|Home | About | Journals | Submit | Contact Us | Français|
Estrogen and growth factors play a major role in uterine leiomyoma (UtLM) growth possibly through interactions of receptor tyrosine kinases (RTKs) and estrogen receptor-alpha (ERα) signaling. We determined the genomic and nongenomic effects of 17β-estradiol (E2) on IGF-IR/MAPKp44/42 signaling and gene expression in human UtLM cells with intact or silenced IGF-IR. Analysis by RT2 Profiler PCR-array showed genes involved in IGF-IR/MAPK signaling were upregulated in UtLM cells by E2 including cyclin D kinases, MAPKs, and MAPK kinases; RTK signaling mediator, GRB2; transcriptional factors ELK1 and E2F1; CCNB2 involved in cell cycle progression, proliferation, and survival; and COL1A1 associated with collagen synthesis. Silencing (si)IGF-IR attenuated the above effects and resulted in upregulation of different genes, such as transcriptional factor ETS2; the tyrosine kinase receptor, EGFR; and DLK1 involved in fibrosis. E2 rapidly activated IGF-IR/MAPKp44/42 signaling nongenomically and induced phosphorylation of ERα at ser118 in cells with a functional IGF-IR versus those without. E2 also upregulated IGF-I gene and protein expression through a prolonged genomic event. These results suggest a pivotal role of IGF-IR and possibly other RTKs in mediating genomic and nongenomic hormone receptor interactions and signaling in fibroids and provide novel genes and targets for future intervention and prevention strategies.
Although the exact etiology of uterine leiomyomas (fibroids) is unknown, the fact that they develop during the reproductive years and regress after menopause indicates that they are hormonally regulated [1–3]. The important role of estrogen in the promotion of uterine leiomyoma growth has been well supported through clinical and biological studies [4–6]. However, the overexpression of growth factors and their receptors, such as the type I insulin-like growth factor (IGF-I) and IGF-I receptor (IGF-IR), shows that sex steroids are not the only modulators of leiomyoma cell proliferation and exuberant extracellular matrix formation observed in many fibroids [2, 7–9]. Studies have revealed that IGF-I expression is most abundant in leiomyomas during the proliferative phase of the menstrual cycle [10, 11]. The expression of IGF-I mRNA increases in leiomyomas, and estrogen receptor alpha (ERα) mRNA is positively correlated with IGF-I mRNA levels, which implies as we and others have shown that estrogen upregulates the gene encoding IGF-I through ERα in leiomyoma tissue and cells [10–13].
The accumulated data from extensive studies of breast cancer, another disease that is often hormonally regulated, have shown that the interactions of estrogen/ERα with IGF-IR/MAPK signaling can occur at different molecular levels [14, 15]. It is known that 17β-estradiol (E2) primarily acts through cognate nuclear ERα leading to regulation of gene expression, which has traditionally been defined as genomic estrogen activity. It has also been reported that many of the E2-responsive genes are key signaling molecules that participate in IGF-IR signaling . Alternatively, a cell membrane-associated form of ERα has been reported to couple with and activate IGF-IR through phosphorylated Shc [17, 18], thereby triggering rapid nongenomic effects through transactivation of the IGF-IR. More recently, our and other studies have shown that E2 and environmental phytoestrogens (genistein) can induce E2-dependent signals prompting major biological responses such as gene expression and human uterine leiomyoma (UtLM) cell proliferation [12, 13, 19]. In addition, E2 is able to upregulate IGF-I gene expression [12, 16, 20] and increases IGF-I synthesis, which leads to activation of IGF-IRβ and MAPKp44/42 [19, 21]. Increased activated MAPKp44/42 with enhanced phosphorylation of ERα-phospho-ser118 has been observed in uterine leiomyomas, but not in uterine smooth muscle tissue .
