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Oxidative/nitrosative stress and generation of pro-inflammatory cytokines are hallmarks of inflammation. Since chronic inflammation is implicated in several pathological conditions in humans, including cancers of the colon, anti-inflammatory compounds may be useful chemopreventive agents against colon cancer. Stilbenes, such as resveratrol, have diverse pharmacological activities, which include anti-inflammation, cancer prevention, a cholesterol-lowering effect, enhanced insulin sensitivity, and increased lifespan. We previously showed that pterostilbene (trans-3,5-dimethoxy-4’-hydroxystilbene), a structural analogue of resveratrol, is present in blueberries and that pterostilbene inhibited expression of certain inflammation-related genes in the colon and suppressed aberrant crypt foci formation in rats. Here, we examined molecular mechanisms of the action of pterostilbene in colon cancer. Pterostilbene reduced cell proliferation, down-regulated the expression of c-Myc and cyclin D1, and increased the level of cleaved PARP. A combination of cytokines (tumor necrosis factor-α, interferon-γ and bacterial endotoxin lipopolysaccharide) induced inflammation-related genes such as inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), which was significantly suppressed by treatment with pterostilbene. We further identified upstream signaling pathways contributing to the anti-inflammatory activity of pterostilbene by investigating multiple signaling pathways including NF-κB, JAK-STAT, ERK, p38, JNK, and PI-3-kinase. Cytokine induction of the p38-ATF2 pathway was markedly inhibited by pterostilbene among the different mediators of signaling evaluated. By silencing the expression of the p38α isoform, there was significant reduction in cytokine induction of iNOS and COX-2. Our data suggest that the p38 MAP kinase cascade is a key signal transduction pathway for eliciting the anti-inflammatory action of pterostilbene in cultured HT-29 colon cancer cells.
The intriguing link between chronic inflammation and cancer has been the subject of numerous studies for more than a century (1). In particular, the development of colon cancer is a characteristic scenario in which inflammatory conditions such as ulcerative colitis increase the risk of colon cancer by 20-fold (2). The presence of certain inflammation markers, such as the C-reactive protein circulating in the blood, is correlated with an increased risk of colon cancer (3). In addition, overexpression of pro-inflammatory enzymes, such as inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), has been reported in human colon cancer (4, 5) and in an azoxymethane (AOM)-induced colon cancer model in rats (6, 7). More importantly, selective inhibitors of these inflammatory genes are effective in reducing the number of colorectal polyps in humans and in suppressing the formation of AOM-induced hyperplastic aberrant crypt foci (ACF) and colon tumors in rats (7-10).
Epithelial cells express iNOS and COX-2 in response to inflammatory cytokines and the bacterial endotoxin, lipopolysaccharide (LPS), and the transcriptional regulation of iNOS and COX-2 is complex (11-14). This process involves a number of transcription factors, including nuclear factor κB (NF-κB), activator protein-1 (AP-1), CCAAT-enhancer binding protein (C/EBP), activating transcription factor/cyclic-AMP response element binding protein (ATF/CREB), and Janus Kinase Signal Transducers and Activators of Transcription (JAK-STAT) family (12, 14, 15). Depending on the cell type, various downstream signaling pathways are also involved in the transcriptional regulation of iNOS and COX-2.
There are several upstream kinase pathways responsible for transcriptional regulation of COX-2 and iNOS including mitogen activated protein kinases (MAPKs). MAPKs are composed of extracellular receptor kinase (ERK), p38 kinase and c-jun NH2 terminal kinase (JNK) (16). These MAPKs are activated by MAPK kinase (MAPKK) and once activated, these MAPKs in turn activate a number of transcription factors such as Elk1, ATF2 and c-jun, which are the major activators of iNOS and COX-2 genes (17, 18). It was reported that COX-2 expression induced by IL-1β in HT-29 cells was upregulated by all three MAPKs (19). Furthermore, p38 MAP kinase has been shown to be the major signaling pathway, other than NF-κB, involved in the regulation of inflammatory cytokine synthesis (20).
