Miconazole Contributes to NRF2 Activation by Noncanonical P62-KEAP1 Pathway in Bladder Cancer Cells.

PURPOSE: Nuclear factor (erythroid-derived 2)-like 2, also known as NFE2L2 or NRF2, a transcription factor capable of upregulating antioxidant response element (ARE)-mediated expression and cytoprotective proteins, plays critical roles in chemoprevention, inflammation and aging. NRF2 has recently been proposed as a novel target for cancer chemoprevention. The fungicide miconazole has shown promising antiproliferative effects in cancer cells.
MATERIALS AND METHODS: After miconazole treatment, the p62-KEAP1-NRF2 activation was analyzed by qPCR and Western blot. The nuclear translocation indicating NRF2 activation was further confirmed by immunofluorescence. Finally, the ROS production was detected by CM-H2DCFDA staining.
RESULTS: We demonstrate in this study that miconazole dramatically increases NRF2 activation in bladder cancer cells, in a dose- and time-dependent manner. Interestingly, levels of expression of p62, a noncanonical pathway that mediates NRF2 activation, appeared to increase in accordance with NRF2. We also investigated levels of the negative regulator kelch-like ECH-associated protein 1 (KEAP1), which is involved in NRF2 activation. As expected, a decrease in KEAP1 expression was found after miconazole exposure. Confirmation of NRF2 nuclear translocation was monitored by immunofluorescence. Miconazole-induced generation of reactive oxygen species (ROS) promoted NRF2 activation. Pretreatment of bladder cancer cells with ROS scavengers abolished NRF2 expression and nuclear translocation, indicating that miconazole activates the noncanonical p62-KEAP1-NRF2 pathway, which is regulated by ROS production.
CONCLUSION: Our study elucidates the mechanisms through which miconazole stimulates NRF2 which may contribute to cancer chemopreventive effects.

Introduction

Nuclear factor erythroid 2-related factor 2 (NRF2) is a 66-kDa transcription factor that coordinates cellular stress response thus against oxidative stress.1 Considerable evidence shows that NRF2 activators can prevent not only tumor progression but also various chronic diseases in which oxidative and inflammatory stress are crucial for pathogenesis.2–4 Ongoing clinical trials are investigating the antitumor activity of several NRF2 activators, including sulforaphane,5 curcumin,6 dimethyl fumarate,7 bardoxolone methyl8 and resveratrol.9 These agents may offer new a strategy for preventing tumor progression.10

It is well established that kelch-like ECH-associated protein 1 (KEAP1)-NRF2 system activation is the major oxidative stress response pathway.11 Analyses of the molecular components involved in NRF2 activation have demonstrated that its transcriptional activity is inhibited by KEAP1, a cytoplasmic, cysteine-rich, actin-bound protein that sequesters NRF2 in the cytoplasm. Under normal conditions, the transcription factor NRF2 is constitutively inactivated by ubiquitin-proteasome degradation. KEAP1, an adaptor of the ubiquitin ligase complex that targets NRF2, plays a major role in NRF2 degradation.12 When cells encounter oxidative stress or NRF2 activators, NRF2 quickly disassociates from KEAP1 and inhibits NRF2 degradation.13 Subsequently, the NRF2 translocates to the nucleus and regulates anti-oxidative stress genes by binding to antioxidant response elements (AREs).14 The noncanonical pathway by which p62/sequestosome 1 (SQSTM1), a key autophagy adaptor, promotes NRF2 nuclear translocation and activates ARE-related genes was reported in 2007.15 Subsequent investigations found that the interaction between p62 and KEAP1 enables p62 to sequester KEAP1 into autophagosomes and abrogate the ubiquitin-proteasome degradation of NRF2, preventing NRF2 activation.16,17 Previous findings have indicated that overexpression of p62 increases the degradation of KEAP1, suggesting that p62 plays a critical role in regulating KEAP1 turnover.18

