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Introduction

Cholangiocarcinoma (CCA; a fatal bile duct cancer) is a major public health concern in the Lower Mekong Basin and South East Asia, which are areas endemic for Opisthorchis viverrini liver fluke infection (1). The prognosis of CCA is principally poor because the majority of patients with CCA are diagnosed at an advanced stage, therefore they are inoperable and there are no effective treatments available (2). Additionally, CCA is prone to developing multidrug chemoresistance (3,4). Therefore, there is a requirement to investigate novel targeted therapies and strategies to enhance chemosensitivity of CCA.

We previously demonstrated that the alteration of cytoprotective enzymes or derangement of intracellular redox balance and the signaling system were involved in the chemoresistance of CCA (5–8). NAD(P)H:quinone oxidoreductase 1 (NQO1; EC 1.6.5.2), one of the detoxifying enzymes with antioxidant properties, has been proposed to be associated with the chemotherapeutic response of CCA (5,8). NQO1 is generally recognized as a ‘cell protector’, its induction in response to various noxious stimuli provides protection for cells against oxidative damage and oxidative stress-associated pathological conditions including cancer (9,10). Conversely, an increasing number of studies revealed abnormal increases in NQO1 expression levels in solid tumors of the adrenal gland, breast, colon, lung, ovary, pancreas, thyroid, skin and bladder (9–16). High-level expression of NQO1 may be associated with cancer progression and it was suggested to be a poor prognostic marker of these types of cancer (14,16,17). Upregulation of NQO1 during carcinogenesis may provide cancer cells with a growth advantage and protection against extreme oxidative stress environments (10,11). Considering the function of NQO1, an increased NQO1 expression level may be associated with disappointing outcomes to certain cancer treatment modalities, including chemotherapy and radiotherapy, which induces cancer cell death by the generation of free radicals and oxidative damage (5,8).

The roles of NQO1 during carcinogenesis and chemotherapeutic response have been demonstrated by numerous previous studies (11,18,19). Inhibition of NQO1 by a pharmacological inhibitor, dicoumarol, suppressed urogenital and pancreatic cancer cell growth and also potentiated cytotoxicity of cisplatin and doxorubicin (18,20). Similarly, the roles of NQO1 in CCA have been previously demonstrated (5,8,17,21). Significant association between high NQO1 expression level in CCA tissues and short survival time of patients was observed (17), implying NQO1 is an independent predictor associated with prognosis of CCA. Furthermore, dicoumarol was able to enhance gemcitabine-induced cytotoxicity in CCA cells with increased NQO1 activity (5). In addition, knockdown of NQO1 expression levels enhanced the cytotoxicity of chemotherapeutic agents; conversely, overexpression of NQO1 protected the cells from chemotherapeutic agents (8). These results suggested roles for NQO1 in CCA chemotherapy; however, the biological role of NQO1 in CCA cells has not yet been clearly demonstrated.

The aim of the present study was to investigate the biological role of NQO1 in CCA cells. The effects of NQO1 knockdown on cell proliferation, cell cycle and migration were assessed in KKU-100 CCA cells, which notably expressed NQO1. Furthermore, the molecular events associated with NQO1 small interfering RNA (siRNA)-induced inhibition of cell proliferation, inducing cell cycle arrest and inhibiting migration of CCA cells were investigated.

Materials and methods

Human cell line and cell culture

KKU-100 cells with high expression levels of NQO1 were provided by Professor Banchob Sripa (Department of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand). KKU-100 cells were established, characterized and derived from CCA tissues (22). Cells were routinely cultured in Ham's F-12 complete medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (Gibco; Thermo Fisher Scientific, Inc.), 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (pH 7.3), 100 U/ml penicillin G and 100 µg/ml streptomycin, and maintained under an atmosphere of 5% CO2 at 37°C. Cells were passaged every 3 days using 0.25% trypsin-EDTA (2).