Recently, we showed that pterostilbene (Fig. 1), a naturally occurring analogue of resveratrol, caused suppression of ACF formation in the AOM-induced colon cancer model in rats, which may be due to a decreased expression of inflammatory genes, such as iNOS, in the colonic crypts and in the ACF (21). Stilbenes, including resveratrol and pterostilbene, are present in small berries such as blueberries and deerberries (22, 23). The discovery of resveratrol as a cancer preventive agent (24) has fostered interest in testing the cancer preventive activity of other naturally occurring stilbenes in many laboratories (25-28). It has been reported that the bioavailability of resveratrol is low when given orally, probably due to three hydroxyl groups (29, 30). Pterostilbene, a stilbene found in several types of blueberries such as rabbiteye blueberries and also in unripe Pinot noir grapes (22), has two methoxy groups and one hydroxyl group (Fig. 1), and this structural difference from resveratrol may contribute to the better bioavailability of pterostilbene in vivo when compared with resveratrol (29-31). Pterostilbene and resveratrol both have strong antioxidant and hypolipidemic activities (25, 32-34). However, Rimando et al have shown that pterostilbene, but not resveratrol, piceatannol, or resveratrol trimethyl ether, is a peroxisome proliferator-activated receptor α (PPARα) agonist, suggesting a difference in their mechanisms of action (33).
In the present study, we indicate that pterostilbene is more potent than resveratrol as an inhibitor of the proliferation of cultured HT-29 colon cancer cells. Although there have been some detailed studies on the chemopreventive effect of resveratrol, very little is known about the mechanism of action of pterostilbene. The present study aims to understand the inhibitory effects of pterostilbene on the induction of inflammatory markers in the HT-29 colon cancer cell line. Based on our studies, the anti-inflammatory property of pterostilbene may be regarded as a key attribute for its role against colon tumorigenesis. The effects of pterostilbene on the activation of upstream signaling pathways and transcription factors involved in NF-κB, JAK-STAT, and MAPK pathways were investigated. Among them, p38 MAP kinase was identified as a key mediator for the inhibitory effect of pterostilbene on the formation of iNOS and COX-2.
Pterostilbene (trans-3,5-dimethoxy-4’-hydroxystilbene; Fig. 1) and resveratrol were synthesized at the National Products Utilization Research Unit, USDA (Mississippi) (purity > 99.9%). The compounds were dissolved in dimethyl sulfoxide (DMSO), and the final concentration of DMSO in the cell culture studies was 0.1% or less. The controls were used DMSO alone in all experiments. Recombinant human IFN-γ and TNF-α were purchased from R & D Systems, Inc. (Minneapolis, MN), and lipopolysaccharide (from Escherichia coli 0111:B4 γ-irradiated) was purchased from Sigma (St. Louis, MO).
Human colon carcinoma cell lines HT-29 was obtained from the American Type Culture Collection (Manassas, VA). The cells were maintained in Dulbecco's modification of Eagle's medium (DMEM) supplemented with 10% FBS and 1% penicillin /streptomycin at 37°C and 5% CO2. The cytokine mixture, consisting of 10 ng/ml of TNF-α, IFN-γ and LPS, was used to induce iNOS and COX-2, unless otherwise mentioned. The cells were treated with the test compound either alone or in combination with cytokines for different time intervals.
HT-29 cells were plated at a density of 20,000 cells/well in a 24 well plate and treated with varying concentrations of pterostilbene for a period of 1, 2 or 3 days at 37°C. Before harvest, the cells were incubated with 1 μCi [3H]thymidine for 4 h at 37°C and were washed with phosphate buffered saline. The cells were precipitated with cold 10% trichloroacetic acid for 10 min and solubilized with 0.5 ml solubilization buffer (0.2 M NaOH, 40 μg/ml salmon sperm DNA) for 2 h at room temperature. The lysate was transferred to 5 ml Ecolume and the [3H]thymidine incorporated into the DNA of HT-29 cells was determined using a scintillation spectrometer (Beckman Coulter, Fullerton, CA).
