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Article

Effects of Platycodin D on Proliferation, Apoptosis and PI3K/Akt Signal Pathway of Human Glioma U251 Cells

by
Chong Xu
1,
Guibo Sun
1,
Guangxin Yuan
2,
Rui Wang
3 and
Xiaobo Sun
1,*
1
Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100193, China
2
Pharmaceutical College, Beihua University, Jilin 132013, China
3
School of Pharmaceutical Sciences, Jilin University, Changchun 130021, China
*
Author to whom correspondence should be addressed.
Molecules 2014, 19(12), 21411-21423; https://doi.org/10.3390/molecules191221411
Submission received: 28 October 2014 / Revised: 5 December 2014 / Accepted: 15 December 2014 / Published: 19 December 2014
(This article belongs to the Section Medicinal Chemistry)
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Abstract

:
Effects of platycodin D (PD) on the proliferation, apoptosis and PI3K/Akt signaling pathway of human glioma U251 cells were investigated. Glioma U251 cells were treated with PD at final concentrations of 0, 16.3, 40.8, 81.6, 163.2 μM, and inhibition rate, early and late apoptotic rate, apoptotic index, expression of apoptosis-related proteins and phosphorylation of the PI3K/Akt signaling pathway were evaluated. The results showed that compared with the control group, PD could increase the proliferation inhibition rate of U251 cells in a dose- and time -dependent manner; PD could also elevate the early and late apoptotic rate, apoptotic index and the level of pro-apoptotic proteins of glioma U251 cells, such as Bax and cleaved caspase-3, but lower the level of apoptosis inhibitory protein, such as Bcl-2; PD could increase the ratio of G0/G1 phase U251 cells, and lower the proportion of Sphase U251 cells and the ratio of G2/M phase U251 cells; PD could reduce the ratio of p-Akt/Akt. The results indicate that PD can inhibit the proliferation, induce the apoptosis and cause the cell cycle arrest in human glioma U251 cells, which may be related to the inhibition of PD on the activation of PI3K/Akt signaling pathway.

1. Introduction

Glioma is the most common intracranial malignant tumor developing in the neuroectoderm. Its incidence accounts for 40%–50% of all intracranial tumors, and it is characterized by high recurrence, high mortality and low cure rates [1]. Glioma includes astrocytoma, oligodendroglioma, ependymoma and choroid plexus papilloma, of which the incidence of astrocytoma developing from astrocytes or astrocyte precursors is highest [2,3]. Although significant progress in the treatment of gliomas with surgery, radiotherapy and chemotherapy has been made, the clinical treatment of gliomas is still far from satisfactory due to their multiple types, invasiveness and difficulty to completely remove them with surgery [4]. The treatment of gliomas with post-operative radiotherapy and chemotherapy is generally accepted, but the tolerance of tumor cells to the radiotherapy may promote the relapse of residual nidus [5]; Numerous anticancer drugs have been studied and developed at home and abroad, but they can induce more adverse reactions and their therapeutic effects are not satisfactory [6,7]. In recent years, many scholars have come to believe that the anti-tumor treatment possible with Traditional Chinese Medicine is unique, and the screening of anti-tumor active ingredients and lead compounds from Traditional Chinese Medicines has become a hot topic in this field [8,9]. Currently, anti-cancer agents derived from botanicals such as paclitaxel, camptothecin, etc., which have become the drugs as the first choice in many tumor therapies, account for more than 30% of all anti-cancer drugs [10,11]. The abundance and variety of medicinal plants in China are rich, so it is more important to screen anti-tumor active ingredients from Traditional Chinese Medicines, confirm their anti-tumor effects and clarify their mechanisms for action for the research and development of new and better anticancer drugs.
Platycodon grandiflorum, a Chinese herbal medicine, is the dried root of a Campanulaceae plant. It is one of most important medicinal and edible plants in China and other Asian countries, widely used in food and for the treatment of bronchitis, asthma, tuberculosis and other chronic diseases [12,13]. Modern pharmaceutical research has demonstrated that triterpenoid saponins are the main active ingredients in this herbal medicine [14,15,16] and that platycodin D (PD, Figure 1) is the most important triterpenoid saponin-like ingredient extracted from P. grandiflorum. As the main effective ingredient in P. grandiflorum, PD has been shown to have some good anti-inflammation [17], anti-virus [18], heptoprotection [19], immunoregulation [20] and anti-tumor [21] pharmacological activities. There have been some reports on the inhibitory effects of platycodin D on liver cancer [22], ovarian cancer [23], breast cancer [24], gastric cancer [25], and leukemia [26], but none on the effect of PD on glioma and the related mechanisms through which PD can exert its tumor inhibition. In this study, the effect of PD on the proliferation and the apoptosis of human glioma U251 cells was investigated, and an attempt was made to study its mechanism of action by exploring the relationship between the effect of PD and cell cycle, and the apoptosis-related signaling pathway, in order to provide an experimental basis for the research and the application of PD in the treatment of glioma.
Molecules 19 21411 g001 550
Figure 1. The chemical structure of platycodin D (C57H92O28, M.W. 1225).
Figure 1. The chemical structure of platycodin D (C57H92O28, M.W. 1225).
Molecules 19 21411 g001

