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. 2014 Dec 10;38(2):151–155. doi: 10.14348/molcells.2015.2229

Galangin and Kaempferol Suppress Phorbol-12-Myristate-13-Acetate-Induced Matrix Metalloproteinase-9 Expression in Human Fibrosarcoma HT-1080 Cells

Yu Jung Choi 1, Young Hun Lee 1, Seung-Taek Lee 1,*
PMCID: PMC4332032  PMID: 25518925

Abstract

Matrix metalloproteinase (MMP)-9 degrades type IV collagen in the basement membrane and plays crucial roles in several pathological implications, including tumorigenesis and inflammation. In this study, we analyzed the effect of flavonols on MMP-9 expression in phorbol-12-myristate-13-acetate (PMA)-induced human fibrosarcoma HT-1080 cells. Galangin and kaempferol efficiently decreased MMP-9 secretion, whereas fisetin only weakly decreased its secretion. Galangin and kaempferol did not affect cell viability at concentrations up to 30 μM. Luciferase reporter assays showed that galangin and kaempferol decrease transcription of MMP-9 mRNA. Moreover, galangin and kaempferol strongly reduce IκBα phosphorylation and significantly decrease JNK phosphorylation. These results indicate that galangin and kaempferol suppress PMA-induced MMP-9 expression by blocking activation of NF-κB and AP-1. Therefore, these flavonols could be used as chemopreventive agents to lower the risk of diseases involving MMP-9.

Keywords: flavonol, galangin, kaempferol, mitogen-activated protein kinase, MMP-9, NF-κB

INTRODUCTION

Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases, and there are 23 different types of human MMPs. These proteases collectively degrade structural components of the extracellular matrix (ECM). Controlled degradation of ECM proteins by MMPs is observed in many normal physiological processes, including embryogenesis, wound healing, and tissue remodeling. In contrast, uncontrolled MMP activity is implicated in pathological situations such as tumor invasion, metastasis, rheumatoid arthritis, osteoarthritis, and cardiovascular diseases (Kim et al., 2013; Visse and Nagase, 2003; Yan and Boyd, 2007).

Gelatinolytic MMPs, including MMP-2 and MMP-9, degrade type IV collagen, a major component of the basement membrane. Basement membrane degradation is involved in the initiation and progression of important diseases, including cancer, atherosclerosis, and inflammatory disorders (Coussens et al., 2002; Liotta et al., 1991; Nelson et al., 2000). MMP-9 is synergistically upregulated by growth factors and inflammatory cytokines (Bond et al., 1998). Therefore, downregulation of MMP-9 would be effective to prevent or alleviate these diseases.

Flavonoids are polyphenolic compounds that are ubiquitously found in foods of plant origin. They are known to have antioxidant and anticarcinogenic effects (Hanneken et al., 2006; Knekt et al., 2002; Scalbert et al., 2005). Flavonols are a class of flavonoids that have a 3-hydroxy flavone backbone. Their diversity comes from phenolic hydroxyl (-OH) groups at different numbers and positions. MMP catalytic activity is regulated at several levels, including transcription, as well as activation and inhibition. We previously showed that phorbol-12-myristate-13-acetate (PMA) transactivates MMP-9 expression in HCC cells in an AP-1 and NF-κB dependent manner (Hah and Lee, 2003). Herein we have evaluated modulation of PMA-induced MMP-9 expression in HT-1080 cells using eight different commercially available flavonols. In addition, we have analyzed the signaling pathways involved in flavonol-mediated MMP-9 suppression.