Whole cell and nuclear protein extracts from different experiments were collected and analyzed by Western blotting. The protein samples were separated on 4−15% SDS-PAGE gels (Biorad, Hercules, CA) followed by transfer to a polyvinylidene fluoride (PVDF) membrane. The membranes were blocked with 5% milk in Tris buffer for 1 h and then incubated with the appropriate primary antibody solutions overnight at 4°C. The membranes were washed with Tris buffer, and incubated with horseradish peroxidase conjugated secondary antibody solutions for 1 h at room temperature. The protein bands were visualized using a chemiluminescence based kit from Amersham Biosciences (Buckinghamshire, UK). The primary antibodies against iNOS, COX-2, IκBα, p65, cyclin D1, c-Myc (Santa Cruz Biotechnology, Santa Cruz, CA), phospho-STAT3, phospho-STAT1, phospho-Erk1/2, phospho-JNK1/2, phospho-p38, phospho-Akt, phospho-ATF2, phospho-Elk1, PARP, p38α, p38β, total p38 (Cell Signaling Technology Inc., Beverly, MA) and actin (Sigma, St. Louis, MO) and secondary antibodies (Santa Cruz Biotechnology, Santa Cruz, CA) were used.
The procedure for quantitative RT-PCR analysis is previously reported (35). Briefly, the cells were incubated with compounds for indicated period and the cells were then lysed using Trizol to extract RNA. RNA was reverse transcribed into cDNA using a high capacity cDNA archive kit (Applied Biosystems, Foster City, CA). The cDNA was used for quantitative PCR which was run on the ABI Prism 700 sequence Detection System. The primers for the iNOS, COX-2, IFN-γ, TNF-α, IL-1β and GAPDH were obtained from Applied Biosystems (Foster City, CA).
HT-29 cells were incubated in a chamber slide (Nunc, Rochester, NY) with cytokines and pterostilbene for 15 min and for 30 min to detect p-p38 and p-ATF2, respectively. Cells were fixed with 4% paraformaldehyde [1X PBS (pH 7.4)] for 20 min and blocked with 10% BSA/0.5%Triton X-100/ 1X PBS for 1 h. Following this, the cells were incubated sequentially with primary antibody (1:100 dilution for p-p38 or 1:25 dilution for p-ATF2) overnight and fluorophore conjugated secondary antibody (Alexa Fluor® 488, Invitrogen, Carlsbad, CA) for 1 h and 4’, 6-diamidino-2-phenylindole (DAPI) for 30 min. The cells were irradiated with green laser at 488 nm for detection of p-p38 and p-ATF2 and UV light at 364 nm for nuclear staining by DAPI.
siRNA against p38α and p38β isoforms were purchased from Dharmacon (Lafayette, CO). HT-29 cells were transfected as given in the manufacturer's protocol. Briefly, the cells were plated at 150,000 cells/ well in 6-well plates. Individual siRNA was mixed with Accell™ siRNA delivery medium and added to the wells to give a final concentration of 1 μM per well. After incubation with the mixture for 72 h, the medium was changed to complete medium and cells were treated with cytokine mixture and pterostilbene for an additional 15 h. Changes in induction of iNOS and COX-2 were measured by Western blot analysis.
Quantitative data are reported as the mean ± standard deviation for the individual experiments as specified in the figure legends. Statistical significance analysis was performed using the Student's t-test. The number of observations for each treatment, represented as n, and the measure of significance of treatments, the p-value, are given in the figure legends.
We evaluated the effect of pterostilbene and resveratrol on the growth of cultured colon cancer HT-29 cells. The cells were incubated with different concentrations of pterostilbene for 1, 2 and 3 days, and cell proliferation was estimated by measuring [3H]thymidine incorporated into DNA. The 3-day incubation gave the strongest growth inhibition, and there was a dose-dependent effect (Fig. 1B). As illustrated in Fig. 1C, pterostilbene was a more potent inhibitor of proliferation (IC50 = 22.4 μM) when compared to resveratrol treatment (IC50 = 43.8 μM) under the same conditions. IC50 values were determined using TableCurve 2D® software (Ver. 5.01) from Systat. In order to evaluate whether pterostilbene potentiates cell cycle arrest or apoptosis in HT-29 cells, we examined the effect of pterostilbene on proteins regulating the cell cycle/apoptosis pathways. Pterostilbene was effective in reducing c-Myc and cyclin D1 levels, after a 9 h incubation (Fig. 1C). However, pterostilbene showed no induction of p21 and p27, which belong to the CIP-KIP family of cyclin dependent kinase inhibitors (data not shown). As a marker for the induction of apoptosis, we determined the level of cleaved PARP. Treatment with pterostilbene for 9 h or 18 h increased the level of cleaved PARP (Fig. 1D).
