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Acta Pharmaceutica Sinica. B logoLink to Acta Pharmaceutica Sinica. B
. 2016 Jul 30;7(1):59–64. doi: 10.1016/j.apsb.2016.06.008

Euphorbia factor L2 induces apoptosis in A549 cells through the mitochondrial pathway

Minting Lin a, Sili Tang a, Chao Zhang a, Hubiao Chen b, Wenjing Huang a, Yun Liu a, Jianye Zhang a,⁎
PMCID: PMC5237708  PMID: 28119809

Abstract

Euphorbia factor L2, a lathyrane diterpenoid isolated from caper euphorbia seed (the seeds of Euphorbia lathyris L.), has been traditionally applied to treat cancer. This article focuses on the cytotoxic activity of Euphorbia factor L2 against lung carcinoma A549 cells and the mechanism by which apoptosis is induced. We analyzed the cytotoxicity and related mechanism of Euphorbia factor L2 with an MTT assay, an annexin V-FITC/PI test, a colorimetric assay, and immunoblotting. Euphorbia factor L2 showed potent cytotoxicity to A549 cells. Euphorbia factor L2 led to an increase in reactive oxygen species (ROS) generation, a loss of mitochondrial electrochemical potential, release of cytochrome c, activation of caspase-9 and caspase-3, and cleavage of poly(ADP-ribose) polymerase, suggesting that Euphorbia factor L2 induced apoptosis through a mitochondrial pathway. The cytotoxic activity of Euphorbia factor L2 in A549 cells and the related mechanisms of apoptotic induction provide support for the further investigation of caper euphorbia seeds.

KEY WORDS: Euphorbia Factor L2, Caper euphorbia seed, Euphorbia lathyris L., Anticancer agent, Apoptosis, Mitochondrial pathway

Graphical abstract

Euphorbia factor L2 from caper euphorbia seed showed potent growth inhibition against A549 cells. Moreover, EFL2 led to an increase of reactive oxygen species generation, loss of mitochondrial potential, release of cytochrome c, activation of caspase-9, caspase-3 and cleavage of poly(ADP-ribose) polymerase. These results indicate that EFL2 induced apoptosis of A549 cells through a mitochondrial pathway. Our study provides evidence for further investigation of caper euphorbia seed.

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1. Introduction

Lung cancer is the leading cause of cancer-related mortality in the world and non-small-cell lung cancer (NSCLC) is the most common form of lung cancer1, 2. Cancer chemotherapy has been regarded as one of the most effective therapy and the development of new anticancer agents is a promising strategy to treat cancer. Indeed, a growing body of evidence suggests that the success of anticancer chemotherapy depends on the discovery of novel anticancer agents3.

Traditional Chinese medicine provides a rich resource in the search for novel anticancer agents, of which caper euphorbia seed has been recorded for treating cancer4. The genus Euphorbia (spurges, Euphorbiaceae) has received worldwide attention as its exceptional diversity of growth forms and near-worldwide distribution5. It is the largest genus in the spurge family (Euphorbiaceae), containing more than 2000 species. The seeds of Euphorbia lathyris L. (caper euphorbia seed) have been used medicinally for the treatment of hydropsy, ascites, terminal schistosomiasis, and snakebites6. What׳s more, the seeds of E. lathyris L. can be used for cancer treatment7.

Multidrug resistance (MDR) is the major impediment to the efficient treatment of tumors. Previous studies revealed that lathyrane diterpenes extracted from the seeds of E. lathyris L., Euphorbia factor L1–L11 (EFL1–11), have been considered as promising P-glycoprotein (P-gp) modulators in MDR-mediated resistance8, 9. We have reported the isolation, identification and anticancer activity of EFL110. On that basis, we further isolated EFL2 (Fig. 1A), and identified the structure using 1H and 13C NMR, DEPT and high resolution electrospray ionization mass spectrometry (HR-EI-MS). The structure was also reported by Appendino and co-workers11 from the same plant species. In this study, we elucidated the mechanism of EFL2 cytotoxicity against the lung cancer cell line A549. Our results reveal that EFL2 does show potent cytotoxicity and induces apoptosis via a mitochondrial pathway in A549 cells.

Figure 1.

Fig. 1

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Structure of EFL2 and its cytotoxicity to A549 cells. (A) Chemical structure of Euphorbia factor L2 (EFL2); (B) EFL2 inhibited viability of A549 cells with log scale of concentration.

