Introduction

Colorectal carcinoma is one of the major causes of cancer patient mortality worldwide. The development, progression and metastasis of this carcinoma are a well-defined series of steps, which among others depend on local nitric oxide (NO) concentration and over-expression of cyclooxygenase (COX) enzymes [1–3].

NO is a short-lived molecule required for physiological functions but also engaged in pathological ones [4]. It can be produced from exogenous sources such as nitrovasodilators or endogenously from L-arginine by NO synthases (NOS) [5]. This molecule exhibits a dual role, stimulating tumor growth and metastasis on the one hand and, on the other hand, inhibiting neoplasia by its antioxidant action, inhibition of angiogenesis, and enhancement of vasodilation, differentiation and apoptosis [6]. These effects are attributed especially to the local NO concentration. At low levels, NO increases tumor growth and development, while higher levels of NO (above optimal concentrations) may express cytotoxic or cytostatic effects [6, 7]. The degree of tumor malignancy is also linked to the amount and activity of NOS proteins [8]. It has been shown that the expression of NOS may promote metastatic behavior of tumor cells [4]. The level of nitrite and nitrate in serum or culture supernatants can be significantly reduced by application of L-NAME, a competitive inhibitor of NOS. Its activity is based on structural similarity to L-arginine, a substrate for NOS, and competitive inhibition of L-arginine metabolization. It has been shown that L-NAME exerts anti-invasive and anti-metastatic effects on many cancers including colon carcinoma [9].

Some reports also demonstrate a cross-talk between NO and NOS levels and COX expression in cancer cells [10]. COX are essential enzymes which catalyze the conversion of arachidonic acid (AA) to prostaglandins (PGs). Especially the COX-2 isoform is important in carcinogenesis and opens new anticancer therapeutic possibilities [11, 12]. Exposure of various human carcinoma cell lines to COX-2 inhibitors has been shown to induce tumor cell apoptosis in laboratory in vitro tests [13]. It has been shown that the selective COX-2 inhibitor NS398 may in a dose-dependent manner inhibit proliferation and induce death in many carcinomas including colon cancer [14]. COX-2-derived bioactive prostaglandins, especially PGE2, have a direct effect on cancer cells by increasing their motility and metastatic potential [15]. However, PGE2 is one of the main pro-inflammatory factors, which is elevated in colorectal cancers and promotes their development by inducing cell proliferation and inhibiting apoptosis [16, 17]. Therefore, selective inhibitors of COX-2 may also block PGE2 generation minimizing its colorectal-tumor-promoting effects.

Selective inhibition of COX-2 and PGE2 production and influencing NO synthesis in the tumor microenvironment may represent important goals for prevention or therapy of colon cancers. The aim of the present study was to determine the reciprocal relations among NO, COX-2 and PGE2 in co-cultures of human colon tumor spheroids derived from different tumor grades with normal human colonic epithelium or myofibroblast monolayers in the presence of selective inhibitors of NOS (L-NAME) or COX-2 (NS398) and after the addition of a substrate for NOS (L-arginine).

Materials and Methods

Cell Culture

Human colon adenocarcinoma cell lines HT29 (ATCC No. HTB-38) derived from grade I tumor, LS180 (ATCC No. CL-187) from grade II tumor and SW948 (ATCC No. CCL-237) from grade III tumor were cultured in RPMI 1640 medium supplemented with 10% fetal calf serum (FCS) (GibcoTM, Paisley, UK) and antibiotics (100 U/ml penicillin and 100 μg/ml streptomycin) (Sigma, St. Louis, MO, USA) at 37°C in a humidified atmosphere with 5% CO2.

Human normal colon myofibroblasts CCD-18Co (ATCC No. CRL-1459) and normal epithelial cells CCD 841 CoTr (ATCC No. CRL-1807) were cultured in RPMI 1640 + DMEM (1:1) medium (Sigma) supplemented with 10% FCS at 37°C (CCD-18Co) or 34°C (CCD 841 CoTr) in a 5% CO2/95% air atmosphere.

Preparation of Tumor Cell Spheroids

Tumor cell spheroids were prepared by the liquid overlay method, as described previously [18]. In brief, tumor cell suspension (200 μl) at a density of 2 × 105 cells/ml in RPMI 1640 medium supplemented with 10% FCS was plated on 1% agarose-coated 96-multiwell culture plates (4 × 104 cells/well). After 4 days’ incubation at 37°C in a humidified atmosphere with 5% CO2, the cells formed spheroids.

