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. 2011 Jul 28;2(7):e185. doi: 10.1038/cddis.2011.64

Celecoxib and acetylbritannilactone interact synergistically to suppress breast cancer cell growth via COX-2-dependent and -independent mechanisms

B Liu 1,2, J K Wen 1, B H Li 3, X M Fang 1, J J Wang 1, Y P Zhang 1, C J Shi 1, D Q Zhang 4, M Han 1,*
PMCID: PMC3199716  PMID: 21796157

Abstract

The use of celecoxib is associated with a significant decrease in breast cancer risk. However, the long-term use of high-dose celecoxib might be limited owing to cardiovascular side effects. In this study, we found that acetylbritannilactone (ABL), extract from a Chinese medicinal herb, could reduce celecoxib dose and potentiate the growth-inhibitory effect in breast cancer cells. ABL enhanced the apoptotic effect of celecoxib in COX-2-expressing cells, but had little effect in COX-2-negative cells. The apoptosis induced by the combination treatment disappeared when COX-2 was knocked down, whereas the lack of apoptotic effects in COX-2-negative cells was reversed after COX-2 transfection. However, the combination treatment induced a G0/G1 phase arrest independent of whether or not the cells expressed COX-2. The G0/G1 arrest was attributed to a decreased expression of cyclinD1, cyclinE, CDK2 and CDK6, especially the upregulation of p21. In addition, inhibition of Akt and p38 signaling pathways was required by the synergism, as the constitutively active Akt and p38 protected cells against apoptosis and cell cycle arrest induced by the combination treatment. In vivo, administration of celecoxib and ABL were more effective than the individual agents against xenograft tumor growth. Thus, our data suggested that the combinatorial approach of celecoxib and ABL might be helpful for breast cancer treatment.

Keywords: acetylbritannilactone, apoptosis, breast cancer, cell cycle, cyclooxygenase-2

Breast cancer is the most common cancer among women in both developed and underdeveloped countries. Abnormally elevated expression of cyclooxygenase-2 (COX-2) has been frequently observed in breast cancer tissues and some researches support the concept that COX-2 could provide an early target for breast cancer prevention.1, 2, 3 Previous studies demonstrated that administration of non-steroidal anti-inflammatory drugs (NSAIDs), such as aspirin, ibuprofen, naproxen, piroxicam or indomethacin, had significant chemopreventive effects against the development of breast cancer.4, 5 On the contrary, the long-term use of them may be limited owing to serious adverse effects among users, such as ulcer complications, bleeding, cardiovascular toxicity, platelet dysfunctions and renal toxicity,6, 7 as a result of interference of COX-1-derived homeostatic functions. Therefore, it is rational to search for specific inhibitors of COX-2 as potential candidates for use as chemopreventive agents. Celecoxib, the first selective COX-2 inhibitor approved by the U.S. Food and Drug Administration, is a widely marketed anti-inflammatory drug with improved safety unlike traditional NSAIDs8 and exerts potent anticancer effects in various tumor types, including the colon, skin, prostate, lung and breast.9, 10, 11, 12, 13, 14 However, the exact molecular mechanisms involved are not yet defined. Many lines of evidence from in vitro studies and animal models indicated that celecoxib exerted its effect by preventing COX-2 protein expression and prostaglandin E2 (PGE2) synthesis.9, 10 Moreover, other studies suggested that celecoxib might suppress cell proliferation and carcinogenesis by downregulating multidrug resistance-associated protein expression12 or inhibiting nuclear factor-kappa B (NF-κB) activation.13, 15

The development of a regimen consisting of a phytochemical with chemopreventive activity combined with celecoxib would be highly desirable for the treatment of cancer, which will reduce the dose of celecoxib16, 17 and may minimize dose-related cardiovascular side effects.18, 19, 20 Acetylbritannilactone (ABL), a new active extract isolated from a traditional Chinese medicinal herb Inula britannica L,21 is commonly used to treat bronchitis and inflammation in China. Previous studies have shown that ABL exhibit potent anti-inflammatory effects in vascular smooth muscle cells21, 22, 23 and anticancer activities against colon, breast, ovary, leukemia and prostate cancer cells.24, 25, 26, 27 Moreover, additional researches reported that ABL could activate caspases via the mitochondrial apoptosis pathway, induce Bcl-2 phosphorylation and suppress NF-κB activation in several types of cell lines.21, 25, 27 Therefore, it is interesting to investigate whether ABL could be a synergist to help increase the efficacy of other chemopreventive agents in cancer therapy. With the goal of enhancing the chemopreventive effects of celecoxib and reduced the dose in chemotherapy, we evaluated the possibility of the combination treatment of celecoxib and ABL on human breast cancer in vivo and in vitro.