All of these studies suggest that the effect of growth promoter IGF-I and its receptor IGF-IR and downstream target MAPK-related genes may be regulated by estrogen at genomic and nongenomic levels, and the interaction of ERα and IGF-IR/MAPKp44/42 may play a pivotal role in fibroid tumorigenesis, but the exact mechanism(s) of how this all occurs is unknown. There are several questions that need to be addressed such as (1) how does estrogen regulate MAPK related gene expression through IGF-I and the IGF-IR/MAPKp44/42 pathway; (2) what is the role of E2 in the activation of IGF-IR leading to MAPKp44/42 phosphorylation of ERα at the serine 118 site; (3) which specific mediators of the signaling pathways are involved in the interactions of IGF-I/IGF-IR and ERα in uterine leiomyomas. In this study, we explored the regulatory effects of E2 on intermediates of the IGF-IR/MAPK signaling cascade and related gene expression in UtLM cells and identified new genomic mediators involved in fibroid growth and development by genomic array profiling. We also determined if the effects of E2 were through genomic and nongenomic interactions of IGF-I, IGF-IR, ERαser118, and MAPKp44/42 by silencing IGF-IR followed by western blotting, immunoprecipitation, and immunofluorescence microscopy. To our knowledge, this is the first study in human leiomyoma research focusing on determining the profile of E2-mediated IGF-IR/MAPK-related genes and exploring the genomic and nongenomic interactions of ERα/IGF-IR/MAPKp44/42 pathways.
UtLM cells (GM10964) were purchased from Coriell Institute for Medical Research (Camden, NJ, USA) and maintained in MEM (Gibco Life Technologies, Grand Island, NY, USA) with supplements at 37°C, with 95% humidity, and 5% carbon dioxide as previously described .
The RT2 Profiler PCR Array System (MAP Kinase Signaling Pathway PCR Array, PAHS-061) from SABiosciences (Frederick, MD, USA) was used to analyze gene expression related to the MAPK signaling pathway in UtLM cells in response to E2 (Sigma, St. Louis, MO, USA) treatment, with and without IGF-IR silencing (siIGF-IR). The transfection of siIGF-IR oligo targeting human IGF-IR gene (5′ to 3′ CGUCUUCCAUAGAAAGAGAtt) and a control scrambled siRNA (siScr) with a nonsense sequence designed to have no significant sequence similarity to mouse, rat, or human transcript sequences (Ambion, Foster City, CA, USA) into cells was done using Lipofectamine (Invitrogen, Carlsbad, CA, USA) as a transfection agent following the manufacturer's protocol. UtLM cells were incubated in serum-free medium containing 0.001% of vehicle (ethanol) for 24h after siIGF-IR, then treated with E2 (10−8M), and harvested at 24h using Trizol Reagent (Invitrogen). Total cellular RNA was extracted from the cells using Qiagen RNeasy Mini Kit (SABiosciences) followed by the RT2 First Strand C-03 Kit (SABiosciences) to remove any residual contamination from the RNA samples with 2μg purified RNA per treatment condition. The template combined with the RT2 SYBR green/ROX qPCR mix (25μL/well) was loaded into a 96-well array plate coated with 84 predispensed MAPK-related gene-specific primer sets (SABiosciences) with each treatment condition per plate and processed on a TaqMan ABI Prism 7900 Sequence Detector System (Applied Biosystems, Foster City, CA, USA) according to the RT2 Profiler PCR Array (SABiosciences) manufacturer's protocol. The data analysis was based on the ΔΔCt method with normalization to GAPDH and HPRT (SABiosciences), (http://www.sabiosciences.com/pcrarraydataanalysis.php).
Real-time (RT) PCR was performed to detect estrogen responsive gene, IGF-I mRNA expression levels following E2 treatment at 0min, 10min, 60min, 24h, and 48h in UtLM cells. Starvation of cells with serum-free medium was the same as described for RT2 Profiler PCR Array and occurred 24h prior to E2 (10−8M) treatment. Cells were harvested with Trizol Reagent, and total cellular RNA was extracted from the cells using a Trizol Plus RNA Purification Kit (Qiagen, Valencia, CA, USA). One microgram total RNA was used to prepare cDNA and reverse-transcribed with Superscript II (Invitrogen). RT-PCR was performed using IGF-I and GAPDH primers  with Applied Biosystems Power SYBR Green PCR Mix on an AB cycler. The results were expressed as fold changes compared to untreated groups and normalized with GAPDH.
