Background
Hepatocelluar carcinoma (HCC) is the third leading cause of cancer-related deaths worldwide, and the burden of this devastating cancer is expected to increase further in the coming years [
1]. Due to the difficulty of effectively diagnosing HCC at its early stage, only about 10 to 20% of patients with hepatocellular carcinoma are currently eligible for surgical intervention [
2‐
6]. Therefore, elucidating the molecular mechanisms involved in HCC is essential for developing cancer prevention strategies and possible guiding disease management in the clinic.
Accumulating evidence suggests that microRNAs (miRNAs) are involved in the initiation and progression of HCC [
7]. First, the 22nt noncoding miRNAs act as key regulators of various fundamental biological processes, such as development, differentiation, apoptosis, and cell proliferation, in which common pathways are shared with cancer [
8‐
11]. Second, bioinformation analyses estimate that miRNAs may regulate as much as 30% of the human protein coding genes, including oncogenes and tumor suppressors, suggesting that these small RNAs may act to coordinate the interplay between complex signal transduction pathways [
12]. Third, increasing evidence shows that the expression of miRNAs is remarkably deregulated in cancer due to multiple epigenetic and genomic alterations. Fourth, several miRNAs themselves have been demonstrated to serve as tumor suppressor genes or oncogenes in tumors [
13‐
15].
The miR-302 family consists of four highly-homologous miRNA members, which are transcribed together as a noncoding RNA cluster containing mir-302b, mir-302c, mir-302a, mir-302d, and mir-367 in a 5′-to-3′ direction [
16]. To date, miR-302 s have been proven to post-transcriptionally regulate CCND1 and CDK4, therefore affecting cell cycle progression. Other studies have demonstrated the tumor suppressive activity of miR-302 in human pluripotent stem cell by both the CCNE-CDK2 and CCND-CDK4/6 pathways in G1-S cell cycle transition. Although miR-302 has been suggested to have tumor suppressor potential, the present studies focused on the self-renewal and proliferation properties of miR-302b in the stemness maintenance of embryonic stem cells (ESCs) or tumor stem cell properties in advanced cancer cells [
17,
18]. So, the relationship between miR-320b and cancers needs to be investigated further.
In this research, we analyzed the miR-302b targets by bioinformatics software, and found that miR-302b can target EGFR. Next, we found that miR-302b was frequently down-regulated in HCC tissues and cells. Further, in vitro experiments proved that the re-expression of miR-302b inhibited HCC proliferation dramatically, and arrested the HCC cell cycle at the G1/S phase. The dual-luciferase reporter assays further demonstrated that EGFR was a novel target of miR-302b. The silencing of EGFR by miR-302b or siEGFR led to the down-regulation of cell-cycle related proteins, such as AKT2, CCND1, and CDK2, strongly suggesting that miR-302b suppresses the growth of SMMC-7721 cells by targeting EGFR involved the EGFR/AKT2/CCND1 pathway.
Methods
Cell lines and tissue specimens
Bel7402, SMMC-7721, HepG2, Hep3B, and HL-7702 cells were maintained in 1640 medium (1640, PAA Laboratories GmbH, Pasching, Austria), supplemented with 10% fetal bovine serum (FBS, PAA Laboratories GmbH, Pasching, Austria). Cells were maintained at 37°C in a humidified chamber with 95% air and 5% CO2. 27 paired HCCs and adjacent non-tumor liver tissues were collected from patients undergoing resection of HCC at the Hepatobiliary Surgery Department of the First Affiliated Hospital of Xi’an Jiaotong University, P.R. China. No local or systemic treatment had been conducted before operation. Tissue samples were immediately snap frozen in liquid nitrogen until RNA extraction. Both tumor and non-tumor tissues were histologically confirmed. Informed consent was obtained from each patient and was approved by the Institute Research Ethics Committee at the Cancer Center, Xi’an Jiaotong University.
Plasmid constructions
pcDNA™6.2-GW/EmGFP-miR vector (Invitrogen) was used to construct vectors of re-expression miR-302b. First, we inserted EcoRI and HindIII sites into the MCS of the vector. Then, the miR-302b was chemically synthesized and cloned into pcDNA™6.2-GW/EmGFP-miR vector between the EcoRI and HindIII sites. RegRNA (A Regulatory RNA Motifs and Elements Finder
http://regrna.mbc.nctu.edu.tw/), TargetScan (
http://www.targetscan.org/) and DIANA (
http://diana.cslab.ece.ntua.gr/microT/) were used for gene-related specified microRNA prediction. Through bioinformatics analysis, we got the predicted fragment of targeted gene (EGFR), which was associated with miR302b. Specified fragments of EGFR were chemically synthesized, and are shown in supporting Table
1. The luciferase-UTR reporter constructions were generated by introducing the Wt/Mut-EGFR 3′-UTR, carrying a putative miR-302b binding site into pmirGLO Dual-Luciferase miRNA Target Expression vector (Promega) between the XhoI and SacI sites.
