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. 2018 Aug 3;16(4):5006–5012. doi: 10.3892/ol.2018.9267

Erianin inhibits human cervical cancer cell through regulation of tumor protein p53 via the extracellular signal-regulated kinase signaling pathway

Mengting Li 1,2, Yulin He 1,2, Cheng Peng 1,2,✉, Xiaofang Xie 1,2,✉, Guanying Hu 1,2
PMCID: PMC6144433  PMID: 30250566

Abstract

Erianin, a natural bibenzyl compound, is present in Dendrobium chrysotoxum Lindl. (commonly known as Shihu in China), which is used as an antipyretic and analgesic in traditional Chinese medicine, and has been reported to exert inhibitory effects on cancer cells in vitro. Cervical cancer is the third-most common cancer in women worldwide, and has the highest morbidity rate of gynecological malignancies. Thus, the identification of effective chemotherapeutical agents to treat this disease is urgent. The aim of the present study was to elucidate the biological functions and molecular mechanism of erianin on HeLa cells. Cellular proliferation was assessed using an MTT assay and flow cytometry assay with propidium iodide (PI) staining. Apoptosis rates were observed using a high content screening system via annexin V-fluorescein isothiocyanate/PI double staining, and measured by flow cytometry. The protein levels of tumor protein p53, extracellular signal-regulated kinase 1/2 (ERK1/2), caspase-3, B-cell lymphoma-2 (Bcl-2) and Bcl-2-associated X (Bax) were assessed by western blot analysis. Erianin inhibited the growth of HeLa cells and induced apoptosis in a dose- and time-dependent manner, inducing cell cycle arrest at the G2/M stage. Erianin treatment also increased the expression of Bax and caspase-3, but decreased levels of Bcl-2 and phosphorylated-ERK1/2. Cells treated with paclitaxel were regarded as the positive group. Together, the results of the present study indicated that erianin could be considered as an effective drug candidate; in HeLa cells it inhibited cellular proliferation and promoted apoptosis via regulation of the ERK1/2 signaling and mitochondrial-based apoptosis pathways. Thus, erianin has the promise to be developed further for cervical cancer therapy.

Keywords: erianin, HeLa, proliferation, apoptosis, extracellular signal-regulated kinase pathway

Introduction

Cervical cancer, which is often induced by human papilloma virus (HPV) infection, is one of the most serious life-threatening diseases among women in developing countries (1,2). Recently, two prophylactic vaccines, Cervarix and Gardasil, against the high-risk strains HPV-16 and HPV-18 have been developed and are used in more than 100 countries worldwide (3). However, these vaccines offer no benefit for patients that are already infected with HPV, have pre-cancerous lesions or cervical cancer (4). The long-term use of routine approaches to treat cervical cancer, including surgical removal, radiotherapy and chemotherapy, further damage the health of patients. Accordingly, seeking effective treatment agents from natural compounds to prevent and treat cervical cancer without these adverse effects is clinically urgent.

Erianin [2-Methoxy-5-(2-(3,4,5-trimethoxyphenyl)-ethyl)-phenol] (Fig. 1) is a natural bibenzyl compound present in Dendrobium chrysotoxum Lindl., which is commonly known as Shihu in China; it has been used as a herbal drug for thousands of years in traditional Chinese medicine (TCM), where it is often used as antipyretic and analgesic medication (5). Previous studies have demonstrated that erianin can elicit multiple pharmacological effects, including anti-oxidative (6) and antitumor activity (7). Erianin has been reported to inhibit cell proliferation and induce apoptosis in human promyelocytic leukemia HL-60 cells (8), and reverse multidrug resistance in B16/hMDR-1 cells (9). However, the effect of erianin on cervical cancer HeLa cells and the underlying molecular mechanisms behind these effects remain unclear. Thus, in the present study, the anticancer effects of erianin in HeLa cells compared with paclitaxel, a frequently used chemotherapeutic drug, were examined. Additionally, the involvement of tumor protein p53 and extracellular signal-regulated kinase (ERK) signaling were also investigated as potential molecular mechanism. The present study aimed to elucidate the effects and potential mechanism of erianin on cervical cancer HeLa cells in vitro.

Figure 1.

Figure 1.

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Chemical structure of erianin. C18H22O5; molecular weight, 318.36.

Materials and methods

Reagents

Erianin and paclitaxel (PTX) were purchased from Chengdu Must Bio-Technology Co. Ltd. (Chengdu, China), purity >98%, and dissolved in dimethyl sulfoxide (DMSO) (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) for use.