Miconazole has long been used as an effective antifungal drug in humans.19 Systemic fungal infection is the major cause of morbidity and mortality in cancer patients, especially those with neutropenia. Antifungals, including miconazole, have been used as adjuvant therapy to decrease mortality in cancer patients with neutropenia.20,21 Miconazole exhibits antiproliferative effects in cancer cells.22 In an antitumor drug screening study, miconazole inhibited cell proliferation in breast cancer and bladder cancer.23 In preclinical testing, miconazole demonstrated antitumor effects through promoting cell apoptosis and G0/G1 cell cycle arrest in colon cancer.24 Miconazole has an inhibitory effect on melanogenesis in B16 melanoma cells25 and its antioxidative effects have already been investigated.26 However, the mechanisms involved in NRF2 activation of miconazole have not been well described. This study describes how miconazole promotes NRF2 activation and the key role played by the p62-KEAP noncanonical pathway in this activation.

Materials and Methods

Materials

Anti-mouse and anti-rabbit IgG-conjugated horseradish peroxidase, rabbit polyclonal antibodies specific for p62 (Abcam; Cambridge, UK; cat. No. ab109012), KEAP1 (Cell Signaling Technology, Inc.; Danvers, MA, USA; cat. No. #8047), NRF2 (GeneTex, Inc.; San Diego, CA, USA; cat. No. GTX103322) and β-Tubulin (Cell Signaling Technology, Inc.; Danvers, MA, USA; cat. No. #2146) were purchased from commercial companies. All other chemicals were obtained from Sigma-Aldrich (St Louis, MO, USA).

Cell Culture

Human bladder cancer cell lines (5637 and T24) were obtained from Bioresource Collection and Research Center (BCRC; Hsinchu, Taiwan) and maintained at 37°C under 5% CO2. 5637 and T24 cells were cultured in RPMI-1640 and McCoy’s 5a media, respectively. Culture media were supplemented with 10% FBS, 2 mM GlutaMAX-1, 100 units/mL penicillin and 100 μg/mL streptomycin. Cells were seeded on 96-well plates (5 x 103/well) or 6-well plates (5 x 105/well) or 10-cm dishes, 2 x 106/dish for cell viability assays and collection of RNA or protein samples.

Western Blot Analysis

The cellular lysates were prepared and proteins were resolved on SDS-PAGE and transferred to Immobilon polyvinyldifluoride (PVDF) membranes. The blots were blocked with 4% BSA for 1 hr at room temperature and then probed with mouse or rabbit primary antibodies (1:1000) overnight at 4°C. After undergoing three TBST washes, the blots were incubated with anti-rabbit or -mouse peroxidase-conjugated secondary antibody (1:1000) for 1 hr at room temperature. After another three washes with TBST, the blots were visualized with enhanced chemiluminescence using a ChemiDoc-It® Imaging System (UVP Inc., Upland, CA, USA). ImageJ software (National Institutes of Health, USA) was used to quantify Western blot results.

Quantitative Real-Time PCR

Quantitative real-time PCR (qPCR) analysis was carried out using Taqman® one-step PCR Master Mix (Applied Biosystems, Foster City, CA, USA). One hundred ng of total cDNA was added per 20-µL reaction with sequence-specific primers and Taqman probes. Sequences for all target gene primers and probes were purchased commercially (β-actin served as the internal control) from Applied Biosystems. Quantitative RT-PCR assays were carried out in triplicate on a StepOnePlus sequence detection system (Applied Biosystems). Cycling conditions consisted of 10 min of polymerase activation at 95°C followed by 40 cycles at 95°C for 15 sec and 60°C for 60 sec. The threshold was set above the non-template control background and within the linear phase of target gene amplification to calculate the cycle number at which the transcript was detected (denoted as CT).

Immunofluorescence Staining

BC cells were seeded on chamber slides (5 x 103 cells/well) for 24 hrs before the experiment. After treatment with miconazole alone or in the presence with ROS inhibitors (catalase, DPI and NAC) for 24 hrs. Cells were washed three times with PBS and fixed in 3.7% formaldehyde for 10 mins at room temperature. Cells were washed three times with PBS and blocked with 4% BSA for 15 mins. Cells were then incubated with the p62 (Abcam; Cambridge, UK; cat. No. ab109012) or NRF2 (Genetex; cat. No. GTX103322) primary antibodies (1:100) overnight at 4°C. Twenty-four hour later, the cells were washed again by PBS for three times and incubated with Alexa Fluor 488 secondary antibody (1:100) for 1 hr. Finally, cells were washed, mounted with DAPI-containing solution, and photographed with a Nikon Ti2 microscopy System.

