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Introduction

Glioblastoma multiforme is the most common type of malignant primary brain tumor in adults (1). Mean progression-free survival is just over 6 months; treatment with surgical resection, chemotherapy and radiation is invariably followed by tumor recurrence (2). Despite the improvement in outcomes with this combined chemoradiotherapy approach, few patients survive beyond 5 years (3). Therefore, future studies on the molecular mechanism of the disease may provide the theoretical basis to identify new targets for effective therapies.

Cytochrome P450, family 27, subfamily A, polypeptide 1 (CYP27A1), also termed CTX\CP27\CYP27 is a ubiquitously expressed mitochondrial enzyme belonging to the cytochrome P450 family (4). CYP27A1 catalyzes the hydroxylation of cholesterol at C-27 to form 27-hydroxycholesterol and cholestenoic acid (5). A single serum measurement of 27-hydroxycholesterol can reliably estimate average levels over a one-year period (6). The role of CYP27A1 in bile acid synthesis in the liver is well established; it catalyzes the initial, rate-limiting step in the alternative bile acid synthetic pathway and the intermediate step in the classic bile acid synthetic pathway (7,8). CYP27A1 is strongly expressed in macrophages within human benign and malignant mammary tissue (4). Breast cancer cell intrinsic expression of CYP27A1 protein is associated with tumor grade (4). However, its roles remain unclear in glioblastoma.

MicroRNAs (miRNAs/miRs) are a class of small RNA found in a diverse range of eukaryotes, including animals, plants and DNA viruses, which range in size between 19 and 24 nucleotides (nts) (9). Aberrant miRNA expression has been linked to glioblastoma (10). miR-204, a direct negative regulator of ezrin gene expression, inhibits glioma cell migration and invasion (11). However, studies continue to emerge with an improved understanding on the mechanism of miR-204 as a tumor suppressive gene in glioblastoma. In the present study, it was observed that CYP27A1 overexpression promoted proliferation, while silencing of CYP27A1 inhibited proliferation in glioblastoma cells, without affecting migration and invasion. It was revealed that CYP27A1 was upregulated in glioblastoma tissues, indicating that CYP27A1 may be an oncogene. The downregulation of specific miRNAs may contribute to the upregulation of oncogenes in glioblastoma (12). A common strategy was used to predict target miRNAs of CPY27A1 using the miRanda algorithm. It was revealed that miR-211 and miR-204 could target the 3′untranslated region (UTR) of CPY27A1 mRNA. Overexpressing miR-204 inhibited CPY27A1 expression in glioblastoma cells. Lastly, the present study demonstrated that miR-204 was downregulated in glioblastoma and its overexpression inhibited proliferation, migration and invasion in glioblastoma cells. Therefore, miR-204 functions as a tumor suppressor gene, at least partly by suppressing CYP27A1 expression in glioblastoma.

Materials and methods

Glioblastoma tissues, cells, CYP27A1-expressing plasmids and short hairpin (sh) CYP27A1 plasmids

A total of 7 Chinese women patients with glioblastoma were recruited from the Department of Neurosurgery, Yishui Central Hospital (Shandong, China). The mean age was 56 years (range, 31–78 years). All tissues were examined histologically, and pathologists confirmed the diagnosis. The present study was approved by the medical ethics committee of Yishui Central Hospital (Shandong, China). Written informed consent was obtained from each individual. The human glioblastoma U87MG cell line was purchased from the Cell Bank of the Chinese Academy of Sciences (Beijing, China). CYP27A1-expressing plasmids/pcDNA3.1 (pcDNA3.1) and shCYP27A1/scramble were purchased from Tiangen Biotech Co., Ltd. (Shanghai, China).