Cell culture

HeLa cells, human cervical cancer cell line, were obtained from American Type Culture Collection (Manassas, VA, USA). HeLa cells were cultured in Dulbecco's modified Eagle's medium (DMEM) (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) with 10% fetal bovine serum (FBS) (Gibco; Thermo Fisher Scientific, Inc.) at 37°C in a humidified atmosphere of 5% CO2.

Cell viability assay

The cytotoxic activity of erianin on HeLa cells was assessed using an MTT assay. HeLa cells were treated with erianin at various concentrations (3.9, 7.8, 15.7, 31.4 or 157.0 µM) for different time points (24, 48 or 72 h), and then incubated with MTT (0.5 mg/ml) at 37°C for 4 h. Meanwhile, HeLa cells were treated with PTX (7.81, 15.63, 31.25, 62.50, 125.0 and 250.0 nM) for 48 h as the positive groups. The purple formazan crystals were dissolved in 0.15 ml of DMSO. Following shaking, the plates read on an automated microplate spectrophotometer at 570 nm. Assays were performed in triplicate in three independent experiments.

Cell cycle assay

Following exposure to erianin (3.9, 7.9, 15.7 and 31.4 µM) and 0.05 µM PTX for 12, 24, 36 and 48 h, the control (without treatment) and experimental groups (3.0×105 cells in a 60-mm dish) were harvested using 0.25% trypsin, washed with ice-cold PBS and collected by centrifugation at 400 × g for 15 min at 4°C. The cells were suspended in PBS and fixed with 70% ethanol (v/v) overnight at 4°C. The following day, subsequent to three washes with ice-cold PBS, the cells were treated with 100 µl RNase at 37°C for 30 min and stained with 400 µl propidium iodide (PI) (Nanjing KeyGen Biotech Co. Ltd., Nanjing, China) for 30 min. Next, cell cycle analysis was performed by flow cytometry (Coulter Epics XL; Beckman Coulter, Inc., Brea, CA, USA). The data were analyzed using MultiCycle software (version 6-16-03-F32; Beckman Coulter, Inc.).

Cell apoptosis assay

For apoptotic cells analysis, HeLa cells were treated with various concentrations of erianin (3.9, 7.9, 15.7, 31.4) µM and 0.05 µM PTX for 12, 24, 36 and 48 h. The cells were then collected and washed with ice-cold PBS. Next, early apoptosis was measured using an Annexin V-Fluorescein Isothiocyanate (FITC)/PI apoptosis detection kit (BD Pharmingen; BD Biosciences, Franklin Lakes, NJ, USA). The cells were suspended with 100 µl of binding buffer and stained with 5 µl annexin V-FITC and 5 µl PI for 20 min at room temperature in the dark and then 400 µl binding buffer was added. The proportion of apoptotic cells were determined by flow cytometry and observed using the ImageXpress® Micro XLS High Content Screening system (Molecular Devices, LLC, Sunnyvale, CA, USA), with Hoechest 33342 staining.

Western blot assay

Cells were treated with 3.9, 7.8, 15.7 or 31.4 µM erianin or 0.05 µM PTX for 48 h, lysed using lysis buffer radioimmunoprecipitation assay (RIPA; 3 ml; cat. no. AR0102; Wuhan Boster Biological Technology, Ltd., Wuhan, China) buffer with phenylmethane sulfonyl fluoride (40 µl; cat. no. AR1778; Wuhan Boster Biological Technology, Ltd.) and a protease inhibitor cocktail (cat. no. P8340; 30 µl Sigma-Aldrich; Merck KGaA) and the lysates were measured for protein concentrations with a total protein quantitative assay (Coomassie brilliant blue method) kit (cat. no. A405-2; Nanjing Jiancheng Bioengineering Institute, Nanjing, China) as described previously (10), according to the manufacturer's protocols. Protein samples (20 µg) were separated by 10% SDS-PAGE and then transferred to a polyvinylidene fluoride membrane. The membrane was blocked for 2 h with 5% non-fat dry skimmed milk. Following incubation overnight at 4°C with antibodies against tumor protein p53 (hereafter p53) (dilution, 1:1,000; cat. no. ab131442; Abcam, Cambridge, UK), ERK1/2 (dilution, 1:1,000; cat. no. ab50011; Abcam), phosphorylated ERK1/2 (dilution, 1:1,000; cat. no. ab36991; Abcam), caspase-3 (dilution, 1:1,000; cat. no. 9665; Cell Signaling Technology, Inc., Danvers, MA, USA), B-cell lymphoma-2 (Bcl-2) (dilution, 1:1,000; cat. no. ab136285; Abcam), Bcl-2-associated X (Bax) (dilution, 1:1,000; cat. no. ab32503; Abcam), GAPDH (dilution, 1:1,000; cat. no. BA2913; Wuhan Boster Biological Technology, Ltd.) and β-actin (dilution, 1:1,000; cat. no. ab3280, Abcam), the membrane was incubated with horseradish peroxidase-conjugated anti-rabbit antibody (dilution, 1:5,000; cat. no. RA1054; Wuhan Boster Biological Technology, Ltd.) at 37°C for 2 h. Finally, the reaction was visualized using SuperLumia enhanced chimiluminescence kit (cat. no. K22020; Abbkine Scientific Co., Ltd, Wuhan, China) and detected using a Molecular Imager® Gel Doc™ XR+ (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The integrated density of the bands was quantified using Image Lab 5.1 software (Bio-Rad Laboratories, Inc.).