Co-Culture of Tumor Spheroids with a Monolayer of Normal Cells

Tumor spheroids were harvested with glass pipettes from the agarose-coated microplates and transferred into a Petri dish filled with warm RPMI 1640 medium. After 5 min washing, 5 spheroids each were transferred onto confluent monolayers of myofibroblasts and colon epithelial cells in 24-well tissue culture plates in RPMI 1640 medium supplemented with 2% FCS and incubated at 37°C in a humidified atmosphere with 5% CO2. Such co-cultures were designed to reflect different stages of tumor metastasis. Parallel experiments with tumor spheroids or normal cell monolayers alone as culture controls were performed. After 24 h of culture, supernatants and cellular lysates were collected and stored at −80°C until estimation of the amounts of NO, PGE2 and COX-2.

Exposure of Cells to L-arginine, L-NAME and NS398

After 24-h incubation of the cells in RPMI 1640 with 10% FCS, the medium was discarded and fresh RPMI 1640 containing 2% FCS and L-arginine (2 mM) (Sigma), L-NAME (2 mM) (Sigma) and NS398 (Sigma) (75 μM) was added.

The incubation with the mentioned substances was performed for 24 h. Culture supernatants and cell lysates were collected and stored in −80°C for no longer than 3 months.

Cell Migration Assessment

Tumor cells were plated at 5 × 105 cells/ml on 4 cm culture dishes (Nunc). After formation of monolayers, culture was scratched with a pipette tip (P300), the medium was discarded and the cells were rinsed twice with PBS. Next, a fresh culture medium was applied and the distance of cell migration into the wound area after 24 h was estimated in the control and the cultures treated with L-arginine, L-NAME and NS398. The plates were stained with the May-Grünwald-Giemsa method. The observation was performed in an Olympus BX51 System Microscope (Olympus Optical CO., LTD, Tokyo, Japan) and the micrographs were prepared using the analySIS® software (Soft Imaging System GmbH, Münster, Germany). The results are a mean distance of migration to 5 selected wound areas taken from 4 micrographs.

ELISA Assay

The level of human PGE2 was tested immunoenzymatically (ELISA) using a commercially available kit (Cayman Chemical Company, Ann Arbor, MI, USA) according to the manufacturer’s instruction. The optical density at 405 nm was determined using a microplate reader (Molecular Devices Corp., Emax, Menlo Park, CA, USA). The concentrations of PGE2 in the analyzed samples were calculated on the basis of a standard curve. The detection limit was 15 pg/ml.

Nitric Oxide (NO) Measurement

Nitrate, a stable end product of NO was determined in culture supernatants by a spectrophotometric method based on the Griess reaction. Briefly, 100 μl of supernatant was plated in 96-well flat-bottomed plates in triplicate and incubated with 100 μl of Griess reagent (1% sulfanilamide/0.1% N-(1-naphthyl)ethylenediamine dihydrochloride) (Sigma) in 3% H3PO4 (POCH Gliwice, Poland) at room temperature for 10 min. The optical density was measured at 550 nm using a microplate reader. A standard curve was performed using 0.5–25 μM sodium nitrite (NaNO2) for calibration.

Immunoblotting

Total lysate of the treated cells was prepared by adding 150 μl of SDS-loading buffer with protease inhibitor cocktail (Sigma) directly to the cells cultured on 24-well plates and detaching them with a cell scraper. The protein concentration was determined using a BCATM Protein Assay Kit (Pierce Biotechnology, Rockford, IL, USA).

The extracts were boiled for 5 min at 95°C and centrifuged at 10.000 rpm for 10 min at 4°C. 15 μl of each protein sample was then loaded onto a 9% SDS-polyacrylamide gel. Following electrophoresis, the proteins were electrotransferred onto Immobilon-P transfer membranes (Millipore, Bedford, MA, USA). The membranes were blocked with 5% skimmed milk for 1 h at room temperature and probed with primary goat anti-COX-2 IgG polyclonal antibody (Santa Cruz Biotechnology, Inc.) for 2 h. After washing in PBS/1% Tween 20 (TBS-T), the membranes were labeled with alkaline phosphatase conjugated donkey anti-goat IgG-AP secondary antibodies (Santa Cruz Biotechnology, Inc) for 1 h at room temperature. After washing with TBS-T, the membranes were visualized with alkaline phosphatase substrates (5-bromo-4-chloro-3-indolyphosphate and nitroblue tetrazolium) (BCIP/NBT) (Sigma) in color development buffer (100 mM Tris with 5 mM Mg2+ at pH 9.5). As an endogenous control to ensure the same protein loading for each sample, we used β-actin.