MATERIALS AND METHODS

Chemicals

3-hydroxyflavone (purity > 98.0%) was obtained from Tokyo Chemical Industry (Japan). Galangin (purity ≥ 95.0%), kaempferol (purity ≥ 90.0%), fisetin (purity ≥ 98.0%), quercetin (purity ≥ 98.0%), morin (purity ≥ 85.0%), and myricetin (purity ≥ 96.0%) were obtained from Sigma-Aldrich (USA). Gossypetin (purity ≥ 97.0%) was obtained from Timtec (USA). 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was obtained from Sigma-Aldrich. PMA was obtained from A.G. Scientific (USA). Anti-MMP-9, anti-phospho-ERK1/2, anti-ERK, anti-phospho-JNK, anti-JNK, anti-phospho-p38 MAPK, anti-phospho-IκBα, and anti-IκBα antibodies were purchased from Cell Signaling Technology (USA). The anti-p38 MAPK antibody was purchased from Santa Cruz Biotechnology (USA). The anti-GAPDH antibody was purchased from AbClon (Korea). Horseradish peroxidase-conjugated goat-anti mouse or rabbit IgG antibodies were purchased from KOMA (Korea).

Cell culture

Human fibrosarcoma HT-1080 cells were maintained in Dulbecco’s modified Eagle media (DMEM) (Thermo Scientific, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/ml penicillin, and 100 μg/ml streptomycin in a humidified culture incubator at 37°C containing 5% CO2. When flavonols were added to cells, they were solubilized in dimethylsulfoxide (DMSO). Cells were incubated in DMEM containing DMSO at a final concentration of less than 0.2%.

Gelatin zymography assays

Subconfluent HT-1080 cells were plated in a 12-well plate and incubated for 24 h with serum-free media with 30 ng/ml PMA and various concentrations of flavonols. Conditioned media were subjected to gelatin zymography assays (Lv et al., 2013, Nam et al., 2011) using 7.5% SDS gels containing 0.1% gelatin. Gels were incubated for 1 h at room temperature in refolding buffer (50 mM Tris-HCl, pH 7.4, 100 mM NaCl, 2.5% Triton X-100) and for 16 h at 37°C in reaction buffer (50 mM Tris-HCl, pH 7.4, 10 mM CaCl2). Gels were then stained with Coomassie brilliant blue R-250.

Cell proliferation assays

Subconfluent HT-1080 cells were plated in 96-well plates and incubated for 24 h in media supplemented with 10% FBS and various concentrations of galangin and kaempferol. After incubation, cells were treated with MTT solution, solubilized with DMSO, and the absorbance at 565 nm was measured using a microplate reader as described previously (Shin et al., 2008).

Dual-luciferase reporter assays

Subconfluent HT-1080 cells were plated in 24-well plates and co-transfected with a firefly luciferase reporter construct pGL3-M9Pwt containing the human wild-type MMP-9 promoter (Hah and Lee, 2003) and a Renilla luciferase reporter vector pRL-TK. Cells were transfected using WelFect-EX plus transfection reagent (Welgene, Korea) according to the manufacturer’s recommendations. After incubation for 24 h in complete media, the media was replaced with serum-free media and cells were then treated for 24 h with 30 ng/ml PMA and 30 μM galangin or kaempferol. Luciferase activity of the cell lysates was measured using a dual-luciferase reporter assay system (Promega, USA).

Western blotting and immunodetection

Cells were lysed using RIPA lysis buffer [50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1% NP-40, 0.5% deoxycholate, 0.1% SDS, 1 mM NaF, 1 mM sodium orthovanadate, protease inhibitor cocktail set I (Calbiochem, Germany)] on ice for 15 min, followed by centrifugation for 15 min at 13,000 × g at 4°C. Supernatants were resuspended in SDS sample buffer (50 mM Tris-HCl, pH 6.8, 2% SDS, 0.1% bromophenol blue, 10% glycerol) containing 100 mM β -mercaptoethanol, and resolved by SDS-PAGE. Proteins were blotted onto nitrocellulose or PVDF membranes and incubated with primary and secondary antibodies. Immunoreactive signals were detected using Immobilon Western Chemiluminescent HRP Substrate (Millipore, USA) and LAS-3000 (Fujifilm, Japan).