Results

The combination treatment of celecoxib and ABL on human breast cancer cell growth

The effects of celecoxib, ABL and their combination on cell growth were assessed by cell counting assays. Three cell lines (MDA-MB-231, MDA-MB-468 and MCF-7) that differ in the COX-2 status (Supplementary Figure S1A) were used to elucidate whether the effects depend on COX-2 expression levels. As shown in Figure 1a, both celecoxib and ABL suppressed cell growth in a dose dependent manner. At the doses tested, neither celecoxib (5 μM) nor ABL (25 or 50 μM) elicited the growth-inhibition effect as a single agent, but the combination treatment significantly suppressed cell growth in all three cell lines. Despite the higher basal level of COX-2 expression in MDA-MB-231 cells, a comparable degree of growth inhibition was observed in the other cell lines, which were not found to differ significantly according to COX-2 expression levels. In the presence of 50 μM ABL, IC50 of celecoxib was 4.6 μM, a 7.5-fold lower dose than the IC50 (34.4 μM) of celecoxib alone in MDA-MB-231 cells, suggesting that ABL may enhance the sensitivity of cancer cells to celecoxib. Moreover, there was a dose-response reduction in MDA-MB-231 cell growth caused by the combination treatment (Supplementary Figure S1B).

Figure 1.

Figure 1

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Effects of celecoxib, ABL or their combination on the growth of breast cancer cells. (a) Cells were treated with different doses of celecoxib, ABL or their combination for 48 h, and growth inhibition was measured by cell counting assays. The data were showed as the percentage of vehicle-treated cells. Results were expressed as mean±S.E.M. *P <0.05, compared with vehicle-treated group. (b) MDA-MB-231 cells were treated with celecoxib (2.5–10 μM) plus ABL (12.5–100 μM) at a fixed ratio of 1:5 or 1:10, and then the CI was calculated as described in Materials and Methods

To do mathematical analysis by the median effect method, MDA-MB-231 cells were treated with both celecoxib and ABL simultaneously at fixed 1: 5 and 1:10 dose ratio for 48 h. Combination index (CI) values were calculated as described previously.28 As shown in Figure 1b, the CI values of the concentration were less than 1, indicating that ABL synergistically enhances celecoxib-induced growth inhibition in MDA-MB-231 cells. Moreover, similar results were obtained in MDA-MB-468 and MCF-7 cell lines (Supplementary Figure S1C). Thus, celecoxib and ABL may be an effective combination for cell growth inhibition due to their synergistic efficacy.

ABL synergistically enhanced celecoxib-induced apoptosis

To evaluate the mechanism for synergistic cytotoxicity between celecoxib and ABL, the extent of apoptosis was assessed using ELISA. In MDA-MB-231 cells, the formation of cytoplasmic histone-associated DNA fragments was observed only when they were exposed to the combination (Figure 2a). DAPI staining assay confirmed the results (Supplementary Figure S2A). However, a very weak effect was seen in MCF-7 cells that expressed no constitutive COX-2 (Figure 2a and Supplementary Figure S2A). Various ABL doses were tested in the MDA-MB-468 cells, but we were unable to detect any apoptotic enhancement effect of celecoxib (5 μM) (Supplementary Figure S2B).

Figure 2.

Figure 2

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Effects of celecoxib, ABL or their combinations on the apoptosis of breast cancer cells. Cells were treated with celecoxib, ABL or their combination as indicated for 48 h. (a) DNA fragmentation of apoptotic cells was evaluated using a Cell Death Detection ELISAPlus kit. *P<0.05, compared with vehicle-treated cells. (b) Apoptotic cells were evaluated by ELISA in Control and KD cells after the combination treatment. Control, MDA-MB-231 cells transfected with a general negative sequence of siRNA; KD, COX-2 KD MDA-MB-231 cells. (c) MCF-7-mock, MCF-7-COX-2 and TPA (0.1 μM)-stimulated MCF-7 cells were treated with combination of celecoxib and ABL for 48 h, and apoptotic cells were evaluated. Results were expressed as mean±S.E.M. from at least three independent experiments

Moreover, apoptosis markers were analyzed by western blot. The combination treatment, instead of individual agents, resulted in marked increased cleavage of PARP in MDA-MB-231 cells and, to a minor degree, in MCF-7 cells (Supplementary Figure S2C). Further experiments indicated that the combination treatment increased the active form of cleaved caspase-3 and cleaved caspase-9 in MDA-MB-231 cells. The absence of caspase-3 activation in MCF-7 cells29 raised the possibility that the combination treatment might induce apoptosis through other caspases or death receptor pathways.