NQO1 siRNA transfection

The transfection of NQO1 siRNA was performed using four sequences of predesigned NQO1 siRNA (siGENOME SMARTpool of siRNA M-005133-02-0010; Dharmacon Inc., Lafayette, CO, USA), as described previously (8). The NQO1 siRNA and the negative control siRNA (siGENOME non-targeting siRNA pool#2 D-001206-14-20) at a final concentration of 100 nM siRNA were introduced to the cells using Lipofectamine™ 2000 (Invitrogen; Thermo Fisher Scientific, Inc.) as a transfection reagent, according to the manufacturer's protocol. The efficiency of the NQO1 knockdown by transient NQO1 siRNA transfection was confirmed by evaluating levels of gene expression by performing the reverse transcription-quantitative polymerase chain reaction (RT-qPCR), protein expression levels by performing western blot analysis and NQO1 enzyme activity using an enzymatic assay.

Clonogenic survival assay

Cells with NQO1 siRNA were used in the colony formation assay. KKU-100 cells were transfected with NQO1 siRNA then seeded in 6-well plates at densities of 300 and 600 cells/well in Ham's F-12 complete medium. Two cell densities were used to confirm the effect of NQO1 siRNA on replicative potential of KKU-100 cells. Cells were cultured at 37°C in a 5% CO2 incubator for another 10 days to obtain cell colonies and the Ham's F-12 complete medium was freshly renewed every 3 days. On the last experiment day, the cell colonies were fixed with absolute methanol at room temperature (25°C) for 20 min, stained with 0.5% crystal violet solution at room temperature (25°C) for 15 min and the number of cell colonies was counted (23).

Cell cycle analysis using flow cytometry

KKU-100 cells were seeded in a 6-well plate with a density of 150,000 cells/well in Ham's F-12 complete medium, transfected with NQO1 siRNA for 24 h and then starved for 12 h using serum-free Ham F-12 medium at 37°C and 5% CO2. At 24 h post-starvation, the cell cycle distribution was evaluated using flow cytometric analysis. On the experimental day, cells were harvested, washed with PBS and fixed overnight with 70% cold ethanol at 4°C. Subsequently, the cell suspension was maintained at −20°C for 3 h, followed by the addition of 0.02 mg/ml propidium iodide and 0.02 mg/ml RNase A (Ameresco, Inc., Framingham, MA, USA). The cell suspension was incubated further for 1 h at 4°C in the dark. The cell cycle stage content was evaluated using a BD FACSCanto II flow cytometer and determined using BD FACSDiva™ software v6.1.3 (BD Biosciences, San Jose, CA, USA). The service was provided by the Research Instrument Center, Khon Kaen University, Thailand.

Cell motility by wound healing and Transwell migration assays

Cells with NQO1 siRNA were used in the wound-healing and Transwell migration assays. For the wound-healing assay, KKU-100 cells transfected with NQO1 siRNA were seeded in a 24-well plate at a cell density of 150,000 cells/well in Ham's F-12 complete medium at 37°C with 5% CO2 overnight to obtain 90–100% cell confluence. On the next day, cells were scratched to create a straight wound using a sterile 200-µl pipette tip. Following scratching, the cells were washed twice with PBS to remove any detached cells and further incubated for 72 h at 37°C and 5% CO2. The width of the wound outline was monitored under a phase-contrast microscope at designed times; 0, 3, 6, 12, 24, 48 and 72 h.

For the Transwell migration assay, KKU-100 cells transfected with NQO1 siRNA were seeded onto a 6.5 mm Transwell insert (Corning Incorporated, Corning, NY, USA) at a cell density of 75,000 cells/well in serum-free Ham's F-12 medium at 37°C with 5% CO2, while the lower parts of the chambers were filled with Ham's F-12 complete medium. Following a 24-h incubation, cells were fixed with absolute methanol for 20 min and stained with 0.05% crystal violet solution for 15 min. The number of migrated cells on the lower surface of the filters was counted under a light microscope (Eclipse Ni-U; Nikon Corporation, Tokyo, Japan).

