Please cite this paper as:
Xiang, S., Dong, C., Yuan, L., Dauchy, R., Blask, D., Frasch, T. and Hill, S. 2020. Retinoic Acid-Related Orphan Receptor alpha 1 (RORα1) Induction of AKR1C3 Promotes MCF-7 Breast Cancer Cell Proliferation and Tamoxifen-Resistance which is Suppressed by Melatonin. Melatonin Research. 3, 1 (Mar. 2020), 81-100. DOI:https://doi.org/https://doi.org/10.32794/mr11250050.
Research Article
Retinoic acid-related orphan receptor alpha 1 (RORa1) induction of AKR1C3 promotes MCF-7 breast cancer cell proliferation and tamoxifen-resistance which is suppressed by melatonin
Shulin Xiang1,2,3, Chunmin Dong1, Lin Yuan1, Robert T Dauchy1,2,3, David E. Blask1,2,3, Tripp Frasch1,3*, Steven M. Hill1,2,3
1Department of Structural and Cellular Biology, Tulane University School of Medicine, New Orleans, LA 70112, USA
2Tulane Cancer Center, Tulane University School of Medicine, New Orleans, LA 70112, USA
3Tulane Center for Circadian Biology, Tulane University School of Medicine, New Orleans, LA 70112, USA
*Correspondence: tfrasch@tulane.edu, Tel: +015049885255
Running title: Melatonin inhibits RORα1 and AKR1C3 expression
Received: November 11, 2019; Accepted: March 17, 2020
ABSTRACT
The retinoic acid-related orphan receptors alpha (RORa) are members of the steroid/thyroid nuclear receptor super-family and core components of the circadian timing system. In the present study, we continue to investigate the role of RORas in human breast cancer. Assays using the RORa response element (RORE)-tk-luciferase reporter demonstrate the functionality of the RORa1 in MCF-7 breast cancer cells and that over-expression of RORa1 stimulates MCF-7 human breast cancer cell proliferation. Genomic analysis revealed that RORα1 over-expression regulated the transcription of numerous genes in MCF-7 breast cancer cells including increasing the expression of connexin 43 (CX43), aldo-keto reductases 1C1 (AKR1C1), and AKR1C3. Furthermore, administration of the pineal hormone melatonin represses RORa1 induction of CX43, AKR1C1, and AKR1C3 in MCF-7 cells. AKR1C3 has been reported to impact in intra-tumoral production of androgens and estrogens and thus, might promote Tamoxifen resistance in breast cancer. Over-expression of RORa1 and subsequently AKR1C3 does promote Tamoxifen resistance, which can be inhibited by melatonin administration.
Key Words: Retinoic acid-related orphan receptor alpha 1, breast cancer, AKR1C3, melatonin.
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1. INTRODUCTION
A number of steroid/thyroid hormone nuclear receptor superfamily including the estrogen receptor (ER), progesterone receptor (PR), and androgen receptor (AR) influence the development and progression of breast cancer (1-3). The retinoic acid-related orphan receptors (RORs) are nuclear orphan receptors that are expressed in human breast cancer (4). There are 4 RORα splice variants [1, 2, 3 and 4] from the same gene located on chromosome 15q21 in humans and chromosome 9 in mice that differ by small sequences in their N-terminal domains (5-7). The RORas bind to their corresponding DNA response elements primarily as monomers (5). The RORa response element (RORE) consists of a tandem repeat of the PuGGTCA motif, spaced by two nucleotides, and proceeded by a 6-bp AT-rich sequence, referred to as Rev-DR2 site. The RORa1 has also been shown to bind as a homodimer to an RORE in the promoter region of the circadian clock gene Rev-erba (8). The RORαs appear to be widely expressed and have been detected by us and others at both the mRNA and protein level in many tissues and even human breast cancer (4, 9-11). By identification of RORE motifs in their regulatory region, several tumor-related genes, including N-Myc, laminin B1, p21, BMAL1, REV-ERBα, NM23, and Aromatase have been designated as RORα responsive genes, suggesting that RORas may play a role in the progression of certain neoplasias (11-16). We and others have reported that RORas cross-talk with other steroid nuclear receptors including RARa and ERa in breast cancer cells (17, 18). The RORs are also core circadian clock genes that regulate the expression of the basic helix-loop-helix gene Brain Muscle and Arnt Protein 2 (BMAL2) of the positive limb of the circadian clock that dimerizes with Circadian Locomoter Clock Kaput (CLOCK) to modulate the expression of E-box genes including Cryptochrome, Period, and even MYC genes (19). These and other studies demonstrate that disruption of peripheral oscillator (clock) genes in the breast, are strongly associated with cancer (20).