The combination-induced apoptosis via a COX-2-dependent manner

To determine whether the combination-induced apoptosis occurs in a COX-2-dependent route, COX-2 knocked-down cells (KD), which transfected COX-2 siRNA, and its mock control cells (Control) were established from MDA-MB-231 cells. The COX-2 expression was markedly reduced in the KD compared with MDA-MB-231 cells, whereas we observed no changes in the Control (Supplementary Figure S3A). PGE2 is a primary product of the COX-2 enzyme, which represents COX-2 activity. PGE2 production of the Control cells was comparable to that in MDA-MB-231 cells. However, PGE2 production in the KD was noted to have decreased to 5% that observed in MDA-MB-231 cells or the Control (Supplementary Figure S3A). Moreover, the combination-induced apoptosis were observed in the Control, but these effects disappeared in the KD (Figure 2b).

Furthermore, additional experiments were performed to determine whether the weak apoptotic induction by combination treatment in MCF-7 cells could be reversed via COX-2 overexpression. For this, we constructed stably transfected MCF-7 cells (MCF-7-COX-2) and mock control cells (MCF-7-mock) as previously described.30 The MCF-7-COX-2 cells exhibited high expression of COX-2 protein, comparable to that of MDA-MB-231 cells, whereas the MCF-7-mock cells expressed no COX-2 (Supplementary Figure S3B). As shown in Figure 2c, MCF-7-COX-2 cells were more sensitive to combination treatment than MCF-7-mock cells. Moreover, TPA (0.1 μM)-stimulated MCF-7 cells were treated with the combination and showed that there was additive proapoptotic effect in the cells (Figure 2c). In addition, exogenous PGE2 partially prevented the combination-induced apoptosis in MDA-MB-231 and MCF-7-COX-2 cells (Supplementary Figure S3C), suggesting that these effects at least partially suppress PGE2 generation.

ABL synergistically improved the effects of celecoxib on COX-2 expression and activity

To determine whether the synergistic effects observed in COX-2 expressing cells were related to COX-2 synthesis, expression of COX-2 mRNA and protein was examined in MDA-MB-231 cells. As shown in Figure 3a, COX-2 was slightly decreased by the single agent, but was markedly decreased by the combination treatment, although COX-1 was not changed under the same treatment conditions. The combination treatment also notably decreased PGE2 in medium collected from the cells (Figure 3b). Consistent with western blot results, the combination treatment on MDA-MB-231 cells led to a drastic decrease in cytoplasmic COX-2, and COX-1 expression was not affected in immunofluorescence staining analyses (Supplementary Figure S4A).

Figure 3.

Figure 3

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Effects of the combination of celecoxib and ABL on COX-2 expression and activity in MDA-MD-231 cells. (a) MDA-MD-231 cells were treated with celecoxib, ABL or their combination for 24 h (left) or 48 h (right). COX-2 mRNA and protein expression was examined using RT-PCR (left) and western blot analysis (right). Quantification of COX-2 mRNA and protein expression normalized to actin levels, were provided at the bottom. (b) MDA-MB-231 cells were treated with the combination for 48 h, and PGE2 levels in the culture medium were measured using ELISA. Results were expressed as mean±S.E.M. from at least three independent experiments

Moreover, luciferase-reporter construct containing a fragment of COX-2 promoter was transfected into MCF-7 cells, which was used to study regulation of COX-2 transcriptional activity.31, 32 It showed that ABL potentiated the inhibitory effect of celecoxib on COX-2 activity (Supplementary Figure S4B). In addition, TPA-induced COX-2 expression was also markedly suppressed by the combination treatment (Supplementary Figure S4C).

