LncRNA RHPN1-AS1 Promotes Cell Proliferation, Migration and Invasion Through Targeting miR-7-5p and Activating PI3K/AKT/mTOR Pathway in Hepatocellular Carcinoma.

Hepatocellular carcinoma (HCC) is a severe disease with high mortality in the world. Emerging evidence has suggested that lncRNAs play an important role in cancer progression, including HCC. This study aimed to comprehensively investigate the effect of lncRNA RHPN1 antisense RNA 1 (RHPN1-AS1) on HCC and its underlying molecular mechanism. In this study, we evaluated the expressions of lncRNA RHPN1-AS1 and miR-7-5p by qRT-RCR in both HCC tissue and HCC cells. Our findings showed that lncRNA RHPN1-AS1 was upregulated in HCC tissue and HCC cells, while miR-7-5p was downregulated. LncRNA RHPN1-AS1 expression in HCC patients was closely related to vascular invasion, tumor-node-metastasis (TNM) stage and barcelona clinic liver cancer (BCLC) stage. Furthermore, we quantified cell clone-formation ability, proliferation, migration and invasion of HCCLM3 and MHCC97 H cells using several assays (colony formation assay, 5-Ethynyl-2'-deoxyuridine (EdU) assay and transwell assay, respectively). Functional experiments confirmed that silencing lncRNA RHPN1-AS1 inhibited cell proliferation, migration and invasion in HCCLM3 and MHCC97 H cells. After that, bioinformatics analysis, dual luciferase reporter gene assay, qRT-PCR and western blot were used to investigate the molecular mechanism of lncRNA RHPN1-AS1 on HCC. Mechanistically, the rescue experiments demonstrated that miR-7-5p inhibitor reversed the inhibition effect of silencing lncRNA RHPN1-AS1 on HCCLM3 cells proliferation, migration and invasion. Moreover, silencing lncRNA RHPN1-AS1 also inhibited the activation of PI3K/AKT/mTOR pathway. Taken together our findings demonstrated that lncRNA RHPN1-AS1 could facilitate cell proliferation, migration and invasion via targeting miR-7-5p and activating PI3K/AKT/mTOR pathway in HCC.

Introduction

Hepatocellular carcinoma (HCC) is one of the most common cancers and ranks as the second most common cause of cancer-associated death all over the world.[1] Despite a variety of therapeutic approaches have been improving in recent years, the survival of HCC patients is still poor due to recurrence and metastasis.[2] Thus, the identification of new therapeutic strategies and molecular targets for the treatment of HCC is critical.

Long noncoding RNA (lncRNAs) are a class of RNA transcripts which are longer than 200 nucleotides and exhibit no protein coding ability.[3] An increasing body of literature suggests lncRNA may be closely related to the pathogenesis of multiple malignancies.[4,5] In HCC, lncRNAs have been demonstrated to participate in cell proliferation, migration and invasion.[6,7] For example, lncRNA-AWPPH has been reported to promote cell proliferation and migration in HCC.[8] Shen et al. have indicated that lncRNA TATDN1 accelerates proliferation and cell cycle progression in HCC.[9] There have been some studies demonstrating abnormal lncRNA RHPN1 antisense RNA 1 (RHPN1-AS1) expression in several types of cancers, including breast cancer,[10] squamous cell carcinoma[11] and non-small cell lung cancer.[12] However, the function of lncRNA RHPN1-AS1 on HCC is unclear.

MicroRNAs (miRNAs) are noncoding endogenous short RNA molecules of 19 to 25 nucleotides of length which are capable of modulating gene expression at the post-transcriptional level.[13] More and more studies have indicated that miRNAs are involved in many types of cancers, including HCC.[14] Numerous miRNAs such as miR-21, miR-141, miR-769-5p and miR-7-5p have been reported to be abnormally expressed in HCC and play an important role in modulating the proliferation, migration and invasion of HCC cells.[15-18] Several recent studies have suggested that lncRNAs, act as “molecular sponges” of miRNAs and can affect the target mRNA expression and ultimately interfere with the occurrence and development of diseases.[12] However, the relationship between lncRNA RHPN1-AS1 and miR-7-5p remains uninvestigated in HCC.

