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. 2020 Jul 22;13:7111–7123. doi: 10.2147/OTT.S243542

Long Non-Coding RNA DUXAP8 Facilitates Cell Viability, Migration, and Glycolysis in Non-Small-Cell Lung Cancer via Regulating HK2 and LDHA by Inhibition of miR-409-3p

Dianhe Yin 1,*, Li Hua 2,*, Jiao Wang 1, Yuru Liu 1,✉, Xiaoyan Li 1
PMCID: PMC7383025  PMID: 32801745

Abstract

Purpose

Long non-coding RNAs (lncRNAs) were confirmed to play important roles in human cancers. In this study, we explored the functional role of lncRNA double homeobox A pseudogene 8 (DUXAP8) in non-small-cell lung cancer (NSCLC).

Methods

Real-time quantitative PCR (RT-qPCR) was used to detect DUXAP8 and microRNA-409-3p (miR-409-3p) expression. CCK-8, cell colony formation assay, and Transwell migration assay were performed to measure cell growth and migration, respectively. The expression of the relative proteins was detected by Western blot. Cell glycolysis was determined by glucose uptake, adenosine triphosphate (ATP) concentration, lactate generation, extracellular acidification rate and oxygen consumption rate assays. Bioinformatics analysis and dual-luciferase reporter assay were used to measure the interaction among DUXAP8, miR-409-3p, hexokinase 2 (HK2) and lactate dehydrogenase A (LDHA). In vivo, subcutaneous tumor formation assay was performed in the nude mice.

Results

DUXAP8 was highly expressed in NSCLC, while miR-409-3p was downregulated. High expression of DUXAP8 was positively related to the grade division and negatively associated with the 5-year survival rate of NSCLC patients. Downregulated DUXAP8 significantly suppressed cell growth, metastasis and glycolysis. Besides, DUXAP8 sponged miR-409-3p to promote HK2 and LDHA expression. DUXAP8 promoted cell viability, migration and glycolysis by regulating miR-409-3p/HK2/LDHA axis. Moreover, DUXAP8 downregulation markedly inhibited tumor growth in vivo.

Conclusion

Our findings demonstrated that DUXAP8 served as an oncogene in the progression of NSCLC.

Keywords: non-small-cell lung cancer, DUXAP8, miR-409-3p, HK2, LDHA

Introduction

Non-small-cell lung cancer (NSCLC), one of the leading causes related to cancer deaths, is the most common type of lung cancer accounting for about 80%.1 Unfortunately, approximately 80% NSCLC patients were diagnosed at the advanced stage.2 Despite the molecular targeting therapy, chemotherapy and surgery had achieved advanced development, the 5-year survival rate of NSCLC patients is extremely poor, even less than 15%.3,4 NSCLC is a particularly complex tumor that is involved in the genetic dysregulation of tumor suppressor genes and protooncogenes, as well as multiple preneoplastic pathways.5 However, the biomarkers and molecular mechanisms for NSCLC early diagnosis, treatment, and prognosis remain largely lack and unclear.

Long non-coding RNAs (LncRNAs), with approximately 200 nucleotides, are a group of transcribed RNA sequences that do not possess the ability to encode proteins.6,7 LncRNAs played crucial regulatory roles in maintaining genome structure, gene transcription and translation, as well as epigenetic regulation.8,9 Accumulating evidence demonstrated the essential biological functions of lncRNAs in the tumorigenesis of multiple malignancies.10 The derived lncRNA double homeobox A pseudogene 8 (DUXAP8) with a length of 2107 bp is located on chromosome 22q11.1. DUXAP8 was confirmed to facilitate the proliferation and metastasis of renal cell carcinoma cells,11 bladder cancer cells,12 and hepatocellular carcinoma cells.13 However, the effects and the underlying molecular mechanisms of DUXAP8 in NSCLC are still largely unknown.

MicroRNAs (miRNAs) are a series of non-coding, single-stranded RNAs with the length of 19~25 nucleotides that can lead to RNA degradation or translation inhibition of target mRNA through pairing with the 3ʹuntranslated region (3ʹUTR) of the target gene.14,15 MiRNAs were involved in the pathogenesis of varieties of human cancers, which could target mRNAs to regulate the tumorigenesis and the crucial biological processes of tumors, including cell growth, differentiation, metastasis, as well as cell apoptosis.16,17 Accumulating evidence revealed that dysregulation of miRNAs was closely correlated with the development of tumors.18 Several researches reported that microRNA-409-3p (miR-409-3p) was aberrantly expressed in many malignant cancers, such as colon cancer,19 breast cancer,20 as well as NSCLC.21 Nevertheless, the functional effects of miR-409-3p on NSCLC are not fully elucidated.

