC cell lines with different metastatic potentials and the immortalized hepatic cell line LO2. **P<0.01.

Then, we examined the expression level of miR-616 in a non-transformed hepatic cell line (LO2) and six types of HCC cell lines (Hep3B, HepG2, Huh7, MHCC97L, HCCLM3 and MHCC97H). Compared with LO2, all HCC cell lines had significantly higher expression level of miR-616 (P<0.01, Fig. 1D). Moreover, it was interesting to find that miR-616 expression in HCCLM3 and MHCC97H, two highly metastatic HCC cell lines, was obviously higher than that in the low metastatic HCC cell lines including Hep3B, HepG2, Huh7 and MHCC97L (P<0.01, Fig. 1D). These data indicated that miR-616 can probably potentiate the invasive ability of HCC cells.

Elevated expression of miR-616 was correlated with adverse clinicopathological features and poor prognosis of HCC patients

The obvious elevation of miR-616 in HCC tissues and its association with HCC recurrence and metastasis prompted us to examine the clinical significance of miR-616 in HCC. The expression level of miR-616 was assessed either low (n=40) or high (n=40) based on the cut-off value which was defined as the median level of miR-616 in the 80 patients cohort. As presented in Table II, elevated expression level of miR-616 in HCC patient was associated with the venous infiltration (P=0.026), high Edmondson-Steiner grading (P=0.001) and advanced TNM stage (P<0.001). Furthermore, Kaplan-Meier analysis was performed to evaluate the prognostic value of miR-616 in HCC. Patients with high-miR-616 expression level had significantly decreased overall survival (P<0.01, Fig. 2A) and disease-free survival (P<0.01, Fig. 2B). These data suggest miR-616 can serve as a prognostic predictor for HCC patients.

Figure 2 Prognostic value of miR-616 in HCC patients. Compared with those with low-miR-616 level, those with high-miR-616 level had significantly decreased (A) overall survival and (B) disease-free survival. The median expression level of miR-616 in 80 HCC patients was chosen as the cut-off value. **P<0.01.

Table II Multivariate Cox regression analysis of 5-year overall and disease-free survival.

Table II

Multivariate Cox regression analysis of 5-year overall and disease-free survival.

Variables	Overall survival			Disease-free survival
	HR	95% CI	P-value	HR	95% CI	P-value
miR-616	1.808	1.044–3.134	0.035a	1.724	1.014–2.932	0.044a
Venous infiltration	1.941	1.012–3.725	0.046a	2.164	1.132–4.139	0.020a
Edmondson-Steiner grading	1.717	1.018–2.897	0.043a	1.730	1.019–2.939	0.042a
TNM stage	2.294	1.126–4.671	0.022a	2.116	1.040–4.303	0.038a

{ label (or @symbol) needed for fn[@id='tfn2-or-35-01-0366'] } HR, hazard ratio; CI, confidence interval.

a Statistically significant.

miR-616 promotes the migration, invasion and EMT of HCC cells

Next, we further explored the functional role of miR-616 in HCC cells. We transfected Hep3B cells with miR-616 mimics, and miR-616 expression level was significantly increased after transfection, as suggested by the qRT-PCR (P<0.01, Fig. 3A). Functionally, as suggested by the Transwell assay, Hep3B cells overexpressing miR-616 (Hep3B-miR-616 cells) showed increased ability of migration (P<0.01, Fig. 3B) and invasion (P<0.05, Fig. 3B). In contrast, miR-616 inhibitor significantly downregulated the expression level of miR-616 in MHCC97H cells (P<0.01, Fig. 3C), and resulted in an obviously reduced number of migrated (P<0.01, Fig. 3D) and invaded (P<0.01, Fig. 3D) MHCC97H cells. These results demonstrated that miR-616 can promote the invasive behavior of HCC cells.