Protein extraction and western blot analysis

Following transfection, cells and tissues were lysed for 48 h using RIPA Lysis and Extraction Buffer (Beijing Solarbio Science & Technology Co., Ltd., Beijing, China), and the protein concentration was measured using Pierce™ BCA Protein Assay kit (Thermo Fisher Scientific, Inc.). Following heating at 100°C for 10 min in the presence of a loading buffer, equal amounts of protein lysates (50 µg) were separated using 10% SDS-PAGE (Bio-West Inc., Logan, UT, USA) at 100 V for 1 h, and transferred onto Invitrogen nitrocellulose membranes (Thermo Fisher Scientific, Inc.) at 120 V for 1 h. Following blocking with 5% skimmed milk (diluted with PBS), the membranes were incubated overnight at 4°C with the following primary antibodies: CYP27A1 (ab126785; 1:500; Abcam, Cambridge, MA, USA), c-myc (ab32072; 1:500; Abcam), RB (ab181616; 1:500; Abcam), Ki-67 (ab15580; 1:500; Abcam), CDK2 (ab32147; 1:500; Abcam), p21 (ab109520; 1:500; Abcam), p53 (ab32049; 1:500; Abcam), PDCD4 (ab51495; 1:500; Abcam), SOX2 (ab92494; 1:500; Abcam), β-actin (ab8227; 1:500; Abcam). Subsequently, the membranes were incubated with secondary goat monoclonal (RMG01) to rabbit IgG Fab region (Biotinylated; ab222772; 1:10,000; Abcam) at room temperature for 2 h, and proteins were detected using enhanced chemiluminescence (Pierce™ ECL Western Blotting Substrate; Thermo Fisher Scientific, Inc.).

MTT assay

A total of 5×103 cells were seeded onto 96-well plates and transfected with CYP27A1 expressing plasmids or empty vector at 37°C for 24 h.

Subsequent to transfection, MTT (5 mg/ml; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) was added to the wells (20 µl/well) and incubated for 4 h at 37°C, and then the supernatants were removed and 2% dimethyl sulfoxide was added to each well. The absorbance of each sample was measured using a UV spectrophotometer at the wavelength of 490 nm.

Bromodeoxyuridine (BrdU) labeling and immunofluorescence

Cells grown on coverslips (Thermo Fisher Scientific, Inc., Waltham, MA, USA) were incubated with BrdU at 37°C for 1 h and stained with anti-BrdU antibody (1:200; cat. no. ab220076; Abcam) according to the manufacturer's protocol. For immunofluorescence analysis, cells were plated on glass coverslips. Following transfection, cells were exposed to anti-CYP27A1 antibody (1:250; ab198970; Abcam) overnight at 4°C and goat anti-rabbit secondary antibody (1:500; ab150079; Abcam). Coverslips were counterstained with DAPI (Molecular Probes; Thermo Fisher Scientific, Inc.) to detect cell nuclei. Microscopic analysis was performed with a confocal laser-scanning microscope (Leica Microsystems, Bensheim, Germany). Fluorescence intensities were measured in three randomly selected viewing areas for 200~300 cells/coverslip and analyzed using ImageJ (version 1.37v; National Institutes of Health, Bethesda, MA, USA).

Migration and invasion assay

Cell suspension (total cells, 3×104) in medium without fetal bovine serum (FBS) was plated into the top chamber with 8-µm pore sized filter inserts of Transwell plates (24-well; Costar, Cambridge, MA, USA). For the Transwell migration assay, the top surface of filter membranes was not coated with Matrigel, while the top surface of filter membranes was coated with Matrigel matrix (BD Biosciences, San Jose, CA, USA) in the Matrigel invasion assay. Medium containing 10% FBS (Sigma-Aldrich; Merck KGaA) was added to the bottom chambers in the two assays. The cells were incubated for 24 h at 37°C, and then the non-migrated or non-invaded cells on top surface of the membrane were removed with a cotton swab, the cells under the filter membrane were fixed with 4% paraformaldehyde for 10 min at room temperature and stained with 0.2% crystal violet for 10 min at room temperature (Sigma-Aldrich; Merck KGaA).

Methods of bioinformatics

The analysis of potential microRNA target sites was performed using the commonly used miRanda prediction algorithm (http://www.microrna.org/).

Reverse transcription-polymerase chain reaction (RT-PCR)

Extraction of total RNA and detection of the mature form of miRNAs was performed with the mirVanami RNA Isolation kit (Ambion; Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. Template DNA was obtained from Dr Xin Shao (Department of Medicine, Jiujiang College, Jiujiang, China). Taq DNA polymerase was purchased from Promega Corporation (Madison, WI, USA). β-actin was used as an experimental control gene. SYBR green (Takara Biotechnology Co., Ltd., Dalian, China) was used as a fluorophore. Quantification was performed using the 2−ΔΔCq method (13).

