- *Corresponding Author:
- B. Pourgheysari
Pathology and Hematology Department, Shahrekord University of Medical Sciences, Shahrekord, Iran
|Date of Submission||29 November 2017|
|Date of Revision||06 May 2018|
|Date of Acceptance||15 January 2019|
|Indian J Pharm Sci 2019;81(2):226-233|
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Antiproliferative and apoptotic effects of pterostilbene were examined in combination with L-asparaginase in Jurkat cell line. Jurkat cells were incubated with different concentrations of pterostilbene alone or in combination with L-asparaginase for 24, 48 and 72 h. Cell viability was evaluated using 3-(4,5-dimethylthiazol-2-yl)-5-3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2htetrazolium assay. Induction of apoptosis was measured by annexin-V fluorescein isothiocyanate and the level of active caspase 3 positive cells by intracellular staining and flowcytometry. Decline of cell viability to 50 % was observed at 67.78±3.88, 60.97±3.36 and 52.11±2.50 µM concentration after 24, 48 and 72 h incubation with pterostilbene, respectively. Pterostilbene at a concentration of 30, 50 and 70 µM in combination with 0.5 and 0.7 IU/ml L-asparaginase reduced relative cell growth to a significant level. The rate of apoptosis was significantly higher than control at 80 µM concentration of pterostilbene and a combination of 60 µM pterostilbene with 0.5 and 0.7 IU/ml L-asparaginase, but not with L-asparaginase alone. The level of caspase 3 positive cells was significantly higher than control at 80 µM concentration of pterostilbene. Pterostilbene increased antiproliferative and apoptotic effects of L-asparaginase in Jurkat cells. These results suggested that pterostilbene might be a potential anticancer agent in lymphoblastic leukaemia and potentiate the effect of L-asparaginase. Unravelling the mechanism of pterostilbene-induced cell apoptosis in this cell line could help in the development of a targeted therapy.
Pterostilbene, L-asparaginase, Jurkat cell line, proliferation, apoptosis, lymphoblastic leukaemia
Acute lymphoblastic leukaemia (ALL) is the most frequent leukaemia in childhood and almost 25 % of cancer cases under 15 y old . The treatment of childhood ALL has developed in the past decade. However common chemotherapy has failed in 20 % of the patients . Most therapy failures have been explained by cellular resistance to antileukemia drugs . Children with T-lineage leukaemia are more resistant to a variety of drugs in vitro than B-cell and acute myeloid leukaemia .
L-asparaginase (L-ASP) is a well-known and prominent growth inhibitory enzyme in oncology clinics and has been successfully used for combination chemotherapy in ALL and some solid tumours . However, this treatment causes anaphylactic reaction and coagulopathy in some patients and may have liver and kidney toxicity. In addition, it is ineffective in some patients [3,6,7]. AntiL-ASP has been produced in some patients following treatment, which can cause undetectable level of enzyme activity and minimize the effect of the drug [8,9]. These limitations point out to looking for alternative or complimentary treatments.
Stilbene-based phytonutrients have attracted the attention of many studies to their wide biological functions. One of such components is resveratrol, which is a phytoalexin found in grapes and some of the other food products and has demonstrated anticancer effects . Pterostilbene (PT), the natural analogue of resveratrol with similar pharmacologic properties, is the main antioxidant in blueberries and has been found in several types of grapes and tree wood. PT contains two methoxy groups, making it more lipophilic and increasing oral absorption and cellular uptake . In oral administration, it showed 95 % bioavailability versus 25 % of resveratrol  and its half-life is seven times higher . Many studies have demonstrated antiproliferative effects of PT. In association with quercetin, PT inhibited metastasis of B16 melanoma cell line. Its anticancer effect has been reported in rodent model . Tolomeo and colleagues used different myeloblastic leukaemia including drug14 resistant cell lines and demonstrated that PT exerted dose-dependent and line-specific inhibitory effect upon cell growth . The anticarcinogenic effect of PT has also been demonstrated in bladder, breast, liver, colon, lung, pancreatic and prostatic cell lines [17-23]. How it can work in combination with common chemotherapy agents needs to be investigated. The aim of our study was to investigate the antiproliferative, apoptosis and caspase 3 activity of PT versus and in combination with L-ASP in Jurkat cell line as a possible chemotherapy compound.