In this study, we therefore explored the effect of lncRNA RHPN1-AS1 on cell proliferation, migration and invasion in HCC and investigated the potential underlying molecular mechanisms. Our results revealed that lncRNA RHPN1-AS1 could facilitate cell proliferation, migration and invasion via targeting miR-7-5p and activating PI3K/AKT/mTOR pathway in HCC. Findings of our study may provide a new theoretical foundation for exploring novel treatments for HCC.

Methods

Patients and Tissue Samples

Paired HCC and adjacent normal liver tissues were obtained from 126 HCC patients at our hospital during July 2015 to June 2018. All samples were pathologically confirmed and immediately frozen in liquid nitrogen after resection. None of the patients received chemotherapy and radiotherapy before surgery. The characteristics of HCC patients were presented in Table 1. The protocol of this research has been approved by the Ethics Committee of our hospital. All patients have signed written informed consent.

Table 1.

Association Between lncRNA RHPN1-AS1 Expression and Clinical Parameters in Patients With HCC.

Clinical parameters	Number of cases = 126	RHPN1-AS1		p-value
		High = 63	Low = 63
Age
<60	51	25	26	0.8560
≥60	75	38	37
Gender
Male	112	58	54	0.2568
Female	14	5	9
HBsAg
Positive	103	53	50	0.4890
Negative	23	10	13
AFP (μg/l)
<400	85	41	44	0.5684
≥400	41	22	19
Tumor size (maximal diameter)
<5cm	60	31	29	0.7213
≥5cm	66	32	34
Number of tumors
Solitary	102	51	53	0.4116
Multiple	24	14	10
Encapsulation
Complete	85	39	46	0.1832
No	41	24	17
Vascular invasion
Yes	102	56	46	0.0233*
No	24	7	17
TNM stage
I-II	103	47	56	0.0379*
III	23	16	7
BCLC stage
A	88	38	50	0.0198*
B-C	38	25	13
Histologic differentiation
I-II	88	42	46	0.4375
III-IV	38	21	17

* p < 0.05. HBeAg, hepatitis B e-antigen; AFP, a-fetoprotein; TNM, tumor-node metastasis; BCLC, barcelona clinic liver cancer

Cell Cultures

The immortalized normal liver epithelial cell line (THLE-3) and 4 human HCC cell lines (Hep-3B, Huh7, MHCC97 H and HCCLM3) were obtained from the American Type Culture Collection (ATCC, USA). All cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco) at 37°C in a humidified incubator containing 5% CO2.

Cell Transfection

The RHPN1-AS1 siRNA, miR-7-5p inhibitor and their corresponding negative controls were purchased from GENECHEM Co., Ltd. (Shanghai, China). HCCLM3 and MHCC97 H cells were seeded into a 24-well plates at a density of 1 × 105 cell/well, and respectively transfected with RHPN1-AS1 siRNA, miR-7-5p inhibitor, UCA1 siRNA negative control (siNC) or miR-7-5p inhibitor negative control (inhibitor NC) by using Lipofectamine® 3000 (Invitrogen, USA). Subsequently, the transfected HCCLM3 and MHCC97 H cells were randomly assigned to 7 groups: Mock group (no treatment), siNC group (transfected with siNC), siRHPN1-AS1 group (transfected with RHPN1-AS1 siRNA), siNC + inhibitor NC group (transfected with siNC and inhibitor NC), siRHPN1-AS1 + inhibitor NC group (transfected with RHPN1-AS1 siRNA and inhibitor NC), siNC + miR-7-5p inhibitor group (transfected with siNC and miR-7-5p inhibitor) and siRHPN1-AS1 + miR-7-5p inhibitor group (transfected with RHPN1-AS1 siRNA and miR-7-5p inhibitor).

Colony Formation Assay

The clonal abilities of HCCLM3 and MHCC97 H cells were measured by using a colony formation assay. In brief, HCCLM3 and MHCC97 H cells were seeded in six-well plates at a concentration of 500 cells per well and cultured for 14 d to form colonies. Subsequently, the colonies were fixed with formaldehyde (4%) and stained with crystal violet (2%) for 20 min. Finally, the stained colonies were imaged and counted.

