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Cytotoxicity of methanol extracts of Annona muricata, Passiflora edulis and nine other Cameroonian medicinal plants towards multi-factorial drug-resistant cancer cell lines

SpringerPlus volume 5, Article number: 1666 (2016) Cite this article

Abstract

Background

Cancer cells rapidly acquire resistance leading to treatment failures. In the present study, we have evaluated the cytotoxicity of 17 methanol extracts from 11 Cameroonian medicinal plants against the sensitive leukemia CCRF–CEM cells and the best ones were further tested on a panel of 8 other human cancer cell lines, including various MDR phenotypes as well as against the normal AML12 hepatocytes.

Methods

The cytotoxicity of the extracts was determined using a resazurin reduction assay meanwhile flow cytometry was used to measure cell cycle, apoptosis, mitochondrial membrane potential (MMP), and reactive oxygen species.

Results

In an initial screening using leukemia CCRF–CEM cells, ten extracts from five plants namely Alchornea floribunda, Annona muricata, Euphorbia prostata, Pachypodanthium staudtii and Passiflora edulis displayed IC50 values below 20 µg/mL. They were further tested in 8 other cell lines as well as in normal AML12 hepatocytes. All selected extracts were active against leukemia CEM/ADR5000 cells with IC50 value below 40 µg/mL. IC50 values ranging from 10.13 µg/mL (towards CEM/ADR5000 cells) to 72.01 µg/mL [towards resistant colon carcinoma HCT116 (p53 −/−) cells] for Pachypodanthium staudtii roots and from 0.11 µg/mL (towards CCRF–CEM cells) to 108 µg/mL (towards P-glycoprotein-over-expressing CEM/ADR5000 cells) for doxorubicin were obtained in the eight other cancer cell lines studied. Extracts from Annona muricata leaves (AML) and seeds (AMS), and Passiflora edulis fruit (PEF) had IC50 values below 1 µg/mL against CCRF–CEM cells and below 10 µg/mL against its MDR subline CEM/ADR5000 cells. AML, AMS and PEF induced MMP-loss-mediated apoptosis in CCRF–CEM cells.

Conclusions

Results of the present study suggest that some of the tested plants namely Alchornea floribunda, Annona muricata, Euphorbia prostata, Pachypodanthium staudtii and Passiflora edulis represent a source of anticancer drugs. Annona muricata and Passiflora edulis are good cytotoxic plants that could be exploited to develop phytomedicine to fight mostly hematological cancers including MDR phenotypes.

Background

The development of resistance to cytotoxic agents represents a major concern in cancer chemotherapy. Multi-drug resistance (MDR) is associated with over-expression of transmembrane glycoprotein (P-gp) which functions as a drug efflux pump, reducing the intracellular levels of cytotoxic drugs (Juranka et al. 1989). P-gp belongs to the ATP-binding cassette (ABC) transport proteins, which also include the multi-drug resistance associated protein 1 (MRP1) (Shen et al. 2011; Biedler and Spengler 1994; Efferth et al. 2003a), or the breast cancer resistance protein (BCRP/ABCG2) (Shen et al. 2011). The oncogene epidermal growth factor receptor (EGFR) (Biedler and Spengler 1994; Efferth et al. 2003a, b) and the deletions or inactivation of tumor suppressor gene p53 (el-Deiry 1997) have also been involved in MDR mechanism of cancer cells. Overcoming this resistance requires a permanent search of new antineoplastic agents. In the past, natural products from plant kingdom have revealed a high potential as cytotoxic drug reservoir (Kuete and Efferth 2011). According to the World Health Organization, about 80 % of the population of developing countries relies on traditional medicines, mostly plant drugs, for their primary health care needs (FAO 1997). It has also been reported that modern pharmacopoeia still contain at least 25 % drugs derived from plants and many others which are synthetic analogues (FAO 1997). Therefore, fighting cancers with botanicals represents a very promising alternative, especially regarding the diversity of plant’s secondary metabolites. African flora has previously been found to be very fruitful in the search of antiproliferative molecules. Many compounds including xanthones: 8-hydroxycudraxanthone G, morusignin I, cudraxanthone I (Kuete et al. 2013a), and xanthone V1 (Kuete et al. 2011a), benzophenones: guttiferone E and isogarcinol (Kuete et al. 2013b), quinone: 2-acetylfuro-1,4-naphthoquinone (Kuete et al. 2011a), flavonoids: 4-hydroxylonchocarpin, 6,8-diprenyleriodictyol (Kuete et al. 2011b), 2′,4′-dihydroxy-3′,6′-dimethoxychalcone and 4′-hydroxy-2′,6′-dimethoxychalcone (Kuete et al. 2014a; Dzoyem et al. 2012) and alkaloids: isotetrandrine (Kuete et al. 2015a) and montrofoline (Kuete et al. 2015b) displayed good antiproliferative effects against various cancer cell lines. In a collaborative research programme between the Council for Scientific and Industrial Research (CSIR) in South Africa and the National Cancer Institute (NCI) in the USA, several South African plant extracts exhibited anticancer activity against a panel of three human cell lines (breast MCF7, renal TK10 and melanoma UACC62) (Fouche et al. 2006, 2008). African medicinal plants such as Fagara heitzii (Dzoyem et al. 2013), Echinops giganteus, Xylopia aethiopica, Piper capense, Imperata cylindrica (Kuete et al. 2011c), Beilschmiedia acuta, Clausena anisata (Kuete et al. 2013c) also displayed good cytotoxicity towards drug-sensitive and drug-resistant cancer cell lines. In our ongoing search of anticancer products from African medicinal flora, we designed the present study to investigate the cytotoxicity of 11 plants traditionally used to manage cancer or disease states bearing relevance to cancer or cancer-like symptoms, such as immune and skin disorders, inflammatory, infectious, parasitic and viral diseases (Kuete et al. 2015a). The study was extended to the evaluation of the ability of the three most active extracts from two medicinal plants, Annona muricata Lin. (Annonaceae) and Passiflora edulis Sims (Passifloraceae) to alter the cell cycle distribution, caspases activity, mitochondrial membrane potential (MMP) and to increase the production of reactive oxygen species (ROS) in leukemia CCRF–CEM cells.

