Background
Prostate cancer (PCa) is the second leading cause of death among men in the United States [
1]. The causes for PCa appear to be multifactorial, however it is well established that the incidence of PCa increases with age [
1,
2]. Several risk factors are associated with PCa including aging [
2], obesity [
3], hormonal imbalance [
3], oxidative stress [
3,
4] and hypercholesterolemia [
5,
6]. Estrogen receptor (ER) signaling has been implicated in PCa; the isoform ERβ, and to a lesser extent ERα, is expressed in prostate epithelial and stromal cells [
7,
8]. ERα is considered pro-proliferative [
9] and ERβ anti-proliferative in the context of PCa [
10‐
12]. However ERβ agonists have not shown clinical promise to combat PCa [
13] and there is a gap in knowledge elucidating the role of ERβ in PCa.
27-Hydroxycholesterol (27-OHC) is the most abundant cholesterol metabolite in the periphery [
14,
15]. Also, 27-OHC in plasma increases with age, especially in men [
16]. Men also have higher basal levels of 27-OHC in the plasma than women [
16]. Moreover, while patients with hypercholesterolemia are at risk for developing PCa [
6], they also have increased 27-OHC levels in the blood [
17‐
19]. Understanding the role of 27-OHC in the context of PCa is critical and may reveal the underlying mechanisms responsible for PCa tumor initiation and progression. 27-OHC is a selective estrogen receptor modulator (SERM) that has been identified to bind to ER and modulate its activity [
20,
21]. 27-OHC levels are higher among those with hypercholesterolemia [
17‐
19] and older men [
16], both of which are at high risk of developing PCa. Also, 27-OHC-induced ER activation has been shown to promote ER+ breast cancer growth and progression [
18,
22‐
24]. Given that 27-OHC, at high levels, is associated with risk factors for PCa (i.e., hypercholesterolemia and aging) and that 27-OHC modulates ER signaling, a pathway that plays a role in PCa development and progression, it is essential to study the role of 27-OHC in the context of PCa. Further understanding of the role of 27-OHC in PCa may innovate alternative therapeutic avenues to those that are currently on the market.
We have previously shown that 27-OHC stimulates cell proliferation and inhibits docetaxel induced apoptosis in non-tumorigenic prostate epithelial cells [
25]. In this study, we determined the extent to which 27-OHC is deleterious to PCa cells involving the activation of ERs.
Methods
Reagents
27-Hydroxycholesterol was purchased from Santa Cruz Biotechnologies (Dallas, TX), docetaxel, 4-[2-phenyl-5,7-bis(trifluoromethyl) pyrazolo[1,5-a]pyrimidin-3-yl]phenol (PHTPP) and fulvestrant from Cayman Chemicals (Ann Arbor, MI) and β-estradiol from Sigma-Aldrich (St. Louis, MO). All cell culture reagents, with the exception of fetal bovine serum (FBS) (Atlanta Biologicals; Flowery Branch, GA) were from Invitrogen (Carlsbad, CA). Human RWPE-1, LNCaP and PC3 cells were purchased from ATCC (Manassas, VA).
Cell culture
Non-tumorigenic human prostate epithelial RWPE-1 cells were maintained in Keratinocyte serum free medium (Invitrogen; Carlsbad, CA) supplemented with 0.05 mg/ml BPE and 5 ng/ml EGF. Metastatic LNCaP cells were maintained in RPMI 1640 medium and highly metastatic PC3 cells were maintained in F-12K medium. LNCaP and PC3 cells were supplemented with 10% FBS. All cells were supplemented with 100 U/ml penicillin, 100 μg/ml streptomycin 0.25 μg/ml amphotericin (Sigma; St. Louis, MO) and cultured at 5% CO
2 and 37 °C. Stock solutions of 27-OHC were prepared in 100% ethanol and stored at −80 °C. 27-OHC stock solution was dissolved in appropriate volumes of media to prepare the working solutions of 1 μM, a concentration that we showed to cause proliferation in prostate epithelial cells [
25]. Stock solutions of β-estradiol were dissolved in 100% ethanol and stored at −80 °C. Stock solutions were diluted to prepare working solutions of 2 nM. Stock solutions of PHTPP and fulvestrant were also dissolved in 100% ethanol, stored at −20 °C, and diluted prior to treatment to prepare working solutions of 10 μM. Concentrations of solvent in treatments were less than 0.1%.
