LncRNA loc285194 inhibits tumor growth of laryngeal squamous cell carcinoma cells by downregulating hexokinase 2
- Yan Gao
- Zhongqiao Wang
- Jing Tong
- Yan Zheng
- Published online on: July 9, 2019 https://doi.org/10.3892/etm.2019.7761
- Pages: 2378-2384
Copyright: © Gao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Tumor growth serves pivotal roles in cancer development and progression. Chemical drugs that inhibit tumor cell growth are used in the treatment of cancer (1). Laryngeal squamous cell carcinoma (LSCC) is a rare malignancy, accounting for ~2% of all cancer cases (2). However, LSCC is considered to be a major cause of cancer-associated mortality due to its aggressive nature and rapid development (3). In spite of the efforts made to prevent and treat LSCC, the survival rate of patients with this disease remains poor (4). Therefore, novel therapeutic approaches with higher efficacies are required to improve treatment outcomes in patients with LSCC. It has been reported that tumor size is associated with the prognosis of patients with LSCC (5). Therefore, the identification of factors that can regulate tumor growth in patients with LSCC may provide guidance for the treatment of LSCC.
Hexokinase 2 (HK-2) is an enzyme in the human body that can phosphorylate glucose to produce glucose-6-phosphate, which is typically the initial step in glucose metabolism (6). The overexpression of HK-2 is frequently observed in the progression of different types of cancer, and the upregulated expression of HK-2 in certain types of cancer accelerates cell growth and promotes cancer progression (7–9). Thus, the inhibition of HK-2 expression is considered to be a promising therapeutic target for cancer treatment (10). HK-2 achieves its biological roles through its interactions with different cellular factors, including long (>200 nucleotides) non-coding RNAs (lncRNAs), which are a heterogeneous group of RNA transcripts with pivotal roles in human diseases due to their regulatory roles in gene expression (11). LncRNA loc285194 has been reported to have tumor suppressive functions in certain types of malignancies (12), while its involvement in LSCC remains unclear. Our preliminary data of microarray revealed an association between HK-2 and loc285194 (data not shown). The present study aimed to assess the involvement of lncRNA loc285194 in the pathogenesis of LSCC via its interaction with HK-2.
Materials and methods
Subjects and specimens
The current study included 66 patients with LSCC, who were diagnosed at the Affiliated Second Hospital Xinjiang Medical University between January 2015 and March 2017. The inclusion criteria were as follows: i) Patients diagnosed through laryngeal biopsies; ii) patients received treatment for the first time; iii) patients willing to join the study. The exclusion criteria were as follows: i) Patients complicated with other malignancies (102 patients were excluded); ii) patients who were treated prior to admission (12 cases were excluded); iii) patients with chronic diseases (45 patients were excluded); iv) blood relatives (2 patients were excluded). Among those patients, 10 cases were in American Joint Committee on Cancer stage II, 12 in stage III, 9 in stage IVA, 12 in stage IVB and 23 in stage IVC. The patients included 36 males and 30 females with ages ranging between 24 and 66 years, and a mean age of 44.5±6.6 years. During the same time period, 92 people received laryngeal biopsies to detect suspected laryngeal lesions and laryngeal lesions were excluded in 39 cases. Among these 39 cases, laryngeal biopsies were obtained from 28 cases to match the age and sex distributions of patient group and to serve as control group. The present study was approved by the Ethics Committee of The Affiliated Second Hospital Xinjiang Medical University. All participants signed informed consent. Laryngeal biopsies were obtained from the specimen library of the Affiliated Second Hospital Xinjiang Medical University. All specimens were stored in liquid nitrogen (−195.79°C) prior to use.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) was used to extract total RNA. All operations were performed in accordance with manufacturer's protocol. cDNA was synthesized through reverse transcription using SuperScript III Reverse Transcriptase (Thermo Fisher Scientific, Inc.) under the following conditions: 50°C for 30 min and 75°C for 15 min. qPCR was performed using SYBR® Green Real-Time PCR Master Mix (Thermo Fisher Scientific, Inc.) with following primers: lncRNA loc285194 forward, 5′-TGTGCCTGTTTGACCTCTGA-3′ and reverse, 5′-AGGAAGGATAAAAGACCGACCA-3′; HK-2 mRNA forward, 5′-AAGGCTTCAAGGCATCTG-3′ and reverse, 5′-CCACAGGTCATCATAGTTCC-3′; β-actin forward, 5′-GACCTCTATGCCAACACAGT-3′ and reverse, 5′-AGTACTTGCGCTCAGGAGGA-3′. The qPCR reaction conditions were as follows: 50 sec at 95°C, followed by 40 cycles of 20 sec at 95°C and 40 sec at 59°C. The 2−ΔΔCq method was used for data normalization (13).