Bioinformatics methods

The data concerning the association between p53 expression and survival ratios in patients with cervical cancer were acquired from The Cancer Genome Atlas (TCGA) database (https://cancergenome.nih.gov/). The interaction regulatory function of p53, ERK1/2, Bax and Bcl-2 was analyzed using Pathway Commons (http://www.pathwaycommons.org/) (11).

Statistical analysis

All experiments were independently repeated three times. All quantitative data were presented as the mean ± standard deviation and analyzed using SPSS 19.0 software (IBM Corp., Armonk, NY, USA). The half-maximal inhibitory concentration (IC50) and combination index values were calculated using a logit regression model. One-way analysis of variance with a least significant difference post-hoc test was used to compare mean values between the control and treatment groups. P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of erianin on the proliferation of HeLa cells

To evaluate the inhibitory effect of erianin on HeLa cells, cell viability was assessed using an MTT assay after 24, 48, or 72 h of treatment. The results showed that erianin inhibited HeLa cells growth in a dose- and time-dependent manner. At doses of 3.9, 7.8, 15.7, 31.4 and 157.0 µM, erianin elicited a significant inhibition in HeLa cell viability after a 48-h treatment (P<0.05). The IC50 values of erianin and PTX after 48 h were 8.3±1.3 and 0.055±0.0017 µM, respectively (Fig. 2).

Figure 2.

Figure 2.

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Changes of proliferation ability of HeLa cells following treatment with erianin and paclitaxel. The viability of HeLa cells at different time points were evaluated by MTT following incubated with different concentrations of erianin. *P<0.05, **P<0.01.

Effects of erianin on cell cycle of HeLa cells. To investigate whether the inhibition in cell proliferation induced by erianin could be attributed to the induction of cell cycle arrest, cell cycle analysis was performed. This analysis revealed that erianin induced cell cycle arrest in a time- and dose-dependent manner (Fig. 3). Compared with the control, the proportion of cells in G0/G1 phase following treatment with erianin and PTX decreased significantly after 12 h of treatment (P<0.01), whereas the proportion of cells in G2/M phase increased significantly (P<0.01) (Fig. 3A), indicating that erianin could at least partly inhibit HeLa cells proliferation via G2/M checkpoint arrest.

Figure 3.

Figure 3.

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Effects of erianin on cell cycle of HeLa. (A) HeLa cells were harvested following treatment with the indicated concentration of erianin or PTX for (A) 12, (B) 24, (C) 36 and (D) 48 h. Data are presented as the mean. PTX, paclitaxel.

Effects of erianin on apoptosis of HeLa cells

Induction of apoptosis is an central mechanism by which anticancer drugs can inhibit cancer cell growth. Flow cytometry analysis demonstrated that erianin at a dose of 7.8 µM induced apoptosis rate compared with the control, 0.22±0.26 vs. 1.52±0.29% at 12 h, 0.10±0.1 vs. 8.12±0.92% at 24 h, 1.83±0.71 vs. 11.53±1.22% at 36 h and 5.99±5.12 vs. 41.83±5.32% at 48 h, respectively (Fig. 4). As shown in Fig. 4D, erianin could increase rates of early apoptosis in HeLa cells, from 5.99±5.12% in the control (untreated cells at 48 h) to 48.91±5.22% in cells treated with 31.4 µM erianin after 48 h of treatment (P<0.05). Therefore, the results of the present study demonstrated that erianin induced apoptosis in HeLa cells in a time- and dose-dependent manner.

