Evaluation of antiproliferative and anti-inflammatory activities of methanol extract and its fractions from the Mediterranean sponge

The samples were defrosted, macerated in distilled water and then air dried at 30°C and finely powdered. 600 g of finely powdered sponge material were packed in small bags (5x10 cm) of Whatman filter paper No. 1 and all bags were sealed and soaked in a methanol bath three times, steeping for 48 h. The methanol extracts were combined and evaporated under vacuum at low temperature (<40°C) and then stored at −20°C until use.

In order to localize the active fraction, methanol extract of Spongia officinalis was purified, using C₁₈ cartridges (Sep-pack, Supelco), by gradient elution with methanol–water mixture (0%, 50% and 80% methanol) to give 3 fractions (F1, F2 and F3). Methanol solvent was removed from fractions recuperated using rotating evaporator at 35°C and distilled water was then added to the residues and the aqueous phases were lyophilized. The powdered fractions were stored at −20°C until use.

Methanol extract, F2 and F3 fractions were diluted to the desired final concentration immediately prior manipulation.

For the anti-inflammatory evaluation of the methanol extract and its semi-purified fractions (F2, F3), adult Wistar rats (150-180 g) of both sex, provided from Pasteur institute (Tunis, Tunisia) were used. All animals were fed a standard diet ad libitum and allowed free access to drinking water. Animals fasted overnight before any experiments. Housing conditions and in vivo experiments were approved according to the guidelines established by the European Union on Animal care (CEE Council 86/609) [11].

The anti-inflammatory activity of our extract and fractions on carrageenan-induced paw edema was determined according to Winter et al. [12]. The animals were divided into three groups consisting of 6 rats each. The control group received 2.5 ml/kg intraperitoneally (i.p.) of saline solution, the standard groups received Acetylsalicylate of Lysine (ASL) (300 mg/kg) (i.p.) and the test group received the methanol extract of Spongia officinalis (25, 50 and 100 mg/kg) and its semi-purified fractions (F2, F3) at 50 mg/kg (i.p.). 30 min after intraperitoneal administration of different substances, 0.05 ml of 1% carrageenan suspension was injected to all animals in the left hind paw. The paw volume up to the tibiotarsal articulation was measured using Plethysmometer (model 7150, Ugo Basile, Italy). The measures were determined at 0 h (V₀) (before carrageenan injection) and 1, 3 and 5 h later (V_T). The volume of paw swelling was determined for each rat and the difference between V_T and V₀ was taken as the edema volume. The percentages of inhibition were calculated according to the following formula:

The human tumor cell lines A549 (lung cell carcinoma), HCT15 (colon cell carcinoma) and MCF7 (breast adenocarcinoma) were obtained from the American Type Culture Collection (ATCC, Manassas, VA). Cells were routinely grown with DMEM supplemented with 10% fetal calf serum and 1% penicillin/streptomycin, all obtained from Biochrom AG (Berlin, Germany). They were grown on Flasks (Nunc, Denmark) at 37°C in a humidified atmosphere containing 5% CO₂. Cells were replicated every 4–5 days and the medium changed once in-between.

The potential effects on cell viability were investigated according to previously reported conditions [13, 14], using the MTT assay [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide, Sigma-Aldrich Chimie, Saint-Quentin-Fallavier, France] as an indicator of metabolically active cells [15].

Known number of A549, HCT15 or MCF7 cells (10³) were transferred into 96-well plates (Nunc, Denmark) in a volume of 200 μl of culture medium and incubated for 24 h before addition of test compounds. Cells were then exposed for 24 h at 37°C to known concentrations of the methanol extract or fractions to be tested. After drug exposure, the cells were washed with phosphate-buffered saline and then reincubated in fresh culture medium for a further 48 h, then the culture medium was removed and 200 μl of MTT reagent (diluted in culture medium, 0.5 mg/ml) was added. Following incubation for 4 h, the MTT/medium was removed and DMSO (200 μl) was added to dissolve the formazan crystals. Absorbance of the colored solution was measured on a microplate photometre (Bio-Tek Instruments) using a test wavelength of 570 nm and a reference wavelength of 630 nm. Results were evaluated by comparing the absorbance of the treated cells with the absorbance of wells containing cell treated by the solvent control. Conventionally, cell viability was estimated to be 100% in the solvent control. All experiments were performed at least twice in triplicate. The concentration of substance required for 50% growth inhibition (IC50) was estimated according to the method described by Dellai [5].