Immunofluorescence staining was performed to detect IGF-I peptide expression at 0min, 10min, 60min, 24h, and 48h, and phospho-ERαser118 and phospho-MAPKp44/42 colocalization at 0min, 10min, and 60min in UtLM cells following E2 treatment. The cells were starved the same as described for the real-time RT2 Profiler PCR Array for 24h prior to E2 treatment at 10−8M. The cells were fixed with 4% paraformaldehyde (Electron Microscopy Sciences, Hatfield, PA, USA), permeabilized with 0.2% Triton X-100 (Sigma), and blocked with 5% BSA (Sigma) and 0.1% gelatin (Sigma) in PBS. The cells were incubated overnight with primary IGF-I goat polyclonal antibody (sc-1422, 1:200 dilution; Santa Cruz Biotechnology, Santa Cruz, CA, USA), phospho-ERαser118 mouse monoclonal antibody (number 2511, 1:50 dilution; Cell Signaling, Danvers, MA) and phosho-MAPKp44/42 rabbit monoclonal antibody (number 9101, 1:100 dilution, Cell Signaling). Alexa Fluor (Invitrogen) 488 goat anti-rabbit for phospho-MAPKp44/42, Alexa Fluor (Invitrogen) 594 donkey anti-mouse for phospho-ERαser118, and 594 donkey anti-goat for IGF-I (1:3000 dilution) were used as secondary antibodies and DAPI (Invitrogen) for nuclear staining. Normal rabbit, normal mouse, or normal goat serum (Jackson Immunoresearch, West Grove, PA, USA) served as negative controls. Confocal images were taken on a Zeiss LSM510-UV meta (Carl Zeiss Inc, Oberkochen, Germany) using a C-Apochromat 40x/1.2 ∞/0.14–0.19 Korr UV-VIS-IR objective. The 488nm laser line from a Krypton/Argon laser was used for excitation of the Alexa 488. A 505–550nm bandpass emission filter was used to collect this image with a pinhole setting of 1.09 airy unit. For the second channel, the 543nm laser line from a Helium Neon laser was used for excitation of the Alexa 594. A 560nm longpass emission filter was used to collect the images with a pinhole setting of 1 airy unit.
Western blot analysis was performed using a standard procedure as described previously  to assess rapid effects of E2 on target protein expression in UtLM cells. The siIGF-IR and siScr transfection procedure were the same as described in siIGF-IR and real-time RT2 Profiler PCR Array. The serum-starved cells were treated with E2 (10−8M) at 0, 10, and 60min. The protein was extracted with a lysis buffer as previously described . Primary antibodies used for the western blotting were as follows: rabbit polyclonal anti-phospho-IGF-1RβTyr1131/IR-βTyr1146 (number 3021, Cell Signaling), rabbit polyclonal anti-IGF-IRβ (sc-713, Santa Cruz Biotechnology), rabbit polyclonal anti-phospho-Shc (number 2434, Cell Signaling), rabbit polyclonal anti-Shc (sc-288, Santa Cruz), rabbit polyclonal anti-ERα (sc-7207, Santa Cruz), mouse monoclonal anti-phospho-ERαSer118 (number 2511, Cell Signaling), rabbit polyclonal anti-MAPKp44/42, and rabbit polyclonal anti-phospho-MAPKp44/42 (number 9201 and number 9101, Cell Signaling). The rabbit anti-ERα, rabbit anti-IGF-IRβ, and rabbit anti-Shc antibodies used in the western blotting studies were used for immunoprecipitation samples. Primary antibodies were detected with horseradish peroxidase-conjugated secondary anti-mouse or anti-rabbit antibodies (GE Healthcare, Buchinghamshire, UK).
A Seize Primary Immunoprecipitation Kit (Pierce Biotechnology, Rockford, IL, USA) was used to detect the association of ERα, IGF-IRβ, and Shc in the cells treated with E2. The kit was used because IgG of anti-ERα, which was used to pull down Shc, and IGF-IRβ, has the same molecular weight as the target protein Shc and this kit allows the immunoglobulin to remain adherent to Aminolink Plus Gel following elution. The procedures were done according to the manufacturer's protocol . Briefly, 200μg of ERα rabbit polyclonal antibody (Santa Cruz) were coupled to 50μL of 50% of Aminolink Plus Gel Slurry in coupling buffer overnight at 4°C. The coupled gel and antibody complex was incubated with 300μg of the total protein harvested from the cells treated with E2 at 0, 10, and 60min same as described in western blotting procedures in binding buffer overnight at 4°C. The gel was washed three times with washing buffer. Only the antigens (Shc and IGF-IR) in the antigen-antibody complexes were eluted by the elution buffer (all buffers were supplied in the kit) and stored for western blot analysis.