Cell proliferation assay
Proliferation assays were conducted on black 96 well plates using CyQUANT Direct Cell Proliferation Assay (Invitrogen; Carlsbad, CA), which quantifies cell number using DNA content and membrane integrity. Cells seeded at 50–60% confluence were treated and incubated for 48 h. Cells were then stained as per the manufacturer’s protocol and read using Spectra MAX GEMINI EM (Molecular Devices; Sunnyvale, CA).
Cell metabolic activity was quantified by measurement of the reduction of MTS to formazan product using CellTiter 96® AQueous One Solution Cell Proliferation Assay (Promega; Madison, WI) according to the manufacturer’s protocol. The assay of the formation of formazan was performed by measuring absorbance change using a microplate reader (Molecular Devices; Sunnyvale, CA) 48 h after treatments.
Western blot analysis
Treated cells were washed with PBS, trypsinized, and centrifuged at 5000g. The pellets were washed with PBS and homogenized in M-PER tissue protein extraction reagent (Thermo Scientific; Waltham, MA) supplemented with protease and phosphatase inhibitors. Denatured proteins (5 µg) were separated in 10% SDS-PAGE gels, transferred to a PVDF membrane (Millipore; Billerica, MA) and incubated with antibodies to ERα (1:1000, Santa Cruz; Dallas,TX) and ERβ (1:1000, Millipore, Billerica, MA). β-actin was used as a gel loading control. The blots were developed with enhanced chemiluminescence (ECL Clarity kit, Bio-Rad). Bands were visualized on a polyvinylidene difluoride membrane and analyzed by LabWorks 4.5 software on a UVP Bioimaging System. Quantification of results was performed by densitometry and the results analyzed as total integrated densitometric values (arbitrary units).
Invasion assay
Invasion assays were conducted using QCM 96-well Cell Invasion Assay kit (Millipore; Billerica, MA). The various treatments were added to the wells of the feeder tray and at least 1 × 104 cells/well re-suspended in serum free medium were added to the invasion chambers. Cells were incubated with treatments for 24 h then stained as per manufacturer’s protocol and transferred to a black 96 well plate to read fluorescence using Spectra MAX GEMINI EM (Molecular Devices; Sunnyvale, CA).
Real-time polymerase chain reaction (RT-PCR)
After treatments, cells were lysed according to QuickGene Mini80 protocol and kit (Autogen). RNA sample were quantitated by spectrophotometry and subsequently, 1 µg total RNA was used as template to synthesize cDNA with the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems; Foster City, CA). We selected genes involved in pathways related to oxysterols, such as 27-OHC, including cholesterol metabolism [
26], liver X receptor (LXR) [
27] and sonic hedgehog (Shh) [
28] signaling. We also selected genes involved in metastasis [
29‐
31], oxysterol binding [
32] and tumor suppression [
33]. The screened genes are included in Table
1. Primers for all assays were designed using Primer Express 3.0 (Applied Biosystems; Foster City, CA). Melting curve analysis was performed to ensure single-product amplification for all primer pairs. Real time PCR was performed on the ABI 7900HT Fast Real Time PCR System (Applied Biosystems; Foster City, CA) using the panel of genes of interest. Data analysis was performed using Sequence Detection System software from Applied Biosystems, version 2.4. The experimental Ct (cycle threshold) was calibrated against the endogenous control products alpha-ACTIN (ACTN1) and beta-2-microglobulin (B2M). Samples were analyzed for relative gene expression by the DDCt method [
34].
Table 1
Selected genes analyzed with their corresponding pathways
CYP27A1 | CYP7B1 | HMGCR | ABCA1 | EZH2 | FOXA1 | GLI1 | GLI2 | GLI3 | CBX1 | CBX5 | CTGF | INSIG2 | OSBP | MDM2 | TAF3 | TNF |
NFKB1 | SRD5A2 | SREBF1 | NR1H2 | NR1H3 | RXRA | PTCH1 | PTCH2 | SHH | FN1 | IGF-1 | IGFBP3 | | | TP53 | | |
| | | RXRB | SIRT1 | TFF1 | SMO | | | MTA1 | MTA3 | SNAI1 | | | | | |
| | | TMPRSS2 | | | | | | SNAI2 | SPARC | VEGFA | | | | | |
Immunocytochemistry (ICC)
Coverslip seeded cells were rinsed with PBS and fixed in cold acetone, blocked with 10% normal goat serum and incubated overnight at 4 °C with human anti-ERβ2 monoclonal antibody (Biorad; Hercules, CA). ERβ2 was conjugated to Alexa Fluor 488. All coverslips were washed and mounted with Vectashield containing DAPI. Slides were visualized using DMI 6000 (Leica Microsystems; Buffalo Grove, IL).