2. Materials and methods

2.1. Chemicals and reagents

EFL2 was isolated from the seeds of E. lathyris L. with a purity of more than 98%. 3-(4,5-Dimethyl-2-thiazolyl)2,5-diphenyl-2H-tetrazolium bromide (MTT), 2ʹ,7ʹ-dichlorofluorescin diacetate (DCFH-DA), 3,3ʹ-dihexyloxacarbocyanine iodide (DiOC6) were obtained from Sigma Chemical Co. (USA). Primary antibodies were obtained as follows: antibodies against GAPDH, anti-mouse IgG-HRP and anti-rabbit IgG-HRP from KangChen Biotechnology Co. (Shanghai, China), antibody against cytochrome c from Santa Cruz Biotechnology Co. Colorimetric assay kits for caspase-9 and caspase-3 were purchased from R&D systems (Minneapolis, MN, US). All tissue culture supplies were products of Life Technologies. Other routine laboratory reagents were obtained from commercial sources of analytical or HPLC grade.

2.2. Cell lines and cell culture

Lung cancer A549 cells were maintained in RPMI 1640 medium containing 100 U/mL penicillin, 100 μmol/L streptomycin, and 10% fetal bovine serum (FBS). Cells were cultured in a humidified atmosphere incubator of 5% CO2 at 37 °C12.

2.3. Cell viability assay

The effect of EFL2 on cell viability was detected by MTT assay. Cells were harvested and transferred into 96-well plates at a density of 5×104 cells/mL. After 24 h incubation, 10 μL EFL2 solution (0, 4.162, 6.243, 9.364, 14.05, 21.07, 31.60, 47.41, 71.11, 106.7, 160 and 240 μmol/L) was added to 96-well plates. After 68 h of treatment, 10 μL MTT (10 mmol/L stock solution in saline) was added to each well and incubated in darkness for 4 h at 37 °C. Subsequently, the supernatant was removed and 100 μL anhydrous dimethyl sulfoxide was added into each well. Cell viability was measured with a Model 550 Microplate reader (BIO-RAD, USA) at 540 nm and 655 nm as reference filter. The growth-inhibitory effect of EFL2 was expressed as IC50 estimated from the concentration–response curve (Bliss׳s software). Cell survival was calculated using the following formula13: Survival (%)=(Mean experimental absorbance/Mean control absorbance)×100.

2.4. Annexin V-FITC/PI assay for apoptosis

Apoptosis was quantified by measuring surface exposure of phosphatidylserine in apoptotic cells using an annexin V-FITC/PI (propidium iodide) apoptosis detection kit (KeyGEN Biotech, Nanjing, China) according to the manufacturer׳s protocol. Briefly, after A549 cells were treated with the indicated concentrations (40 and 80 μmol/L) of EFL2 for 48 h, the cells were collected and washed twice with ice-cold phosphate-buffered saline (PBS). Then 5×105 cells were resuspended with 0.5 mL binding buffer containing Annexin-V (1:50 according to the manufacturer׳s instruction) and 40 ng/sample of PI for 30 min at 37 °C in the dark. Subsequently, the cells were assayed by flow cytometer (Becton Dickinson, USA) and analyzed with the CellQuest software (Becton Dickinson, USA). At least 10,000 cells were analyzed for each sample. The apoptosis rate was calculated using the following formula14: Apoptosis rate (%)=(Number of apoptotic cells/Number of total cells observed)×100.

2.5. Measurement of ROS generation

The fluorescence intensity of 2ʹ,7ʹ-dichlorofluorescein (DCF) is proportional to the amount of reactive oxygen species (ROS) produced by the cells. After exposure to the indicated concentrations (40 and 80 μmol/L) of EFL2 for 24 h, 5 ×105 cells were harvested, washed with PBS and incubated with DCFH-DA (50 μmol/L in a final concentration) at 37 °C for 20 min in the dark. Then the cells were washed twice and resuspended in 1 mL PBS. ROS generation was determined from 10,000 cells in each sample by FACS (fluorescence-activated cell sorting) with a Caliber flow cytometer (Beckman-coulter, Elite) at the excitation wavelength of 488 nm and emission wavelength of 530 nm. The data were analyzed by CellQuest software (Becton Dickinson, USA) and expressed as median fluorescence intensity (MFI)15.

