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Introduction

Cancer is characterized by uncontrolled growth and spreading of abnormal cells. It is one of the most life-threatening and challenging diseases of modern time, caused by a number of internal factors, including immune condition and inherited mutation, and external factors, including radiation, tobacco and chemical exposure (1). Liver, breast, colorectal, lung, cervical and nasopharyngeal cancer are the most prevalent cancer types in the modern age. The present study focused on liver and breast cancer due to their high occurrence rates. In 2006, hepatocellular carcinoma (HCC) was identified to account for 70–85% of total primary liver cancer types (2). HCC is primarily caused by chronic viral hepatitis B or C infection, iron overload, aflotoxin exposure, obesity, alcohol-associated cirrhosis and possibly non-alcoholic fatty liver disease (3,4). Breast cancer continues to be the leading cause of cancer-associated mortality among women (5), and the occurrence rate has increased in China and other Asian countries (6,7). Breast cancer can be categorized into two main types, ductal carcinoma and lobular carcinoma. Ductal carcinoma begins in the ducts that transport milk from the breast to the nipple, whereas lobular carcinoma starts in the lobules that produce milk. Atypical hyperplasia of the breast, family history, early menarche, late menopause and Li-Fraumeni syndrome are some of the known risk factors for breast cancer (8–10).

To date, the common treatments for cancers are surgical removal of the tumour tissue, chemotherapy and ionizing radiation. Apart from destroying adjacent normal cells (11), these treatments also cause severe side effects (12–14). Therefore, current studies have focused on the search for alternative medicines from plant-based sources. Alternative medicine not only improves the efficacy of conventional medicines, it reduces the side effects of chemotherapy (15) and strengthens the immune system to fight against cancer (16).

Among the medicinal plants, one of the commonly found plants in tropical countries is Strobilanthes crispa Blume. It is traditionally known as daun pecah beling in Jakarta and enyoh kilo, kecibeling or kejibeling in Java (17). In Malaysia, it is known as pecahkaca or jinbatu (17). This bush-like plant is scattered throughout the regions of Madagascar to Malay Archipelago (18). S. crispa has high mineral and phenolic content, and exhibits high antioxidant activity (19,20). In addition, this plant contains alkaloids, tannins, polyphenols, water-soluble vitamins, caffeine, catechins (19,20) and bioactive compounds, including β-sitosterol, and stigmasterol (21). A previous study demonstrated that S. crispa leaves possess anti-diabetic, diuretic and blood pressure lowering properties (17). Furthermore, a number of studies have recorded the potency of S. crispa extracts in inhibiting cancer cell growth (22–25).

Thus, the aim of the present study was to investigate the cytotoxic and anti-proliferative effects of S. crispa extracts on HepG-2 and MDA-MB-231 cancer cell lines. Furthermore, one of the aims was to determine the effects of the extracts on cell cycle and caspase-8 activation.

Materials and methods

Preparation of plant extracts

The botanical identity of S. crispa was determined and authenticated by a taxonomist from the Forest Research Institute Malaysia (Kuala Lumpur, Malaysia; sample no. PID 040114–04). Fresh plant materials (leaves and stems) were collected and dried in an oven at 40°C until a constant weight was obtained. Dried leaves and stems were separated, crushed into fine pieces and then ground with a mill grinder into powder form. A total of four organic solvent extracts of the leaves and stems were prepared individually. The organic solvents used were hexane, chloroform, ethyl acetate and methanol (all Friendemann Schmidt, Parkwood, WA, USA). The extraction was performed by mixing 500 ml of solvent into 100 g of powdered leaves or stems, and then macerating in the dark at room temperature for 3 days. The suspensions were filtered using Whatman paper (Thermo Fisher Scientific, Inc., Waltham, MA, USA) and then evaporated using a rotary evaporator (Büchi R-2154; Büchi Labortechnik AG, Flawil, Switzerland) to obtain desired crude extracts. The extracts obtained were as follows: Leaf hexane (LH), leaf chloroform (LC), leaf ethyl acetate (LEA), leaf methanol (LM), stem hexane (SH), stem chloroform (SC), stem ethyl acetate (SEA) and stem methanol (SM).

The dried plant materials (10 g) were mixed with 500 ml distilled water and kept at 60°C for 3 h. The resulting suspensions were then filtered and followed by freeze drying. The extracts obtained were designated as leaf water (LW) and stem water (SW).