Statistical analysis
The significance of differences were assessed by unpaired t test and One Way Analysis of Variance (One Way ANOVA) followed by Tukey’s post hoc test. Statistical analysis was performed with GraphPad Prism software 4.01. Quantitative data for experimental analysis are presented as mean values ± SEM with unit value assigned to control and the magnitude of differences among the samples being expressed relative to the unit value of control.
Discussion
This study investigated the role of 27-OHC in PCa cell models. We demonstrate that 27-OHC induces cell proliferation in PCa cells through ER. We further show that 27-OHC regulates ERβ expression over ERα. Moreover, we demonstrate that 27-OHC-induced cell proliferation is dependent on ERβ activation. We also show that 27-OHC reduces ECM cell invasion in PCa cells but not in non-tumorigenic cells. Additionally, we found that among pre-selected genes, several genes that are related to oxysterol biology and PCa were significantly upregulated/downregulated following 27-OHC treatment in non-tumorigenic and PCa cells. These include TFF1 and TMPRSS2 in non-tumorigenic cells and CTGF and RXRB in PCa cells. We also demonstrated that 27-OHC may regulate ERβ2 levels and its cellular localization. Thus, our data show for the first time a potential link between 27-OHC and PCa pathogenesis by demonstrating the deleterious effect of 27-OHC in PCa cellular models.
Previously, we have reported that 27-OHC stimulates cell proliferation in non-tumorigenic prostate epithelial cells [
25]. Subsequently, in this report, we demonstrate the effect of 27-OHC in PCa cells. Given that cell proliferation is associated with tumor growth, we measured cell proliferation upon 27-OHC treatment. We found that 27-OHC significantly increases cell proliferation in tumorigenic LNCaP and PC3 cells. Interestingly, the magnitude of 27-OHC-induced cell proliferation in LNCaP is higher than PC3. Also, the magnitude of 27-OHC-induced cell proliferation is higher in RWPE-1 than in LNCaP and PC3. The three epithelial cell lines have different morphologies, androgen receptor (AR) status, and depict different stages of PCa pathology. RWPE-1 are non-tumorigenic [
44], LNCaP are androgen sensitive and with low tumorigenicity [
45], and PC3 are androgen insensitive and highly tumorigenic [
46]. Taking tumorigenicity of the cells into account, it appears that 27-OHC increases cell proliferation to a greater magnitude in prostate cells with low or non-tumorigenic phenotypes versus highly tumorigenic phenotype.
The role of estrogens and estrogen receptors in the context of PCa is currently being explored. Recently, estrogens have been associated with the development and progression of PCa [
47]. Moreover, the discovery of 27-OHC as a SERM [
21] adds another dimension to the growing phenomena of estrogenic actions as well as cholesterol metabolism role in PCas. Our previous [
25] and current data strongly suggest that 27-OHC-induced cell proliferation in non-tumorigenic prostate cells and in PCa cells is ER dependent. When cells were treated concomitantly with 27-OHC and the ER inhibitor fulvestrant, proliferation was substantially attenuated. Given that 27-OHC is known to bind and activate ER [
21,
23], our results suggest that activation of ER is required to ensue 27-OHC-induced cell proliferation in PCa cells. This observation suggests a potential link between 27-OHC, ER and PCa.
It is worth noting that being an ER modulator, 27-OHC can act as an agonist or antagonist depending on the target tissue. For example, 27-OHC activates ER in breast tissue [
18,
22,
23] and inhibits the receptor in the vasculature [
20]. We propose an additional novel concept that 27-OHC activates ER signaling in prostate cells and may thus play a pivotal role in PCa development and progression.
Furthermore, we demonstrate that 27-OHC-induced cell proliferation in non-tumorigenic and PCa cells is ERβ dependent. When cells are treated with the ERβ specific inhibitor PHTPP, the 27-OHC-induced cell proliferation is attenuated, suggesting the 27-OHC-induced ERβ activation as the underlying factor leading to cell proliferation.
