The GSE35988 dataset was downloaded from GEO database (http://www.ncbi.nlm.nih.gov/geo) and re-analyzed with R (11). Pearson's correlation in MATLAB was used to analyze the relationship between SP1 and all identified genes (P<0.05).

Two human PCa cell lines, namely, DU145 and PC3, were purchased from Nanjing KeyGen Biotech, Co., Ltd. (Nanjing, China). The cells were cultured at 37°C in a 20% O₂ humidified atmosphere with 5% CO₂ in RPMI-1640 medium that was supplemented with 10% fetal bovine serum (FBS; 100–700; Gemini Bio Products, Woodland, CA, USA), 50 U/ml penicillin and 50 mg/ml streptomycin (15140-122; Gibco Laboratories, Gaithersburg, MD, USA). Hypoxia experiments were performed in a hypoxic chamber (Coy Laboratory Products, Inc., Grass Lake, MI, USA) at 1% O₂ at 37°C in a 5% CO₂ humidified environment.

Oligonucleotides were chemically synthesized by Shanghai GenePharma, Co., Ltd., (Shanghai, China), based on the following sequences: Sp1 siRNA, 5-GGUCAGUUGGCAGA CUCUATT-3 (sense); siRNA negative control(NC), 5-UUC UCCGAACGUGUCACGUTT-3 (sense); hsa-miR-361-5p mimics: 5-ACCCCUGGAGAUUCUGAUAAUU-3; negative control (NC): 5-UUCUCCGAACGUGUCACGUTT-3. Cells that were 60–70% confluent were transfected with Lipofectamine 2000 (11668-019; Invitrogen, Albuquerque, NM, USA). Oligonucleotides or plasmids formed transfection complexes with Lipofectamine 2000. The transfection complexes were then added to DU145 and PC3 cells at different concentrations and incubated for 6–8 h before changing the medium.

Total RNA was extracted from cells using TRIzol (15596018; Invitrogen) in accordance with the manufacturers instructions. RNA concentration was measured using NanoDrop 2000c (Thermo Scientific, Wilmington, DE, USA). For miR-361-5p, the RT-qPCR reaction was performed with a HiScript RT kit (R132-01; Vazyme Biotech, Co., Ltd., Nanjing, China) and AceQ SYBR-Green PCR Master Mix (Q141-02/03; Vazyme Biotech) following the manufacturers protocols. Primers were chemically synthesized by Nanjing Springen Biotech, Co., Ltd. (Nanjing, China). The miR-361-5p primers for amplification were as follows: stem-loop reverse transcription primer: 5-CTCAACTGGT GTCGTGGAGTCGGCAATTCAGTTGAGGTACCCCT-3; specific forward primer, 5-ACACTCCAGCTGGGTTATC AGAATCTCC-3 and specific reverse primer: 5-TGGTGTCG TGGAGTCG-3. The U6 snRNA primers were as follows: forward: 5-CTCGCTTCGGCAGCACA-3 and reverse, 5-AA CGCTTCACGAATTTGCGT-3. PCR was conducted with a 20 µl reaction volume that contained 2 µl of RT products, 1 µl of 10 µM miR-361-5p or U6 primer set, 10 µl of 2X SYBR-Green PCR Master Mix, and 7 µl of ddH₂O. Cycling conditions were as follows: 95°C for 3 min, 95°C for 15 sec, and 60°C for 60 sec. The last two steps were conducted with 40 cycles. RT-qPCR was performed using 7500 Real-Time PCR System (Applied Biosystems, Inc., Carlsbad, CA, USA). The gene expression threshold cycle (CT) values of miRNAs were calculated by normalizing to the internal control U6. Relative quantification values were calculated via the 2^−ΔΔCt method (12).

DU145 and PC3 cells were seeded in a 6-well plate and cultured overnight. The cells were transfected with oligonucleotides and cultured overnight. Subsequently, the cells were trypsinized and seeded at 2,000 cells/well (200 µl/well) in a 96-well plate. At 24-h post-transfection, cell proliferation was measured with a CCK-8 assay kit (KGA317; Nanjing KeyGen Biotech) in accordance with the manufacturers instructions. Absorbance was detected at a wavelength of 450 nm. Five wells were measured for cell viability in each treatment group. All independent treatments were performed in triplicate.

Cell cycle distributions were analyzed using FACS (Becton-Dickinson, Franklin Lakes, NJ, USA). Cell cycle assay kits were procured from Nanjing KeyGen Biotech (KGA514). At 48 h post-transfection, cells were harvested and fixed with 75% ethanol at −20°C overnight. Subsequently, the cells were incubated in 50 µg/ml propidium iodide and 1 mg/ml RNase for 30 min at room temperature and analyzed using flow cytometry. The experiments were performed in triplicate.