Cell culture

Hepatocellular carcinoma HepG-2, breast cancer MDA-MB-231 and normal rat kidney NRK-52E cell lines were obtained from the American Type Culture Collection (Manassas, VA, USA). The cells were cultured in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 100 U/ml penicillin and 100 mg/ml streptomycin (all Gibco; Thermo Fisher Scientific, Inc.), and maintained at 37°C in a humidified atmosphere of 5% CO2.

MTT assay

HepG-2, MDA-MB-231 and NRK-52E cells were seeded at a density of 1×105 cells/ml into a 96-well plate and treated with varying concentrations of S. crispa extracts (12.5, 25, 50, 100 and 200 µg/ml) including LH, LC, LEA, LM, LW, SH, SC, SEA, SM and SW for 72 h at 37°C. Subsequently, 10 µl MTT solution (Bio Basic, Inc., Amherst, NY, USA) was added into each well and cells were incubated for 4 h at 37°C. Subsequently, the solution in each well was removed and 100 µl of dimethyl sulphoxide (Friendemann Schmidt) was added. The coloured solution was measured using a Dynex Opsys MR microplate reader (Dynex Technologies Inc., Chantilly, VA, USA) at 570 nm wavelength. Cell viability (%) was calculated according to the following formula: Optical density (OD) of samples/OD of control ×100, where the control represents untreated cells. The control cells were incubated with DMEM supplemented with 10% FBS, 100 U/ml penicillin and 100 mg/ml streptomycin (all Gibco; Thermo Fisher Scientific, Inc.) for 72 h at 37°C. The half maximal inhibitory concentration (IC50), which is defined as the concentration required to inhibit cell viability by 50%, was determined through the construction of a dose-response curve.

HepG-2 and MDA-MB-231 cells were also treated with 5-flurouracil (5-Fu; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany), the positive control of the experiment, at the concentrations of 12.5, 25, 50, 100 and 200 µg/ml for 72 h at 37°C. IC50 values were determined and the cytotoxicity of S. crispa extracts were compared to the effects of the known anti-cancer drug, 5-Fu.

The selectivity index (SI) in the present study was calculated from the IC50 of the extracts in normal rat kidney cells (NRK-52E) vs. cancer cells. The extract was considered to have high selectivity for cancer cells if the SI was >3 (26).

Observation of morphological changes

HepG-2 and MDA-MB-231 cells were seeded at a density of 1×106 cells/well into 6-well plates and treated with the SH at their respective IC50 concentrations for 72 h at 37°C. Untreated and treated cells were then observed under an inverted microscope (Nikon Eclipse TS100; Nikon Corporation, Tokyo, Japan) and images were captured with the attached camera.

Determination of cell doubling time

HepG-2 and MDA-MB-231 cells were seeded into a 24-well plate at the density of 1×104 cells/ml. Subsequently, the cells were treated with SH and incubated at 37°C for 72 h. Two different concentrations were used: The pre-determined IC50; and 2x the IC50. On the third day, the treated cells were trypsinised and stained with trypan blue (Gibco; Thermo Fisher Scientific, Inc.). Live cells were counted under an inverted microscope (Nikon Eclipse TS100) using a hemocytometer (Paul Marienfeld GmbH & Co. KG, Lunda-Königshofen, Germany). The cell doubling time was calculated by dividing the total duration (h) by the total number of generations. The number of generations was calculated using the following formula: 3.32 (logNN-logN1), where NN is the number of cells counted and N1 is the number of cells seeded (27).

Cell cycle analysis

HepG-2 and MDA-MB-231 cells were seeded into 6-well plates at a density of 1×106 cells/well and treated with SH at IC50 for 72 h at 37°C. The cells were fixed with 70% ethanol subsequently. Then the cells were washed twice with cold phosphate buffer saline (PBS) and resuspended in 1 ml of PBS at a concentration of 1×106 cells/ml. Subsequently, 5 µl of 10 mg/ml RNase (Sigma-Aldrich; Merck KGaA) was added to the cell suspension and incubated at 37°C for 1 h. Subsequently, 10 µl propidium iodide (1 mg/ml; Sigma-Aldrich; Merck KGaA) was added and the suspension was incubated in the dark for 30 min at 37°C. Finally, the samples were analysed using flow cytometry (FACScan; BD Biosciences, Franklin Lakes, NJ, USA) and CELLQuest™ software (BD Biosciences), version 3.0. Flow cytometric analysis of the samples stained with propidium iodide was run by collecting 25,000 events per sample.