Western blot analysis

In order to determine the expression levels of p21, cyclin D1 and cyclin A protein, western blot analysis was performed. KKU-100 cells were seeded in a 6-well plate at a cell density of 150,000 cells/well in Ham's F-12 complete medium and transfected with NQO1 siRNA for 24 h. Then cells were serum-starved for 12 h using serum-free Ham F-12 medium at 37°C in at atmosphere containing 5% CO2 and grown in Ham's F-12 complete medium for a further 24 h. Following this, the cells were harvested for western blot analysis. Cells were washed twice with PBS and lysed with radioimmunoprecipitation assay cell lysis buffer supplemented with dithiothreitol, phenylmethylsulfonyl fluoride (PMSF) and protease inhibitor cocktail (Ameresco, Inc.) at 4°C for 15 min. The concentration of extracted proteins was determined using Bradford reagent, according to the manufacturer's protocol (Bio-Rad Laboratories, Inc., Hercules, CA, USA). Whole cell lysate containing 30 mg protein was separated by SDS-PAGE using a 10% polyacrylamide gel. The separated proteins were then transferred onto polyvinylidene difluoride membranes (EMD Millipore, Billerica, MA, USA). The membranes were blocked for 1 h at room temperature with 5% non-fat milk in PBS supplemented with 0.1% Tween-20. They were then probed with rabbit polyclonal anti-human cyclin D1 (dilution, 1:1,000; #sc-718), rabbit polyclonal anti-human cyclin A (dilution, 1:2,000; #sc-751), mouse monoclonal anti-human p21 (dilution, 1:500; #sc-56335) or horseradish peroxidase (HRP)-conjugated goat polyclonal anti-human β-actin (dilution, 1:5,000; #sc-1616) primary antibodies for 12 h at 4°C (all antibodies were from Santa Cruz Biotechnology, Inc., Dallas, TX, USA). The membranes were then incubated with HRP-conjugated goat anti-mouse IgG (dilution, 1:5,000; #sc-2005) or HRP-conjugated goat anti-rabbit IgG (dilution, 1:5,000; #sc-2004) secondary antibodies for 2 h at room temperature (both from Santa Cruz Biotechnology Inc.). The membranes were incubated with enhanced chemiluminescence (ECL) substrate solution (Amersham™ ECL™ Prime Western Blotting detection reagent; GE Healthcare Life Sciences, Chalfont, UK) for 1 min at room temperature (25°C). The optical densities of the protein bands were determined using ImageQuant™ LAS4000 (GE Healthcare Life Sciences) (8).