2. Results and Discussion

2.1. Effects of Different Concentrations of PD on the Proliferation of Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD, the MTT assay was used to observe the effect of different concentration of PD on the proliferation activity of U251 cells. As shown in Figure 2, in addition to 16.3 μM of PD at 24 h, inhibition rates of different concentrations of PD on the proliferation activity of U251 cells at 24, 48, 72 and 96 h after the treatment were significantly higher than those of 0 μM of PD at the same time points (p < 0.05 or p < 0.01), and the inhibition of PD presented an approximate dose- and time-dependent manner.
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Figure 2. Effects of PD on cell growth inhibition of U251. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 24, 48, 72 and 96 h. Cell growth inhibition was measured by using MTT assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Figure 2. Effects of PD on cell growth inhibition of U251. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 24, 48, 72 and 96 h. Cell growth inhibition was measured by using MTT assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g002

2.2. Effects of Different Concentrations of PD on the Apoptotic Rate of Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h, Annexin V-FITC/PI double staining flow cytometry was applied to detect the apoptotic rates. The results (Figure 3) showed that PD could increase early and late apoptotic rates of U251 cells early, and the apoptotic rates of 0, 16.3, 40.8, 81.6 and 163.2 μM of PD were significantly higher than those of 0 μM of PD (p < 0.01).
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Figure 3. PD induced apoptosis in U251 cells. (A) flow cytometric analysis; (B) cell apoptosis rate. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with FITC-conjugated Annexin V and PI for flow cytometric analysis. Each value is presented as mean ± SD (n = 3). ** p < 0.01 compared with 0 μM PD.
Figure 3. PD induced apoptosis in U251 cells. (A) flow cytometric analysis; (B) cell apoptosis rate. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with FITC-conjugated Annexin V and PI for flow cytometric analysis. Each value is presented as mean ± SD (n = 3). ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g003

2.3. Effects of Different Concentrations of PD on the Apoptotic Index Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h, Hoechst staining detection showed that the apoptotic indexes in the 16.3, 40.8, 81.6 and 163.2 μM PD groups which were in turn 2.12%, 6.24%, 11.03% and 15.91 (p < 0.01), were significantly higher than those in the 0 μM PD group, indicating that PD could increase the apoptotic index of U251 cells in a dose-dependent way. The data are shown in Figure 4.
Molecules 19 21411 g004 550
Figure 4. The effect of PD on cells apoptosis index in U251 cells. (A) Hoechst 33258 staining (×200); (B) cell apoptosis index. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with Hoechst 33258. Each value is presented as mean ± SD (n = 3). ** p < 0.01 compared with 0 μM PD.
Figure 4. The effect of PD on cells apoptosis index in U251 cells. (A) Hoechst 33258 staining (×200); (B) cell apoptosis index. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with Hoechst 33258. Each value is presented as mean ± SD (n = 3). ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g004

2.4. Effects of Different Concentrations of PD on the Expression of Apoptosis-Related Genes in Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h, western blotting analysis showed that compared with those in the 0 μM group, Bax and cleaved caspase-3 protein levels were elevated, but Bcl-2 protein levels were reduced in the other PD groups (p < 0.05 or p < 0.01). The results are shown in Figure 5.
Molecules 19 21411 g005 550
Figure 5. The effect of PD on the expressions of Bcl-2, Bax and cleaved caspase-3 in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then the expressions of target protein were evaluated by western blot assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Figure 5. The effect of PD on the expressions of Bcl-2, Bax and cleaved caspase-3 in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then the expressions of target protein were evaluated by western blot assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g005