The clonogenic inhibition assay was performed as described previously by Nicolas et al. [16] with some modifications. Known number of A549, HCT15 or MCF7 cells (2.10⁴) were transferred into six-well plates (Becton Dickinson Labware, USA) in a volume of 2 ml of culture medium and incubated for 24 h before addition of test compounds. Cells were then exposed for 24 h at 37°C to known concentrations of the compound to be tested. After drug exposure, the cells were washed with phosphate-buffered saline and subsequently re-plated in appropriate dilution in triplicate to assess clonogenic ability. After incubation for 14 days, each plate was stained with crystal violet and colonies were counted with a “colony counter pen”. The surviving fraction was calculated as the ratio of the number of colonies formed after treatment to the product of the number of cells plated and the plating efficiency. The IC₅₀ value is the concentration of the drug which is capable of bringing about 50% inhibition of colony formation.

For all our experiments, a one-way ANOVA was used to analyze the differences between groups, followed by a Duncan’s test with a threshold of significance of p < 0.01 and p < 0.001 to detect specific differences, using a statistical software package (STATISTICA edition 99 Maisons-Alfor- France). We used this post hoc test or multiple comparison tests, to determine the significant differences between a single control group mean and the remaining treatment group means in an analysis of variance setting.

Results of the carrageenan induced rat paw edema are shown in Table 1. The i.p. administration of the methanol extract of Spongia officinalis (25, 50 and 100 mg/kg) produced a significant reduction of the edema throughout the entire period of observation in a dose related manner. Interestingly the highest reduction of the edema was at 3 h with respectively 42.5, 52.7 and 61.71%. After i.p. administration of the semi-purified fractions F2 and F3 obtained by fractionation of the methanol extract, significant activity was observed with fraction F3 at the dose of 50 mg/kg, at the third hour after carrageenan injection, with 72.85% reduction in paw volume, whereas at the same time, F2 inhibited edema by 58.05. Standard drugs, ASL (300 mg/kg), decreased paw edema by 62.3% at the third hour (Table 1). The present results indicate that methanol extract and its semi-purified fractions exhibit anti-inflammatory effects.

In the first experiment, F2 was tested for its effect on inhibition of cell growth against three human tumor cell lines A549, HCT15 and MCF7 over a concentration range (100–2000 μg/ml) to determine their potency (IC₅₀-50% inhibition of cell growth), results are shown in Table 2. Assay was performed in vitro on exponentially growing cells. The activity was evaluated by measuring the levels of surviving cell after incubation for 24 h with the test samples, using the MTT colorimetric assay [15, 17]. This is the first step in our anticancer drug development program and is designed to identify those extracts with cytotoxic activity. The results of this primary screening are reported in Figure 1. F2 exhibited a rather moderate cytotoxicity. 50% inhibition of cell growth was obtained at concentrations of 1225 and 980 μg/ml respectively against human tumor cell lines A549 and MCF7. However within the series studied, F3 revealed a significant activity against A549, HCT15 and MCF7 cell lines at concentration related manner (25–500 μg/ml), the results are shown in Figure 2. 50% inhibition of cell growth was obtained at concentrations of 231, 212.5 and 72 μg/ml respectively against human tumor cell lines tested A549, HCT15 and MCF7 (Table 2). Since the inhibitory effects of F2 and F3 on the inhibition of cell growth using the MTT colorimetric assay were established, we then examined their effects on cell viability by clonogenic inhibition assay against the same three human tumor cell lines (A549, HCT15 and MCF7) with the same range of concentrations. The latter allows the chemosensitivity study but is more time consuming than the other [18]. Results of this assay are presented in Table 3. In our experiments, data for antiproliferative effect of F2 on A549 and MCF7 cells showed a significant clonogenic inhibition at concentration-related manner, results are reported in Figure 3. 50% inhibition of cell growth was obtained at concentrations of 875 and 375 μg/ml respectively against human tumor cell lines tested A549 and MCF7 (Table 3). In a further experiment, F3 produced significant clonogenic inhibition too (Figure 4). IC₅₀ are 137.5, 139.25 and 37.5 μg/ml respectively against human tumor cell lines tested A549, HCT15 and MCF7 (Table 3).

Both F2 and F3 semi-purified fractions of Spongia officinalis showed, in vitro, significant antiproliferative activities. The IC₅₀ values clearly indicated that the semi-purified fraction F3 had a much more potent effect, on the three human tumor cell lines tested, than F2. In term of cell line sensitivity, different responses were observed against the three human tumor cell lines, and no effect was observed on HCT15 cells with the semi purified F2.