Leiomyomas and other mesenchymally derived tumors are the most common neoplasms of the female reproductive tract. Presently, very little is known about the etiology and progression of these tumors, which are the primary indication for hysterectomies. Dysregulated WNT signaling through beta-catenin is a well-established mechanism for tumorigenesis. We have developed a mouse model that expresses constitutively activated beta-catenin in uterine mesenchyme driven by the expression of Cre recombinase knocked into the Müllerian-inhibiting substance type II receptor promoter locus to investigate its effects on uterine endometrial stroma and myometrium. These mice show myometrial hyperplasia and develop mesenchymal tumors with 100% penetrance that exhibit histological and molecular characteristics of human leiomyomas and endometrial stromal sarcomas. By immunohistochemistry, we also show that both transforming growth factor beta and the mammalian target of rapamycin are induced by constitutive activation of beta-catenin. The prevalence of the tumors was greater in multiparous mice, suggesting that their development may be a hormonally driven process or that changes in uterine morphology during pregnancy and after parturition induce injury and repair mechanisms that stimulate tumorigenesis from stem/progenitor cells, which normally do not express constitutively activated beta-catenin. Additionally, adenomyosis and endometrial gland hyperplasia were occasionally observed in some mice. These results show evidence suggesting that dysregulated, stromal, and myometrial WNT/beta-catenin signaling has pleiotropic effects on uterine function and tumorigenesis.
Mesenchymal uterine tumors are the most common neoplasms found in the human female reproductive tract. The vast majority of these tumors are uterine leiomyomas (uterine fibroids), which are benign lesions that form in the myometrium of an estimated 25%–50% of American women. Uterine leiomyomas are clonal in origin and hormone responsive . Patients may have a single uterine fibroid, but many have multiple fibroids, and they can be located anywhere in myometrial tissue. These tumors are commonly associated with severe pelvic discomfort during menstruation (dysmenorrhea), heavy menstrual bleeding (menorrhagia), infertility, abortion, ascites, and polycythemia. On the basis of their location in the uterus, fibroids are subdivided into three broad categories: subserosal, submucosal, and intramural. The size of the fibroids can vary greatly from microscopic to tumors weighing more than 1 kg, are often associated with significant morbidities, and are the leading cause of hysterectomies . Other uterine tumors such as leiomyosarcomas, endometrial stromal sarcomas (ESSs), perivascular epitheliod cell tumors (PEComa), and adenocarcinomas are less common but still pose a significant burden on a women's health and are often fatal. The etiology of any of these mesenchymal tumors is largely unknown.
One of the major mechanisms of neoplastic transformation is dysregulated β-catenin signaling. β-Catenin is the core component of the canonical wingless-type MMTV integration site family member (WNT) signaling pathway whose activation leads to the translocation of β-catenin from the cytoplasm to the nucleus and transcription of targeted genes . The role of WNT signaling in carcinogenesis in other tissues is well documented , but evidence for its contribution to mesenchymal uterine tumor development has been limited [5–7]. WNT signaling is indispensible for normal uterine development from the primordial Müllerian duct [8–10], and there is accumulating evidence to support a role for WNT signaling in postnatal uterine functions, including implantation , decidualization [12, 13], and perhaps remodeling after parturition.
We have been investigating β-catenin signaling in uterine development and function using a mouse Cre recombinase model system [14, 15] that exploits the uterine mesenchyme-specific expression of the Müllerian inhibiting substance type II receptor, which is also known as anti-Müllerian hormone 2 (AMHR2). We have shown that conditional deletion of β-catenin in uterine mesenchyme leads to progressive cell fate change from myogenesis to an adipogenic lineage . The aim of the present study was to investigate the role of β-catenin in uterine development further by expressing a constitutively activated form of β-catenin in uterine mesenchyme driven by Amhr2-Cre. When Amhr2tm3(cre)Bhr (Amhr2-Cre) mice are crossed with Ctnnb1tm1Mmt mice , Amhr2-driven Cre recombinase, which is expressed in ovary, oviduct, and uterus, deletes exon3 and leads to formation of a stable form of β-catenin in Amhr2-Cre-expressing cells and in their progeny. This form of β-catenin is resistant to phosphorylation by the adenomatosis polyposis coli complex and its subsequent degradation. We show that dysregulated WNT signaling in the uteri of these mice causes mesenchymal tumorigenesis in all mice examined and occasional adenomyosis, with probable indirect stromal support for the induction of adenocarcinoma.
