Human glioma tissue samples were obtained from the Department of Neurosurgery, Shandong Provincial Hospital Affiliated to Shandong University (Jinan, China). The patients included 38 World Health Organization (WHO) grade I; 39 WHO grade II; 44 WHO grade III and 40 WHO grade IV cases) (18). The patients comprised 60 women and 111 men, with a mean age of 58 years (range, 31–78 years). The human tissue samples were used according to internationally recognized guidelines, as well as local and national regulations. Investigations involving humans followed international and national regulations. The medical ethics committee of Shandong Provincial Hospital Affiliated to Shandong University (Shandong, China) approved the experiments of the present study. Informed consent was obtained from each individual. Human A172 glioblastoma cell lines were donated by Dr Rosalind Segal (University of Heidelberg, Heidelberg, Germany). The A172 cells were maintained at 37°C in Dulbecco's modified Eagle's medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; Hyclone; GE Healthcare Life Sciences, Logan, UT, USA). GAB2-expressing plasmids were donated by Dr Xiao Yao (University of Heidelberg).

The miR-197 miRNA precursor (pre-miR-197) and a control precursor (control miR) were purchased from Ambion (Thermo Fisher Scientific, Inc.).

For the transfection experiments, 5×10⁴ A172 cells were cultured in serum-free medium without antibiotics to 60% confluence for 24 h at 37°C, prior to being transfected with Invitrogen Lipofectamine^® 2000 transfection reagent (Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. Following incubation at 37°C for 6 h, the medium was removed and replaced with normal culture medium for 48 h at 37°C, unless otherwise specified.

Paraffin-embedded specimens of gliomas and adjacent normal tissue were obtained from the Pathology Department of the Shandong Provincial Hospital affiliated to Shandong University. Sections (5 µm) were deparaffinized in 70% xylene (Tiangen Biotech Co., Ltd., Beijing, China) and then rehydrated through a series of graded ethanol dilutions (100–25%). The sections on slides and submerged in diethyl pyrocarbonate-treated water (Tiangen Biotech Co., Ltd.) and subjected to proteinase K (Tiangen Biotech Co., Ltd.) (10 µg/ml) digestion and 0.2% glycine treatment, refixed in 4% paraformaldehyde (Tiangen Biotech Co., Ltd.), and treated with acetylation solution (Tiangen Biotech Co., Ltd.) containing 66 mmol/l HCl, 0.66% (v/v) acetic anhydride and 1.5% (v/v) triethanolamine. The slides were rinsed three times with 1X phosphate-buffered saline (PBS) between treatments. The slides were then prehybridized in hybridization solution (Tiangen Biotech Co., Ltd.), containing 50% formamide, 5X saline sodium citrate (SSC), 500 µg/ml yeast tRNA and 1X Denhardt's solution, at 50°C for 30 min. Subsequently, 5-10 pmol fluorescein isothiocyanate-labeled, LNA-modified DNA probe (Exiqon A/S, Vedbeak, Denmark) complementary to miR-197 was added to the 180 µl hybridization solution and hybridized for 2 h at a temperature 20–25°C below the calculated melting temperature of the LNA probe (37°C). Following washes in SSC at increasing stringency (2-0.2X) at the same temperature as hybridization, a tyramide signal amplification reaction was performed using a GenPoint Fluorescein kit (Dako, Glostrup, Denmark), according to the manufacturer's protocol. Finally, the slides were mounted with Prolong Gold solution (Invitrogen; Thermo Fisher Scientific, Inc.). The signals were visually quantified by Dr Li-Qiang Tian and Dr En-Qin Liu using a quick score system (scores 0-5), which combines the intensity of the signal and the percentage of positive cells (signal: 0, no signal; 1, weak signal; 2, intermediate signal; 3, strong signal; percentage: 0, 0%; 1, <30%; 2, >30%). The tissue sections were then examined by Jian Li and Guang-Ming Xu in a blinded-manner, who reported results in agreement with the initial quantifications.

Total RNA from the cultured A172 cells, with efficient recovery of small RNAs, was isolated using an mirVana miRNA Isolation kit (Ambion; Thermo Fisher Scientific, Inc.). In addition, detection of the mature form of miRNAs was performed using an mirVana qRT-PCR miRNA Detection kit, according to the manufacturer's protocol. Reverse Transcription system (Promega Corporation, Madison, WI, USA) was used with the miR-197 primer as follows: 5′-TTC ACC ACC TTC TCC ACC CAGC-3′. The U6 small nuclear RNA was used as an internal control. The RT-qPCR and quantification were conducted as described previously (19).

