Abstract
Uterine fibroids (UFs) are associated with irregular or excessive uterine bleeding, pelvic pain or pressure, or infertility. Ovarian steroid hormones support the growth and maintenance of UFs. Ulipristal acetate (UPA) a selective progesterone receptor (PR) modulator (SPRM) reduce the size of UFs, inhibit ovulation and lead to amenorrhea. Recent liver toxicity concerns with UPA, diminished enthusiasm for its use and reinstate the critical need for a safe, efficacious SPRM to treat UFs. In the current study, we evaluated the efficacy of new SPRM, EC313, for the treatment for UFs using a NOD-SCID mouse model. EC313 treatment resulted in a dose-dependent reduction in the fibroid xenograft weight (p < 0.01). Estradiol (E2) induced proliferation was blocked significantly in EC313-treated xenograft fibroids (p < 0.0001). Uterine weight was reduced by EC313 treatment compared to UPA treatment. ER and PR were reduced in EC313-treated groups compared to controls (p < 0.001) and UPA treatments (p < 0.01). UF specific desmin and collagen were markedly reduced with EC313 treatment. The partial PR agonism and no signs of unopposed estrogenicity makes EC313 a candidate for the long-term treatment for UFs. Docking studies have provided a structure based explanation for the SPRM activity of EC313.
Similar content being viewed by others
Introduction
The unmet need for medical management of uterine fibroids (UFs) has led to the discovery of various novel agents in recent years. These includes GnRH agonist, antagonists and selective progesterone receptor modulators (SPRMs). Various SPRMs are found to be very effective in range of biological activity including contraception, preoperative treatment of uterine leiomyomas1. UFs are the most common benign tumors in reproductive age women, are asymptomatic in at least 50% of afflicted women, in others, they cause significant morbidity and affect quality of life2. Women with UFs have abnormal uterine bleeding, dysmenorrhea, pelvic pain unrelated to menstruation, as well as pressure symptoms such as bloating, urinary frequency and bowel disturbances3. Current options for the management of UFs include medical therapy, minimally invasive procedures (e.g. uterine artery embolization, ultrasonic ablation), and surgery.
UFs growth requires ovarian steroid hormones estradiol (E2) and progesterone (P4). Even though the endocrine support is from steroid hormones, interactions of sex steroids with growth factors cytokines were documented in UFs4,5,6,7. Recent interventions approaches have targeted inhibition of steroid hormones using antiestrogens/estrogen receptor modulators (SERMs) and SPRMs. Recent FDA-approved SPRMs, UPA and asoprisnil (ASO) (Fig. 1B,C) were withdrawn from the market due to the endometrial changes8,9. Another approach is gonadotropin-releasing hormone (GnRH) agonists, upon binding GnRH-analogues to GnRH receptors, an initial increase in the release of gonadotropins is followed by to GnRH receptor downregulation leads to reduced levels of sex hormones10. Often GnRH agonists are used as preoperative therapy11,12. GnRH agonists achieved decreasing menstrual bleeding and reducing fibroid volume by approximately 50%13. Adverse effects of GnRH agonist therapy involves the full range of menopausal symptoms including vasomotor symptoms and decreased bone mineral density14. The GnRH antagonists Elagolix was recently approved for endometriosis treatment and is expected to be submitted for market authorization for treatment of heavy menstrual bleeding associated with UFs9,15. Other antagonists such as relugolix and linzagolix are in development for the treatment of endometriosis and UFs. GnRH antagonists for UFs are often used in combination with estrogenic add-back medication to reduce the menopausal symptoms and loss of bone mineral density (BMD). Despite the concomitant add-back medication, the loss of BMD may be a major drawback for long-term treatment1. UFs often shows accumulation of extracellular matrix proteins and smooth muscle actin (α-SMA) in entwined bundles16. Collagenase treatment resulted a reduction of uterine fibroids from 5.3% to 2.4% in 96 hours17. It seems the structure of small fibroids differs considerably from large fibroids at cellular level, small fibroids are more cellular, whereas more vascularization was noted in large fibroids. It is also noted that a greater proportion of smooth muscle cells to fibroblasts is present in small fibroids18. Targeted agents that affect collagen or smooth muscle actin could be potential therapeutic agents for treating uterine fibroids.