The RORas were initially classified as orphan receptors with no defined ligands, however, using X-ray crystallography, Kallen et al. (21) identified cholesterol and its derivatives as potential ligands of RORa, while Kane and Means (22) demonstrated that calcium/calmodulin-dependent kinase IV (CaMKIV) enhanced RORa transactivation. It was initially reported by Becker-Andre et al. (23) that circadian hormone, melatonin, a known inhibitor of mammary tumorigenesis (24), was a ligand for the RORas, however this report has been retracted as melatonin was not confirmed as a ligand for these receptors (25). We have reported that RORa receptors are constitutively active in MCF-7 breast tumor cells and their transcriptional activity can be inhibited/suppressed by melatonin in MCF-7 human breast cancer cells in a ligand-independent manner (4).
Melatonin (N-acetyl-5-methoxytryptamine) is the major hormonal product of the pineal gland that regulates circadian rhythms, reproduction in seasonally breeding mammals, and has been demonstrated to have anti-tumorigenic effects on breast cancer (26). Studies with the ERa-positive MCF-7 human breast cancer cell line demonstrated that physiological concentrations of melatonin significantly inhibit breast tumor cell proliferation and induce a more differentiated phenotype (24). Furthermore, we have reported that melatonin can modulate various nuclear receptors, including inhibiting ERα, GR, and RORa transactivation, while promoting RAR, RXR, and VDR transcriptional activity in breast cancer cells (26, 27).
In the present study, we demonstrate that expression of RORa1 promotes the proliferation of ERa-positive MCF-7 cells, and induces the expression of numerous genes including CX43, AKR1C1, and AKR1C3. Finally, we show that MCF-7 cells over-expressing RORa1 with subsequent induction of AKR1C3 protein expression show resistance to the anti-estrogen tamoxifen which can be reversed by the administration of melatonin.
2. MATERIALS AND METHODS
2.1. Materials.
All chemicals and tissue culture reagents were purchased from Sigma Chemical Co. (St. Louis, MO). RPMI-1640 medium, fetal bovine serum (FBS), and lipofectamine were purchased from Gibco BRL (Gaithersburg, MD). TRIzol, the pcDNA3.1/Zeo (+) plasmid and zeocin were purchased from Invitrogen (Carlsbad, CA). Molecular biology enzymes were purchased from Promega (Madison, WI) and RORa primers were synthesized by integrated DNA technologies, Inc. (Coralville, IA). The chemiluminescence reagents were purchased from Amersham Pharmacia Biotech (Arlington Heights, IL) and Kodak X-Omat AR films were purchased from Eastman Kodak Co. (Rochester NY). The pCMV-b-galactosidase plasmid was provided by Dr. Jean Lokeyer (New Orleans, LA); the pCMX-RORa expression vectors and the ROREa23TKLUC reporter plasmid were kindly provided by Dr. Vincent Giguere from McGill University (Montreal, Quebec, Canada).
2.2. Cell lines and breast tumors.
MCF-7 ERa-positive breast cancer cells were purchased from American Type Culture Collection (ATCC) (Manassas, VA), expanded and frozen in liquid nitrogen. MCF-7 cells below passage 20 were employed for these studies. Breast cancer cell lines were routinely maintained at 37° C in a humidified atmosphere of 5% CO2 and 95% air in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS), 2 mM glutamine, 50 mM MEM non-essential amino acids, 1 mM sodium pyruvate and 10 mM BME.
2.3. Expression vector and stable transfection.
The plasmid pCMX-RORa1 was digested with the restriction enzymes KpnI and BamHI to obtain the full-length RORa1 cDNA which as then cloned into the KpnI-BamHI sites of the pcDNA3.1/Zeo (+) expression vector to generate the expression construct pcDNA3.1-RORa1, that was stably transfected into MCF-7 cells. The pcDNA3.1/Zeo (+) (pcDNA3.1-vt) vector was used to transfect MCF-7 cells, which were then used as controls in studies of RORa1-transfected cells. Details regarding stable transfection and RORa1 expression can be found in the supplemental materials.
2.4. Growth studies.
Vector-transfected and RORa1-transfected MCF-7 human breast cancer cells were plated onto 6-well plates at a density of 5 ´ 104 cells/well in RPMI-1640 medium supplemented with 10% FBS, in triplicate. On Days 1, 3, 5 and 7, cells were harvested in phosphate-buffered saline (PBS) solution containing 0.1% EDTA and passed through a 21-gauge needle to generate a single cell suspension. Cell numbers were determined by counting on a hemocytometer using the trypan blue dye exclusion method.