Table 1
Primers and oligonucleotides used in this work
Pri-miR-302b-S | 5′-AATTCGCTCCCTTCAACTTTAACATGGAAGTGCTTTCTGTGACTTTAAAAGTAAGTGCTTCCATGTTTTAGTAGGAGTA-3′ |
Pri-miR-302b-A | 5′-AGCTTACTCCTACTAAAACATGGAAGCACTTACTTTTAAAGTCACAGAAAGCACTTCCATGTTAAAGTTGAAGGGAGCG-3′ |
EGFR 3′UTR-S | 5′-CAAGAAGCTTGCTGGTAGCACTTGC- 3′ |
EGFR 3′UTR-A | 5′-TCGAGCAAGTGCTACCAGCAAGCTTCTTGAGCT- 3′. |
EGFR 3′UTR-MS | 5′-CAAGAAGCTTGCTGGCAGCGTTTGC-3′ |
EGFR 3′UTR-MA | 5′-TCGAGCAAACGCTGCCAGCAAGCTTCTTGAGCT-3′ |
siRNA-ctrl-S | 5′-ACCGAACGTGTCACGT-3′ |
siRNA-ctrl-A | 5′-ACGTGACACGTTCGGAGAATT-3′ |
siEGFR-S | 5′-AACACAGTGGAGCGAATTCCT-3′ |
siEGFR-A | 5′-AGGAATTCGCTCCACTGTGTT-3′ |
miR-302b RT | 5′-TGCTTAAGTGCTTCCATGTT-3′ |
miR-302b-F | 5′-ATCCAGTGCGTGTCGTG-3′ |
miR-302b-R | 5′-TGCTTAAGTGCTTCCATGTT-3′ |
Inhibitor-ctrl | 5′-TGACTGTACTGACTCGACTG-3′ |
MiR-302b inhibitor | 5′ -TGATTTTGTACCTTCTGGAAT-3 |
EGFR-F | 5′-GCCTTGACTGAGGACAGCA-3′ |
EGFR-R | 5′-TTTGGGAACGGACTGGTTTA-3′ |
β-actin-F | 5′-CGGGAAGCTTGTCATCAATGG-3′ |
β-actin-R | 5′-GGCAGTGATGGCATGGACTG-3′ |
U6 RT | 5′-GTCGTATCCAGTGCAGGGTCCGAGGTGCACTGGATACGACAAAATATGG-3′ |
U6-F | 5′-TGCGGGTGCTCGCTTCGGCAGC-3′ |
U6-R | 5′ CCAGTGCAGGGTCCGAGGT 3′ |
Quantitative real-time PCR
Total RNA was extracted using Trizol solution (Invitrogen, USA) according to the manufacturer’s protocol, and RNAse-free DNase was used to remove DNA contamination. Total RNA concentration and quantity were assessed using a DNA/Protein Analyzer (GeneQuant pro RNA/DNA). cDNA was synthesized from RNA, using a PrimeScript™ RT reagent Kit (TaKaRa). The special primer was used to synthesize miR-302b cDNA, which is shown in Table
1. The cDNA specimens were amplified using an SYBR Premix Ex Taq™ II (TaKaRa). The polymerase chain reaction (PCR) primers used are shown in Table
1. PCR amplification was performed on the IQ5 Optical System real-time PCR machine. β-actin and U6 were used to normalize mRNA and miRNA respectively. Relative quantification of mRNA expression levels was determined using the relative standard curve method according to the manufacturer’s instructions (Bio-Rad).
MTT assay
The cells were seeded into 96-well plates at a density of 1 × 105 cells/well with 100 uL of 1640, supplemented with 10% fetal bovine serum without antibiotics for 24 h. Thereafter, 0.2 ug of the miR-302b ctrl (empty vector), miR-302b expression vector, siEGFR or siRNA-ctrl oligonucleotide in 25 μl of 1640 and 0.5 μl of lipofectamine 2000 (Invitrogen, USA) in 25 μl of 1640 were preincubated for 5 min at room temperature, respectively, and then mixed together and incubated for additional 25 min at room temperature. After the addition of 50 μl of 1640, the entire mixture was added to the well, and the cells were further cultivated for an additional 1–3 days. Cell viability was assessed using the 3-(4, 5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay on FLUOstar OPTIMA (BMG). Each experiment contained three replicates and was repeated at least twice. The data were summarized as mean ± s.d.