RT-qPCR

In order to determine the mRNA expression levels of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs), RT-qPCR was performed. KKU-100 cells were seeded in a 6-well plate with density of 150,000 cells/well in Ham's F-12 complete medium, transfected with NQO1 siRNA for 24 h and then starved for 12 h using serum-free Ham F-12 medium at 37°C and 5% CO2. At 24 h post-starvation, total RNA was extracted from CCA cells using TRIzol® reagent was obtained from Thermo Fisher Scientific, Inc., according to a previously described method (8). A cDNA synthesis mixture consisting of 1 µg total RNA and 4 µl 5x iScript™ Reverse Transcription Supermix for RT-qPCR (170–8841; Bio-Rad Laboratories, Inc.) was mixed with RNase-free water in a total volume of 20 µl. cDNA synthesis was performed using a C1000™ thermal cycler (Bio-Rad Laboratories, Inc.). The cDNA synthesis conditions included priming for 5 min at 25°C and reverse transcription for 30 min at 42°C, and the reaction was stopped by incubation for 15 min at 70°C. The reverse transcription products served as templates for qPCR. PCR amplification was performed using specific primers for the MMP2, MMP3, MMP9, TIMP1, TIMP2 and the internal control β-actin. The primer sequences were as follows: i) MMP2 (NM_004530) (24), forward primer 5′-AGCTCCCGGAAAAGATGGATG-3′ and reverse primer 5′-CAGGGTGCTGGCTGAGTAGAT-3′; ii) MMP3 (NM_002422) (25), forward primer 5′-GCGTGGATGCCGCATATGAAGTTA-3′ and reverse primer 5′-AAACCTAGGGTGTGGATGCCTCTT-3′; iii) MMP9 (NM_002422) (26), forward primer 5′-GAAGATGCTGCTGTTCAGCG-3′ and reverse primer 5′-ACTTGGTCCACCTGGTTCAA-3′; iv) TIMP1 (NM_003254) (27), forward primer 5′-AGGCTCTGAAAAGGGCTTCCA-3′ and reverse primer 5′-GAGTGGGAACAGGGTGGACA-3′; v) TIMP2 (NM_003255) (28), forward primer 5′-GACGGCAAGATGCACATCAC-3′ and reverse primer 5′-GAGATGTAGCACGGGATCATGG-3′; vi) β-actin (NM_001101) (8), forward primer 5′-TGCCATCCTAAAAGCCAC-3′ and reverse primer 5′-TCAACTGGTCTCAAGTCAGTG-3′. The reverse-transcription fluorescence PCR, based on EvaGreen® dye, was performed in a final volume of 20 µl of 1x SsoFast™ EvaGreen® Supermix (172–5201; Bio-Rad Laboratories, Inc.), 0.5 µmol/l MMP2, MMP3, MMP9, TIMP1 or TIMP2 primer and 0.25 µmol/l β-actin primer. A negative control (no cDNA template) was included in the experimental runs. The qPCR was performed for each gene in duplicate on cDNA samples in 96-well reaction plates using LightCycler® 480 Real-Time PCR System (Roche Applied Science, Madison, WI, USA). The cycling conditions for qPCR were: 95°C for 3 min, followed by 40 cycles of 95°C for 15 sec and 60°C for 31 sec. To verify the purity of the products, a melting curve analysis was performed following each run. The concentration of PCR products was evaluated on the basis of an established standard curve derived from serial dilutions of the positive control for MMP2, MMP3, MMP9, TIMP1, TIMP2 and β-actin.

Statistical analysis

Data were expressed as the mean ± standard error of the mean from three independent experiments (SigmaPlot Version 10.0; Systat Software, Inc., San Jose, CA, USA). Statistical comparison between the control and treatment groups was performed using Student's t-test. P<0.05 was considered to indicate a statistically significant difference (SigmaStat Version 3.11; Systat Software, Inc.).

Results

Knockdown of NQO1 expression suppresses the cell proliferation of KKU-100 cells

The efficiency of NQO1 siRNA transfection in KKU-100 cells was established using qPCR, western blot analysis and NQO1 enzymatic assay (Fig. 1). Knockdown of NQO1 transcripts using siRNA transfection efficiently decreased NQO1 expression at the mRNA and protein levels, and enzymatic activity by ~90, ~60 and ~50%, respectively compared with the non-targeting siRNA-transfected control cells (P<0.001; Fig. 1). To investigate the role of NQO1 on CCA cell proliferation, NQO1-knockdown cells using siRNA were subjected to the clonogenic survival assay. The colony formation, as an index of long-term cell proliferation, was observed by plating the cells at low densities (300 and 600 cells/well; Fig. 2). NQO1-knockdown CCA cells exhibited a decreased number of colonies formed compared with control cells (Fig. 2). A significant antiproliferative effect of NQO1 siRNA was observed between days 6 and 10. At 10 days of culture, the NQO1 siRNA decreased colony formation by ~24 and ~37% when cells were plated at 300 and 600 cells/well, respectively, compared with the non-targeting siRNA-transfected control cells (P<0.05; Fig. 2). These results suggested that knockdown of NQO1 transcripts using siRNA transfection decreases the ability of CCA cells to grow and proliferate, resulting in a decrease in colony formation. Therefore, these results implied that NQO1 may serve a role in CCA cell growth and proliferation.

