Effects of COX-2 inhibition on expression of vascular endothelial growth factor and interleukin-8 in lung cancer cells
© Zhu et al. 2008
Received: 29 June 2007
Accepted: 31 July 2008
Published: 31 July 2008
Skip to main content
© Zhu et al. 2008
Received: 29 June 2007
Accepted: 31 July 2008
Published: 31 July 2008
Cyclooxygenase (COX)-2 has been implicated in tumour progression, angiogenesis and metastasis in non-small cell lung cancer (NSCLC). We speculated that inhibition of COX-2 activity might reduce expression of the pro-angiogenic factors vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8) in lung cancer cells.
The levels of IL-8, VEGF and prostaglandin E2 (PGE2) were measured by ELISA. Expression of COX-1 and COX-2 was determined by Western blotting. Inhibition or knockdown of COX-2 was achieved by treating NSCLC cells with specific COX-2 inhibitor NS-398 or COX-2 siRNA, respectively.
We found that NSCLC cell lines produced more IL-8 than VEGF (p < 0.001). In contrast, small cell lung cancer (SCLC) cell lines produced more VEGF than IL-8 (p < 0.001). COX-1 was expressed in all cell lines, but COX-2 was expressed only in NSCLC cell lines. Consistent with this, PGE2 was significantly higher in NSCLC cell lines than SCLC cell lines (p < 0.001). We tested these cell lines with a potent specific COX-2 inhibitor NS-398 at concentrations of 0.02, 0.2, 2, 20 μM for 24 or 48 h. The COX-2 activity was reduced in a dose-dependent fashion as shown by reduced PGE2 production. VEGF was significantly reduced following the treatment of NS-398 in A549 (by 31%) and MOR/P (by 47%) cells lines which expressing strong COX-2, but not in H460 cell line which expressing very low COX-2. However, IL-8 was not reduced in these cell lines. To confirm these results, we knocked down COX-2 expression with COX-2 siRNA in these cell lines. VEGF was significantly decreased in A549 (by 24%) and in MOR/P (by 53%), but not in H460 whereas IL-8 was not affected in any cell line.
We conclude that NSCLC cells produce much higher levels of IL-8 than SCLC cells whereas both NSCLC and SCLC cells produce similar levels of VEGF. COX-2 is only expressed in NSCLC cells, but not in SCLC cells. VEGF is produced in both NSCLC and SCLC cells regardless of COX-2 expression. However, VEGF production is, at least partly, COX-2 dependent in NSCLC cells expressing COX-2. In contrast, IL-8 production is COX-2 independent in both NSCLC and SCLC cells. We speculate that combined targeting of COX-2 and IL-8 may be useful in the treatment of patients with NSCLC and targeting VEGF may be useful in the treatment of patients with SCLC.
Lung cancer remains the leading cause of cancer death in many countries worldwide. There is considerable interest in anti-angiogenic drugs as therapeutic agents for lung cancer. Angiogenesis in tumours is promoted through the secretion of a variety of pro-angiogenic factors. Among these, vascular endothelial growth factor (VEGF) is important in many tumour types due to both its potent activity and markedly elevated expression level. Several studies have shown that high levels of VEGF are associated with increased tumour vascularity, advanced stage and poor prognosis in patients with non-small cell (NSCLC) and small cell lung cancer (SCLC) [1–5]. In addition to its angiogenic effects, functional VEGF receptors are expressed on SCLC cells and VEGF induces cell proliferation and migration in these cells . Treatment with a humanized monoclonal antibody to VEGF, bevacizumab (Avastin), prolongs the survival of patients with NSCLC .
Interleukin-8 (IL-8), one of the ELR+ CXC family of chemokines, is another potent pro-angiogenic factor and its expression is associated with angiogenesis, tumour progression and survival in patients with NSCLC [8–11]. In addition to its angiogenic effects, IL-8 receptors (CXCR1 and CXCR2) are expressed on lung cancer cells and IL-8 can act as growth/survival factor to these cells . Hence, both VEGF and IL-8 contribute to lung cancer progression through angiogenic and direct mitogenic effects [13, 14]. The relative contributions of different angiogenic factors to lung cancer growth are unknown.
Cyclooxygenases (COX) are key enzymes in the conversion of arachidonic acid to prostaglandin (PG) and other eicosanoids including PGE2, PGD2, PGF2α, PGI2 and thromboxane A2. COX-1 is present in nearly all cells whereas COX-2 is normally undetectable but is inducible under circumstances such as inflammation and cancer. Cancer cells, including NSCLC cells, express high levels of COX-2 protein [15–17]. COX-2 overexpression has been associated with poor prognosis in NSCLC, although a recent meta-analysis challenges this . It is correlated to VEGF and IL-8 expression in NSCLC [19, 20]. Selective COX-2 inhibitors have been shown to inhibit the growth and metastasis of several types of cancers . Celecoxib (Celebrex) and rofecoxib (Vioxx) have been tested in clinical trials, but their utilities are limited by cardiac adverse effects. Nevertheless, COX-2 could be a potential target to limit lung cancer growth. However, the mechanism underlying inhibition of angiogenesis and metastasis by targeting COX-2 is not fully understood. The aim of this study was to establish whether there is a direct relationship between COX-2 expression and VEGF and IL-8 production in lung cancer cells.