Western blot
The culture of SMMC-7721 cells and the transfection of miR-302b expression vector, miR-ctrl, siEGFR, and siRNA-ctrl were performed as above. All RNA transfections were performed at a final concentration of 100 nM unless otherwise indicated. SMMC-7721 cells were lysed using RIPA buffer, supplemented with protease inhibitor (invitrogen). Protein concentration was estimated by quantitative analyzer (GeneQuant pro RNA/DNA). Protein was then separated with a 8% to 10% SDS-PAGE (Invitrogen), transferred to a nitrocellulose membrane, incubated with the EGFR, pAKT2, AKT2, CCND1, CDK2, p27, and β-actin antibodies (Bioworld, diluted 1/500). After washed three times with TBST, the membrane was incubated with a goat anti-rabbit antibody (Bioworld, diluted 1/5000). Relative protein expression was then normalized to β-actin levels in each sample.
Immunofluorescence microscopy
To determine the effect of miR-302b/siEGFR on cell proliferation, we also performed immunofluorescence staining using the Ki-67 antibody (Millipore, diluted 1/100). Plasmid miR-302b or siEGFR was transfected into SMMC-7721 cells using Lipofectamine 2000 (Invitrogen Co., Carlsbad, CA, USA) into SMMC-7721 cells, miR-ctrl and siRNA-ctrl as respective controls. After 48 h, transfected SMMC-7721 cells were fixed with 4% formaldehyde for 20 min, then incubated with 0.5% Triton X-100. Anti-Ki-67 antibody (Bioworld, 1:100) was used for immunofluorescence staining. After washed three times with PBS, the cells were incubated with a goat anti-mouse antibody (Millipore, diluted 1:500), and measured by immunofluorescence microscopy.
Dual luciferase assay
PmirGLO-EGFR-3′UTR-wt vector or pmirGLO-EGFR-3′UTR-mut vector were co-transfected with miR-302b or miR-ctrl into SMMC-7721 cells using lipofectamine 2000 (Invitrogen). Then, reporter gene assays were performed 24 h and 48 h post-transfection using the Dual luciferase Reporter assay system (Promega) according to the manufacturer’s protocol. The normalized firefly luciferase activity was obtained by firefly luciferase activity/Renilla luciferase activity. All experiments were performed at least three times.
Colony assay
Post-transfected SMMC-7721 cells were resuspended and seeded onto 12-well plates at a density of 2000 cells/well, incubated two weeks later, and then were stained with 0.5% crystal violet for 30 min. Excess dye was rinsed off twice with PBS. The pictures were obtained by using computer software (Bio-Rad quantity one).
Cell cycle analysis
The SMMC-7721 cells were transfected with miR-302b re-expression vector, miR-ctrl, siEGFR or siRNA-ctrl. Cells were harvested by trypsinization, and 1 × 106 cells were used for analysis after 24 h, 48 h, and 72 h. The cells were washed in PBS and fixed in ice-cold ethanol overnight at 4°C. The cells were then washed in PBS and incubated in 1 ml staining solution (20 ug/ml propidium iodide and 10 U/ml RNaseA) for 30 min at room temperature. Cell cycle distributions were assayed by fluorescence-activated cell sorting using a flow cytometer (FACSort; Becton).
Statistical analysis
Each experiment was repeated at least three times. Numerical data were presented as mean ± s.d.. Unless indicated, the differences between the two groups were analyzed using a Student’s t-test (two-tailed). All statistical analyses were performed using SPSS13.0 software (SPSS, Chicago, IL, USA). The linear correlation coefficient (Pearson’s r) was calculated to estimate the correlation between miR-302b values and EGFR levels in the matched HCC tumor specimens.