At 48 h post-transfection, A172 cells were seeded in 96-well plates in triplicate at a density of 5×10³ cells/well in 100 µl RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc.) containing 10% FBS and 1% antibiotics (Hyclone; GE Healthcare Life Sciences). Cell proliferation was evaluated using a Cell Counting kit-8 (Dojindo Molecular Technologies, Inc., Kumamoto, Japan), according to the manufacturer's protocol, and the absorbance value for each well was measured at 450 nm using a microplate reader (Spectra Max 180; Molecular Devices, LLC, Sunnyvale, CA, USA).

For the colony formation assay, 5×10⁴ A172 cells were transfected with pre-miR-197 or control miR for 24 h, prior to being seeded into a 6-well plate. A total of 0.2 ml FBS was added per well on day 5. Following 9–10 days incubation at 37°C, the plates were washed with PBS and stained with 0.1% crystal violet (Tiangen Biotech Co., Ltd.). Colonies with >50 cells were manually counted (IX-70 inverted microscope; Olympus Corporation, Tokyo, Japan). Plating efficiency was calculated by dividing the number of colonies formed in the treated group by that in the control.

The A172 cells (8.0×10⁵ cells) were seeded into a 100 mm culture plate and allowed to attach overnight. The cells were transfected, as previously described, for 24 h at 37°C, washed twice with NaCl/P_i (Tiangen Biotech Co., Ltd.), and then centrifuged at 200 × g at room temperature for 10 min. The pellet was resuspended in 1 ml cold NaCl/P_i and fixed in 70% ethanol for ≥12 h at 4°C. The fixed cells were incubated with 100 µl DNase-free RNaseA (200 µg/ml; Tiangen Biotech Co., Ltd.) for 30 min at 37°C, prior to the addition of 1 mg/ml propidium iodide (Tiangen Biotech Co., Ltd.). The stained cells were analyzed using a fluorescence-activated cell sorter (BD Accuri C6; BD Biosciences, San Jose, CA, USA). The percentages of cells in the G₁, S and G₂/M phases of the cell cycle were determined using Cell Quest Pro software (FlowJo; Tree Star, Inc., Ashland, OR, USA).

Cell proliferation was assessed using a colorimetric BrdU Proliferation kit, according to the manufacturer's protocol (Roche Diagnostics, Indianapolis, IN, USA). Briefly, the transfected A172 cells were labeled with BrdU for 4 h at 37°C. The genomic DNA was fixed and denatured by BrdU, and then incubated with a rat peroxidase-conjugated anti-BrdU antibody (Sigma-Aldrich, St. Louis, MO, USA; cat. no. 11202693001) for 90 min. A substrate for the conjugated peroxidase, a component included in the kit, was then added, and the reaction product was quantified by measuring the absorbance at a wavelength of 270 nm using a SpectraMax M5 (Molecular Devices, LLC). The results were then normalized to the number of total viable cells.

Confluent A172 cells were washed twice with cold PBS and denatured in a radioimmunoprecipi-tation assay lysis buffer (containing 20 mM Tris-HCl, 200 mM NaCl, 0.2% Nonidet P-40, 0.5% Triton X-100 and protease inhibitors; Beijing Solarbio Science and Technology Co., Ltd., Beijing, China) and boiled at 100°C for 10 min. Protein was quantified by BCA Protein assay kit (Beyotime Institute of Biotechnology, Haimen, China) and western blot analysis was performed, as described previously (20). Equal quantities of protein (5 µg) were separated by 10% sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (Beijing Solarbio Science and Technology Co., Ltd.) and then transferred onto polyvinylidene difluoride membranes (Bio-Rad Laboratories, Inc., Hercules, CA, USA). Following blocking in Tris-buffered saline (TBS; Beijing Solarbio Science and Technology Co., Ltd.) with 0.1% Triton X-100 and 5% milk, the membranes were incubated with the following primary antibodies: Rabbit polyclonal anti-proliferating cell nuclear antigen (PCNA; 1:500; Abcam, Cambridge, MA, USA; cat. no. ab18197), rabbit polyclonal anti-retinoblastoma (Rb; 1:500; Abcam; ab1765), rabbit polyclonal anti-Ki67 (1:500; Abcam; ab15580), rabbit monoclonal anti-cyclin-dependent kinase (CDK)2 (1:500; Abcam; ab32147), rabbit monoclonal anti-CDK4 (1:500; Abcam; ab108357), rabbit monoclonal anti-E2F transcription factor 1 (E2F1; 1:500; Abcam; ab179445), rabbit monoclonal anti-GAB2 (1:500; Abcam; ab32365) and mouse monoclonal anti-β-actin (1:500; Abcam; ab129348) overnight at 4°C. Following washing with TBS three times, the membranes were incubated with donkey anti-mouse Alexa Fluor 488 secondary antibodies (1:5,000; Abcam; cat. no. ab150105) and goat anti-rabbit immunoglobulin G biotin-conjugated secondary antibodies (1:5,000; Abcam; cat. no. ab6720) for 30 min at room temperature. Signal detection was conducted with an enhanced chemiluminescence system (GE Healthcare Life Sciences, Chalfont, UK). The specific proteins were visualized and analyzed using an Odyssey™ Infrared Imaging system (Gene Company, Ltd., Hong Kong, China).