Figure 4.

Figure 4.

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Effects of erianin on apoptosis of HeLa. (A) HeLa cells were harvested and stained following erianin or PTX treatment for 12, (B) 24, (C) 36 and (D) 48 h. (E) Images were acquired when HeLa were exposed to erianin for 48 h, and early apoptotic cells were marked. *P<0.05, **P<0.01. PTX, paclitaxel; PI, propidium iodide.

Effects of erianin on the expression of p53, ERK1/2, caspase-3, Bcl-2 and Bax proteins

It has been reported that the p53 and ERK pathways are involved in mitochondrial-based apoptosis (12,13). Therefore, whether erianin induced mitochondrial-based apoptosis through the inhibition of ERK1/2 signaling and activation of p53 was examined. The results of western blot analysis revealed that erianin could reduce the levels of p53 expression and phosphorylated-ERK1/2 expression without decreasing total ERK1/2 expression, indicating that erianin could affect ERK1/2 phosphorylation in a concentration-dependent manner, compared with the control (P<0.05; Fig. 5A and B). Further study indicated that administration of erianin for 48 h evidently promoted caspase-3 cleavage, upregulated the expression of Bax and downregulated the expression of Bcl-2 (P<0.05; Fig. 5C and D), Note that, since the effect of erianin on p-ERK1/2 and caspase-3 expression at a concentration of 1.9 µM was similar to that at 3.9 µM, these data were therefore not included in the figure. A concentration of 3.9 µM as the minimum concentration was selected for the further investigation.

Figure 5.

Figure 5.

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Effect of erianin on p53/ERK1/2 signaling. (A) The levels of p53, ERK1/2 and its phosphorylated protein were tested after treatment for 48 h by 0.05 µM PTX and erianin at concentrations of 3.9, 7.8, 15.7 and 31.4 µM for HeLa cells, with (B) quantification of this expression. (C) The levels of caspase-3, Bcl-2 and Bax proteins were measured following treatment with compounds, with (D) quantification of this expression. **P<0.01. p53, tumor protein p53; p-ERK1/2, phosphorylated extracellular signal-regulated kinase 1/2; PTX, paclitaxel; Bcl-2, B-cell lymphoma-2; Bax, Bcl-2-assocated X; PTX, paclitaxel.

ERK and p53 expression are associated with mitochondrial-based apoptosis in cervical cancer

p53 is an essential tumor suppressor gene in various types of cancer (14). According to data from TGCA, high expression of p53 was positively associated with the survival rates in patients with cervical cancer (P=0.038) (https://cancergenome.nih.gov/), indicating that promoting p53 expression may represent a promising approach to treating cervical cancer (Fig. 6A). Furthermore, data from Pathway Commons (http://www.pathwaycommons.org/) in cervical cancer revealed that p53 serves essential roles in numerous different pathways, including apoptosis. Specially, p53 could control the expression and activation of Bcl-2 and Bax, and control phosphorylation of ERK1/2. The activation of the ERK1/2 pathway could control the activity of Bcl-2 (Fig. 6B).

Figure 6.

Figure 6.

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Role of p53 and ERK in mitochondrial-based apoptosis of cervical cancer. (A) Association between p53 expression and survival ratio. (B) Association between p53, ERK, Bax, and Bcl-2. p53, tumor protein p53; ERK, extracellular signal-regulated kinase; Bcl-2, B-cell lymphoma-2; Bax, Bcl-2-associated X.

Discussion

An epidemiological study indicated that in 2008, cervical cancer was the third-most common cancer in women worldwide and the gynecological malignancy with the highest morbidity, with an estimated 529,000 new cases occurring, resulting in 274,000 mortalities (15). Treatments for cervical cancer, including surgery, chemotherapy, radiation therapy, and chemotherapy combined with radiation therapy, can have a curative effect; however, these treatments are accompanied by adverse effects and recurrence within a short time (16–20). Accordingly, seeking effective chemotherapeutical agents to increase the curative rate, reduce the risk of recurrence and metastasis, and improve patient quality of life is highly desirable.

The development of antitumor drugs, particularly those based on natural products, is receiving considerable attention. Erianin, a naturally occurring product isolated from Dendrobium chrysotoxum Lindl., was reported to exert antitumor (21–23) and anti-oxidative effects (8). However, the anti-cervical cancer activity and the potential mechanisms of erianin have, to the best of our knowledge, not been assessed. The present study aimed to elucidate the effects of erianin on cell growth and apoptosis, and clarify the potential mechanism by which this occurred, which was associated with regulation of the ERK1/2 signaling and mitochondrial pathways.