Methods

Plant material and extraction

All medicinal plants tested are traditionally used in the management of cancer or disease states with symptoms related to cancer. Plants were collected in different regions of Cameroon in January 2012. They included Pachypodanthium staudtii, Alchornea floribunda, Annona muricata, Canarium schweinfurthii, Hibiscus esculentus, Colocasia esculenta, Moringa oleifera, Triumphetta pentandra, Xanthosoma mafaffa, Euphorbia prostata and Passiflora edulis. The plant parts investigated are shown in Table 1. The plants were identified at the National Herbarium (Yaoundé, Cameroon), where voucher specimens were deposited under the reference numbers shown in Table 1. The air-dried and powdered plant material (50 g) was soaked in methanol (200 mL) for 48 h, at room temperature. The methanol extract was concentrated in vacuum under reduced pressure at 68 °C to give the crude extract. This extract was completely dried at room temperature, then conserved at 4 °C until further use.

Table 1 General information and reports on evidence of biological activities and chemistry of the studied plants
Full size table

Chemicals

Doxorubicin 98.0 % and vinblastine ≥96 % from Sigma-Aldrich (Munich, Germany) were provided by the University Pharmacy of the Johannes Gutenberg University (Mainz, Germany), dissolved in phosphate buffer saline (PBS; Invitrogen, Eggenstein, Germany) at a concentration of 10 mM and used as positive control drugs. Geneticin >98 % (Sigma-Aldrich), stored at a stock concentration of 72.18 mM was used to maintain the resistance patterns of MDR carcinoma cell lines.

Cell cultures

The cell lines used in the present study included drug-sensitive leukemia CCRF–CEM and multidrug-resistant P-glycoprotein-over-expressing subline CEM/ADR5000 cells (Efferth et al. 2003a; Kimmig et al. 1990; Gillet et al. 2004), breast cancer MDA-MB-231-pcDNA3 cells and its resistant subline MDA-MB-231-BCRP clone 23 (Doyle et al. 1998), colon cancer HCT116 (p53 +/+) cells and its knockout clone HCT116 (p53 −/−), glioblastoma U87MG cells and its resistant subline U87MG.ΔEGFR (Kuete et al. 2013a, b; Dzoyem et al. 2013). Leukemia CCRF–CEM and CEM/ADR5000 cells were maintained in RPMI 1640 medium (Invitrogen) supplemented with 10 % fetal calf serum in a humidified 5 % CO2 atmosphere at 37 °C.

Sensitive and resistant cells were kindly provided by Dr. J. Beck (Department of Pediatrics, University of Greifswald, Greifswald, Germany). Breast cancer cells transduced with control vector (MDA-MB-231-pcDNA3) or with cDNA for the breast cancer resistance protein BCRP (MDA-MB-231-BCRP clone 23) were maintained under standard conditions as described above for CCRF–CEM and CEM/ADR5000 cells. Human wild-type HCT116 (p53 +/+) colon cancer cells as well as knockout clones HCT116 (p53 − / −) derived by homologous recombination were a generous gift from Dr. B. Vogelstein and H. Hermeking (Howard Hughes Medical Institute, Baltimore, MD). Human glioblastoma multiforme U87MG cells (non-transduced) and U87MG cell line transduced with an expression vector harboring an epidermal growth factor receptor (EGFR) gene with a genomic deletion of exons 2 through 7 (U87MG.ΔEGFR) were kindly provided by Dr. W. K. Cavenee (Ludwig Institute for Cancer Research, San Diego, CA). MDA-MB-231-BCRP, U87MG.ΔEGFR and HCT116 (p53 − / −) were maintained in DMEM medium containing 10 % FBS (Invitrogen) and 1 % penicillin (100 U/mL)-streptomycin (100 μg/mL) (Invitrogen) and were continuously treated with 800 ng/mL and 400 µg/mL geneticin, respectively. The multidrug resistance profile of these cell lines has been reported (Doyle et al. 1998). Human liver hepatocellular carcinoma HepG2 and the AML 12 normal heptocytes were obtained from ATCC (USA). The above medium without geneticin was used to maintained MDA-MB-231, U87MG, HCT116 (p53 +/+), HepG2 and AML 12 cell lines. The cells were passaged twice weekly. All experiments were performed with cells in the logarithmic growth phase.

Resazurin reduction assay

The cytotoxicity of the tested samples was performed by resazurin reduction assay as previously described (Kuete et al. 2013b; O’Brien et al. 2000). The assay is based on reduction of the indicator dye, resazurin, to the highly fluorescent resorufin by viable cells. Non-viable cells rapidly lose the metabolic capacity to reduce resazurin and thus produced no fluorescent signal. Briefly, adherent cells were detached by treatment with 0.25 % trypsin/EDTA (Invitrogen) and an aliquot of 1 × 104 cells was placed in each well of a 96-well cell culture plate (Thermo Scientific, Germany) in a total volume of 200 µL. Cells were allowed to attach overnight and then were treated with different concentrations of the studied sample. For suspension cells, aliquots of 2 × 104 cells per well were seeded in 96-well-plates in a total volume of 100 µL. The studied sample was immediately added in varying concentrations in an additional 100 µL of culture medium to obtain a total volume of 200 µL/well. After 24 or 48 h, 20 µL resazurin (Sigma-Aldrich, Germany) 0.01 % w/v in ddH2O was added to each well and the plates were incubated at 37 °C for 4 h. Fluorescence was measured on an Infinite M2000 Pro™ plate reader (Tecan, Germany) using an excitation wavelength of 544 nm and an emission wavelength of 590 nm. Each assay was done twice, with six replicates each. The viability was evaluated based on a comparison with untreated cells. IC50 values representing the sample’s concentrations required to inhibit 50 % of cell proliferation were calculated from a calibration curve by linear regression using Microsoft Excel (Kuete et al. 2011a; Dzoyem et al. 2012). In a preliminary step, all samples were tested against the sensitive CCRF–CEM cells at various concentrations ranging from 0.16 to 80 µg/mL (crude extracts) or 0.08 to 10 µg/mL (doxorubicin), and samples displaying IC50 values below 20 µg/mL were further investigated in 8 other tumor cell lines as well as in normal AML12 hepatocytes. Doxorubicin was used as positive control, while dimethylsulfoxide (DMSO) used to dissolve the samples was used as negative control. The highest concentration of DMSO was less than 0.4 %.