Aerobic glycolysis (also known as the Warburg effect), accompanying with the upregulated levels of lactate production and glucose uptake even in the condition with abundant oxygen, is regarded as a common and essential feature of cancer cells that can facilitate tumor growth.22,23 Thus, increasing researchers focused on the ectopic energy metabolism of cancer cells, which might be the novel potential pathway for cancer treatment. Hexokinase 2 (HK2) and lactate dehydrogenase A (LDHA) are essential drivers in the processes of glycolysis. HK2 is an enzyme participating in the initial and rate-limiting step of glycolysis that can convert glucose to glucose-6-phosphate. LDHA participates in the process through converting pyruvate into lactate, which is the final step of glycolysis.24,25 Increasing evidence suggested that HK2 and LDHA played promotion roles in human cancers.26,27 Thus, it is necessary to explore the functional effects of HK2 and LDHA on NSCLC progression.

In this research, the expression of DUXAP8 was determined in NSCLC. Functionally, the effects of DUXAP8 on the progression of NSCLC were explored both in vivo and in vitro. Mechanistically, the potential regulatory mechanism of DUXAP8 in the development of NSCLC was investigated.

Patients and Methods

Patients and Tissue Samples

66 pairs of NSCLC tissues and the adjacent normal tissues were collected from 66 NSCLC patients, who were pathologically diagnosed as NSCLC and underwent surgery at Huaihe Hospital of Henan University. NSCLC patients did not treat with any preoperative anti-tumor methods. All participants provided the written informed consents. This study was approved by the Human Research Ethics Committee of Huaihe Hospital of Henan University.

Cell Lines and Culture

The normal human lung epithelial cells BEAS-2B and NSCLC cell lines (H1299, A549, H460 and PC-9) were used in this study. BEAS-2B, H1299, A549 and H460 cells were purchased from American Type Culture Collection (Manassas, VA, USA), and PC-9 cells were bought from Shanghai Zeye Biological Technology Co. Ltd. (Shanghai, China). BEAS-2B and A549 cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM, Gibco, Carlsbad, CA, USA) and H1299, H460 and PC-9 cells were incubated with Roswell Park Memorial Institute 1640 (RPMI-1640) medium (Gibco), while DMEM and RPMI-1640 were supplemented with streptomycin/penicillin (100 U/mL; Invitrogen, Carlsbad, CA, USA) and 10% fetal bovine serum (FBS; Invitrogen). All the cells were cultured in a humidified chamber at 37°C with a condition of 5% CO2.

Cell Transfection

Small interfering RNAs (siRNAs) targeting DUXAP8 (si-DUXAP8 #1: 5ʹ- AAGATAAAGGTGGTTTCCACAAGAA-3ʹ; si-DUXAP8 #2: 5ʹ-GGAACTTCCCAAACCTCCATGATTT-3ʹ; si-DUXAP8 #3: 5ʹ-CAGCATACTTCAAATTCACAGCAAA-3ʹ) and the control si-NC (5ʹ-UUCUCCGAACGUGUCACGUTT-3ʹ), miR-409-3p mimic and the corresponding control group (NC mimic), DUXAP8 overexpression vector (DUXAP8) and the control vector (Vector), miR-409-3p inhibitor and the control (NC inhibitor) purchased from Genepharma (Shanghai, China) were transfected into A549 and H1299 cells using Lipofectamine 3000 Reagent (Invitrogen).

Real-Time Quantitative Polymerase Chain Reaction (RT-qPCR)

Total RNA was isolated from NSCLC tumorous tissues and the adjacent normal tissues, as well as NSCLC cells and BEAS-2B cells using Trizol reagent (Invitrogen). Briefly, total RNA was reverse-transcribed using SuperScript III RT (Invitrogen) under standard conditions, and then the amplified transcript level of the specific gene was determined by a real-time quantitative PCR system. The expression of miR-409-3p and DUXAP8 was normalized by U6 and glyceraldehyde 3-phosphate dehydrogenase (GAPDH), respectively. The primer sequences of specific genes were as follows, DUXAP8: AGACGCCATGGAACAT (sense) and AAGCGGAGACCTGAGGAG (antisense), miR-409-3p: GGGGAATGTTGCTCGGTGA (sense) and CAGTGCGTGTCGTGGAGT (antisense), U6: CTCGCTTCGGCAGCACA (sense) and AACGCTTCACGAATTTGCGT (antisense), GAPDH: AAGGCTGAGAATGGGAAAC (sense) and TTCAGGGACTTGTCATACTTC (antisense). The relative expression of DUXAP8 and miR-409-3p was determined by the 2 −∆∆Ct method.

