Characterization of the antiproliferative activity of Xylopia aethiopica
© Choumessi et al; licensee BioMed Central Ltd. 2012
Received: 7 October 2011
Accepted: 12 March 2012
Published: 12 March 2012
Xylopia aethiopica, a plant found throughout West Africa, has both nutritional and medicinal uses. The present study aims to characterize the effects of extracts of this plant on cancer cells.
We report that X. aethiopica extract prepared with 70% ethanol has antiproliferative activity against a panel of cancer cell lines. The IC50 was estimated at 12 μg/ml against HCT116 colon cancer cells, 7.5 μg/ml and > 25 μg/ml against U937 and KG1a leukemia cells, respectively. Upon fractionation of the extract by HPLC, the active fraction induced DNA damage, cell cycle arrest in G1 phase and apoptotic cell death. By using NMR and mass spectrometry, we determined the structure of the active natural product in the HPLC fraction as ent-15-oxokaur-16-en-19-oic acid.
The main cytotoxic and DNA-damaging compound in ethanolic extracts of Xylopia aethiopica is ent-15-oxokaur-16-en-19-oic acid.
KeywordsXylopia aethiopica ent-15-oxokaur-16-en-19-oic acid cytotoxicity DNA damage
Natural compounds have attracted considerable attention as preventive and therapeutic agents against cancer . Indeed, 74% of anticancer compounds are natural products or their derivatives. According to the World Health Organization (WHO), 80% of the population in Africa and in some Asian countries still use plant preparations to treat their illnesses, including cancer. The cloves of the plant Xylopia aethiopica, a member of the custard apple family, Annonaceae, are used as a spice in various traditional dishes of Western and Central Africa. The plant is also used in decoction to treat dysentery, bronchitis, ulceration, skin infection and female sterility. Several studies have shown that X. aethiopica extracts possess antibacterial [2–5], antifungal  and anti-plasmodial  activities. X. aethiopica extract contains an antioxidant activity ; it also increases antioxidant defense and protects rats from the adverse effects of irradiation [9, 10].
Although some extracts of this plant have antioxidant properties, others have cytotoxic effects on a wide range of cancer cell lines . A recent study of various Cameroonian spices  found that extract of X. aethiopica had cytotoxic activity against pancreatic and leukemia cells sufficient for the plant to be considered a potential source of cytotoxic compounds, according to the plant-screening program of the National Cancer Institute. In this report, we confirm the cytotoxic activity of X. aethiopica extract against a panel of cancer cell lines and identify the main compound responsible for this cytotoxic effect: ent-15-oxokaur-16-en-19-oic acid (EOKA). Furthermore, we show that EOKA triggers DNA damage and accumulation of the cells in the G1 phase of the cell cycle, followed by apoptosis.
Human cancer cell lines HCT116 (from a colorectal cancer), U2OS (from an osteosarcoma) and SUM-159PT (from a breast carcinoma) were cultured in DMEM. The human pancreas adenocarcinoma cell line Capan-2 and normal human skin primary fibroblasts (kindly provided by P. Descargues, Toulouse) were cultured in DMEM F-12. Leukemia cell lines KG1a and U937 were grown in IMDM. All culture media were supplemented with 10% foetal calf serum, 100 u/ml penicillin and 100 μg/ml streptomycin.
Extraction of X. Aethiopica
Dried fruits of X. aethiopica were collected from spice vendors and the voucher specimen was identified at the Cameroon National Herbarium. Dried fruits were ground and extracted with 70% ethanol (100 mg/ml) for 2 h at 55°C with shaking every 30 minutes. The suspension was centrifuged at 4000 rpm for 10 minutes at 25°C and the resulting supernatant extract was filtered and stored at -20°C.
Stability assessment of the dried residue by LC/MS
Analytical liquid chromatography-mass spectrometry (LC/MS) was carried out using Waters equipment: an Xbridge C18 column (4.6 × 150 mm; 5 μm particle) for separation, a Waters 2996 photodiode array detector and a Waters 3100 mass detector (ES mode) for detection. Compounds were eluted with a gradient of water and acetonitrile containing 0.05% of formic acid at a rate of 17 ml/min. Ten microlitres of sample solution were injected for each analysis.
Each LC/MS analysis was performed by injecting 500 μl of the X. aethiopica extract diluted with 500 μl methanol. To check the stability of the extract, 20 ml was dried under vacuum and the dried residue was stored at room temperature for a week; it was then solubilized in a mixture of 20 ml of methanol and 2 ml of DMSO and analyzed by LC/MS. The resulting chromatograms were identical, thus we conclude that the dried residue is stable at room temperature.
HPLC fractionation of X. Aethiopica extract
Fractionation by HPLC was carried out using a Waters Xbridge C18 column (19 × 150 mm; 5 μm particle), a Waters 2996 photodiode array detector and a Waters 3100 mass detector (ES mode) for detection. Compounds were eluted with a gradient of water and acetonitrile at 1 ml/min. For each fractionation run, we injected 350 μl of the solubilized residue in methanol/DMSO as previously described.
Cell proliferation was assessed first by measurement of viable cell number. HCT116, U2OS, SUM-159PT, Capan-2, U937, KG1a and normal fibroblasts were seeded in six-well plates (5 × 104 cells/well). Cells were treated 24 hours later with X. aethiopica extract (25 μg od dry powder per ml). After 4 days, the number of cells in each well were counted on a cell counter.