The experiments for RT-PCR of IGF-I mRNA expression, immunoprecipitation, and western blot analysis were repeated at least three times independently. The data obtained from RT-PCR were expressed as mean ± SEM, and the two-tailed Student's t-test was used to compare statistical significance between different groups and between various time points. Most data obtained from immunoprecipitation and western blot analyses were not normally distributed, hence, nonparametric statistical methods and Mann-Whitney tests  were used to determine statistically significant differences between silenced and nonsilenced IGF-IR groups at various time points after E2 treatment in UtLM cells with respect to ratio of band intensity of phosphorylated/total protein (mean ± SEM) of IGF-IR, Shc, MAPKp44/42, and ERαser118 expression. The statistical significance was defined as one-sided P < 0.05.
For the RT2 Profiler PCR Array data, the receptor tyrosine kinase IGF-IR, MAPK signaling pathway, and fibrosis-related genes were chosen to be analyzed. The fold changes in response to E2 treatment were calculated separately for silenced and non-silenced IGF-IR groups (<−2 or >2 for either groups) and examined with scatter plots.
In order to explore signaling intermediates of the IGF-IR/MAPK cascade and related genes regulated by E2 and find new genomic mediators of fibroid growth and development, we performed genomic arrays to determine MAPK-related gene profiles mediated by E2 with and without IGF-IR gene knockdown. We found 35 genes related to the IGF-IR/MAPK signaling pathway and fibrosis that were differentially expressed between the groups with or without E2 treatment at 24h with a functional IGF-IR (scrambled siRNA; siScr), compared to those groups under siIGF-IR conditions (Table 1, Figure 1) within a total of 62 differentially expressed MAPK-related genes (see supplementary material available online at doi:10.1155/2012/204236, Table 1). The PCR array showed that E2 exposure in UtLM cells with a functional IGF-IR (siScr) resulted in >2-fold upregulation of 27 genes and <−2-fold downregulation of 3 genes involved in the IGF-IR/MAPK signaling cascade at 24h as shown in a heat map (Figure 1(a)) and by fold changes (Figure 1(b)); the other 5 genes were unchanged (<2-fold and >−2-fold). Those genes upregulated >2-fold in the presence of an intact IGF-IR included several D-type cyclins and other cyclin-dependent kinases involved in cell cycle progression, growth factor receptor-bound protein (GRB2), and ARAF associated with IGF-IR signaling through MAPK, MAPKs, and MAPK kinases involved in proliferation, differentiation, and survival. Collagen type I alpha I (COL1A1) which is involved in collagen synthesis and fibrosis, a prominent feature of fibroids, and transcriptional factors ELK1, E2F1, and EGR1 were upregulated as well. Also, RAC1, a Rho GTPase, involved in the regulation of several cellular processes and often activated following stimulation of RTKs , such as IGF-IR was increased.
The upregulated genes induced by E2 in the presence of an intact IGF-IR were mostly abrogated, and the 5 unchanged genes observed in the presence of a functional IGF-IR were upregulated after IGF-IR was silenced in UtLM cells. The E2 treatment with siIGF-IR resulted in differential expression of >2-fold upregulation of additional genes such as epidermal growth factor receptor (EGFR) involved in cell growth and survival, cyclin D2 (CCND2) and D3 (CCND3) involved in cell cycle progression, v-Ets erythroblastosis virus E26 oncogene homolog 2 (ETS2), a transcriptional factor involved in cell development and tumorigenesis, delta-like 1 homolog (DLK1) involved in fibrosis, and the glucose-regulated protein 78kDa (HSPA5) associated with monitoring protein transport (Table 1, Figures 1(a) and 1(b)). Alternatively, COL1A1 and GRB2, typically increased in the presence of a functional IGF-IR, showed decreased expression with silenced IGF-IR. However, the transcriptional factor EGR1 showed further upregulation when IGF-IR was silenced.