2.6. Determination of mitochondrial membrane potential (ΔΨm)

A549 cells (5×105 cells/mL) were treated with EFL2 at the indicated concentrations (40 and 80 μmol/L) for 24 h to determine ΔΨm. The cells were collected, centrifuged at 600g for 5 min, and washed with PBS. Thereafter cells were incubated with 40 nmol/L DiOC6(3) at 37 °C for 20 min in the dark. Subsequently, the stained cells were washed twice with chilled PBS prior to suspension in 1 mL PBS, and then the amount of DiOC6(3) retained by 10,000 cells per sample was analyzed by FASCanto Flow Cytometer (Beckman Coulter Inc., USA) with the excitation wavelength of 484 nm and emission wavelength of 501 nm. The data obtained from flow cytometry were analyzed with CellQuest software (Becton Dickinson, USA) and expressed as MFI16.

2.7. Activities measurement of caspase-9 and caspase-3 by colorimetric assay

The activities of caspase-9 and caspase-3 were measured with a caspase colorimetric assay kit according to the manufacturer׳s protocol. Briefly, 1×106 cells were treated with 80 μmol/L EFL2 for 12, 24, 36 or 48 h. Subsequently, cells were collected, washed with ice-cold PBS and lysed in lysis buffer. The lysates were assayed for protease activity with the caspase-specific peptide conjugated with the color reporter molecule p-nitroanaline. The chromophore p-nitroanaline cleaved by caspases was quantified with the spectrophotometer at a wavelength of 405 nm. The caspase enzymatic activities in cell lysates were proportional to the color intensity11.

2.8. Western blot analysis of cytosolic cytochrome c, caspase-9, caspase-3 and PARP

Expression of cytochrome c, caspase-9, caspase-3, and poly (ADP-ribose) polymerase (PARP) was detected by Western blot analysis as previously reported17. Approximately 3.5×106–4.0×106 cells/well were seeded into culture dishes, incubated with 80 μmol/L EFL2 for 0, 12, 24, 48 h and then washed with ice-cold PBS.

For whole cell lysates, the pellet was lysed in 1× loading buffer [50 mmol/L Tris–HCl (pH 6.8); 10% glycerol, v/v; 2% sodium dodecylsulphate, w/v; 0.25% bromphenol blue, w/v; 0.1 mol/L d,l-dithiothreitol (DTT)]. After treatment at 100 °C for 20 min, the lysates were centrifuged and the supernatant was collected18.

For subcellular fractionation of cytosol, cells were harvested and resuspended in a 5-fold volume of ice-cold cell extract buffer [20 mmol/L HEPES-KOH (pH 7.5), 10 mmol/L KCl, 1.5 mmol/L MgCl2, 1 mmol/L EDTA, 1 mmol/L EGTA, 1 mmol/L DTT, 250 mmol/L sucrose, 0.1 mmol/L phenylmethanesulfonyl fluoride (PMSF) and 0.02 mmol/L aprotinin] at 4 °C for 40 min. Then, the final supernatant after repeated centrifugation was collected and dissolved in 5×loading buffer [250 mmol/L Tris–HCl (pH 6.8); 50% glycerol, v/v; 10% sodium dodecylsulphate, w/v; 1.25% bromphenol blue, w/v; 0.5 mol/L DTT]. The samples were heated at 100 °C for 15 min and subjected to Western blot analysis. Equal amounts of protein were loaded onto 8%–12% sodium SDS-PAGE and transferred to PVDF membranes (Millipore, USA) and the membranes were incubated with specific primary antibodies. Proteins were then visualized using HRP-conjugated secondary antibody and a PhototopeTM-HRP detection kit (Cell Signaling, USA) on Kodak medical X-ray processor (Kodak, USA). The cytochrome c protein was detected by anti-cytochrome c antibody in a ratio of 1:100019, 20.

2.9. Statistical analysis

Results were analyzed by t-test or one-way ANOVA with SPSS 13.0 software (SPSS Inc., USA). Data are presented as mean±SD of at least triplicate determinations. *P<0.05 and **P<0.01 were considered significant differences.

3. Results

3.1. EFL2 exerted potent cytotoxicity against A549 cells

The cytotoxicity of EFL2 was measured by MTT assay. The IC50 of EFL2 was 36.82±2.14 μmol/L for A549 cells (Fig. 1B), suggesting that EFL2 exhibited potent cytotoxicity to A549 cells.