Figure 1. NQO1 siRNA was effectively transfected in KKU-100 cells. NQO1-knockdown cells using siRNA were used to assess levels of (A) NQO1 mRNA, (B) NQO1 protein and (C) NQO1 enzyme activity by quantitative polymerase chain reaction, western blot analysis and enzymatic assays, respectively. Data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 vs. control. NQO1, NAD(P)H:Quinone oxidoreductase 1; siRNA, small interfering RNA; NT, non-targeting siRNA; OD, optical density.

Figure 2. NQO1 siRNA reduced KKU-100 cell proliferation. NQO1-knockdown cells using siRNA were subjected to clonogenic survival assay. NQO1-knockdown CCA cells were plated at cell densities of (A) 300 and (B) 600 cells/well and cultured for another 10 days. The cell colonies were counted at 6, 8 and 10 days. (C) Representative images of the clonogenic survival assay of the cell density at 600 cells/well cultured for 8 days. Data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 vs. control. NQO1, NAD(P)H:quinone oxidoreductase 1; siRNA, small interfering RNA; NT, non-targeting siRNA.

Knockdown of NQO1 expression arrests the cell cycle progression of KKU-100 cells

To investigate the role of NQO1 on the regulation of the CCA cell cycle, NQO1-knockdown cells using siRNA were subjected to cell cycle analysis using a flow cytometer. The results demonstrated that NQO1-knockdown CCA cells significantly accumulated at the G1 phase with a decreased proportion of cells at the S phase compared with the non-targeting siRNA-transfected control cells (P<0.05; Fig. 3A). Therefore, these results suggested that NQO1 serves a role in cell cycle progression in CCA cells.

Figure 3. NQO1 siRNA (A) induced cell cycle arrest and (B) altered the expression of cell cycle and proliferation-associated proteins in KKU-100 cells. NQO1-knockdown cells using siRNA were synchronized by 12-h starvation, cultured for another 24 h and then subjected to flow cytometric analysis. (A) The cell cycle distribution at 24 h post-synchronization. (B) western blot analysis was performed using anti-p21, -cyclin D1, -cyclin A and β-actin antibodies. The expression levels of proteins were normalized using β-actin as a loading control for each band. Data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 vs. control. NQO1, NAD(P)H:quinone oxidoreductase 1; siRNA, small interfering RNA; NT, non-targeting siRNA.

Knockdown of NQO1 expression contributes to altered levels of p21 and cyclin D1 protein

The suppression of cell proliferation and arrestment of cell cycle in KKU-100 cells by NQO1 siRNA transfection led to further experiments investigating the influence of NQO1 knockdown on the expression levels of proteins which are associated with cell proliferation and cell cycle. The effect of NQO1 siRNA on the expression levels of p21, cyclin A and cyclin D1 protein was observed by western blot analysis. Knockdown of NQO1 transcripts using siRNA transfection significantly increased p21 and decreased cyclin D1 protein expression levels compared with in the non-targeting siRNA-transfected control cells (P<0.05; Fig. 3B); however, cyclin A protein expression levels remained the same. As p21 and cyclin D1 are important cell cycle regulator proteins for G1 and S phases, altered expression levels of p21 and cyclin D1 protein in NQO1-knockdown cells may induce CCA cells arrest at the G1 phase. These results provided evidence for the biological role of NQO1 in cell proliferation and cell cycle regulation of CCA cells.