ROS Detection

Molecular Probes™ CM-H2DCFDA was purchased from Thermo Fisher Scientific (Waltham, MA, USA) to examine the production of ROS in bladder cancer cells. The cells were incubated with different concentrations of miconazole (0, 12.5, 25, or 50 μM) for 24 hrs, were washed twice with PBS, trypsinized into PBS and centrifuged at 5000 g for 3 mins at 4°C. Then, collected cells were incubated with 25 μM CM-H2DCFDA for 45 mins at 37°C. The cells were washed, and CM-H2DCFDA fluorescence in the cells was monitored using a flow cytometer.

Statistics

All experiments were performed at least three times, each time in triplicate. Data from two experimental groups were analyzed using the Student’s t test and multiple group comparisons were performed using one-way analysis of variance (one-way ANOVA) with Bonferroni’s post hoc tests. Statistical significance was expressed as the mean ± standard deviation (S.D.). A p-value of <0.05 was considered statistically significant.

Results

Miconazole Treatment Contributes to NRF2 Protein Expression in Bladder Cancer Cells

To examine the effects of miconazole on NRF2 expression, T24 and 5637 bladder cancer cells were incubated with miconazole (24 hrs) in different concentrations (0, 6.25, 12.5, or 50 μM). Levels of NRF2 protein expression were investigated by Western blot. As shown in Figure 1, the treatment of bladder cancer cells with miconazole increased NRF2 protein expression in a dose-dependent manner.

Figure 1

Miconazole promotes protein expression of NRF2 in bladder cancer cells. (A and B; upper panels) T24 and 5637 BC cells were treated with increased concentrations of miconazole for 24 h, total proteins were extracted and expression levels of NRF2 were detected by Western blot. (A and B; lower panels) The relative band intensities of proteins presented in (A and B) were quantitated by densitometric scanning and are presented as the fold of control group; and the statistical calculation from blots more than three independent experiments are shown (n=4). The results are presented as the means ± S.D. *P<0.05 compared with Con. group.

Miconazole Treatment Activates a P62-KEAP1 Noncanonical Pathway Responsible for NRF2 Activation

To explore the mechanism that regulates NRF2 activation, we investigated levels of KEAP1 and p62 expression, which lead to noncanonical activation of NRF2 after miconazole incubation. We found that miconazole treatment inhibited KEAP1 protein expression and increased p62 expression, suggesting the activation of the p62-KEAP1 noncanonical pathway (Figure 2). When we examined the effect of miconazole on NRF2 expression in bladder cancer cells incubated with miconazole (25 μM) for different time intervals (0, 12, 24, or 48 h), miconazole promoted NRF2 protein expression level in a time-dependent manner (Figure 3A and B), via the p62-KEAP1 noncanonical pathway examined by p62 siRNA (Figure 3C). In order to confirm NRF2 activation after miconazole treatment, we investigated NRF2 nuclear translocation by cell immunofluorescence. The data revealed dose-dependent increases in NRF2 nuclear translocation and p62 protein expression in the presence of miconazole in bladder cancer cells (Figure 4).

Figure 2

Miconazole stimulates noncanonical p62-KEAP1 pathway in bladder cancer cells. (A and B; upper panels) T24 and 5637 BC cells were treated with increased concentrations of miconazole for 24 h, total proteins were extracted and expression levels of p62 and KEAP1 were detected by Western blot. (A and B; lower panels) The relative band intensities of proteins presented in (A and B) were quantitated by densitometric scanning and are presented as the fold of control group; and the statistical calculation from blots more than three independent experiments are shown (n=4). The results are presented as the means ± S.D. *P<0.05 compared with Con. group.