Statistical analyses

Data are shown as the mean ± standard deviation of at least three independent experiments. Comparisons of group means were performed using Student’s t-tests.

RESULTS

Some flavonols decrease secretion of MMP-9

We analyzed the effect of eight different flavonols (Supplementary Fig. S1) on PMA-induced MMP-9 expression in HT-1080 cells using gelatin zymography assays. As expected, we found that PMA treatment significantly increased secretion of proMMP-9 (Fig. 1A). When each flavonol was added at a concentration of 30 μM, PMA-induced MMP-9 secretion was clearly reduced by galangin and kaempferol, moderately reduced by fisetin, and weakly reduced by quercetin (Fig. 1A). Dose-dependent treatment of galangin, kaempferol, and fisetin showed that galangin and kaempferol reduce MMP-9 secretion more efficiently than fisetin (Fig. 1B). Western blot analysis also demonstrated that galangin, kaempferol, and fisetin decrease the PMA-induced MMP-9 secretion (Fig. 1C).

Fig. 1.

Fig. 1.

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Effect of flavonols on the amount of secreted MMP-9 in human fibrosarcoma HT-1080 cells. Subconfluent HT-1080 cells were incubated for 24 h with serum-free media in the presence of 30 μM flavonols (A, C) or the indicated concentrations (B) and 30 ng/ml PMA. Conditioned media were subjected to gelatin zymography assays (A, B) or Western blot analysis with MMP-9 antibody (C). GAPDH immunoblots in cell lysates are shown to normalize the cell number used in this experiment. -, DMSO; Hy, 3-hydroxyflavone; Ga, galangin; Ka, kaempferol; Fi, fisetin; Qu, quercetin; Mo, morin; My, myricetin; Go, gossypetin.

Galangin and kaempferol did not affect cell proliferation at concentrations up to 30 μM

To examine whether reduced MMP-9 secretion induced by galangin and kaempferol may result from their cytotoxicity, we used MTT assays to analyze the effect of galangin and kaemp-ferol on HT-1080 cell proliferation. Cell proliferation was not affected by 30 μM galangin or kaempferol and was only weakly inhibited by 100 μM galangin (79.4%) and kaempferol (74.3%) (Fig. 2). Thus, 30 μM galangin or kaempferol did not affect cell viability and was selected as the concentration for the following experiments.

Fig. 2.

Fig. 2.

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Effect of galangin and kaempferol on HT-1080 cell proliferation. Cells (1 × 104 per well) were plated in 96-well plates. Subconfluent cells were incubated for 24 h with various concentrations of galangin or kaempferol. The number of viable cells was determined by measuring absorbance at a wavelength of 565 nm after incubating cells with MTT reagent. The relative viable cell number (%) in the presence of flavonols is expressed relative to the cell number in the absence of flavonols. Each value is the mean ± standard deviation from at least three independent determinations. *p < 0.05; **p < 0.01 vs. no flavonol.

Galangin and kaempferol inhibit MMP-9 gene transcription

To analyze whether galangin- and kaempferol-mediated inhibition of MMP-9 secretion is due to suppression of MMP-9 transcription, we performed promoter assays using cells transiently transfected with a luciferase reporter gene linked to the MMP-9 promoter sequence (pGL3-M9Pwt). Luciferase activity driven by the MMP-9 promoter increased up to 22-fold in cells treated with PMA compared to untreated cells (Fig. 3). The addition of galangin or kaempferol (30 μM) to cells decreased luciferase activity to approximately 40% of control. This result demonstrates that galangin and kaempferol suppress PMA-induced transcription of the MMP-9 gene.

Fig. 3.

Fig. 3.

