The human U87 cell line, which is likely to be a glioblastoma cell line of unknown origin (12), was obtained from the American Type Culture Collection (Manassas, VA, USA). U87 cells were cultured at 37°C and 95% humidity in minimum essential medium (cat. no. M2297; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) containing 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA). The medium was refreshed every other day, and cells were passaged prior to reaching 100% confluence.

The following primary antibodies were employed in the present study: Anti-caspase 3 (cat. no. 9662; dilution, 1:1,000; rabbit; Cell Signaling Technology, Inc., Danvers, MA, USA); anti-GAPDH (cat. no. SC-25778; dilution, 1:2,000; rabbit; Santa Cruz Biotechnology, Inc., Dallas, TX, USA); anti-poly (ADP) ribose polymerase (PARP; cat. no. SC-8007; dilution, 1:1,000; mouse; Santa Cruz Biotechnology, Inc.); anti-microtubule-associated proteins 1A/1B light chain 3A (LC3; cat. no. L7543; dilution, 1:1,000; rabbit; Sigma-Aldrich; Merck KGaA); anti-autophagy protein 5 (ATG5; cat. no. sc-133158; dilution, 1:500; mouse; Santa Cruz Biotechnology, Inc.) and anti-p62 (cat. no. ab109012; dilution, 1:1,000; rabbit; Abcam, Cambridge, UK). The PARP antibody was used to detect PARP and cleaved PARP, the LC3 antibody was used to detect LC3 I and LC3 II, and the caspase 3 antibody was used to detect pro-caspase-3 and cleaved-caspase-3. Horseradish peroxidase-conjugated goat anti-mouse IgG (cat. no. A21010; dilution, 1:5,000) and anti-rabbit IgG (cat. no. A21020; dilution, 1:5,000) were purchased from Abbkine Scientific Co., Ltd. (Wuhan, China). Cisplatin was purchased from Sigma-Aldrich; Merck KGaA (cat. no. P4394), and the phosphoinositide 3-kinase (PI3K) inhibitor, 3-methyladenine (3-MA), was purchased from R&D Systems, Inc. (Minneapolis, MN, USA). 3-MA inhibits autophagy by preventing autophagosome formation via the inhibition of PI3K catalytic subunit type 3 (13). 3-MA was resuspended in water, as organic solvents, such as dimethyl sulfoxide (DMSO), may be cytotoxic. Due to its instability in aqueous solutions, 50 mM stocks of 3-MA were freshly prepared, and cells were treated with 5 mM 3-MA to inhibit autophagy.

The lentiviral transduction particles for short hairpin (sh)RNA-mediated knockdown of ATG5 were purchased from Sigma-Aldrich; Merck KGaA. The shRNA sequence targeting ATG5 was 5′-CCTTTCATTCAGAAGCTGTTT-3′ and the pLKO.1 vector (Sigma-Aldrich; Merck KGaA) was used as negative control. The shRNA was cloned using the PLKO.1 vector. Stable knockdown of ATG5 in cells was achieved as previously described (14). The primer sequences, 5′-AGACGGCGGAGAGCAGAG-3′ and 5′-CACATTTATTGAGAGCACAGTGG-3′, were used to generate plasmids encoding the full-length MEG3 sequence. RNA was extracted from U87 cells using RNAiso Plus (Takara Biotechnology Co., Ltd., Dalian, China) MEG3 cDNA was then reverse transcribed using 100 µg total RNA from U87 cells and the Advantage RT-For PCR kit (Takara Biotechnology Co., Ltd.), and was amplified for 40 cycles of 95°C for 1 min, 54°C for 1 min and 72°C for 30 sec. To generate lentiviral vectors expressing MEG3, HEK293T cells (1×105/well) cultured on a 6-cm dish were transfected with 2 µg pCDH-MEG3 or pCDH vector (System Biosciences, Inc., Palo Alto, CA, USA), together with 1.5 µg psPax2 (System Biosciences, Inc.) and 0.5 µg pMD2 G (System Biosciences, Inc.) vectors using Lipofectamine 3000 (Thermo Fisher Scientific, Inc.). At 24 h following transfection, the medium was replaced with Dulbecco's modified Eagle's medium containing 10% FBS, and cells were incubated for a further 24 h. The culture medium containing lentiviral particles was centrifuged at 1,000 × g for 5 min at room temperature. Viral particles were collected in the supernatant and the concentration was determined using the Lenti-Pac™ Lentivirus Concentration Solution (GeneCopoeia, Inc., Rockville, MD, USA). The virus titer was determined by calculating the multiplicity of infection. For infection of U87 cells (1×105), 100 µl viral particles (1×108/ml) were used for 12 h. In order to establish a stable cell line, at 24 h after infection was performed, 1×105 cells that were infected by viral particles (1×108/ml) at 37°C were seeded in a 6-well plate and puromycin (5 µM) was used as a selection marker for the infected cells for 24 h at 37°C. The expression efficiency was evaluated by western blot analysis.

