ABSTRACT

Objectives:

Dehydroepiandrosterone (DHEA) is an endogenous hormone that acts as a ligand for several cellular receptors. An age-dependent decline in circulating levels of DHEA is linked to changes in various physiological functions. In gynecological clinical practice, DHEA is commonly prescribed to induce ovulation. Some clinical studies report a positive association between high serum concentrations of DHEA and an increased risk of developing ovarian cancer. However, the in vitro physiological effects of DHEA on ovarian cancerous cells have not been explored thus far. In this study, we aimed to investigate the physiological effects of DHEA treatment (0-200 μM, 24-72 hours) on MDAH-2774 human ovarian cancer cell line and primary HuVeC human endothelial cells.

Materials and Methods:

The physiological effects of DHEA treatment (0-200 μM, 24-72 hours) on MDAH-2774 human ovarian cancer cell line and primary HuVeC human endothelial cells were investigated with the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) test, acridine orange/ethidium bromide staining, and scratch assay.

Results:

DHEA treatment promoted proliferation of the MDAH-2774 cancer cell line in a dose-dependent manner (r=0.6906, p<0.0001, for 24 hours) (r=0.6802, p<0.0001, for 48 hours) (r=0.7969, p<0.0001, for 72 hours). In contrast, DHEA inhibited proliferation of the primary HuVeC cells (r=0.9490, p<0.0001, for 24 hours) (r=0.9533, p<0.0001, for 48 hours) (r=0.9584, p<0.0001, for 72 hours). In agreement with these observations, DHEA treatment resulted in a dose-dependent increase in the number of necrotic cells in the primary HuVeC cells (r=0.97, p<0.0001). However, the number of necrotic or apoptotic cells did not change significantly when the MDAH-2774 cells was exposed to DHEA. Moreover, we found that DHEA treatment reduced the migration rate of HuVeC cells in a dose-dependent manner (r=0.9868, p<0.0001), whereas only a slight increase was observed in the MDAH-2774 ovarian cancer cell line (r=0.8938, p<0.05).

Conclusion:

Our findings suggest that DHEA promotes the proliferation of ovarian cancer cells in a dose-dependent manner in vitro. Moreover, DHEA induced necrosis and inhibited proliferation in endothelial cells. Although mechanistic evidence is required, our preliminary findings imply that exposure to high doses of DHEA may be associated with an increased risk of developing ovarian cancer.

Keywords:

Dehydroepiandrosterone, MDAH-2774, HuVeC, ovarian cancer

INTRODUCTION

Dehydroepiandrosterone (DHEA) is one of the most abundant circulating steroid hormones produced by adrenal glands¹ and it can also serve as a precursor of other steroids in the brain.² DHEA is involved in the biosynthesis of sex steroids, and it may act as a ligand for several nuclear receptors as well as G-protein-coupled receptors. Physiological levels of DHEA in human serum range between 1 and 1000 nm,³ whereas prescribed pharmacological doses range between 10 and 100 µM.⁴ An age-dependent decline in circulating levels of DHEA can induce changes in cardiovascular tissues,⁵ female fertility,⁶ and metabolic and neuronal/central nervous system functions.⁷

Clinical findings show that DHEA administration can increase serum androgen levels, improve mood, improve sexual function, and decrease fatigue.⁸ DHEA is also widely used to induce ovulation in gynecological clinical practice. However, data also suggest that high doses or prolonged use of DHEA is associated with an increased risk of developing ovarian cancer.^9,10 Cameron and Braunstein⁸ have reported that DHEA activates estrogen receptors¹¹ in breast cancer and endothelial cell lines.^4,12,13 In line with these observations, clinical findings also implicate DHEA as a risk factor for developing breast cancer.¹⁴ In contrast, in vitro findings suggest an inhibitory effect of DHEA on the proliferation of breast, myeloma, hepatoma, prostate, human colon adenocarcinoma, cervical, and leukemia cancer cell lines.^{15,16,17,18,19,20,21} Thus, our understanding of the role of DHEA as a risk factor for developing cancer is limited.

At present, the in vitro effects of DHEA on normal and ovarian cancer cell lines have not been compared. Therefore, we aimed to investigate the physiological effects of DHEA on MDAH-2774 human ovarian cancer and non-cancerous HuVeC human endothelial cell lines. A better understanding of the differential effects of DHEA on normal and cancer cell lines can have important implications in clinical research.