Luciferase (Luc) assays

Total RNA was isolated from the U87MG cells using TRIzol reagent (cat no. 101472; Invitrogen; Thermo Fisher Scientific, Inc.). cDNA was synthesized from 1 µg of total RNA in a 20 µl reverse transcription system followed by PCR amplification in a 50 µl PCR system performed using an RT-PCR kit (cat no. A3500; Promega Corporation). The 3′UTR of CYP27A1 was amplified [10X buffer 3 ul, MgCl2 (25 mM) 3 ul, dNTP (25 mM) 0.36 ul, forward primer (10 µM) 1 ul, reverse primer (10 µM) 1 µl, Taq enzyme (5 U/µl) 0.3 µl, ddH2O 19.34 µl and cDNA 2 µl; 95°C for 2 min; 95°C for 30 sec; 55°C for 60 sec; 72°C for 30 sec] using cDNA from U87MG cells, cloned into pRL-TK (Promega Corporation), checked for orientation, sequenced and termed Luc-CYP27A1-wild-type (WT). For reporter assays, U87MG cells were transiently transfected with WT-reporter plasmid and precursor (pre)-miR-204 using Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.). Reporter assays were performed 36 h post-transfection using the dual-luciferase assay-system (Promega Corporation), normalized for transfection efficiency by co-transfected Renilla-luciferase.

Northern blot analysis

Northern blot analysis of miRNAs was performed as described previously (14). Probes were labeled with (γ-32P) ATP complementary to miR-204 and U6 small nuclear RNA.

Statistical analysis

All experimental data are presented as the mean ± standard error, with the number of independent experiments (n=3), and were analyzed using Student's t-test. P<0.05 was considered to indicate a statistically significant difference. Analysis was performed using GraphPad Prism software (version 5.0; GraphPad Software, Inc., La Jolla, CA, USA).

Results

CYP27A1 promotes proliferation of glioblastoma cells

To investigate whether CYP27A1 could promote the proliferation of glioblastoma U87MG cells, firstly using western blot analysis, it was examined whether CYP27A1-expressing plasmids could stably express CYP27A1 protein in U87MG cells. The results demonstrated that CYP27A1 protein could be significantly increased by CYP27A1-expressing plasmids in the cells (Fig. 1A). In order to identify the effect of CYP27A1 on proliferation, an MTT assay was performed. The results demonstrated that overexpression of CYP27A1 significantly upregulated the proliferation rate of U87MG cells following transfection (Fig. 1B). To show the effects of CYP27A1 on proliferation, a BrdU incorporation assay was performed to analyze its effects on DNA synthesis. The results confirmed that CYP27A1 significantly promoted DNA synthesis in the cells, and representative micrographs and quantification of BrdU incorporating-cells following transfection with CYP27A1 or empty vector (mock) are shown (Fig. 1C). Subsequently, western blot analysis was performed to identify whether proliferation-associated markers were affected by CYP27A1 in the cells. The results of western blot analysis revealed that c-myc, sex determining region Y-box 2 (SOX2), Ki-67 and cyclin-dependent kinase 2 were promoted and p21, p53and programmed cell death protein 4 (PDCD4) were inhibited by CYP27A1 (Fig. 1D). Meanwhile, it was observed that CYP27A1 protein was increased by CYP27A1 expression plasmids (Fig. 2A) and overexpression of CYP27A1 promoted proliferation in LN-229 glioblastoma cells (Fig. 2B). These data supported that CYP27A1 promoted proliferation in glioblastoma cells.

Figure 1. CYP27A1 promotes proliferation in glioblastoma U87MG cells. (A) Western blot analysis for CYP27A1 in U87MG cells. U87MG cells were transfected with CYP27A1-expressing plasmids or the empty vector (mock). β-actin was used as the loading control. n=3. (B) MTT assay for U87MG cells. U87MG cells were transfected with CYP27A1-expressing plasmids or the empty vector (mock) and cellular viability was then measured at the indicated time points using an MTT assay. n=3. (C) BrdU incorporation assay for U87MG cells. Representative micrographs and quantification of BrdU incorporating-cells following transfection with CYP27A1-expressing plasmids or the empty vector (mock). n=3. (D) Western blot analysis for c-myc, RB, Ki67, CDK2, p21, p53, PDCD4 and SOX2 in U87MG cells transfected with CYP27A1-expressing plasmids or the empty vector (mock). β-actin was used as the loading control. n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1; BrdU, bromodeoxyuridine; RB, retinoblastoma; CDK2, cyclin-dependent kinase 2; PDCD4, programmed cell death protein 4; SOX2, sex determining region Y-box 2.