2.5. Tamoxifen resistance growth studies.
MCF-7 vector (control) and MCF-7 RORa1 expressing cells were seeded at the density of 10 x 104 cells/well into 35 mm 6-well plates. After 24 h cells were administered 4-hydroxy-tamoxifen (4-OHT) or melatonin at concentrations of 5 mM and 10 nM, respectively, for 96 h (4 days). Before staining with trypan blue to test for cell viability, cells were dislodged with trypsin and rinsed with PBS. Viable and dead cells were counted on the hemocytometer using a microscope.
2.6 Transient transfection and luciferase transcriptional reporter assays.
Parental MCF-7 cells were plated onto 35 mm 6-well plates at a density of 2 ´ 105 cells/well in RPMI-1640 medium supplemented with 10% FBS. After 24 h of serum-starvation, cells were transfected in serum-free RPMI-1640 medium for 6 h with 2 mg of the ROREa23-tk-LUC reporter construct or 1 mg of pCMVb control plasmid per well, using 6 ml of lipofectamine (Life Technologies, Inc.). Luciferase was measured using a Model 2010 luminometer (Analytical Luminescence) and luminescence was normalized to both the protein concentration and the b-galactosidase activity, as previously described (28).
2.7 Western blot analysis.
The concentrations of total cellular protein in extracts from cell line lysates were determined using the Bio-Rad protein assay (Bio-Rad, Hercules, CA, USA). Total protein (50 μg per sample) from cell line lysates was electrophorectically separated on 10% SDS polyacrylamide gels and electro-blotted onto a Hybond membrane. After incubation with 5% nonfat milk in Tris-buffered saline containing 0.1% Tween-20, the blots were probed with antibodies against RORa (Santa Cruz Biotechnology, Inc. Santa Cruz, CA), AKR1C1, AKR1C3 (Abcam, Cambridge, MA), and b-actin (Cell Signaling Technology). The same blots were subsequently stripped and re-probed with a b-actin antibody as an internal loading control (Cell Signaling Technology Inc.). Band intensity was quantified using ImageJ v1.50e (NIH, Bethesda MD) to normalize to internal control.
2.8 cDNA microarray analysis.
Total RNA from the MCF-vt, MCF-ROR#3, and MCF-ROR#8 cell clones was isolated by RNeasy Mini kits (Qiagen, Valencia, CA) following the manufacturer’s instructions. The cDNA microarray analysis was performed by the Tulane University Gene Therapy Center employing Affymetrix Gene Chip microarray (Affymetrix, Santa Clara, CA). Technical and experimental details are described in the Supplemental Materials. In brief, Twenty-five micrograms of biotinylated cRNA was fragmented and hybridized to Affymetrix HG-U133A array, which contains 22,215 oligonucleotides representing 15,003 human genes. The array was stained with streptavidin-phycoerythrin (Molecular Probes, Eugene, OR) and the staining signal was amplified by biotinylated anti-streptavidin (Vector Laboratories, Burlingame, CA) and by a second staining with streptavidin-phycoerythrin, and then scanned on a Hewlett-Packard Gene Array Scanner. The expression data were analyzed using Microarray Suite 5.0 (MAS5.0).
2.9. Northern blot analysis of Cx43 mRNA expression.
Fifty micrograms of total cellular RNA isolated from RORa1-over expressing clones (#3 and #8), pcDNA3.1 vector-transfected, and parental MCF-7 cells was separated by electrophoresis on a 1% agarose gel containing 2.2 M formaldehyde and transferred onto Hybond-XL membranes, as previously described (23, 28). The membranes were then hybridized with full-length a-[32P]–labeled RORa1 or CX43 probes purchased from American Type Culture Collection (ATCC). The membranes were then washed and exposed to Kodak X-Omat AR film.
2.10. Quantitative real time PCR (qPCR).
qPCR was performed using an iCycler iQ apparatus (Bio-Rad) associated with the iCycler Optical System Interface software (version 2.3; Bio-Rad) as we described previously (28). The sequences of primers used are shown in Supplementary Table 1. For the analysis of AKR1C1 and AKR1C3 mRNA expession, qPCR analysis was performed in triplicate. The differences in the expression of all the gene transcripts were normalized with respect to GAPDH expression. The relative level of expression was calculated with the formula 2−Δct.
2.11. Statistical analysis.
Statistical difference in cell proliferation and RORa transcriptional activity was determined by two-way analysis of variance (ANOVA) followed by a Newman-Kuels post-hoc test. P-values < 0.05 were considered statistically significant.