Flow cytometry for cell cycle analysis and detection of apoptotic cells

Extracts from Passiflora edulis fruit (PEF), Annona muricata leaves (AML), Annona muricata seeds (AMS) that displayed the best cytotoxicity as well as doxorubicin were used to treat CCRF–CEM cells (1 × 106) at their IC50 values. Thus, CCRF–CEM cells were cultured in RPMI medium as described above, in the presence of each sample at a concentration corresponding to the IC50 values obtained in the cell line. The cell cycle was then analyzed after incubation for 24, 48 and 72 h. All reagents, experimental conditions and apparatus were identical to those previously reported (Kuete et al. 2013a; Dzoyem et al. 2013). Briefly, cell cycle analysis was performed by flow cytometry using Vybrant® DyeCycle™ (Invitrogen, Darmstadt, Germany). Cells were measured after Vybrant® DyeCycle™ Violet staining (30 min at 37 °C) on a LSR-Fortessa FACS analyzer (Becton–Dickinson, Heidelberg, Germany) using the violet laser. Vybrant® DyeCycle™ Violet stain was measured with 440 nm excitation. Cytographs were analyzed using FlowJo software (Celeza, Switzerland). All experiments were performed at least in triplicate.

Caspase-Glo 3/7, caspase-Glo 8 and caspase-Glo 9 assay

The influence of extracts on caspase 3/7, caspase 8 and caspase 9 activity in leukemia CCRF–CEM cell line was detected using Caspase-Glo 3/7, Caspase-Glo 8 and Caspase-Glo 9 Assay kits (Promega, Germany). Cells cultured in RPMI medium were seeded in 96-well plates and treated with the sample (2 × IC50; IC50) or DMSO (solvent control). After 6 h incubation in a humidified 5 % CO2 atmosphere at 37 °C, 100 µL of caspase reagent were added to each well, mixed and incubated for 1 h at room temperature. Luminescence was measured using well Infinite M2000 Pro™ instrument (Tecan). Caspase activity was expressed as percentage relative to the untreated control (Kuete et al. 2014b).

Analysis of mitochondrial membrane potential (MMP)

The effects of extracts on the MMP were analyzed by 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolylcarbocyanine iodide) (JC-1; Biomol, Germany) staining (Kuete et al. 2013c). JC-1 is a dye that can selectively enter into mitochondria and exhibits an intense red fluorescence in healthy mitochondria with normal membrane potentials. In cells with reduced MMP, the red fluorescence disappears. Briefly, 1 × 106 CCRF–CEM cells treated at different concentrations with PEF, AML, AMS or vinblastine for 24 h were incubated with JC-1 staining solution according to the manufacturer`s protocol for 30 min. Subsequently, cells were measured in a LSR-Fortessa FACS analyzer (Becton–Dickinson). For each sample, 1 × 104 cells were counted. The JC-1 signal was measured with 561 nm excitation (150 mW) and detected using a 586/15 nm bandpass filter. The samples signal was analyzed with 640 nm excitation (40 mW) and detected using a 730/45 nm bandpass filter. All parameters were plotted on a logarithmic scale. Cytographs were analyzed using FlowJo software (Celeza, Switzerland). All experiments were performed in triplicate.

Measurement of reactive oxygen species (ROS) by flow cytometry

The 2′,7′-Dichlorodihydrofluorescein diacetate (H2DCFH-DA) (Sigma-Aldrich, Germany) is a probe used for the highly sensitive and quantifiable detection of ROS. The non-fluorescent H2DCFH-DA diffuses into the cells and is cleaved by cytoplasmic esterases into 2′,7′-dichlorodihydrofluorescein (H2DCF) which is unable to diffuse back out of the cells. In the presence of hydrogen peroxide, H2DCF is oxidized to the fluorescent molecule dichlorofluorescein (DCF) by peroxidases. The fluorescent signal emanating from DCF can be measured and quantified by flow cytometry, thus providing an indication of intracellular ROS concentration (Kuete et al. 2011c; Bass et al. 1983; Cossarizza et al. 2009). Briefly, 2 × 106 CCRF–CEM cells were resuspended in PBS and incubated with 2 µM H2DCFH-DA for 20 min in the dark. Subsequently, cells were washed with PBS and resuspended in RPMI 1640 culture medium containing different concentrations of PEF, AML, AMS or DMSO (solvent control), or hydrogen peroxide (H2O2; positive control). After 24 h of incubation, cells were washed and suspended in PBS. Subsequently cells were measured in a FACSCalibur flow cytometer (Becton–Dickinson, Germany). For each sample 1 × 104 cells were counted. DCF was measured at 488 nm excitation (25mW) and detected using a 530/30 nm bandpass filter. All parameters were plotted on a logarithmic scale. Cytographs were analyzed using FlowJo software (Celeza, Switzerland). All experiments were performed in triplicate.

