Original Articles

In Vitro Cytotoxic and Anti-inflammatory Activities of Tanacetum argenteum (Lam.) Willd. subsp. argenteum Extract


  • Gökay ALBAYRAK
  • Şüra BAYKAN

Received Date: 28.11.2016 Accepted Date: 23.02.2017 Turk J Pharm Sci 2017;14(3):231-236 PMID: 32454618


The objective of this study was to examine the anti-inflammatory and cytotoxic potential of n-hexane, ethyl acetate, and methanolic extracts of Tanacetum argenteum subsp. argenteum.

Materials and Methods:

Tanacetum L. is the third largest genus of Asteraceae family and is represented by 60 taxa in Turkish flora. Sesquiterpene lactones and pyrethrins are the main chemical groups of the genus. T. argenteum subsp. argenteum is an endemic taxa that is distributed in the Central and South Anatolia.


In vitro anti-inflammatory activity was assayed using iNOS and NF-κB inhibition tests on RAW264.7 and HeLa cells. The cytotoxic activities were tested against ten cell lines using MTT assays.


As a result, the n-hexane extract was found more active than the positive control parthenolide in iNOS test (IC50: 0.627±0.16 μg/mL) and cytotoxic experiments against PC3 and MPANC-96 cell lines (IC50: 2.85±0.51 μg/mL and 5.35±1.24 μg/mL, respectively).

Keywords: Tanacetum argenteum subsp. argenteum,anti-inflammatory,NF-κB,iNOS,cytotoxicity,MTT


The genus Tanacetum L. consists of around 160 species in the world1 and 60 taxa of the genus exist in Turkey, 26 of which are endemic.2 The genus is distributed in Europe and West Asia and all over Turkey, excluding the Aegean side.3,4 Tanacetum sp. are used as insecticides, tonic, appetizers, anthelmintics, diuretics, carminatives, stimulants, emmenagogues, antipyretics, and antimigraine agents in Turkey.5 Tanacetum parthenium (L.) Schultz Bip. (feverfew) is the most prominent species. It is known as having antimigraine properties and is used to relieve menstrual pain in traditional medicine, and standardized capsules of leaf extract are available on the market.3,6 Eudesmane sesquiterpenes are the main components of the genus. Tanacetum argenteum. (Lam.) Willd., subsp. argenteum is an endemic perennial plant with 20-30 cm stem length and deeply divided or 2-pinnatisect leaves. The involucre is 3-4 (-5) mm broad and campanulate. Its flowers are yellow, female flowers are absent, and achenes are brown, 2-2.25 mm. It grows on rocks and limestone cliffs, ranging from 990 to 2500 m. The plant is mainly distributed in Inner and South Anatolia.4 The main chemical constituents of T. argenteum subsp. argenteum are sesquiterpenoids and flavonoids. Phytochemical studies on this species also resulted with the isolation of β-sitosterol and β-amyrin, desacetyllaurenobiolide, spiciformin, tatridin-A, tatridin-B, desacetyl-β-cylclopyrethrosin, desacetyltulipinolide-1β, 10α-epoxide and 8α-angeloyloxycostunolide.7 Sesquiterpenoids are thought to be the bioactive constituents of this taxon.3 The major compounds of the essential oil of the plant are reported as monoterpenes; α-pinene, β-pinene and santolinatriene by previous studies.7,8,9 Caryophyllene oxide and α-thujone were found as the main constituents of the oil of T. argenteum subsp. canum var. canum in Gören and Tahtasakal10 study.