3. RESULTS
3.1. Stable expression of RORa1 receptor in MCF-7 human breast cancer cells lines.
RORa1 was expressed at high levels in ERa-positive MCF-7 human breast cancer cells following stable transfection with the pcDNA3.1-RORa1 construct. Nine clones of MCF-7 breast cancer cells were characterized for RORa1 expression. Two clones, MCF-ROR#3 and MCF-ROR#8, which exhibited the greatest levels of RORa1 mRNA (Figure 1A) and protein (Figure 1B) expression levels were chosen for further analysis. To confirm the functionality of the RORa1 receptor in these cells, RORE luciferase assays were conducted. These assays showed that the RORa1 over-expressing cell lines possessed significantly greater RORa transcriptional activity than their parental or vector transfected counterparts. As illustrated in Figure 1C, the relative luciferase activities increased 2 to 3-fold in RORa1 over-expressing MCF-7 cells in comparison with their corresponding vector-transfected control cells. These data demonstrate that expressed recombinant RORa1 receptors are functional in MCF-7 cells.
Fig. 1. Northern and Western blot analyses of RORa in MCF-7 human breast cancer cells and RORa1 transactivation in RORa1-transfected ERa-positive MCF-7 breast cancer cells.
In the Northern blot analysis (A), fifty micrograms of total cellular RNA from different RORa1-transfected cell clones (MCF-ROR#3, MCF-ROR#8), pcDNA3.1 vector-transfected (MCF-vt) or MCF-7 parental cells (MCF-p) were separated on a 1% denaturing agarose gel and transferred to Hybond-XL membranes. The RORa1 and 36B4, loading control, mRNA signals were detected on the blot by probing with the RORa1 and 36B4 cDNAs. In the Western blot analysis (B), fifty micrograms of cellular protein from each cell clone was subjected to a 12% SDS-PAGE and transferred to nitrocellulose paper. Expression of RORa and b-actin were detected by ECL reagents following a sequential incubation with a pan RORa and b-actin antibodies. (C) RORa1 transactivation ROREa23-TKLUC reporter assays in ERa-positive MCF-7 breast cancer cells. Transient transfection with the ROREa23-TKLU reporter construct was conducted on different RORa1-over-expressing MCF-7 cell clones (MCF-ROR#3, MCF-ROR#8), pcDNA3.1 vector-transfected (MCF-vt), or MCF-7 parental cells (MCF-p). Cells were harvested 24 h following transfection and subjected to luciferase assays. The transfection efficiency was normalized by b-galactosidase activities. (* P< 0.05 vs. MCF-p or MCF-vt, n=3).
3.2. Effects of RORa1 on MCF-7 human breast cancer cell proliferation.
The role of the RORa1 receptor on human breast cancer cell proliferation was determined by comparing the growth rates between RORa1 over-expressing cells and vector-transfected control cells. RORa1 over-expressing MCF-7 cells grew significantly faster (p < 0.05) than their corresponding parental and vector-transfected cells. As illustrated in Figure 2, the cell number in the MCF-ROR#3 and MCF-ROR#8 clones increased by 150% and 166%, respectively, in comparison with vector-transfected cells after 7 days of culture.
Fig. 2. Mitogenic effect of RORa1 in ERa-positive MCF-7 cells.
Different RORa1 over-expressing MCF-7 cell clones (MCF-ROR#3, MCF-ROR#8), vector-transfected (MCF-vt) or MCF-7 parental cells (MCF-p) were plated onto 6-well plates at a density of 5 ´ 104 cells/well in RPMI-1640 medium supplemented with 10% FBS and the cell numbers were determined by trypan blue dye exclusion method on days 1, 3, 5 and 7 following plating. (* P< 0.05 vs. MCF-p or MCF-vt at the same time point, n=3).
3. Genes modulated by RORa1 overexpression in MCF-7 cells.
To explore the function of RORa1 in human breast cancer we conducted a cDNA microarray analysis to compare the gene expression profiles of MCF-7 cells transfected with and over-expressing RORa1 vs. the vector-transfected cells. In this study, Human U133A genomic gene chips, which contain 22, 215 oligonucleotides representing 15,003 human genes, were used. To increase the reliability of the results, we examined two RORa1 over-expressing MCF-7 clones (#3 and #8) in this study. As shown in Table 1, the cDNA microarray results revealed 38 genes, whose expression was altered (either up- or down-regulated) significantly and consistently between two RORa1 over-expressing MCF-7 cell clones versus the control cell RNA samples. Twenty-three genes were elevated and 15 genes were down regulated in the RORa1 over expressing cell clones compared to the control cells. Genes regulated by RORa1 were grouped into seven functional categories: 1. cell proliferation and cell cycle, 2. apoptosis, 3. invasion and metastasis, 4. cell adhesion, 5. signaling transduction molecules and transcriptional factors, 6. calcium signaling, and 7. lipid metabolism as shown in Table 1. Our results suggest that RORa1 is involved in a variety of cellular activities in breast cancer cells. Of the genes induced by RORa1 some are also reported to be estrogen regulated, including; insulin-like growth factor binding protein 3, transforming growth factor alpha and beta, CX43, and bone morphogenetic protein 7 genes.