To determine the cytokines or the combination of cytokines that will give maximal induction of iNOS and COX-2 in HT-29 cells, we treated the cells with TNF-α, IFN-γ, LPS and IL-1β either alone or in combination for 15 h (Fig. 2A). Addition of the cytokines individually to HT-29 cells did not cause a noticeable induction of iNOS. Although the addition of IFN-γ plus LPS caused a strong induction, even stronger induction of iNOS amongst the combinations tested was exhibited by a triple combination of TNF-α, IFN-γ and LPS. COX-2 was induced by TNF-α, LPS or IL-1β individually, and TNF-α was the most potent inducer. The combination of TNF-α with either IL-1β or LPS yielded the strongest induction of COX-2. The triple combination induced both iNOS and COX-2, and this combination was selected for additional studies. Since pterostilbene is a naturally occurring analog of resveratrol, we first compared the inhibitory effects of pterostilbene and resveratrol against the induction of iNOS and COX-2 protein in this condition. At the concentration tested (30 μM), pterostilbene showed better inhibitory activity than resveratrol against induction of iNOS and COX-2 proteins (Fig. 2B).
To determine the kinetics of induction of iNOS and COX-2 in HT-29 colon cancer cells, the cells were treated with the cytokine mixture of TNF-α, IFN-γ and LPS for periods of 9, 12 and 15 h. The induction of iNOS was highest at 15 h while the COX-2 level was high at 9−12 h and low at 15 h (Fig. 2C). These data show that maximal induction of COX-2 occurs earlier than that of iNOS. As also shown in Fig. 2C, pterostilbene at 50 μM markedly blocked the induction of iNOS and COX-2 by the cytokine mixture at each time point. In addition, we determined the effect of treatment of the cells with different concentrations of pterostilbene on the induction of iNOS and COX-2 by the cytokine mixture. Pterostilbene inhibited the induction of iNOS and COX-2 in a dose-dependent manner (Fig. 2D).
The gene-mediated expression of iNOS and COX-2 are regulated both at the transcriptional and translational levels (13, 14). In order to evaluate the effect of pterostilbene on cytokine-induced expression of pro-inflammatory enzymes and cytokines, the induction of mRNA levels of iNOS, COX-2, IL-1β, IFN-γ and TNF-α genes were analyzed by quantitative RT-PCR after HT-29 cells were treated with cytokines and/or pterostilbene. Pterostilbene at 30 μM strongly inhibited iNOS, COX-2, and IL-1β mRNA induction by the cytokine mixture (Fig. 3). Induction of TNF-α mRNA by cytokines was observed, but pterostilbene showed only a weak inhibitory effect (Fig. 3). We also measured the mRNA level of IFN-γ induced by the cytokine mixtures, but it was too low to be detected in HT-29 cells (data not shown).
Cytokines induce iNOS and COX-2 through various signaling pathways (13, 15). To elucidate the mechanism responsible for the anti-inflammatory action of pterostilbene, we examined the upstream pathways for iNOS and COX-2 formation, which are activated rapidly after cytokine treatment. As shown in Fig. 4A, the NF-κB/IκBα and JAK-STAT pathways were investigated. Cytokine treatment for a short time (15 min) decreased IκBα levels. Pterostilbene, however, did not block the degradation of IκBα protein induced by the cytokines (Fig. 4A). In addition, the accumulation of the p65 subunit of NF-κB in the nucleus was not affected by pterostilbene (data not shown), confirming that NF-κB signaling is not regulated by pterostilbene in colon cancer cells.
The significance of the JAK-STAT pathway in HT-29 cells was evaluated by the level of phospho-STAT1 and phospho-STAT3 proteins. Cytokines activated the STAT pathway, as shown by a strong induction of phospho-STAT1 and phospho-STAT3. However, pterostilbene did not alter the level of induced phospho-STAT1 and phospho-STAT3 (Fig. 4A). When we determined the activation of ERK1/2 and p38 kinases by cytokines by measuring the levels of phosphorylated ERK1/2 and p38, we found that pterostilbene did not block ERK1/2 activation but strongly inhibited activation of p38 (Fig. 4B). Cytokine-induced increase in p-JNK protein was noticeable, but there was little or no inhibitory effect of pterostilbene on this increase. Cytokine or pterostilbene treatment did not change the level of p-Akt, which is the downstream effector of the PI3-kinase pathway (Fig. 4B).