The combination-induced cell growth inhibition is mediated partly through G0/G1 arrest

As cell growth suppression often occurs as a consequence of cell cycle block, we were interested in knowing whether the effects of the combination treatment were related to cell cycle regulation. As determined by flow cytometry, the combination of celecoxib and ABL induced a significant inhibition of cell cycle progression from the G0/G1 to S phase in both MDA-MB-231 and MCF-7 cells (Figure 4a). Moreover, a marked reduction of cyclinD1 and cyclinE expression was observed when cells were treated with the combination (Figure 4b). CDK2 and CDK6 levels also decreased. Conversely, expression of p21 was significantly induced after the combination treatment. In addition, other tested cell lines treated with celecoxib and ABL also exhibited considerably increased rates of G0/G1 phase cells (for Control, KD, MCF-7-COX-2, MCF-7-mock and MDA-MB-468 cells, respectively), and supplementation with PGE2 (50–200 pg/ml) did not affect the G0/G1 block (Supplementary Figure S5A). As p21 has a critical role in mediating G0/G1 arrest, we performed experiments to examine whether overexpression of COX-2 would alter its expression. As shown in Supplementary Figure S5B, although the COX-2 protein was induced in MCF-7-COX-2 and TPA-stimulated MCF-7 cells, p21 level was not altered after the combination treatment. Thus, the results suggested that the combination-induced cell growth inhibition was mediated, at least in part, through G0/G1-cell cycle arrest, which was independent of whether the cells expressed COX-2 or not.

Figure 4.

Figure 4

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Effects of the combination of celecoxib and ABL on cell cycle progression. (a) MDA-MB-231 and MCF-7 cells were treated with celecoxib, ABL alone or their combination for 24 h. Cell cycle distributions were determined by flow cytometry analysis. The bar graph reflected the percentage of cells in G0/G1, S, G2/M phase of cell cycle. (b) Cells were treated with the combination for 24 h and subjected to western blot with specific antibodies directed against cyclin D1, cyclin E, CDK-2, CDK-4, CDK-6, p21 and p27. Densitometric analyses of western blot, normalized to actin levels, were provided. Each column represents the mean±S.E.M.

The combination-induced cell growth inhibition associated with Akt and p38 signaling

To investigate the common mechanistic basis of apoptosis and cell cycle arrest for the synergistic effects between celecoxib and ABL, we determined the changes on the survival signaling pathways represented by Akt, and also the mitogen-activated protein kinases cascades.33 Western blot analysis showed that exposure of MCF-7 cells to celecoxib or ABL alone for 2 h resulted in a slight decrease in Akt and p38 phosphorylation induced by TPA (Figure 5a). However, the combination treatment reduced active Akt and p38 to a greater degree versus either agent alone. In addition, combined exposure of cells to celecoxib and ABL resulted in a modest but discernible decline in the phosphorylation of downstream Akt target GSK-3β. In contrast, JNK and ERK1/2 activation were barely affected (Figure 5a), suggesting that they were unlikely to be involved in these processes. Focusing on Akt and p38, modulation of these pathways was not cell line specific, as similar results were observed in MDA-MB-231 cells after combination treatment.

Figure 5.

Figure 5

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Effects of the combination of celecoxib and ABL on signaling pathways in MCF-7 cells. (a) MCF-7 cells were cotreated with TPA and the combination for 2 h, then cell lysates were analyzed by western blot for p-Akt, p-GSK-3β, p-p38, p-JNK and p-ERK1/2. Densitometric analyses of western blot, normalized to actin levels, were provided. (b) MCF-7 cells were transfected with the Ca-Akt or MKK6b vector and then treated with TAP and the combination in the presence of Akt inhibitor (LY294002) or p38 inhibitor (SB203580) for 48 h as indicated. The percentage of apoptotic cells was determined by ELISA. (c) The transfected cells were treated with the combination in the presence of LY294002 or SB203580 for 24 h. Cell cycle distribution was analyzed by flow cytometry. Results were expressed as mean±S.E.M.

To address the question on whether the observed changes in signaling were responsible for the apoptosis, MCF-7 cells were transfected with Ca-Akt or MKK6b vectors. It showed that Ca-Akt or MKK6b protected cells from combination-induced apoptosis, whereas inhibition of these pathways enhanced pro-apoptotic effects (Figure 5b). Moreover, MCF-7 cells were transfected with COX-2-Luc along with Ca-Akt or MKK6b vectors and it could restore the TPA-induced COX-2 activity after the combination treatment (Supplementary Figure S6A). Further works were addressed to evaluate the ability of celecoxib plus ABL on COX-2 mRNA decay, and similar effects were observed (Supplementary Figure S6B). These results indicated that the combination treatment modulated the activation of Akt and p38, beyond the primary effect on COX-2.