2.5. Effects of Different Concentrations of PD on the Cell Cycle of Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h, the detection with PI staining flow cytometry found that ratios of G0/G1 phase cells were increased in all PD dose groups except for those in the 0 μM PD group, in which those in 40.8, 81.6 and 163.2 μM groups were significantly increased (p < 0.05 or p < 0.01); meanwhile, PD could also significantly reduce the ratio of S and G2/M phase cells, which was dose-dependent (p < 0.05 or p < 0.01), as shown in Figure 6.

2.6. Effects of Different Concentrations of PD on the PI3K/Akt Signaling Pathway of Human Glioma U251 Cells

After U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h, the ratio of p-AKT/AKT evidently was reduced with the increase of concentrations of PD (p < 0.05 or p < 0.01). The results indicated that PD could inhibit the activation of PI3K/Akt signal pathway, as shown in Figure 7.
Molecules 19 21411 g006 550
Figure 6. The effect of PD on the cell cycle in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with PI for flow cytometric analysis. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Figure 6. The effect of PD on the cell cycle in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then they were stained with PI for flow cytometric analysis. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g006
Molecules 19 21411 g007 550
Figure 7. The effect of PD on the PI3K/Akt signaling pathway in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then the expressions of p-AKT and AKT were evaluated by western blot assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Figure 7. The effect of PD on the PI3K/Akt signaling pathway in U251 cells. U251 cells were treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h. Then the expressions of p-AKT and AKT were evaluated by western blot assay. Each value is presented as mean ± SD (n = 3). * p < 0.05 compared with 0 μM PD; ** p < 0.01 compared with 0 μM PD.
Molecules 19 21411 g007

2.7. Discussion

Currently, research on the anti-tumor activity of the active ingredients from P. grandiflorum has become a hot spot. PD is a triterpenoid extracted from the Traditional Chinese Medicine P. grandiflorum [27]. Many studies have verified that PD has a broad cytotoxic activity and effectively inhibits the growth of a variety of tumor cells, such as liver cancer, ovarian cancer, breast cancer, stomach cancer and leukemia and other cancers [22,23,24,25,26]. At present, there has been no study yet to show the biological activity of PD in human glioma U251 cells, so in this study, human glioma U251 cells were treated with PD for the observation on its activity against human glioma. The study found that PD could inhibit the proliferation of U251 cells, in which the inhibition was dose- and time- dependent at dose range from 40.8–163.2 μM, the proliferation inhibition rates of these dosages of PD were higher than those at 0 μM of PD. These results indicate that PD can inhibit the proliferation of human glioma U251 cells.
Inducing the apoptosis of tumor cells is an important way through which anti-tumor drugs exert their therapeutic effects, and the anti-tumor effect of plant extracts and the relationship between their effects and the induction of tumor cell apoptosis is currently a research hot spot [28,29,30]. Apoptosis is a cell suicide phenomenon regulated by genes and biologically significant in the occurrence and development of tumors, and many chemotherapeutic drugs exert their inhibitory effects on tumors by inducing the apoptosis of tumor cells [31,32]. In our study, an Annexin V-FITC/PI double staining flow cytometry and a Hoechst staining were applied to investigate effects of PD on the apoptosis of human glioma U251 cells. The results showed that compared with the none-PD treatment of U251 cells, the treatment of U251 cells with PD could significantly increase the apoptosis and apoptotic index of U251 cells, indicating that PD can induce the apoptosis of U251 cells.
Two pathways including mitochondria and death receptors are primarily involved in apoptosis, and the mitochondrial pathway is composed of Bid and Bad that are members of Bcl-2 family containing the BH3 domain and can be activated after they receive intracellular death signals [33]. The Bcl-2 family proteins are important regulators of mitochondrial apoptosis, including two types of proteins with opposite functions, namely, inhibition or promotion. The interaction between Bcl-2 family protein members plays a regulatory role in the mitochondrial-mediated apoptosis [34,35]. The interaction between anti-apoptotic binding protein Bcl-2 and pro-apoptotic protein Bax or Bak that binds to the outer membrane surface of mitochondria or exists in the cytoplasm can activate the caspase pathway, ultimately inducing apoptosis [36]. The results of this study showed that PD could reduce the Bcl-2 protein level of human glioma U251 cells, and elevate the level of Bax and cleaved caspase-3 protein, indicating that PD may induce the apoptosis of U251 cells by changing the expression of Bcl-2 and Bax proteins to activate the caspase pathway.
The cell cycle of normal cells is a strictly regulated process and cell cycle disorder is a basic characteristic of tumor cells so that anti-tumor effects can be exerted by disturbing the cell cycle of tumor cells [37,38,39]. This study found that PD could affect the cell cycle of U251 cells, in which the ratio of U251 cells treated with different concentrations of PD for 48 h was lower in S phase and G2/M phase, while that in G0/G1 phase was higher, suggesting that PD can arrest the cells in the G0/G1 phase. Besides the excessive proliferation of cells and the cell cycle abnormality, the occurrence of malignancies is also related to the reduction of cell apoptosis [40]. The phosphatidyl-inositol 3-kinase/serine-threonine kinase (PI3K/Akt) signaling pathway plays an important role in the regulation of cell biological behaviors, such as the proliferation and the apoptosis, in which this pathway is in an active state in most tumors [41,42]. It is reported that many chemotherapeutic drugs can exert their anti-tumors effects by blocking this pathway [43,44]. Akt is an important component of PI3K/Akt signaling pathway; when this pathway is activated, the activity of PI3K is enhanced, the phosphorylated form of Akt is predominant and the ratio of p-Akt (p-Akt/Akt) is increased [45]. The experimental results showed that compared with the treatment without PD, the treatment of U251 cells with PD could reduce the ratio of p-Akt/Akt, suggesting that PD may inhibit the activation of PI3K/Akt signaling pathway of U251 cells.