EC313 is a steroidal progestin with differential binding towards steroids receptors such as PR and glucocorticoids (GR). Regarding E313’s binding affinity towards PR shows that it is <0.28% agonistic and 79.1% antagonistic when compared to R5020 and mifepristone respectively. EC313 binds to glucocorticoids minimally about 6.4% compared mifepristone and exert 100% antinidation (antiovulation/contraception) in rats. EC313 does not bind to ER. Also, we have shown that EC313 inhibits breast cancer cell proliferation and dichotomous branching of mammary glands in mice (44). Based on the previous studies we hypothesize that EC313 as an SPRM with preferential receptor binding capabilities, could be used to treat non-malignant estrogen driven gynecological conditions such as UFs. Here we assessed the potential therapeutic effect of EC313 (Fig. 1A) for the treatment of UFs. The efficacy of EC313 was tested in a patient derived UF xenograft in NOD-SCID mouse model and tissue markers of proliferation and fibrosis were analyzed by immunohistochemistry (IHC).
Materials and Methods
Materials
UPA, EC313, and ASO (Fig. 1) were synthesized by Evestra, Inc. release E2 pellets (0.05 mg/60day) were purchased from Innovative Research of America, Sarasota, FL. IHC was done at the University of Texas Health Science Center at San Antonio pathology core facility. Hydroxyl methyl cellulose was purchased from Sigma Aldrich, St. Louis, MO.
Animal model
Animals
The in vivo study was approved by the Institutional Animal Care and Use Committee of the University of Texas Health Science Center at San Antonio (Protocol #20170019AP). The established murine model of transplantation of human UF tissue to immunodeficient NOD-SCID mice was used (1). Immunodeficient female, (NOD-SCID) mice were obtained from Charles River laboratories (USA), were housed according to institutional guidelines. Animals had the access to food and water ad libitum.
Collection of uterine fibroid tissue
All experimental protocols were approved by the institutional animal care and use committee of University of Texas Health Science Center at San Antonio (Protocol #20170019AP). Informed consent was obtained to collect human UF tissue. All experiments were performed in accordance with relevant regulation and guidelines of the University of Texas Health Science Center at San Antonio - Institutional Review Board (Protocol # HSC20070728H). The UF tissue used for current study is obtained from a single patient. The samples was transported to the laboratory on ice in Viaspan® buffer (Bristol –Myers Squibb) within 4 hours of collection. Tissue samples were cut aseptically into 2 × 2 × 2 mm sections and weighed. Equal weight grafts were used for transplantation.
Tissue transplantation
The mice were anesthetized using 1.5% isoflurane (4% for induction) in an oxygen/nitrous oxide 30%/70% mixture. Dorsal incisions were made, bilateral oophorectomy was performed, and wounds were stapled. Animals were monitored carefully during the recovery phase and 5 mg Rimadyl/kg bodyweight was administered s.c. for pain relief. Three weeks after ovariectomy, the UF tissue pieces, were transplanted s.c. using a trocar. During the same surgery, mice were supplemented s.c. with (60 day release estrogen) E2 pellets (Innovative Research of America, Sarasota, FL, USA). Animals received EC313 0.1 mg/kg, N = 6, or 1 mg/kg, N = 6), or UPA (5 mg/kg, N = 5) by subcutaneous injection (s.c) for five days per week for 8.5 weeks. E2 control animals received E2 + vehicle (N = 5). 0.2% hydroxymethyl cellulose (Sigma Aldrich, St. Louis, MO) in phosphate buffered saline (Life technologies, Carlsbad, CA) was used as vehicle. At termination of the study animals were weighed, sacrificed, and the uterus and fibroid xenografts were excised and weighed. Tissues were harvested, fixed in 10% formalin, and processed for immunohistochemistry (IHC) for ER, PR, Ki67, desmin and α-SMA.