The differences in gene expression in response to E2 treatment with and without IGF-IR silencing indicate the important role of IGF-IR and its signaling molecules in E2-mediated activation of MAPK and MAPK-related pathways in UtLM cells.
To determine if the regulatory effects of E2 on MAPK-related gene expression could also occur through the genomic action of E2 on the expression of one of its early response genes and a MAPK and IGF-IR activating peptide, IGF-I, we assessed IGF-I mRNA and protein levels in UtLM cells. We performed real-time RT PCR at 0, 10, 60min, 24h, and 48h after E2 treatment and found that E2 at 10−8M induced a time-dependent increase in IGF-I gene expression. A prolonged response started at 24h and reached maximum levels by 48h in UtLM cells (P < 0.05, Figure 2(a)).
Confocal microscopy of immunofluorescence staining for IGF-I protein in UtLM cells further revealed that IGF-I peptide expression was increased by E2 and mostly localized in the cytoplasm, but appeared to translocate to the nucleus at 24h and 48h (Figure 2(b)). Interestingly, to date, IGF-I protein expression has only been reported to occur in the cytoplasm of uterine leiomyoma cells, although there has been one report of its localization in the nucleus of kidney cells .
To determine the rapid nongenomic actions of E2, we treated UtLM cells with a functional IGF-IR with E2 at 10−8M for 0, 10, and 60min and measured phosphorylated IGF-IRβ, Shc, and MAPKp44/42 using western blot analysis. We found that there was a quick phosphorylation of IGF-Rβ, Shc, and MAPKp44/42 at 10min until 60min in UtLM cells when treated with E2 (Figure 3). It has been previously shown that estrogen treatment can cause an increase in MAPKp44/42 activation and phosphorylation of ERα at serine118 site in estrogen-responsive breast cancer cell lines . It has also been shown that the IGF-IR downstream protein Shc can act as a transporter for the ER leading to activation of the MAPK signaling cascade . Additionally, in earlier studies, we found that fibroid tissue samples from women in the proliferative phase expressed more phosphorylated ERαser118 and had more nuclear colocalization and immunoprecipitation of phospho-MAPKp44/42 and ERαser118 compared to patient-matched myometrial controls . We therefore examined whether administration of estrogen could produce similar effects in human uterine leiomyoma cells in vitro. As shown in Figures 3(a) and 3(b), the phosphorylation level of ERα at serine 118 rapidly increased at 10min and continued until 60min in UtLM cells following E2 treatment. These effects were not present with siIGF-IR. Confocal microscopy further revealed that there was increased colocalization of phosphorylated ERαser118 and MAPKp44/42 in E2 treated UtLM cells at 10min (Figure 4).
Immunoprecipitation studies (Figure 5) further revealed that ERα is associated with both IGF-IRβ and Shc proteins following E2 treatment, and the amounts of both proteins were decreased when the IGF-IR gene was knocked down, which indicates that there is an association between IGF-IR and ERα and between Shc and ERα in UtLM cells exposed to E2.
The collective view of extranuclear ERα signaling suggests that its transduction pathways and its interaction with IGF-IR/MAPK pathways may connect the nongenomic actions of estrogen to genomic responses, since many of them interact and regulate the phosphorylation status and activities of multiple transcription factors, which affect gene expression [14, 27–30]. Therefore, in this study we first investigated the gene profile involved in the MAPK pathway to explore the effects of E2 treatment on IGF-IR/MAPK pathway related gene expression using siIGF-IR and real-time PCR array technology. As shown in Table 1 and Figure 1, UtLM cells treated with E2 in the presence of an intact IGF-IR had a high induction of 27 genes including genes encoding Cyclins, Cyclin Kinases, MAPKs, MAPK kinases, and transcription factors all involved in the cell proliferation, differentiation and survival. However, by silencing the IGF-IR the effects induced by E2 were diminished in UtLM cells and further indicated that E2-mediated MAPK pathway activation requires the presence of the IGF-IR in UtLM cells.