MATERIALS AND METHODS
The mice used in this study were housed under standard animal housing conditions. All protocols involving animal experimentation were approved by the Institutional Animal Care and Use Committee at Massachusetts General Hospital. Mice were maintained on C57BL/6;129/SvEv mixed genetic background. Amhr2tm3(cre)Bhr (Amhr2-Cre) mice  (Dr. Richard Behringer, M.D. Anderson, Houston, TX) were mated with Ctnnb1tm1Mmt/tm1Mmt  to generate Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice. The DNA from tail biopsies was used to genotype mice using the standard PCR protocols. The uterus collected from Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ and control mice were photographed by using a Nikon SMZ1500 microscope with an attached Spot camera (Diagnostic Instruments, Sterling Heights, MI).
Oocyte and Blastocyst Collection and Assessment
The 6- to 7-wk-old mutant and control mice were superovulated with i.p. injections of 7.5 IU equine chorionic gonadotropin (eCG; Sigma Chemical Co., St. Louis, MO) followed by 7.5 IU human chorionic gonadotropin (hCG; Sigma) after 48 h. Fourteen hours after hCG injection, females were euthanized, and their oviducts were removed. The cumulus-oocyte complexes were released from the ampullary region of each oviduct by puncturing the oviduct. Cumulus cells were removed by exposure to 80 IU/ml hyaluronidase (Irvine Scientific, Santa Ana, CA) in Hepes buffer and washed out with human tubal fluid (HTF; Irvine Scientific) with 10% fetal bovine serum (FBS). Isolated oocytes were transferred into HTF media with 10% FBS and assessed by morphology. Oocytes were classified into four groups as mature, germinal vesicle break down, immature, and atretic. For blastocysts, the 6- to 7-wk-old mutant and control mice were superovulated with 7.5 IU eCG and 7.5 IU hCG as above then mated with wild-type males. Mice were euthanized at 3.5 days after mating, and uteri were removed. Blastocysts were flushed from the uteri and transferred into HTF media with 10% FBS and assessed by morphology. Blastocysts were classified as 4-cell to morula, expanded blastocyst, and early blastocyst.
Human myometrial and fibroid samples were collected using Institutional Review Board approved protocols. Murine uteri and human samples were fixed by immersion in 4% paraformaldehyde for 10–12 h and then transferred to 70% ethanol until processing. The fixed tissues were dehydrated in a graded ethanol series, cleared in xylene, and embedded in paraffin wax. Embedded tissue samples were sectioned at 5-μm thickness and mounted on slides. Hematoxylin and eosin (H&E) staining was performed using standard histological techniques. Photomicrographs of nontumorous myometria (n = 3 mice for each group) were measured to determine the ratio of the width of myometria to total uterine width.
In Situ Hybridization
Analyses for Amhr2 mRNA are described in a detail in a previous study [14, 15]. Briefly, urogenital ridges were collected from timed pregnant dams and at Embryonic Day 13.5 (E13.5) and fixed overnight at 4°C in 4% paraformaldehyde. Tissues were pretreated with protease prior to overnight hybridization with either Amhr2 full-length  digoxigenin-labeled antisense riboprobes in 50% formamide hybridization solution at 70°C. The resultant hybrids were detected with alkaline phosphatase-conjugated antidigoxigenin antibodies and BM purple colorimetric solution (Roche Molecular Biochemicals, Indianapolis, IN).
Serial sections of tissues were deparaffinized with xylene and rehydrated with graded series of ethanol (absolute, 95%, 80%, and 50%, respectively, and distilled water), followed by two washes of 5 min each in PBS containing 0.05% Tween 20 (PBS-T). After a wash with PBS-T, antigen retrieval was performed by boiling the tissue sections in 0.01 M citrate buffer (pH 6) for 20 min. Sections were then washed for 5 min in PBS-T and blocked at room temperature for 1 h by using 2% normal donkey or goat serum, 2% bovine serum albumin, and 0.1% triton-X in PBS. Tissue sections were then incubated in a humidified chamber overnight at 4°C with primary antibody. Sections were subsequently washed with PBS-T, incubated at room temperature for 1 h with secondary antibody, then counterstained with 4′,6′-diamidino-2-phenylindole (DAPI). Images were photographed using a microscope (Nikon Eclipse TE 2000-S; Micro Video Instruments, Avon, MA) equipped with a Spot digital camera. DAPI-stained nuclei and phospho-histone H3 (pH3)-positive cells from sections of three different lesions were counted with the nucleus-counting analysis plugin of Image J software (v1.37; NIH, Bethesda, MD) after setting a black and white threshold at 27–30 in Photoshop (v10; Adobe Systems Inc., San Jose, CA).