Cell Viability

Cell viability was detected by Cell Counting Kit-8 (CCK-8) assay. 100 μL cell suspension containing 2 × 103 cells was plated into the 96-well plates and then incubated for 24 h. Then, cells were cultured with 10 μL CCK-8 solution (Dojindo, Tokyo, Japan). Finally, the absorbance was determined at 450 nm after transfection for 24 h, 48 h, and 72 h.

Colony Formation Assay

The selected A549 and H1299 cells with the density of 0.5 × 103 cells per well were seeded into the 6-well plates after transfection for 48 h. Then, cells were incubated for 2 weeks. Subsequently, cells were washed using phosphate-buffered saline, fixed with methanol, stained with 0.1% crystal violet, and counted by a microscope (Bio-Rad Laboratories Inc., Hercules, CA, USA).

Cell Migration

The number of the migrated NSCLC cells was measured by transwell migration assay. After transfection, 3 × 104 cells maintained in serum-free medium were added into the higher chamber, while the lower chamber was supplemented with 500 μL medium. After 48 h incubation, the not migrated cells were removed, while the migrated NSCLC cells on the lower chamber were fixed with 4% paraformaldehyde. Then, the migrated cells were stained with crystal violet, followed by counting in 5 randomly selected fields.

Western Blot

The involved protein expression was examined by Western blot analysis. Total protein was extracted from the transfected A549 and H1299 cells, as well as the mice tumor tissues by RIPA lysis buffer (Beyotime, Shanghai, China). 30 μg total protein was separated by 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Then, the proteins were transferred onto a polyvinylidene difluoride (PVDF) membrane (Thermo Fisher Scientific, Waltham, MA, USA). Subsequently, the membrane was incubated with 5% skim milk (dissolved in TBST buffer) for 1 h at room temperature. The proteins were incubated with the primary antibodies against c-myc (1:1000, 18,583, Cell Signaling Technology (CST), Boston, MA, USA), Cyclin D1 (1:200, ab16663, Abcam, Cambridge, UK), matrix metalloprotein 9 (MMP9, 1:1000, 13,667, CST), E-cadherin (E-cad, 1:1000; 14,472, CST), HK2 (1:1000, ab104836, Abcam), LDHA (1:2000, ab101562, Abcam) and GAPDH (1:1000, ab8245, Abcam) overnight at 4°C, followed by incubating with the secondary antibodies including goat anti-mouse IgG H&L (1:2000, ab205719, Abcam) or goat anti-rabbit IgG H&L (1:2000, ab6721, Abcam) for 2 h. Finally, the signals of proteins were visualized by an electrochemiluminescent system (PerkinElmer Life Science, Waltham, MA, USA).

Determination of Glucose Uptake, Lactate and ATP

The levels of lactate production, glucose uptake, and ATP production were detected by Lactate Assay Kit II, Glucose Uptake Colorimetric Assay Kit, and ATP Colorimetric Assay Kit (BioVision, Milpitas, CA, USA) according to the manufacturer’s instructions, respectively. For the examination of glucose uptake, the transfected cells with the density of 1 × 104 cells per well were seeded into the 96-well plate, followed by culturing in 100 mL Krebs-Ringer-Phosphate-HEPES (KRPH) buffer supplemented with 2% albumin from bovine serum for 40 min. Then, 10 mM 2-deoxyglucose (2-DG) was added and the cells were cultured for 20 min. For the measurement of lactate and ATP production, 1 × 104 cells were suspended in the buffer from the corresponding assay kit. Then, the samples were centrifuged at 4°C for analyzing the soluble fraction.

Extracellular Acidification (ECAR) and Oxygen Consumption Rate Assays (OCR)

In the present study, we used the Seahorse Extracellular Flux Analyzer XF96 (Seahorse Bioscience, North Billerica, MA, USA) to calculate ECAR and OCR in NSCLC cells. After 48 h transfection, cells (2 × 104 per well) were plated into the XF96-well plate and cultured overnight. For ECAR determination, glucose, oligomycin (oxidative phosphorylation inhibitor), and 2-DG (glycolytic inhibitor) were sequentially added into the NSCLC cells in culture. For OCR determination, cells were sequentially cultured with oligomycin, the reversible inhibitor of oxidative phosphorylation FCCP, and Rotenone/antimycin A. Data were analyzed by Seahorse XF-96 Wave software. ECAR detection was noted as mpH/min, and OCR was represented as pmol/min.