To confirm that RORa1 regulates the expression of these genes, we chose to examine connexin 43 which were increased by 13.9-fold, as well as AKR1C1 and AKR1C3 genes, also known as dihydrodiol dehydrogenases 1 and 3, which RORa1 induced by 19- and 25-fold, respectively. Interestingly, AKR1C3 has been implicated in the progression of prostate and breast cancers and is reported to be involved in promoting drug resistance and in intra-tumoral endocrine production in these cancers (29).
3.3. Over-expression of RORα1 up-regulates the expression of CX43 mRNA.
It is reported that elevated expression of CX43 is involved in tumorigenesis, tumor cell migration, and metastasis in breast cancer (30). Recent studies support the therapeutic potential of targeting CX43 as a treatment in breast cancer (31, 32). Thus, we decided to determine if RORa1 over-expression could induce CX43 expression in MCF-7 breast cancer cells. As shown in Figure 3, Northern blot analysis of CX43 shows CX43 mRNA expression is increased by approximately 37-fold in MCF-7 cells stably over-expressing RORa1.
Fig. 3. RORa1 over-expression up regulates the expression of Cx43 mRNA.
Cx43 mRNA expression measured by Northern blot. Fifty micrograms of total RNA isolated from parental (MCF-p), pCDNA3.1 vector-transfected (MCF-vt), and RORa1-overexpressing MCF-7 cell clones (MCF-ROR#3 and MCF-ROR#8) were subjected to 1% MOPS/formaldehyde agarose gel and transferred to Hybond-XL membranes. Full-length human Cx43 cDNA was radiolabeled and used as probe to hybridize with membranes. The blots were stripped and re-probed with 36B4 cDNA, which is a loading control.
3.4. Over-expression of RORα1 up-regulates AKR1C1 and AKR1C3 mRNA and protein expression in MCF-7 breast cancer cells which can be suppressed by treatment with melatonin.
To confirm the effect of RORα1 on regulating AKR1C1 and AKR1C3 mRNA and protein expression in MCF-7 cells and to define if melatonin inhibition of RORa1 transcriptional activity might repress AKR1C1 and AKR1C3 expression, we employed both real time PCR (qPCR) and Western blot analysis. As shown in figure 4 over-expression of RORα1 in MCF-7 cells increase the expression of AKR1C1 mRNA (Figure 4A) and protein (Fig.4B/C), which was significantly inhibited by 72% and 54%, respectively, in response to administration of physiologic levels (1 nM) of melatonin. Figure 5 shows that RORa1 over-expression greatly up regulated the expression AKR1C3 mRNA (Figure 5A) and protein (Figure 5B/C) in MCF-7 cells and the administration of physiologic levels of melatonin (1 nM) significantly suppressed AKR1C3 mRNA and protein by 78% and 91%, respectively.
Fig. 4. Effects of melatonin on RORα1 over-expression induction of AKR1C1 mRNA and protein expression in MCF-7 cells.
(A) AKR1C1 mRNA expression was measured by qPCR in parental MCF-7 cells, vector transfected (Vect.) MCF-7 cells, MCF-7 cells transiently transfected with pcDNA3.1-RORa1, and RORa1 transfected MCF-7 cells treated with 10-9 M melatonin (RORa1+MLT) for 48 hours. Cells were collected and lysed and 5 μg total mRNA was used for qPCR analysis of AKR1C1 mRNA expression using primers and described in mateirals in methods. AKR1C1 protein expression (B) in the same groups above after total protein was extracted and determined by Western blot analyisis using a rabbit anti-AKR1C1 antibody at 1: 1000 and anti-GAPDH antibody at 1:750, as described in “Materials and Methods”. Graphical data (C) represents the mean of 3 independent experiments.
Fig. 5. Effects of melatonin on RORα1 over-expression induction of AKR131 mRNA and protein expression in MCF-7 cells.