5-Ethynyl-2′-Deoxyuridine (EdU) Assay

The proliferation abilities of HCCLM3 and MHCC97 H cells were determined by using the an EdU kit (Roche, Germany) according to the manufacturer’s protocol. Simply, the transfected HCCLM3 and MHCC97 H cells were seeded into 6-well plate and then incubated with EdU solution. Subsequently, cell nuclei were stained with DAPI. Finally, the EdU staining was visualized on a microscope (Carl Zeiss, Oberkochen, Germany).

Transwell Assay

The migration and invasion abilities of HCCLM3 and MHCC97 H cells were detected by using a transwell chamber (Corning, USA) according to the manufacturer’s protocol. Simply, the transfected HCCLM3 and MHCC97 H cells were plated into the upper chamber at a density 5 × 104 cells/well. For the invasion assay, the upper chamber was pre-coated with Matrigel (BD Biosciences, USA). The bottom chamber was filled with 500 µL DMEM containing 10% FBS. After incubation for 24 h at 37°C, the upper chamber cells were carefully removed. And the lower membrane cells were fixed in formaldehyde for 20 min, and then stained with crystal violet (Beyotime, China) for 30 min. Finally, images were collected using an optical microscope (Olympus, Tokyo, Japan).

Dual Luciferase Reporter Gene Assay

Starbase3.0 was used to predict the relationship between lncRNA RHPN1-AS1 and miRNA. For the luciferase assay, the fragments of lncRNA RHPN1-AS1 containing the miR-7-5p targeting sites were inserted into pGL3 vector (Promega, USA) for constructing wild pmirGLO-WT-RHPN1-AS1-3′-UTR (RHPN1-AS1-WT) and mutant pmirGLO-MUT-RHPN1-AS1-3′-UTR (RHPN1-AS1-MUT). Subsequently, reporter vectors with miR-7-5p mimics and miR-7-5p mimics negative control (mimics NC) were respectively co-transfected into HCCLM3 and MHCC97 H cells by Lipofectamine 3000 (Invitrogen, USA). At 48 h after transfection, the fluorescence intensity was measured using a dual luciferase kit (Promega, USA).

Real-Time Fluorogenic PCR Assays

Total RNA from HCC tissue, normal liver tissue, normal liver cells and HCC cells was extracted using TRIZOL (TaKaRa, Shanghai, China). The total RNA was reverse transcribed into cDNA using Revert Aid First Strand cDNA Synthesis Kit (Thermo, USA). Subsequently, qRT-PCR was performed using SYBR green qPCR Master Mix (Thermo Scientific, USA) according to the manufacturer’s protocol. Primers sequences were as follows: lncRNA RHPN1-AS1 F: 5′-GCTCCTGGTCATCAAGTTCCTCT-3′, R: 5′-GCACAGGCACCAGAATGATCC-3′; GAPDH F: 5′-TCCTCTGACTTCAACAGCGACAC-3′, R: 5′-CACCCTGTTGCTGTAGCCAAATTC-3′; miR-7-5p F: 5′-TGTTGTTTTGTGAT-3′, R: 5′-GTGCAGGGTCCGAGGT-3′; U6 F: 5′-CACTGGGTGCGGCAGGT-3′, R: 5′-TCATCACCGATCGATACGATGA-3′. GAPDH and U6 were respectively used as internal controls of lncRNA RHPN1-AS1 and miR-7-5p.

Western Blot Analysis

Total proteins from HCCLM3 and MHCC97 H cells were extracted using RIPA lysis buffer. Protein samples (50 μg) were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and then transferred to a polyvinylidene difluoride membrane. The membranes were blocked with 5% non-fat milk for 2 h at room temperature. The membranes were then incubated with the primary antibodies against PI3 K (#4249, 1:1000, Cell Signal, USA), p-PI3 K (#3241, 1:500, Cell Signal), Akt (#9272, 1:1000, Cell Signal), p-Akt (#0016, 1:500, Cell Signal), mTOR (#2972, 1:1000, Cell Signal), p-mTOR (#3308, 1:500, Cell Signal), GAPDH (#5174, 1:1000, Cell Signal) at 4°C overnight. Subsequently, HRP-conjugate secondary antibodies (1:5000, Santa Cruz, USA) were used to incubate membranes for 2 h at room temperature. The immunoreactive signals were visualized by an ECL system (Thermo, USA).