MATERIALS AND METHODS

RESULTS

First, we investigated the effects of DHEA on cell viability by comparing the changes in proliferation rates of MDAH-2774 (human ovarian carcinoma epithelial cell) and HuVeC (human non-cancerous umbilical vein endothelial) cell lines. For this purpose, we used the MTT assay, which is a relatively simple and well-established procedure for the evaluation of cell viability and proliferation.²⁵ We tested the effects of four different concentrations (10 µM, 50 µM, 100 µM, and 200 µM) of DHEA for 24, 48, and 72 hours. The concentration range was determined according to literature data.⁴

Data analysis obtained from the MTT assay showed that DHEA treatment (10-200 µM) promoted the proliferation of the MDAH-2774 cell line in a dose-dependent manner (r=0.6906, p<0.0001, for 24 hours; r=0.6802, p<0.0001, for 48 hours; r=0.7969, p<0.0001, for 72 hours). In contrast to the MDAH-2774 ovarian cancer cell line, DHEA treatment inhibited proliferation of the non-cancerous HuVeC cells. Although, 10 µM (24 hours) DHEA treatment did not appear to affect the rate of cell proliferation, higher doses of DHEA (≥50 µM for 24, 48, and 72 hours) significantly inhibited proliferation of HuVeC cells in a dose-dependent fashion (r=0.9490, p<0.0001, for 24 hours; r=0.9533, p<0.0001, for 48 hours; r=0.9584, p<0.0001, for 72 hours) (Figure 1b, d, f).

As seen in Figure 1, 48 and 72 hours of DHEA exposure had the greatest effect on cell proliferation. In this context, to avoid the possible toxic effects that might arise due to prolonged drug exposure, we selected 48 hours as the optimum exposure time. Thus, subsequent experiments were carried out by exposing the cells to 10 µM, 50 µM, 100 µM, and 200 µM DHEA for 48 hours.

Next, we used the AO/EtBr dual staining protocol to compare changes in the ratio of apoptotic/necrotic cells. Dual AO/EB staining is a reliable and inexpensive technique to detect apoptotic and necrotic cells in cell culture experiments.²³ The changes in the ratio of apoptotic and necrotic cells were evaluated upon exposure to DHEA (10-200 µM for 48 hours). Our findings demonstrated that DHEA treatment did not induce apoptosis or necrosis in MDAH-2774 cells (Figure 2a, b). On the other hand, we detected a dose-dependent increase in the number of necrotic cells when HuVeC cells were treated with DHEA (48 hours, by 5% ± 1% for 10 µM, 14.33% ± 6% for 50 µM, 32% ± 3% for 100 µM, 54.33% ± 5% for 200 µM, p<0.05). Suggesting that DHEA treatment induces necrotic death in the HuVeC cell line. Representative microscope images from AO/EtBr-stained samples are shown in Figure 3.

Then, we investigated whether or not DHEA treatment could cause changes in cell migration rates. To this end, we performed the scratch assay. This is a simple in vitro method that serves as a powerful tool for analyzing cell migration rates in two dimensions.²⁶ In this context, we tested the effect of 10-200 µM DHEA (48 hours) treatment on cell migration rates by the in vitro scratch assay protocol. Our findings indicated that DHEA treatment triggered a slight increase in the migration rate of MDAH-2774 ovarian cancer cells (48 hours, by 7% ± 1% for 10 µM, 8% ± 1% for 50 µM, 9% ± 1% for 100 µM, 10% ± 1% for 200 µM, p<0.05) (Figure 4a). In contrast, DHEA reduced the migration rate of non-cancerous HuVeC cells in a dose-dependent manner (48 hours, by 5% ± 3% for 10 µM, 14% ± 1% for 50 µM, 31% ± 3% for 100 µM, 52% ± 4% for 200 µM, p<0.05) (Figure 4b). Representative microscope images from scratch assay experiments are shown in Figure 5.

DISCUSSION

DHEA is one of the most widespread adrenal steroids in humans. DHEA is the precursor of bioactive steroids, such as estrogen and testosterone.²⁷ Although DHEA is shown to be capable of activating estrogen receptors,¹¹ it can also act independently of estrogen and androgen receptors in endothelial and breast cancer cells.^4,12,13 In gynecological clinical practice, DHEA is also prescribed to induce ovulation. There are conflicting findings as to the role of DHEA as a risk factor for developing cancer. Higher levels of DHEA have been correlated with an increased risk of developing breast cancer.²⁸ On the other hand, Yoshida et al.²⁹ proposed that DHEA can reduce the risk of developing breast cancer by blocking estrogen receptors. For the most part, DHEA appears to inhibit the proliferation of cancer cells, according to in vitro findings.^{15,16,17,18,19,20,21} Several different groups have demonstrated that DHEA inhibits the proliferation of hepatoma, breast, myeloma, prostate, human colon adenocarcinoma, leukemia, and cervical cancer cell lines.^{15,16,17,18,19,20,21} On the other hand, clinical data also suggests that DHEA may be positively associated with breast cancer.¹⁴ For example, Michels et al.³⁰ have identified an increased risk of endometrial cancer with high levels of adrenal androgens and estrogens. A review of the literature revealed that sufficient data were not available regarding the in vitro physiological effects of DHEA on ovarian cancer cell lines.