Knockdown of NQO1 expression delays CCA cell migration

To investigate the role of NQO1 on CCA cell migration, wound healing and Transwell migration assays were performed. Knockdown of NQO1 transcripts using siRNA transfection efficiently delayed cell migration, and this suppressive effect was observed early at 6 h and continued until 72 h (P<0.05; Fig. 4A). To confirm the anti-migration effect of NQO1 siRNA, a Transwell migration assay was additionally performed. The results revealed that NQO1-knockdown CCA cells significantly lost their migration ability, as presented in Fig. 4B (P<0.05). The cell migration of NQO1-knockdown CCA cells decreased by ~60% compared with the non-targeting siRNA-transfected control cells. Therefore, NQO1 siRNA exhibited anti-migration ability on CCA cells as observed using wound healing and Transwell migration assays, and it was concluded that NQO1 serves a role in the migration of CCA cells.

Figure 4. NQO1 siRNA delayed cell migration in KKU-100 cells. NQO1-knockdown cells using siRNA were subjected to (A) wound healing and (B) Transwell migration assays. (A) Representative images of the wound healing assays. The distance of cell migration into the scratched area was imaged (x4 phase-contrast microscope) and measured at various times. The wound space was determined as the percentage of wound distance at initial time (0 h). (B) The Transwell migration assay was performed using modified Transwell chambers. Representative images of the Transwell migration assay. By systematical selection, 6 fields/well were imaged (x10 phase-contrast microscope) at 24 h. The number of cells migrated to the lower surface was evaluated as a percentage of the control relative migration. The scale bar shows 100 µm. Data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 vs. control. NQO1, NAD(P)H:quinone oxidoreductase 1; siRNA, small interfering RNA; NT, non-targeting siRNA; T, time.

Knockdown of NQO1 expression contributes to altered MMP/TIMP mRNA ratios

Further to demonstrating the biological role of NQO1 in CCA cell migration, the effects of NQO1 knockdown on expression levels of migration-associated genes were investigated using RT-qPCR. The RT-qPCR results revealed that knockdown of NQO1 transcripts using siRNA transfection did not alter expression levels of MMP2, MMP3 and MMP9, but tended to increase level of TIMP1 and significantly increased the expression level of TIMP2 mRNA compared with control cells (data not shown). The effects of NQO1 knockdown on the MMP/TIMP mRNA ratios, which are generally recognized as the index of the relative inhibition of MMP activity (24,29), were analyzed. NQO1-knockdown CCA cells demonstrated a decreased MMP9/TIMP1 ratio compared with in the control cells (P<0.05; Fig. 5); suggesting that NQO1 siRNA has an inhibitory effect on MMP activity. The suppression of MMP activity in NQO1-knockdown cells provided evidence of the biological role of NQO1 in the migration of CCA cells.

Figure 5. NQO1 siRNA decreased MMP/TIMP ratios. NQO1-knockdown cells using siRNA were subjected to RT-qPCR analysis. The mRNA levels of MMP2, MMP3, MMP9, TIMP1 and TIMP2 were normalized using β-actin mRNA as an internal control of each gene expression. The (A) MMP/TIMP1 and (B) MMP/TIMP2 mRNA ratios were determined in order to evaluate the relative inhibition of the MMP activity. Data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 vs. control. RT-qPCR, reverse transcription-quantitative polymerase chain reaction; NQO1, NAD(P)H:quinone oxidoreductase 1; siRNA, small interfering RNA; MMP, matrix metalloproteinase; TIMP, tissue inhibitor of metalloproteinases; NT, non-targeting siRNA.

Discussion

The involvement of NQO1 in various types of cancer has previously been demonstrated (9–16). The upregulation of NQO1 in certain types of solid tumor, including CCA (17), was associated with poor prognosis, thus NQO1 targeting has therapeutic potential (10,11). The present study investigated the biological role of NQO1 in cell proliferation, cell cycle and migration of CCA. The in vitro experiments revealed that knockdown of NQO1 expression compromised the proliferation and reproductive ability of cells, arrested cell cycle progression and inhibited the motile capacity of CCA cells. Therefore, suppression of NQO1 may be a potential target for the treatment and/or strategy to enhance the chemosensitivity of CCA and other types of cancer with increased NQO1 activity.