(A) AKR1C3 mRNA expression was measured by qPCR in parental MCF-7 cells, Vector transfected (Vect.) MCF-7 cells, MCF-7 cells transiently transfected with pcDNA3.1-RORa1, and RORa1 transfected MCF-7 cells treated with 10-9 M melatonin (RORa1+MLT) for 48 hours. Cells were collected and lysed and 5 ug total mRNA was used for qPCR analysis of AKR1C3 mRNA expression using primers and described in mateirals in methods. AKR1C3 protein expression (B) was determined in the same groups above after total protein was extracted was determined by Western blot analyisis using a rabbit anti-AKR1C3 antibody at 1: 1000 and anti-GAPDH antibody at 1:750, as described in “Materials and Methods”. Graphical data (C) represents the mean of 3 independent experiments.
3.5. Melatonin suppresses RORa1 transcriptional activity in MCF-7 breast cancer cells.
We previously reported that physiologic concentrations of melatonin inhibited RORa1 transcriptional activity to suppress the proliferation of MCF-7 human breast cancer cells (4, 28). In the present study, RORα1 over-expression significantly stimulated MCF-7 cell growth. To test whether the inhibitory effect of melatonin on MCF-7 proliferation is due to its repression of RORα1 transcriptional activity, we used transcriptional reporter assays to evaluate the effect of melatonin on the transactivation of RORα1. As shown in Figure 6, physiologic concentrations of melatonin (10-9 M and 10-8 M) significantly repressed the transactivation of RORα1 as measured in a RORE-Luc reporter assay.
Fig. 6. Melatonin represses the transactivation of RORα1.
Two mg of the ROREa23-TKLUC reporter construct and 1 mg of pCMVb control plasmid per well were transfected into MCF-7 cells by 6 mg of lipofectamine for 6 h. Following transfection, cells were treated with melatonin (10-11 M to 10-6 M) or diluent ethanol control (Med) for 24 h. The RORa transcriptional activities were determined by luciferase assays and the transfection efficiency was normalized by b-galactasidase assay. (* P< 0.05 vs. ethanol control group, n=3).
3.6. RORa1 expression drive tamoxifen resistance in MCF-7 breast cancer cells.
To determine if elevated expression of RORa1 contributes to tamoxifen resistance we examined the response of MCF-7RORa1 cells (clone #3) to 4-OH TAM in the presence or absence of 17-b estradiol (E2) and melatonin. As shown in Figure 7A, administration of E2 to MCF-7RORa1 cells induced as significant 41% increase in cell number, while treatment with 4-OH TAM did not significantly decrease cell proliferation after 4 days of treatment. However, treatment of RORa1 expressing cells with physiologic levels of melatonin significantly diminished cell proliferation by 27% and treatment of RORa1 expressing cells with the combination of 4-OH TAM and melatonin blocked cell proliferation and promoted a decrease in cell number. As shown in Figure 7B, Western blot analysis showed strong AKR1C3 protein expression in RORa1 expressing cells that was further increased when cells were treated with E2. Conversely, AKR1C3 levels were diminished in cells treated with melatonin and almost completely abolished in the presence of 4-OH TAM and melatonin.
Fig. 7. Effects of melatonin administration on RORa1-induced AKR1C3 expression and RORa1/ARK1C3-mediated tamoxifen resistance in MCF-7 breast cancer cells.
(A) MCF-7 breast cancer cells were plated at a density of 10 x 104 cells per ml in six-well plates and 5 hours after seeding, cells were treated with diluent (0.01% ethanolic cell culture media), E2 (10 nM), 4-OH TAM (4.5 mM), MLT (10 nM), or TAM + MLT for 96 h, (4 days). On specific days total and viable cells counted on a haemocytometer. n = 3 independent studies, and a = p<0.05 difference vs. RORa1, b = p<0.05 vs. RORa1 and RORa1 + TAM, and c = p< 0.005 vs. RORa1 and p<0.05 vs. RORa1 + TAM. (B) Expression of AKR1C3 was determined by Western blot analysis as described in materials and methods from cells harvested after 4 days in treatments described above. Densitometric levels of AKR1C3 protein expressed in each treatment group is noted, with the control RORa1 group normalized to 1.0.
4. DISCUSSION
We and others have reported that the RORas are constitutively active and their transcriptional activity in human breast cancer cells can be induced by cholesterol but repressed by melatonin (4, 13-15). In addition, Kane and Means (22) demonstrated that CaMKIV enhances RORa1 transactivation via phosphorylation of co-activators, such as CBP/p300 (33).