MDAH-2774 is a widely used ovarian cancer cell line³¹ with a high mean tumor volume and is accepted as a suitable model for human ovarian cancer.³² Endothelial cells are one of the key players in maintaining physiological hemostasis³³ and are involved in many important processes, including regulation of cell migration, proliferation, and apoptosis.³⁴ Therefore, we have chosen a well-established endothelial cell model, the HUVEC cell line, as a non-cancerous cell model. In this context, we investigated the physiological effects of DHEA on MDAH-2774 human ovarian cancer cells in comparison with the non-cancerous HuVeC human endothelial cell line.

We have assessed the effect of DHEA on cell proliferation via the MTT assay, which is a relatively simple and well-established procedure for evaluating cell viability.²⁵ Our findings revealed that DHEA inhibits proliferation in the non-cancerous HuVeC cells in a dose-dependent manner (Figure 1). In line with our observation, Liu et al.³⁵ showed that DHEA inhibited cell proliferation of non-cancerous primary rat Leydig cells. They suggested that this cell type-specific response could be due to the differences in the way DHEA was processed or metabolized inside the cell. Surprisingly, we found that DHEA promoted proliferation of MDAH-2774 cancer cells in a dose-dependent manner (Figure 1). This finding supports the notion that DHEA may exert its effect in a cell type-specific manner. Similarly, Joshi et al.³⁶ reported cell type-specific differential effects of DHEA between mouse and human melanoma cell lines.

We have employed dual AO/EB staining technique to assess the DHEA-induced effects on apoptotic activity in cells.²³ We did not observe a significant change in the number of necrotic or apoptotic cells in the ovarian cancer cell line MDAH-2774 (Figure 2). However, our findings revealed that DHEA can induce necrotic cell death in the non-cancerous HuVeC cell line. Girón et al.¹⁹ previously reported that DHEA treatment induced both apoptotic and necrotic cell death in cervical cancer cell lines. Interestingly, supplementation of the medium with DHEA was reported to increase the number of primordial follicles by inhibiting apoptotic activity in mice.³⁷ In contrast, Kim et al.³⁸ demonstrated that DHEA administration can induce apoptosis in the mouse ovaries. More recent evidence also suggests that DHEA supplementation can protect ovarian cells in rats rather than inducing apoptotic activity.³⁹ Similarly, DHEA was found to inhibit H₂O₂-induced oxidative stress damage and apoptosis in Leydig cells.⁴⁰ The presence of contradictory findings further supports the idea that DHEA can exert its effects in a cell-type-specific manner.

Available data on the signaling mechanisms involved in DHEA-mediated physiological changes are also scarce. Girón et al.¹⁹ suggested that DHEA can exert its effects through the mitogen-activated protein kinase signaling pathway, independently of either estrogen receptor or androgen receptor. Jimenez et al.⁴¹ showed that DHEA may inhibit the pentose phosphate pathway and thereby alter oocyte lipid metabolism in mice. DHEA is shown to be able to directly act on plasma membrane receptors, such as the G-protein-coupled receptor in endothelial cells and aminobutyric-acid-type A in neurons. DHEA also binds androgen and estrogen receptors and can inhibit voltage-gated T-type calcium channels.⁴² Nevertheless, molecular and mechanistic approaches are necessary to dissect the mechanisms involved in this cell type-specific action of DHEA.

Previously, the migration of cervical cancer cell lines was found to be suppressed by DHEA.⁴³ In line with these reports, López-Marure et al.²⁰ proposed that DHEA inhibited the proliferation of all breast cancer cell lines. Consistently, we found that DHEA treatment can reduce the migration rate of non-cancerous HuVeC cells in a dose-dependent manner (Figure 4). Curiously, however, we detected a slight increase in the migration rate of the MDAH-2774 ovarian cancer cell line (Figure 4). This observation suggests that DHEA may induce the migration of ovarian cancer cells. In agreement with our observations, Montt-Guevara et al.⁴⁴ showed that DHEA stimulates cell invasion via moesin activation in the T47D breast cancer cell line.

CONCLUSION

Although DHEA inhibited proliferation of the non-cancerous HuVeC cells, DHEA treatment was able to promote the proliferation of the MDAH-2774 cancer cell line in a dose-dependent manner. We detected a dose-dependent increase in the number of necrotic cells in the non-cancerous HuVeC cell line in response to DHEA treatment. However, the number of necrotic or apoptotic cells did not change significantly in the MDAH-2774 cell line. DHEA treatment reduced the migration rate of non-cancerous HuVeC cells, whereas only a slight increase was observed in the MDAH-2774 ovarian cancer cell line. Our findings suggest that DHEA promotes the proliferation of ovarian cancer cells in a dose-dependent manner in vitro. Moreover, we found that DHEA induced necrosis and inhibited proliferation in a non-cancerous endothelial cell line. Although molecular and mechanistic evidence is required, our preliminary findings imply that exposure to high doses of DHEA may be associated with an increased risk of developing ovarian cancer.