Following are the primary and secondary antibodies used in this study: anti-β-catenin (1:250; BD Transduction Laboratories, San Jose, CA); anti-KIT (1:200; R&D Systems, Minneapolis, MN); anti-TGFB3 (1:200; Abcam, Cambridge, MA); anti-HMGA2 and anti-PECAM1 (1:200; Santa Cruz Biotechnology, Santa Cruz, CA); anti-vimentin (1:200; Santa Cruz Biotechnology); anti-Ecadherin (1:100; Santa Cruz Biotechnology); anti-pH3 (1:200; BD Transduction Laboratories); anti-CD11B (1:100; eBiosciences, San Diego, CA); anti-CD140B (1:200; Ebiosciences); anti-ACTA2, CY3-conjugated (Sigma); anti- PCNA (ready to use; Zymed, San Francisco, CA); anti-FRAP1 (1:200; Cell Signaling, Danvers, MA); AlexaFluor secondary antibodies (1:500; Invitrogen, Carlsbad, CA); and biotinylated donkey anti-mouse or anti-rabbit antibody F(ab)2 (1:1000; Jackson ImmunoResearch Laboratories, West Grove, PA).
A previous study has shown that despite normal ovarian functions, Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mutant mice were subfertile . In our study we also observed that Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice have smaller litters in younger mice despite their having histologically normal ovaries (data not shown). Further analyses showed that neither oocyte nor 3-day-old embryo quality appeared to be significantly affected by constitutive activation of β-catenin in the ovary (Table 1). However, fewer oocytes and embryos were collected from the mutant uteri (Table 1), which is likely in part because of structural blockage we observed in some of the mutant oviducts (data not shown). We next analyzed the uteri to determine if the subfertility in mutant mice might also be due, in part, to defective development in mutant uteri. Below we show evidence that expression of constitutively activated β-catenin in mouse uteri results in the appearance of two types of mesenchymal tumors that resemble human leiomyomas and ESSs (Table 2).
Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mutant and Amhr2tm3(cre)Bhr/+ or Ctnnb1tm1Mmt/+ control mice were examined for phenotypic analysis. Initial gross examination of adult nulliparous mutant uteri occasionally showed hemorrhagic areas (data not shown) along both horns and an extraneous layer of tissue with protruding nodules at the anti-mesometrial side of the uteri (Fig. 1A). Examination of mutant uteri from multiparous mice revealed the presence of large tumorous growths and consistent multiple hemorrhagic sites on the surface of the uteri (Fig. 1B). No abnormalities were detected in the uteri collected from control mice (Fig. 1C). Histological examination of noncycling 4-wk-old uteri showed that the nodules observed on the surface of uteri appear to originate from the longitudinal myometrial layer of the uterus (shown with a red arrowhead in Fig. 1D). We also observed a small area of dysplasia (shown with a black arrowhead and outlined in white) in the mutant uteri, which otherwise appear similar to controls (Fig. 1E), suggesting that tumorigenesis starts before the mice begin estrous cycling. Staining of the mutant and control uteri for α-smooth muscle actin (ACTA2) shows that the polyps are derived from the myometrium and that there was expansion of the myometrium in the mutants (Fig. 1, F and G). The ratio of the width of ACTA2-positive myometrium to total uterine width in the mutant (0.45 ± 0.04, n = 3) was significantly higher (P = 0.009) than that of control uteri (0.22 ± 0.03, n = 3) suggesting smooth muscle hyperplasia. Normal WNT signaling is highly active at the coelomic epithelium of the Müllerian duct . The nodules we observe in the mutant mice may be the result of constitutively activated β-catenin on the coelomic epithelium and adjacent mesenchyme of the presumptive anti-mesometrial side of the E13.5 urogenital ridge where Amhr2 is highly expressed (Fig. 1H).