Detection of caspase-8

The caspase-8 assay kit was purchased from Calbiochem (Merck KGaA). The caspase activity in SH-treated cells was measured according to the manufacturer's protocol. Briefly, cells were seeded at a density of 1×106 cells/ml into 6-well plates. Cells were trypsinised following treatment with the SH at IC50 for 72 h at 37°C. The cells were then transferred into an Eppendorf tube. Subsequently, 1 µl staining reagent was added to the cell suspension and incubated at 37°C for 30 min. Cells were washed with PBS and transferred into a black well plate. Fluorescence intensity at excitation 485 nm and emission 535 nm was then recorded.

Statistical analysis

Statistical analysis was performed using one-way analysis of variance with Tukey's honest significant difference post-hoc test with GraphPad Instat software (version 3.0; GraphPad Software, Inc., La Jolla, CA, USA) or Student's t-tests with Microsoft Excel (version 2013; Microsoft Corporation, Redmond, WA, USA). All data are presented as the mean ± standard deviation. P<0.05 was considered to indicate a statistically significant difference.

Results

Cytotoxic effect of S. crispa extracts

The effect of S. crispa on the growth activities of HepG-2 and MDA-MB-231 cells was investigated using MTT assays (Fig. 1). In total, 5 extracts (LH, LC, LEA, SH and SC) were demonstrated to induce cell death in the two cell lines in a concentration-dependent manner (P<0.05) while SEA displayed moderate cytotoxicity. However, methanolic and water extracts of S. crispa (LM, LW, SM and SW) revealed no evident cytotoxic activity against the cell lines. In fact, the extracts promoted the growth of cancer cells, when compared with the untreated control (Fig. 1). However, the differences were not statistically significant.

Figure 1. Dose-response curve of Strobilanthes crispa extracts on HepG-2 liver cancer and MDA-MB-231 breast cancer cell lines. Cells were treated with various concentrations (12.5, 25, 50, 100 and 200 µg/ml) of S. crispa extracts for 72 h and percentage of cell viability was determined using an MTT assay. HepG-2 cells treated with extracts derived from the (A) leaves and (B) stems of Strobilanthes crispa. MDA-MB-231 cells treated with extracts derived from the (C) leaves and (D) stems of Strobilanthes crispa. Data are presented as the mean following 3 independent experiments. *P<0.05, compared with the untreated control (representing 100% of cell viability). LH, leaf hexane; LEA, leaf ethyl acetate; LC, leaf chloroform; LM, leaf methanol; LW, leaf water; SH, stem hexane; SEA, stem ethyl acetate; SC, stem chloroform; SM, stem methanol; SW, stem water.

Based on the dose-response curve generated, IC50 of each extracts was determined and summarized in Table I. Among the extracts tested, SH exhibited the highest potency with the lowest IC50 values in mediating HepG-2 and MDA-MB-231 cell death. The IC50 value obtained from HepG-2 cells (38.8 µg/ml) was comparable to the commercially available anti-cancer drug, 5-Fu (IC50, 37.3 µg/ml). The IC50 determined in MDA-MB-231 cells, 42.5 µg/ml was 1.4 times lower compared with the 5-Fu (IC50, 60 µg/ml).

Table I. IC50 and SI values of extracts of Strobilanthes crispa on HepG-2 and MDA-MB-231 cells.

Table I.

IC50 and SI values of extracts of Strobilanthes crispa on HepG-2 and MDA-MB-231 cells.

	IC50, µg/ml (SI)
Extract/treatment	HepG-2	MDA-MB-231
Leaf
Hexane	N/A	192.50±3.54 (0.44)
Chloroform	175.70±35.40 (1.05)	N/A
Ethyl acetate	176.70±15.30 (0.94)	N/A
Methanol	N/A	N/A
Water	N/A	N/A
Stem
Hexane	38.80±8.50 (0.28)	42.50±39.67 (0.26)
Chloroform	173.30±5.80 (>1.15)	N/A
Ethyl acetate	N/A	N/A
Methanol	N/A	N/A
Water	N/A	N/A
5-Fluorouracil	37.30±6.75 (0.26)	60.00±14.14 (0.16)

[i] Data are presented as the mean ± standard deviation following 3 independent experiments. IC50, half maximal inhibitory concentration; SI, selectivity index; N/A, not available.