DU145 and PC3 cells were seeded in a 24-well plate that contained 200 µl of media/well. To determine glucose and lactate levels in cells, the supernatants of the cell culture media were collected and assayed for glucose and lactate levels by using a glucose assay kit (K686; BioVision, Inc., San Francisco, CA, USA) and lactate assay kit (K627; BioVision), respectively, in accordance with the manufacturers instructions. OD values of the supernatants were analyzed at 72 h after different treatments. The remaining glucose and lactate production were calculated based on the standard curve and normalized to the cell number.

Cells were harvested 48 h post-transfection with Sp1 siRNA and NC siRNA. The samples were then pelleted and fixed in 2.5% glutaraldehyde (G5882; Sigma-Aldrich, St. Louis, MO, USA) in phosphate buffer (pH 7.4). Next, the samples were rinsed with phosphate buffer (pH 7.4) and postfixed with 2% OsO₄ (75633; Sigma-Aldrich) for 1 h. The samples were then rinsed with water, dehydrated in a graded ethanol series [70% ethanol (20 min), 96% ethanol (20 min), and then 100% ethanol (2×20 min)] followed by propylene oxide (2×10 min) (SAJ-24-6210; Sigma-Aldrich), and maintained overnight in Epon 812 (45347-1L-F; Sigma-Aldrich). Subsequently, the samples were embedded in Epon 812 and then fumigated in a microwave oven at 60°C. Ultrathin sections were obtained using Reichert Ultracut E microtome and then stained with uranyl acetate and lead citrate. Samples were imaged using an H-7650 transmission electron microscope (Hitachi, Ltd., Tokyo, Japan).

Radioimmunoprecipitation assay buffer (KGP701; Keygentec, Inc., Nanjing, China) was used to lyse cells for total proteins. Protein concentration was determined via the BCA method (KGP902; Keygentec). Protein samples (30 µg) were electrophoresed on 10% sodium dodecyl sulphate-polyacrylamide electrophoresis gels (KGP113K; Keygentec) and transferred onto polyvinylidene fluoride membranes (IPVH00010; Millipore, Billerica, MA, USA). The membranes were blocked with 5% skim milk at room temperature for 1 h and incubated overnight at 4°C with diluted primary antibodies. Subsequently, the membranes were washed thrice with TBST buffer (pH 7.6, 20 mM Tris-HCl, 137 mM NaCl, 0.01% Tween-20) and then incubated with HRP-conjugated secondary antibodies at 37°C for 1 h. After being washed with TBST buffer, the membranes were visualized using enhanced chemiluminescence ECL (WBKLS0050; Millipore). Protein levels were normalized to GAPDH levels. The related antibodies were HRP-conjugated monoclonal mouse anti-GAPDH (KC-5G5, 1:1,000; Shanghai Kangchen), rabbit polyclonal anti-LC3B (18725-1-AP, 1:1,000; Proteintech Group, Inc., Chicago, IL, USA), rabbit monoclonal anti-Beclin-1 (3495, 1:1,000; Cell Signaling Technology, Danvers, MA, USA), rabbit monoclonal anti-PKM2 (4053, 1:1,000; Cell Signaling Technology), rabbit monoclonal anti-SP1 (9389S, 1:1,000; Cell Signaling Technology), HRP-labeled goat anti-rabbit secondary antibody (ZB-2301, 1:3000; Beijing Zhongshan Golden Bridge Biotechnology, Co., Ltd., Beijing, China).

The 3-UTR segment of Sp1 mRNA with miR-361-5p binding site was amplified via PCR with human genomic DNA. To generate the Sp1 3-UTR reporter, PCR products were cloned into the XhoI and NotI restriction sites that were downstream of the open reading frame of luciferase in the psiCHECK-2™ Vector (c8021; Promega, Madison, WI, USA). Deleting the binding site for miR-361-5p generated the mutant reporter. For reporter assays, the cells were transfected with Sp1 3′UTR, mutant reporter plasmid and miR-361-5p mimics, or NC. Luciferase activity was measured by Dual-luciferase assays (E1910; Promega) 48 h after co-transfection.

Each value in this study was obtained from at least three independent experiments and presented as mean ± SD. The significance of differences was calculated using t-tests for two-group comparisons with the SPSS 22.0 (IBM Corp., Armonk, NY, USA). A probability of P<0.05 was considered statistically significant.

First, we used the GEO database to analyze the SP1 expression in benign prostatic hyperplasia tissues and PCa tissues at different stages. The results indicated that SP1 expression is significantly higher in CRPC than in androgen-dependent prostate cancer (ADPC) (Fig. 1A). To verify the function of Sp1 in CRPC, we transfected CRPC cells with Sp1 siRNA or NC. SP1 protein was detected by western blot analysis, and results showed that Sp1 siRNA efficiently silenced Sp1 gene expression (Fig. 1B). CCK-8 assays demonstrated that Sp1 depletion significantly decreased proliferative index of PC3 and DU145 cells compared with NC (Fig. 1C and D). Flow cytometry assay revealed that CRPC cells that were transfected with Sp1 siRNA demonstrated a higher rate of G1 cell cycle arrest (Fig. 1E and F). Moreover, Sp1 siRNA significantly decreased glucose consumption and lactate production in CRPC cells compared with those in the NC group (Fig. 2A and B).