Densitometric Analysis

Semiquantitative densitometric analysis of the bands was carried out with the Bio-Profil Bio-1D Windows Application V.99.03 program. The results were presented as density/volume of the bands.

Statistical Analysis

Results are presented as means ± SD of three independent experiments. The data were analyzed using one-way analysis of variance ANOVA followed by Bonferroni’s multiple comparison post-hoc test. Differences of p ≤ 0.05 were considered significant.

Immunoblots after semiquantitative densitometry were calculated using Student’s t-test. p-values lower than 0.05 were considered significant.

Results

In the presented study we analyzed the cross-talk among NO, COX-2 and PGE2 in co-cultures of human colon carcinoma spheroids with human normal colonic epithelium and myofibroblasts mimicking the early steps of colon tumor cell metastasis.

Cell Viability Analysis

The viability of colon tumor and normal cells was analyzed by the neutral red (NR) uptake assay and the MTT test.

Both tests revealed that L-arginine had no effect on the viability of the tumor and normal cells (data not shown).

Cell Motility Analysis

Tumor cell migration was analyzed using the wound assay model. The quantitative results of the measurement of migration distances are presented in Table 1 and Fig. 1a–e. We found that treatment of colon tumor cells with NS398 reduced the migration capacities of the cells. L-NAME also blocked the migration of tumor cells but the effect was weaker than that obtained using NS398. Treatment of cells with L-arginine had no significant influence on the motility of colon tumor cells.

Table 1 Colon tumor cell migration assay. The quantitative results of the measurement of migration distances after colon tumor cells treatment with L-arginine, NS398 and L-NAME
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Fig. 1
figure 1

The effect of L-arginine (2 mM), L-NAME (2 mM) and NS398 (75 μM) on the migration capacity of colon tumor HT29 cells. a wounded monolayer, b tumor cell migration after 24 h in control culture, c tumor cell migration after 24-h incubation with L-arginine, d tumor cell migration after 24-h incubation with L-NAME and e tumor cell migration after 24-h incubation with NS398. Bar = 500 μm

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NO Production

Tumor cell spheroids, especially LS180 and SW948, produced higher amounts of NO than an equal number of normal cells cultured as monolayers. Colon epithelial cells produced similar amounts of NO to myofibroblasts. In co-cultures, similar concentrations of NO were detected when HT29, LS180 and SW948 cell spheroids were implanted onto normal cell monolayers. Generally, in comparison to tumor cell spheroids (LS180, SW948) cultivated alone, in co-cultures composed of two kinds of cells a decrease in NO production was detected. Exposure of the cells to L-arginine (2 mM) for 24 h enhanced NO production both in the mono- and co-cultures with significant increase in HT29 and LS180 tumor spheroids and SW948 tumor spheroids co-cultured with 18Co normal cells. On the other hand, L-NAME (2 mM) significantly inhibited NO secretion as compared to an appropriate sample control. Finally, NS398 had no significant influence on NO production (Fig. 2a–c).

Fig. 2
figure 2

a–c Nitric oxide (NO) production in co-cultures of colon carcinoma cell spheroids HT29 (a), LS180 (b) and SW948 (c) with normal colon epithelial cells (841CoTr) and myofibroblasts (18Co) during 24 h of incubation with L-arginine (2 mM), L-NAME (2 mM), and NS398 (75 μM). Exposure of cells to L-arginine non-significantly enhanced NO production, while L-NAME significantly inhibited NO secretion as compared to an appropriate sample control. NS398 had no significant influence on NO production. *p ≤ 0.05—a co-culture of tumor/normal cells compared to an appropriate monoculture of normal cells. # p ≤ 0.05—a culture of tumor and/or normal cells after treatment compared to an appropriate non-treated culture

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COX-2 Expression

COX-2 expression analysis was performed using the immunoblotting method (Fig. 3) followed by densitometry (Fig. 4a–c). We found that in normal colonic epithelium, there was very low or undetectable COX-2 expression. Conversely, colon tumor cells over-expressed COX-2 protein. Additionally, normal stromal myofibroblasts were found to produce COX-2 but in lower amounts than cancer cells. In tumor spheroids co-cultured with normal myofibroblasts, COX-2 expression increased above the sum of the enzyme level observed in the respective monocultures. In contrast, in tumor spheroid co-cultures with normal colonic epithelium very low amounts of COX-2 were detected. L-arginine added to normal or tumor cell cultures had no significant influence on COX-2 expression, but in tumor cells co-cultured with myofibroblasts the amino acid significantly decreased the enzyme level as compared to a non-treated co-culture. In mono- and co-cultures treated with L-NAME, non-significant decrease in COX-2 expression was detected as compared to a non-treated co-culture control. The exposure of tumor cells and their co-culture with myofibroblasts to NS398 resulted in a significant inhibition of COX-2 expression.