Materials and Methods
Jurkat cells were purchased from Pasteur Institute (Tehran, Iran). RPMI 1640 medium, penicillin/ streptomycin, trypan blue and PT were obtained from Sigma-Aldrich (Germany). Bovine foetus serum was obtained from GIBCO (USA), apoptosis kit from BD, and caspase 3 assay kit and 3-(4,5-dimethylthiazol-2- yl)-5-3-carboxymethoxyphenyl)-2-(4-sulfophenyl)- 2H-tetrazolium (MTS) from Promega (USA).
Jurkat cells were grown in RPMI 1640 supplemented with 0.3 mg/ml L-glutamine, 10 % fetal calf serum, 100 IU/ml penicillin and 100 μg/ml streptomycin (complete media) at a concentration of 2×105/ml. The cells were incubated at 37° in a 5 % CO2 atmosphere.
Cell viability assay:
To evaluate the number of living and dead cells, the cells were stained with trypan blue and counted on a haemocytometer. Cell viability was assessed by MTS assay in a 96-well plate according to the manufacturer instructions. Briefly, 1×104 live cells were seeded per well in above complete media and incubated for 24 h. 10 mg of PT was dissolved in 1 ml dimethyl sulfoxide (DMSO, stock). Working solution was prepared at 400 μm in culture media. The cells then were treated with different concentrations of PT (0-100 μm), L-ASP (0.01-1 IU/ml) or a combination of them and incubated for 24, 48 and 72 h. 20 μl of MTS was added to each well and incubated at 37° in 5 % CO2 for an additional 3 h. The absorbance of the wells was measured against the background (culture medium with DMSO) at 490 nm (the optical density is proportional to the total number of living cells). At least 3 wells were used for each concentration of the used drugs and values were expressed as mean±SD.
Determination of apoptosis and necrosis:
Cells were seeded in a six well plate with 2×105 cells per well in complete media and incubated for 24 h. The cells were then treated with different concentration of PT (0-100 μm), L-ASP (0.01-1 IU/ml) or a combination of them and incubated for 24 and 48 h. The cells were washed twice with PBS after the incubation time and resuspended in binding buffer at a concentration of 106/ml. 1×105 cells were incubated with annexin V conjugated with fluorescein isothiocyanate (FITC) and propidium iodide (PI) for 20 min. The cells were analysed afterward by flowcytometry (Partec, Germany). Phosphatidyl serine migrates to the outer surface of cell membrane in early apoptosis and bind to annexin V FITC. PI negative and FITC positive cells are in first stage of apoptosis whereas PI and FITC positive cells are in final stage of apoptosis. Both early and final apoptotic cells were recorded as apoptotic cells. The control was treated with highest concentration of DMSO in treated cells for comparison.
Detection of active caspase 3 positive cells:
The active caspase 3 positive cells were detected using intracellular staining and flowcytometry according to the manufacturer instructions (BD). Briefly, the cells were seeded in a 6 well plate at a concentration of 200 000 cells/well in 2 ml media and treated with different concentrations of PT. After 48 h incubation, the cells were washed and re-suspended in cytofix/ cytoperm and incubated for 20 min on ice. The cells were then washed with perm/wash buffer and incubated with PE conjugated anticaspase 3 in a perm/wash buffer suspension for 30 min in darkness at room temperature. The cells were washed and re-suspended in perm/wash buffer and analysed by flowcytometry.
Values are expressed as the mean±SD. All experiments were done at least in triplicate. Data were analysed by SPSS using Kruskal-Wallis multiple comparison and Dunn’s test and the difference between control and each experimental condition considered significant if p value was less than 0.05. EC50 was calculated using probit analysis.
Results and Discussion
Cells were incubated with different concentrations of PT. Percent living cells was calculated over a period of 24, 48 and 72 h and expressed as a percent of the cells incubated with media alone (figure 1). EC50 was calculated as a drug concentration, which is capable of inhibiting 50 % cell growth. PT displayed an EC50 of 67.78±3.88 μM at 24 h, 60.97±3.36 μM at 48 h and 52.11±2.50 at 72 h of incubation. Cell viability declined to 32.51±4.93 % and 22.33±4.72 % at 80 and 100 μM concentrations of PT, respectively. The proportion of living cells decreased more over a period of 72 h incubation time with the same concentrations as it was 11.21±2.65 % at 100 μM. As figure 1 shows, PT decreased cell viability in a time and dose-dependent manner.