Results

Cytotoxicity of the studied samples

In this study, we first screened the cytotoxicity of 17 crude extracts belonging to 11 plants towards drug-sensitive CCRF–CEM leukemia cells. The results are shown in Table 2. All tested extracts had IC50 values below 80 µg/mL. Ten extracts from five plants including Alchornea floribunda bark (AFB), Annona muricata fruit pericarp (AMP), leaves (AML) and seeds (AMS), Euphorbia prostata whole plant (EPW), Pachypodanthium staudtii bark (PSB), leaves (PSL) and roots (PSR), and Passiflora edulis fruit pericarp (PEP) and fruit (PEF) displayed IC50 values below 20 µg/mL in CCRF–CEM cells (Table 2). These extracts were further selected for IC50 determination towards a panel of sensitive and MDR cell lines. The results summarized in Table 3 indicate that all selected extracts were also active against P-glycoprotein-over-expressing CEM/ADR5000 leukemia cells with IC50 values below 40 µg/mL. IC50 values ranged from 10.13 µg/mL (towards CEM/ADR5000 cells) to 72.01 µg/mL (on resistant colon carcinoma HCT116 (p53 −/−) cells) for PSR, from 14.97 µg/mL (on CEM/ADR5000 cells) to 65.68 µg/mL (against HCT116 (p53 −/−) cells) for PSB, from 18.21 µg/mL (against CEM/ADR5000 cells) to 65.21 µg/mL (on HCT116 (p5 +/+) cells) for PSL and from 0.11 µg/mL (towards CCRF–CEM cells) to 108 µg/mL (against CEM/ADR5000 cells) for doxorubicin in the 8 other cancer cell lines studied. Apart from extract from P. staudtii, other extracts were less active on carcinoma cells including normal AML12 hepatocytes, with IC50 values above 80 µg/mL. Collateral sensitivity (or hypersensitivity: higher toxicity to resistant than to sensitive cells with a degree of resistance below 1) (Kuete et al. 2013a) was observed in CEM/ADR5000 cells to PSB (degree of resistance of 0.87-fold) and PSR (0.59-fold) (Table 3). Hypersensitivity of resistant carcinoma cells was also recorded in many cases to PSL, PSB or PSR even though they were moderately active. However, if cross-resistance of CEM/ADR5000 cells to the tested extracts were observed, the degrees of resistance were in all cases lower than that of doxorubicin (Table 3). AMS, AML and PEF had IC50 values below 1 and 10 µg/mL in sensitive CCRF/CEM cells and it resistant subline CEM/ADR5000 cells respectively; they were subsequently selected for mechanistic studies.

Table 2 IC50 values of the tested plant extracts towards leukemia CCRF–CEM cells and as determined by the resazurin assay
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Table 3 Cytotoxicity of the tested extracts and doxorubicin towards sensitive and drug-resistant cancer cell lines and normal cells as determined by the resazurin assay
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Cell cycle distribution and apoptosis

The best extracts (AMS, AML and PEF) as well as doxorubicin were used to treat CCRF–CEM cells at their IC50 values, and the cycle distribution was analyzed. Results depicted in Fig. 1 show dose-dependent and significant modifications of the cell cycle phases after treatment of cells with all samples. Both PEF and AML induced cell cycle arrest in G0/G1 phase while AMS induced cell cycle arrest in S-phase. After treatment with these three extracts, CCRF–CEM cells underwent apoptosis with dose-dependent increases in sub-G0/G1 phase. The percentages of cells in sub-G0/G1 phase varied from 9.31 % (in 24 h) to 48.69 % (72 h), from 8.87 % (in 24 h) to 33.98 % (72 h) and from 11.03 % (24 h) to 21.63 % (72 h) after PEP, AML and AMS treatments respectively, while doxorubicin increased apoptosis in a range of 6.02 % (24 h) to 51.87 % (72 h). The highest percentage of sub-G0/G1 phase in non-treated cells was only 6.42 % after 72 h.

Fig. 1
figure1

Cell cycle distribution of CCRF–CEM leukemia cells treated with extracts from PEF, AML and AMS or doxorubicin. PEF, AML and AMS were tested at 0.69, 0.57 and 0.36 and 8.02 µg/mL respectively while doxorubicin was tested at 0.11 µg/mL corresponding to their IC50

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Effects on the activity of caspases, MMP and ROS

After treating CCRF–CEM cells for 6 h at different concentrations of PEF, AML and AMS, no changes of caspase 3/7, caspase 8 and caspase 9 activities were observed. No increase in ROS production was also not found in CCRF–CEM cells treated with the three extracts (data not shown). PEF, AML and AMS induced significant MMP loss in the respective ranges of 35.3 % (1/2-fold IC50 treatment) to 46.7 % (2-fold IC50), 28.2 % (1/2-fold IC50) to 53.8 % (2-fold IC50) and 36.6 % (1/2-fold IC50) to 51.0 % (2-fold IC50) (Fig. 2). A 48.6 % loss of MMP at 2-fold IC50 of vinblastine was previously reported under similar experimental conditions in CCRF–CEM cells (Kuete et al. 2013a).

Fig. 2
figure2

Effect of PEF, AML and AMS on the mitochondrial membrane potential in CCRF–CEM cells. C control; PEF was tested at 24 h at 0.35 µg/mL (PEF1), 0.69 µg/mL (PEF2), and 1.38 µg/L (PEF3) while AML was tested at 0.29 µg/mL (AML1), 0.57 µg/mL (AML2), and 1.14 µg/mL (AML3) and AMS was tested at 0.18 µg/mL (AML1), 0.36 µg/mL (AML2), and 0.72 µg/mL (AML3) corresponding to 1/2-fold, IC50 and 2-fold IC50. Data for the positive control, vinblastine in similar experimental conditions were previously reported (Kuete et al. 2013b); Loss of MMP (Q1), intact cells (Q2), ruptured cell membrane (Q3 and Q4)