Recently, Orhan et al.11 measured parthenolide levels using liquid chromatograph-mass spectrometry and total flavonoid contents of three subspecies of T. argentum. Among all T. argenteum subsp. argenteum has the highest parthenolide and total flavonoid contents. The authors also investigated the cholinesterase inhibitory potential of these plants. Among them, the leaf extract of T. argenteum subsp. flabellifolium has the strongest cholinesterase inhibitor activity.11 Gören and Tahtasakal10 isolated guaian-type sesquiterpene lactones from T. argenteum subsp. canum var. canum and T. argenteum subsp. Flabellifolium.12,13

The aim of this study was to investigate the anti-inflammatory and the cytotoxic activity of n-hexane, ethyl acetate, and methanolic extracts of T. argenteum subsp. argenteum. For this purpose, nuclear factor kappa B (NF-κB) and induced nitric oxide synthesis (iNOS) methods were used as anti-inflammatory assays and MTT(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) was used for cytotoxic activity. Thin-layer chromatography (TLC) analysis of extracts were also performed to obtain an overview on the chemical compounds of the extract.


Plant material

Plants were collected from Nemrut Mountain, 1600 m, Kahta, Adıyaman on May 30th, 2012, and identified by Şüra Baykan. Voucher specimens have been deposited in the Ege University Herbarium, Faculty of Pharmacy, İzmir, Turkey (IZEF 6029) (www.izef.ege.edu.tr).


Dried and powdered plant parts (250 g) were extracted sequentially with n-hexane, ethyl acetate and methanol (2x300 mL for each), sonicated at room temperature for 6 h, and then filtered. The combined extracts were evaporated using a rotary evaporator to dryness at 40°C.

Thin-layer chromatography analysis

TLC analysis of n-hexane, EtOAc, and methanolic extracts of the plant was made. A silica gel-coated aluminum plate was used as the stationary phase and n-hexane:ethyl acetate (5:5) solvent system was used as the mobile phase. Comparisons was performed using parthenolide as the reference compound.


All cells were obtained from American Type Culture Collection (ATCC, Rockville, MD).

Chemicals and other materials

MTT, n-hexane, parthenolide, Griess reagent, 100 µ/mL penicillin G sodium, 100 µ/mL streptomycin were from Sigma (St. Louis, MO); ethyl acetate and methanol were from Merck, Germany; RPMI 1640, fetal bovine serum (FBS), 1% L-glutamine and 1% gentamicin were obtained from PAA Laboratories GmbH, Cölbe, Germany; DMEM/F12 and RPMI-1640 were from Invitrogen (Carlsbad, CA); 1 mM calcium and magnesium were from Packard Instrument Company (Meriden, CT); bovine calf serum and FBS were from Atlanta Biologicals (Lawrenceville, GA); and the Luciferase Assay Kit was obtained from Promega (E1500).

Assay for in vitro cytotoxicity

n-hexane, EtOAc, and MeOH extracts of T. argenteum subsp. argenteum were tested against ten cell lines using MTT assays. These cell lines included A549 (human alveolar epithelial cells), CaCo-2 (human epithelial colorectal adenocarcinoma), MCF-7 (human breast adenocarcinoma), MPANC-96 (human pancreatic cancer), MDA-MB-231 (metastatic human breast cancer), 253J-BV (bladder cancer cells), U87-MG (human glioblastoma-astrocytoma, epithelial-like), prostate cancer (PC3), human cervical carcinoma (HeLa) as cancerous cells and human embryonic kidney (HEK)-293 as noncancerous cells. Parthenolide was used as a positive control. Cells were cultivated in DMEM-F12 medium, passaged twice a week. Cells (104 cells/well) were seeded to the wells of 96-well plates and cultivated for 24 h in an incubator. Extracts with different dilutions (0.5, 5, 50 µg/mL) and the positive control were added and cells were incubated for 48 h. After 48 h, the number of viable cells was determined using an MTT assay. For this purpose; in order to count the number of living cells, 25 µL MTT (stock solution of 2.5 mg/mL) physiologic saline (9% NaCl) was added to the wells and incubated for 4 h. After a while, the medium was removed to dissolve the formazan crystals; 150 µL DMSO was added and the absorbance was read at 520 and 620 nm. All measurements were performed in triplets and the half-maximum inhibitory concentration (IC50) was determined using GraphPad Prism 5.