In mutant mouse uteri, we observed dysplastic lesions in myometria with 100% penetrance that appeared to increase in size and number with age and parity (Fig. 2, A and B, and Table 2). The mutant murine tumors were composed of plump spindle cells surrounded by an extracellular matrix that formed fascicles (Fig. 2C) that are remarkably similar to those typically found in human uterine leiomyomas  (Fig. 2D). The largest tumors were often necrotic with hemorrhagia and fibrosis (data not shown). The murine smooth muscle tumors are ACTA2-positive (Fig. 2, E–G), which is also characteristic of human uterine leiomyomas (Fig. 2H). Typically, human uterine leiomyomas are very slow-dividing tumors and are usually present with a low proliferative index (0–2 mitoses per 10 high power field) . We analyzed proliferation in the uterine smooth muscle tumors observed in mutant mice by performing pH3 expression analysis and found few pH3-positive cells (5–6 per high-powered filed or 2.4 ± 0.2/1000 cells) in these tumors, whereas pH3 expression was high in luminal epithelium (LE; Fig. 2, I and J). Proliferating cell nuclear antigen (PCNA) expression was also analyzed with similar results (data not shown). These data suggest that, similar to human uterine leiomyomas and unlike most other more aggressive tumors, these mouse uterine smooth muscle tumors also have a low mitotic activity. Another characteristic of many human uterine leiomyomas is that leiomyomas express higher levels of TGFB, particularly TGFB3, than the surrounding myometrium [22–26]. Analysis of TGFB3 in the uteri of mutant mice showed much higher levels of expression by immunohistochemistry in the epithelium and endometrial stroma, as well as in the central areas of the leiomyoma-like lesions, than in surrounding areas and the remaining myometrium and at levels consistent with those observed in human leiomyoma (Fig. 2, K and L). Together with the appearance of polyps shown above, these results suggest that constitutively activated β-catenin induces smooth muscle hyperplasia, which can then lead to smooth muscle tumor development.
The oncogenic serine/threonine kinase, mammalian Target of Rapamycin (FRAP1), which lies downstream of the PI3K signaling pathway and is a master regulator of cell proliferation , is up-regulated in the Eker rat leiomyoma model because of a mutation in tuberous sclerosis 2 (Tsc2) . We assayed whether FRAP1 is also induced in these tumors by constitutively activated β-catenin using immunohistochemistry (Fig. 3). In the mutant with CA β-catenin, FRAP1 appears highly expressed in the central portion of the leiomyoma-like lesion, with little expression observed in the surrounding hypocellular areas (Fig. 3A). Relatively strong FRAP1 expression was also observed in both the circular and longitudinal myometrial layers (Fig. 3B). In the normal myometrium of control mice, FRAP1 expression appears to be limited to the endothelial cells or pericytes (Fig. 3, C and D).
In addition to uterine smooth muscle tumors, Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mutants also developed ESS-like neoplastic lesions that were restricted to the endometrial stroma (ES; Fig. 4A). These lesions were ACTA2-negative (Fig. 4B), which we used as a marker to distinguish between ESS and ACTA2-positive leiomyomas. These tumors expressed high levels of nuclear β-catenin, indicating their origin from Amhr2-Cre-expressing mesenchymal cells (Fig. 4C). As expected, only membranous β-catenin is detected in LE and endometrial glands (EG) of both mutant (Fig. 4C) and control uterus (Fig. 4D), since Amhr2 is not expressed in these cells . Some cells at the junction of the longitudinal and circular smooth muscle layers also expressed nuclear β-catenin (Fig. 4D). The ESS-like tumors expressed vimentin, a mesenchymal marker, suggesting the mesenchymal origin of these tumors (Fig. 4E). Consistent with a previous study , vimentin is also expressed in ES and blood vessels of both the mutant and control uteri (Fig. 4F).
