Harmine suppresses the proliferation and migration of human ovarian cancer cells through inhibiting ERK/CREB pathway

Introduction

Ovarian cancer is the sixth most common cause of cancer related death among Western women. Although it represents 30% of cancers of the female genital tract, ovarian cancers are responsible for more than half of the deaths (1). Significant progress has been made in surgery and the improvement of chemotherapeutic agents in ovarian cancer which led to improved 5-year survival rate, however, ovarian cancer remains the leading cause of death of all gynecological cancers (1,2). The main challenge of current chemotherapies for ovarian cancer treatment is due to drug resistance or relapse. Thus, identification of novel anticancer drugs and understanding the underlying molecular mechanisms will be of great help in the treatment of ovarian cancer.

Natural products have attracted considerable attention due to their potent anticancer effects in the past decades (3,4). It is estimated that over 46% of the new drugs and new drug candidates for cancer therapy approved by US Food and Drug Administration (FDA) between 1989 and 1995 were natural products or natural products derivatives (5). Notably, recent studies have demonstrated that the β-carboline alkaloids, a large group of natural and synthetic indole alkaloids that extensively exist in extracts from the leaves, barks, roots and seeds of a variety of plants, possess a broad range of psychopharmacological and neuropharmacological effects (6). Many alkaloids have been widely used in the clinical treatment of cough, hypertension and inflammation. Among them, harmine (7-methoxy-1-methyl-9Hpyrido [3,4-b] indole), which was originally isolated from the seeds of Peganum harmala and Banisteriopsis caapi and has been traditionally used as folk medicine in the Middle East, Central Asia, and South America (7), appears to exhibit various pharmacological effects both in vitro and in vivo, such as anti-Alzheimer, anti-inflammatory anxiolytic and antidepressant effects (8). Notably, recent studies also indicate that harmine shows to have significant anticancer effect in several cancer cells including hepatoblastoma HepG2 cells (9), B16F-10 melanoma cells (10) and gastric cancer MGC-803 cells (11). However, the effect of harmine on the proliferation and migration of ovarian cancer cells remains unknown.

To this end, the present study was aimed to investigate the anticancer effect and the possible mechanisms of harmine-mediated cell proliferation and migration in human SKOV-3 cells. Our results demonstrated that harmine significantly suppressed the proliferation and migration of ovarian cancer cells via inhibition of the ERK/CREB pathway. Moreover, the reduced expression of vascular endothelial growth factor (VEGF), matrix metalloproteinase (MMP)-2 and MMP-9 may be involved in harmine-mediated SKOV-3 cell proliferation.

Materials and methods

Antibodies and reagents

Antibodies to phospho-ERK1/2 (Thr202/Tyr204) (cat. no. 9101), ERK1/2 (cat. no. 9102), phospho-CREB (Ser133) (antibodies to phospho-ERK1/2 (Thr202/Tyr204) (cat. no. 9198), CREB (antibodies to phospho-ERK1/2 (Thr202/Tyr204) (cat. no. 9197), β-actin (antibodies to phospho-ERK1/2 (Thr202/Tyr204) (cat. no. 4970), goat anti-rabbit horseradish peroxidase (HRP)-linked antibody (antibodies to phospho-ERK1/2 (Thr202/Tyr204) (cat. no. 7074) as well as U0126 (specific ERK1/2 inhibitor) were purchased from Cell Signaling Technology (Beverly, MA, USA). Harmine, epidermal growth factors (EGF), dimethyl sulfoxide (DMSO) and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Culture medium and other solutions used for cell culture were purchased from Invitrogen (Shanghai, China). SYBR® Premix Ex Taq™ II was obtained from Takara Bio, Inc. (Otsu, Japan).

Cell culture and treatment

Human SKOV-3 ovarian cancer cells were grown in RPMI-1640 medium supplemented with 10% fetal bovine serum, 50 µg/ml streptomycin, 50 IU/ml penicillin. Cultures were maintained at 37°C in a humidified atmosphere containing 5% CO2. Cells were regenerated every 3 days when they reached 70–90% confluence. Harmine was dissolved in DMSO and diluted to appropriate concentrations with culture medium. The final concentration of DMSO in the culture medium did not exceed 0.1%.