To determine the role of RORas in human breast cancer cell proliferation, we developed clones of ERa-positive (MCF-7) breast cancer cells that are stably transfected with and constitutively over-express the RORa1. Comparison of the growth rates of RORa1-transfected MCF-7 cells with vector-transfected and parental controls, demonstrates significantly increased proliferation (Figure 2) in RORa1 expressing MCF-7 breast cancer cells. The RORas have been reported to cross-talk with other steroid hormone receptors, such as TR and RARa (16-17) and we have reported that they cross-talk with the ERa (28), all of which play important roles in promoting breast cancer cell proliferation. The observation that response elements for RORa are present in the promoter region of various tumor-related genes, such as N-MYC, P21WAF1/CIP1, NM23, and aromatase (CYP19A), support RORa’s role in breast tumor growth and metastasis (11-14, 16). Based on these studies and our earlier reports, we conclude that RORas are expressed in primary breast tumor and that RORa1 play an important role in stimulating the proliferation of ERa-positive breast cancer.
Our cDNA microarray results (Table 2) revealed that the expression of 38 genes was significantly altered in two MCF-7 RORa1 over-expressing cell clones, compared to vector-transfected controls. Five of these genes are E2-regulated, including insulin-like growth factor binding protein 3 (IGFBP3) (34), transforming growth factor alpha (TGFa) (35), transforming growth factor beta (TGFb) (36), CX43(32), and bone morphogenetic protein 7 (BMP7) (37). These genes are up regulated by E2 and by RORa1 over-expression and these data are in agreement with our earlier reports that RORa cross-talks and augments ligand-mediated ERa transcriptional activity in MCF-7 cells (28). At the present time however, it is still not clear which genes are regulated directly by RORa1 over-expression and which are regulated via RORa1/ERa cross talk.
Review of the literature shows that RORa1 regulated genes impact variety of cellular signaling pathways to regulate various cellular functions including cell proliferation and cancer. We were able to group RORa1 regulated genes into seven functional categories, including, cell proliferation and cell cycle, apoptosis, invasion and metastasis, cell adhesion, signal transduction molecules and transcriptional factors, calcium signaling, and lipid metabolism (Table 1). For example, TGFa and TGFb are well-known growth factors that play important roles in regulation of breast cancer cell proliferation, with TGFa promoting cell proliferation, but TGFb in many cases decreasing proliferation (38). As shown in Table 1, RORa1 over-expression up regulated TGFa but down-regulated TGFb expression in MCF-7 cells, both of which play important roles in mediating E2’s mitogenic effect on human breast cancer. As RORa/ERa cross-talk (4, 28), it is possible that the mitogenic effect of RORa1 is mediated via its regulation of TGFa and TGFb alone or in concert with ERa. The expression of IGFBP3, an known inhibitor of breast cancer proliferation (34), was also induced by RORa1. Conversely, fibroblast growth factor 2 receptor (FGFR-2), which is over-expressed in many breast cancers and mediates cell proliferation (39, 40), was down-regulated in response to RORa1 expression. Furthermore, RORa1 over-expression also induced the expression of v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 epidermal growth factor tyrosine kinase receptor 3 (ERBB3) that modulates breast cancer activities by heterodimerizing with ErbB2 to activate survival and mitogenic pathways in breast cancer cells (41).
Although it is clear from the literature and our cDNA microarray data above that RORa1 expression can induce the expression of numerous genes known to be involved in breast cancer such as IGFBP, TGFb, CX43 and BMP7, we chose to focus our efforts in understanding if RORa1 regulated AKRC1 and AKR1C3 mRNA expression in MCF-7 breast cancer cells and if AKR1C3 elevated expression and its’ impact on aromatase activity might be tied to the development of Tamoxifen resistance in these cells.
It has been reported that RORα1 can regulate the expression of genes encoding several phase I and phase II metabolic enzymes (42), such as cytochrome P450 enzymes and AKR1Cs (43, 44). The ARK1Cs, also termed dihydrodiol dehydrogenases, are phase 1 drug-metabolizing enzymes involved in the steroid biosynthesis and prostaglandin metabolism (45). As shown in Table 1, RORa1 over-expression induced the expression of AKR1C1 and AKR1C3 mRNA by 19- and 25-fold respectively, (clone #3) in MCF-7 breast cancer cells. Furthermore, RORα1 over-expression also increased AKR1C1 and AKR1C3 protein expression in MCF-7 breast cancer cells and that administration of the circadian hormone melatonin (1nM) significantly repressed AKR1C1 and AKR1C3 protein levels. The up regulation of AKR1C3 expression in response to RORa1 expression suggests that RORa1 may significantly impact the progression of luminal A breast cancer as AKR1C3 has been shown to play a central role in intratumoral endocrine production of testosterone and E2 in both prostate and breast tumor cells, driving the conversion androstenedione to testosterone and esterone to E2 (44). Elevated testosterone is a key precursor for the generation of E2 by Aromatase (CYP19A1). Given the report by Odawara et al. (16) that RORa can induce the expression of Aromatase, it would appear that RORas may play a critical role in driving E2-mediated breast cancer progression. Furthermore, as luminal A breast cancer cells typically express both androgen receptor (AR) and ERa (46) the elevated intratumoral levels of testosterone and E2 in response to increased AKR1C3 expression/activity could promote breast tumor growth via activation of not only ERa but also AR.