Further analysis of the ESS-like neoplastic lesions with various markers used in the diagnosis of human tumors was performed to determine how well the murine tumors compare. The ESS-like neoplastic growths observed in mutant uterus are strongly estrogen receptor alpha (ESR1) positive (Fig. 5A), suggesting that these tumors can be responsive to changes in the levels of estrogen. KIT (CD117) is the tyrosine kinase receptor for the stem cell factor that has been shown to be expressed at relatively high levels in uterine sarcomas and mesenchyme-derived tumors of the uterus [30, 31]. We also find high levels of KIT expression in the ESS-like tumors (Fig. 5B). Co-staining with ITGAM (CD11B), a monocyte/macrophage cell marker, was performed to ensure that the KIT+ cells were not hematopoietic cells that had infiltrated the lesion. In the rest of the endometrial stroma, KIT is only expressed in a few cells, probably of hematopoietic origin. In addition, these tumorous lesions do not express PECAM1, an endothelial cell marker, except for the endothelial cells of blood vessels present inside the tumorous area (Fig. 5C). HMGA2 is a member of the high mobility group (HMG) of proteins. The disruption and misexpression of HMGA2 has been reported in various benign mesenchymal tumors such as lipomas, uterine leiomyomas, endometrial polyps, and salivary gland adenomas [32, 33]. In mutant uteri, we detected very high expression of HMGA2 in ESS-like tumor lesions compared with the normal adjacent tissue (Fig. 5D). Although E-cadherin, an epithelial cell marker, and PDGFRB (CD140B), a fibroblast marker, were expressed in normal LE and a few scattered cells of ES and myometrium, respectively, they were not expressed in ESS-like tumors of mutant uteri (Fig. 5, E and F). These results suggest that the ESS-like tumors in Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice strongly resemble ESS tumors found in human uteri both by histology and by marker profile.
The mutations in phosphorylation sites on exon 3 of the β-catenin gene have been shown to occur in various tumors [34, 35]. In humans, 38% of cases of endometrial carcinoma show nuclear and/or cytoplasmic accumulation of β-catenin, suggesting that β-catenin plays an important role in the development of this disease . In the present study, we observed hyperplasia and pseudostratification of epithelia of EGs in 14% of the mutant uteri (Table 2). We also observed aberrant EGs in the myometrium of the mutant uteri (Fig. 6A). The colocalization of ACTA2 and E-cadherin further confirms the presence of EGs in the myometrial layer of the mutant uteri (Fig. 6B). These phenotypic changes observed in EGs were surprising because Amhr2-Cre is only expressed in the stromal and myometrial compartments of the uterus , and the activation of β-catenin only occurred in these two compartments (Fig. 2). However, correctly functioning uterine stroma is required for normal adenogenesis , and our previous study has shown that conditional deletion of β-catenin from ES and the myometrium leads to fewer EGs . Collectively, our findings suggest that tight regulation of the β-catenin signaling in ES and possibly myometrium is essential for the maintenance of normal EGs.
WNT signaling plays an important role in the development of the female reproductive tract [8–10, 20]. Wnt4 mutant females have a defect in the development of Müllerian duct and show gonadal characteristics of males . Similarly, deletion of Wnt5a leads to posteriorization of the female reproductive tract and causes a decrease in the thickness of myometrium . The Wnt7a mutant males showed a defect in the regression of Müllerian duct, whereas females were infertile due to abnormal development of oviduct and uterus . Wnt7a mutant uteri showed a lack of EGs and a decrease in the thickness of the myometrial layer of uterus as well . Misregulated WNT signaling has been associated with the development of uterine tumors [7, 36]. The decrease in expression of secreted frizzled related proteins 4, an antagonist of WNT signaling, and concomitant increase in nuclear β-catenin is observed in the human ESS .
Consistent with a previous report , we observed that constitutive activation of β-catenin driven by the Amhr2-Cre induced ovarian anomalies in mice by 6 wk that were described as solid nests of disorganized cells. However, they showed that these mutant mice still had normal follicular and luteal structures and that a subset of older mutant mice developed ovarian tumors, which we also observed. Here we show that dysregulated WNT signaling in murine uterine mesenchymal cells via constitutively activated β-catenin leads to pleiotropic effects on uterine tumorigenesis as well. The unknown etiology of uterine mesenchymal tumors could be a primary reason for the limited progress toward development of therapeutics to prevent or manage leiomyomas. Currently, there are no mouse models that display uterine-specific mesenchymal tumors available for in-depth mechanistic analyses. In this study, we have shown that sustained activation of the WNT signaling pathway in ES and myometrium leads to the development of mesenchymal tumors in 100% of the mutant animals. In future studies we will use this mutant mouse model system to explore the molecular mechanisms and signaling pathways involved in leiomyoma and ESS tumorigenesis, with the goal of developing better treatment options.