Figure 3 miR-616 promotes the migration, invasion and EMT phenotype of HCC cells. (A and B) miR-616 overexpression increased the migration and invasion of Hep3B cells. n=3 repeats with similar results; *P<0.05, **P<0.01. (C and D) Inhibiting the expression of miR-616 significantly decreased the number of migrated and invaded MHCC97H cells as compared with control cells. n=3 repeats with similar results; **P<0.01. (E) Representative western blot analysis of E-cadherin and vimentin in Hep3B cells transfected with miR-616 mimics and MHCC97H cells transfected with miR-616 inhibitor are shown. n=6; **P<0.01.

Since the EMT process, which is regarded as a hallmark of metastasis (18), increased the migratory and invasive ability of HCC cells (19), we next investigated whether miR-616 could modulate EMT phenotype of HCC cells. Overexpression of miR-616 in Hep3B cells resulted in decreased level of E-cadherin (P<0.01, Fig. 3E) and increased expression of vimentin (P<0.01, Fig. 3E). In addition, inhibition of miR-616 in MHCC97H cells led to increased level of E-cadherin (P<0.01, Fig. 3E) and decreased expression of vimentin (P<0.01, Fig. 3E). These results suggested that miR-616 can promote EMT of HCC cells.

PTEN is a downstream target of miR-616 in HCC cells

To clarify the underlying mechanisms by which miR-616 regulates the invasive behavior and EMT of HCC cells, we used two publicly available databases (TargetScan 6.2 and miRanda) to search potential downstream target of miR-616. PTEN, which is a well-recognized tumor suppressor and an important regulator of HCC metastasis (20,21), was predicted as a downstream target of miR-616. As shown in Fig. 4A, the 3′-UTR of PTEN mRNA was found to contain the complementary sequence of miR-616. This suggests that miR-616 can potentially regulate the expression of PTEN by binding to the 3′-UTR of PTEN. To confirm this prediction, Hep3B cells transfected with miR-616 expression vector were subjected to western blotting. Overexpression of miR-616 in Hep3B cells resulted in significantly reduced expression of PTEN (P<0.05, Fig. 4B). It is well recognized that inhibiting PTEN expression can lead to increased phosphorylation of AKT (22). Accordingly, the phosphorylation of AKT was significantly increased after overexpressing miR-616 in Hep3B cells (P<0.05, Fig. 4B). Conversely, inhibiting the expression of miR-616 in MHCC97H cells resulted in significantly increased expression of PTEN (P<0.01, Fig. 4B) and reduced phosphorylation of AKT (P<0.01, Fig. 4B). Next, we performed the dual-luciferase reporter assay to elucidate whether miR-616 regulated PTEN expression by directly binding to its 3′-UTR. Overexpressing miR-616 significantly inhibited the luciferase activity of PTEN with a wild-type (wt) 3′-UTR (P<0.01, Fig. 4C), but had no influence on the activity of PTEN with a mutant (mt) 3′-UTR. Additionally, when anti-miR-616 was transfected, the luciferase activity of wt PTEN 3′-UTR obviously increased (P<0.01, Fig. 4C) while the luciferase activity of mt PTEN 3′-UTR remained unchanged.

Figure 4 PTEN is identified as a direct downstream target of miR-616 in HCC. (A) miR-616 and its putative binding sequence in the 3′-UTR of PTEN. The mutant miR-616 binding site was generated in the complementary site for the seed region of miR-616 (wt, wild-type; mt, mutant type). (B) Western blot analysis of PTEN, AKT and p-AKT expression in Hep3B cells transfected with miR-616 mimics or MHCC97H cells transfected with miR-616 inhibitors. n=6; *P<0.05, **P<0.01. (C) miR-616 overexpression significantly suppressed the luciferase activity that carried wt but not mt 3′-UTR of PTEN. Anti-miR-616 led to an obvious increase in luciferase activity of wt 3′-UTR of PTEN. n=3 repeats with similar results; *P<0.05, **P<0.01.