Figure 1: Effect of pterostilbene on Jurkat cell viability
a period of 24, 48 and 72 h. Controls are the cells incubated with media after 72 h incubation. The antiproliferative effect of PT on Jurkat cells is time-dependent. B) Cells incubated with different concentrations of PT for 24, 48 and 72 h and MTS assay was performed to detect the viable cells. Cell viability decreases in a concentration-dependent manner. All experiments were done in triplicate. PT is pterostilbene (μM). 24 h; 48 h; 72 h
Jurkat cells were seeded in a concentration of 1×104 cells per well in a 96 well plate and incubated with different concentration (0.01-1 IU/ml) of L-ASP alone or in combination with different concentrations of PT. Cell viability declined slightly after 24 h incubation with L-ASP (EC50 of 1.86±0.23), but fell to less than 40 % after 72 h incubation with 0.7 IU/ml concentration of the drug. L-ASP declined cell viability to 71.12±2.08, 52.34±3.06 and 47.21±3.06 % at the concentration of 0.1, 0.5 and 0.7 IU/ml with an EC50 of 0.66±0.08 IU/ml after 48 h incubation, respectively (figure 2A). The viability decreased to 33.17±4.16 and 28.12±4.0 % when the cells were treated with a combination of 30 μm concentration of PT and 0.5 or 0.7 IU/ml L-ASP, respectively. The cell viability declined to 55.14±4.36, 30.32±3.06 and 21.41±3.0 % using a combination of 50 μm concentrations of PT and 0.1, 0.5 and 0.7 IU/ml L-ASP, respectively. Viable cells reduced to 35.61±6.01, 25.23±3.0 and 18.52±2.01 % in the presence of 0.1, 0.5 and 0.7 IU/ml L-ASP, respectively, when used with 70 μm concentration of PT (p<0.05, figure 2B).
Figure 2: Cell viability in the presence of L-asparaginase alone or in combination with PT
A) Cells incubated with different concentrations of L-ASP for 24, 48 and 72 h and MTS assay was performed to detect the viable cells. Cell viability decreased after 48 and 72 h with a concentration-dependent manner. All experiments were done in triplicate. B) Cell viability was detected after 48 h incubation with different concentrations of L-ASP alone or in combination with different concentrations of PT. Each experiment was performed in triplicates or more and cell viability compared to control. Cell viability decreased to a significant level when a concentration of 0.5 and 0.7 IU/ml of L-asparaginase was combined with 30, 50 and 70 μM concentration of PT. Kruskal- Wallis multiple comparison and Dunn’s test, (*shows significant difference compared to control and indicates p<0.05). ASP is asparaginase (IU/ml), PT is pterostilbene (μM). 24 h; 48 h; 72 h
Cell apoptosis was analysed after treatment with different concentration of PT. Forty eight hours after incubation with the drug, percent apoptotic cells was determined by flowcytometry considering the annexin V FTIC positive cells. Higher apoptosis was observed at higher concentration of PT. Figure 3A demonstrates an example of apoptosis at 40 and 60 μM concentration of PT compared to control. As shown in figure 3B, PT at the concentrations of 40, 60 and 80 μM induced 27.17±6.56, 49.41±7.02 and 60.71± 8.62 % cell apoptosis, respectively. There was a significant difference between control and PT at 80 μM.
Figure 3: Analysis of apoptosis
Cells were incubated with different concentration of PT or media for 48 h, then stained for apoptosis and analysed by flowcytometry. The annexin V positive cells were considered as apoptotic cells and the treated cells were compared to control. A) A representative sample of flowcytometric analysis: apoptosis in (a) 40 and (b) 60 μM concentration (black) was compared to control (grey). B) The apoptosis was 27.17±6.56, 49.41±7 and 60.71±8.62 % at the concentrations of 40, 60 and 80 μM, respectively compared to 4.8.01±1.12% in control. Each experiment was performed in triplicate. *p<0.05 compared to control
Apoptosis was analysed in the presence of L-ASP alone or in combination with PT. Cells were incubated with different concentrations of L-ASP alone or in combination with 60 μm concentration of PT for 48 h. As figure 4A illustrates, the apoptosis was 22.75±5.31 and 57.49±9.70 % after treatment with 0.5 IU/ml L-ASP alone or in combination with 60 μm PT (p<0.05), respectively. The apoptosis increased to 34.05±9.08 and 69.41±9.59 % in the presence of 0.7 IU/ml L-ASP alone and in combination with 60 μm PT, respectively compared to 8.32 % in control (p<0.05). As figure 4B demonstrates, the combination induced more apoptosis than L-ASP or PT alone.