For example, we have shown evidence that FRAP1 is affected by activated β-catenin in mutant mouse uteri. Uterine leiomyomas have also been observed in patients suffering from tuberous sclerosis and lymphangioleiomyomatosis, and there is evidence that half of human uterine leiomyomas show loss of tuberin, a protein product of tuberous sclerosis complex (TSC) 2 . TSC 1/2 is the upstream regulator of FRAP1, and mutations in TSC1/2 lead to activation of FRAP1 signaling, which can lead to lymphangioleiomyomatosis and tuberous sclerosis in human patients . A germline mutation in the TSC2 gene in rats leads to the development of uterine leiomyomas and leiomyosarcoma-like tumors in up to 65% of animals . Additionally, activation and deletion of β-catenin in gastrointestinal stromal tumors both in vivo and in vitro have been shown to activate and down-regulate, respectively, the FRAP1 signaling pathway . In other mouse model systems, mutations in Pten, a downstream inhibitor of the PI3 kinase pathway, have also been shown to correlate with more aggressive ovarian tumorigenesis when coupled with activated WNT signaling [34, 36, 40]. These findings suggest that WNT signaling and PI3 kinase signaling interactions could play an important role in the development of uterine tumors.
Alternatively, changes in uterine morphology during pregnancy and after parturition induce injury and repair mechanisms that stimulate tumorigenesis from stem/progenitor cells, which normally do not express constitutively activated β-catenin. This hypothesis is supported by the observation that the leiomyomas appeared near areas with prominent hemorrhaging and inflammation in multiparous mutant mice. The concept that uterine leiomyomas might be the end result of dysregulated fibrotic response and hypertrophic scarring has also been proposed by others . These investigators suspected that uterine fibroids retained myofibroblasts, which are different from myometrial smooth muscle cells and which are also the extracellular matrix-depositing cells active in wound healing [23, 42–45]. Using their own published studies and those of others comparing leiomyoma and normal myometrium by microarray hybridizations [23, 42–45], they found, perhaps unsurprisingly, that the genes most consistently differentially regulated were those involved in extracellular matrix formation. The most consistently up-regulated gene was TGFB3, a member of the well-known TGFB cytokine family and a potent promoter of fibrosis . They also showed electron microscopic evidence that the leiomyoma cells were indeed myofibroblasts and speculated that uterine fibroids were similar to keloids, in which repair of the injury extends beyond its original border. Furthermore, they made the interesting correlation that, as with keloids, leiomyomata uteri are disproportionally observed in African-American women, suggesting a genetic link between hypertrophic scarring and ethnicity.
We also observed ESS-like tumors in the Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice with 100% penetrance. These ESS-like tumor lesions were positive for ESR1, vimentin, KIT, and HMGA2 and negative for E-cadherin (CDH1), ACTA2, PDGFRB (CD140B), and PECAM1. A similar immunohistochemical expression pattern is also observed in human cases of ESS . Additionally, genetic alternations in exon 3 of the β-catenin gene and subsequent stabilization of β-catenin in nucleus and/or cytoplasm are a common feature of various human tumors, including ovarian and uterine tumors [34, 36, 40]. Other human stromal tumors that express high levels of or have activating mutations in KIT are being relatively successfully treated with receptor tyrosine kinase inhibitors . We suspect that human ESS might be amenable to similar therapies.
Recently, Jeong et al.  have shown that conditional activation of β-catenin with progesterone receptor (PGR)-driven Cre leads to the development of endometrial glandular hyperplasia. As PGR-Cre is expressed in all three compartments of the uterus (LE, ES, and myometrium), their study was unable to show whether the development of endometrial glandular hyperplasia is a direct result of activation of β-catenin in the epithelial cells or an indirect effect of activation in adjacent stromal cells. In the present study, we occasionally found both abnormal localization and hyperplasia of endometrial glands in the mutant uteri without constitutive activation of β-catenin in the epithelial cells, suggesting that dysregulated β-catenin signaling in stroma can also induce development of endometrial glandular hyperplasia. In summary, we have developed a mouse model to analyze the origin and progression of leiomyomas, ESSs, and adenomyosis and to devise novel treatment paradigms based on the molecular pathways we identify as targets for intervention.
We would like to thank Drs. Patricia K. Donahoe, Henry L. Chang, and James K. Pru for their helpful suggestions and for reviewing this manuscript. We would like to thank Dr. Richard Behringer for providing us with the Amhr2tm3(cre)Bhr (Amhr2-Cre) mice.
Oocyte and embryo analysis in Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice.*
Incidence of mesenchymal tumors in Amhr2tm3(cre)Bhr/+;Ctnnb1tm1Mmt/+ mice.