Dual-Luciferase Reporter Assay

HEK293T cells were seeded into the 6-well plates and cultured for 24 h. The wild-type sequences of DUXAP8 (WT-DUXAP8), HK2 (WT-HK2 3ʹUTR) and LDHA (WT-LDHA 3ʹUTR) were constructed and inserted into pGL3 promoter vector (Invitrogen). The primer sequences for cloning DUXAP8 or the 3ʹ-UTR of HK2 and LDHA were as below: 5ʹ-GGTGGGTTCCATGTGATGGT-3ʹ (Forward) and 5ʹ-GTCTTCTGAGAAACATTGTGCCA-3ʹ (Reverse) for DUXAP8; 5ʹ-TGGTGTTAGGAAAGTCGCCC-3ʹ (Forward) and 5ʹ-AGGAAGGGCCTACTCACAGT-3ʹ (Reverse) for HK2; 5ʹ-TAGTCTGATTTCCGCCCACC-3ʹ (Forward) and 5ʹ-ACCGCTTCCAATAACACGGT-3ʹ (Reverse) for LDHA. The potential DUXAP8, HK2 and LDHA binding sites for miR-409-3p were mutated by Quick-change site-directed mutagenesis kit (Agilent Technologies, Santa Clara, CA, USA), named as MUT-DUXAP8, MUT-HK2 3ʹUTR and MUT-LDHA 3ʹUTR reporter plasmids. Then, HEK293T cells were co-transfected with 400 ng of these constructed plasmids (WT-DUXAP8, WT-HK2 3ʹUTR, WT-LDHA 3ʹUTR or MUT-DUXAP8, MUT-HK2 3ʹUTR, MUT-LDHA 3ʹUTR), 50 ng of renilla luciferase reporter plasmid (pRL-TK) and 50 nM of miR-409-3p mimic or NC mimic using Lipofectamine 3000 (Invitrogen). After 48 h transfection, the relative luciferase activity was measured by a dual-luciferase reporter assay system (Promega, Madison, WI, USA). Renilla luciferase activity was used as normalization.

Xenograft Experiment

The 4–6 weeks old BALB/c nude mice bought from Beijing Laboratory Animal Center (Beijing, China) were used in this study. A549 cells were stably transfected with short hairpin RNA against DUXAP8 (sh-DUXAP8) or sh-NC (Genepharma, Shanghai, China). Approximately 1 × 106 sh-DUXAP8/sh-NC-infected A549 cells were subcutaneously inoculated into the flanks of the nude mice (5 per group). Tumor volume was detected every 3 days from 6 day using a caliper. After 30 days, the mice were euthanized and tumor weight was assessed. All experiments were performed in line with the Guide for the Care and Use of Laboratory Animals and approved by the Huaihe Hospital of Henan University Experimental Animal Ethics Committee.

Statistical Analysis

All data were represented as the mean ± the standard deviations (SD) and analyzed by SPSS 18.0 software. Comparisons between groups were calculated using Student’s t-test or One-way ANOVA. Pearson correlation analysis was used to analyze the relationship between miR-409-3p and DUXAP8. Kaplan–Meier was used to measure the overall survival. P < 0.05 was regarded as statistically significant.

Results

DUXAP8 Was Upregulated and Associated with Low Overall Survival in NSCLC Patients

We detected the expression of DUXAP8 in 66 tumorous tissues and the paired adjacent normal tissues from NSCLC patients using RT-qPCR. A significant increase of DUXAP8 was observed in tumor tissues compared with the normal tissues (Figure 1A). The data showed that DUXAP8 expression was markedly upregulated in 51 NSCLC tissues (Figure 1B). The data in Figure 1C suggested that DUXAP8 was significantly higher in the advanced Tumor Node Metastasis stage (Stage III+IV) relative to the low Stage I+II. We also determined the association between DUXAP8 and lymph node metastasis and found that high expression of DUXAP8 was positively correlated with lymph node metastasis in NSCLC patients (Figure 1D). Besides, the overall survival of NSCLC patients with high DUXAP8 expression was shorter than the low DUXAP8 expression group (Figure 1E). These results demonstrated that DUXAP8 served as an oncogenic role in NSCLC and higher expression of DUXAP8 was correlated with shorter overall survival.

Figure 1.

Figure 1

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DUXAP8 was upregulated and associated with the low overall survival rate in NSCLC patients. (A) The expression of DUXAP8 in NSCLC tissues (n=66) and the adjacent normal tissues (n=66) was detected by RT-qPCR. (B) RT-qPCR analysis was used to measure DUXAP8 expression in 66 pairs of NSCLC tissues and the corresponding non-tumor lung tissues. (C) DUXAP8 expression was examined in tumor tissues isolated from various TNM stage (I+II (n=31), III+IV (n=35)) NSCLC patients by RT-qPCR. (D) DUXAP8 expression in lymph node metastatic (n=41) and nonmetastatic (n=25) NSCLC tissues was assessed by RT-qPCR. (E) Kaplan–Meier survival curves and Log rank tests were used to explore the relationship between DUXAP8 expression and the 5-year overall survival rate of NSCLC patients; low DUXAP8 expression group (n=33) and high DUXAP8 expression group (n=33).