Figure 2. CYP27A1 promotes proliferation in glioblastoma LN-229 cells. (A) Western blot analysis for CYP27A1 in LN-229 cells. LN-229 cells were transfected with CYP27A1-expressing plasmids or the empty vector (mock). β-actin was used as the loading control. n=3. (B) MTT assay for LN-229 cells. LN-229 cells were transfected with CYP27A1-expressing plasmids or the empty vector (mock) and cellular viability was then measured at the indicated time-points using an MTT assay. n=3. Error bars indicate standard error of the mean.

CYP27A1 overexpression does not affect migration and invasion in glioblastoma cells

Considering that CYP27A1 evidently promoted U87MG cellular proliferation, it was then determined whether CYP27A1 has an impact on the migration and invasion of glioblastoma cells. The migration and invasion assay results demonstrated that the overexpression of CYP27A1 did not affect migration and invasion in U87MG and LN-229 cells (Fig. 3A and B).

Figure 3. CYP27A1 overexpression does not affect migration and invasion in glioblastoma U87MG and LN-229 cells. (A) Matrigel invasion and Transwell migration assays for U87MG cells transfected with CYP27A1-expressing plasmids or the empty vector (mock). n=3. (B) Matrigel invasion and Transwell migration assays for LN-229 cells transfected with CYP27A1-expressing plasmids or the empty vector (mock). n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1.

Silencing CYP27A1 inhibits proliferation in glioblastoma cells

It was demonstrated that CYP27A1 overexpression promoted proliferation in U87MG and LN-229 cells. To provide additional evidence that CYP27A1 is involved in the proliferation of glioblastoma cells, the effects of an inhibitor of CYP27A1, shCYP27A1, were studied. Following stable transfection, CYP27A1 expression was detected by western blot analysis. The results demonstrated that exogenous shCYP27A1 significantly downregulated CYP27A1 expression in U87MG cells (Fig. 4A). An MTT assay was performed to detect the proliferation of U87MG cells transfected with shCYP27A1 and scramble. The results demonstrated that shCYP27A1 inhibited proliferation in U87MG cells compared with scramble-transfected groups, and that the inhibition was dose-dependent (Fig. 4B). To demonstrate the effects of silencing CYP27A1 on cellular proliferation, BrdU incorporation assay was performed to detect DNA synthesis in the cells. The results confirmed that shCYP27A1 significantly suppressed DNA synthesis in the cells and representative micrographs and quantification of BrdU incorporating-cells following transfection with shCYP27A1 or scramble are presented (Fig. 4C). Subsequently, western blot analysis was performed to identify whether proliferation-associated markers were affected by shCYP27A1 in the cells. The results of western blot analysis demonstrated that the proliferating cell nuclear antigen was downregulated and p21, as well as p53, were upregulated by silencing CYP27A1 (Fig. 4D).

Figure 4. Silencing CYP27A1 inhibits proliferation in glioblastoma U87MG cells. (A) Western blot analysis for CYP27A1 in U87MG cells infected with shCYP27A1 or scramble. β-actin was used as the loading control. n=3. (B) MTT assay for U87MG cells transfected with shCYP27A1 or scramble. n=3. (C) BrdUincorporation assay for U87MG cells. Representative micrographs and quantification of BrdU incorporating cells following transfection with shCYP27A1 or scramble. n=3. (D) Western blot analysis for PCNA, p21, p53 and RB in U87MG cells transfected with shCYP27A1 or scramble. β-actin was used as the loading control. n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1; BrdU, bromodeoxyuridine; sh, short hairpin; PCNA, proliferating cell nuclear antigen; RB, retinoblastoma.