Cell lines, cell culture and cell transfection
Human LSCC cell line UM-SCC-17A (EMD Millipore, Billerica, MA, USA) and normal larynx cell line HuLa-PC (American Type Culture Collection, Manassas, VA, USA) were used in this study. Cells of each cell line were cultured with DMEM containing 10% fetal bovine serum (FBS; Sangon Biotech Co., Ltd. Shanghai, China) at 37°C with 5% CO2. Full-length loc285194 and HK-2 cDNAs were amplified through PCR using primers with NheI cutting site at the 5′ end. Loc285194 and HK-2 cDNAs were inserted into pIRSE2 vector (Clontech Laboratories, Inc., Mountainview, CA, USA) to construct loc285194 and HK-2 expression vectors. Loc285194 and HK-2 expression vectors were transfected into 5×105 cells at a dose of 10 nM using Lipofectamine 2000 reagent (Thermo Fisher Scientific, Inc.). Cells without transfection were used as control cells. Cells transfected with empty vector were used as negative control cells. The expression of loc285194 and HK-2 was confirmed by RT-qPCR 12 h after transfection. Subsequent experiments were performed only in cases where an overexpression rate of >200% compared with control cells and negative control cells was reached.
Cell Counting Kit-8 (CCK-8) assay
Cell proliferation was detected using a CCK-8 assay. Briefly, cell suspensions (1% FBS) with a cell density of 5×104 cells/ml were prepared. Subsequently, 5×103 cells in 0.1 ml cell suspension were added into each well of a 96-well plate. Cells were cultured at 37°C in a 5% CO2 incubator, followed by addition of 10 µl CCK-8 solution (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) 24, 48, 72 and 96 h later. Cells were cultured for additional 4 h and Fisherbrand™ accuSkan™ GO UV/Vis microplate spectrophotometer (Thermo Fisher Scientific, Inc.) was used to measure the optical density values at 450 nM.
Western blot analysis
RIPA solution (Thermo Fisher Scientific, Inc.) was mixed with cultured cells to extract total protein. Subsequently, a bicinchoninic acid assay was performed to measure protein concentration. Protein samples were denatured and subjected to 10% SDS-PAGE gel electrophoresis with 45 µg protein/lane. Subsequently, PVDF membranes were blocked in 5% skimmed milk at room temperature for 1 h, followed by incubation with rabbit anti-human primary antibodies against HK-2 (1:1,200; cat. no. ab37593; Abcam, Cambridge, UK) and GAPDH (1:2,000; cat. no. ab8245; Abcam) at 4°C overnight. The following day, a goat anti-rabbit IgG-horseradish peroxidase secondary antibody (1:1,000; cat. no. MBS435036; MyBioSource, San Diego, CA, USA) was used to further incubate with membranes at 25°C for 2 h. Then, ECL (Sigma-Aldrich, Merck KGaA) was added to develop the signals. Signals were normalized using ImageJ v1.46 software (National Institutes of Health, Bethesda, MD, USA).
Data analyses were performed using GraphPad Prism 6 software (GraphPad Software, Inc., La Jolla, CA, USA). Gene expression and cell proliferation data are presented as the mean ± standard deviation. One-way analysis of variance followed by the least significant difference test among multiple groups or unpaired t-test between two groups was used. Associations between loc285194 expression and clinicopathological data of LSCC patients were analyzed using the Chi-square test. Correlations between expression of loc285194 and HK-2 mRNA were analyzed using the Pearson correlation coefficient. The diagnostic value of loc285194 and HK-2 mRNA for LSCC was evaluated using receiver operating characteristic curve analysis (ROC). Origin Pro 8.0 (OriginLab, Northampton, MA, USA) was used to calculate statistical power. Statistical power >90% was reached in all cases. All data provided sufficient statistical power. P<0.05 was considered to indicate a statistically significant difference.