A cascade of MAPKs can be induced by a variety of signaling molecules [31, 32]. Transduction of the signals is achieved by a sequential series of phosphorylation reactions, wherein each downstream kinase serves as a substrate for the upstream activator. For example, in the mitogenic extracellular signal regulated kinase (ERK1/2) cascade, the two related mammalian MAPKs, ERK1 and ERK2 (p44mapk and p42mapk), are phosphorylated by MAP kinase/ERK kinase (MEK), which is activated primarily by the protein kinase Raf-1 after having been recruited to the plasma membrane by Ras [33, 34]. In our previous studies, the MAPKp44/42 cascade, preferentially regulating cell growth and differentiation, was upregulated in leiomyomas [9, 22]. The MAPK-related gene profiling RT-PCR array applied in this study further proves that the expression of genes involved in MAPK pathway, such as MAPK1, MAPK3, and GRB2, and the genes encoding transcriptional factors, ELK1, E2F1, MYC, and MAX are mediated by E2, and their expression levels are elevated when UtLM cells are exposed to E2 in the presence of a functional IGF-IR.
In the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance throughout the cell cycle, cyclin D1 can complex with and function as a regulatory subunit of CDK4 or CDK6, which is required for cell cycle G1/S progression . In this study, cyclin D1 and CDK4 expression levels were increased, which further indicates that E2 not only upregulates the MAPK/ERK1/2 pathway, but can also induce cyclin family proteins leading to cell cycle progression from G1 to S phase, thereby increasing cell proliferation. It was interesting to note that some genes encoding cyclin kinase inhibitors, such as CDKN2B, were also increased following E2 exposure and may have been increased to counterbalance the extremely high expression of CDK4. These findings are consistent with the concept of different cyclins and their kinases exhibiting distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event .
The abrogation of upregulation of genes by E2 in the presence of siIGF-IR in UtLM cells further strengthened our hypothesis that IGF-IR plays an important role in the crosstalk between the estrogen/ERα and IGF-I/MAPKp44/42 pathways. However, other genes were differentially expressed by E2 treatment in UtLM cells with and without siIGF-IR, which indicates that with silencing of the IGF-IR, other mechanisms compensated in response to E2 exposure, resulting in differential gene expression. The increased EGFR, EGR1, CCND2, and CCND3 gene expression pattern with siIGF-IR suggests that E2 treatment promotes alternative pathways for growth and survival when IGF-IR levels are decreased in UtLM cells. In other genes, such as DLK-1, involved in fibrosis , the expression level was increased, and COL1A1, a gene involved in collagen synthesis and fibrosis, which is typically increased in the presence of a functional IGF-IR [37, 38], was decreased after siIGF-IR further indicating that IGF-IR may play an important role in fibrosis in uterine leiomyomas.
We next investigated whether E2 upregulates IGF-I and IGF-IR, and their target proteins in leiomyoma cells, and what mechanisms are involved in the interaction between E2/ERα and IGF-I/IGF-IR pathways. We found that IGF-I gene and protein expression levels increased during the course of E2 exposure with a peak fold-change at 48 hours in UtLM cells; this prolonged response indicates a possible mechanism of IGF-I gene expression mediated by E2 at a genomic level. We also found that phosphorylated ERαser118, IGF-IRβ, and their target protein MAPKp44/42 were all increased within minutes after E2 treatment. The rapid activation of IGF-IR and its target downstream proteins indicates that the interaction between E2 and IGF-IR is mediated by nongenotropic signaling, that is, by kinase-initiated events that do not involve estrogen receptor binding to canonical steroid response elements on DNA [18, 28]. Furthermore, increased colocalization of phospho-MAPKp44/42 and ERαser118 occurred in UtLM cells 10 minutes after E2 treatment. These results are consistent with the findings that several mechanisms are associated with E2 exposure, including rapid activation of IGF-IR and MAP kinase, a nongenomic process observed in estrogen-responsive breast cancer cell lines , which could lead to ERα activation at serine 118 [14, 28].