Silencing CYP27A1 does not affect migration and invasion in glioblastoma cells

It was then determined whether silencing CYP27A1 would have any impact on migration and invasion in U87MG cells. The migration and invasion assays revealed that silencing CYP27A1 did not affect migration and invasion of them (Fig. 5).

Figure 5. Silencing CYP27A1 does not affect migration and invasion in glioblastoma U87MG cells. Matrigel invasion assay and Transwell migration assay for U87MG cells transfected with shCYP27A1 plasmids orscramble. n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1; sh, short hairpin.

Aberrant expression of CYP27A1 in glioblastoma tissues

In order to identify CYP27A1 protein expression in glioblastoma tissues, western blot analysis was performed to detect CYP27A1 protein between glioblastoma tissues and adjacent normal tissues. It was revealed that CYP27A1 was increased in cancer tissues of 6 patients, compared with adjacent normal tissues (Fig. 6).

Figure 6. CYP27A1 is upregulated in glioblastoma tissues. Differential expression of CYP27A1 in 6 pairs of human glioblastoma tissues (C) and corresponding adjacent normal tissues (N) were detected by western blot analysis. β-actin was used as an endogenous control. n=6. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1.

CYP27A1 is a target of miR-204 in glioblastoma U87MG cells

Having demonstrated that CYP27A1 expression is specifically upregulated in glioblastoma and it can promote proliferation in glioblastoma cells, the mechanisms promoting CYP27A1 expression in the disease were then studied. miRNAs are a new class of small (~22 nt) noncoding RNAs, which negatively regulate protein-coding gene expression by targeting mRNA degradation or translation inhibition (15). Downregulation of specific miRNA may contribute to oncogene overexpression (16). Thus, it was reasoned whether CYP27A1 was upregulated by defect of specific miRNA. To confirm this reason, a commonly used prediction algorithm, miRanda (http://www.microrna.org/), was used to analyze the 3′UTR of CYP27A1.

The algorithm predicted that miR-204 and miR-221 could target the 3′UTR of CYP27A1 and the predicted target is shown in Fig. 7A. To study the biological function of miR-204, it was investigated whether miR-204 expression could be increased by pre-miR-204 in U87MG cells. RT-PCR was performed to detect miR-204 expression in the cells transfected with pre-miR-204 and the results demonstrated that pre-miR-204 could significantly upregulate miR-204 expression in U87MG cells (Fig. 7B). In order to identify that CYP27A1 could be downregulated by miR-204, immunofluorescence and western blot analyses were performed to study whether miR-204 could affect CYP27A1 protein expression. Immunofluorescence analyses demonstrated that CYP27A1 was significantly downregulated in U87MG cells transfected with pre-miR-204 and representative micrographs, and the quantification of immunofluorescence is shown in Fig. 7C. Consistent with immunofluorescence analysis, the results of western blot analysis demonstrated that CYP27A1 protein was significantly downregulated by miR-204 in U87MG cells (Fig. 7D).

Figure 7. CYP27A1 is a target of miR-204 in glioblastoma U87MG cells. (A) Diagram demonstrating that CYP27A1 is a target gene of miR-204 and miR-211, predicted by miRanda. (B) Detection of miR-204 by RT-PCR in U87MG cells transfected with precursor-miR-204 or the control miR (mock). (C) Immunofluorescence analyses of U87MG cells transfected with pre-miR-204 or the control miR (mock). Upper panel shows microscopic images of immunofluorescence staining of one representative experiment (magnification, ×100). Bottom panel shows graphic presentation of mean fluorescence intensities of three independent experiments. (D) Western blot analysis for CYP27A1 in U87MG cells. U87MG cells were transfected with pre-miR-204 or control-miR (mock). β-actin was used as the loading control. (E) RT-PCR for CYP27A1 in U87MG cells. U87MG cells were transfected with pre-miR-204 or control-miR (mock). GAPDH was a loading control. (F) Reporter assay, with cotransfection of 500 ng WT-reporter and 50 nM control-miR, or pre-miR-204 as indicated. 36 h after transfection, cells were harvested for luciferase reporter assay. + represents existing inserted fragments; - represents no existing inserted fragments; n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1; miR, microRNA; RT-PCR, reverse transcription-polymerase chain reaction; WT, wild-type; has, Homo sapiens; UTR, untranslated region.