Fig. 3
figure 3

Western blot analysis of COX-2 after 24 h of incubation with L-arginine, L-NAME or NS398 in HT29 colon carcinoma cells, myofibroblasts and their co-culture. The increase in band density indicates an increase in protein levels. L-arginine limited COX-2 expression and in tumor cells co-cultured with myofibroblasts the amino acid significantly decreased the enzyme level as compared to a non-treated co-culture. L-NAME non-significantly decreased COX-2 expression as compared to a non-treated co-culture control. NS398 caused a significant inhibition of COX-2 expression

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Fig. 4
figure 4

a–c Semiquantitative results of a densitometric analysis of the bands of COX-2 protein detected by immunoblotting performed on material obtained from co-cultures of tumor cell spheroids HT29 (a), LS180 (b) and SW948 (c) with normal cells. Only co-cultures of tumor spheroids with colonic epithelium and myofibroblasts were analyzed. Note the lack of COX-2 expression in normal colonic epithelial cells. *p < 0.05—co-cultures treated with L-arginine, L-NAME or NS398 compared to an untreated co-culture

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PGE2 Expression

The level of PGE2 closely reflected the expression of COX-2 protein. Tumor cells produced significantly higher PGE2 than normal cells. Among the normal cells, myofibroblasts expressed significantly higher PGE2 than colonic epithelium. In co-cultures, the prostaglandin level was lower than the sum of PGE2 produced by the respective monocultures. Addition of L-arginine had no significant influence on PGE2 production either in tumor or normal cells. However, in tumor cell co-cultures with colonic epithelium the decreases of that prostanoid were significant as compared to non-treated controls. L-NAME had no significant influence on PGE2 level, which remained unchanged or slightly decreased in tumor cells, normal cells and their co-cultures as compared to untreated controls. In tumor spheroids, and co-cultures exposed to NS398, a significant inhibition of PGE2 production was found. In normal cell monolayers inhibition of PGE2 after NS398 addition was non-significant (Fig. 5a–c).

Fig. 5
figure 5

a–c PGE2 production in co-cultures of colon carcinoma cell spheroids HT29 (a), LS180 (b) and SW948 (c) with normal colon epithelial cells and myofibroblasts during 24 h of incubation with L-arginine, L-NAME or NS398. ELISA test. Tumor cells produced significantly higher PGE2 than normal cells. Myofibroblasts expressed significantly higher PGE2 than colonic epithelium. L-arginine limited PGE2 production in tumor cells, myofibroblasts and their co-cultures. L-NAME had no significant influence on PGE2 level, which remained unchanged or slightly decreased in tumor cells, normal cells and their co-cultures as compared to untreated controls. NS398, inhibited PGE2 production in the tested cells. *p ≤ 0.05—a co-culture of tumor/normal cells compared to an appropriate monoculture of normal cells. # p ≤ 0.05—a culture of tumor and/or normal cells after treatment compared to an appropriate non-treated culture

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Discussion

Cyclooxygenases (COX) are essential rate-limiting enzymes catalyzing the conversion of arachidonic acid to prostaglandins (PGs) and other eicosanoids in cells [11, 19]. Three isoforms of COX have been identified: COX-1 and its spliced version COX-3 constitutively expressed in tissues and COX-2, which is regulated by growth factors, cytokines or oncogenes [20, 21]. It has been clearly shown that COX-2 has tumor-promoting properties. This enzyme has been found to be expressed in approximately 40–50% of colonic adenomas and to be significantly over-expressed in 80–90% of colorectal carcinomas [22, 23]. To date, several mechanisms by which COX-2 contributes to carcinogenesis have been identified. They include inhibition of apoptosis, enhancement of angiogenesis and invasiveness, modulation of inflammation and immunosuppression or conversion of procarcinogens to cancerogenic factors [24]. Finally, COX-2 up-regulation is closely linked with increased production of PGs, especially PGE2, which supports tumor growth by induction of angiogenesis and inhibition of tumor cell apoptosis and exerts immunomodulating effects via, e.g. T-cell response inhibition [17, 25, 26].