Figure 4: Apoptosis in the presence of ASP or in combination with PT
Jurkat cells were treated with L-ASP alone or in combination with 60 μM concentration of PT for 48 h, then stained and analysed by flowcytometry. A) A representative sample of apoptosis was induced by 0.5 and 0.7 IU/ml L-ASP in combination with 60 μM of PT. B) Apoptosis level in the presence of ASP alone and in combination with 60 μM concentration of PT. Untreated cells served as control. A significant difference was observed between control and a combination of 0.5 or 0.7 IU/ml L-ASP with 60 μM PT. Kruskal-Wallis multiple comparison and Dunn’s test, *significant compared to control at p<0.05. Pterostilbene is in μM, ASP is Asparaginase concentration in IU/ml
Intracellular active caspase 3 was measured by flowcytometry after permeabilization and fixation of the cells and incubation with anticaspase 3 PIconjugated monoclonal antibody. After 48 h incubation with different concentration of PT, the percentage of positive cells was detected by flowcytometry. The mean value of positive cells in three experiments was 18.37±1.01, 25.38±3.06 and 40.85±1.25 % in the presence of 40, 60 and 80 μm concentrations of PT, respectively compared to 7.32±2.01 %. Although the ratio of positive cells increased in all concentrations, there was more than two and three-fold increase at 40 and 60 μm compared to control, the difference was significant only at the 80 μm concentration (figure 5).
Figure 5: Alteration of the level of caspase 3 positive cells in the presence of PT
Cells treated with different concentrations of PT or incubated with media alone as control. A) A representative sample of flowcytometric analysis of intracellular caspase 3 positive cells treated with 0, 40, 60, and 80 μM concentration of PT. B) The mean frequency of caspase 3 positive cells were 18.37±1.01, 25.38±3.06, and 40.85 ±1.28 % at concentrations of 40, 60 and 80 μM, respectively, compared to 7.32±2.01 % in control. The experiments were performed in triplicate. *p<0.05 compared to control
The treatment approaches of ALL were developed in the last decade, however common chemotherapy has failed in some patients. The development of therapies that could improve the quality of life without compromising survival is promising. In the present study we represented the enhancement of the effect of L-ASP in combination with PT on cell viability and apoptosis of a lymphoblastic leukaemia cell line. Different studies have reported anticancer activity, induction of apoptosis and inhibition of proliferation of PT on some tumor cell lines. Here we demonstrated the effect of PT, on inhibiting cell proliferation, inducing apoptosis and increasing caspase 3 in Jurkat cell line. The drug also increased the antiproliferative and apoptotic effect of L-ASP.
The current data demonstrated that PT decreased viability of Jurkat cells in a time- and dose-dependent manner and viability fell to around 50 % at 61 μm concentration after 48 h incubation. Different studies have demonstrated that the EC50 of PT is variable and dependent to the cell line [16,24,25]. Tolomeo et al. studied PT effect on seven cell line including human myeloid cell line and drug resistant myeloid cells. They concluded that PT had dose-dependent inhibitory effect on cell growth .
PT also increased antiproliferative effect of L-ASP in our study. L-ASP is a part of combination chemotherapy for ALL and some of the solid tumours and has demonstrated antitumor activity on leukemic cell lines including Jurkat cells. Abakumova et al. demonstrated the cytotoxicity of ASP on different cell lines at the concentration of 0.02-10 IU/ml including Jurkat cells . Apparently different cell lines have different sensitivity to L-ASP . In the present study dose-dependency of this effect was demonstrated as maximal inhibition of cell growth was at the highest concentration of 1 IU/ml used. The important finding was the enhancement of this antiproliferative effect in the presence of PT. In fact the combination of 0.7 IU/ml of L-ASP with 70 μm of PT led to 82 % growth inhibition. As more intensive treatment with conventional combination chemotherapy can lead to increased side effects, the addition of PT to those combinations could improve the outcome. The additive or synergistic antiproliferative effect of a plant-derived constituent with another ALLchemotherapy agent, doxorubicin, was reported on lymphoblastic leukaemia cells . The present work also demonstrated the dose-dependency of apoptosis upon treatment with PT as such effect with other plantderived compounds, epigallocatechin-3-gallate and gallic acid in lymphoblastic cell line was previously reported [29,30].