DUXAP8 Knockdown Inhibited Cell Viability and Migration of NSCLC Cells

Next, we measured the expression of DUXAP8 in NSCLC cells and BEAS-2B cells. RT-qPCR showed that DUXAP8 expression was higher in NSCLC cells (Figure 2A). To determine the biological functions of DUXAP8 in NSCLC, siRNAs against DUXAP8 were transfected into A549 and H1299 cells, which had the highest expression of DUXAP8. The data suggested that siRNAs against DUXAP8 significantly decreased the expression of DUXAP8 in both A549 and H1299 cells (Figure 2B). Next, si-DUXAP8 #1 was selected to perform the following experiments, which exerted the best knockdown efficiency in NSCLC cells. CCK-8 assay indicated that cell viability in A549 and H1299 cells transfected with si-DUXAP8 at 48h and 72 h was markedly inhibited in comparison to the control group (Figure 2C and D). Consistently, the number of colonies was significantly attenuated by DUXAP8 knockdown (Figure 2E). Moreover, transwell migration assay demonstrated that DUXAP8 knockdown could decrease the number of migrated NSCLC cells (Figure 2F). Subsequently, we detected the expression of cell viability-related proteins c-myc and Cyclin D1, as well as metastasis-related proteins MMP9 and E-cad. As described in Figure 2G and H, DUXAP8 knockdown significantly suppressed the expression of c-myc, Cyclin D1 and MMP9, and enhanced E-cad expression in both A549 and H1299 cells. All these results indicated that DUXAP8 downregulation inhibited cell growth and metastasis in NSCLC cells.

Figure 2.

Figure 2

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DUXAP8 knockdown inhibited the viability and migration of NSCLC cells. (A) DUXAP8 expression in BEAS-2B, H1299, A549, H460 and PC-9 cells was detected by RT-qPCR (n=3). (B) RT-qPCR was used to measure the expression of DUXAP8 in A549 and H1299 cells transfected with siRNAs against DUXAP8 or si-NC (n=3). (C and D) CCK-8 assay was used to determine the viability of NSCLC cells transfected with si-DUXAP8 or si-NC (n=3). (E) The number of colonies of NSCLC cells transfected with si-DUXAP8 or si-NC was detected by cell colony formation assay (n=3). (F) The migratory ability of NSCLC cells transfected with si-DUXAP8 or si-NC was examined by transwell migration assay (n=3). (G and H) The protein expression of c-myc, Cyclin D1, MMP9 and E-cad in NSCLC cells transfected with si-DUXAP8 or si-NC was detected by Western blot (n=3).

DUXAP8 Downregulation Dampened Glycolysis in NSCLC Cells

Glycolysis is related to multiple reactions that each glucose molecule can be converted to pyruvate to produce 2 adenosine triphosphate (ATP). The consumption of glucose in cancer cells can produce lactate, which is the final metabolism product of glycolysis, even in the environment with oxygen. Thus, we investigated whether DUXAP8 affected the glycolysis of NSCLC cells. DUXAP8 knockdown decreased glucose uptake, lactate production and ATP generation (Figure 3A–C). Additionally, the indicators of glycolysis, including ECAR and OCR, were calculated. ECAR can reflect overall glycolytic flux, while OCR can reflect mitochondrial oxidative respiration. As shown in Figure 3D and E, downregulation of DUXAP8 could significantly enhance OCR in both A549 and H1299 cells. DUXAP8 knockdown markedly suppressed ECAR in NSCLC cells (Figure 3F and G). We further measured the glycolysis-related proteins including HK2 and LDHA. The data suggested that DUXAP8 knockdown significantly reduced the expression of HK2 and LDHA in both A549 and H1299 cells (Figure 3H and I). These results collectively demonstrated that DUXAP8 knockdown inhibited the glycolysis in NSCLC cells.

Figure 3.

Figure 3

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DUXAP8 downregulation dampened the glycolysis in NSCLC cells. (A–C) Glucose uptake (A), lactate release (B), and ATP production level (C) were measured in A549 and H1299 cells transfected with si-DUXAP8 or si-NC by Glucose Uptake Colorimetric Assay Kit, Lactate Assay Kit II, and ATP Colorimetric Assay Kit, respectively (n=3). (D–G) The quantification of OCR (D and E) and ECAR (F and G) in NSCLC cells transfected with si-DUXAP8 or si-NC was measured by Seahorse Extracellular Flux Analyzer XF96 assays (n=3). (H and I) The protein expression of HK2 and LDHA in NSCLC cells transfected with si-DUXAP8 or si-NC was examined by Western blot analysis (n=3).