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Discussion

According to the U.S. National Cancer Institute (NCI) plant screening program, plant extracts with IC50 values below of 20 µg/mL following incubation between 48 and 72 h (Boik 2001) are recognized as potential cytotoxic substances. In the present study, multi-factorial drug-resistant cancer cell lines such as leukemia CEM/ADR5000 cells over-expressing P-gp, breast adenocarcinoma MDA-MB-231-BCRP clone 23 expressing BCRP, EGFR-transfected U87MG.ΔEGFR glioblastoma cells and p53 knockout HCT116 (p53 −/−) colon cancer cells (Efferth et al. 2003a; Kuete et al. 2013a, b, 2014c; Kimmig et al. 1990; Gillet et al. 2004; Doyle et al. 1998) were used to determine the cytotoxicity the selected plant extracts. In the first step of the investigations, we carried out a preliminary assays with the sensitive leukemia CCRF–CEM cells. In regards to the NCI threshold, AFB, AMP, AML, AMS, EPW, PSB, PSL, PSR, PEP and PEF (Table 2) displaying IC50 values below 20 µg/mL were selected and further tested on a panel of 8 other cell lines. Interestingly, the P-gp over-expressing leukemia CEM/ADR5000 was also sensitive to most of the extracts with IC50 value below 20 µg/mL obtained with AML, AMS, PSL, PSB, PSR, PEF and PEP. This suggests that these extracts can be used to manage hematological cancers including resistant phenotypes. Data obtained with AML, AMS and PEP are very interesting as they displayed IC50 values below 10 µg/mL in the resistant CEM/ADR5000 cells and even below 1 µg/mL in its sensitive counterpart CCRF–CEM cells. Nonetheless, they were not active in carcinoma cells, clearly indicating their selectivity to leukemia cells. Alteration of MMP has been reported as a mode of apoptosis induction of plant extracts (Kuete and Efferth 2015). AML, AMS and PEP induced MMP loss but no caspase activation nor increase ROS production. Hence, MMP is the main mode of induction of apoptosis of AML, AMS and PEP in CCRF–CEM cells as observed in this study.

To the best of our knowledge, the cytotoxicty of the five most active plants, Alchornea floribunda, Annona muricata, Euphorbia prostata, Pachypodanthium staudtii and Passiflora edulis towards the cell line panel tested in this study is being reported for the first time. Nevertheless, the leaves ethanol extract of Annona muricata was reported to have antiproliferative effect against leukemia HL-60 cells with an IC50 value of 14 µg/mL, and also induced apoptosis through the loss of MMP with G0/G1 phase cell arrest (Pieme et al. 2014). This is in accordance with data reported herein. The ethyl acetate extract of the leaves of this plant harvested in Malaysia was also found active against colon carcinoma HCT-116 and HT-29 cells with the respective IC50 values of 11.43 and 8.98 µg/mL (Zorofchian Moghadamtousi et al. 2014). In the present study, IC50 were not detected at up to 80 µg/mL, either indicating that the active constituents of the plant against carcinoma cells might not be well extracted with methanol or that the geographic distribution influences the cytotoxic potential of the plant. Also the methanol extracts of the leaves and fruits of Passiflora edulis harvested in Egypt were screened at 100 µg/mL against HCT-116 cells, HepG2 cells as well as against the breast carcinoma MCF-7 cells and lung carcinoma A-549 cells; As results, less than 50 % growth inhibition was recorded (Moustafa et al. 2014), coroborating the low activity obtained with various parts of this plant against carcinoma cells.

Conclusions

In this study, ten extracts from five medicinal plants, Alchornea floribunda, Annona muricata, Euphorbia prostata, Pachypodanthium staudtii and Passiflora edulis had good cytotoxicity against CCRF–CEM leukemia cells and its resistant subline CEM/ADR5000 cells. Their selectivity to these two cell lines, indicates that they can be sources for the development of novel anticancer drugs to fight leukemia. AML, AML and PEF were the most cytotoxic extracts and induced apoptosis in CCRF–CEM cells mediated by loss of MMP. Further phytochemical investigations of these extracts will be done to isolate their active constituents.

Abbreviations

ABC:

adenosine triphosphate-binding cassette

AFB:

Alchornea floribunda bark

AML:

Annona muricata leaves

AMP:

Annona muricata fruit pericarp

AMS:

Annona muricata seeds

BCRP:

breast cancer resistance protein

DCF:

dichlorofluorescein

DMSO:

dimethylsufoxide

EGFR:

epidermal growth factor receptor

EPW:

Euphorbia prostata whole plant

H2DCFH-DA:

2′,7′-dichlorodihydrofluorescein diacetate

IC50 :

inhibitory concentration 50 %

JC-1:

5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolylcarbocyanine iodide

MDR:

multi-drug resistant

MMP:

mitochondrial membrane potential

PBS:

phosphate buffer saline

PEF:

Passiflora edulis fruit

PEP:

Passiflora edulis fruit pericarp

P-gp:

P-glycoprotein

PSB:

Pachypodanthium staudtii bark

PSL:

Pachypodanthium staudtii leaves

PSR:

Pachypodanthium staudtii roots

ROS:

reactive oxygen species

References

  1. Abrams B, Duncan D, Hertz-Picciotto I (1993) A prospective study of dietary intake and acquired immune deficiency syndrome in HIV-seropositive homosexual men. J Acquir Immune Defic Syndr 6(8):949–958

  2. Adjanohoun J, Aboubakar N, Dramane K, Ebot M, Ekpere J, Enow-Orock E et al (eds) (1996) Traditional medicine and pharmacopoeia: contribution to ethnobotanical and floristic studies in Cameroon. OUA/STRC, Lagos

  3. Bass DA, Parce JW, Dechatelet LR, Szejda P, Seeds MC, Thomas M (1983) Flow cytometric studies of oxidative product formation by neutrophils: a graded response to membrane stimulation. J Immunol 130(4):1910–1917

  4. Biedler JL, Spengler BA (1994) Reverse transformation of multidrug-resistant cells. Cancer Metastasis Rev 13(2):191–207