Reverse transcription PCR

Total RNA was extracted using TRIzol reagent. Reverse transcription was performed according to the manufacturer's instructions from Invitrogen. PCR analysis was performed using the following sense and antisense primers: The VEGF primers were forward 5′-CTGGGCTGTTCTCGCTTCG-3′ and reverse 5′-CTCTCCTCTTCCTTCTCTTCTTCC-3′. The MMP-2 primers were forward 5′-CCGTCGCCCATCATCAAGTTC-3′ and reverse 5′-GCAGCCATAGAAGGTGTTCAGG-3′. The MMP-9 primers were forward 5′-TGGTCCTGGTGCTCCTGGTG-3′ and reverse 5′-GCTGCCTGTCGGTGAGATTGG-3′. The GAPDH primers were forward 5′-ACAACTTTGGTATCGTGGAAGG-3′ and reverse 5′-GCCATCACGCCACAGTTTC-3′. The amplification steps were as follows: 94°C for 5 min, 30 cycles of denaturation for 45 sec at 95°C, 45 sec of annealing at 60°C, elongation at 72°C for 45 sec, and extension at 72°C for 1 min. After amplification, the PCR products were electrophoresed on a 1.5% agarose gel and visualized by ethidium bromide staining.

Quantitative real-time PCR (qRT-PCR)

cDNA was obtain as described above. PCR primers used for the analysis are listed above. The 20 µl PCR system was composed of 2 µl cDNA, 10 µl SYBR Premix Ex Taq II, 0.4 µl ROX Reference Dye II, 0.8 µl 10 µM forward primer, 0.8 µl 10 µM reverse primer and 6 µl ddH2O. The qRT-PCR amplification was performed under the following conditions: 1 cycle of initial denaturation for 30 sec at 95°C, 40 cycles of denaturation for 5 sec at 95°C, followed by DNA synthesis for 30 sec at 60°C. After amplification, real-time data acquisition and analysis were performed.

Western blot analysis

After treated with different compounds, cells were harvested at indicated time, washed, and lysed in ice-cold lysis buffer. The cell lysates were sonicated and centrifuged at 12,000 × g at 4°C for 5 min. The protein concentration of extracts was determined by using the Bradford reagent from Bio-Rad Laboratories. Equal amounts of protein (20 µg/lane) were resolved with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to nitrocellulose membranes (Millipore, Bedford, MA, USA). Next, the membrane was blocked in 5% non-fat dry milk in Tris-buffered saline with Tween-20 for 2 h at room temperature and then incubated with different primary antibodies overnight at 4°C. HRP-conjugated secondary antibodies (1:20,000) were used subsequently for 2 h at room temperature. Immunoreactive bands were visualized by enhanced chemiluminescence (Pierce, Rockford, IL, USA) and quantified by using ImageJ software (National Institutes of Health, Bethesda, MD, USA).

MTT assay

Cell viability was assessed by MTT assay. Briefly, cells were seeded in a 48-well flat-bottomed plate (3×104 cells per well) and cultured overnight. Then, the cells were starved overnight and treated with different drugs as indicated later. For dose course experiment, the cells were treated with concentrations of harmine and incubated 48 h. For time course experiment, the cells were incubated with 10 µM harmine for 12, 24, 36, and 48 h. After incubation, 20 µl MTT (5 mg/ml) was added to each well, and the cells were allowed to grow in complete media at 37°C for 3 h. The supernatant was removed, then 500 µl DMSO was added to each well and swung for 10 min to dissolve the crystal. Subsequently, and absorbance was determined by using a microplate spectrophotometer assay reader at 570 nm.

Wound healing assay

SKOV-3 cells were seeded in 6-well plate and cultured to a confluent monolayer. The cells were pretreated with hydroxyurea (5 mmol/l) to prevent cell proliferation. A pipette tip (200 µl) was used to scratch a wound on the midline of each well and the cells were then washed twice with PBS. Following 0, 12, 24, 36 h of culture in RPMI-1640 supplemented with 10% serum (control) or harmine stimulants, the migration of the cells was evaluated by measuring the difference in the area of the wounds with a Leica DM2500 image analysis system (Leica, Mannheim, Germany).