Cell culture and chemicals

Human ovarian carcinoma epithelial cell [MDAH-2774 (ATCC^® CRLM10303^TM)] and human umbilical vein endothelial [HUV-EC-C (HuVeC) ATCC^® CRL-1730^TM)] cell lines were used. The cell lines were cultured in high-glucose Dulbeccos modified eagle medium (DMEM) (Sigma, 5546) supplemented with 1% 2 mM L-glutamine (Biological Industries, BI03-020-1B), P/S (50 U/mL penicillin and 50 µg/mL streptomycin; Biological Industries, 03-031-1B), 10% fetal bovine serum (Biowest, S1810-500). Each cell line was seeded into 10 cm plates (1.5x10⁶ cells/plate) and Biotest divided 72 hours later. DHEA tablets [approximately 0.6-1.2 g (2-3 pieces)] were dissolved in 50 mL of absolute ethanol as stock solutions. A 0.45-µm membrane filter was used for sterilization and the solution prepared fresh for every test.⁴ As a negative control, cells were treated with ethanol (the solvent of DHEA) containing DMEM.

(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) assay

12 mM stock solution of MTT (Neofrox 3580 MTT) was prepared as described by Mosmann.²² Cells were seeded into each well of a 96-well plate (approximately 10⁴ cells/well) in a volume of 100 µL. The MTT assay was conducted as follows: 10 µL of 12 mM MTT stock solution was added to each well and incubated at 37°C for 4 hours. Cell-free wells containing only 100 µL of medium were included as negative controls. After incubation with MTT for 4 hours, 75 µL of medium was removed from the wells, and the formazan crystals were then dissolved in 50 µL of DMSO by mixing the wells with a pipette. After a further 10 minutes of incubation at 37°C, the samples were mixed briefly again and the absorbance recorded at 540 nm.

Acridine orange/ethidium bromide (AO/EtBr) dual staining

The AO/EtBr dual staining technique was performed as described by Liu et al.²³ Briefly, the cells were seeded in a 96-well plate at a density of approximately 10⁴ cells per well. After 48 hours of incubation with DHEA, the cells were trypsinized, and 10-25 µl of the cell suspension was transferred to glass slides. One microliter of AO/EtBr staining (dye mixture containing 100 µg/mL AO and 100 µg/mL EtBr) solution was added to the cell suspension, and then the sample was covered with a cover glass. Within 20 minutes after addition of AO/EtBr dye, the cell morphology was checked under a fluorescence microscope (Carl-Zeiss/Axio Observer 3., Zen 2.3 Blue Edition software). For statistical analysis, at least 200 cells were counted and the results expressed as the average of at least three independent experiments. Both live and dead cells stained with AO, while only the dead cells that had lost membrane integrity stained with ethidium bromide. Living cells appeared uniformly green, while cells that were in the early apoptotic stage showed green dots in their nuclei. Late apoptotic cells stained orange and showed nuclear condensation and/or frequent fragmentation. Necrotic cells stained orange, and their nuclear morphology was similar to that of living cells, but without concentrated chromatin.²³

In vitro scratch assay

The in vitro scratch assay was carried out to evaluate the migration rates according to the protocol described by Liang et al.²⁴ Briefly, the surface of the wells in a 6-well plates was scratched with a 10 µL sterile pipette tip. After gentle washing with culture medium, images of the scratches at 0-24 hours were taken under a microscope with a magnification of 10x (Carl-Zeiss/Axio observer 3). By using ImageJ software, the gap size was analyzed and the cell migration rate calculated by comparing the cell-free areas of scratches at 24 hours after injury and the scratched areas at 0 hours. The results are expressed as the average of three repeated experiments.

Statistical analysis

Statistical analysis was performed using GraphPad (Prism 5) software. The statistical significance of differences between groups was assessed by One-Way ANOVA and Tukey’s post-hoc test (n=3).

Study limitations

In this study, we presented reproducible data to support our observations as to the physiological effects of DHEA on ovarian cancer and non-cancerous cells. However, we were not able to provide insight into the underlying molecular mechanisms and pathways due to a lack of molecular evidence. We were not able to provide mechanistic evidence to support our descriptive findings.

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Investigation of Physiological Effects Induced by Dehydroepiandrosterone in Human Endothelial Cells and Ovarian Cancer Cell Line