Molecular docking studies
To understand the possible agonistic and antagonistic activities of EC313, two stages of molecular docking studies have been performed. In stage-1 docking, we mainly explored the binding affinity of EC313 towards PR and compared with that of ASO and UPA (widely studied SPRMs). While in stage-2 docking, we investigated the affinities of four co-regulators (two co-activators: SRC1 and AIB1 and two co-repressors: SMRT and NCoR) towards the PR-SPRM complexes obtained from the stage-1 docking and compared with that of PR-P4 and PR-mifepristone complexes.
According to the previous studies, the ligand-bound PR interacts with DNA at P4 response elements to activate or repress the transcription activity through the recruitment of coregulatory proteins19,20,21,22. The binding of agonists or antagonists to PR induces conformational switching to the helix-12, which is a determining factor for the recruitment of co-activators or co-repressors. Molecules such as SPRMs exhibited mixed profiles of action, i.e., inducing decreased transcriptional activity compared with full agonists and increased transcriptional activity compared with full antagonists23,24,25,26. Studies postulated that SPRMs can induce an intermediate state of interactions between receptor and co-modulators27,28,29. These molecules partly stabilize at the agonist bound conformation of the receptor30,31,32,33,34 and allow co-activators to bind but with less efficacy than full agonists. The crystal structure of one of the well characterized SPRM ASO in complex with PR is reported in both agonist and antagonist bound conformations35,36. In the agonist bound conformation, the positioning of helix-12 is close to the ligand binding domain (LBD) and facilitates a binding site for co-activator proteins, whereas in the antagonist bound conformation, the helix-12 is positioned away from the LBD. These crystal structures (PDB IDs: 4a2j and 2ovh35,36) were used for the stage-1 docking studies. We have used an induced fit docking (IFD) protocol (Schrödinger LLC), to assess the binding of ligands towards the LBD. IFD predicts the ligand binding modes in a realistic way by applying concomitant structural changes in the receptor. No co-regulators were included in the receptor structure during stage-1 docking to avoid the conformational restrictions of the side chains of PR residues especially at the LBD upon ligand binding. The binding of ASO and UPA were also investigated in the same way. The corresponding poses obtained from docking studies were used for the MM-GBSA calculations and their binding energies were compared between the SPRMs. The detailed docking protocols including the protein and ligand preparations were explained in the supplementary text.
In stage-2 docking, the binding modes and affinities of four co-regulators towards PR-SPRM complexes were predicted. Three dimensional structures of all these co-regulators were extracted from different PDB entries and used for the docking studies (details shown in Supplementary Table 1). The co-activators and co-repressors were docked against agonist and antagonist bound conformations respectively using Hex 8.0.037,38 and subsequently energy minimized using Maestro (Schrödinger LLC). The affinities of co-activators towards PR-P4 and affinities of co-repressors towards PR-mifepristone complexes were also calculated separately and compared with that of PR-SPRM complexes. The binding sites (grid) for co-regulators were defined on the PR based on the available literature information. The co-regulators were allowed only to probe at a defined grid space. After the docking, the best pose was selected based on the docking energy and was used for the MM-GBSA calculations followed by per-residue decomposition energy analyses.
Statistical analysis
Quantitative data are expressed as the mean ± standard deviation and statistical significance was determined by Student’s t test.
Results
In this study we have demonstrated an in vivo xenograft model of human UF in immunodeficient NOD-SCID mice. The optimum dose of E2 was required to support the growth of subcutaneous grafts. E2 dose were selected based on previous studies2. The grafted tissues showed UF cellular characteristics such as collagen bundles and abundance of smooth muscle actin as observed by Fritsch et al.2. The levels of ERα and PR stay expressed in UF grafts after 60 days in mice. The graft weights at the termination of the experiment was the primary endpoint, while histology and IHC were as secondary endpoints. The treatment didn’t affect the body weight of the animals when compared to untreated control animals (Fig. 2). The UF weight in all treated groups were found reduced. Both 0.1 and 1 mg/kg of EC313 were statistically superior to control in reducing the fibroid weight (Fig. 3, Table S2) (p < 0.001). ER as a target gene of PR was found upregulated in IHC staining in E2 treated control grafts versus treated ones. We have not observed a significant change in frequency or intensity of PR staining among these grafts, however reduced ER staining was noticed among treatment groups (Fig. 4). Alpha-SMA, was prominent in non-treated animals when compared to EC313 and UPA treated groups (Fig. 5). ER as a target gene of PR was found upregulated in IHC staining in E2 treated control grafts versus treated ones. Ki67 was decreased in EC313 treated mice compared to controls. The strongest staining observed in fibroid grafts of control animals, correlated with the highest grafted tissue weight gain (Fig. 5). Desmin staining established that the grafts maintained the intermediate filament features of smooth muscle cells in both treated and untreated mice (Fig. 5) as reported by Fritsch et al.2.