Our results demonstrate that 27-OHC reduces cell invasion in PCa cells but not in non-tumorigenic cells. The finding that 27-OHC increases cell proliferation but reduces cell invasion is unexpected, however it is in accordance with the current environment of diagnosed PCa in which over 90% of PCa diagnosed are reported to be localized PCas [
48,
49]. Additionally, it is important to note that cell invasion and proliferation are two different parameters in cancer. Moreover, androgen deprivation therapy (ADT) for patients with localized PCa does not improve survival or delay the use of secondary cancer therapy [
50], suggesting a potential role of 27-OHC-induced estrogenic signaling in localized PCa.
Our study determined the expressions of genes regulated by 27-OHC in non-tumorigenic cells and PCa cells. In non-tumorigenic RWPE-1 cells, we found that 27-OHC treatment upregulated TFF1 (ps2) and TMPRSS2, downstream targets of ER [
48] and AR [
49], respectively. The upregulation of these target genes by 27-OHC demonstrates that this oxysterol activates target genes to both ER and AR activation. This corroborates with our earlier report that AR and ER are necessary to induce cell proliferation in the 27-OHC-treated RWPE-1 cells [
25]. This observation also substantiates the idea that ER and AR activation simultaneously play a significant role in PCa tumor initiation. For instance, when Noble rats are concomitantly treated with estradiol and testosterone almost rats develop PCa tumors, while only 40% of them develop PCa when treated with testosterone alone [
50,
51].
Unlike in RWPE-1 cells, we did not find upregulation of ps2 and TMPRSS2 genes by 27-OHC in PCa cells. This may be attributed to the fact that LNCaP has a mutated AR [
52] and that PC3 has no AR [
53]. In PCa cells, we found that the connective tissue growth actor(CTGF), which plays a vital role in tumorigenesis and wound healing processes [
54] is upregulated by 27-OHC. Also, specific to LNCaP, we found a significant upregulation of insulin-like growth factor binding protein-3(IGFBP-3) which has been implicated in PCa tumors. IGFBP-3 is an anti-angiogenic and anti-metastatic protein that is upregulated and localized in the nucleus of PCa tumor cells [
55].
Moreover, our results demonstrate that ERβ2 can be regulated by 27-OHC. In RWPE-1, the cells which obtained the most increase in cell proliferation upon 27-OHC treatment, ERβ2 expression increased. Surprisingly while no change was observed in LNCaP, PC3 demonstrated a reduction in nuclear ERβ2 expression, which corresponds to the decreased cell invasion upon 27-OHC treatment (Fig.
5c). This finding corroborates with the observation that nuclear ERβ2 abundance is associated with poor PCa prognosis and increased cell invasion [
43].
Given the observations that 27-OHC induced AR transactivation and increased cell proliferation in an AR dependent manner in RWPE-1 cells, and 27-OHC does not directly bind to AR [
25], RWPE-1 is the only cell line in this study with a wild type AR [
44] and it is also the only cell line to show an increase in ERβ2 expression upon 27-OHC treatment. Furthermore, 27-OHC augmented cell proliferation at a greater magnitude in non-tumorigenic (RWPE-1) compared to low tumorigenic (LNCaP) and highly tumorigenic (PC3) PCa cells. Taken together, we hypothesize that 27-OHC binds and activates ERβ, inducing downstream AR-ERβ2 crosstalk signaling events leading to increased cell proliferation which may result into early stages of PCa. Further studies are warranted to test this hypothesis and determine the relationship between AR and ERβ2 in the presence of 27-OHC in the context of wildtype AR + prostate cancers.
Although there are variations between the both the PCa cells due to their difference in phenotypes, they have notable similarities. Both having mutated ARs; LNCaP having a mutated AR for increased androgen sensitivity and PC3 having the mutated AR for decreased androgen sensitivity, hence each cell line depicts a different stage of PCa. Also, 27-OHC increased proliferation, decreased cell invasion and increased expression of CTGF in both cell lines, CTGF is known to play anti-metastatic roles [
56,
57]. These results establish a rationale and prelude to the potential role of 27-OHC in promoting tumor growth in localized prostate cancers.
Authors’ contributions
SR, MM and CG carried out experiments; SR drafted the manuscript a; KH and BG participated in the design and interpretation of the study; OG conceived the study, designed and coordinated the experiments, interpreted the data and conceived the final draft of the manuscript. All authors read and approved the final manuscript.