Betulinic acid is a pentacyclic plant compound obtained from the bark of white birch trees and has been demonstrated to exhibit notable pharmacological properties. In the present study, the anticancer potential of betulinic acid on paclitaxel-resistant lung cancer cell line (H460) was evaluated. Cell viability was evaluated by an MTT assay, and a clonogenic assay was performed to assess the effects on cancer cell colony formation. DAPI staining using fluorescence microscopy and flow cytometry were employed to evaluate the effects of betulinic acid on apoptosis. The effects of betulinic acid on the cell cycle and mitochondrial membrane potential were also evaluated by flow cytometry. The effects of betulinic acid on the protein expression of B-cell lymphoma-2 (Bcl-2)/Bcl-2-associated X (Bax) were evaluated by western blot analysis. The results of the present study indicated that the half-maximal inhibitory concentration value of betulinic acid on paclitaxel-resistant H460 lung cancer cells was 50 µM. The treatment with betulinic acid was able to inhibit the colony formation potential in a dose-dependent manner. A lower cytoxicity by betulinic acid against normal human epithelial FR2 cells was observed compared with H460 cells. The betulinic acid exerted anticancer activity via the induction of apoptosis by regulating the Bcl-2/Bax signaling pathway. Additionally, treatment with betulinic acid resulted in cell cycle arrest of paclitaxel-resistant lung cancer H460 cells at the G2/M phase. Betulinic acid was also reported to cause reductions in the mitochondrial membrane potential in a dose-dependent manner. In conclusion, the results of the present study indicated that betulinic acid may be a useful drug candidate for the management of drug-resistant lung cancer.
Lung cancer is one of the major causes of cancer-associated mortality, particularly in China (
Betulinic acid, propidium iodide (PI), RNase A Triton X-100 and dimethyl sulfoxide (DMSO) were obtained from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany). All primary and secondary antibodies were purchased from Santa Cruz Biotechnology Inc. (Dallas, TX, USA). The fluorescent probes (dichloro-dihydro-fluorescein diacetate DCFH-DA, DiOC6 and DAPI), fetal bovine serum (FBS), RPMI-1640 medium, L-glutamine and antibiotics were obtained from Invitrogen (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Paclitaxel-resistant human lung cancer cell line (H460) and non-cancerous FR2 cells were procured from Cancer Research Institute of Beijing (Beijing, China), which were maintained in Dulbecco's modified Eagle's medium and was supplemented with 10% FBS and antibiotics (100 µg/ml streptomycin and 100 U/ml penicillin G) in incubator at 37°C (5% CO2 and 95% air).
The cytotoxic effect of betulinic acid in paclitaxel-resistant human lung H460 cancer cells was determined using an MTT assay. The cells were cultured at 1×106 cells per well in 96-well plates for a time period of 12 h and then administrated with varying concentrations of betulinic acid (0–500 µM) for 48 h. MTT solution (20 µl) was added to each well. Prior to the addition of 500 µl DMSO, the media was completely removed and replaced with fresh media. To solubilize MTT formazan crystals, 500 µl DMSO was added. ELISA plate reader was used for the determination of optical density at 570 nm. H460 lung cancer cells were then subjected to 0, 25, 50 and 100 µM betulinic acid for further experiments. To evaluate colony formation, lung cancer H460 cells at the exponential growth phase were harvested and counted with a hemocytometer. The cells were plated at 200 cells per well. This was followed by incubation for a time period of 48 h at 37°C to allow the cells to adhere and then various doses (0, 25, 50 and 100 µM) of betulinic acid were added. Following administration of betulinic acid, the cells were again incubated for 6 days at 37°C and washed with PBS. Methanol was used to fix the colonies at −20°C for 4 min and then stained with crystal violet at room temperature for ~30 min prior to analysis under a light microscope (10 fields).