3. Experimental Section

3.1. Materials and Chemicals

PD (purity > 98%) was purchased from Best-Reagent (Chengdu, China) and human glioma cell line (U251) was purchased from ATCC (Rockefeller, MA, USA). Fetal calf serum, trypsin and RPMI 1640 were obtained from Gibco Co. (Grand Island, NY, USA) and MTT, PI and Triton X-100 were obtained from Sigma Chemical Co. (St. Louis, MO, USA). Antibodies of Bax, Bcl-2, Cleaved caspase-3, AKT, and p-AKT were gained from Cell Signaling Technology (Danvers, MA, USA). All of other reagents were of analytical grade from Sinopharm Chemical Reagent Co (Beijing, China).

3.2. Detection of Cell Proliferation Activity

Thawed U251 cells were routinely cultured under the condition of 37 °C and 5% CO2 in a culture medium containing 15% fetal bovine serum, the medium was changed every other 24 h, a light microscope was used to observe the cells, and the cells were subcultured 3–5 generations with 0.25% trypsin digestion and subculture when the confluence reached 80%–90%. Logarithmic growth phase U251 cells were seeded in a 96-well culture plate at a density of 1 × 105/well; 24 h later, PD at its final concentration of 0, 16.3, 40.8, 81.6 and 163.2 μM was in turn added to the culture medium respectively, in which the well containing 0 μM of PD was taken as the control group and the remaining wells containing different concentrations of PD were the experiment groups. All the cells were cultured under normal conditions, 10 μL of 5 mg/mL MTT solution were added to each well at 48, 72 and 96 h after the culture; 4 h later, absorbance values (A) of each group were recorded with a microplate reader (Thermo, Franklin, MA, USA) at the wavelength of 492 nm, which was repeated 3 times at the same time points for each concentration group and the proliferation inhibition rates were calculated according to the following formula:
Proliferation inhibition rate (%) = (1 − Aexperiment/Acontrol) × 100%

3.3. Detection of Cell Apoptosis and Cell Cycle

The cell apoptosis was detected with an Annexin V-FITC/PI double staining flow cytometry and the cell cycle was observed with a PI single staining flow cytometry. U251 cells were seeded in 6-well culture plates at a density of 1 × 106/well, and 24 h later, PD at the final concentration of 0, 16.3, 40.8, 81.6 and 163.2 μM was respectively added to the plates in turn, and the cells were cultured under conventional conditions; 24 h later, the cells were harvested and washed with PBS, Annexin V/FITC and PI were respectively added to them for the staining for 15 min, and then the cell apoptosis and cell cycle were detected with a flow cytometry (BD Biosciences, San Jose, CA, USA) and PI single staining flow cytometry separately, based on the kit instructions.