  5. Boik J (2001) Natural compounds in cancer therapy. Oregon Medical Press, Minnesota

  6. Bouquet A, Debray M (1974) Plantes médicinales de Côte d’Ivoire. Mission ORSTOM, Paris

  7. Cancer in Africa (2012) http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-031574.pdf1. Accessed 13 Aug 2012

  8. Cossarizza A, Ferraresi R, Troiano L, Roat E, Gibellini L, Bertoncelli L et al (2009) Simultaneous analysis of reactive oxygen species and reduced glutathione content in living cells by polychromatic flow cytometry. Nat Protoc 4(12):1790–1797

  9. Daly D (1997) Alternative medicinal course taught at the United States Medical School. J Altern Complement Med 3:406–410

  10. Doyle LA, Yang W, Abruzzo LV, Krogmann T, Gao Y, Rishi AK et al (1998) A multidrug resistance transporter from human MCF-7 breast cancer cells. Proc Natl Acad Sci USA 95(26):15665–15670

  11. Dzotam JK, Touani FK, Kuete V (2016) Antibacterial activities of the methanol extracts of Canarium schweinfurthii and four other Cameroonian dietary plants against multi-drug resistant Gram-negative bacteria. Saudi J Biol Sci. 23(5):565–570

  12. Dzotam JK, Touani FK, Kuete V (2016) Antibacterial and antibiotic-modifying activities of three food plants (Xanthosoma mafaffa Lam., Moringa oleifera (L.) Schott and Passiflora edulis Sims) against multidrug-resistant (MDR) Gram-negative bacteria. BMC Complement Altern Med 16(1):9

  13. Dzoyem JP, Nkuete AH, Kuete V, Tala MF, Wabo HK, Guru SK et al (2012) Cytotoxicity and antimicrobial activity of the methanol extract and compounds from Polygonum limbatum. Planta Med 78(8):787–792

  14. Dzoyem J, Guru S, Pieme C, Kuete V, Sharma A, Khan I et al (2013) Cytotoxic and antimicrobial activity of selected Cameroonian edible plants. BMC Complement Altern Med 13(1):78

  15. Efferth T, Sauerbrey A, Olbrich A, Gebhart E, Rauch P, Weber HO et al (2003a) Molecular modes of action of artesunate in tumor cell lines. Mol Pharmacol 64(2):382–394

  16. Efferth T, Sauerbrey A, Halatsch ME, Ross DD, Gebhart E (2003b) Molecular modes of action of cephalotaxine and homoharringtonine from the coniferous tree Cephalotaxus hainanensis in human tumor cell lines. Naunyn Schmiedebergs Arch Pharmacol 367(1):56–67

  17. el-Deiry WS (1997) Role of oncogenes in resistance and killing by cancer therapeutic agents. Curr Opin Oncol 9(1):79–87

  18. Fahey J (2005) Moringa oleifera: a review of the medical evidence for its nutritional, therapeutic and prophylactic properties. Trees Life J. 1(5):1–15

  19. Fankam AG, Kuiate JR, Kuete V (2014) Antibacterial activities of Beilschmiedia obscura and six other Cameroonian medicinal plants against multi-drug resistant Gram-negative phenotypes. BMC Complement Altern Med 14:241

  20. FAO (Food and Agriculture Organization of the United Nations) (1997) Non-wood forest products: 11-Medicinal plants for forest conservation and health care. www.faoorg/3/a-w7261epdf. Accessed on Jan 2014

  21. Fouche G, Khorombi E, Kolesnikova N, Maharaj VJ (2006) Investigation of South African plants. Pharmacologyonline 3:494–500

  22. Fouche G, Cragg GM, Pillay P, Kolesnikova N, Maharaj VJ, Senabe J (2008) In vitro anticancer screening of South African plants. J Ethnopharmacol 119(3):455–461

  23. Fuglie L (1999) The miracle tree Moringa oleifera: natural nutrition for the tropics. Church World Service, Dakar

  24. Gillet J, Efferth T, Steinbach D, Hamels J, de Longueville F, Bertholet V et al (2004) Microarray-based detection of multidrug resistance in human tumor cells by expression profiling of ATP-binding cassette transporter genes. Cancer Res 64(24):8987–8993

  25. Gupta PJ (2011) The efficacy of Euphorbia prostrata in early grades of symptomatic hemorrhoids—a pilot study. Eur Rev Med Pharmacogn Sci 15:199–203

  26. Ichimura T, Yamanaka A, Ichiba T, Toyokawa T, Kamada Y, Tamamura T et al (2006) Antihypertensive effect of an extract of Passiflora edulis rind in spontaneously hypertensive rats. Biosci Biotechnol Biochem 70(3):718–721

  27. Irvine R (1961) Woody plant of Ghana. Oxford University Press, London

  28. Jiofack T, Ayissi I, Fokunang C, Guedje N, Kemeuze V (2009) Ethnobotany and phytomedicine of the upper Nyong valley forest in Cameroon. Afr J Pharm Pharmacol 3:144–150

  29. Juranka PF, Zastawny RL, Ling V (1989) P-glycoprotein: multidrug-resistance and a superfamily of membrane-associated transport proteins. FASEB J 3(14):2583–2592

  30. Kannan S, Parimala B, Jayakar B (2011) Antibacterial evaluation of the methanolic extract of Passiflora edulis. HygeiaJDMed 3(1):46–49

  31. Kimmig A, Gekeler V, Neumann M, Frese G, Handgretinger R, Kardos G et al (1990) Susceptibility of multidrug-resistant human leukemia cell lines to human interleukin 2-activated killer cells. Cancer Res 50(21):6793–6799

  32. Koudou J, Abena AA, Ngaissona P, Bessiere JM (2005) Chemical composition and pharmacological activity of essential oil of Canarium schweinfurthii. Fitoterapia 76(7–8):700–703