During tumor development and metastasis, a significant role is also attributed to nitric oxide (NO). This molecule is implicated in the regulation of tumorigenesis depending on its local concentration, tumor stage, local microenvironmental conditions or even direct interactions between tumor and stromal cells.

In this study we tried to find a link between NO and COX-2 and PGE2 levels in co-cultures of colon cancer spheroids prepared from tumor cells isolated from different tumor grades with normal colonic epithelium and myofibroblasts. We analyzed COX-2 and PGE2 levels in the presence of an excess concentration of L-arginine, a substrate for NOS activity and L-NAME, or NS398 as NOS or COX-2 inhibitors, respectively (Fig. 6).

Fig. 6
figure 6

Schematic graph showing reciprocal relations among nitric oxide (NO), nitric oxide synthases (NOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2)

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In our study we used single doses of each agent. However, it was intended, because we did not want to analyze the effects depending on different concentrations of inhibitors or L-arginine but the relationship between COX-2, NO and PGE2 in specific culture conditions. We wanted to show that there are changes in specific molecules concentration or whole cells reaction (motility) when other molecules concentration is limited or inhibited their activity. It was only to show that such cross-talk among analyzed molecules exists. The detailed explanation of these observations, obviously, needs further study.

The selection of the dose of each agent was performed multistage. On the basis of the literature we selected a few concentrations. Next, they were tested for their cytotoxicity because in the further experiments we wanted to show often slight and delicate changes in specific molecules amounts. We had to be sure that under any circumstances we did not influence on cells amount or their viability. Thereafter, different concentrations were analyzed on their influence on NO level on normal colon epithelial cells. After that, the most appropriate concentration of inhibitors and L-arginine adapted to our experimental model has been selected.

We had to choose either different concentrations of inhibitors and L-arginine analysis or expand cellular model. The idea of our study was to analyze the relationship among selected parameters and therefore only single doses of inhibitors and L-arginine were used. If different concentrations of these agents and different cellular model combination were analyzed then, as we suppose, the results would be difficult to explain and in consequence difficult to understand.

We showed that COX-2 was over-expressed in colon tumor cells and stromal myofibroblasts but its level was relatively low in normal colon epithelial cells. Some authors have shown that COX-2 expression differs depending on colon tumor grade. Zhang and Sun [11] revealed that frequencies of COX-2 expression were greater in advanced colon tumors (Duke’s B-D) than in Duke’s A. Similar observations were performed by Williams et al. [27], who showed that higher COX-2 expression was associated with tumors that were advanced and larger in size. In our study we confirmed these clinical observations showing in vitro higher COX-2 and PGE2 amounts in LS180 (grade II) and SW948 (grade III) cells than in the HT29 (grade I) colon cancer culture. In co-cultures, similarly to COX-2, also NO level was comparable to that observed in tumor spheroid monocultures. The lower amounts of NO in co-cultures than in tumor cells cultured alone may be partially due to the general reduction of NO production in tumor cells after their contact with normal cells [28].

