- Open Access
Polyphenol extract of Phyllanthus emblica (PEEP) induces inhibition of cell proliferation and triggers apoptosis in cervical cancer cells
© Zhu et al.; licensee BioMed Central Ltd. 2013
- Received: 30 July 2013
- Accepted: 21 October 2013
- Published: 19 November 2013
The aim of this study is to investigate the effects of polyphenol extract from Phyllanthus emblica (PEEP) on cervical cancer cells and to explore the underlying mechanism.
MTT assay was used to measure inhibition of proliferation of cervical cancer (HeLa) cells after treatment with PEEP at concentrations of 0, 50, 100, 150, and 200 mg/ml for 48 hours. HeLa cells were treated with PEEP (150 mg/ml) for 48 hours in the following analysis. Karyomorphism was assessed by immunofluorescence using DAPI staining, and cell apoptosis and cell cycle were assessed using flow cytometry. Three apoptotic marker proteins, namely, Fas, FasL, and cleaved caspase-8, were assessed by western blotting.
PEEP inhibited the growth of HeLa cells, and the optimum concentration of PEEP was 150 mg/ml. In addition, the karyomorphism of HeLa cells after treatment with PEEP was abnormal. Furthermore, PEEP induced arrest of the HeLa cell cycle at G2/M phase, and triggered apoptosis. PEEP also induced significant Fas and FasL activation, and cleavage of caspase-8.
Our study indicates that PEEP is effective in inhibiting HeLa cell proliferation by inducing cell cycle arrest at G2/M phase and inducing apoptosis.
- Phyllanthus emblica polyphenol extract
- Cervical cancer
- Cell cycle arrest
Cervical cancer is ranked as the second leading cause of female cancer mortality worldwide, with an annual incidence of approximately 200,000 deaths and more than 500,000 new cases diagnosed [1–3]. The incidence of cervical cancer is high in developing countries, and more than 28.8% of the world’s cases occur in China .
Human papillomavirus (HPV) infection is considered the greatest risk factor in the development of cervical cancer . Although HPV vaccines have been licensed in several areas, such as the USA, Europe, Canada, and Australia, the incidence of HPV infection-related cervical cancer has not been eliminated . This is because the vaccines are effective only against some types of HPV, and they are not yet widely used in developing countries . Curative surgery is the first option for patients with early-stage cervical cancer, while radiotherapy and chemotherapy have proven to be effective treatments for patients in the advanced stages. However, the curative effect of traditional chemotherapeutic drugs is limitedm and their side effects, such as neurological and/or renal  and cardiac  toxicity, are serious. Therefore, research into novel chemotherapeutic drugs is essential for effective treatment of cervical cancer.
Phyllanthus emblica (PE; syn. Emblica officinalis, also known as the Indian or Nepalese gooseberry or emblic leaf-flower) is a species belonging to the family Euphorbiaceae, which is used as a traditional medicine, especially in Asia . A previous study showed that PE could induce apoptosis in mouse and human carcinoma cell lines, including Dalton’s lymphoma ascites and CeHa cell lines . In addition, Ngamkitidechakul et al. reported that PE was able to inhibit proliferation of a series of cancer cell lines, including A549, HepG2, HeLa, MDA-MB-231, SK-OV3, and SW620, suggesting potential for PE in oncotherapy .
The ingredients of PE are complex, and include tannin and phenolic glycosides, flavonoids, terpenes, sterols, and several human essential trace elements such as vitamins and amino acids . In the present study, we isolated polyphenol extract from PE (PEEP), and measured its effect on the proliferation, cell cycle and apoptosis of cervical cancer (HeLa) cells. We also assessed karyomorphism of the cells after incubation with PEEP for 48 hours, and assessed expression of three apoptotic marker proteins: Fas, FasL, and cleaved caspase-8, using western blotting.
Preparation of PEEP
Polyphenols were extracted from the leaves of PE plants as described previously . Briefly, the leaves were homogenized for 5 minutes with chilled 70% acetone, followed by homogenization at high speed for 5 minutes, then the homogenate was centrifuged for 10 minutes. This process was performed in triplicate. Finally, the extract was dissolved in dimethyl sulfoxide (DMSO, Sigma, St Louis, MO,USA) and stored at −20°C until used.
HeLa cells were obtained from the Cell Bank of Type Culture Collection of the Chinese Academy of Sciences, (Shanghai, China), and were maintained in RPMI1640 (Gibco, Uxbridge, UK) with 10% fetal bovine serum (Hyclone, UT, USA) at 37°C in an atmosphere of 5% CO2. HeLa cells in the logarithmic phase were seeded into 96-well tissue culture plates at a density of 1 × 105 cells per well, and allowed to grow for 24 hours before being treated with PEEP. Cells were exposed to different concentrations (50, 100, 150, and 200 mg/ml) of PEEP, with phosphate-buffered saline (PBS) used as a negative control.