  33. Kuete V, Efferth T (2011) Pharmacogenomics of Cameroonian traditional herbal medicine for cancer therapy. J Ethnopharmacol 137(1):752–766

  34. Kuete V, Efferth T (2015) African flora has the potential to fight multidrug resistance of cancer. BioMed Res Int. Article ID 914813

  35. Kuete V, Wabo HK, Eyong KO, Feussi MT, Wiench B, Krusche B et al (2011a) Anticancer activities of six selected natural compounds of some Cameroonian medicinal plants. PLoS ONE 6(8):e21762

  36. Kuete V, Ngameni B, Wiench B, Krusche B, Horwedel C, Ngadjui BT et al (2011b) Cytotoxicity and mode of action of four naturally occurring flavonoids from the genus Dorstenia: gancaonin Q, 4-hydroxylonchocarpin, 6-prenylapigenin, and 6,8-diprenyleriodictyol. Planta Med 77(18):1984–1989

  37. Kuete V, Krusche B, Youns M, Voukeng I, Fankam AG, Tankeo S et al (2011c) Cytotoxicity of some Cameroonian spices and selected medicinal plant extracts. J Ethnopharmacol 134(3):803–812

  38. Kuete V, Sandjo L, Nantchouang Ouete J, Fouotsa H, Wiench B, Efferth T (2013a) Cytotoxicity and modes of action of three naturally occurring xanthones (8-hydroxycudraxanthone G, morusignin I and cudraxanthone I) against sensitive and multidrug-resistant cancer cell lines. Phytomedicine 21(3):315–322

  39. Kuete V, Tchakam PD, Wiench B, Ngameni B, Wabo HK, Tala MF et al (2013b) Cytotoxicity and modes of action of four naturally occurring benzophenones: 2,2′,5,6′-tetrahydroxybenzophenone, guttiferone E, isogarcinol and isoxanthochymol. Phytomedicine 20(6):528–536

  40. Kuete V, Sandjo LP, Wiench B, Efferth T (2013c) Cytotoxicity and modes of action of four Cameroonian dietary spices ethno-medically used to treat cancers: Echinops giganteus, Xylopia aethiopica, Imperata cylindrica and Piper capense. J Ethnopharmacol 149(1):245–253

  41. Kuete V, Nkuete AHL, Mbaveng AT, Wiench B, Wabo HK, Tane P et al (2014a) Cytotoxicity and modes of action of 4′-hydroxy-2′,6′-dimethoxychalcone and other flavonoids toward drug-sensitive and multidrug-resistant cancer cell lines. Phytomedicine 21(12):1651–1657

  42. Kuete V, Sandjo LP, Djeussi DE, Zeino M, Kwamou GM, Ngadjui B et al (2014b) Cytotoxic flavonoids and isoflavonoids from Erythrina sigmoidea towards multi-factorial drug resistant cancer cells. Invest New Drugs 32:1053–1062

  43. Kuete V, Sandjo LP, Kwamou GM, Wiench B, Nkengfack AE, Efferth T (2014c) Activity of three cytotoxic isoflavonoids from Erythrina excelsa and Erythrina senegalensis (neobavaisoflavone, sigmoidin H and isoneorautenol) toward multi-factorial drug resistant cancer cells. Phytomedicine 21(5):682–688

  44. Kuete V, Sandjo LP, Mbaveng AT, Zeino M, Efferth T (2015a) Cytotoxicity of compounds from Xylopia aethiopica towards multi-factorial drug-resistant cancer cells. Phytomedicine 22:1247–1254

  45. Kuete V, Fouotsa H, Mbaveng AT, Wiench B, Nkengfack AE, Efferth T (2015b) Cytotoxicity of a naturally occurring furoquinoline alkaloid and four acridone alkaloids towards multi-factorial drug-resistant cancer cells. Phytomedicine 22(10):946–951

  46. Lee S, Najiah M, Wendy W (2010) In vitro antimicrobial activities of Colocasia esculenta extracts against Vibrio spp. Agricultura 7:5–7

  47. Mesia GK, Tona GL, Nanga TH, Cimanga RK, Apers S, Cos P et al (2008) Antiprotozoal and cytotoxic screening of 45 plant extracts from Democratic Republic of Congo. J Ethnopharmacol 115(3):409–415

  48. Moustafa SMA, Menshawi BM, Wassel GM, Mahmoud K, Mounier MM (2014) Screening of some plants in Egypt for their cytotoxicity against four human cancer cell lines. Int J PharmTech Res 3:1074–1084

  49. Musuyu Muganza D, Fruth BI, Nzunzu Lami J, Mesia GK, Kambu OK, Tona GL et al (2012) In vitro antiprotozoal and cytotoxic activity of 33 ethonopharmacologically selected medicinal plants from Democratic Republic of Congo. J Ethnopharmacol 141(1):301–308

  50. Nakade D, Mahesh S, Kiran N, Vinayak S (2013) Phytochemical screening and antibacterial activity of western region wild leaf of Colocasia esculenta. Int Res J Biol Sci 2:18–21

  51. Ngadjui BT, Lontsi D, Ayafor JF, Sondengam BL (1989) Pachypophyllin and pachypostaudins A and B: three bisnorlignans from Pachypodanthium staudtii. Phytochemistry 28(1):231–234

  52. Ngbede J, Yakubu R, Nyam D (2008) Phytochemical screening for active compounds in Canarium schweinfurthii (Atile) leaves from Jos North, Plateau State, Nigeria. International Research Journal of Biological Sciences 3:1076–1078

  53. Ngondi J, Etame S, Oben J (2005) Effect of Triumphetta cordifolia on body weight and blood lipids in normolipidemic Guinea pigs. J Food Technol 3:469–471

  54. Nwaiwu N, Mshelia F, Raufu I (2012) Antimicrobial activities of rrude extracts of Moringa oleifera, Hibiscus sabdariffa and Hibiscus esculentus seeds against some Enterobacteria. J Appl Phytotechnol Environ Sanit 1:11–16