For knockdown of MEG3 in U87 cells, small interfering (si)RNA molecules were custom designed and synthesized by Sigma-Aldrich; Merck KGaA. The sequences of the siRNAs were as follows: Control, 5′-TACGTCCAAGGTCGGGCAGGAAGA-3′; and MEG3, 5′-GACUUAAACCAAUGCCCUA-3′. This was transfected into U87 cells (2×10⁵/well) for 24 h using Lipofectamine 3000 and, at 36 h after transfection, cells were treated with 10 µM cisplatin for 0 or 36 h. For certain experiments, cells with or without knockdown of MEG3 were pretreated with 5 mM 3-MA or mock treatment (water) at 36 h after transfection for 6 h at 37°C to inhibit autophagy, immediately prior to treatment with 10 µM cisplatin for 0 or 36 h.

U87 cells (1×105/well) were seeded into the six well cell culture plate and subjected to various treatments as described in the above paragraphs. Total protein extracted from U87 cells using radioimmunoprecipitation assay lysis buffer (Shanghai Qcbio Science and Technologies Co., Ltd., Shanghai, China) was used for immunoblotting. Briefly, cell lysates were centrifuged at 9,000 × g for 10 min at 4°C, and the supernatant was collected. The protein concentration was determined using a BCA Protein assay kit (Pierce; Thermo Fisher Scientific, Inc.). Total protein (30–60 µg) was separated on a 12% SDS-PAGE mini-gel, followed by transfer to a nitrocellulose membrane. The membranes were blocked with 5% fat-free dry milk in a Tris-buffered saline plus Tween-20 solution, consisting of 50 mM Tris-HCl, 0.15 M NaCl and 0.1% Tween-20 (pH 7.5), overnight at 4°C. Membranes were then incubated with primary antibodies overnight at 4°C and incubated with the secondary antibodies (1:5,000) at room temperature for 1 h. An enhanced chemiluminescence detection system (GE Healthcare, Chicago, IL, USA) was used to visualize the expression of target proteins. Three samples from each group were analyzed, and the results were quantified using the Gel-Pro analyzer software (version, 4.0, GE Healthcare).

U87 cells (2×104/well) were seeded in 96-well plates and incubated for 24 h. Cells were then treated with 10 µM cisplatin for 36 h at 37°C. MTT reagent (0.5 mg/ml; Cayman Chemical Company, Ann Arbor, MI, USA) was subsequently added, and cells were incubated for 4 h before the medium was removed and 100 µl DMSO was added. Cell viability was quantified by measuring the optical density (OD) at 490 nm using a microplate reader (Bio-Rad Laboratories, Inc., Hercules, CA, USA). At least three independent experiments were performed, and the final inhibitory rate of cell viability was calculated using the following formula: Inhibitory rate = [1 - (OD490compound/OD490solvent)] × 100.

The staining protocol was performed using a FITC Annexin V Apoptosis Detection kit I (BD Biosciences, Franklin Lakes, NJ, USA), according to the manufacturer's protocol. Briefly, 5×105 cells were transfected with 100 µl pLKO.1 (1×108/ml) as a control or 100 µl shRNA ATG5 (1×108/ml) for 12 h at 37°C and, immediately following infection, the cells were transfected with control or MEG3 siRNA at 37°C. After transfection for 24 h, the cells were treated with 10 µM cisplatin for 36 h at 37°C. Cells were subsequently centrifuged at 1,000 × g for 5 min at 4°C and resuspended in 195 µl binding buffer. This was followed by incubation with 5 µl Annexin V-FITC for 10 min at room temperature in the dark. The cells were centrifuged again at 1,000 × g for 5 min at 4°C, before they were resuspended in 190 µl binding buffer and 10 µl propidium iodide stain and gently agitated. FACS analysis was performed using the BD Accuri C6 Flow Cytometer (BD Biosciences) in order to detect cell apoptosis and the apoptosis was analyzed using CFlow Plus software (version, 1.0264.15; BD Biosciences).