Paclitaxel-resistant H460 cells (density, 2×105 cells/well) that were plated in 6-well plates were administrated with 0, 25, 50 and 100 µM betulinic acid for 48 h at 37°C. The cells were harvested by trypsinization and fixed with acetic acid and methanol (1:3) for 6 h at −20°C. Following incubation at −20°C for 6 h, the cells were centrifuged for 10 min at 8,000 × g at 4°C and pellets were resuspended in methanol:acetic acid (1:3). The cells were then plated on a chilled glass slide. DAPI was added for 20–30 min at 25°C in the dark at a concentration of 1 µg/ml, and the images were captured using fluorescence microscope (excitation wavelength, 488 nm; 10 different fields). For Annexin V/PI staining, the cells were harvested and stained with Annexin V/PI for 15 min in dark at room temperature. Subsequently, analysis was performed with a flow cytometer (IX-70; Olympus Corporation, Tokyo, Japan) as previously described (
The cells were seeded into 6-well plates (2×105 cells/well), and betulinic was administrated to the cells at 0, 25, 50 and 100 µM, followed by 24 h of incubation at 37°C. DMSO was used as a control. For estimation of the DNA content, PBS was used to wash the cells, which were then fixed in ethanol at −20°C for 24 h. This was followed by re-suspension in PBS, containing 40 µg/ml PI, RNase A (0.1 mg/ml) and Triton X-100 (0.1%), for 30 min in a dark room at 37°C. Subsequently, analysis was conducted with a flow cytometer (IX-70; Olympus Corporation). The estimated percentage of cells in each phase of the cell cycle was quantified using WinMDI software version 2.0 (Informer Technologies, Inc., Los Angeles, CA, USA).
H460 cells were seeded at a density of 2×105 cells/well in a 6-well plate, which were maintained for 24 h and treated with 50 µM betulinic acid for 0, 12, 24 and 48 h at 37°C in 5% CO2 and 95% air. Thereafter, the cells from all treatment groups were collected, washed twice with PBS and re-suspended in 500 µl 3,3′-dihexyloxacarbocyanine iodide (1 µmol/l) for MMP at 37°C in a dark room for 30 min. The samples were then analyzed immediately using a fluorescence microscope (IX-70; Olympus Corporation) and a flow cytometer with WinMDI software version 2.0 (Informer Technologies, Inc.).
The betulinic acid-treated cells (concentration, 0, 25, 50 and 100 µM) were harvested and lysed in lysis buffer [20 mM 4-(2-hydroxyethyl)-1-piperazineethanesulphonic acid, 350 mM NaCl, 20% glycerol, 1% Nonidet P 40, 1 mM MgCl2, 0.5 mM EDTA, 0.1 mM EGTA, 1 mM DTT, 1 mM PMSF, protease inhibitor cocktail and phosphatase inhibitor cocktail]. The protein concentrations of the lysates were quantified by a bicinchoninic acid assay using specific antibodies. β-actin was used as a control. From each sample, equal quantities of protein (0.5 µg) were loaded and separated by electrophoresis on a 12% denaturing SDS gel. Subsequently, the proteins were transferred onto polyvinylidene difluoride membranes (pore size, 0.45 µm). Following transfer, the membranes were blocked with 3% bovine serum albumin (Thermo Fisher Scientific, Inc.) in tris-phosphate-buffered saline (200 mM Tris/pH 7.0, 1.37 M NaCl and 1% Tween-20) for 1 h at room temperature. The membranes were then incubated with appropriate primary antibodies (rabbit polyclonal β-actin; sc-58673, Bax; sc-6236, BCl2; sc-509) overnight at 4°C, followed by incubation with horseradish peroxidase-conjugated alkaline phosphatase secondary antibody (sc-2372; dilution 1:1,000) for 1 h at room temperature. Super Signal West Dura Extended Duration Chemiluminescent substrate was used for the enhanced chemiluminescence reaction, and the signal was detected and quantified using the ImageQuantLAS4000 imaging system (GE Healthcare Life Sciences, Little Chalfont, UK).
All experiments were conducted in triplicate and expressed as the mean ± standard deviation. Statistical analysis was carried out using a Student's t-test and one-way analysis of variance followed by Tukey's test. GraphPad prism software (version 5.0; GraphPad Software, Inc., La Jolla, CA, USA) was used. P<0.01 was considered to indicate a statistically significant difference.