Subsequently, the roles of the above signal pathways were determined in cell cycle regulation. As shown in Figure 5c, activation of the Akt or p38 pathway significantly decreased cell number in G0/G1 phase, whereas inhibition of these pathways enhanced cell G0/G1 cycle arrest by the combination treatment. Thus, it indicated that the synergism reflected inhibition of Akt and p38 that occurred upstream of combination-initiated cell cycle arrest.

Therapeutic effects of combination treatment against MDA-MB-231 xenograft model

As the combination treatment of celecoxib and ABL was more effective than the individual agents in vitro, effects of them on tumor development were examined in athymic nude mice. As shown in Figure 6a, treatment with celecoxib (5 mg/kg) or ABL (15 mg/kg) had weak inhibitory effect on MDA-MB-231 tumor growth, whereas the combination treatment significantly reduced tumor volume by 50% (P<0.05) after 30 days. All the groups were well tolerated without obvious signs of drug-related toxicity throughout the course of this study.

Figure 6.

Figure 6

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Effects of celecoxib and ABL individually and in combination on MDA-MB-231 Xenograft model. Female nude mice bearing MDA-MB-231 tumors were treated with vehicle, celecoxib (5 mg/kg) and ABL (15 mg/kg) individually, or in combination. (a) Tumors were measured with calipers on alternate days. Points, mean tumor volume in each experimental group containing six mice. *P<0.01 versus vehicle group. (b) The expression of COX-2, COX-1, p21, PARP, p-Akt, Akt, p-p38 and p38 were determined by western blot analysis in protein extracted from the tumor specimens. Total protein samples from two mice for each group representing control and experiment were used for western blot. Densitometric analyses of western blot (average of two samples) were provided. Each column represents the mean±S.E.M. (c) A strong positive correlation (data shown were obtained from Supplementary Figure S7A and B) between serum PGE2 level and COX-2 expression in xenograft specimens (Pearson's correlation coefficient, 0.900; P<0.001, two-tailed)

Furthermore, the COX-2 expression at tumor specimens was measured. Compared with the individual use of one agent, it clearly indicated that tumor specimens from celecoxib plus ABL-treated mice stained more weakly positive COX-2 expression (Supplementary Figure S7A). Similar results were also determined by western blot analysis in protein extracted from the tumor tissue (Figure 6b). The findings from ELISA assay for serum PGE2 level showed a significant decrease in mice that received the combination treatment (Supplementary Figure S7B). Further, in-depth analysis indicated a positive correlation between the serum PGE2 level and tumor COX-2 expression (Pearson's correlation coefficient, 0.900; P<0.001, two-tailed) (Figure 6c). Moreover, augmented expression of p21 and marked increased cleavage of PARP (Figure 6b) was evident in the mice that received the combination treatment, confirming in vitro data.

We finally evaluated whether the effects of the combination treatment on signal transduction could be also observed in vivo. As shown in Figure 6b, although the inhibitory effects exerted by the individual agents were mild, total and phosphorylated Akt and p38 were downregulated among the mice that received the combination treatment.

Discussion

In this study, we found that the phytochemical ABL synergistically augmented the growth-inhibitory effects of celecoxib on breast cancer cells via COX-2-dependent apoptosis and COX-2-independent cell cycle regulation involving Akt and p38 pathways. Moreover, the therapeutic potential of this combination was shown in its superior activity in suppressing the xenograft tumor growth comparing with that of individual agents.

The combinatorial strategies in cancer therapies can provide more synergistic tumor inhibition and less systemic toxicity than each of the monotherapeutic regimens alone.34, 35, 36 Current results showed that ABL was useful to increase the anticancer activity of celecoxib and reduce its dose. Low dose of celecoxib (5 μM) plus ABL (50 μM) was sufficient to suppress breast cancer cell growth in vitro. This effect was more than that exerted by a higher dose of celecoxib (>40 μM) when administered alone. The dose of celecoxib using here was lower than clinically achievable plasma levels.37 It might be clinically useful, because it could be achieved in the patients who receive the standard dose of celecoxib to cure the neoplastic disease and also avoids the related cardiovascular risk.18, 19, 20 Moreover, we found that ABL primarily affects the sensitization of COX-2-expressing cells to celecoxib and does not tend to confer this sensitivity to COX-2-nonexpressing cells. Thus, it would be reasonable to suppose that ABL-augmented celecoxib-induced apoptosis occurs via a COX-2-dependent mechanism. Furthermore, we observed that only the combination treatment decreased COX-2 expression, activity and notably reduced PGE2 production in COX-2-overexpressing cells. It can be inferred that the synergistic effects may be not only mediated by COX-2 protein itself or by substrates or enzymes in the upstream regions of this protein, but also by its end product. In addition, the combination treatment has no effect on COX-1 expression in vitro and in vivo experiment, it is reasonable to assume that it may be avoid of the side effects associated with the suppression of COX-1-derived prostanoids.