Analysis of the potential miRNA target sites was performed using the TargetScan algorithm (http://www.targetscan.org).

Total RNA was isolated from A172 cells using TRIzol^® reagent (Invitrogen; Thermo Fisher Scientific, Inc.). First-strand cDNA was synthesized from the total RNA using Moloney Murine Leukemia Virus Reverse Transcriptase (Promega Corporation), 2.5 µl 5X buffer and 2 µl random hexamer primers (Sangon Biotech, Co., Ltd., Shanghai, China). The concentration of the cDNA was quantified using a NanoDrop 1000 spectrophotometer (Thermo Fisher Scientific, Inc.). The reaction was performed with the following thermo-cycling conditions: Denaturation for 30 sec at 95°C, annealing for 45 sec at 52–58°C, depending on the primers used, and extension for 45 sec at 72°C. The PCR products were visual-ized on 2% agarose gels (Tiangen Biotech Co., Ltd.) stained with 20% ethidium bromide (Tiangen Biotech Co., Ltd.) under ultra violet transillumination. RT-qPCR was performed using Power SYBR^® Green PCR Master mix (Applied Biosystems; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. The primer sequences for GAB2 were forward, 5′-CTG AGA CTG ATA ACG AGG AT-3′ and reverse, 5′-GAG GTG TTT CTG CTT GAC-3′.

For immunofluorescence analysis, 5×10⁴ A172 cells were plated on glass coverslips in six-well plates and transfected with 50 nM pre-miR-197 or control miR. At 36 h post-transfection, the coverslips were stained with the previously mentioned anti-GAB2 antibodies. Alexa Fluor 488 goat anti-rabbit IgG antibody was used as a secondary antibody (Invitrogen; Thermo Fisher Scientific, Inc.). The coverslips were counterstained with DAPI (Invitrogen; Thermo Fisher Scientific, Inc.) for visualization of the nuclei. Microscopic analysis was performed using a confocal laser-scanning microscope (FV300; Olympus Corporation). Fluorescence intensity was measured in a small number of viewing areas with 200–300 cells per coverslip, and analyzed using ImageJ 1.37 software (National Institutes of Health, Bethesda, MD, USA).

Luciferase reporter plasmids were purchased from Tianjin Biotech Co., Ltd. (Tianjin, China). Briefly, the 3′-UTR of human GAB2 mRNA was cloned into pRL-TK (Promega Corporation) using three PCR-generated fragments, including positions of 3885–3891, 1151–1158, 2044–2050 in the 3′UTR of GAB2. Site-directed mutagenesis of the miR-197 target sites in the GAB2-3′-UTR was performed using a Quik Change Mutagenesis kit (Agilent Technologies GmbH, Waldbronn, Germany), with GAB2-WT-luc (containing position 1151–1158) a template. For reporter assays, the A172 cells were transiently transfected with wild-type or mutant reporter plasmid and miRNA using Lipofectamine^® 2000. Reporter assays were performed 36 h post-transfection using a Dual Luciferase Assay system (Promega Corporation), normalized for transfection efficiency with co-transfected Renilla luciferase (Tiangen Biotech Co., Ltd.).