Since pterostilbene is effective in down-regulating the cytokine-induced activation of p38, we further examined the involvement of pterostilbene on some of the known upstream effectors and downstream targets of p38 kinase. Phospho-MKK3/6 is known as the major molecule responsible for activating p38 MAPK which, in turn, is activated by the upstream kinase in the MAPK cascade. We found that pterostilbene was effective in inhibiting cytokine-induced phosphorylation of MKK3/6 at 15 min (Fig. 5A). Furthermore, the activation (phosphorylation) of well-known downstream targets of p38, ATF2 and Elk-1, was also blocked by pterostilbene at 30 min (Fig. 5B).
Changes in the intracellular expression pattern of p-p38 and p-ATF2 were detected by immunofluorescence. With regard to p-p38, cytokine treatment induced p-p38 and its localization mainly in the nucleus and perinuclear region. Recently, Siddiqui et al have reported similar localization pattern for activated p38 in endothelial cells (36). Pterostilbene treatment attenuated this increase (Fig. 5C), parallel to the observations from Western blot analysis (Fig. 4B). Activated transcription factor, p-ATF2, was prominent in the nucleus by cytokine treatment and pterostilbene virtually nullified these elevated levels (Fig. 5D). Thus, significantly lower levels of the activated p38 and ATF-2 were observed in the nucleus of HT-29 cells after treatment with the stilbene.
Four mammalian p38 isoforms, p38α, p38β, p38γ and p38δ, have been identified: p38α and p38β forms are ubiquitously expressed, whereas p38γ is present mostly in skeletal muscle, heart, lung and thymus, and p38δ in lungs, pancreas, testis, kidney and small intestine (37). SB203580, a pharmacological inhibitor that specifically targets the p38α and p38β isoforms (38), was shown to lower cytokine-induction of iNOS and COX-2 in our study (data not shown). Thus to delineate the role of different isoforms of p38 MAPK for the induction of iNOS and COX-2, we used siRNA against p38α and p38β. Results showed that absence of p38α expression almost completely blocked the induction of iNOS (Fig. 6). Since deletion of p38α expression by itself resulted in almost no induction of iNOS, there was hardly any change by co-treatment of pterostilbene with the cytokine mixture in the p38α siRNA treated group. In addition, siRNA against p38α also markedly reduced COX-2 induction. Moreover, p38α is the most abundant isoform of p38 (Fig. 6; total p38 blot). These results suggest that p38α is the key molecule in inducing iNOS and COX-2 with the cytokine mixture, and pterostilbene may be acting through this p38α isoform to block the inflammatory enzyme expression in HT-29 cells.
In the present study, we investigated the mechanisms of action of pterostilbene in HT-29 colon cancer cells. The results of our study indicate that pterostilbene is more effective than resveratrol as an inhibitor of DNA synthesis in the human adenocarcinoma HT-29 cell line (Fig.1C). In addition, pterostilbene showed better activity than resveratrol for inhibiting the induction of inflammatory genes, such as iNOS and COX-2 (Fig. 2B). The better activity of pterostilbene over resveratrol may, in part, be explained by structural differences. Pterostilbene with two methoxy groups and one hydroxyl group has improved lipophilicity and a better potential for cellular uptake compared to resveratrol which has trihydroxy groups. We showed that pterostilbene inhibited the growth of HT-29 cells and altered markers of cellular proliferation and apoptosis, as shown by lower protein levels of c-Myc and cyclin D1 as well as an increased level of cleaved PARP in pterostilbene treated cells (Fig. 1). These data are consistent with the results of recent studies indicating that pterostilbene and resveratrol induce apoptosis and down-regulate genes that are directly involved in cell proliferation including cyclin D1 in vivo and in vitro (39, 40).
In our study with HT-29 colon cancer cells, a triple combination of TNF-α, IFN-γ and LPS resulted in a marked induction of iNOS and COX-2 (Fig. 2A), and pterostilbene reduced the induction of iNOS and COX-2 in a dose-dependent fashion (Fig. 2D). Quantitative RT-PCR data showed that the regulation of iNOS and COX-2 occurred at the transcriptional level with pterostilbene effectively down-regulating the cytokine induction of iNOS and COX-2 mRNA (Fig. 3). Treatment with a mixture of cytokines induced mRNA synthesis for pro-inflammatory cytokines, such as IL-1β, and this was significantly inhibited by pterostilbene. These results underscore the anti-inflammatory potential of pterostilbene.