Figure 3

Miconazole activates p62-KEAP1-NRF2 pathway in a time-dependent manner in bladder cancer cells. (A and B; upper panels) T24 and 5637 BC cells were treated with the increased time course of miconazole (25 μM), total proteins were extracted and expression levels of p62, KEAP1 and NRF2 were detected by Western blot. (C; upper panel) T24 BC cells were transfected with p62 siRNA or negative control siRNA for 24 h, followed by treated with miconazole (25 μM) for further 24 hrs, and expression levels of p62 and NRF2 were evaluated by Western blot. (A–C; lower panels) The relative band intensities of proteins presented in (A–C) were quantitated by densitometric scanning and are presented as the fold of control group; and the statistical calculation from blots of three independent experiments are shown (n=3). The results are presented as the means ± S.D; *P<0.05 compared with Con.; #P<0.05 compared with the miconazole treatment group.

Figure 4

Miconazole promotes NRF2 nuclear translocation in bladder cancer cells. (A and B) T24 and 5637 bladder cancer cells were treated with increased concentrations of miconazole for 24 h, then subjected to immunofluorescence staining by anti-p62 and -NRF2 antibodies. Nuclei were counterstained with DAPI. Representative microscopy images were shown.

Miconazole Increases P62 and NRF2 Transcription Levels in Bladder Cancer Cells

We next evaluated the transcription levels of NRF2 and its corresponding regulators, p62 and KEAP1, after miconazole treatment in bladder cancer cells. The cells were treated with miconazole in dose- and time-course experiments as described in Figures 1 and 3, and real-time qPCR determined NRF2, p62 and KEAP1 mRNA expression. Miconazole promoted increases in mRNA expression levels of NRF2 and p62 (Figures 5 and 6), although no significant changes in KEAP1 transcription levels were observed following miconazole exposure. This lack of response suggests that miconazole may suppress KEAP1 protein expression through post-translation regulation such as p62-dependent proteasomal degradation.

Figure 5

Miconazole increases transcriptional levels of NRF2 and p62 but not KEAP1 in a dose-dependent manner. (A and B) T24 and 5637 bladder cancer cells were treated with different concentrations of miconazole for 24 hrs, total mRNA were extracted from cells, and expression levels of NRF2, p62 and KEAP1 were detected by qPCR. Results are expressed as the mean ± S.D of triplicate samples (n=6). *P < 0.05 compared to the Con. group.

Figure 6

Miconazole increases transcriptional levels of NRF2 and p62 but not KEAP1 in a time-course investigation. (A and B) T24 and 5637 bladder cancer cells were treated with 25 μM of miconazole for 0 hrs, 12 hrs, 24 hrs and 48 hrs, total mRNA were extracted from cells, and expression levels of NRF2, p62 and KEAP1 were detected by qPCR. Results are expressed as the mean ± S.D of triplicate samples (n=6). *P < 0.05 compared to the Con. group.

ROS Generation Is Required for Activation of the P62-KEAP1-NRF2 Noncanonical Pathway After Miconazole Exposure

NRF2 activation is the major regulator of cytoprotective responses to ROS-induced oxidative stress and restores redox balance.27 We, therefore, evaluated ROS production after miconazole incubation. We found that miconazole increased ROS levels in bladder cancer cells, and pretreatment with the ROS scavenger N-acetylcysteine (NAC) reversed ROS production (Figure 7A). To ascertain whether ROS production is responsible for the p62-KEAP1 noncanonical pathway that activates NRF2, we pretreated bladder cancer cells with ROS scavengers including catalase, diphenyleneiodonium (DPI) and NAC, followed by miconazole exposure. Levels of p62 and NRF2 expression were assessed by Western blot and real-time qPCR. We found that NAC and DPI, but not catalase, dramatically abrogated p62 and NRF2 up-regulation after miconazole treatment, suggesting that miconazole-induced NRF2 activation is mediated through the superoxide-generating NADPH oxidase (NOX) (Figure 7B–D).