NO is produced from L-arginine, a semiessential amino acid which by modulating host immune functions causes variable responses against tumor growth [29, 30]. L-arginine, in experimental settings, has been shown to exert anti-tumor effects by reducing tumor size and incidence, and retarding tumor growth and metastasis [31]. Generally, L-arginine may reduce chemically induced colorectal carcinomas influencing host immune system functions [32]. Supplementation with this amino acid also leads to increased NO formation by the oxidative deaminase pathway. In turn, an increased local NO level may induce cytostasis by inhibiting hyperproliferation of tumor cells or cytotoxicity in tumor cells by, e.g. formation of toxic peroxynitrite [33]. Moreover, there is also a cross-talk between products of the NOS and COX pathways. In our study, we showed that L-arginine supplementation slightly increased NO level but had no significant influence on the amount of COX-2, and in consequence on PGE2 production in tumor and normal cell monocultures. The interactions between NO and COX-2 and PGE2 occur at multiple levels and therefore it is difficult to unequivocally speculate about them and give simple answers or solutions. The significant reduction of PGE2 levels by L-arginine was found in co-cultures of tumor spheroids with colonic epithelium rather than with myofibroblasts, which may suggest an important role of NO in chemoprevention of tumor-epithelial cell interactions rather than its effect on tumor-stromal development, activity and viability. Our results are in agreement with the findings of Clancy et al. [34] and Ghosh et al. [35], who showed that NO inactivates COX-2 functions through inhibiting its enzymatic activity by reacting with iron in the enzyme’s heme group. Moreover, we demonstrated that L-NAME, an inhibitor of NO synthases which decreased NO level and motility of tumor cells in the experiment had a relatively weak effect on COX-2 level. These results are in agreement with the findings of other authors showing a balance and interference with each other’s synthesis between NO, COX-2 and PGE2 [36, 37]. These interactions are important for maintaining homeostasis in normal cells and influence invasiveness in tumors. There exist contradictory reports describing the relationships between NO and COX, showing that blockade of NOS by L-NAME may either increase or decrease COX-2 and PGE2 synthesis [38–40]. We suppose, on the basis of our study, that the NO and COX-2 relationship is closely dependent on the kind of cells that have been used, their direct interactions, the kind of inhibitor applied and the local microenvironmental conditions. These elements together influence COX-2 and PGE2 synthesis after NO imbalance. This hypothesis is confirmed by Ohno et al. [40], who showed that mucosal PGE2 was decreased by SC-560, a COX-2 inhibitor, but not by L-NAME. Moreover, other authors have shown that L-NAME reduces PGE2 generation via limitation of COX-2 expression [41]. Therefore, L-NAME may limit the invasion and migration of tumor cells and serve as a cancer prevention factor [10, 42]. Finally, NS398, a specific COX-2 inhibitor, decreased the enzyme and PGE2 levels and tumor cell motility with slight effects on NO production. These results are in agreement with the findings of West et al. [43] and Payá et al. [44], who revealed that NS398 strongly reduced COX-2 and PGE2 levels without affecting NO metabolites and NOS activity. We can only speculate on the mechanism by which COX-2 inhibitor also causes inhibition of the enzyme expression. It may be associated with cell cycle arrest by COX-2 inhibitor what may result in potential decrease in enzyme level. NS398, which acts by inducing a conformational change of COX-2, may also lead to unrecognizing of the protein by specific antibodies. The inhibitor may also cross-influence on molecular pathways and signal transduction connected with enzyme activity and expression. Finally there may be a feedback between COX-2 and PGE2 levels and activity. However, these are only speculations which need experimental confirmation. Moreover, there is strong evidence indicating that specific COX-2 inhibition could down-regulate the antiapoptotic Bcl-2 protein, thus inhibiting proliferation and progression of different carcinomas including colon cancer [14, 45, 46]. At present, there is no uniform explanation of the mechanism of the cross-talks between NO and COX-2 and PGE2 in tumor/normal cell co-cultures. Some evidence indicates that NO produced from L-arginine contributes to COX-2 and PGE2 activation [47]. However, no answer has been offered to the question of the influence of the NO + O −2 product (ONOO−), which is locally produced during direct tumor/normal cell interactions, on COX-2 expression. In our previous work we showed that during direct tumor/normal cell contact O −2 anion is overproduced [18]. However, our data obtained so far do not allow to determine whether this is mainly free NO or its reaction product peroxynitric acid, generated through the interaction between tumor cell-derived superoxide anions and NO. In order to distinguish reaction products, additional methods should be applied. Nevertheless, NO as a short-lived and highly reactive molecule will be converted into nitrate, a stable end product of NO, and will react with free oxygen radicals forming reactive oxygen/nitrogen species. The exact kind of molecules formed needs further studies. On the other hand, a large number of experimental results indicate that NO, under certain conditions, down-regulates the prostaglandin biosynthetic pathway mainly via COX-2 inhibition [48]. We showed that in tumor or normal cell monocultures NO had no significant influence on COX-2 and PGE2 expression. However, in specific culture conditions when tumor cells directly interacted with normal cells, especially myofibroblasts, the addition of L-arginine resulted in a limitation of COX-2 expression; PGE2 level was decreased when tumor cells were implanted onto normal colon epithelium. Based on these results, we may speculate that NO and COX-2 and PGE2 cross-talks should be considered in relation to the experimental conditions and the cell culture model used.

In conclusion, we have shown the existence of cross-talks among NO, COX-2 and PGE2. This relationship is rather unidirectional where NO level influences COX-2 and PGE2 levels. Moreover, any imbalances in NO level caused by exogenous factors influence COX-2 and PGE2 amounts depending on the kind of cells, their reciprocal interactions and the local microenvironmental conditions. The knowledge of these effects may be useful in limiting colon carcinoma progression and invasion.