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Effect of galangin and kaempferol on MMP-9 transcription. HT-1080 cells were transiently co-transfected with pGL3-M9Pwt luciferase reporter constructs and pRL-TK. Cells were treated for 24 h with galangin and kaempferol (30 μM) and PMA (30 ng/ml). Luciferase activity was measured using a dual-luciferase reporter assay system. Luciferase activity was normalized to Renilla luciferase activity. Each value is the mean ± standard deviation from three independent determinations. †††p < 0.001; **p < 0.01 vs. PMA alone. -, DMSO; Ga, galangin; Ka, kaempferol.

Galangin and kaempferol abrogate PMA-induced MMP-9 expression by blocking the NF-κB and AP-1 pathways

MMP-9 gene transcription is activated predominantly by the mitogen-activated protein kinases (MAPKs) and NF-κB pathways (Gum et al., 1997; Sato and Seiki, 1993; Sato et al., 1993). We first investigated whether galangin and kaempferol modulate MAPK signaling pathways. To determine the optimal time point for PMA-induced activation of MAPKs, HT-1080 cells were stimulated with PMA for various time intervals. PMA induced phosphorylation of MAPKs, with maximal activation of ERKs and JNK after 30–60 min and activation of p38 MAPK after 10–30 min (Fig. 4A). Pre-incubation of cells with galangin or kaempferol does not affect PMA-induced ERK1/2 and p38 MAPK phosphorylation, similar to gossypetin treatment that does not induce MMP-9 secretion. However, galangin and kaempferol significantly decreased PMA-induced JNK phosphorylation (Fig. 4B).

Fig. 4.

Fig. 4.

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Effect of galangin and kaempferol on PMA-induced activation of MAPKs. (A) To determine the optimal time point for PMA-induced activation of MAPKs, cells were starved for 24 h and then stimulated with 30 ng/ml PMA for the indicated time intervals. (B) Cells were starved for 24 h, preincubated for 30 min with 30 μM of galangin, kaempferol, or gossypetin (as a negative control), and stimulated for 30 min with 30 ng/ml PMA. Cell lysates were subjected to 10% SDS-PAGE and analyzed by Western blotting. ERK, JNK, and p38 MAPK levels in cell lysates were analyzed as loading controls. Ka, kaempferol; Ga, galangin; Go, gossypetin.

Next, we investigated whether galangin and kaempferol control the NF-κB signaling pathway. As expected, PMA treatment transiently increased IκBα phosphorylation and decreased IκBα levels in HT-1080 cells (Fig. 5A). Interestingly, galangin and kaempferol significantly decreased IκBα phosphorylation with a concomitant increase in IκBα levels (Fig. 5B). Taken together, these results suggest that galangin and kaempferol reduce PMA-induced MMP-9 expression by hampering NF-κB activation and, to a lesser extent, by inhibiting JNK activation and thereby decreasing AP-1 activation.

Fig. 5.

Fig. 5.

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Effect of galangin and kaempferol on PMA-induced activation of NF-κB. (A) Cells were starved for 24 h and then stimulated with 30 ng/ml PMA for the indicated time intervals. (B) Cells were starved for 24 h, preincubated for 30 min with 30 μM of galangin, kaempferol, or gossypetin (as a negative control), and stimulated for 10 min with 30 ng/ml PMA. Cell lysates were subjected to 10% SDS-PAGE and analyzed by Western blotting. GAPDH level in cell lysates were analyzed as loading controls. Ka, kaempferol; Ga, galangin; Go, gossypetin.