In addition, RT-PCR was also performed to detect CYP27A1 mRNA in the cells transfected with pre-miR-204. The results demonstrated that miR-204 downregulated CYP27A1 mRNA level in U87MG cells (Fig. 7E). To demonstrate the direct regulation of CYP27A1 by miR-204, luciferase reporters with the targeting sequences of wild-type (CYP27A1-wt-luc) were used to detect whether miR-204 targets 3′UTR of CYP27A1 mRNA. A luciferase assay was performed. The results demonstrated that miR-204 significantly inhibited CYP27A1-WT-luc plasmids in the cells (Fig. 7F). Meanwhile, we observed that miR-204 inhibits CYP27A1 expression in LN-229 glioblastoma cells by targeting 3′UTR of CYP27A1 mRNA (Fig. 8). The results confirmed that miR-204 negatively regulates protein-coding gene CYP27A1 expression by targeting its 3′UTR in glioblastoma cells.

Figure 8. CYP27A1 is a target of miR-204 in glioblastoma LN-229 cells. (A) Detection of miR-204 by RT-PCR in LN-229 cells transfected with pre-miR-204 (precursors miRNA) or the control miR (mock). (B) Western blot analysis for CYP27A1 in LN-229 cells. LN-229 cells were transfected with pre-miR-204 or control-miR (mock). β-actin was used as the loading control. (C) RT-PCR for CYP27A1 in LN-229 cells. LN-229 cells were transfected with pre-miR-204 or control-miR (mock). GAPDH was a loading control. (D) Reporter assay, with cotransfection of 500 ng WT-reporter and 50 nM control-miR, or pre-miR-204 as indicated. 36 h after transfection, cells were harvested for luciferase reporter assay. + represents existing inserted fragments; - represents no existing inserted fragments; n=3. Error bars indicate standard error of the mean. CYP27A1, cytochrome P450, family 27, subfamily A, polypeptide 1; miR, microRNA; RT-PCR, reverse transcription-polymerase chain reaction; WT, wild-type.

miR-204 is downregulated in glioblastoma and its overexpression inhibits proliferation, migration and invasion in glioblastoma cells

To assess the expression of miR-204 in glioblastoma tissues, northern blot analysis was conducted in 7 pairs of glioblastoma tissues and matched adjacent normal tissue samples. The expression of miR-204 was consistently lower in the glioblastoma tissues compared with normal tissues (Fig. 9A). In an attempt to identify the role of miR-204 in regulating proliferation of U87MG cells, the cells were transfected with pre-miR-204. Following stable transfection, the proliferation rates of U87MG cells were tested by an MTT assay. The results demonstrated that overexpression of miR-204 significantly inhibited the proliferation rate of U87MG cells and that the inhibition of cellular proliferation was dose-dependent (Fig. 9B). This was revealed by BrdU incorporation analysis showing that transfection with miR-204 resulted in decreased DNA synthesis activity per viable cell in U87MG cells (Fig. 9C). Considering that miR-204 evidently inhibited the proliferation of U87MG cells, the present study then sought to determine whether miR-204 would have any impact on migration and invasion in U87MG cells. The migration and invasion assay demonstrated that the overexpression of miR-204 not only inhibited migration of U87MG cells, but also suppressed their invasion (Fig. 9D). Moreover, we observed that miR-204 inhibits proliferation in LN-229 glioblastoma cells (Fig. 10).

Figure 9. miR-204 is downregulated in glioblastoma and its overexpression inhibits proliferation, migration and invasion in glioblastoma U87MG cells. (A) Northern blot analysis for miR-204 in glioblastoma tissues (C) and adjacent normal tissues (N). β-actin was used as the loading control. n=7. (B) MTT assay for U87MG cells. U87MG cells were transfected with pre-miR-204 (precursors miRNA) and control miR (mock) and cell viability was then measured at the indicated time points using an MTT assay. n=3. (C) BrdU incorporation assay for U87MG cells transfected with pre-miR-204 or control miR (mock). n=3. (D) Matrigel invasion assay and Transwell migration assay for U87MG cells transfected with pre-miR-204 or control miR (mock). n=3. Error bars indicate standard error of the mean. miR, microRNA; BrdU, bromodeoxyuridine.