Our molecular docking studies of EC313 against agonist and antagonist bound conformations revealed a similar orientation for the ligand at LBD of PR (Fig. 6A). Further superimposition of PR-EC313 complexes (both agonist and antagonist bound form) has revealed a negligible structural deviation (~0.7 Å) for EC313 and shared a similar pattern of interactions. The orientation of steroid ring of EC313 is exactly same as other reported oxosteroid molecules.
Stage-1 docking - docking towards agonist bound conformation
The ketone group located at the A-ring of EC313 anchors to R766 and Q725 through hydrogen bonds (Fig. 6B). The 17 α substitution in EC313 has oriented towards the hydrophobic sub-pocket (constituted by residues such as L715, L718, F794, L797, M801 and Y890) and favors a hydrophobic interaction. However, a halogen bond between one of the F atom of EC313 and the hydroxyl group of the Y890 was observed at a distance 3.2 Å, which were absent in ASO and UPA. The O atom in the oxolane of EC313 is oriented in such a way that it can readily accept a proton from the side chain of C891 and involved in a hydrogen bond. The phenyl furan ring of EC313 is involved in an edge to face stacking interactions with W755. In order to avoid the steric clashes and to facilitate the binding, side chains of M908 and M909 in helix-12 have adopted a different orientation compared to the ASO bound PR crystal structure. Apart from these interactions, several hydrophobic residues, especially L887, M756 and F778 and residues from helix-12, are involved in hydrophobic interactions with EC313.
Although the co-crystal structure of PR with ASO in the agonist bound conformation was available in the PDB, we repeated the docking calculations for ASO as a control experiment. The docking exactly reproduced the binding mode as in the crystal structure. However, a slight conformational change was observed for the amino acid side chains located at the LBD due to the ligand binding. The docking studies of UPA towards agonist bound conformation revealed a similar orientation for the oxosteroid ring as observed in EC313 and ASO. Hence, the hydrogen bonds between the ketone group of UPA and R766 and Q725 were maintained as in the previous cases. The MM-GBSA calculations suggested that EC313 exhibited an improved energy (−99 ± 14 kcal/mol) compared to ASO (−92 ± 8 kcal/mol) and UPA (−77 ± 7 kcal/mol) (Fig. 6D). Due to the substitution of bulky furan ring in EC313 compared to the N-hydroxymethanimine (in ASO) and N,N-dimethylmethanamine (in UPA) at the corresponding positions, more hydrophobic interactions with the side chains of helix 12 was observed for EC313 which may be partly contributed for the improved binding energy.
Docking towards antagonist bound conformation
The binding mode of EC313 towards antagonist bound conformation was exactly the same as that of agonist bound conformation and hence almost similar type of interactions were produced by the ligand at the LBD (Fig. 6C). However, due to outward positioning of helix-12 in the antagonist bound conformations, no interactions were observed with the side chains of helix-12. Although the co-crystal structures of ASO and UPA in the antagonist bound conformations were available in the PDB, we repeated the docking studies as a control experiment. As expected, the bound poses were very similar to the crystal pose. Further, our MM-GBSA calculations revealed a significant reduction in the binding energies for all ligands in the antagonist bound conformations when compared to the agonist bound conformations. The difference in the energy might be due to the absence of interactions with the helix-12. The EC313 exhibited slightly improved binding energy (−73 ± 2 kcal/mol) towards PR compared to the asoprisnil (−63 ± 5 kcal/mol) and UPA (−63 ± 13 kcal/mol) (Fig. 6D).