Previous studies have suggested possible growth-inhibitory effects triggered by NQO1 suppression (11,18,19). Dicoumarol, a potent inhibitor of the NQO1 enzyme, inhibited cell growth of pancreatic cancer cells in a dose-dependent manner (30), whereas a higher dose of dicoumarol decreased colony formation on soft agar of pancreatic cancer cells (18). For HeLa cells, treatment with dicoumarol resulted in a marked decrease in the viability of cells and proliferation rate (28). In accordance with these findings, the results of the present study demonstrated that knockdown of NQO1 in CCA cells significantly impaired cell proliferative ability. These results provide evidence suggesting the role of NQO1 in maintaining the ability of cell proliferation and replication.

The cell cycle, a series of events leading to cell division and duplication, is a key regulatory process in cell growth and proliferation (31). In the present study, flow cytometric analysis revealed that NQO1 knockdown induced G1 phase arrest and decreased the proportion of cells at the S phase, which may have contributed to the inhibition of proliferation in the NQO1-knockdown cells. In order to elucidate the possible molecular mechanism underlying NQO1-mediated inhibition of the proliferation and reproductive capacities of CCA cells, western blot analysis was performed to identify the influence of NQO1 siRNA on the expression levels of p21, cyclin A and cyclin D1 proteins. The results of the present study demonstrated that the upregulation of p21 and downregulation of cyclin D1 proteins were associated with the NQO1 expression level, which indicated that these two proteins serve important roles in the process of antiproliferation and cell cycle arrest triggered by NQO1 siRNA. A similar observation was previously revealed in melanoma cells, where knockdown of NQO1 decelerated the transition of melanoma cells from G1 to G2-M phase (32). Knockdown of NQO1 in melanoma cells also induced downregulation of cyclins D1, A2 and B1 (32). Furthermore, treatment with dicoumarol increased the number of cells that accumulated in the sub-G1 phase (33).

Cell migration serves an important role in the cancer progression (34). The ability of NQO1 to drive human aortic vascular smooth muscle cell migration and invasion was previously demonstrated (35). Treatment with dicoumarol or transfection with NQO1 siRNA suppressed tumor necrosis factor α-induced cell migration by inhibiting MMP9 protein and mRNA expression (35,36). In the present study, NQO1 siRNA significantly decreased the migratory ability of CCA cells, which suggested a role for NQO1 in promoting the metastasis of CCA. In order to elucidate the potential molecular mechanism underlying NQO1-mediated inhibition of the motility of the CCA cells, RT-qPCR analysis was performed to investigate the influence of NQO1 siRNA on the expression levels of MMP2, MMP3, MMP9, TIMP1 and TIMP2 mRNA. It was revealed that NQO1 siRNA exhibited an inhibitory effect on MMP activity by altering the MMP/TIMP mRNA ratio, which indicated that NQO1 serves a role in the process of cell migration of CCA.

In conclusion, to the best of our knowledge, the results of the present study provided evidence for the first time that NQO1 serves a key role in cell proliferation, cell cycle and migration of CCA cells. Furthermore, NQO1 siRNA demonstrated an antiproliferative effect in KKU-100 cells by upregulation of p21 and downregulation of cyclin D1 proteins. Additionally, NQO1 siRNA revealed an anti-migratory effect by decreasing the MMP9/TIMP1 mRNA ratio. Therefore, the results of the present study highlighted the biological role of NQO1 maintaining the ability of cell proliferation and replication and migration in CCA. Thus, NQO1 may be a potential molecular target to enhance CCA treatment and other types of cancer with increased NQO1 activity.

Acknowledgements

This present study was supported by Khon Kaen University Thailand Research Fund (grant no. RMU5380027), Faculty of Medicine (grant no. I57206) and a scholarship from the National Research University Project and Office of Higher Education Commission through the Specific Health Problem in Greater Mekong Sub-region project of Khon Kaen University to S.B.

References