HeLa cells in the logarithmic phase that had been treated with PEEP (150 mg/ml) for 48 hours were seeded at a density of 2 × 105 cells onto coverslips, and maintained at 37°C in an atmosphere of 5% CO2 for another 48 hours. After that, cells were washed three times with PBS, and fixed in 3.7% paraformaldehyde for 20 minutes. The nuclei were stained with DAPI (4′, 6-diamidino-2-phenylindole; Roche, Mannheim, Germany) for 15 minutes. Images were captured using a confocal microscope.
Cell cycle analysis
HeLa cells in the logarithmic phase were seeded on a 96-well plate at a density of 1 × 105 cells per well and treated with PEEP (150 mg/ml), with PBS used as a control. At 48 hours after treatment, the cells were harvested and washed twice with PBS. The cells were then stained with 0.1% Triton X-100 containing propidium iodide (Amersham, Buckinghamshire, UK) and RNase (NEB, Ipswich, USA). Fluorescence from the propidium iodide-DNA complex was measured by flow cytometry (Millipore, Billerica, USA).
Analysis of apoptosis
For analysis of cell apoptosis, HeLa cells in the logarithmic phase were seeded at a density of 1 × 105 cells per well and treated with PEEP (150 mg/ml) for 48 hours before harvesting. Cells were washed twice with PBS and resuspended in PBS at a density of 1 × 105 cells/ml. Before being analyzed by fluorescence-activated cell sorting (FACS) (FACSCaliburl Milipore, Billerica, USA), 100 μl of cells were mixed with 100 μl Guava Nexin reagent (Milipore, Billerica, USA) for 20 minutes. All experiments were carried out in triplicate.
Cells in the logarithmic phase were harvested and lysed on ice for 30 minutes. After centrifugation at 2,000 rpm (626 g) for 10 minutes, the supernatant was collected, and protein concentrations were determined by bicinchoninic acid assay (BCA). Proteins were separated by 10% SDS-PAGE (20 μg protein per well). Then proteins were transferred to PVDF membrane (Bio-Rad, Hercules, USA). The membrane was blocked in Tris-buffered saline containing 5% non-fat milk (Wyeth) for 2 hours, and subsequently incubated with primary caspase-8 (1:200 dilution), Fas (1:200 dilution), FasL(1:200 dilution), and GAPDH antibodies (Abcam, Cambridge, USA) overnight at 4°C, followed by incubation with secondary antibody (Abcam, Cambridge, USA) at room temperature for 1 hour. The proteins of interest were visualized using an enhanced chemiluminescence (ECL) system (Millipore). GAPDH expression was used as internal control.
PEEP inhibits HeLa cell proliferation
PEEP induces G2/M arrest of HeLa cells
PEEP changes the karyomorphism of HeLa cells
PEEP induce apoptosis of HeLa cells
PE is a traditional medicine that has been investgated fo antiviral [14, 15] and anti-cancer  propertied, with satisfactory results. Although PE seems to have an anti-cancer effect, the active ingredients of PE are not very clear. The structure of PEEP contains an aromatic nucleus, one or more phenolic hydroxyl groups, and other elements. In the present study, we isolated polyphenols from PE and determined that in HeLa cells, this extract is capable of inhibiting cell proliferation, inducing cell cycle arrest at G2/M phase, and triggering apoptosis. We suggest that these effects were mainly due to the unique characteristics of polyphenols.
There are two common mechanisms identified in drug-induced inhibition of cancer cell proliferation [16–18]. First, chemotherapeutic drugs induce cell cycle arrest, especially in S or G2/M phase, with consequent inhibition of cell growth. Second, such drugs trigger the apoptotic pathway in cells. Fas, FasL, and caspase-8 are all molecular markers in the apoptotic pathway . Zhang et al. indicates that polyphenols extracted from fruit juice or from PE leaves had a strong inhibitory effect on melanoma cells . In addition, PEEP is efficient in facilitating the cytotoxicity of other drugs, such as doxorubicin and cis-platinum, when co-administered . In the current study, we determined that the inhibition of HeLa cell proliferation increased as PEEP concentration increased, reaching a maximum inhibition level of 39% at 150 mg/ml PEEP. Further experiments showed that PEEP inhibited HeLa proliferation by inducing cell cycle arrest at G2/M phase and triggering apoptosis.
It has been reported previously that PEEP induced G2/M phase arrest of lung cancer cells and triggered cell apoptosis . Our data suggest that PEEP similarly induces HeLa cell cycle arrest at G2/M phase. Further experiment showed that cell apoptosis was also triggered. Consistent with this, three apoptotic markers, Fas, FasL and cleaved caspase-8, were increased, suggesting that PEEP inhibits cell proliferation by inducing cell cycle arrest at G2/M phase and triggering apoptosis in cervical cancer cells.
PEEP was able to inhibit proliferation and promote apoptosis of cervical cancer HeLa cells by inducing cell cycle arrest at G2/M phase and triggering apoptosis. PEEP may be a potential future chemotherapy drug with definite functional components.
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