The lung cancer cell lines used were A549, H460, MOR/P (NSCLC) and GLC19, H69, H345, H711, Lu165 (SCLC). All cell lines were grown in RPMI 1640 (Bio Whittaker) with 10% fetal calf serum (Biosera) at 37°C in 5% CO2, 95% air. To collect supernatants for VEGF and IL-8 detection, NSCLC (adherent) cells were seeded in 6 well tissue culture plates and SCLC (suspension) cells were seeded in 24 well plates before being treated with various concentrations of the COX-2 inhibitor NS-398 (Cayman Chemical and Calbiochem) in triplicate for 24 h or 48 h. Anti-COX-1 and anti-COX-2 antibodies were purchased from Cayman Chemical. Anti-actin antibody was purchased from Sigma. Antibodies to VEGF and IL-8 for ELISA were purchased from R&D systems. PGE2 enzyme immunoassay kit was purchased from R&D systems. The siRNA-COX-2 and siRNA-control were purchased from Dharmacon.
Total VEGF and IL-8 concentrations were determined by ELISA kits as previously described for IL-8 . PGE2 was measured using a highly sensitive PGE2 competitive ELISA kit according to the manufacturer's instruction. The intensity of colour developed was measured using a Dynatech MR5000 microplate reader at 450 nm optical density (OD) with correction at 570 nm.
Whole cell lysates were prepared by resuspending cell pellets in CelLytic™M lysis buffer (Sigma) and incubating on ice for 15 minutes before centrifuging at 13,000 rpm for 15 minutes. Protein concentrations were measured in triplicate with the quick start Bradford reagent (Bio-Rad), and 20 μg of protein was added to loading buffer (62.5 mM Tris.HCl pH 6.8, 2% SDS, 10% glycerol, 50 mM DTT and 0.01% bromophenol blue), boiled, and electrophoresed on a 12% polyacrylamide/SDS gel, before being transferred to a Hybond P membrane (Amersham Biosciences). Membranes were incubated in primary anti-COX-2 (1:1000 dilution) or anti-COX-1 antibody (1:200 dilution) for 2 h at room temperature with gentle agitation, and in peroxidase-conjugated rabbit anti-mouse IgG for 2 hour at room temperature before being treated with the ECL detection system and exposed to hyperfilm ECL film (Amersham Biosciences). In some experiments, the membranes were washed and re-probed with anti-actin antibody as control of equal loading.
Cell growth was determined by direct cell counting under the microscope after cells were treated with various concentration of NS-398 for 24 or 48 h. The cells were trypsinized and resuspended in PBS. 50 μl of cell suspension was added to 50 μl of 0.4% Trypan Blue solution, mixed thoroughly and left for 10 min. Viable cells and dead cells (staining blue) were counted in four 1 mm corner squares of a hemocytometer slide. Total cells = (average count/square) × (dilution factor) × 104 × (predilution volume).
On-target COX-2 plus SMARTpool (COX-2 siRNA) and SiCONTROL Non-Targeting siRNA#1 (control siRNA) were purchased from Dharmacon. The sequences of On-target COX-2 plus SMARTpool (COX-2 siRNA) [GenBank: NM_000963] were GGACUUAUGGGUAAUGUUAUU (duplex 6); GAUAAUUGAUGGAGAGAUGUU (duplex 7); GUGAAACUCUGGCUAGACAUU (duplex 8) and CGAAAUGCAAUUAUGAGUUUU (duplex 9). The siRNAs were transfected into the cells in 12-well plate using DharmaFECT1 transfection reagent according to manufacturer's instructions. Four hours after transfection, the media was replaced by fresh media with 10% FCS. After further 48 h, the media were collected for ELISA and cells were collected for protein extraction.
The results were expressed as mean ± standard error of the mean (SEM). Statistical significance was obtained using unpaired student's t-test. Each experiment was repeated at least 3 times. Values with p < 0.05 were considered significant.
Several studies have shown that COX-2, VEGF and IL-8 are overexpressed in lung cancer compared to normal bronchial epithelium. Most studies have focused on NSCLC since clinical specimens of SCLC are difficult to obtain for research because SCLC patients are rarely operated on. Tas et al [23, 24] recently reported that serum VEGF levels were significantly higher in lung cancer patients than healthy controls. Mean serum VEGF levels appeared to be slightly higher in SCLC (1350 pg/ml, range 170 – 3810 pg/ml, n = 34) than NSCLC patients (402 pg/ml, range 121 – 1800 pg/ml, n = 52), but this was not tested statistically.