Statistical Analysis

All statistical analyses were performed using SPSS 22.0 Statistical Software (Chicago, IL). The data were presented as the mean ± SD. Statistical significance was tested using the Student’s t-test or one-way ANOVA followed by the Tukey’s post hoc test. A level of P < 0.05 was considered to be statistically significant.

Results

The Expression of lncRNA RHPN1-AS1 Is Upregulated in HCC and Associated With Clinical Parameters

qRT-PCR of HCC tissue compared to normal liver tissue showed a significantly increased expression of lncRNA RHPN1-AS1 in HCC (P < 0.0001) (Figure 1A). Similarly, the expression of lncRNA RHPN1-AS1 in THLE-3 cells was markedly lower than that in Hep-3B (P = 0.0038), Huh7 (P = 0.0013), MHCC97 H (P = 0.0006) and HCCLM3 cells (P = 0.0004) (Figure 1B). These results suggested that lncRNA RHPN1-AS1 was highly expressed in HCC. Furthermore, the results of our further analysis (presented in Table 1) indicated that lncRNA RHPN1-AS1 expression was closely related to vascular invasion (P < 0.05), tumor-node-metastasis (TNM) stage (P < 0.05) and barcelona clinic liver cancer (BCLC) stage (P < 0.05) in HCC patients.

Figure 1.

The expression of lncRNA RHPN1-AS1 was upregulated in HCC. (A) The expression of lncRNA RHPN1-AS1 was detected by qRT-PCR in HCC tissue and normal liver tissue. (B) The expression of lncRNA RHPN1-AS1 was detected by qRT-PCR in THLE-3, Hep-3B, Huh7, MHCC97 H and HCCLM3 cells. ****P < 0.0001, vs. Normal group (A); **P < 0.01, ***P < 0.001, vs. THLE-3 group (B).

lncRNA RHPN1-AS1 Promotes Cell Proliferation, Migration and Invasion in MHCC97 H and HCCLM3 Cells

As shown in Figure 2A, the transfection of si-RHPN1-AS11 or si-RHPN1-AS12 treatment significantly inhibited lncRNA RHPN1-AS1 expression in HCCLM3 (P = 0.0056; P = 0.0033) and MHCC97 H cells (P = 0.0213; P = 0.0036), suggesting that the transfection was successful. Colony formation assay showed that cell clone numbers of HCCLM3 and MHCC97 H cells were dramatically decreased after siRHPN1-AS1 transfection when compared to siNC group (P = 0.0012; P = 0.0021) (Figure 2B). Moreover, EdU assay revealed that silencing lncRNA RHPN1-AS1 significantly suppressed the proliferation of HCCLM3 (P = 0.0011) and MHCC97 H cells (P = 0.0029) (Figure 2C). In addition, the transwell assay revealed that silencing lncRNA RHPN1-AS1 also markedly inhibited the migration and invasion of HCCLM3 (P = 0.0001; P = 0.0003) and MHCC97 H cells (P = 0.0002; P = 0.0007) (Figure 2D). Therefore, these results indicated that lncRNA RHPN1-AS1 could promote cell proliferation, migration and invasion in HCCLM3 and MHCC97 H cells.

Figure 2.

lncRNA RHPN1-AS1 promoted cell proliferation, migration and invasion in HCCLM3 and MHCC97 H cells. (A) The expression of lncRNA RHPN1-AS1 was measured by qRT-PCR in HCCLM3 and MHCC97 H cells. (B) Cell clones number of HCCLM3 and MHCC97 H cells was detected by colony formation assay. (C) The cell proliferation ability of HCCLM3 and MHCC97 H cells was measured by EdU assay. (D) The cell migration and invasion abilities of HCCLM3 and MHCC97 H cells were detected by transwell assay. *P < 0.05, **P < 0.01, ***P < 0.001, vs. siNC group.