SI calculated based on predetermined IC50 values on NRK-52E cells demonstrated that none of the extracts, apart from SC, exhibited high selectivity towards cancer cells because the SI values were <3 (Table I). Furthermore, the anti-cancer drug, 5-Fu exhibited poor selectivity. The SI value of SC was markedly higher compared with the other extracts (>1.15).

Effect of SH on cell morphological changes

HepG-2 and MDA-MB-231 cells were observed under an inverted microscope for morphological changes and the results are presented in Fig. 2. Fig. 2A demonstrates confluent HepG-2 cells that are flattened, grossly polygonal in shape and arranged in monolayer. In the SH-treated HepG-2 cells, morphological changes, including the formation of vacuoles within the cell were observed. Furthermore, floating dead cells and a reduction in cell number were also noted (Fig. 2B).

Figure 2. Microscopic observation of (A) untreated control and (B) treated HepG-2 liver cancer cells, and (C) untreated control and (D) treated MDA-MB-231 breast cancer cells. The cells were treated with the predetermined half maximal inhibitory concentration of Strobilanthes crispa stem hexane extract (38.8 µg/ml for HepG-2 cells; 42.5 µg/ml for MDA-MB-231 cells) for 72 h. The cells were then observed under an inverted microscope (magnification, ×200). The white arrow indicates vacuolation of cells and the black arrows indicate floating dead cells.

SH also induced MDA-MB-231 cell death as more floating cells were observed in the treated compared with the control cells. Untreated MDA-MB-231 cells remained normal, healthy and confluent throughout the treatment period (Fig. 2C). However, vacuolation of cells was noted in the treated cells (Fig. 2D).

Effect of SH on cell doubling time

Fig. 3 demonstrates the effect of SH on HepG-2 and MDA-MB-231 cell proliferation. When HepG-2 cells were exposed to SH at the IC50, no significant differences in the cell population doubling time were observed. However, cells treated with double the IC50 of SH exhibited a significant increase in the cell doubling time compared with the untreated control group (P<0.001). However, MDA-MB-231 cells responded to SH in a dose-dependent manner. SH treatment at the IC50 caused a 2.5-fold delay in cell proliferation while twice the IC50 of SH delayed cell doubling by 3.4-fold. The delayed cell doubling in cells treated with the higher dose was statistically significant when compared with the untreated control cells (P<0.05).

Figure 3. Effects of Strobilanthes crispa stem hexane extract on the cell doubling time of HepG-2 liver cancer and MDA-MB-231 breast cancer cells. Cells were treated with two different concentrations of stems hexane extract (38.8 and 77.6 µg/ml for HepG-2 cells; 42.5 and 85 µg/ml for MDA-MB-231 cells) for 72 h, and the number of cells was counted to determine the cell doubling time. Data are presented as the mean ± standard deviation following 3 independent experiments. *P<0.05 and ***P<0.001, compared with the untreated control. IC50, half maximal inhibitory concentration.

Effect of SH on cell cycle profile

Treatment with SH caused HepG-2 cell cycle arrest at the G0/G1 phase. This in turn caused a decrease in percentage of cells that entered the S and G2/M phases. The percentage of cells in sub-G phase in SH-treated group was ~50% compared with that of the control cells (Table II).

Table II. Effect of S. crispa stem hexane extract on cell cycle progression of HepG-2 cells.

Table II.

Effect of S. crispa stem hexane extract on cell cycle progression of HepG-2 cells.

	Percentage of cells
Cell cycle phase	Control	Stem hexane	P-value
Sub-G	0.79±0.01	0.41±0.01	0.017
G0/G1	60.68±1.22	71.16±0.68	0.009
S	2.22±0.05	1.80±0.01	0.008
G2/M	35.37±0.71	26.13±0.25	0.003

[i] Data are presented as the mean ± standard deviation following 3 independent experiments. P-values were determined using the t-test in which the stem hexane-treated group was compared with the control group.

Table III shows the distribution of MDA-MB-231 cells in different cell cycle phases following treatment with SH. Increased sub-G and S phases were noted following the treatment; however, no significant differences were identified.