3.4. Detection of Apoptotic Index

U251 cells in a single cell suspension were seeded on sterile small slides placed at the bottom of plates in advance and were observed under a light microscope; after the cells adhered to the wall of plates, PD was added to them, in which the final concentrations of PD in wells were 0, 16.3, 40.8, 81.6 and 163.2 μM respectively; after the cells were cultured for 48 h, the slides were fixed with paraformaldehyde, then after washing with PBS, stained with Hoechst 33258 (5 μg/mL) staining at room temperature in the dark; 30 min later, they were observed under a fluorescence microscope (Nikon, Chiyoda-ku, Tokyo, Japan) and five high-power visual fields were randomly selected for each slide. The apoptotic index was calculated according to the following formula:
Apoptotic index = Number of apoptotic cells/total cells × 100%

3.5. Western Blotting Analysis

U251 cells treated with 0, 16.3, 40.8, 81.6 and 163.2 μM of PD for 48 h were centrifuged at 1000 r/min for 5 min. The cell lysate was added to the precipitated cells and the cells were lysed on an ice bath, and then the protein concentration was measured by BCA method; a quantitative protein was taken from each sample, and the transfer film was performed routinely with 10% SDS-PAGE gel electrophoresis and semi-transfer method (Bio-Rad, Hercules, CA, USA) after the protein was mixed with the loading buffer; according to the size of film, an appropriate amount of the primary antibody was added to it at a dilution ratio of 1:2000 in addition to the ratio of 1:1000 for Bax, which was incubated at 4 °C overnight; after the film was washed with TBST, the secondary antibody (1:3000) was added to, which was kept at room temperature for 2 h and then the coloration with ECL was conducted; Gel-Pro analyzer software was used to the optical density of each band, in which in addition to the p-Akt-related expression amount expressed in the ratio of Akt optical density, the rest are expressed in the ratio of optical density of the target protein to that of GAPDH.

3.6. Statistical Analysis

All results were expressed as mean ± SD. Data were analyzed by standard t-test. p values less than 0.05 or 0.01 were considered statistically significant.

4. Conclusions

PD can inhibit the proliferation, induce apoptosis and cause cell cycle arrest in human glioma U251 cells, which may be related to the inhibition of PD on the activation of PI3K/Akt signaling pathway.

Acknowledgments

This work was supported by the Major Scientific and TechnologicalSpecial Project for “Significant New Drug Formulation” (grant No. 2012ZX09501001004 and 2012ZX09301002-001).

Author Contributions

C.X. and X.S. designed the research; C.X., G.S., and G.Y. performed the experimental work; C.X. and R.W. wrote the manuscript. All authors discussed, edited and approved the final version.

Conflicts of Interest

The authors declare no conflict of interest.

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  • Sample Availability: Samples of the compounds platycodin D are available from the authors.

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MDPI and ACS Style

Xu, C.; Sun, G.; Yuan, G.; Wang, R.; Sun, X. Effects of Platycodin D on Proliferation, Apoptosis and PI3K/Akt Signal Pathway of Human Glioma U251 Cells. Molecules 2014, 19, 21411-21423. https://doi.org/10.3390/molecules191221411

AMA Style

Xu C, Sun G, Yuan G, Wang R, Sun X. Effects of Platycodin D on Proliferation, Apoptosis and PI3K/Akt Signal Pathway of Human Glioma U251 Cells. Molecules. 2014; 19(12):21411-21423. https://doi.org/10.3390/molecules191221411

Chicago/Turabian Style

Xu, Chong, Guibo Sun, Guangxin Yuan, Rui Wang, and Xiaobo Sun. 2014. "Effects of Platycodin D on Proliferation, Apoptosis and PI3K/Akt Signal Pathway of Human Glioma U251 Cells" Molecules 19, no. 12: 21411-21423. https://doi.org/10.3390/molecules191221411

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