Melatonin, synthesized and secreted at night by the pineal gland in response to darkness, has been reported to inhibit the proliferation of ERα-positive MCF-7 human breast cancer cells (24). Melatonin has been shown to modulate the transcriptional activity of various nuclear receptors, inhibiting the transcriptional activity of the ERα, glucocorticoid receptor (GR), while enhancing the transcriptional activation of the retinoic acid receptor alpha (RARα) and Vitamin D receptor in human breast cancer cells (26, 27). RORαs were originally reported by Wiesenberg and Carlberg to be nuclear melatonin receptors, but the direct binding of melatonin to these receptors could not be repeated and thus, the report has been retracted (47). Therefore, ROR receptors, including the RORa1 receptor, are not melatonin receptors, as melatonin does not bind to them to initiate or inhibit their transcriptional activity (26). Although, our previous studies demonstrate that melatonin, when administered at physiologic (nM) concentrations decreased RORα DNA binding activity (4, 28) and transcriptional activity suppressing clock gene BMAL1 expression in MCF-7 breast cancer cells (20), we believe this is most likely mediated by phosphor-inhibition of RORa1, similar to what we have reported with the ERa in breast cancer. The current study further confirms that RORa1 transcriptional activity can be suppressed by melatonin to significantly suppress RORα1’s inductive effect on AKR1C1 and AKR1C3 mRNA and protein expression.
AKR1C3 also converts prostaglandin (PG) H2 to PGF2α and PGD2 to 9α,11β-PGF2 (48). The PGF2 isomers bind to the F prostanoid receptor and induce MAPK signaling cascades that promote cell proliferation (49). Furthermore, by removing PGD2, AKR1C3 inhibits the formation of the anti-proliferative and anti-inflammatory prostaglandin 15-deoxy-Δ(12, 14) -PGJ2 (15dPGJ2) that promotes anti-proliferative effects on breast cancer cells (50). Thus, the mitogenic actions of RORa1 we observed may not only be through enhancing AR and ERα signaling but possibly by its regulation of the prostaglandin pathway to induce expression mitogenic 9α,11β-PGF2, while inhibiting the production of the anti-proliferative 15dPGJ2.
These effects of melatonin on RORα1 transcriptional activity are likely mediated via post-translational modification of RORa1 to repress its DNA-binding activity, but possibly through other mechanisms including modulation of key co-regulators to profoundly impact breast cancer progression. Melatonin, by inhibiting RORα expression and/or transcription activity and the suppression of AKR1C1 and ARK1C3 expression may impact the regulation of aromatase and intra-tumoral endocrinology in breast cancer, and thus, could have promising clinical applications for adjunctive treatment of breast cancer patients which display resistance to endocrine therapies.
ACKNOWLEDGEMENTS
This work has been generously supported by a National Institutes of Health-National Cancer Institute R56 grant (1 R56 CA193518-01), SMH and DEB Principal Investigators, entitled "Circadian Disruption by Light at Night Induces Intrinsic Tamoxifen Resistant Breast Cancer" and by funds from the Edmond and Lily Safra Chair for Breast Cancer Research and the Tulane Center for Circadian Biology.
We gratefully thank Suzanne Fuqua and her team at Baylor College of Medicine in Houston for contributing breast tumors used in this study and Dr. Vincent Giguere for the pCMX-RORa expression vectors and the ROREa23-TKLUC reporter construct.
AUTHORSHIP
The following authors contributed to concept/design (SMH, DEB, SX), acquisition of data (SX, CD, RTD, Ly), data analysis/interpretation, drafting of the manuscript (SX, SMH, DEB, RTD, SMH), critical revision of the manuscript (SX, SMH RTD, DEB, TF), and approval of the article (SX, CD,LY, RD, DEB, TF, SMH).
CONFLICT OF INTEREST
The authors disclose no potential conflicts of interest.
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