Glycolysis positively regulates autophagy via various mechanisms (13). The transcription factor HIF-1α is an important regulator of glycolysis, and its upregulation is the mechanism through which autophagy is induced under hypoxia or nutrient starvation (14,15). Given that previous studies have indicated that decreased glycolysis decreases HIF-1 and inhibits autophagy (16), we investigated whether the inhibition of metabolism by Sp1 depletion affects hypoxia-induced autophagy in CRPC.

PC3 and DU145 cells were cultured at 37°C in 1% O₂ and 5% CO₂ humidified environment and were simultaneously transfected with Sp1 siRNA or NC. The cells were harvested for TEM at 48 h post-transfection. Autophagosomes, spherical structures with mono- or bilayer membranes, engulf degraded or abandoned organelles and deliver cytoplasmic components to lysosomes. As expected, hypoxic conditions significantly induced autophagy in PCa cells, as evidenced by large areas of autophagosomes or autolysosomes that were revealed by TEM. By contrast, Sp1 downregulation markedly inhibited hypoxia-induced autophagy, as indicated by the significantly decreased number of autophagosomes or autolysosomes in the Sp1 siRNA group in both CRPC cell lines (Fig. 2C).

To further evaluate the potential role of aberrantly expressed SP1, Pearson correlation was used to analyze the relationship between Sp1 and all identified genes (Fig. 3A). The SP1-specific gene signature included 2,357 genes that are positively correlated with SP1 expression (R>0.4, P<0.05) and 3,418 genes that are negatively correlated with SP1 expression (R≤0.4, P<0.05) (data available upon request). Among these genes, a set of glycometabolism-related genes are positively correlated with SP1 expression. PKM2, a metabolic enzyme that executes the last step of aerobic glycolysis, is included in this set of genes, and its expression is significantly higher in CRPC than in androgen-dependent prostate cancer (Fig. 3B and C). Previous studies that identified Sp1 binding motifs in PKM2 promoter sequences have also asserted that Sp1 activates PKM2 promoter activity (10,17); thus, western blot analysis was conducted in this study to confirm if Sp1 inhibition could decrease PKM2 expression. After 48 h of hypoxia experiments with Sp1 siRNA transfection, the cells were harvested for western blot analysis. Results indicated that transfection with Sp1 siRNA downregulated PKM2. Microtubule-associated protein 1 LC3, a specific marker of autophagy, is converted from LC3-I (inactivated form) to LC3-II (cleaved form) during autophagy. Western blot analysis showed that the conversion from LC3-I to LC3-II was inhibited in the Sp1 siRNA group, and that Beclin-1 expression also decreased (Fig. 3D). The signal ratio between LC3-II and LC3-I indirectly showed the extent of autophagy in PCa. The result indicated that the LC3-II/LC3-I ratio decreased in the Sp1 siRNA group and that autophagy decreased with Sp1 depletion (Fig. 3E).

To identify the potential targets of miR-361-5p in PCa, bioinformatics analysis was performed with the website microRNA.org. Bioinformatics analysis revealed that miR-361-5p could bind to target sequences in the 3′UTR of Sp1 mRNA (Fig. 4A). Moreover, western blot analysis revealed that Sp1 protein expression was inhibited by treatment with miR-361-5p mimics (Fig. 4B). To confirm the direct miRNA-target interaction, Sp1 3-UTR was cloned into a Dual-luciferase reporter cloning site in the psiCHECK-2 Dual-luciferase vector. Luciferase activities remarkably decreased with increasing miR-361-5p levels (Fig. 4C).

RT-qPCR was utilized to examine miR-361-5p expression in cells at 48 h post-transfection with miR-361-5p mimics or NC into DU145 (PC3). miR-361-5p was expressed at higher levels in the miR-361-5p mimic group than in the NC group (Fig. 5A). Cell cycle analysis was conducted to determine the effect of miR-361-5p on cell proliferation. At 48 h post-transfection, the percentage of miR-361-5p-transfected cells in the G1 phase was higher than that of the NC-transfected cells (Fig. 5B). This result indicated that miR-361-5p induced G1 cell cycle arrest in CRPC cell lines. CCK-8 assays revealed that miR-361-5p overexpression significantly inhibited DU145 (PC3) proliferation (Fig. 5C and D). Moreover, miR-361-5p significantly reduced glucose consumption and lactate production in the CRPC cells relative to that in the NC group (Fig. 6A and B).

miR-361-5p mimics or NC were transfected into CRPC cells, which were cultured under hypoxic conditions. The cells were harvested for western blot analysis at 48 h post-transfection. miR-361-5p overexpression significantly decreased PKM2, Beclin-1 and LC3B expression levels. Moreover, the LC3-II/LC3-I ratio of the miR-361-5p group was also lower than that in the NC group, indicating that miR-361-5p negatively regulates autophagy in PCa cells (Fig. 6C and D).