DUXAP8 Targeted MiR-409-3p to Regulate HK2 and LDHA Expression

To explore whether DUXAP8 functioned as a competing endogenous RNA, we searched DUXAP8 binding miRNAs using StarBase v2.0, which was further used to predict the potential binding miRNAs of HK2 and LDHA. Venn diagram showed that 101 miRNAs harbored the binding sites of DUXAP8, 197 miRNAs harbored the binding sites of HK2, and 85 miRNAs harbored the binding site of LDHA (Figure 4A). We found that there were 11 miRNAs simultaneously contained the binding sits of DUXAP8, HK2 and LDHA. Among the 11 miRNAs, miR-409-3p was identified as a candidate miRNA. RT-qPCR showed that the expression of miR-409-3p was significantly decreased in NSCLC tissues and cells (Figure 4B and C). Besides, we discovered a negative relationship between DUXAP8 and miR-409-3p in NSCLC tissues (Figure 4D). As described in Figure 4E, miR-409-3p harbored the binding sites of DUXAP8, HK2 and LDHA. To verify the predicted relationships, dual-luciferase reporter assay was carried out and the results suggested that the luciferase activity of the wild-type (WT) of DUXAP8, HK2 3ʹUTR and LDHA 3ʹUTR reporter vectors, but not (MUT) vectors, was markedly decreased in HEK293T cells transfected with miR-409-3p mimic compared with NC mimic group (Figure 4F–H).

Figure 4.

Figure 4

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DUXAP8 targeted miR-409-3p to regulate HK2 and LDHA expression. (A) The overlapped binding miRNAs were analyzed by Venn diagram. (B) The expression of miR-409-3p in NSCLC tissues was detected by RT-qPCR (n=3). (C) RT-qPCR was used to measure the expression of miR-409-3p in BEAS-2B, A549 and H1299 cells (n=3). (D) The relationship between DUXAP8 and miR-409-3p in NSCLC tissues was analyzed by Kaplan–Meier analysis (r = −0.322, P = 0.008) (n=3). (E) StarBase v2.0 predicted that miR-409-3p contained the binding sites of DUXAP8, HK2 and LDHA. (F and H) Dual-luciferase reporter assay was performed to determine the relative luciferase activity in 293T cells co-transfected with wild type (WT-) or mutant (MUT-) of DUXAP8, HK2 3ʹUTR or LDHA 3ʹUTR and miR-409-3p mimic or NC mimic (n=3). (I) The expression of DUXAP8 in NSCLC cells transfected with DUXAP3 or Vector was detected by RT-qPCR (n=3). (J) RT-qPCR was used to determine miR-409-3p expression in NSCLC cells transfected with si-NC, si-DUXAP8, Vector, or DUXAP8 (n=3). (K) RT-qPCR was used to detect the expression of miR-409-3p in NSCLC cells transfected with NC mimic, miR-409-3p mimic, NC inhibitor, or miR-409-3p inhibitor (n=3). (L) The protein expression of HK2 and LDHA in NSCLC cells transfected with NC mimic, miR-409-3p mimic, NC inhibitor, or miR-409-3p inhibitor was measured by Western blot (n=3).

Moreover, RT-qPCR indicated a successful overexpression efficiency of DUXAP8 in both A549 and H1299 cells (Figure 4I). As shown in Figure 4J, the expression of miR-409-3p was significantly increased by downregulating DUXAP8 and decreased by overexpressing DUXAP8 in NSCLC cells. Furthermore, miR-409-3p expression was upregulated in NSCLC cells transfected with miR-409-3p mimic, while the expression of miR-409-3p was downregulated in NSCLC cells transfected with miR-409-3p inhibitor (Figure 4K). We also detected the expression of HK2 and LDHA in A549 and H1299 cells transfected with miR-409-3p mimic, NC mimic, miR-409-3p inhibitor, or NC inhibitor, and the results suggested that the expression of HK2 and LDHA was markedly inhibited by overexpression of miR-409-3p, but enhanced by downregulation of miR-409-3p (Figure 4L). Taken together, we observed that DUXAP8 sponged miR-409-3p to regulate the expression of HK2 and LDHA.

MiR-409-3p Inhibitor Reversed Downregulation of DUXAP8-Mediated Cell Viability and Migration

To explore whether miR-409-3p was involved in DUXAP8-induced promotion effects on NSCLC cell viability and migration, we performed rescue experiments by co-transfecting si-DUXAP8 and miR-409-3p inhibitor into A549 and H1299 cells. As described in Figure 5A and B, downregulation of DUXAP8-impaired cell viability of NSCLC cells was reversed by miR-409-3p inhibitor. Besides, miR-409-3p downregulation rescued the reduction of the number of colonies and the migrated NSCLC cells transfected with si-DUXAP8 (Figure 5C and D). Subsequently, the involvement of protein expression, including c-myc, Cyclin D1, MMP9 and E-cad, was detected by Western blot. DUXAP8 downregulation induced the decrease of c-myc, Cyclin D1 and MMP9 expression, as well as the increase of E-cad expression in NSCLC cells, which were reversed by downregulating miR-409-3p (Figure 5E and F).