The effect of X. aethiopica extract on cell proliferation was also examined with the colorimetric reagent WST-1 (Roche). HCT116 cells were seeded into 96-well plates (3 × 103 cells/well). After 24 h, increasing concentrations of X. aethiopica extract or fractions obtained by HPLC were added (six wells for each concentration). After 4 days, cell viability was estimated according to the manufacturer instructions, by measuring the optical density of each well at 450 nm with a microplate reader (Labsystems Multiskan).
Statistical tests were performed using Excel and PRISM softwares.
Flow cytometry analysis
HCT116 cells were seeded in 60 mm plates (3 × 105 cells/plate) then treated 24 hours later with HPLC fractions of X. aethiopica extract. Cells were harvested after various times of treatment, fixed in ice-cold 70% ethanol, washed with PBS containing1% bovine serum albumin, and permeabilized with 0.25% Triton X-100 for 10 minutes. Cells were stained with a mouse monoclonal antibody against phosphorylated γ-H2AX (diluted 1/1000; Upstate Biotechnology) followed by an Alexa 488-conjugated anti-rabbit antibody (diluted 1/500;). DNA was stained with propidium iodide (10 μg/ml) in the presence of RNAase (10 μg/ml) for 1 h at room temperature. The cell cycle phase and presence of γ-H2AX staining in individual cells was determined by flow cytometry analysis (Accuri C6 cytometer, Cflow plus software).
U2OS cells were seeded in six-well plates (5 × 104 cells/well) containing 12 mm coverslips and subsequently treated for various times with peak 1 (20 μg/ml) or with doxorubicin (10 mM). Cells were fixed with 4% formaldehyde (Diapath), permeabilized in 0.1% (w/v) Triton X-100 for 5 min, washed in PBS and stained with DAPI.
Western blot analysis
U2OS cells were treated for various times with peak 1 (20 μg/ml). Cells were washed with PBS and lyzed in ice-cold lysis buffer (Tris-HCl pH 7.5, 250 mM NaCl, 5 mM EDTA, 1 mM DTT, 0.1% Triton X-100, 50 mM sodium fluoride, 1 mM sodium orthovanadate, 100 μg/ml PMSF and TPCK, 50 μg/ml TLCK, 2 μg/ml leupeptin, 1 μg/ml pepstatin and 1 μg/ml aprotinin). Proteins (100 μg) were separated by SDS-polyacrylamide gel electrophoresis and transferred to nitrocellulose membranes by semi-dry blotting. Membranes were hybridized with antibodies against PARP (diuted 1/500; BD Pharmingen), p21 (antibody sc-397, diluted 1/2000) and p53 (antibody sc-126, dilted 1/2000) (both from Santa Cruz Biotechnology,). To control for equal loading, the western blot was probed with an antibody against actin (diluted 1/10000, Chemicon,).
Identification of the cytotoxic natural product
The chemical structure of the cytotoxic natural product (peak 1 of the HPLC profile) was determined by mass spectrometry (positive and negative electrospray ionization) with a Waters 3100 mass detector and by NMR analyses. 1H and 13 C spectra NMR spectra were carried out in either methanol-d4 or deuteriochloroform as solvents and were recorded with a Brucker Avance 300 spectrometer at 300 and 75 MHz, respectively. Carbon multiplicities were determined by either DEPT135 or Jmod experiments. Diagnostic correlations were determined by two-dimensional NMR correlation spectroscopy (COSY), heteronuclear multiple-quantum correlation spectroscopy (HMQC) and heteronuclear multiple-bond correlation spectroscopy (HMBC).
Results and discussion
Our data indicate that X. aethiopica extract is cytotoxic to cells from a variety of cancers: carcinoma, osteosarcoma and leukemia. These data confirm and extend those of Kuete et al. , who reported that, among the 34 Cameroonian spices and plant tested, a crude extract of X. aethiopica was one of the most cytotoxic against MiaPaCa-2 pancreatic cancer cell line and CCRF-CEM leukemia cells. Another study characterized the antiproliferative effect of X. aethiopica extract on human cervical cancer cells .
Screening of some medicinal plants commonly used in Nigeria found that X. aethiopica had mutagenic activity . This mutagenic activity could be due to the DNA damage we found induced by peak 1 in the X. aethiopica extract. raising the issue of the use of this medicinal plant as spice. By contrast, other studies have found that X. aethiopica extract protects rats against the adverse effects of γ irradiation [9, 10], suggesting that X. aethiopica extract contains both DNA damaging agents and protecting agents against the DNA damaging effect of irradiation.
To determine unambiguously the chemical structure of the active compound corresponding to peak 1 of HPLC profile, we first analyzed our mass spectrometry data and found a molecular weight of 316, possibly indicating a C20H28O3 diterpene. We elucidated the structure by using standard and multi-dimensional NMR spectroscopy. Finally, we compared our 1H and 13 C NMR data with those of the known compound ent-15-oxokaur-16-en-19-oic acid (EOKA) (Figure 2B) and proved to be identical to the literature data [17–19].
Taken together, our data demonstrate that EOKA is the main cytotoxic compound in extract of X. aethiopica.
Aphrodite Choumessi was a recipient of a PhD student travel grant from the French embassy in Cameroon. This work was supported by the CNRS, the University of Toulouse and the Région Midi-Pyrénées.
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