Immunohistochemistry was performed using standard laboratory techniques. Antigen retrieval was performed by autoclaving at 121°C for 8 min (model, V8879l; Tiangen Biotech Co., Ltd.), following which the above-mentioned glioma tissue sample sections were incubated with 10% normal goat serum in PBS for 15 min at 37°C to eliminate non-specific staining. Incubation with anti-GAB2 antibody was then performed. Finally, the sections were coun-terstained with 10% Mayer hematoxylin (Tiangen Biotech Co., Ltd.), dehydrated, mounted, and observed. Staining was evaluated by a neuropathologist and an investigator in a blinded-manner (H-7000 electron microscope; Hitachi, Ltd., Tokyo, Japan). The sections were classified as - (negative), + (focal and weak immunoreactivity), ++ (diffuse and weak or focal and intense immunoreactivity) or +++ (diffuse and intense immunoreactivity). The data were analyzed using SPSS 11.5 (SPSS, Inc., Chicago, IL, USA). Quantitative image analysis was performed, as previously described (21). The comparison between high expression levels was achieved using a χ² test.

The effect on cell proliferation was assessed using MTT (Sigma-Aldrich). A172 cells were suspended in 200 µl medium and seeded in 96-well plates (1×10⁴/ml and grown to 50% confluence and synchronized with serum-free medium for 24 h prior to adding serum to a concentration of 10%. MTT reagent (20 µl; 5 mg/ml; Amresco, LLC, Solon, OH, USA) was added at 48 h. The cells were incubated at 37°C for 4 h and following centrifugation at 500 × g for 5 min at room temperature, 150 µl dimethyl sulfoxide (Beijing Solarbio Science and Technology Co., Ltd.) was added to halt the reaction. The cell confluence was determined by absorbance at a wavelength of 570 nm on a spectrophotometer (UV-16; Shimadzu Corporation, Kyoto, Japan) and absorbance was directly proportional to the number of surviving cells.

Total RNA from the cultured A172 cells, with efficient recovery of small RNAs, was isolated using an mirVana miRNA Isolation kit (Ambion; Thermo Fisher Scientific, Inc.). The cRNA for each sample was synthesized using a 3′ IVT Express kit (Affymetrix, Inc., Santa Clara, CA, USA), according to the manufacturer's protocol. The purified cRNA was fragmented by incubation in fragmentation buffer (provided in the 3′ IVT Express kit) at 95°C for 35 min, and chilled on ice. The fragmented labeled cRNA was applied to a microRNA 2.0 array (Affymetrix, Inc.) and hybridized in a Genechip hybridization oven 640 (Affymetrix, Inc.) at 45°C for 18 h. Following washing and staining in a Genechip fluidics station 450 (Affymetrix, Inc.), the arrays were scanned using a Genechip Scanner 3000 (Affymetrix, Inc.). The gene expressions levels of the samples were normalized and compared using Partek GS 6.5 (Partek, Inc, St. Louis, MO, USA). The average-linkage hierarchical clustering of the data was applied using Cluster (http://rana.lbl.gov) and the results were displayed using TreeView (http://rana.lbl.gov) (22).

Northern blot analysis of miRNAs was performed, as previously described (23). Total RNA was fractionated on a denaturing 12% polyacrylamide gel containing 8 M urea (Tiangen Biotech Co., Ltd.). The RNA was transferred to a Nytran N membrane (Schleicher & Schuell Bioscience GmbH, Dassel, Germany) by capillary method and fixed by ultraviolet cross-linking. The membranes were probed with ³²P-labelled standard DNA and LNA-modified oligonucleotides, complementary to the mature miRNA-197 and U6 snRNA, 10 pmol of each probe was end-labeled with [γ-³²P] ATP using T4 polynucleotide kinase. Prehybridization of the filters (Tiangen Biotech Co., Ltd.) was conducted in 50% formamide, 0.5% SDS, 5X SSPE, 5X Denhardt's solution (all from Tiangen Biotech Co., Ltd.) and 20 µg/ml sheared and denatured salmon sperm DNA (Beijing Solarbio Science and Technology Co., Ltd.). Hybridizations were performed in the same solution at 34–45°C. The labeled probes were heated for 1 min at 95°C prior to addition of the filters in the prehybridization solution. Following hybridization, the membranes were washed at low stringency in 2X SSC and 0.1% SDS at 34–45°C twice for 5 min each time or at high stringency in 0.1 SSC and 0.1% SDS at 65°C twice for 5 min. The results of the northern blot were visualized by Quantity One software (Bio-Rad Laboratories, Inc.)

Each experiment was repeated at least three times. All results are expressed as the mean ±standard deviation. The difference between the means was analyzed using the Student's t-test or the χ² test. All statistical analyses were performed using SPSS 16.0 software (SPSS, Inc.) and P<0.05 indicated a statistically significant difference.