Loc285194 is downregulated and HK-2 mRNA is upregulated in patients with LSCC compared with healthy controls
The expression of loc285194 and HK-2 mRNA in laryngeal biopsies of patients with LSCC or healthy controls was detected using RT-qPCR. As shown in Fig. 1A, loc285194 expression was significantly downregulated in patients with LSCC compared with that in healthy controls (P<0.05). In contrast, HK-2 mRNA was significantly upregulated in LSCC patients compared with that in healthy controls (Fig. 1B; P<0.05).
Loc285194 is downregulated and HK-2 mRNA is upregulated in patients with LSCC compared with in healthy controls. Comparison of loc285194 and HK-2 mRNA expression revealed (A) significantly downregulated loc285194 expression and (B) significantly upregulated HK-2 mRNA expression in patients with LSCC compared with in healthy controls. *P<0.05. LSCC, laryngeal squamous cell carcinoma; HK-2, hexokinase 2.
Loc285194 and HK-2 mRNA are potential diagnostic biomarkers for LSCC
ROC curve analysis was performed to evaluate the diagnostic values of loc285194 and HK-2 mRNA for LSCC (Fig. 2). For loc285194, the area under the curve (AUC) was 0.8810 [standard error (SE), 0.03499; 95% confidence interval (CI), 0.8124–0.9405; P<0.0001]. For HK-2 mRNA, the AUC was 0.8239 (SE, 0.04211; 95% CI, 0.7413–0.9064; P<0.0001).
Loc285194 and HK-2 mRNA are potential diagnostic biomarkers for LSCC. Receiver operating characteristic curve analysis revealed that (A) downregulation of loc285194 and (B) upregulation of HK-2 mRNA effectively distinguished patients with LSCC from healthy controls. LSCC, laryngeal squamous cell carcinoma; HK-2, hexokinase 2; AUC, area under the curve.
loc285194 and HK-2 mRNA expression levels are inversely correlated in patients with LSCC, but not in healthy controls
The correlation between the expression levels of loc285194 and HK-2 mRNA was analyzed using the Pearson correlation coefficient. A significantly inverse correlation was identified between the expression levels of loc285194 and HK-2 mRNA in patients with LSCC (Fig. 3A). In contrast, no significant correlation between loc285194 and HK-2 mRNA expression levels was observed in healthy controls (Fig. 3B).
Expression of loc285194 and HK-2 mRNA is inversely correlated in LSCC patients, but not in healthy controls. Pearson correlation coefficient revealed a significant inverse correlation between the expression of loc285194 and HK-2 mRNA in (A) patients with LSCC, but not in (B) healthy controls. LSCC, laryngeal squamous cell carcinoma; HK-2, hexokinase 2.
Expression of loc285194 is significantly associated with tumor size, but not distant tumor metastasis
Patients were divided into high and low expression groups according to the median expression level of loc285194 (1.72). The association between loc285194 and clinicopathological data of patients with LSCC was analyzed using the Chi-square test. As shown in Table I, loc285194 expression was not significantly associated with the age, sex, smoking and drinking habits of patients as well as the presence of tumor metastasis. In contrast, a significant association was observed between loc285194 expression and primary tumor size.
Loc285194 is an upstream activator of HK-2 in LSCC cells
Cells with transient loc285194 and HK-2 were produced, and the expression of loc285194 and HK-2 was detected by RT-qPCR and western blot analysis. As shown in Fig. 4A, compared with the control cells and negative control cells, loc285194 overexpression significantly inhibited the expression of HK-2 in the human LSCC UM-SCC-17A cell line, but not in the normal HuLa-PC larynx cell line (P<0.05). In contrast, HK-2 overexpression demonstrated no significant effects on loc285194 expression in the UM-SCC-17A and HuLa-PC cell lines (Fig. 4B).
Loc285194 is an upstream activator of HK-2 in LSCC cells. The data demonstrates (A) the effects of loc285194 overexpression on HK-2 expression and (B) the effects of HK-2 overexpression on loc285194 expression. *P<0.05. LSCC, laryngeal squamous cell carcinoma; HK-2, hexokinase 2; C, control; NC, negative control.
Loc285194 overexpression inhibits HK-2 expression and LSCC cell proliferation
A CCK-8 assay was performed to detect cell proliferation following loc285194 and HK-2 overexpression. As shown in Fig. 5, loc285194 overexpression led to significantly inhibited HK-2 expression and LSCC cell proliferation compared with the control and negative control groups (P<0.05). In addition, HK-2 overexpression attenuated the inhibitory effects of loc285194 overexpression on LSCC cell proliferation (P<0.05). Loc285194 and HK-2 overexpression showed no significant effects on the proliferation of normal HuLa-PC cells.