Discussion
HCC is a primary lethal neoplasm of the liver and the third cause of cancer-related deaths worldwide [
21]. However, its underlying molecular mechanism remains largely unknown. In the past ten years, microRNAs (miRNAs) have been found to be involved in the initiation and progression of HCC. According to its tumorigenesis function, miRNAs can be divided in two classes:oncogenes and tumor suppressor genes [
22]. Many oncogenic miRNAs, such as miR-221 and miR-222, are involved in sustaining proliferative signaling, resisting growth suppression and apoptosis, enabling immortality, prompting angiogenesis, invasion and metastasis, evading and so on [
23‐
28], whereas tumor suppressor miRNAs are involved in the reverse processes. Let-7 family and miR-101, as potential tumor suppressors, were markedly decreased in HCC cells [
29,
30]. Recent studies proved that the miR-302-367 cluster is down-regulated in cervical cancer cells and gastric adenocarcinoma [
31,
32]. Our study showed that the expression of the miR-302b was frequently down-regulated in clinical HCC tissues and in SMMC-7721 cells (Figure
1). Thus, we supposed that miR-302b might be a novel tumor-suppressor miRNA.
Human epidermal growth factor receptor (EGFR/HER/ErbB) family of tyrosine kinases plays a major role in the etiology and progression of many carcinomas, including HCC. Increased expression of EGFR/HER1 occurs frequently in different human tumor types, and is involved in the early stages of human hepatocarcinogenesis [
33,
34]. In our study, increased expression of EGFR was observed in the HCC samples and HCC cells (Figure
1D and E). Over-expression of EGFR is also related to the gene amplification of EGFR and deficiency of EGFR targeting miRNA. There seemed to be a negative correlation between the expression of EGFR and that of miR-302b in HCC tissues (Figure
1A and B), implying that EGFR might be a novel target of miR-302b. Further bio-information analysis showed that there was a miR-302b-binding site at 4259–4284 nt of the EGFR 3′ UTR. The dual-luciferase reporter assays demonstrated that miR-302b targeted directly to EGFR through the suppression of translation (Figure
2B). In this research, we examine the relationship between miR-302b and EGFR at both of the transcription level and translational level, in which miR-302b was verified to silence EGFR at translational level from in vitro and in vivo clinical samples. At the transcription level, we tested relationship between miR-302b and EGFR by using Pearson’s correlation coefficient test in 27 paired HCC tissues and found that they have inverse correlation in mRNA level (Figure
2D). Whereas in SMMC-7721 cell lines, the correlation between miR-302b and EGFR didn’t show significant difference (Figure
2C), but it exhibited the correlation trend, which were consistent with the results of that in HCC tissues.
EGFR induces activation of the Ras/Raf/MEK/MAPK pathway through either Grb2 or Shc adaptor proteins, and that of PI3K/AKT/CCND1 pathway by recruitment of the p85 regulatory subunit to the activated receptors [
35]. The activation of EGFR/AKT/NF-kB/CCND1 survival signaling pathway has been certified in cholesteatoma epithelium [
36]. Function of dominant negative EGFR shows that dominant negative EGFR induces G0/G1 arrest by decreasing the expression of phosphorylated retinoblastoma protein, phosphorylated GSK-3β, CCND1, and by increasing expression of p21 and p27 in human gastric cancer cells SGC-7901 and NCI-N87 [
37]. AKT2 is essential for progressing from the G0/G1 to the S-phase by activating the positive regulator of G1/S transition, including CCND1, CCND2, and CCNE1, during cell cycle progression [
38]. CCND1, as a AKT2 downstream gene, is expressed in the G1 phase of the cell cycle, together with its CDK partner, CDK2. p27, as a CDK inhibitor, could be combined with CCND1-CDK2 complex to restrain CDK2 activity [
39]. Our results showed that miR-302b may inhibit the growth of SMMC-7721 cells through targeting EGFR, and that the cell cycle progression was arrested at the G0/G1-phase (Figure
3). At the same time, the expression of AKT2 was down-regulated, and CCND1 and CDK2 were reduced by miR-302b, while the expression of CDK inhibitor p27 was up-regulated (Figure
4). A few of the miR-302b targets have been found, including AKT1, CCNA, CDK2, CCND1/D2, and BMI-1 [
40]. These genes are involved in the regulation of the cell cycle. In order to prove the biological effects of miR-302b on inhibition of EGFR, siEGFR was used. The results showed that the effect of miR-302b re-expression on the cell proliferation was consistent with that of siEGFR in SMMC-7721cells, suggesting that miR-302b may suppress the growth of SMMC-7721 cells by targeting the EGFR/AKT2/CCND1 signaling pathway.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
CH and JYY developed the hypotheses. LMW and LLH executed the experiments. JYY, TSS and ZFL provided the experimental facilities and research funds. LMW, JYY, XS, and CH wrote and revised the paper. All authors read and approved the final manuscript.