Figure 5.

Figure 5

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MiR-409-3p inhibitor reversed DUXAP8 downregulation-mediated cell viability and migration. A549 and H1299 cells were transfected with si-NC, si-DUXAP8, si-DUXAP8+NC inhibitor, or si-DUXAP8+miR-409-3p inhibitor. (A and B) Cell viability was detected by CCK-8 assay (n=3). (C and D) The number of colonies was assessed by cell colony formation assay (n=3). (E and F) The protein expression of c-myc, Cyclin D1, MMP9 and E-cad was determined by Western blot analysis (n=3).

MiR-409-3p Inhibitor Reversed the Inhibitory Effect of DUXAP8 Downregulation on Glycolysis

To confirm whether DUXAP8 might affect glycolysis via targeting miR-409-3p in NSCLC cells, we measured glucose uptake, lactate production and ATP generation. The data demonstrated that miR-409-p knockdown blocked the inhibitory effects of DUXAP8 knockdown on glucose uptake, lactate and ATP production in both A549 and H1299 cells (Figure 6A–C). Subsequently, we detected the ECAR and OCR in NSCLC cells transfected with si-NC, si-DUXAP8, si-DUXAP8+NC inhibitor, or si-DUXAP8+miR-409-3p inhibitor. OCR was facilitated by DUXAP8 downregulation in NSCLC cells, while miR-409-3p inhibitor could significantly attenuate OCR in both A549 and H1299 cells (Figure 6D and E). We also discovered that miR-409-3p inhibitor significantly reversed the reduction of ECAR induced by DUXAP8 knockdown in NSCLC cells (Figure 6F and G). Besides, Western blot analysis indicated that the suppressive effects of DUXAP8 knockdown on HK2 and LDHA expression were reversed by downregulating miR-409-3p in both A549 and H1299 cells (Figure 6H and I). Overall, these data suggested that miR-409-3p inhibitor reversed downregulation of DUXAP8-mediated NSCLC cell glycolysis.

Figure 6.

Figure 6

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MiR-409-3p inhibitor reversed the inhibitory effect of DUXAP8 downregulation on the glycolysis. A549 and H1299 cells were transfected with si-NC, si-DUXAP8, si-DUXAP8+NC inhibitor, or si-DUXAP8+miR-409-3p inhibitor. (A–C) The relative glucose uptake (A), lactate production (B), and ATP production (C) in A549 and H1299 cells were measured by Glucose Uptake Colorimetric Assay Kit, Lactate Assay Kit II, and ATP Colorimetric Assay Kit, respectively (n=3). (D–G) The quantification of OCR (D and E) and ECAR (F and G) in A549 and H1299 cells was calculated by Seahorse Extracellular Flux Analyzer XF96 assays (n=3). (H and I) Western blot analysis was used to examine the expression of HK2 and LDHA in A549 and H1299 cells (n=3).

DUXAP8 Knockdown Suppressed Tumor Growth in vivo

To validate the effect of DUXAP8 on tumor growth in vivo, we constructed A549 cells stably transfected with sh-DUXAP8 or sh-NC. Then, A549 cells stably transfected with sh-DUXAP8 or sh-NC were inoculated into the nude mice. We found that tumor volume was markedly suppressed in the sh-DUXAP8 mice group compared with the control group (Figure 7A). Moreover, tumor weight was also lower in the sh-DUXAP8 group than that in the si-NC group (Figure 7B). RT-qPCR analysis showed that the expression of DUXAP8 was lower, while miR-409-3p expression was higher in tumor tissues from the mice of the sh-DUXAP8 group than that in the control group (Figure 7C). We further determined the protein expression of HK2 and LDHA and discovered that downregulation of DUXAP8 could significantly decrease HK2 and LDHA expression in the tumor tissues from the nude mice (Figure 7D). These in vivo findings confirmed that DUXAP8 was essential for promoting tumor growth in NSCLC.

Figure 7.

Figure 7

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DUXAP8 knockdown suppressed tumor growth in vivo. (A and B) Tumor volume (A) and weight (B) of the nude mice injected with sh-NC or sh-DUXAP8 were measured (n=5). (C) RT-qPCR was used to measure the expression of DUXAP8 and miR-409-3p in tumor tissues (n=3). (D) The protein expression of HK2 and LDHA in tumor tissues was detected by Western blot analysis (n=3).