The chemical structure of betulinic acid is displayed in
DAPI staining indicated that betulinic acid was able to induce apoptosis in H460 paclitaxel-resistant cancer cells in a dose-dependent manner (
The results of the present study indicated that betulinic acid may have induced cell cycle arrest of H460 lung cancer cells. It was observed that the percentage of cells was notably increased at G2. G2 arrest was detected following treatment with 25, 50 and 100 µM betulinic acid (
TheH460 cells were administrated with 50 µM betulinic acid for various time intervals, and the levels of MMP were evaluated. A marked reduction in the level of MMP (
The expression levels of Bcl-2and Bax were determined to confirm if betulinic acid induced-apoptosis followed the mitochondrial apoptotic pathway. The findings are presented in
Lung cancer is one of the most lethal types of cancer detected worldwide and thousands of patients are diagnosed with this disease annually (
In the present study, betulinic acid revealed potential growth-inhibiting activity against paclitaxel-resistant lung H460 cancer cells as evident from the proliferation assay. As reported previously, numerous drugs exhibit antiproliferative effects via the induction of apoptosis. For instance, several chemotherapeutic drugs, including cisplatin, taxol and 5-fluorouracil (
Flow cytometry using PI as a probe was used to analyze the effects of betulinic acid on cell cycle progression in the present study. Treatment with betulinic acid induced G2/M cell cycle arrest and led to a marked increase of G2/M cells in a dose-dependent manner. Furthermore, it was reported that betulinic acid may inhibit H460 cancer cells in a concentration-dependent manner. These findings are promising as it is well established that paclitaxel-resistant lung cancer is one of the cancer types with a high mortality rate, and betulinic acid may a potential compound for treatment (
The effects of betulinic acid on Bcl-2/Bax signaling were investigated using western blot analysis. A concentration-dependent downregulation of Bcl-2 and upregulation of Bax were observed in betulinic acid-treated cells, which may ultimately induce apoptosis.
Collectively, betulinic acid may be a potential candidate for the treatment of lung cancer by regulating the Bcl-2/Bax signaling pathway. With limited drug options available and limited toxicity associated with naturally occurring betulinic acid, this molecule appears to be a viable option, but further investigation is required.
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No funding was received.
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
XZ and JL conceived and designed the experiments; XZ, JL, SZ, PX and MF performed the experiments; JL and MF analysed the data; XZ, JL and SZ drafted the manuscript. All authors reviewed and approved the manuscript.
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The authors declare that they have no competing interests.
(A) Chemical structure of betulinic acid. (B) Effect of indicated doses of betulinic acid on paclitaxel-resistant H460 lung cancer cells. (C) Effect of indicated doses of betulinic acid on non-cancerous FR2 human epithelial cells. All experiments are representative of three biological replicates ± standard deviation. *P<0.01, **P<0.001, ***P<0.0001; H460 lung cells vs. the control FR-2 cells.
Colony forming potential of betulinic acid paclitaxel cancer H460 cells. (A) Plates showing cell colonies that were treated with betulinic acid at the indicated doses. (B) Quantification of the colonies. All experiments are representative of three biological replicates and expressed as the mean ± standard deviation. *P<0.01, **P<0.001, ***P<0.0001 vs. control.
Induction of apoptosis by betulinic acid at indicated doses as depicted by (A) DAPI staining and (B) flow cytometry. All experiments are representatives of three biological replicates and expressed as the mean ± standard deviation. *P<0.01, **P<0.001, ***P<0.0001 vs. control.
Analysis of cell apoptosis in betulinic acid-treated paclitaxel-resistant lung cancer H460 cells by (A) Annexin V/propidium iodide staining. (B) Quantification of the apoptotic cell populations. All experiments are representatives of three biological replicates and expressed as the mean ± standard deviation. *P<0.01, **P<0.001, ***P<0.0001 vs. control.
Effect of the indicated doses of betulinic acid on cell cycle distribution of H460 cancer cells. All experiments are representative of three biological replicates.
Effect of 50 µM betulinic acid at indicated time intervals on mitochondrial membrane potential of paclitaxel-resistant lung cancer H460 cells. All experiments are replicates of three biological replicates. FITC, fluorescein isothiocyanate.
Effect of indicated doses of betulinic acid on the expression of (A) Bcl-2 and Bax proteins by western blotting. (B) Quantification was carried out by densitometric analysis. All experiments are representatives of three biological representatives. Bcl-2, B-cell lymphoma 2; Bax, Bcl-2-associated X.*P<0.01, **P<0.001, ***P<0.0001 vs. control.