Assay for the inhibition of NF-κB activity

The NF-κB Luciferase Reporter HeLa Stable Cell Line (Signosis, CA) was used for this assay. Cells were cultured in DMEM-F12 supplemented with 10% FBS, 100 U/mL penicillin G sodium and 100 µg/mL streptomycin at 37°C in an atmosphere of 5% CO2 and 95% humidity.

Cells (5x105 cells/well/90 µL) were added to 96-well plates and incubated for 24 h. Then, test samples at different concentrations (0.5, 5, 50 µg/mL) were added to the medium and incubated for 30 min. After that, cells were induced with PMA (70 ng/mL) for 24 h, and the medium then was removed and the cells were washed with 200 µL PBS. Cells were incubated with 20 µL lysis buffer on a shaker at room temperature for 1 h. Absorbance was measured using a luminometer subsequent to adding 20 µL Luciferase substrate. Parthenolide was used as a positive control.

Assay for inhibition of iNOS activity

The mouse macrophage (RAW264.7) cells cultured in phenol red-free RPMI medium with 10% bovine calf serum and 100 U/mL penicillin G sodium and 100 µg/mL streptomycin. Cells (105 cells/well) were seeded in 96-well plates and incubated for 24 h. Test samples at different concentrations (0.5, 5, 50 µg/mL) were prepared from 10 mg/mL stock solution and 20 µL were added for each.

After 60 µL serum-free medium were added and 30 min of incubation, LPS (5 µg/mL) was added to the cells to induce iNOS and cells were incubated for 24 h. The concentration of nitric oxide produced as a result of iNOS activity was determined by measuring the level of nitrite in the cell culture supernatant using Griess reagent. The absorbance was read at 540-630 nm. IC50 values were obtained from dose curves. Parthenolide was used as a positive control and DMSO was used in the tests as a vehicle control.14 Extracts were also evaluated using MTT analyses to detect cytotoxic activity against RAW264.7 cells, in addition to the iNOS inhibition test.


Parthenolide was detected in n-hexane and EtOAc extracts of the plant. RF values of n-hexane and EtOAc extracts and parthenolide were 0.69 and their distances from origin of all three spots were equal and all three spots were blue. Based on this results, it was concluded that the major compound of n-hexane and EtOAc extracts of T. argenteum subsp. argenteum was parthenolide. The TLC result is also given as fig1|Table 1.

The results of the cytotoxic activity tests are shown in table1|Table 1. Among the extracts, significant cytotoxic activity of the n-hexane extract was observed against CaCo-2, MPANC-96, HEK-293, MDA-MB-231, and PC3 (IC50 values of 3.959±0.62, 5.353±1.24, 1.651±0.43, 4.154±0.18, 2.847±0.51 µg/mL, respectively). Our results showed that the n-hexane extract is more effective than parthenolide against MPANC-96 and PC3. It also had cytotoxic activity as strong as parthenolide against CaCo-2, HEK-293, MDA-MB-231. The viability percentage of n-hexane extract is shown in fig2|Figure 2. Microscopy images of the cells are shown in fig3|Figure 3.

In many studies, cytotoxic activities of various Tanacetum species have been reported. Rateb et al.15 found that hydroalcoholic and aqueous extracts of different parts of T. parthenium L. had cytotoxic effects. The alcoholic extracts of the flowers of the plant showed significant cytotoxic effects (15% cell viability) with 50 µg/mL concentration on Ehrlich ascites carcinoma. This activity is considered as a result of synergy of flavonoid and sesquiterpene lactone contents. Rosselli et al.16 investigated the cytotoxic activity of eudesmanolides isolated from flowers of Tanacetum vulgare subsp. siculum against an A549 cell line.