U87 cells (2×105/well) were treated with 5 or 10 µM cisplatin for 0, 24 or 36 h, prior to RNA extraction using RNAiso Plus. RNA quality was examined by gel electrophoresis, and only high quality RNA was used for subsequent analyses. A total of 1 µg total RNA was used to synthesize cDNA using the PrimeScript™ RT reagent kit (Perfect Real Time; Takara Biotechnology Co., Ltd.) according to the manufacturer's instructions. qPCR was performed using SYBR premix ExTaq (Takara Biotechnology Co., Ltd.) and ROX, and amplified with the Stratagene Mx3000P qPCR system (Agilent Technologies, Inc., Santa Clara, CA, USA). The primer sequences used for qPCR analysis were as follows: Actin forward, 5′-CTCCATCCTGGCCTCGCTGT-3′, and reverse, 5′-GCTGTCACCTTCACCGTTCC-3′; MEG3 forward, 5′-GCATTAAGCCCTGACCTTTG-3′, and reverse, 5′-TCCAGTTTGCTAGCAGGTGA-3′. The mRNA expression was normalized to the expression of actin using the 2-∆∆Cq method (15).

Data are presented as the mean ± standard deviation, and statistical analysis was performed using SPSS software (version, 22.0; IBM Corp., Armonk, NY, USA). Statistical analysis was performed using one-way analysis of variance followed by Dunnett's test. P<0.05 was considered to indicate a statistically significant difference.

In order to evaluate MEG3 expression in response to cisplatin treatment of GBM, human U87 cells were treated with 0, 5 or 10 µM cisplatin for 36 h. As shown in Fig. 1A, U87 cells were treated with 0, 5 or 10 µM cisplatin for 24 h and cell apoptosis was increased at 10 µM cisplatin as indicated by increased PARP and caspase-3 cleavage. Subsequently, the mRNA expression of MEG3 was detected using RT-qPCR and the results demonstrated that the mRNA expression levels of MEG3 were increased in a dose-dependent manner following treatment of U87 cells with cisplatin (Fig. 1B). The cells were subsequently treated with 10 µM cisplatin for 0, 24 or 36 h. As shown in Fig. 1C, cell apoptosis was increased at 24 and 36 h, as indicated by increased PARP and caspase-3 cleavage. In addition, the expression levels of MEG3 were significantly upregulated in a time-dependent manner in U87 cells (Fig. 1D).

To determine whether elevated MEG3 affected cell survival following cisplatin treatment, MEG3 expression was inhibited by siRNA in U87 cells. The expression level of MEG3 was markedly downregulated in MEG3-siRNA transfected U87 cells when compared with those transfected with control siRNA (Fig. 2A). The cells were subsequently treated with cisplatin for 0 or 36 h. When compared with cells transfected with control siRNA, inhibition of MEG3 reduced the protein expression levels of cleaved PARP (Fig. 2B). Similarly, decreased MEG3 expression attenuated the cisplatin-induced reduction in cell viability (Fig. 2C). Conversely, exogenous expression of MEG3 efficiently enhanced the effects of cisplatin on the protein expression levels of cleaved PARP and cell viability (Fig. 2D-F).

A previous study demonstrated that loss of MEG3 expression activated autophagy and increased the proliferation of bladder cancer cells (9). In order to investigate the effect of MEG3 on autophagy induced by cisplatin, U87 cells transfected with control MEG3 siRNA were treated with cisplatin for 0 or 36 h. Compared with the control cells, silencing of MEG3 expression increased the protein expression of LC3 II relative to GAPDH and promoted p62 degradation (Fig. 3A-C). By contrast, overexpression of MEG3 attenuated cisplatin-induced autophagy in U87 cells (Fig. 3D-F).

Autophagy has been demonstrated to be a key mechanism that induces chemoresistance in cancer cells (9). Therefore, the present study investigated whether the effects of MEG3 in promoting cisplatin-induced apoptosis was dependent on the inhibition of autophagy. U87 cells transfected with control or MEG3 siRNA were pretreated with 3-MA (5 mM) for 6 h and exposed to 10 µM cisplatin for 0 or 36 h. Cell apoptosis was analyzed. Compared with control siRNA-transfected cells, inhibition of MEG3 markedly decreased the expression of apoptosis-associated proteins, which was reversed following treatment with the autophagy inhibitor, 3-MA (Fig. 4A and B). To confirm these observations, cells were infected with lentiviruses expressing shRNA targeting ATG5, which is a key molecule involved in the formation of autophagic vacuoles and induces autophagy (16). The cells were treated with control or MEG3 siRNA. When compared with control shRNA-transfected U87 cells that were transfected with MEG3 siRNA, knockdown of ATG5 significantly increased the level of apoptosis (Fig. 4C-F). These data indicated that inhibition of autophagy by MEG3 promoted cisplatin-induced apoptosis of U87 cells.