Figure 10. Overexpression of miR-204 inhibits proliferation in glioblastoma LN-229 cells. MTT assay for LN-229 cells. LN-229 cells were transfected with pre-miR-204 and control miR (mock) and cell viability was then measured at the indicated time points using an MTT assay. n=3. Error bars indicate standard error of the mean.

Discussion

Increased CYP27A1 expression was detected in aberrant crypt foci, and adenomatous polyps, as well as the expression of CYP27A1 protein is associated with tumor grade in breast cancer (4,14). In the present study, it was identified that overexpression of CYP27A1 promoted proliferation in glioblastoma cells and silencing it inhibited proliferation, indicating that it may be an oncogene. However, its overexpression and silencing it did not affect migration and invasion in glioblastoma cells. PDCD4, a known tumor suppressor gene, has been identified as a functional target of miR-21 (15,16). Silencing of SOX2 in glioblastoma tumor-initiating cells causes the cessation of proliferation and loss of tumorigenicity (17). It was observed that CYP27A1 overexpression significantly downregulated PDCD4 and upregulated the SOX2 protein in glioblastoma cells, indicating that CYP27A1 may perform an important role in the regulation of tumor-initiating cells.

In addition, CYP27A1 was found to be upregulated in glioblastoma tissues. However, only collected 6 pairs of glioblastoma tissues and adjacent normal tissues were collected. Thus, future studies should use a bigger sample size.

Previous studies have reported that miR-204 is a tumor suppressor miRNA: miR-204 can suppress head and neck tumor metastasis (18); higher tumor grade of human clear cell renal cell carcinomas was associated with a concomitant decrease in miR-204 (19); loss of miR-204 expression enhances glioma migration and stem cell-like phenotype (20); miR-204 targets B-cell lymphoma-2 expression and enhances responsiveness of gastric cancer (21); and miR-204 downregulates sirtuin 1 (SIRT1) and reverts SIRT1-induced epithelial-mesenchymal transition, anoikis resistance and invasion in gastric cancer cells (22). Dysregulation of miR-204 mediates migration and invasion of endometrial cancer by regulating fork head box C1 (23). miR-204 increases sensitivity of neuroblastoma cells to cisplatin and is associated with a favorable clinical outcome (24). Consistent with these previous studies (18–24), it was identified that miR-204 was not only downregulated in glioblastoma, and inhibited proliferation, migration and invasion in glioblastoma cells. The present study also revealed that overexpressing miR-204 inhibited CYP27A1 expression in glioblastoma cells, indicating that the downregulation of miR-204 is associated with the upregulation of CYP27A1 in the disease. It was concluded that miR-204 inhibited proliferation by suppressing CYP27A1 expression. However, it was observed that CYP27A1 did not affect migration and invasion in glioblastoma cells, although miR-204 inhibited migration and invasion. This observation indicated that there are other target genes regulated by miR-204, which may regulate migration and invasion in glioblastoma cells.

Recently, the U-87 MG cell line from ATCC was reported to be contaminated or misidentified (25). It has been proposed as a glioblastoma cell line whose origin is unknown (25). However, the U-87 MG cell line is still widely used for glioblastoma research (25). In the present study, U87MG and LN-229 cells were used. The results were same from the 2 cell lines. Thus, the contamination or misidentification does not affect the conclusion presented.

Elucidating the mechanism by whichmiR-204 inhibits proliferation by suppressing CYP27A1 may help to improve the understanding of the molecular mechanism of proliferation in glioblastoma. Thus, restoration of miR-204 may represent a promising therapeutic way to inhibit CYP27A1-mediated proliferation regulation. However, the roles of CYP27A1 require confirmation in vivo.

Acknowledgements

Not applicable.

Funding

The present study was supported by Yishui Central Hospital and Linyi People's Hospital.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

JX and LQT conceived the study, collected the experimental data and wrote a draft of the manuscript. LMZ, DKS, XFL, and PX contributed to the experimental work and data analysis. All authors edited and approved the final version of the manuscript.

Ethics approval and consent to participate

Ethics approval was obtained from ethics committee of Yishui Central Hospital. All subjects provided written informed consent at the time of enrollment.

Consent for publication

Consent for publication was obtained from each patient.

Competing interests

The authors declare that they have no competing financial interests.

References