  55. Obame L, Koudou J, Kumulungui B, Bassolè I, Edou P, Ouattara A et al (2007) Antioxidant and antimicrobial activities of Canarium schweinfurthii Engl. essential oil from Centrafrican Republic. Afr J Biotechnol 6:2319–2323

  56. O’Brien J, Wilson I, Orton T, Pognan F (2000) Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem 267(17):5421–5426

  57. Okoli R, Aigbe O, Ohaju-Obodo J, Mensah J (2007) Medicinal herbs used for managing some common ailments among Esan people of Edo State, Nigeria. Pak J Nutr 6:490–496

  58. Okoye FB, Osadebe PO, Nworu CS, Okoye NN, Omeje EO, Esimone CO (2011) Topical anti-inflammatory constituents of lipophilic leaf fractions of Alchornea floribunda and Alchornea cordifolia. Nat Prod Res 25(20):1941–1949

  59. Pieme CA, Kumar SG, Dongmo MS, Moukette BM, Boyoum FF, Ngogang JY et al (2014) Antiproliferative activity and induction of apoptosis by Annona muricata (Annonaceae) extract on human cancer cells. BMC Complement Altern Med 14:516

  60. Rajeswari V (2012) Vijayalakshmi, Gajalakshmi S. Phytochemical and pharmacological properties of Annona muricata. International. J Pharm Pharm Sci 4:3–6

  61. Sandjo L, Kuete V (2013) 15—ceramides, cerebrosides, and related long chains containing derivatives from the medicinal plants of Africa. In: Kuete V (ed) Medicinal plant research in Africa: pharmacology and chemistry. Elsevier, Oxford, pp 607–620

  62. Sandjo L, Hannewald P, Yemloul M, Kirsch G, Ngadjui T (2008) Triumphettamide and Triumphettoside Ic, two ceramides and other secondary metabolites from stems of wild Triumphetta cordifolia A. RICH. (Tiliaceae). Helv Chim Acta 91:1326–1335

  63. Shen B, Li D, Dong P, Gao S (2011) Expression of ABC transporters is an unfavorable prognostic factor in laryngeal squamous cell carcinoma. Ann Otol Rhinol Laryngol 120(12):820–827

  64. Shrama GD, Tripathi SN (1983) Experimental studies on Euphorbia prostata w. Ait. Anc Sci Life. 2(4):199–204

  65. Silva JR, Campos AC, Ferreira LM, Aranha Junior AA, Thiede A, Zago Filho LA et al (2006) Extract of Passiflora edulis in the healing process of gastric sutures in rats: a morphological and tensiometric study. Acta Cir Bras 21(Suppl 2):52–60

  66. Siwe Noundou X, Krause RW, van Vuuren SF, Tantoh Ndinteh D, Olivier DK (2014) Antibacterial activity of the roots, stems and leaves of Alchornea floribunda. J Ethnopharmacol 151(2):1023–1027

  67. Uraku A, Ajah P, Okala A, Ubiam U, Onu P (2010) Effects of crude extracts of Abelmoshus esculentus on albumin and total bilirubin of diabetic albino rats. Int J Sci Nat 1:38–41

  68. Vieira G, Maurao A, Angelo M, Costa A, Vieira R (2010) Antibacterial effect (in vitro) of Moringa oleifera and Annona muricata against Gram-postive and Gram-negative bacteria. Rev Inst Med Trop São Paulo 52:129–132

  69. Viera GH, Mourao JA, Angelo AM, Costa RA, Vieira RH (2010) Antibacterial effect (in vitro) of Moringa oleifera and Annona muricata against Gram positive and Gram negative bacteria. Rev Inst Med Trop Sao Paulo 52(3):129–132

  70. Yapi TA, Boti JB, Félix TZ, Ahibo AC, Tomi F, Bighelli A (2012) Pachypodanthium Staudtii Engl & Diels from Côte d’Ivoire: composition of leaf, stem bark and roots oils. Eur J Sci Res 69:137–142

  71. Zorofchian Moghadamtousi S, Karimian H, Rouhollahi E, Paydar M, Fadaeinasab M, Abdul KH (2014) Annona muricata leaves induce G(1) cell cycle arrest and apoptosis through mitochondria-mediated pathway in human HCT-116 and HT-29 colon cancer cells. J Ethnopharmacol 156:277–289

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Authors’ contributions

VK, JKD, IKV and AGF carried out the study; VK wrote the manuscript; TE supervised the work; VK and TE designed the experiments, TE provided the facilities for the study. All authors read the manuscript and approved the final version. All authors read and approved the final manuscript.

Acknowledgements

Authors acknowledge the Cameroon National Herbarium (Yaoundé) for the plant identification. VK is very grateful to the Alexander von Humboldt Foundation for the 2015–2018 Linkage program and 18 months’ fellowship in Germany through the ‘‘Georg Foster Research Fellowship for Experienced Researcher’’ program.

Competing interests

The authors declare that they have no competing interests.

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Affiliations

  1. Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, University of Mainz, 55128, Mainz, Germany
    • Victor Kuete
    •  & Thomas Efferth
  2. Department of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon
    • Victor Kuete
    • , Joachim K. Dzotam
    • , Igor K. Voukeng
    •  & Aimé G. Fankam
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Kuete, V., Dzotam, J.K., Voukeng, I.K. et al. Cytotoxicity of methanol extracts of Annona muricata, Passiflora edulis and nine other Cameroonian medicinal plants towards multi-factorial drug-resistant cancer cell lines. SpringerPlus 5, 1666 (2016). https://doi.org/10.1186/s40064-016-3361-4

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Keywords

  • Annona muricata
  • Apoptosis
  • Cameroon
  • Cytotoxicity
  • Medicinal plants
  • Passiflora edulis