To further validate the regulatory effect of miR-616 on PTEN expression, we compared the expression of PTEN and p-AKT in HCC tissues with low-miR-616 expression level with that of high-miR-616 expression. The IHC results showed that the PTEN expression in high-miR-616 expression group was significantly decreased when compared with that in the low-miR-616 expression group (P<0.01, Fig. 5A). Accordingly, the expression of p-AKT was significantly increased in high-miR-616 expression group compared to the low-miR-616 expression group (P<0.01, Fig. 5B). In all, these data demonstrated that PTEN is a direct downstream target of miR-616 and miR-616 can inhibit the expression of PTEN by binding to its 3′-UTR.

Figure 5 An inverse correlation between miR-616, PTEN and p-AKT expression is observed in HCC. (A) Representative immunostaining showed weaker staining of PTEN in miR-616-high expressing HCC tissue and higher expression of PTEN in miR-616-low expressing tissue. (B) Representative immunostaining showed increased expression of p-AKT in miR-616-high expressing HCC tissue and decreased level of p-AKT in miR-616-low expressing tissue. **P<0.01.

miR-616 promotes EMT and metastatic ability of HCC cells through inhibiting PTEN

To further clarify the functional significance of PTEN in miR-616-mediated EMT and metastatic ability of HCC cells, we transfected pCMV5-PTEN plasmids into Hep3B cells overexpressing miR-616 (Hep3B-miR-616 cells). The results of western blotting showed that transfection of pCMV5-PTEN plasmids resulted in significant increase of PTEN level in Hep3B-miR-616 cells (P<0.01, Fig. 6A), and led to upregulation of E-cadherin (P<0.05, Fig. 6A) and reduced expression of vimentin (P<0.05, Fig. 6A), indicating that restoring PTEN expression can reverse the EMT phenotype of Hep3B cells induced by miR-616 overexpression. Furthermore, forced expression of PTEN partly abrogated the promoting effects of miR-616 on the migration (P<0.05, Fig. 6B) and invasion (P<0.05, Fig. 6B) of HCC cells. These data indicated that miR-616 promotes EMT and metastatic ability of HCC cells by targeting PTEN.

Figure 6 miR-616 induces HCC cell migration, invasion and EMT by inhibiting PTEN. (A) Western blot analysis of the expression of E-cadherin and vimentin in pCMV5-PTEN transfected miR-616 overexpressing Hep3B cells. n=6; *P<0.05, **P<0.01. (B) Restoration of PTEN in miR-616 overexpressing Hep3B cells inhibited the promoting effect of miR-616 on cell migration and invasion. n=3 repeats with similar results; *P<0.05.

Discussion

The initiation and progression of HCC is a complex process in which various molecules, and numerous signaling pathways are involved (23,24). Emerging studies have confirmed that abnormal expression and function of miRNAs play a critical role in this process (25,26). miR-616 is a novel cancer-associated miRNA which has been found to be abnormally expressed in gastric (15), lung (16) and prostate cancer (17,27). In the present study, we initially examined the expression status of miR-616 in clinical specimens of HCC. We confirmed for the first time that compared with adjacent non-tumor tissues, the expression level of miR-616 was significantly elevated in HCC tissues. In addition, patients with recurrence and metastasis had significantly higher miR-616 levels than those without recurrence and metastasis. The clinical analysis further demonstrated that increased expression level of miR-616 was associated with adverse clinicopathological features including venous infiltration, high Edmondson-Steiner grading and advanced TNM tumor stage. Importantly, Kaplan-Meier analysis showed that increased expression of miR-616 was associated with poorer prognosis of HCC patients including overall and disease-free survival. Moreover, the expression level of miR-616 in HCC cell lines, particularly in those with high metastatic ability (HCCLM3 and MHCC97H), was significantly higher than that in the non-transformed hepatic cell line LO2. Taken together, these results indicated that miR-616 is an important participant in the development and progression of HCC, and can serve as a prognostic marker of HCC patients.