Colony formation assay

SKOV-3 cells in the logarithmic growth phase were seeded in a 6-well plate and cultured in RPMI-1640 medium supplemented with 10% FBS overnight. Then, the cells were treated with the indicated concentrations of harmine for another two weeks. Then, the supernatants were discarded, and the cells were carefully washed three times with phosphate-buffered saline (PBS). Subsequently, cells were fixed with a fixative composed of methanol-glacial acetic acid (3:1) for 10 min. Finally, the cells were stained in crystal violet for 20 min. Images of the colonies were captured by a digital camera.

Statistical analysis

Data are indicated as mean ± SEM from at least 3 independent experiments. Statistical analysis was performed using the Student's t-test (comparison of two groups) or one-way analysis of variance (ANOVA) followed by the Dunnett's or Tukey's test (comparison of more than two groups). A value of p<0.05 was considered statistically different. All statistical analyses were conducted using Prism version 6.0 (GraphPad Software).

Results

Harmine inhibits the basal cell proliferation level in SKOV-3 cells

We first investigated the influence of harmine on the proliferation of SKOV-3 cells. The SKOV-3 cells were incubated with various concentration of harmine (0, 1, 2, 5, 10, 20 and 30 µM) for 48 h and then cell viability was measured by MTT assay. As shown in Fig. 1A, harmine markedly inhibited the growth of SKOV-3 cells in a dose-dependent manner as concentration of less than 2 µM had little effect while concentrations of more than 5 µM progressively inhibited the growth of SKOV-3 cells (Fig. 1A). We next explored the effects of harmine at different treatment times on SKOV-3 cell viability, the cells were incubated with 10 µM harmine for 12, 24, 36 or 48 h. Cell viability assays revealed that harmine significantly inhibited SKOV-3 cell growth except 12 h incubation, with the strongest effect at 48 h (Fig. 1B).

Figure 1. Harmine inhibits the basal cell proliferation level in SKOV-3 cells. (A) Dose-dependent effects of harmine on the proliferation of SKOV-3 cells. Cells were treated with increasing concentrations of harmine as indicated above for 48 h. (B) Time-dependent effects of harmine on the proliferation of SKOV-3 cells. Cells were treated with harmine (10 µM) for 12, 24, 36 and 48 h. MTT assay was performed to measure the cell viability. Data are representative of triplicate samples from at least three independent experiments and are expressed as the mean ± SEM. (C) Effects of harmine on colony formation capacity of SKOV-3 cells. Cells were treated with harmine at the indicated concentrations for two weeks. The colony number in the area outlined in white was calculated. (D) Quantitation of colony formation results as shown in (C). (E) The expression of PCNA in SKOV-3 cells was measured by western blot analysis after harmine treatment. (F) Quantitation of western blotting results as shown in (E). *p<0.05, **p<0.01, ***p<0.001 vs. control group.

To further confirm the inhibitory effect of cell proliferation of harmine, colony formation assays were performed. As shown in Fig. 1C, consistent with the MTT assay, harmine significantly suppressed the colony formation of SKOV-3 cells in a dose-dependent manner (Fig. 1C and D). To provide additional evidence, we then detected the expression of proliferating cell nuclear antigen (PCNA), a protein marker that has been widely used for indicating cell proliferation. We found that the expression of PCNA was significantly reduced by harmine treatment for either 24 or 48 h (Fig. 1E and F). Taken together, our above results strongly indicated that harmine showed significant inhibitory effect toward the cell growth in SKOV-3 cells.

Harmine inhibits EGF-induced proliferation of SKOV-3 cells

It is widely known that epidermal growth factor receptor (EGFR) is often overexpressed in numerous human cancers including ovarian cancer, and activation of EGFR is known to be involved in the growth and progression of a variety of malignancies (12,13). We next asked whether harmine was able to inhibit EGF-induced cell proliferation of SKOV-3 cells. To do this, the cells were treated with harmine in the absence or presence of EGF (50 ng/ml) for 48 h and then cell viability was measured by MTT assay. As shown in Fig. 2A, EGF significantly increased the proliferation of SKOV-3 cells, while this EGF-enhanced proliferation was remarkably suppressed by harmine treatment (Fig. 2A). Consistent with the previously results, harmine not only inhibited EGF-enhanced proliferation, but also inhibited basal proliferation level of the SKOV-3 cells in the absence of EGF (Fig. 2A). Similar results were observed by colony formation assay. As expected, harmine significantly inhibited EGF-induced colony formation capacity (Fig. 2B and C). These results further confirmed that harmine could obviously inhibit ovarian cancer cell proliferation.