Here, we have compared and contrasted SCLC and NSCLC using a panel of cell lines. Basal expression of VEGF, IL-8, COX-1, COX-2 and PGE2 was determined in three NSCLC and five SCLC cell lines. VEGF was produced at similar levels in all cell lines. NSCLC cell lines produced much more IL-8 than SCLC cell lines. COX-1 was expressed at similar levels in all cell lines, whereas COX-2 was only expressed in NSCLC cell lines, albeit at low levels in H460. Interestingly, high levels of PGE2 were not only produced in MOR/P and A549 cell lines as a result of strong COX-2 expression, but also in H460 cell line in which COX-2 expression was weak. This could result from reduced catabolism of PGE2 due to low levels of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), a primary enzyme responsible for PGE2 metabolism . Previous studies showed that NSCLC cells expressed COX-2 protein [17, 26]. However, one study showed that a subset of 20% of SCLC patients (11 out of 54) expressed COX-2 . These data, together with our results and those of Pold et al , appear to suggest an association between COX-2 expression and IL-8 production in lung cancer cells. In contrast, VEGF production did not seem to be solely related to COX-2 expression as both COX-2 positive and negative cell lines produced similar levels of VEGF in our study.
COX-2 expression has previously been associated with VEGF in patients with NSCLC [19, 20]. Two reports from Dubinett's lab showed that expressions of IL-8 and VEGF were enhanced in NSCLC cell lines transfected with retroviral COX-2 vector [20, 28]. The aim of this study was to exam the causal relationship between COX-2 and IL-8 or VEGF in lung cancer cell through inhibition of endogenous COX-2 using either a potent and specific COX-2 inhibitor, NS398 or COX-2 siRNA. NSCLC cell lines were incubated with NS-398 for 24 h and 48 h. NS-398 exerts its effects by directly inhibits COX-2 activity. We demonstrated that COX-2 activity was inhibited by NS-398 as evidence of reduced production of PGE2 in these cell lines. We decided to use a maximum concentration of 20 μM in this study because COX-2 inhibition had been demonstrated and cell growth was not significantly inhibited in NSCLC cell lines as shown in Figure 5 at this level. NS-398 has been shown to induce 16% apoptosis in H460 cells at 300 μM in another study . Unexpectedly, IL-8 production was not altered after treatment with NS-398 in these cell lines. However, VEGF was significantly decreased by NS-398 in A549 and MOR/P cell lines, but not in H460. Both of A549 and MOR/P cell lines expressed high levels of COX-2 whereas H460 expressed very low level of COX-2 in our experiments. In some reports, H460 was considered as COX-2-negative cell line . These results suggested that VEGF production was independent of COX-2 in H460 and other COX-2-negative cells such as SCLC cell lines. We further confirm the direct involvement of COX-2 on VEGF production using COX-2 siRNA, and similar results were found. VEGF was significantly reduced in both of A549 and MOR/P, but not in H460. IL-8 was not affected following treatment with COX-2 siRNA in all tested NSCLC cell lines. These results suggest that VEGF is, at least partly, COX-2 dependent in COX-2-expressing NSCLC cells such as A549 and MOR/P. This finding is in agreement with other findings [19, 20, 28, 30]. However, VEGF production is clearly not depend on COX-2 status in other lung cancer cells such as SCLC cells, which expressing no COX-2, and some NSCLC cells including H460, which expressing very low level of COX-2. Our results also suggest that IL-8 is COX-2 independent in lung cancer cells. This finding seems to contradict others . The different findings may be due to the different experiments systems (e.g. to introduce ectopic overexpression of COX-2 or to knock down endogenous COX-2 by siRNA) employed in these studies. Interestingly, Raut et al  reported that blocking COX-2 production by NS-398 in pancreatic cancer cell lines did not affect VEGF, bFGF and IL-8 production, but Singh et al  found that NS-398 downregulated IL-8 by 30% in a COX-2 transfected MDA-231 breast cancer cell line. These contradictory findings suggest that the relationship between COX-2, VEGF and IL-8 is complex. More studies are required to establish the causal relationship between COX-2 and IL-8 and VEGF in lung cancer. COX-2 inhibitors have been shown to reduce angiogenesis and metastasis in lung cancer , our results suggest that anti-angiogenic effects of COX-2 inhibitors might be, at least partly, mediated by inhibition of VEGF, but not IL-8. As IL-8 seems to be independent of COX-2, therefore, there is a strong rationale for combining treatments with inhibitors of COX-2 and IL-8 in NSCLC.
Our results suggest that NSCLC cells produce much more IL-8 than SCLC cells whereas both NSCLC and SCLC cells produce similar levels of VEGF. COX-2 is only expressed in NSCLC cells, but not in SCLC cells. VEGF can be produced in lung cancer cells regardless of COX-2 expression. However, VEGF production is, at least partly, COX-2 dependent in NSCLC cells expressing COX-2. In contrast, IL-8 production is COX-2 independent in both NSCLC and SCLC cells. We speculate that combined targeting of COX-2 and IL-8 may be useful in the treatment of patients with NSCLC and targeting VEGF may be useful in the treatment of patients with SCLC.
We thank medical students Philip Sadler and Russell Robb for their contributions, and Weston Park Hospital Cancer Appeal (WPHCA) and Yorkshire Cancer Research (YCR) for financial support. YMZ was funded by YCR. This study was part of projects funded by WPHCA.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.