Loc285194 overexpression inhibits and HK-2 overexpression promotes LSCC cell proliferation *P<0.05. The experiment was performed six times. LSCC, laryngeal squamous cell carcinoma; HK-2, hexokinase 2; C, control; NC, negative control.
One of the key findings of the present study demonstrated that loc285194, a well-studied tumor suppressor lncRNA in several types of human malignancies, may also participate in the regulation of tumor growth, but not tumor metastasis in patients with LSCC. The action of loc285194 in LSCC is likely to be achieved though interactions with HK-2.
LncRNA loc285194 is a tumor suppressor gene that is downregulated in several types of cancer, including esophageal squamous cell carcinoma (14), pancreatic ductal adenocarcinoma (15) and colorectal cancer (16). In the present study, significantly downregulated expression of lncRNA loc285194 was observed in patients with LSCC comparing with healthy controls. The downregulation of lncRNA loc285194 effectively distinguished patients with LSCC from healthy controls, indicating the potential role of lncRNA loc285194 as a tumor suppressor in LSCC.
Accelerated glucose metabolism distinguishes cancer cells from normal cells (17). HK-2 is a key player in glycolysis and is usually upregulated in the development of cancer (18). In a study on LSCC, Chen et al (9) reported that HK-2 is overexpressed in patients with LSCC and the overexpression of HK-2 promotes tumor growth. Consistent with this study, the results of the current study reported that HK-2 was significantly upregulated in patients with LSCC compared with in healthy controls and HK-2 overexpression significantly promoted the proliferation of LSCC cells cultured in vitro. In addition, the overexpression of HK-2 effectively distinguished patients with LSCC from healthy controls.
In the present study, lncRNA loc285194 expression was demonstrated to be significantly associated with tumor size, but not the existing of tumor metastasis, indicating the involvement of lncRNA loc285194 in the regulation of tumor growth. It has been reported that the expression of HK-2 can be regulated by certain lncRNAs (11,19). The results of the current study suggest that lncRNA loc285194 serves as an upstream inhibitor of HK-2 in LSCC. This conclusion may be made based on following observations: i) lncRNA loc285194 overexpression led to a significantly upregulation of HK-2 expression in LSCC cells; ii) HK-2 overexpression showed no significant effects on lncRNA loc285194 expression; iii) the overexpression of HK-2 significantly attenuated the inhibitory effects of lncRNA loc285194 on LSCC cell proliferation. However, the regulatory role of lncRNA loc285194 on HK-2 is unlikely to be direct due to the lack of significant correlation between lncRNA loc285194 on HK-2 in healthy controls and the absence of inhibitory effects of loc285194 expression on HK-2 expression.
Notably, lncRNA loc285194 overexpression demonstrated no significant effects on biological behaviors of normal larynx cells. Therefore, lncRNA loc285194 may serve as a potential therapeutic target for LSCC. However, a previous study has reported that smaller LSCC tumor size is more significantly correlated with an unfavorable prognosis of patients with LSCC (5). Therefore, the correlation between lncRNA loc285194 expression and the prognosis of LSCC patients remains to be further investigated. Overexpression of lncRNA loc285194 also failed to affect the expression of other players in glucose metabolism, such as glucose transporter protein type 1–3 (data not shown). Therefore, lncRNA loc285194 may specifically regulate HK-2. The present study failed to perform HK-2 and loc285194 knockdown assays due to the unsatisfactory knockdown rate. Future studies intend to perform knockdown assays.
In conclusion, the results of the current study demonstrated that lncRNA loc285194 is significantly downregulated in patients with LSCC. LncRNA loc285194 may participate in the regulation of tumor growth in LSCC through the inhibition of HK-2 expression.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
YZ guaranteed the integrity of the entire study. YZ, YG and ZW provided the study concepts. YG and ZW were responsible for the study design, the definition of intellectual content, and for literature research. YG, ZW and JT were responsible for clinical and experimental studies. JT was responsible for data acquisition. YG and ZW were responsible for data analysis, statistical analysis, manuscript preparation, manuscript editing and manuscript review.
Ethics approval and consent to participate
This study got approval from the ethics committee of the Affiliated Second Hospital Xinjiang Medical University. All participants signed informed consent.
Patient consent for publication
The authors declare that they have no competing interests.
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