Discussion

Growing evidence confirmed that lncRNAs with ectopic expression were commonly observed in various human cancers, which might be biomarkers for the prediction, diagnosis, or prognosis of cancers.28 NSCLC is the most common malignancy in the lung, and the underlying mechanisms of NSCLC progression remain largely unknown. Recently, lncRNA DUXAP8 was confirmed to serve as an essential role in the occurrence and development of various cancers. For instance, Huang and his colleagues indicated that DUXAP8 expression was dramatically increased in glioma tissues, which was closely associated with the prognosis of glioma patients and exhibited significant promotion effects on cell growth.29 Thus, we determined the expression and functional role of DUXAP8 in NSCLC. Consistent with the results in the research from Sun and his colleagues,30 we discovered that the expression of DUXAP8 in NSCLC tissues and cells was significantly increased. Moreover, DUXAP8 expression was correlated with the TNM stage and positively related to the lymph node metastasis in NSCLC patients. Then, we performed the functional experiments to investigate the biological functions of DUXAP8 in NSCLC. We found that downregulation of DUXAP8 exerted significant inhibition effects on cell growth and migration in both A549 and H1299 cells. Meanwhile, DUXAP8 knockdown markedly reduced the expression of c-myc, Cyclin D1 and MMP9, and upregulated E-cad expression in NSCLC cells. We demonstrated that DUXAP8 played a promotion role in the progression of NSCLC in vitro. Furthermore, DUXAP8 knockdown suppressed tumor growth in NSCLC in vivo.

Recently, multiple researchers reported that the ectopic metabolism in cancer cells with the upregulated glucose uptake and lactate production was proved to improve the biological processes of cancer.31 Several lncRNAs were demonstrated to be intimately related to regulating aerobic glycolysis to facilitate cancer cell survival and growth.32 For example, PCGEM1 acted as a key regulator to reprogram energy metabolism through directly targeting c-myc in cancer.33 LINC01123 was highly expressed in NSCLC and facilitated cell growth, as well as aerobic glycolysis through targeting miR-199a-5p.34 In another study, lncRNA UCA1 exerted promotion effects on tumorigenesis through overexpressing the expression of HK2 in bladder cancer.35 Consistent with the previous research, our results indicated that DUXAP8 downregulation could inhibit uptake glucose, lactate release and ATP production in NSCLC cells. Furthermore, the key metabolic enzymes HK2 and LDHA played crucial roles in the processes of aerobic glycolysis, which participated in the progression of cancers.36,37 In this study, knockdown of DUXAP8 markedly repressed the expression of HK2 and LDHA in NSCLC cells.

Recently, multiple miRNAs, such as miR-181b,38 miR-98,39 and miR-449a,40 were confirmed to suppress HK2 or LDHA expression. In our study, we discovered that miR-409-3p harbored the binding sites of DUXAP8, HK2 and LDHA. Besides, DUXAP8 could directly sponge miR-409-3p to regulate HK2 and LDHA in NSCLC cells. Previous researches indicated that miR-409-3p functioned as a suppressor in the progression of lung cancer.41,42 Consistently, we observed that miR-409-3p was lowly expressed in NSCLC tissues and cells. Besides, miR-409-3p downregulation could reverse the effects of DUXAP8 knockdown on cell growth, migration and glycolysis, which further rescued by the reduction of HK2 and LDHA expression in NSCLC cells.

Conclusion

In conclusion, DUXAP8 was confirmed to be highly expressed in NSCLC tissues and cells, which was associated with the grade division and prognosis of NSCLC patients. Functionally, DUXAP8 promoted NSCLC cell growth, metastasis and glycolysis. Mechanistically, we found that DUXAP8 was involved in NSCLC progression by inhibiting miR-409-3p to regulate HK2 and LDHA expression. Our study provided a potential target for the treatment and prognosis of NSCLC, which could help to further understand the molecular mechanisms and progression of NSCLC.

Funding Statement

No funding was received.

Highlights

  1. DUXAP8 was highly expressed in non-small-cell lung cancer tissues and cells.

  2. DUXAP8 enhanced non-small-cell lung cancer cell viability, migration and glycolysis.

  3. DUXAP8 increased HK2 and LDHA expression by targeting miR-409-3p.

  4. DUXAP8 promoted non-small-cell lung cancer cell viability, migration and glycolysis via targeting miR-409-3p to regulate HK2 and LDHA expression.

Data Sharing Statement

The analyzed data sets generated during the present study are available from the corresponding author on reasonable request.

Ethics Approval and Consent to Participate

The present study was approved by the ethical review committee of Huaihe Hospital of Henan University.

Author Contributions

All authors contributed to data analysis, drafting or revising the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.

Disclosure

The authors declare that they have no competing interests.

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