The obvious elevation of miR-616 expression in HCC prompted us to examine the functional role of miR-616 in HCC. Since our results showed that the expression of miR-616 was associated with the recurrence and metastasis of HCC patients, we speculated that miR-616 probably influenced the migration and invasion of HCC cells. Transwell assay showed that over-expression of miR-616 promoted the migration and invasion of HCC cells while downregulation of miR-616 inhibited the metastatic behavior of HCC cells. These data suggested that miR-616 can play an active role in HCC by promoting the migration and invasion of HCC cells. EMT, a process in which epithelial cells lose cell polarity and intracellular junctions and acquire mesenchymal features (19,28), can potentiate the migratory and invasive ability of HCC cells (19,29). Increasing evidence has demonstrated that miRNAs, which could regulate the expression of EMT-related genes, played a critical role in the EMT process (28,30,31). In the present study, we found that overexpression of miR-616 reduced the expression of E-cadherin, the epithelial marker and increased the expression of vimentin, the mesenchymal marker. Downregulation of miR-616 resulted in elevated expression of E-cadherin and reduced expression of vimentin. These results suggested that miR-661 promotes the EMT of HCC cells. Altogether, miR-616 may increase the invasive ability of HCC cells by inducing EMT.

Phosphatase and tensin homolog (PTEN) is a well-recognized tumor suppressor which is frequently mutated or deleted in human cancers (22). However, instead of the mutation or the deletion of PTEN, abnormal expression of PTEN was confirmed in HCC (32) and was found to promote the progression of HCC (20). However, the molecular mechanisms responsible for the abnormal expression of PTEN remains unclear. PTEN has been found to be the downstream target of several miRNAs including miR-21 (20,33), miR-216a and 217 (21), miR-221 and 222 (34), miR29a (35) and miR-32 (36). In the present study, we confirmed that PTEN was a direct downstream target of miR-616 in HCC. Firstly, putative binding sequences of miR-616 were found in the 3′-UTR of PTEN after searching two publicly available databases (TargetScan and miRanda). Secondly, transfecting miR-616 mimics into Hep3B cells resulted in decreased expression of PTEN while downregulation of miR-616 in MHCC97H cells led to increased PTEN expression. The phosphorylation of Akt, which is inhibited by PTEN (37), was reduced after miR-616 overexpression and was increased after miR-616 suppression, supporting that miR-616 regulated the expression of PTEN. Additionally, the expression of PTEN in HCC tissues with high-miR-616 level was significantly lower than that in those with low-miR-616 level. This further validates the regulatory effect of miR-616 on PTEN expression. Furthermore, altering the expression level of miR-616 in Hep3B cells significantly influenced the luciferase activity of wt 3′-UTR of PTEN, while had no obvious influence on the luciferase activity of mt 3′-UTR of PTEN, suggesting that miR-616 can regulate the expression of PTEN by directly interacting with the 3′-UTR of PTEN.

Functionally, PTEN was able to influence the migration of glioma cells by modulating its downstream PI3K/Akt pathway (38). Therefore, we performed rescue experiments in Hep3B-miR-616 cells to clarify whether PTEN was involved in the promoting effect of miR-616 on the metastatic ability and EMT phenotype of HCC cells. We found that restoring the expression of PTEN abrogated the promoting effects of miR-616 on EMT and metastatic abilities of HCC cells. Therefore, our results suggest that PTEN is not only a direct target of miR-616 but also a functional mediator downstream of miR-616 in HCC. Of interest is that a study of prostate cancer (17) found TFPI-2 was a direct downstream target of miR-616, and miR-616 induced androgen-independent growth of prostate cancer cells by suppressing TFPI-2 expression. Therefore, the downstream targets and the functional significance of miRNAs in human cancers seem to be cancer-type specific.

In summary, our results demonstrated for the first time that miR-616 expression is elevated in HCC tissues, and its increased expression is associated with adverse prognostic features of HCC patients. Moreover, miR-616 is a valuable biomarker in predicting the prognosis of HCC patients. In vitro experiments demonstrated that miR-616 can promote the migration, invasion and EMT of HCC cells. Mechanistically, we found that PTEN is a downstream target of miR-616 in HCC and miR-616 exerts its functional significance on HCC cells by suppressing PTEN. Taken together, the findings from the present study indicated that miR-616 can serve as a valuable clinical biomarker, and may potentially be a promising therapeutic target in HCC.

References