Table III. Effect of S. crispa stem hexane extract on cell cycle progression of MDA-MB-231 cells.

Table III.

Effect of S. crispa stem hexane extract on cell cycle progression of MDA-MB-231 cells.

	Percentage of cells
Cell cycle phase	Control	Stem hexane	P-value
Sub-G	0.56±0.59	5.04±3.44	0.181
G0/G1	70.25±9.68	57.86±10.23	0.270
S	0.94±0.86	8.57±8.02	0.293
G2/M	28.31±8.29	28.98±13.75	0.956

[i] Data are presented as the mean ± standard deviation following 3 independent experiments. P-values were determined using the t-test in which the stem hexane-treated group was compared with the control group.

Effect of SH on caspase-8 activation

SH treatment significantly induced caspase-8 activation in HepG-2 cells (P<0.01). SH treatment appeared to induce caspase-8 activation in MDA-MB-231 cells, although this was not significant (Fig. 4).

Figure 4. Caspase-8 activity in HepG-2 liver cancer and MDA-MB-231 breast cancer cells following treatment with Strobilanthes crispa stem hexane extract for 72 h. The cancer cells were treated with the extract at their respective half maximal inhibitory concentrations extract (38.8 µg/ml for HepG-2 cells; 42.5 µg/ml for MDA-MB-231 cells), and the fluorescent expression of caspase-8 was measured. Data are presented as the mean ± standard deviation following 3 independent experiments. **P<0.01, compared with the untreated control.

Discussion

Cancer remains one of the leading causes of mortality worldwide. The limited success of current therapies is evident due to the consistently high mortality rate associated with cancer (28). Therefore, the identification of novel potential anti-cancer therapeutic agents is warranted to provide more treatments options. Natural products serve as a valuable source that offer cytotoxic properties, and have gained significant recognition for their role in the management of cancer. The present study evaluated the anticancer effects of S. crispa extracts on HepG-2 liver cancer and MDA-MB-231 breast cancer cells.

An MTT assay was used in the present study to screen the plant extracts for their anti-cancer properties. As demonstrated by the MTT assay LH, LEA, LC, SH and SC reduced cell viability in a concentration-dependent manner in both cell lines. Previous studies have revealed that S. crispa extracts are able to kill liver and breast cancer cells (22–24,29). For example, the chloroform extract of S. crispa was demonstrated to possess cytotoxic effects against HepG-2 cells (22,23), while the methanolic extract exhibited strong cytotoxicity on MDA-MB-231 and HepG-2 cells (22). Furthermore, the ethanolic extract (29) and a sub-fraction of the dichloromethane extract of S. crispa (24) demonstrated the ability to consistently kill breast cancer cells. Notably, the IC50 values obtained in the present study were higher compared with that in the previous studies mentioned. For instance, Asmah et al (22) identified the IC50 value of the S. crispa chloroform extract in HepG-2 cells to be 28 µg/ml, while the present study reported an IC50 value of 175.7 µg/ml. The methanolic extracts demonstrated no cytotoxic effect on HepG-2 and MDA-MB-231 cells in the present study, but Asmah et al (22) reported that the extract inhibited the growth of the cells with IC50 values of 29.3 and 27.2 µg/ml, respectively (22). These contradicting observations may be due to the differences in the geographical areas from which the plants were collected. In fact, a study by Chinkwo et al (30) reported that the bioactivity of extracts from the medicinal plant Sutherlandia frutescens that was collected from different areas varied so much that only plants grown in a specific province exhibited a chemotherapeutic effect. Differences in environmental factors, including soil composition and temperature may influence the production of the bioactive compounds in the plants (31). In addition, the maturity of plants may influence the amount of bioactive compounds produced; generally older plants accumulate a greater amount of content (19).

Among the extracts tested, the hexane extract from the stem of S. crispa demonstrated the most potent cytotoxic effect with the lowest IC50 values in the current study. This suggests that the anti-cancer compounds are extractable by hexane, a hydrophobic solvent. Previous studies have revealed that hexane is useful for the extraction of stigmasterol (32–34) and β-sitosterol (33–36). Stigmasterol and β-sitosterol extracted from S. crispa have been demonstrated to possess anti-cancer effects on liver, breast, and colon carcinoma (22). Other anti-cancer compounds that may be extracted include alkaloids and tannins (20), which have been documented to exhibit anti-cancer properties (37–40). In order to identify the compounds responsible for the anti-cancer effects, further studies on the isolation and purification of the bioactive compounds from S. crispa are required.