To investigate the mechanism of antitumor effect of PT, cell apoptosis was investigated using flowcytometry. Apoptosis is a mechanism, which an organism applies to delete harmed or unnecessary cells. In the process of cancer development, existing mutations allow cells to avoid apoptosis. Therefore, induction of apoptosis in pro-cancer and cancer cells could be an approach to prevention and treatment . In the present investigation, the concentration of PT associated with highest apoptosis rate by flowcytometric analysis caused remarkable decrease in cell viability in cell proliferation assay as well. An increase in caspase 3 positive cells to a significant level at 80 μM concentration of PT was also observed. This finding in Jurkat cells is in accordance with other cell lines.
These results demonstrated that apoptosis increased in the presence of PT and PT enhanced L-ASP-induced cell apoptosis. The induction of apoptosis by L-ASP is controversial. Holleman et al. have already reported a significant inverse correlation between cellular resistance to L-ASP and the percentage of cells with phosphatidyl serine externalization in children with ALL . The inhibitory effect on cancer cell growth is mediated by the modulation of genes involved in cell cycle, apoptosis and metastasis . Abakumova et al. demonstrated that treatment with L-ASP for 72 h did not change cell cycle distribution and did not increase the number of apoptotic cells. A combination with doxorubicin increased apoptosis of Jurkat cells up to 40 %. They concluded that apoptosis might not be the main reason for tumor cell death after treatment with L-ASP . This interpretation could explain findings of this investigation in the presence of a combination of PT and L-ASP, as significant increase in the apoptosis was observed compared to that with L-ASP alone. L-ASP induced extracellular asparagine hydrolysis, stopped asparagine-dependent proteins, prevented DNA synthesis and decreased leukemic cell proliferation . It was reported that asparagine deficiency stopped cells dividing rather than killing them . Some cell lines increase asparagine synthesis in response to amino acid deprivation . It appeared that similar effect was encountered in the current experiments with Jurkat cells, as no remarkable apoptosis was noticed with L-ASP alone. This finding is compatible with some of the previous studies where ASP did not induce remarkable apoptosis in Jurkat cell line. This phenomenon might be related to the high expression of antiapoptotic proteins of BCL2 family in these cells . Resveratrol was shown to be involved in the type I and type II pathways of apoptosis in human cancer cells  and to have cytotoxic effect on tumor cells but not normal tissue . Schneider et al. demonstrated the inhibitory effect of PT on melanoma cell line, which was associated with an increase in caspase activity . Previous studies have also reported the effect of PT on apoptosis through caspase cascade activation in pancreatic cancer .
PT was involved in inducing depolarization of mitochondrial membrane in breast cancer cell line and an increase in caspase 3/7. PT enhanced mitochondrial pro-apoptotic Bax and decreased mitochondrial antiapoptotic Bcl-2 . Current study demonstrated that the induction of apoptosis was not considerable with L-ASP, but PT enhanced this apoptotic effect up to a significant level. Wang et al. found the potentiation of antitumor activity of ASP by curcumin , which demonstrated the effect of combination treatment and is in accordance with our findings on proliferation assay and apoptosis.
Overall, PT might be a potential anticancer compound against lymphoblastic leukaemia and increase the effect of ASP, however these effects on ALL patients’ lymphoblasts need to be investigated. As PT, a resveratrol analogue, can have cytotoxic effect on tumor cells but not normal tissue, it can be considered as a potential choice of ALL chemotherapy. The study of the mechanism of PT-induced apoptosis and signalling pathways in lymphoblastic cell lines besides in vivo studies of experimental models could be a step toward targeted therapy.
The authors would like to thanks the Deputy of Research and Technology of Shahrekord University of Medical sciences for financial support, with the grant number 1316. Authors also thank Medical Plants Research Center of this university. The results described in this paper were part of the first author’s thesis.
Conflict of interest
Authors declared that there is no conflict of interest.
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