In order to determine the expression levels of miR-197 in glioblastoma, in situ hybridization was performed to analyze the expression levels of miR-197 between glioblas-toma tissues and adjacent normal tissues. An LNA-modified DNA probe complementary to the indicated miRNA was used on consecutive 5 µm sections obtained from archived FFPE. The results of in situ hybridization demonstrated that miR-197 was markedly downregulated in the majority of the glioblastoma tissue samples, compared with adjacent normal tissue samples (Fig. 1A). These results suggested that miR-197 functioned as a tumor suppressor gene in glio-blastoma. The roles of miR-197 in glioblastoma were then investigated in A172 cells. To examine whether the expression levels of miR-197 were upregulated by pre-miR-197, the A172 cells were transfected with pre-miR-197. Pre-miR-197 significantly upregulated the expression levels of miR-197 in the A172 cells (Fig. 1B). The effects of miR-197 on proliferation were also examined in the cells using a cell counting assay. miR-197 inhibited proliferation 24–96 h post-transfection in the A172 cells, compared with the untreated or control miR-treated groups (Fig. 1C). A colony formation assay was also performed for the A172 cells trans-fected with pre-miR-197 or control miR. Consistent with the results of the cell counting assay, the colony formation assay demonstrated that miR-197 significantly inhibited colony formation in the A172 cells (Fig. 1D). To further investigate the effects of miR-197 on proliferation, cell-cycle analysis was performed to analyze its effects on cell cycle. The A172 cells transfected with pre-miR-197 exhibited lower S phase fractions compared with the cells transfected with control miR (Fig. 1E). To examine whether the inhibition of DNA synthesis contributed to lower S phase fractions in the A172 cells transfected with pre-miR-197, a BrdU incorporation assay was performed to detect DNA synthesis within the cells. miR-197 significantly suppressed DNA synthesis in the cells (Fig. 1F). In addition, western blotting was performed to identify whether the protein expression levels of the proliferation markers were affected by miR-197 in the cells. The expression levels of PCNA, Rb, Ki67, CDK2, CDK4 and E2F1 were downregulated by miR-197 in the cells (Fig. 1G). These results suggested that miR-197 inhibited the proliferation of A172 cells.

miRNAs are short, non-coding RNAs, which regulate the target mRNA by binding predominantly to the 3′-UTR, inducing either translational repression or the degradation of the target (1-3). The target genes of miR-197 were screened using TargetScan (http://www.targetscan.org/vert_61/), which identified a large number of target genes, however, GAB2 was examined as several reports have demonstrated that GAB2 is an oncogene in malignant tumors (10–16). Target sites on the 3′-UTR of GAB2 are shown in Fig. 2A. It was hypothesized that miR-197 downregulates the expression of GAB2 in A172 cells. Western blot and RT-qPCR analyses were performed to detect the expression levels of GAB2 in the A172 cells transfected with pre-miR-197. The protein expression levels of GAB2 (Fig. 2B) were markedly downregulated in the cells transfected with pre-miR-197, however, mRNA expression levels remained unchanged (Fig. 2C and D). Concordant with the results of the western blot analysis, immunofluorescence analyses in the A172 cells transfected with pre-miR-197 or control miR revealed that the protein expression levels of GAB2 were significantly suppressed in the A172 cells transfected with pre-miR-197 (Fig. 2E and F). Fig. 2E shows microscopy images of immunofluorescence staining of a representative experiment (magnification, ×100), and Fig. 2F shows the mean fluorescence intensities of three independent experiments.

To further demonstrate the direct regulation of GAB2 by miR-197, luciferase reporters were constructed with three targeting sequences: Wild-type-GAB2-WT-luc-1 (Fig. 2G), GAB2-WT-luc-2 (Fig. 2H) and GAB2-WT-luc-3 (Fig. 2I). Following GAB2-WT-luc-1 introduction into the A172 cells, miR-197 did not inhibit GAB2-WT-luc-1 plasmids (Fig. 2J). Therefore, GAB2-WT-luc-2 plasmids were investigated to determine whether they targeted by miR-197 in the A172 cells. The luciferase reporter assays demonstrated that the luciferase activities of the GAB2-WT-luc-2 plasmids were significantly suppressed in the cells (Fig. 2K). To further examine whether miR-197 targeted the 3′-UTR of GAB2 in the predicted sites, four bases were mutated (Fig. 2H). The mutant reporters were subsequently introduced into the A172 cells and demonstrated that the luciferase activity levels of GAB2-MUT-luc-2 were not suppressed in the cells (Fig. 2K). Having demonstrated that GAB2-WT-luc-2 plasmids were inhibited by miR-197, luciferase reporter assays were used to investigate whether miR-197 targeted GAB2-WT-luc-3. miR-197 did not affect the luciferase activity levels of GAB2-WT-luc-3 in the cells (Fig. 2L). These results suggested that miR-197 suppressed the protein expression levels of GAB2 by targeting its 3′-UTR at position 1151–1158.