DISCUSSION

Some flavonols have been reported to control the function of specific MMPs by inhibiting their catalytic activity (Phromnoi et al., 2009; Sartor et al., 2002). Recently, we also found that one flavonol, fisetin, inhibits the catalytic activity of various MMPs, including MMP-14, and reduces MMP-dependent cellular processes, such as tumor cell invasion and endothelial cell tube formation (Park et al., 2013). In addition MMP inhibition, it has recently been shown that flavonols can regulate MMP function through transcriptional suppression. For example, kaempferol suppresses PMA-induced MMP-9 expression in glioblastoma GBM8401 cells (Lin et al., 2010), MMP-2 expression in tongue squamous cell carcinoma SCC4 cells (Lin et al., 2013), and MMP-2 and MMP-9 expression in human osteosarcoma U-2 OS cells (Chen et al., 2013). Quercetin downregulates oxidized LDL-induced expression of MMP-1, MMP-2, and MMP-9 in human umbilical vein endothelial EA.hy926 cells (Yi et al., 2012), decreases phenazine methosulfate-induced expression and activation of MMP-2, as well as decreases MMP-9 expression in HT-1080 cells (Lee et al., 2013). Morin decreases MMP-2 and MMP-9 expression during diethylnitrosamine-induced hepatocellular carcinoma in rats (Sivaramakrishnan and Niranjali Devaraj, 2009). However, the effect of diverse flavonols on MMP-9 expression in a cellular system has not yet been evaluated.

Here we investigated the effect of eight commercially available flavonols on PMA-induced MMP-9 secretion in HT-1080 cells using gelatin zymography assays. Although suppression of MMP-9 expression by kaempferol, quercetin, and morin was reported in different conditions (Chen et al., 2013; Lee et al., 2013; Lin et al., 2010; 2013; Sivaramakrishnan and Niranjali Devaraj, 2009; Yi et al., 2012), our study showed that MMP-9 secretion from HT-1080 cells was severely decreased by galangin as well as kaempferol, and moderately decreased by fisetin. Interestingly, quercetin weakly affected and morin did not affect MMP-9 secretion. Because galangin and kaempferol did not affect cell proliferation at concentrations up to 30 μM, the reduced MMP-9 secretion by galangin and kaempferol could not be attributed to their cytotoxicity.

As expected, we found that the galangin- and kaempferol-mediated decrease in MMP-9 secretion results from suppression of MMP-9 mRNA transcription. It is known that AP-1 and NF-κB transcription factors are important for MMP-9 induction by growth factors, cytokines, and PMA in various cell types (Lee et al., 2014; Lianxu et al., 2006; Shin et al., 2002). We found that galangin and kaempferol drastically decrease IκBα phosphorylation and increase IκBα levels. In addition, galangin and kaempferol significantly reduce JNK phosphorylation and thus are expected to decrease AP-1 activation. However, neither flavonol changes phosphorylation of other MAPKs. These results demonstrate that galangin and kaempferol suppress PMA-induced MMP-9 transactivation by inhibiting both the NF-κB and AP-1 pathways.

In conclusion, this is the first comparative study regarding the effect of various flavonols on MMP-9 suppression. We found that galangin is able to downregulate MMP-9 expression as efficiently as kaempferol, which is a well-known MMP-9 suppressor in various cell types (Chen et al., 2013; Lin et al., 2010). We also demonstrated that galangin and kaempferol suppress MMP-9 transcription by inhibiting both the NF-κB and AP-1 pathways. The identification of galangin and kaempferol as suppressors of MMP-9 expression is meaningful because they are natural components present in a wide variety of fruits, vegetables and plants (e.g., ginger, broccoli, tomato, strawberry, and apple). In particular, enhanced MMP-9 expression is associated with several pathologies, such as tumor invasion and metastasis as well as inflammation (Watanabe et al., 1993; Zheng et al., 2006). Therefore, galangin and kaempferol might be used as chemopreventive compounds to control inflammation and malignant diseases.

Supplementary Data

Note: Supplementary information is available on the Molecules and Cells website (www.molcells.org).

Acknowledgments

This work was supported by grants from the National Research Foundation of Korea funded by the Ministry of Education (2013R1A2A2A01013884) and the Ministry of Science, ICT & Future Planning (2014M3C9A2064536). Y.J.C. and Y.H.L. were graduate student trainees of the Brain Korea 21 plus program from the Ministry of Education, Republic of Korea.

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Note: Supplementary information is available on the Molecules and Cells website (www.molcells.org).

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