SI, an indicator of the safety of drug use, was determined for the compounds investigated in the present study. A compound is considered to have high selectivity towards cancer cells if the SI value is >3 (26). In the present study, all SI values determined were <3, except for SC, indicating the effect of the extracts was not specific to the cancer cells as they were also killing the normal cells. Furthermore, the anti-cancer drug, 5-Fu also demonstrated poor selectivity for tumouricidal activity (41,42). The non-selectiveness of compounds may impose severe side effects on patients with cancer, as they are capable of damaging healthy cells (43). In the current study, SC possessed a relatively high SI value, indicating that it may cause less side effects compared with the other extracts evaluated. In order to improve the selectivity of a compound towards cancer cells, drug modification can be performed (44). Strategies to improve the affinity towards target cells and at the same time lower the affinity towards off-target molecules should be considered (45). Previously, a number of antiepileptic drugs, including levetiracetam, carbamazepine and felbamate, have undergone drug modification to improve their tolerability and efficacy (46). Thus, drug modification to increase the selectively of SH to cancer cells may be an ideal option to further improve its anticancer potency and limit the side effects.

Treatment with SH was observed to delay the doubling time of HepG-2 and MDA-MB-231 cells in the current study. The cell cycle analysis demonstrated that HepG-2 cells were arrested at the G0/G1 phase, indicating that SH inhibited liver cancer cell growth through cell cycle modulation. However, no significant changes in the cell cycle phases were reported in MDA-MB-231 cells. Thus, the reduction in MDA-MB-231 cell proliferation was independent of cell cycle progression and may be attributed to other mechanisms.

Cell apoptosis, an important event in controlling the programmed cell death, may serve an important role in the SH-mediated cytotoxicity observed in the current study. This is evident through the presence of cytoplasmic vacuolation in the HepG-2 and MDA-MB-231 cells, which is a typical feature of apoptosis (47,48). Cell apoptosis is an autonomous dismantled process, which removes individual cell components while avoiding inflammation that usually occurs during necrosis. Thus, apoptosis is only limited to single cells and does not affect normal adjacent cells (49). In cancer studies, induction of apoptosis and inhibition of cellular proliferation are considered as imperative properties in chemoprevention and chemotherapy (50–52). To further confirm the apoptotic activity of SH, caspase activation was determined in the present study.

Caspases can be activated through the intrinsic or extrinsic signalling pathway. Mitochondrial integrity is disrupted by cellular stress in the intrinsic pathway while stimulation of death receptors in the plasma membrane is initiated in the extrinsic pathway (53). In response to cellular stress, the initiator caspases (caspase-2, −8, −9 and −10) cleave and activate the effector caspases (caspase-3, −6 and −7); in turn the effector caspases execute the apoptotic process (54). The present study demonstrated that SH significantly activated caspase-8 in HepG-2 but not MDA-MB-231 cells.

Taken together, the results of the present study demonstrated that SH induced cytotoxicity and reduced cell proliferation in HepG-2 cells through cell cycle modulation and caspase-8 activation. However, the anti-cancer effect of SH was independent of cell cycle and caspase-8 activation in MDA-MB-231 cells. This suggests that SH exhibited cytotoxic effects in MDA-MB-231 cells via other mechanisms. One of the possible mechanisms could be due to the down-regulation of c-myc gene expression (23). C-myc oncogene has been verified to account for the growth and progression of breast cancer in hormone-dependent and -independent breast cancer cell lines (55). Other possible mechanisms that may be involved include the p53-dependent signalling pathway (56), tumour necrosis factor-related apoptosis-inducing ligand mechanism (57) and p73-dependent signalling pathway (58). Hence, further studies investigating these mechanisms are warranted to confirm the mechanism of action of SH on the MDA-MB-231 cell line.

In conclusion, S. crispa extracts were revealed to exert strong anti-cancer effects on liver and breast carcinoma cells. Among the extracts tested, the SH extract demonstrated the most potent activity and could be further developed as a potential anti-cancer therapeutic drug in the future.

Acknowledgements

The present study was supported by the International Medical University, Kuala Lumpur, Malaysia [grant no. BMSc I01/09 (03) 2011].

References