Figure 2. Harmine inhibits EGF-induced SKOV-3 cell proliferation. (A) The cells were treated with harmine (10 µM) in the absence or presence of EGF (50 ng/ml) for 48 h and then cell viability was measured by MTT assay. (B) Effects of harmine on EGF-induced colony formation capacity of SKOV-3 cells. The colony number in the area outlined in white was calculated. (C) Quantitation of colony formation results as shown in (B). Data presented are mean ± SEM from at least three independent experiments. ***p<0.001 vs. control group; ##p<0.01, ###p<0.001 vs. EGF-treated group.

Harmine significantly suppresses the migration of SKOV-3 cells

Cell migration plays an important role during cancer progression. To explore the effect of harmine on the migration of SKOV-3 cells, a typical scratch wound healing assay was performed to measure the migration ratio. As our above results indicated that harmine was able to inhibit the proliferation of SKOV-3 cells, this may interfere with the analysis of cell migration results. Thus, to exclude the proliferation inhibitory effect of harmine on migration, the wound healing assay were performed in the presence of hydroxyurea which prevents cell proliferation by inhibiting the DNA synthesis. As shown in Fig. 3, harmine significantly inhibited the migration of SKOV-3 cells at 24 and 36 h after treatment while had little effect at 12 h (Fig. 3A and B).

Figure 3. Harmine significantly suppresses the migration of SKOV-3 cells. (A) Cells were treated with hydroxyurea (5 mmol/l) to prevent proliferation then effect of harmine on the migration of SKOV-3 cells was measured by wound healing assay. (B) Relative closed-wound distance was calculated by measuring the width of at least four wounds and normalized to control. Data presented are mean ± SEM. *p<0.05, ***p<0.001 vs. control group.

Harmine blocks ERK1/2 and CREB phosphorylation in SKOV-3 cells

We demonstrated that harmine significantly suppressed SKOV-3 cell growth. This raised the question how harmine acts to inhibit SKOV-3 cell growth. Mitogen-activated protein kinase (MAPK) pathways constitute a large modular network that regulates a variety of physiological processes including cell growth and differentiation. Thus, we firstly monitored ERK1/2 phosphorylation levels following harmine treatment. As shown in Fig. 4, harmine caused a rapid decrease in the phosphorylation level of ERK1/2 with no changes in total ERK1/2 expression levels (Fig. 4A). Similarly, the phosphorylation level of CREB, an important transcription factor that plays important roles in cell proliferation, was also decreased in the same manner as ERK1/2 (Fig. 4B), which might suggest that harmine inhibited ERK1/2 phosphorylation which in turn suppressed CREB activation.

Figure 4. Harmine inhibits ERK1/2 and CREB phosphorylation in SKOV-3 cells. Upper panel, dose course of the ERK1/2 (A) and CREB (B) phosphorylation after incubation with various concentration of harmine. Lower panel, typical immunoblots used to quantify the phosphorylated ERK1/2 (pERK1/2) (A) and CREB (B). Data represent the mean ± SEM from at least four independent experiments. *p<0.05, ***p<0.001 vs. control group.

Harmine inhibits EGF-induced ERK1/2 and CREB phosphorylation in SKOV-3 cells

Harmine significantly inhibited the cell proliferation and ERK1/2 and CREB phosphorylation in SKOV-3 cells, however, we do not know whether the inhibitory effect of harmine on cell proliferation was mediated by ERK1/2/CREB pathway. To verify this, we next investigated whether harmine could block EGF-induced ERK1/2 and CREB phosphorylation. As shown in Fig. 5, we first confirmed that EGF treatment significantly increased the phosphorylation of ERK1/2 and CREB (Fig. 5A and B). However, both EGF-induced ERK1/2 and CREB phosphorylation were remarkably inhibited by harmine treatment (Fig. 5A and B). To demonstrate that CREB phosphorylation was downstream of ERK1/2, we evaluated the effect of the EKR1/2 selective inhibitor on EGF-induced CREB phosphorylation in SKOV-3 cells. Cells were pretreated for 30 min with U0126 (10 µM) and then stimulated with EGF. We found that U0126 blocked EGF-induced ERK1/2 and CREB (Fig. 5C and D) phosphorylation, suggesting CREB acted as a downstream factor of ERK1/2.