Figure 7

ROS scavengers reverse p62-KEAP1-NRF2 pathway activation in bladder cancer cells. (A) T24 cells were pretreated with or without ROS scavenger NAC (1mM) for 1 hr, followed by incubated with different concentrations of miconazole for 24 hrs. The cells were stained with ROS detection probe, then subjected to flow cytometry to analyze ROS generation. The quantification of relative intensity was shown in the lower panel. (B and C) T24 cells were pretreated with different ROS scavengers (catalase, an H2O2 scavenger, 3500 U; DPI, a NOX-specific inhibitor, 10 μM; NAC, a general ROS scavenger, 1 mM) for 1 hr followed by treated with miconazole (25 μM) for 24 hrs. The protein and mRNA expression of p62, NRF2 and KEAP1 were evaluated by Western and qPCR. (D) T24 cells were pretreated as described above, then immunofluorescence staining was performed with anti-p62 and -NRF2 antibodies. Nuclei were counterstained with DAPI. Representative microscopy images were shown. Results are expressed as the mean ± S.D of triplicate samples (n=5). *P<0.05 compared with Con.; #P<0.05 compared with the miconazole treatment group.

Discussion

It is well established that NRF2 plays a critical role in adaptive cellular responses to oxidative stress.1 The discovery of novel NRF2 activators has attracted attention for their therapeutic potential in chronic inflammation and cancer. Our present study shows that miconazole, a widely used antifungal agent, promotes NRF2 expression through the noncanonical p62-KEAP1 pathway in bladder cancer cells. Miconazole also promotes ROS generation, which is responsible for p62-KEAP1-NRF2 expression in bladder cancer. Many natural and synthetic compounds have been identified as NRF2 activators and implicated in cancer therapy including sulforaphane, curcumin, resveratrol, lycopene, oleanane triterpenoid.28 Our findings conclusively support the use of miconazole in a novel application, as an NRF2 activator in the treatment of bladder cancer.

Typical NRF2 activation is accompanied by modification of KEAP1 cysteine residues that protect NRF2 from ubiquitylation, allowing NRF2 accumulation and subsequently nuclear translocation. Finally, NRF2 binds to its responsible DNA element AREs and exerts cytoprotective functions.29,30 Here, we found that miconazole improved levels of p62 protein expression, whereas miconazole suppressed KEAP1 in bladder cancer cells. qPCR results indicated a close alignment between p62 mRNA expression and protein levels. However, transcription levels of KEAP1 were not decreased after treatment with miconazole. This finding does not match with our investigations in protein expression levels, revealing that KEAP1 down-regulation is caused by translational or post-translational regulation. A previous report indicates that p62 accumulation in the noncanonical pathway interacts with KEAP1, sequestering KEAP1 into the autophagosomes, abrogating the ubiquitin-proteasomal degradation of NRF2 and leading to activation of the NRF2 response genes.31 Moreover, a previous study has indicated that KEAP1 serves as a p62-regulated substrate for autophagy-mediated degradation.18 Our results suggest that miconazole-induced inhibition of KEAP1 protein expression may be controlled by p62-mediated degradation. The detailed mechanisms need to be explored in future research.

NRF2 is a major cellular defense regulator responsible for controlling those genes whose biological functions participate in the elimination of reactive oxidants. Through binding to its cis-acting element ARE, NRF2 can drive the expression of various antioxidant enzymes such as glutathione-s-transferase (GST), NAD(P)H quinone reductase 1 (NQO1) and heme oxygenase (HO-1).32 Alteration of the cellular redox balance elevates ROS and triggers the transcriptional activity of NRF2.1 Our results demonstrate that miconazole improved ROS production in bladder cancer cells, which in turn elicited NRF2 activation. Pretreatment with ROS scavengers abolished NRF2 expression and nuclear translocation, revealing the pivotal role of ROS in miconazole-induced NRF2 activation. Interestingly, only the ROS scavenger NAC and the NOX-specific inhibitor DPI reversed this response, whereas hydrogen peroxide (H2O2) scavenger catalase had no such effect, suggesting that miconazole triggered the NRF2 pathway via NOX-dependent regulation.

Conclusion

Miconazole is a commonly used antifungal agent in the treatment of fungal infection, and more recently, has been used in the treatment of different tumors.23–25 We have identified that miconazole is a novel NRF2 activator that may possess chemoprotective properties against antioxidant stress as well as chemopreventive properties. Our study confirms that miconazole promotes NRF2 activation through the p62-KEAP1 noncanonical pathway. In conclusion, our data add to the growing body of evidence indicating that NRF2 activators could be used as safe and effective agents for the chemoprevention of cancer and many other diseases.33 Preclinical testing of miconazole is warranted.