lncRNA RHPN1-AS1 Targets Negatively Regulating miR-7-5p Expression

More and more studies have confirmed that lncRNAs may be function as a molecular sponge or a competing endogenous RNA (ceRNA) via competitively binding to miRNAs in modulating the progression of cancers.[19] To shed some light on the potential molecular mechanisms by which lncRNA RHPN1-AS1 exerted its role on HCC, StarBase online tool was used to predict the miRNAs that binds to lncRNA RHPN1-AS1. As Figure 3A showed, there was the binding site between lncRNA RHPN1-AS1 and miR-7-5p. Dual luciferase reporter gene assay showed that the fluorescence intensity in HCCLM3 and MHCC97 H cells was significantly reduced by miR-7-5p mimics in the RHPN1-AS1-WT group (P = 0.0041; P = 0.0046), but there was no significant difference in the RHPN1-AS1-MUT group (P = 0.1744; P = 0.1545) (Figure 3B). The results of qRT-PCR revealed that the expression of miR-7-5p was decreased in HCC tissue compared with normal liver tissue (P < 0.0001) (Figure 3C) and the expression of miR-7-5p was negatively correlated with the expression of lncRNA RHPN1-AS1 in HCC tissue (P < 0.0001) (Figure 3D). In addition, miR-7-5p expression was lower in Hep-3B (P = 0.0032), Huh7 (P = 0.0020), MHCC97 H (P = 0.0008) and HCCLM3 cells (P = 0.0001) than in THLE-3 cells, as shown by qRT-PCR (Figure 3E). All the results demonstrated that lncRNA RHPN1-AS1 could target negatively regulating miR-7-5p expression.

Figure 3.

lncRNA RHPN1-AS1 targeted negatively regulating miR-7-5p expression. (A) The binding target of lncRNA RHPN1-AS1 and miR-7-5p was predicted by StarBase. (B) The luciferase activity was measured by dual luciferase reporter gene assay. (C) The expression of miR-7-5p was detected by qRT-PCR in HCC tissue and normal liver tissue. (D) Correlation analysis between the expression of lncRNA RHPN1-AS1 and miR-7-5p. (E) The expression of miR-7-5p was detected by qRT-PCR in THLE-3, Hep-3B, Huh7, MHCC97 H and HCCLM3 cells. **P < 0.01, vs. mimics NC group (B); ****P < 0.0001, vs. Normal group (C); **P < 0.01, ***P < 0.001, vs. THLE-3 group (E).

lncRNA RHPN1-AS1 Promotes Cell Proliferation, Migration and Invasion by Regulating miR-7-5p in HCCLM3 Cells

To further confirm the interaction between lncRNA RHPN1-AS1 and miR-7-5p in HCC, siRHPN1-AS1, miR-7-5p inhibitor, siNC and inhibitor NC were co-transfected into HCCLM3 cells. As shown in Figure 4A, the expression of miR-7-5p was significantly increased in siRHPN1-AS1 + inhibitor NC group compared with siNC + inhibitor NC group (P = 0.0004). Conversely, the expression of miR-7-5p was significantly decreased in siNC + miR-7-5p inhibitor group compared with siNC + inhibitor NC group (P = 0.0043). The expression of miR-7-5p in siRHPN1-AS1 + miR-7-5p inhibitor group was markedly lower than that in siRHPN1-AS1 + inhibitor NC group (P = 0.0002), while its expression was dramatically higher than that in siNC + miR-7-5p inhibitor group (P = 0.0097), suggesting that the transfection was successful. Colony formation assay (Figure 4B) showed that cell clone numbers of HCCLM3 cells were dramatically decreased in siRHPN1-AS1 + inhibitor NC group compared with siNC + inhibitor NC group (P = 0.0013). Meanwhile, cell clone numbers in siNC + miR-7-5p inhibitor group were significantly higher than that in siNC + inhibitor NC group (P = 0.0106). When compared with siRHPN1-AS1 + miR-7-5p inhibitor group, cell clone numbers were decreased in siRHPN1-AS1 + inhibitor NC group (P = 0.0017), but were increased in siNC + miR-7-5p inhibitor group (P = 0.0177). In addition, the EdU assay (Figure 4C) and transwell assay (Figure 4D) revealed that the the proliferation, migration and invasion abilities of HCCLM3 cells were significantly reduced in siRHPN1-AS1 + inhibitor NC group compared with siNC + inhibitor NC group (P = 0.0021; P = 0.0111; P = 0.0002), while they were elevated in siNC + miR-7-5p inhibitor group (P = 0.0004; P = 0.0083; P = 0.0161). Meanwhile, compared with siRHPN1-AS1 + miR-7-5p inhibitor group, the proliferation, migration and invasion abilities of HCCLM3 cells were decreased in siRHPN1-AS1 + inhibitor NC group (P = 0.0019; P = 0.0069; P = 0.0014), but increased in siNC + miR-7-5p inhibitor group (P = 0.0032; P = 0.0066; P = 0.0171). Therefore, our data revealed that lncRNA RHPN1-AS1 could promote cell proliferation, migration and invasion by regulating miR-7-5p in HCCLM3 cells.