3.2. EFL2-induced cell apoptosis in A549 cells

To explore whether the anti-tumor effect of EFL2 on A549 cells was associated with apoptosis induction, the cells were treated with 40 and 80 μmol/L of EFL2 for 48 h and apoptosis was monitored by flow cytometry following annexin V and PI staining. The results showed that apoptosis rates were 6.2±1.5%, 23.7±3.4%, 36.9±2.4% for control, 40 and 80 μmol/L EFL2, respectively (Fig. 2).

Figure 2.

Fig. 2

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EFL2-induced cell apoptosis in A549 cells. (A) A549 cells were treated with 0, 40 and 80 μmol/L of EFL2 for 48 h, apoptosis rates were then detected by annexin V-FITC/PI double staining and flow cytometer. D4 quadrant represented cells stained mainly by annexin-V (early apoptotic cells) and D2 quadrant represented cells stained by both PI and annexin-V (late apoptotic). D1 quadrant represented cells stained mainly by PI and viable cells negative for both annexin-V and PI appeared in the D3 quadrant. (B) The apoptosis rate was showed in the bar graph.

3.3. EFL2-induced increase of intracellular ROS levels in A549 cells

It is well-known that an increase in intracellular ROS can lead to apoptosis21. For this purpose, the generation of ROS was assessed by a flow cytometric method with DCFH-DA used as the fluorescent probe. After A549 cells were exposed to 40 and 80 μmol/L EFL2 for 24 h, the intracellular ROS levels were 266.23±38.53% and 363.64±40.26% of control, respectively (Fig. 3). These results imply that EFL2 might cause the loss of ΔΨm via ROS, which was subsequently shown by mitochondrial membrane-potential assay.

Figure 3.

Fig. 3

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EFL2 increased ROS levels in A549 cells. (A) ROS generation was increased in A549 cells; (B) ROS levels in A549 cells were calculated as percentage of control.

3.4. EFL2-induced loss of mitochondrial membrane potential (ΔΨm) in A549 cells

Apoptosis is a complex and multifactorial process in which mitochondria are involved. Generally, generation of ROS induced by chemotherapeutical drugs would trigger mitochondrial pathway, leading to the loss of ΔΨm22. To investigate the mechanisms of EFL2-induced apoptosis in A549 cells, the effects of EFL2 on ΔΨm were determined by flow cytometric analysis. After A549 cells were treated with the indicated concentrations of EFL2 for 24 h, the decrease in ΔΨm was observed in a concentration-dependent manner (Fig. 4). After treatment, the ΔΨm was 90.39±6.91% and 75.47±9.35% of control for 40 and 80 μmol/L EFL2, respectively. These data indicate that mitochondrial dysfunction is involved in the apoptosis induced by EFL2.

Figure 4.

Fig. 4

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EFL2 decreased ΔΨm in A549 cells. (A) The decrease of ΔΨm level was observed in A549 cells; (B) ΔΨm level in A549 cells was calculated as percentage of control.

3.5. EFL2-induced release of cytochrome c

The increase in intracellular ROS and loss of ΔΨm have been demonstrated to cause the release of cytochrome c. The release of cytochrome c from mitochondria into the cytosol is a vital factor in the mitochondrial pathway of apoptosis. In this regard, Western blot analysis was used to determine the cytosolic levels of cytochrome c. After A549 cells were treated with 80 μmol/L EFL2 for indicated time, the release of cytochrome c was detected in A549 cells (Fig. 5A).

Figure 5.

Fig. 5

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EFL2 activates the expression of cytochrome c in A549 cells. (A) Release of cytochrome c was discovered in A549 cells; (B) activation of caspase-9 and caspase-3 were detected in A549 cells.

3.6. EFL2 activated the expression of caspase-9 and caspase-3, and the cleavage of PARP

After release of cytochrome c, the caspase cascade would subsequently be activated. For this, the activation of caspase-9 and caspase-3, and the cleavage of PARP were measured in A549 cells (Figs. 5B and 6). After A549 cells were incubated with 80 µmol/L apicidin for 0, 12, 24, 48 h, cells were harvested and Western blot analysis was used to determine relative levels of each protein. Densitometric ratios of cleaved caspase-9 were 5.33±0.72%, 26.06±2.36%, 35.10±1.72% and 46.51±2.83%, at the respective time-points. Densitometric ratios of cleaved caspase-3 were 5.51±1.47%, 23.68±1.15%, 35.99±5.30% and 52.04±3.29%, respectively. Densitometric ratios of cleaved PARP were 2.01±0.42%, 41.24±4.11%, 59.76±4.07% and 77.51±2.86%, respectively.