This is the first report to demonstrate the cytotoxic activity of T. argenteum subsp. argenteum against CaCo-2, MPANC-96, MDA-MB-231, 253J-BV, U87-MG, and PC3 cell lines. In a previous report, the plant was analyzed for its cytotoxic property on MCF-7, the cell viability inhibition value of methanolic extract was found as 52.58% at a concentration of 100 µg/mL, whereas we found no serious activity with MeOH extracts. The difference is likely due to the extraction methods.17

Recently, Şen et al.18 investigated the cytotoxic activity of aerial parts of T. argenteum subsp. argentum against four cell lines [A549, HeLa, HT-29 (human colorectal adenocarcinoma), MCF-7] using MTT assays. The authors found that an n-hexane extract of the plant inhibited growth of A-549 and HT-29 cells, and a chloroform extract of the plant inhibited growth of A-549 and HeLa cells at the concentrations of 30 µg/mL. Both extracts of the plant inhibited more than 50% proliferation of cells. When compared their results with ours on the same cell lines; the stronger results observed in our study with the same extracts are likely associated with the quantitative superiority of secondary metabolites responsible for the cytotoxic activity. Thus, the disparity between the two studies could be attributed to the different localities of the plant materials.

Apolar sesquiterpene lactones with γ lactone moiety pass into the n-hexane fraction could be responsible of the effect because sesquiterpene lactones have a broad spectrum of biologic activities including anti-inflammatory and cytotoxic properties. The lactone ring and exocyclic methylene group of sesquiterpene lactones are considered to be the liable units for biologic activities of sesquiterpenoids.3

It is known that parthenolide, a germacranolide-type sesquiterpene lactone, plays a significant role for anti-inflammatory and cytotoxic activities.19 Notably T. parthenium, T. vulgare, Tanacetum densum subsp. amani, T. argenteum subsp. Flabellifolium, and T. argenteum subsp. canum var. canum contain parthenolide.3 The activities of the n-hexane extract and the ethyl acetate extract may be associated with the plant’s major component parthenolide.

The anti-inflammatory activity of T. argenteum subsp. argenteum was evaluated using NF-κB and iNOS methods. As the results can be seen in table2|Table 2, n-hexane extract had significant anti-inflammatory activity with an IC50 of 6.159±0.45 µg/mL for NF-κB, and 0.627±0.16 µg/mL for iNOS methods, respectively. Anti-inflammatory activities of various Tanacetum species using in vitro and in vivo methods have been reported.20,21 The anti-inflammatory activities of Tanacetum spp. are related to their flavonoid and sesquiterpene contents. In a previous report, Nasri et al.22 investigated the hydroalcoholic extract of Tanacetum balsamita and found anti-inflammatory activity related to quercetin, a flavonoid, and we found the anti-inflammatory activity of the plant through apolar fractions related to sesquiterpene lactones, most probably parthenolide. Bukhari et al.23 noted that the n-hexane extract of Tanacetum artemisioides showed stronger in vivo anti-inflammatory activity than that of polar aqueous fractions.

As postulated, sesquiterpene lactones are generally known to impair the activity of the NF-κB.24 Hehner et al.25 noted that parthenolide, the main compound of T. parthenium, is a well-known anti-inflammatory agent that inhibits the NF-κB pathway. López-Franco et al.26 showed parthenolide’s inhibiting role using the NF-κB method against murine cells. The n-hexane extract is more effective than parthenolide in iNOS methods, whereas parthenolide is stronger than n-hexane extracts with NF-κB. The n-hexane extract’s potency could be related to a synergistic effect of different secondary metabolites of the extract. The results can also be seen in fig4|Figure 4 and fig5|5.


Our results indicated that the n-hexane extract of T. argenteum subsp. argenteum has promising cytotoxic activity on CaCo-2, MPANC-96, HEK-293, MDA-MB-231, and PC3 cells, and also anti-inflammatory activity. Parthenolide, a well-known anti-inflammatory and cytotoxic agent was detected in n-hexane and EtOAc extracts of the plant using TLC analysis. n-hexane extract’s activity may be associated with its major component parthenolide and other substances in the plant. Phytochemical experiments are ongoing with n-hexane extracts of T. argenteum subsp. argenteum.

Conflict of Interest: No conflict of interest was declared by the authors.

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