Figure 4.

Silencing lncRNA RHPN1-AS1 inhibited cell proliferation, migration and invasion by regulating miR-7-5p in HCCLM3 cells. (A) The expression of miR-7-5p was measured by qRT-PCR in HCCLM3 cells. (B) HCCLM3 cells clones number was detected by colony formation assay. (C) HCCLM3 cells proliferation ability was measured by EdU assay. (D) HCCLM3 cells migration and invasion abilities were detected by transwell assay. *P < 0.05, **P < 0.01, ***P < 0.001, vs. siNC + inhibitor NC group; #P < 0.05, ##P < 0.01, vs. siRHPN1-AS1 +inhibitor NC and siNC + miR-7-5p inhibitor group.

lncRNA RHPN1-AS1 Activates the PI3K/AKT/mTOR Pathway in HCCLM3 and MHCC97 H Cells

As shown in Figure 5, silencing lncRNA RHPN1-AS1 significantly inhibited the phosphorylation of PI3 K, AKT and mTOR in HCCLM3 (P = 0.0001; P = 0.0019; P = 0.0013) and MHCC97 H cells (P = 0.0002; P = 0.0004; P = 0.0015). However, pretreatment with a PI3 K activator (740Y-P, 10 μM, MCE, USA) resulted in a significant increase in the phosphorylation of PI3 K, AKT and mTOR in HCCLM3 (P = 0.0003; P = 0.0002; P = 0.0011) and MHCC97 H cells (P = 0.0002; P = 0.0010; P = 0.0007). The results above suggested that lncRNA RHPN1-AS1 could activate PI3K/AKT/mTOR pathway in HCCLM3 and MHCC97 H cells.

Figure 5.

lncRNA RHPN1-AS1 activated PI3K/AKT/mTOR pathway in HCCLM3 and MHCC97 H cells. The expressions of PI3 K, p-PI3 K, Akt, p-Akt, mTOR and p-mTOR in HCCLM3 and MHCC97 H cells were measured by western blot. **P < 0.01, ***P < 0.001, vs. siNC group; ##P < 0.01, ###P < 0.001, vs. siRHPN1-AS1 group.

Discussion

HCC is a global medical issue with a high incidence, especially in China. Although therapeutic approaches have been improving recently, the survival of HCC patients is still poor.[2] It is therefore urgent to clarify the mechanisms of HCC progression and to explore innovative and effective treatment strategies for this disease. In this research, we demonstrated that lncRNA RHPN1-AS1 could facilitate cell proliferation, migration and invasion via targeting miR-7-5p and activating PI3K/AKT/mTOR pathway in HCC.