Figure 5. Harmine inhibits EGF-induced ERK1/2 and CREB phosphorylation in SKOV-3 cells. (A) Effects of harmine on EGF-induced ERK1/2 and CREB phosphorylation. (B) The relative densities of protein bands shown in (A) were analyzed and normalized to β-actin. (C) Effects of MEK1/2 inhibitor U0126 on EGF-induced ERK1/2 phosphorylation. (D) The relative densities of protein bands shown in (C) were analyzed and normalized to β-actin. Data represent the mean ± SEM from at least three independent experiments. ***p<0.001 vs. control group, ###p<0.001 vs. EGF-treated group.

Harmine reduces the expression of VEGF, MMP-2 and MMP-9 in SKOV-3 cells

Since vascular endothelial growth factor (VEGF) and matrix metalloproteinases (MMPs), particularly the gelatinases MMP-2 and MMP-9, have been shown to play important roles in the proliferation, migration and metastasis of many primary epithelial tumors (14,15), we then examined the effect of harmine on the expression of VEGF, MMP-2 and MMP-9 in SKOV-3 cells. As shown in Fig. 6A, reverse transcription-PCR analysis showed that the gene transcription of VEGF, MMP-2 and MMP-9 were significant downregulated in the presence of harmine (10 µM) for 48 h (Fig. 6A and B). Consistently, quantitative real-time PCR analysis also indicated that harmine markedly suppressed the mRNA level of VEGF (Fig. 6C), MMP-2 (Fig. 6D) and MMP-9 (Fig. 6E).

Figure 6. Harmine reduces the expression of VEGF, MMP-2 and MMP-9 in SKOV-3 cells. (A) Cells were treated with 10 µM harmine for 48 h, mRNA level of VEGF, MMP-2 and MMP-9 were detected by reverse transcription PCR. (B) Quantitation of reverse transcription PCR results as shown in (A). RT-qPCR was performed to detect the mRNA level of VEGF (C), MMP-2 (D) and MMP-9 (E). Data are shown as means ± SEM of three triplicate experiments. *p<0.05, **p<0.01, ***p<0.001 vs. control group.

Discussion

In the present study, we investigated the antitumor effect and potential mechanism of harmine on human ovarian cancer cells. Our results showed that harmine not only significantly inhibited the proliferation and migration of SKOV-3 cells, but also suppressed the EGF-induced proliferation of SKOV-3 cells. Moreover, this antitumor effect of harmine might be through inhibiting the EKR1/2/CREB pathway and downregulation the expression of VEGF and MMPs.

Many natural alkaloids such as camptothecin, vincristine and ellipticine are found to be potent anticancer agents in recent years (16). These alkaloids kill tumor cells by different biochemical modes of action, such as inhibition of apoptosis, inhibition of topoisomerase I and II and inhibition of microtubule formation. However, the molecular mechanisms for the antitumor activity of β-carbolines are not fully defined. Of note, it is reported that some β-carbolines and their related compounds appear to have cytotoxic effects on several cell lines including cancer cells and cerebellar granule neurons. Though cytotoxic agents which result in cell death and eventually tumor shrinkage are conventional anticancer drugs and still the most widely used around the world (17), the non-cytotoxic, molecularly targeted drugs that inhibit tumor growth without direct cytotoxicity is of greatest concern (18). In our study, the inhibitory effect of cell growth in the presence of harmine may result from two possible reasons, from the unspecific cytotoxic effect of harmine that killed the cancer cells acutely, or that harmine may suppress the proliferation of SKOV-3 cells without inducing acute cellular damage. To discern the later from the former, we measured the cell viability of SKOV-3 cells treated with or without 10 µM harmine for 12 h. Our results showed that there was no significant difference between the cell viability of control cells and harmine-treated cells. On the other hand, a recent study indicated that treatment with harmine increased proliferation of cultured neural progenitor cells without DNA damage or cell death (19). Moreover, harmine was found to promote cell proliferation as exposure of chick embryos to harmine markedly increased BrdU incorporation and number of mitotic cells in the spinal cord (20). Together with our results, one can speculate that the inhibition of the proliferation of SKOV-3 cells by harmine may not be due to its unspecific cytotoxic effect.