Investigating the molecular mechanisms of cancer cell growth is critically important. Cell cycle dysregulation is a major factor in cancer cell growth (24). ERKs have a key role in promoting cell survival and cellular proliferation (25,26) and have been considered to be significant targets for cancer therapeutics (27). Evidence indicates that erianin affects cell cycle progression, evidenced by inhibition of gastric carcinoma SGC-7901 cell proliferation by blocking progression to S phase (28), and arresting progression at the G2/M phase in hepatocellular carcinoma Huh7 cells (23) and human colorectal cancer SW480 cells (29). In the present study, erianin exhibited potent anti-proliferative activities against HeLa cells (IC50=8.3±1.3 µM; Fig. 2) at 48 h, induced the arrest of HeLa cells at the G2/M phase (Fig. 3), and suppressing the phosphorylation of ERK1/2.

As a tumor suppressor, p53 has a pivotal role in cell cycle progression, the DNA damage response and apoptosis (12). Previous studies confirmed that p53 was one of the most commonly mutation genes in cancer (30–32). Additionally, the upregulation of p53 in cancer cells may prevent cancer cell proliferation by promoting cell cycle arrest and apoptosis (33–36). Liu et al (37) revealed that the p53 pathway in human cervical cancer cells is activated by reversion-inducing-cysteine-rich protein with Kazal motifs overexpression, which induces cancer cell apoptosis and reduces migration. In the present study, erianin treatment of HeLa cells could promote the activation of p53.

Apoptosis maintains the healthy survival/death balance in metazoan cells. Defects in apoptosis can cause cancer autoimmunity, whereas enhanced apoptosis may cause degenerative diseases (38). Mitochondria have a notable role in the intrinsic pathway of mammalian apoptosis. In various types of cancer, inhibitors of apoptosis are highly expressed whereas apoptosis promoters are mostly inactivated, resulting in a certain degree of drug resistance. Thus, reactivation of the normal apoptosis response in cancer cells through regulating apoptotic regulators is a desirable treatment approach (39,40). Developing therapeutic approaches has involved modifying the activity of Bcl-2 family proteins to reactivate apoptosis, eradicating cancer cells (41–43). It is generally recognized that Bcl-2, regarded as an anti-apoptotic protein, was suppressed and pro-apoptotic proteins like Bax was overexpressed following cleavage of caspase-family proteins once cytochrome C was released from the mitochondria into the cytoplasm (44,45). Evidence indicates provided that baicalein and betulinic acid induced apoptosis in HeLa cells by downregulating Bcl-2 expression and upregulating that of expression and caspase-8. When HeLa cells were exposed to erianin, the apoptotic rate was increased and expression of Bax was upregulated, caspase-3 was activated and Bcl-2 levels reduced, which was consistent with the results of previous studies (46,47), indicating that apoptosis induced by erianin was associated with the activation of the proteolytic caspase family and the Bcl-2 family.

Paclitaxel exerts an anticancer function and has been manufactured into albumin-bound paclitaxel (nab-paclitaxel), which received US Food and Drug Administration approval for the treatment of metastatic breast cancer, non-small cell lung cancer and pancreatic cancer (48). The National Comprehensive Cancer Network recommends paclitaxel combined with carboplatin or cisplatin for treatment of recurrent or metastatic cervical cancer. Therefore, in the current study paclitaxel was used as positive control agent and was compared with erianin in terms of effects on HeLa cell proliferation, cell cycle and apoptosis. The results of this analysis revealed that erianin arrested progression at the G2/M phase and enhanced the apoptotic rate, similar to paclitaxel, indicating that erianin has the potential to serve as an anti-cervical cancer drug.

In conclusion, erianin is a promising anticancer compound, owing to its ability to inhibit growth of HeLa by arresting progression at the G2/M phase transition and inducing apoptosis. The potential mechanism of action involves regulation of the ERK1/2 signaling and mitochondrial pathways.

Acknowledgements

Not applicable.

Funding

The present study was financially supported by the National Natural Science Foundation of China (grant no. J1310034).

Availability of data and materials

All data generated or analyzed during the present study are included in this published article.

Authors' contributions

ML performed the cell cycle and apoptosis experiments. YH performed the cell viability experiments. GH participated in statistical analyses and wrote the manuscript. XX and CP designed the research and wrote the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to publish

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Associated Data

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Data Availability Statement

All data generated or analyzed during the present study are included in this published article.

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