An increasing number of studies have suggested that lncRNAs play important roles in the progression of HCC.[20] Previous reports have proved that the expression of lncRNA RHPN1-AS1 is upregulated in many malignancies, such as breast cancer,[10] uveal melanoma[21] and glioma.[22] In our study, we demonstrated lncRNA RHPN1-AS1 was highly expressed in both HCC tissue and HCC cells, which was in line with previous findings. Furthermore, we also found that lncRNA RHPN1-AS1 expression was closely related to certain clinical parameters including vascular invasion, TNM stage and BCLC stage in HCC patients. Accumulating evidences have indicated that lncRNAs participate in a series of cellular processes, such as cell proliferation, migration, invasion and apoptosis.[23,24] For example, lncRNA FAM83H-AS1 is reported to facilitate cell proliferation, migration and invasion in HCC.[25] Liu et al.[26] have indicated that lncRNA MEG3 could inhibit cell proliferation and promote cell apoptosis in HCC. A study by Zhang et al.[27] has confirmed that lncRNA XIST could promote cell proliferation and migration through targeting PDCD4 in HCC. In our present study, we investigated the effect of lncRNA RHPN1-AS1 on HCC cells and found that lncRNA RHPN1-AS1 could facilitate HCC cell proliferation, migration and invasion.

The molecular mechanism underlying the roles of lncRNAs is complex. One of the most common mechanisms of lncRNAs is to competitively bind miRNAs and regulate the effect of miRNAs on their targets.[28] In recent years, lncRNA RHPN1-AS1 has been reported to act as a ceRNA of miRNAs and play a vital role in multiple tumors by antagonizing miRNAs functions and regulating the expression of miRNA targets.[12] Cui et al.[22] have reported that lncRNA RHPN1-AS1 could facilitate proliferation and invasion of glioma cells through targeting miR-625. This study focused on downstream miRNAs of lncRNA RHPN1-AS1, as a large number of miRNAs act as tumor suppressors and oncogenes in HCC. In this study, bioinformatics analysis and dual luciferase reporter gene assay confirmed that miR-7-5p was a target gene of lncRNA RHPN1-AS1. It is reported that miR-7-5p is a tumor suppressor miRNA capable of modulating the development of various cancers.[29,30] Our results showed that miR-7-5p expression was downregulated in HCC, which was consistent with previous studies. Hu et al. have suggested that miR-7-5p mimics could markedly suppress the growth, migration and colony formation of human hepatoma cells.[18] Similarly, our data also confirmed that miR-7-5p inhibitor could reverse the inhibitory effect of silencing lncRNA RHPN1-AS1 on proliferation, migration and invasion of HCCLM3 cells, indicating that lncRNA RHPN1-AS1 could promote these activities by regulating miR-7-5p in HCC.

Previous studies have confirmed that PI3K/Akt/mTOR pathway is a key pathway in many human cancers,[31] and it is reported to be the most widely studied pathway in HCC, active in 40-50% of HCC patients.[32] In addition, the Akt pathway has been identified as a key mechanism of drug resistance in HCC.[32] Currently, studies have reported that lncRNAs could regulate cell proliferation, migration, invasion and apoptosis through modulation of the PI3K/AKT/mTOR pathway in HCC.[33,34] For example, downregulation of lncRNA NR027113 could suppress cell proliferation, migration and invasion by modulating the PI3K/AKT pathway in HCC.[35] Huang et al.[36] have indicated that lncRNA CDKN2B-AS1 could promote cell proliferation and metastasis of human HCC by activating the PI3K/Akt/mTOR signaling pathway. Previous researches have confirmed that lncRNA PTTG3P could promote cell growth and metastasis through upregulating PTTG1 and activating the PI3K/AKT pathway in HCC.[37] In this study, we demonstrated that silencing lncRNA RHPN1-AS1 could inhibit the phosphorylation of PI3 K, AKT and mTOR. In addition, 740Y-P could reverse the inhibitory effect of silencing lncRNA RHPN1-AS1 on the phosphorylation of PI3 K, AKT and mTOR, suggesting that lncRNA RHPN1-AS1 could promote cell proliferation, migration and invasion by activating PI3K/AKT/mTOR pathway in HCC.

Conclusion

In conclusion, our work confirmed that lncRNA RHPN1-AS1 expression was upregulated in both HCC tissue and HCC cells. In addition, we further demonstrated that lncRNA RHPN1-AS1 could facilitate cell proliferation, migration and invasion via targeting miR-7-5p and activating PI3K/AKT/mTOR pathway in HCC. Our research provides a novel regulatory mechanism of lncRNA RHPN1-AS1 on HCC and may provide a reference for the future treatment of HCC.