To assess the expression levels of GAB2 in glioblastoma, western blot analysis was performed in seven pairs of glioblastoma tissue and matched adjacent normal tissue samples. The expression levels of GAB2 were higher in the majority of the glioblastoma tissue samples, compared with the normal tissue samples (Fig. 3A).

To demonstrate the importance of GAB2 in the pathogenesis and progression of glioblastoma, immunohistochemistry was performed to detect the expression of GAB2 in human glioma tissue specimens. The protein expression levels of GAB2 (++/+++) in glioma grades I, II, III and IV were 23.68, 38.46, 59.09 and 75%, respectively (Fig. 3B). Statistical analysis demonstrated that the expression levels of GAB2 were higher in the high-grade glioblastoma tissues, compared with the low grade glioma tissues: Grade I, vs. IV, P<0.001; grade II, vs. grade IV, P<0.001; grade I, vs. grade III, P<0.001.

In order to further confirm that high expression levels of GAB2 were associated with high-grade human glioblas-toma, quantitative image analysis was performed to analyze the protein expression of GAB2 in the tissue sections. The expression levels of GAB2 were positively correlated with glioma grade (Fig. 3C).

In order to identify the role of GAB2 in the regulation of A172 cell proliferation, the cells were transfected with GAB2-expressing plasmids. Following stable transfection, protein expression levels of GAB2 were quantified by western blot analysis. The GAB2-expressing plasmids increased the protein expression levels of GAB2 in the A172 cells (Fig. 4A). Furthermore, the proliferation of the A172 cells was determined using an MTT assay. Overexpression of GAB2 significantly increased the proliferation of A172 cells, in a dose-dependent manner (Fig. 4B). These data supported the hypothesis that GAB2 acts as a tumor suppressor in glioblastoma.

Due to the fact that miR-197 directly targets GAB2 through its 3′-UTR, the present study hypothesized that ectopic expression of GAB2 by transfection with cDNA lacking the predicted 3′-UTR target (in the present study, the GAB2 expression plasmids did not contain 3′-UTR position 1151–1158) can escape the regulation of miR-197, and thus attenuate or decrease miR-197 function. The GAB2-expressing plasmid or empty vector plasmid (pcDNA3.1) were transfected into the control miR or pre-miR-197 treated-A172 cells. Immunoblotting revealed that transfection with the GAB2 plasmids attenuated the effects of miR-197 on GAB2 (Fig. 5A).

As the overexpression of miR-197 in glioblastoma A172 cells inhibited proliferation, the present study investigated whether GAB2 suppressed the function of miR-197 in proliferation by treating the control miR or pre-miR-197-transfected A172 cells with either GAB2-expressing plasmids or empty vector (pcDNA3.1). MTT and BrdU incorporation assays were performed, which demonstrated that the pre-miR-197-treated A172 cells exhibited a ~30–50% decrease in proliferation (Fig. 5B) and DNA synthesis (Fig. 5C), compared with the control miR-treated cells. Overexpression of GAB2 sufficed to reverse the loss of proliferation (Fig. 5B) and DNA synthesis (Fig. 5C) observed in the pre-miR-197-treated cells.

Tumor suppressor genes can exert their functions by regulating miRNA expression in glioma (24), several of which function as tumor suppressor genes or oncogenes (5,25,26). The present study hypothesized that GAB2 functions as an oncogene by regulating relevant miRNAs. An miRNA microarray was performed, in which RNAs isolated from A172 cells transfected with GAB2 or empty vectors were hybridized to a custom miRNA microarray platform. Following three cycles of hybridization, quantification and normalization, several miRNAs, specifically miR-197, were downregulated >1,000-fold in the cells (Fig. 6A). To further examine the regulation of GAB2, northern blotting was performed to detect the expression levels of miR-197. Concordant with the previous results, the results of the northern blot (Fig. 6B) demonstrated that GAB2 significantly downregulated the expression of miR-197. Furthermore, RT-qPCR was performed to quantify the expression levels of miR-197 in the A172 cells transfected with GAB2-expressing plasmids or empty vectors. As with the results of the northern blot analysis, the RT-qPCR analysis demonstrated that the expression levels of miR-197 were significantly suppressed by GAB2 (Fig. 6C).