Many studies have showed that COX-2 might be associated with drug resistance. Several treatment, such as paclitaxel,38 mitomycin C,39 and radiation therapy,40 induced COX-2 overexpression, resulting in some adverse effects associated with inflammation, angiogenesis, invasion and metastasis.1, 10, 41 Therefore, downregulation of COX-2 expression might provide effective approaches to treat cancer patients who were sufferings drug resistance. Previous studies showed that the prototype tumor promoter TPA induced COX-2 expression in MCF-7 cells by activating transcription factors such as NF-κB and activator protein-1 (AP-1).31, 32 In the present study, we used TAP-induced MCF-7 cells to simulate the condition of drug resistance related to COX-2 overexpression. Surprisingly, the combination treatment suppressed COX-2 activation and induced significant apoptosis in TPA-stimulated MCF-7 cells, suggesting that the therapeutic regimen might be helpful in drug resistance related to COX-2 expression.

As cell growth inhibition often occurs as a result of cell cycle arrest, we determined the second mechanism underlying the synergistic effects. Previous studies have shown that treatment with low dose of celecoxib (<20 μM) alone for a short time (<72 h) may not affect cell viability and cell cycle distribution.14, 42 Conversely, we found that the combination treatment of celecoxib (5 μM) and ABL (50 μM) for 24 h induced G0/G1 arrest in all the tested cells. The incomplete protection by addition of PGE2 or COX-2 overexpression, and the fact that overexpression or depletion of COX-2 failed to alter the cell cycle indicated the existence of COX-2-independent mechanism. Moreover, the combination-mediated cell cycle arrest could be caused by the suppression of cyclinD1, cyclinE, CDK2 and CDK6 activities, especially the upregulation of p21, which were significant and consistent with the earlier studies that increased p21 expression were associated with inactive of CDKs/cyclin complexes and induced of G0/G1 arrest.43, 44

Another important observation in this study was that celecoxib combined with ABL suppressed phosphorylated Akt and p38. Activated Akt and p38 targeted multiple factors involving in cell proliferation, survival and also mediating cell cycle alteration and apoptosis. Recently, many studies have demonstrated that the cytotoxic compounds could suppress cancer cell growth through these signaling pathways. Flavopiridol could interfere with Akt and p38 and enhanced cell apoptosis.45 Furthermore, Akt and p38 were identified as key signaling responsible for paclitaxel in metastatic breast cancer.46 In the presence of ABL, celecoxib dramatically downregulated Akt and p38 pathways so as to facilitate apoptosis and cell cycle arrest. Thus, we hypothesize that Akt and p38 signaling represent a therapeutically relevant target for ABL to sensitize these cells to celecoxib via two potential mechanisms. First, the suppression of these pathways by the combination treatment would lead to the inhibition of COX-2 expression and activity, which triggered the apoptosis regulators to facilitate apoptosis. Second, ABL interacted synergistically with celecoxib, which could block Akt and p38 activation. Thereby, this process influenced the cell cycle regulator proteins and induced G0/G1 phase cell arrest.

In summary, ABL synergistically enhanced the activity of celecoxib on breast cancer growth inhibition through COX-2-dependent and COX-2-independent mechanisms. Findings from this study concluded that the combination treatment of celecoxib and ABL could improve the chemopreventive efficacy certainly in breast cancer and help to explain the anticancer properties of these chemopreventive agents.