The molecules involved in the nongenomic signaling process have been identified. More recently, it has been shown that a pool of ERs resides in or is associated with the plasma membrane. These ERs utilize the membrane IGF-IR to rapidly signal through various kinase cascades that influence both transcriptional and nontranscriptional actions of estrogen . In this study, UtLM cells treated with E2, showed upregulation of RAC1, a Rho GTPase involved in the regulation of several cellular processes that is often activated following stimulation of RTKs . This gene expression of RAC1 was decreased upon IGF-IR silencing. These data indicate that E2 can directly, or through the involvement of the ERα, activate IGF-IR and MAPK signaling. The IGF-IR may serve as an anchor for the plasma membrane-associated ERα. Estradiol causes rapid phosphorylation of IGF-IR and Shc. It has been reported that activated Shc, after binding to ERα, serves as a transporter, which carries ERα to Shc-binding sites on the activated IGF-I receptors , which subsequently signals to MAPKs and other pathways. Our immunoprecipitation results also show that these three proteins, ERα, IGF-IR, and Shc, are associated with each other when UtLM cells are treated with E2. Therefore, we proposed that IGF-IR should be a key mediator in this interaction, and applied siIGF-IR methodology to knockdown the IGF-IR gene to block the E2 effect on the interaction of these two pathways through their respective receptors. We found that siIGF-IR decreased the phosphorylation of IGF-IRβ and the activation of MAPKp44/42 induced by E2. At same time, ERα phosphorylation at the serine118 site was also attenuated. These findings indicate that IGF-IRβ activation is required in the rapid nongenomic response of ERα following E2 exposure in UtLM cells. Silencing of IGF-IR abrogated the ERα activity at the serine118 site induced by E2 confirming a potential relationship between membrane-related signals and intracellular ERα, in agreement with the findings that E2 binds to cell membrane-associated ERα, which physically associates with the adaptor protein Shc through IGF-IR activation and induces its phosphorylation . In turn, Shc binds GRB2 and Sos, which also results in the rapid activation of MAP kinase, and we have shown an association between IGF-IR and Grb2 and MAP kinase activation in fibroid tissue samples taken from women in the proliferative phase of the menstrual cycle [9, 40].
Therefore, the possible convergence of distinct ERα-mediated genomic and/or nongenomic actions at multiple response elements provides an extremely fine control system in the regulation of target gene transcript  leading to the alternation of gene expression profiles found in this study. In conclusion, the results obtained in this study indicate that the two growth regulatory pathways, E2/ERα and IGF-I/IGF-IR, are tightly linked in UtLM cells. The E2 effects can occur through both genomic and nongenomic events, which involve IGF-IR activation of MAP kinase cascades mediated by the association between ERαser118 and MAPKp44/42 (Figure 6). The observations that: (1) IGF-IR is required for the interaction and the differential expression of MAPK pathway-related genes mediated by E2; (2) IGF-I gene expression is responsive to E2; (3) the activation of alternative pathways induced by E2 when IGF-IR is silenced enhances our understanding of IGF-I/IGF-IR and E2/ERα interactions and may suggest a multipronged or cocktail approach to fibroid treatment. Considering that the pure antiestrogen or anti-IGF-IR agents may only be partially effective in antagonizing E2-induced IGF-I/MAPK pathway activation and because other alternative pathways (EGFR) could compensate, it suggests that inhibitors of small downstream molecules, such as Src and ERKs, or transcription factors may better block these effects and could possibly serve as noninvasive adjuvant therapies for fibroids.
The RT2 Profiler PCR Array was used to analyze MAPK pathway-related gene expression in human uterine leiomyoma (UtLM) cells mediated by E2 in the presence of scrambled siRNA (siScr) or IGF-IR silencing (siIGF-IR). There were 62 genes related to the MAPK signaling differentially expressed between the UtLM cells with a functional IGF-IR (siScr) compared to UtLM cells under siIGF-IR conditions in the presence or absence of E2 treatment at 24 h(>2-fold, upregulation and <−2-fold, downregulation).
No conflict of interests, financial or otherwise, is declared by the authors.
This paper may be the work product of an employee or group of employees of the NIEHS, NTP, and NIH, however, the statements, opinions, or conclusions contained therein do not necessarily represent the statements, opinions, or conclusions of NIEHS, NTP, NIH, or the United States government.
The authors would like to thank Dr. Kyathanahalli Janardhan and Ms. Retha R. Newbold for their critical review of this paper. This research was supported, in part, by the National Toxicology Program (NTP) and the Intramural Research Program of the National Institutes of Health (NIH), National Institute of Environmental Health Sciences (NIEHS).