Our results showed that harmine inhibited the basal proliferation level of SKOV-3 cells. Noteworthy, it also significantly suppressed EGF-induced proliferation of SKOV-3 cells, suggesting an ideal antitumor effect of harmine. Aberrant expression and signaling of the EGFR-mediated pathway are associated with various human cancers including breast, colon, head and neck, pancreatic, lung and ovarian cancers. Undoubtedly, EGFR and its family members have emerged as the most useful biomarkers and rational target for cancer therapy (21). It is worth noting that EGFR has been reported to be overexpressed in up to 60% of ovarian cancers (22), while increased expression and activation of EGFR is related to high cell proliferation index, high migration and stromal invasion rate (23,24). This may explain, to some extent, why harmine inhibits the basal proliferation level of SKOV-3 cells. However, how harmine affect EGFR signaling pathway needs to be further investigated.

Mitogen-activated protein kinase (MAPK) pathways such as ERK1/2 play an important role in the regulation of proliferation and migration of cancer cells. Consistent with the results showing harmine inhibited the proliferation of SKOV-3 cells, the phosphorylation of ERK1/2 was profoundly blocked by harmine treatment. Moreover, harmine also blocked the CREB phosphorylation which was reported to suppress apoptosis, induce cell proliferation, migration and mediate tumor metastasis (25). Since the inhibition manner of CREB phosphorylation was quite in accordance with ERK1/2, suggesting that CREB acts downstream of ERK1/2. This hypothesis was confirmed by the following data. First, we observed that the phosphorylation of ERK1/2 and CREB mediated by EGF were markedly inhibited in the presence of harmine. Second, the EGF-induced CREB phosphorylation can be significantly blocked by U0126, an inhibitor widely used to block ERK1/2 activity, which indicates EGF-induced CREB phosphorylation is mediated by ERK1/2. Thus, we conclude that inhibition of MEK/ERK pathway which in turn blocked CREB activity is involved in harmine's suppressive effect on EGF-induced cell proliferation in human ovarian cancer cells.

Degradation of extracellular matrix (ECM) and basement membranes by the tumor cells is a critical step in the processes of tumor invasion and metastasis (26). Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that regulate various cell behaviors with relevance to cancer biology through degradation of extracellular matrix surrounding tumors (14). In our study, we found that harmine can inhibit the expression of MMP-2 and MMP-9. Early adhesion and metastasis of ovarian cancer cells are mediated by the MMP family of proteins, the expression of which is upregulated during ovarian cancer progression (27). Though MMPs have been considered to be closely correlated with tumor invasion and metastasis (27), studies also show that inhibition of the activities of MMP-2 and MMP-9 can result in reduced ECM remodeling and suppression of endothelial cell proliferation and migration (28). Moreover, consistent with our results, a recent study indicates that activation of ERK1/2/CREB pathway promotes the expression of MMP-2 and MMP-9 which may account for lung cancer cell proliferation (29). On the other hand, our results also showed that harmine can inhibit the expression of VEGF. Since VEGF is the most important mitogenic and survival factors involved in angiogenesis while angiogenesis is pre-requisite for the growth of solid tumors, vascular targeting has been explored as a potential strategy to suppress tumor growth and metastasis. Thus, this result further confirmed the antitumor effect of harmine. However, whether harmine is able to inhibit angiogenesis in the development of a solid tumor needs further study.

Acknowledgements

The present study was supported by grants from the Traditional Chinese Medicine Research (no. 2016B032), Science and Technology Planning Project (no. 20175032) of Jiangxi Provincial Health and Family Planning Commission, the Guiding Science and Technology Program of Nanchang (no. 2016-ZDXXM-039).

Glossary

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References