Materials and Methods

Reagents, antibodies and plasmids

Celecoxib was provided by LKT Laboratories, Inc. (Minneapolis, MN, USA). Silica gel column chromatography was used to isolate ABL from Inula britannica L grown in Shan-xi Province in China. The effects of ABL and celecoxib in our experiments were compared with the same concentration of dimethyl sulfoxide (DMSO) as vehicle. The antibodies specific for Poly (ADP-ribose) polymerase (PARP), phospho-c-Jun NH2-terminal kinase (p-JNK), phospho-p38 MAP kinase (p-p38) and p38 were obtained from Cell Signaling Technology (Beverly, MA, USA). Antibodies against COX-1, COX-2, β-actin, caspase-3, caspase-9, phospho-extracellular signal-regulated kinase1/2 (p-ERK1/2), phospho-Akt (p-Akt), Akt, phospho-GSK-3β (p-GSK-3β), the secondary antibodies, small interfering RNA (siRNA) specific for human COX-2 mRNA and control siRNA were from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Unless otherwise indicated, all other reagents used in this study were obtained from Sigma Chemicals (St. Louis, MO, USA). Constitutively active p38 construct MKK6b was kindly provided by Dr. Han (The Scripps Research Institute, CA, USA). Constitutively active Akt construct Ca-Akt was gifts from Dr. Woodgett (Ontario Cancer Institute, Toronto, Canada).

Cell lines and culture conditions

The human breast cancer cell lines (MDA-MB-231, MDA-MB-468 and MCF-7) were from American Type Culture Collection (Manassas, VA, USA). Cells were grown in a 5% CO2 atmosphere at 37°C in DMEM (Invitrogen, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum. All treatments were carried out on cells at 60–80% confluence.

Cell growth inhibition assays

The cells were plated in duplicate in 12-well plates. After 24 h, celecoxib, ABL and their combination were added at the selected doses to the culture medium. The number of viable cells was determined by a Coulter counter 48 h later. We calculated the IC50 by using a standard sigmoidal Emax model. To determine whether the combined effects were synergistic, the cells were treated with the combination of the indicated doses of celecoxib and ABL for 48 h and the CI was determined using the method of Chou and Talalay through the commercial software package Calcusyn (Biosoft, Cambridge, UK).28

Apoptosis assays

Apoptosis was determined by two independent methods.47 For fluorescence microscopy, cells were treated with agents for 48 h. Apoptotic cells were detected by nuclear morphologic changes using DAPI staining. Cells were harvested, washed with PBS and fixed in 70% ethanol for 30 min. The fixed cells were placed on slides and stained with 1 mg/ml DAPI for 15 min. Excess dye was removed and the monolayer was thoroughly washed with PBS. The stained nuclei were observed via a fluorescence microscope.

For ELISA, the cells seeded in 96-well plates were treated with agents for 48 h. The induction of apoptosis by the agents was evaluated with a Cell Death Detection ELISAPlus kit (Roche Diagnostics, Mannheim, Germany) according to the manufacturer's instruction. Measurements were made using an ELISA reader at 405 nm and the results were calculated as the ratio of the absorbance of the agents-treated cells/absorbance of vehicle-treated cells.

Cell cycle analysis

Cells were treated with agents at selected doses and harvested by trypsinization, washed with PBS, fixed with ethanol, incubated for 5 min with 0.5% Triton X-100 and stained with propidium iodide in PBS containing 25 μg/ml RNase. Stained cells were analyzed by flow cytometry (Becton Dickinson, San Jose, CA, USA).

Immunohistochemistry

Paraffin-embedded tumor specimens were subjected to immunohistochemistry according to the antibody protocol. Specimens were developed using secondary antibodies linked to HRP and DBA as a substrate.

Immunofluorescence microscopy

Cells were treated with agents at selected doses for 48 h, then fixed on coverslips with 4% paraformaldehyde, permeabilized with 0.2% Triton X-100 and blocked in 5% goat serum, and then incubated overnight at 4°C with antibodies, followed by incubation with FITC-conjugated secondary antibody for 1 h at room temperature in the dark. Nuclear counterstaining was performed with PI for 10 min at room temperature. Fluorescence was visualized under a fluorescence microscope (Olympus, Tokyo, Japan).

Reverse transcription-PCR (RT-PCR)

Total RNA was isolated from cells using TRIzol Reagent (Invitrogen) and equal amounts were reverse transcribed into cDNA using the oligo dT primer, then the cDNAs were used as DNA templates for PCR. Primers used for COX-2 were 5′-TTCAAATGAGATTGTGGGAAAAT-3′and 5′-AGATCATCTCTGCCTGAGTATCTT-3′. β-actin was used to ensure equal loading. The PCR products were separated on 1% agarose gel and visualized by ethidium bromide.