Figure 6.

Fig. 6

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EFL2 activates the expression of caspase-9 and caspase-3, and the cleavage of PARP in A549 cells in a time-dependent manner. (A) Activation of caspase-9 and caspase-3, and the cleavage of PARP were detected in A549 cells; (B) densitometric analysis of Western blot results of (A). The molecular weight of activated (cleaved) caspase-9, caspase-3 and cleaved PARP were 37, 17 and 89 kD, respectively. GAPDH (36 kD) was used to confirm equal protein loading. Results were expressed as mean±SD of at least three determinations.

Taken together, EFL2 led to an increase in ROS generation, a loss of mitochondrial potential, release of cytochrome c, activation of caspase-9 and caspase-3, and the cleavage of PARP, which suggests that EFL2-induced apoptosis of A549 cells through a mitochondrial pathway.

4. Discussion

Lung cancer continues to be the most common cause of cancer-related mortality worldwide, killing more people than prostate, breast, pancreas and colon cancers combined23. The trend in five-year relative survival rates of lung cancer patients is only 15%. Although some therapeutic advances have been achieved, such as chemotherapy that provides useful palliation, therapies for advanced lung cancer are far from satisfactory. A major problem in the treatment of lung cancer is the MDR. Thus, novel approaches to enhance the antitumorigenic effects of chemotherapeutic agents are required24. Numerous natural cancer chemopreventive agents have already been isolated and are being used for the treatment of cancers.

Recent research has revealed that herbal medicines and natural products isolated from plants could provide additional strategies for monotherapy or combination treatments. EFL2 was isolated from the seeds of E. lathyris L. (Caper Euphorbia Seed). Our study showed that it was able to inhibit the growth of human lung cancer A549 cells potently with an IC50 value of 36.82±2.14 μmol/L. Herein, we carried out further investigations to elucidate the mechanisms involved.

As is well known, many chemotherapeutic drugs act by inducing apoptosis. The apoptotic mechanism of cancer cells is composed of both upstream regulators and downstream effector components. The regulators can be divided into two major circuits. One receives and processes extracellular death–inducing signals which involve the Fas ligand/Fas receptor (the extrinsic apoptotic program). The other senses and integrates a variety of signals of intracellular origin (the intrinsic program). Each culminates in the activation of caspases-8 and caspases-9, respectively. As to the activation of protease, a cascade of proteolysis of effector caspases directly responsible for the execution phase of apoptosis is activated. In this way, the cancer cells are progressively disassembled and then consumed both by neighboring cells and phagocytic cells. Currently, the intrinsic apoptotic mechanism is more widely implicated in cancer pathogenesis22, 25.

Indeed, release of cytochrome c and activation of caspase-9 and caspase-3 in time-dependent manner were observed in A549 cells after exposure to EFL2 (Figure 5, Figure 6). Caspase activity measured by colorimetric assay (Fig. 5B) was essentially in agreement with results obtained by Western blot (Fig. 6). What׳s more, the cleavage of PARP was detected in our experiments (Fig. 6). Taken together, EFL2 induced apoptosis of A549 via a mitochondrial pathway.

Generally, loss of mitochondrial membrane potential (ΔΨm) is involved in the mitochondrial pathway. Consistently, ΔΨm of A549 was decreased after treatment with EFL2 for 24 h showing concentration-dependent pattern (Fig. 4). Furthermore, an increase of ROS was noted (Fig. 3), which could cause the loss of ΔΨm.

5. Conclusions

In summary, our study shows that the anticancer activity of EFL2 against lung cancer A549 cells involves mitochondrially-mediated apoptosis, and provides evidence for the further investigation of caper euphorbia seed.

Acknowledgments

The work was supported by National Natural Science Foundation of China (No. 81473320), Fund from Guangdong Science and Technology Department & Guangdong Academy of Traditional Chinese Medicine (2016A020226024), Fund of Guangdong Education Department (2015KTSCX112), the Science Fund of the Education Bureau of Guangzhou City (1201410039 and 2012C208).

Footnotes

Peer review under responsibility of Institute of Materia Medica, Chinese Academy of Medical Sciences and Chinese Pharmaceutical Association.

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