TNF-α, IFN-γ, IL-1β and LPS are effective inducers of the expression of inflammatory genes in macrophages and epithelial cells, although expression levels vary with cell type (41). The upregulation of iNOS and COX-2 is mediated by multiple pathways, which vary with cell type and cytokines used. The involvement of NF-κB, AP-1, MAPKs and JAK-STAT in the expression of these genes has been evaluated for a variety of compounds with anti-inflammatory potential. Resveratrol, which is structurally similar to pterostilbene, reduced iNOS and COX-2 induction in rat glioma cells and inhibited iNOS induction by LPS in macrophages by reducing NF-κB (42, 43). Recently, pterostilbene was found to suppress the activation of ERK, p38, PI-3-kinase and NF-κB in LPS-induced murine macrophages, suggesting that these pathways play crucial roles in the action of pterostilbene to inhibit iNOS and COX-2 in macrophages (44). However, our results demonstrate the p38 MAP kinase cascade as a major signaling pathway inhibited by pterostilbene in HT-29 colon cancer cells, suggesting that cell type specificity may contribute to this difference (Fig. 4). In addition, our preliminary data revealed that pterostilbene does not affect cell proliferation-related events via the p38 pathway (data not shown), indicating that there may be two distinct mechanisms of pterostilbene for its anti-proliferation and anti-inflammatory actions.
The p38 MAPK cascade is activated by its upstream kinase MKK3/6, which is the MAPK kinase for p38, and we found that pterostilbene strongly inhibited the activation of both MKK3/6 and p38 (Fig. 5A and 5B). This suggests that pterostilbene may activate p38 MAPK through the conventional kinase cascade which has small GTP proteins, such as Rac, Rho, cdc42 acting on MAPKKK or MAP3K followed by its substrate, MAPKK or MAP2K (MKK3/6) and finally p38 MAPK (45). In the MAPK cascade, we also observed that pterostilbene acts on downstream targets of p38, namely ATF2 and Elk-1 (Fig. 5B). There are a myriad of transcription factors and kinases that are affected by p38 such as MEF2, MSK, CHOP and MAPKAP (46), but we examined two key mediators, ATF2 and Elk-1, which are known to play important roles in inflammatory gene responses (47). ATF2 is a subunit of the AP-1 complex and binds to the CRE promoter sequence on iNOS and COX-2, and Elk-1 belongs to the ETS transcription factor and binds to the ETS DNA-binding domain on the promoter sequence of inflammatory genes (14). In the present study, we found that pterostilbene blocked the phosphorylation and nuclear translocation of p38 and ATF-2 induced by cytokine mixture (Fig. 5B-D), providing evidence for the involvement of the p38 MAPK-ATF-2 pathway for the anti-inflammatory action of pterostilbene in HT-29 colon cancer cells.
Among the different isoforms of p38 MAPKs, p38α is known to play a key role in inflammatory processes (48). This MAPK was originally identified as a molecular target of the pyridinyl imidazole class of compounds, such as SB203580, that were known to inhibit pro-inflammatory cytokine synthesis, and many of these inhibitors have entered clinical trials for inflammatory diseases (38). Since the p38 inhibitor, SB203580, suppresses activation of both p38α and p38β, it is difficult to distinguish the effects produced by each isoform independently. In our study, we employed RNA interference to show that p38α is the most abundant isoform in HT-29 colon cancer cells, and p38α is the key molecule involved in iNOS and COX-2 expression (Fig. 6). This observation along with coordinated results from short time point experiments (Fig. 4 and and5)5) indicate that pterostilbene may inhibit iNOS and COX-2 expression primarily through its action on p38α MAPK.
In conclusion, the data presented here indicates that pterostilbene inhibits growth and exerts an anti-inflammatory action in HT-29 colon cancer cells. Pterostilbene-induced inhibition of p38 MAPK signaling may be a key effect of pterostilbene required for reduction of inflammatory markers, such as iNOS and COX-2. Overall, pterostilbene is a promising anti-inflammatory agent for inhibition of colon carcinogenesis.
The authors thank the Department of Chemical Biology for their technical assistance and Dr. Allan Conney for helpful comments on our manuscript.
Grant Information: This work was supported in part by NIH R03 CA112642, NIH R01 CA127645, NIEHS P30 ES005022, and a CINJ new investigator award.