Western blot analysis

Equal amounts of proteins were subjected to SDS-PAGE analysis and subsequent immunoblotting was carried out with specific antibodies. Levels of immunocomplexes for β-actin were used as an internal standard for equal loading. All experiments were repeated at least thrice and yielded similar results.

PGE2 production

PGE2 from the collected cell medium or the animal serum was determined by a commercially available PGE2-specific ELISA (R&D Biosystems, Abingdon, UK) according to manufacturer's instructions.

Transfection of siRNA

siRNAs specific for COX-2 (COX-2 siRNA) and control siRNA were transfected into cells using transfection reagent Lipofectamine 2000 (Invitrogen). RT-PCR and western blot were used to confirm adequate silencing of the COX-2 genes at 48 h.

Transfection of cells

Cells were transfected either with empty vector or the same vector containing a cDNA encoding constitutively active p38 construct MKK6b, constitutively active Akt construct Ca-Akt.

The stably transfected cells were conducted using COX-2 expression plasmid (full-length human COX-2 cDNA cloned in pcDNA3 vector) and G418 geneticin (Invitrogen) as described previously.30 Individual drug-resistant colonies were isolated and expanded. The selected cells with successful overexpression of COX-2 protein were used for subsequent experiments.

Luciferase assays

The COX-2 luciferase reporter construct (COX-2-Luc) (−1432/+59), containing the wild-type COX-2 promoter fragment, was prepared and cloned into the pGL3 basic vector. Cells were plated in 24-well plates. Transient transfections were performed using the transfection reagent Lipofectamine 2000. Each well was co-transfected with COX-2-Luc plasmid and the internal control plasmid renilla luciferase (pRL-TK). The cells were harvested after the indicated times of treatment, and the activities of both firefly luciferase and pRL-TK luciferase were measured.

Xenograft model

The animal study was performed via a protocol approved by the governmental committee for animal research. Female BALB/c nude mice (4–5 weeks old) were injected s.c. with MDA-MB-231 cells (6 × 106) per mice at both flanks and randomly assigned to treatment groups (six mice per group). After 6 days, when a small vascularized tumor (50–100 mm3) had developed, control group was treated with vehicle (10% DMSO, 10% ethanol in water) daily by i.p. injection. The celecoxib group (5 mg/kg) was treated daily by oral administration as described previously.10 ABL group (15 mg/kg) was given daily by i.p. injection. The group treated with the combination was dosed in the same manner as both single-agent groups. Mice were weighed at least twice a week and the tumor size was measured every other day using calipers and their volumes were calculated according to a standard formula: width2 × length/2. Mice were killed after 36 days of treatment and the tumor specimens were removed for immunohistochemistry and western blot analysis.

Statistical analysis

All of the experiments were repeated a minimum of three times. Data were presented as mean±S.E.M. Statistical analyses of the differences between the groups were determined with the two-sided unpaired Student's t-test using SPSS software (SPSS, Inc., Chicago, IL, USA), and a value of P<0.05 was considered as significant.

Acknowledgments

This work was supported by a grant from the National Natural Science Foundation of PR China (No. 30973820) and a grant from the Hebei Province Natural Science Foundation of PR China (No. C2011206163 and C2011206146).

Glossary

ABL

acetylbritannilactone

COX-2

cyclooxygenase-2

ERK

extracellular signal-regulated kinase

JNK

c-Jun NH2-terminal kinase

MAPKs

mitogen-activated protein kinases

NF-κB

nuclear factor-kappa B

NSAIDs

non-steroidal anti-inflammatory drugs

p38

p38 MAP kinase

PARP

poly (ADP-ribose) polymerase

PGE2

Prostaglandin E2

siRNA

small interfering RNA

The authors declare no conflict of interest.

Footnotes

Supplementary Information accompanies the paper on Cell Death and Disease website (http://www.nature.com/cddis)

Edited by A Stephanou

Supplementary Material

Supplementary Figure S1
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Supplementary Figure S2
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Supplementary Figure S3
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Supplementary Figure S4
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Supplementary Figure S5
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Supplementary Figure S6
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Supplementary Figure S7
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Supplementary Figure Legends
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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Figure S1
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Supplementary Figure S2
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Supplementary Figure S3
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Supplementary Figure S4
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Supplementary Figure S5
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Supplementary Figure S6
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Supplementary Figure S7
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Supplementary Figure Legends
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