Stage-2 docking - docking of co-activators towards the agonist bound conformations
The docking studies of two co-activators revealed that SRC-1 binds to all of the PR-SPRM complexes with similar affinity (−36 ± 4 kcal/mol, −35 ± 4 kcal/mol and −34 ± 8 kcal/mol towards PR- ASO, PR-EC313 and PR-UPA complexes respectively) (Fig. 6E). However, compared to SRC-1, AIB-1 exhibited an improved binding affinity towards the PR-SPRM complexes (−57 ± 1 kcal/mol, −59 ± 1 kcal/mol and −58 ± 1 kcal/mol towards PR-ASO, PR-EC313 and PR-UPA complex respectively) (Fig. 6E). Furthermore, the binding of these co-regulators towards the PR-P4 complex revealed a remarkable difference in the affinities for both of the co-regulators. Both SRC-1 (−46 kcal/mol) and AIB-1 (−73 kcal/mol) exhibited improved binding affinity towards the PR-P4 complex. We further investigated the mode of interactions of these co-regulators towards PR-P4 complex to understand the reason for improved binding energies. When SRC-1 binds to the PR-P4 complex, the presence of a few salt bridges (between D745 (PR) and H6 (SRC1); E911 (PR) and H2 (SRC-1)) were noticed which were absent in the PR-SPRM complexes. Interestingly, the E911 located at the helix-12 had adopted a small rearrangement to facilitate a salt bridge interaction in PR-P4 complex. As discussed earlier, due to the bulkier size of the SPRMs and to accommodate them in the LBD, the side chains of M908 and M909 have rearranged. However, in the presence of a smaller sized agonist, these residues adopted different conformations in PR-P4 complex. The side chains of M908 and M909 are located at the vicinity of E911 and hence these conformational changes propagated a slight movement for E911 and facilitated the salt bridges. Due to the conformational rearrangement, several hydrophobic contacts were also observed between M908 and residues of SRC-1. At the same time, when AIB1 was docked to the PR-P4 complex, two unique salt bridges (between E907 (PR) and K3 (AIB-1); E911 (PR) and H2 (AIB-1)) were observed, which were absent in the PR-SPRM complexes. Several other hydrophobic interactions, especially with M908 and L727 were found to stabilize the interactions of AIB-1 with PR-P4 complex. As mentioned earlier, the side chains of M908 and M909 have adopted a similar conformation as observed in the PR-P4-SRC-1 complex. The role of M908 and M909 were reported previously to stabilize the agonist bound conformation of helix-1235. The result of our studies highlighted the importance of the conformational flexibility of residues at helix-12 in the determination of agonistic and partial agonistic activities.
The docking of two co-repressors, SMRT and NCoR, towards PR-SPRM complexes revealed that co-repressors have slightly better binding energies than co-activators, which may be due to the differences in the amino acid sequences between the co-regulators (Fig. 6F,G). It was reported that the SPRMs possess increased transcriptional activity compared with full antagonists23,24,25,26,35. The transcriptional repression activity is usually regulated via the binding of co-repressors. Based on this fact, we expected an improved binding affinity for the co-repressors towards PR-SPRM complex compared to the PR-antagonist complex. However, in our docking studies, both SMRT (−61 kcal/mol) and NCoR (−69 kcal/mol) exhibited better binding affinity towards the PR-mifepristone complex than PR-SPRM complexes (Fig. 6F). The affinities of SMRT and NCoR towards PR-ASO complex were −58 kcal/mol and −66 kcal/mol respectively. Similarly, the binding affinities of SMRT and NCoR towards PR-EC313 complexes were −53 kcal/mol and −65 kcal/mol respectively. The affinities of SMRT and NCoR towards PR-UPA were −60 kcal/mol and −67 kcal/mol respectively. Although the reason for improved antagonistic activities of EC313 compared to full antagonists remain unknown, our studies clearly explained partial agonistic activities of EC313.
Discussion
UFs are often asymptomatic, 20–50% of women acknowledge menorrhagia, pregnancy loss, pelvic pressure and uterine pain39. A systematic review estimated total expenses for patients per year succeeding diagnosis or surgery to be $11,717 to $25,02340. Current pharmacological interventions including oral contraceptives, progestins, nonsteroidal anti-inflammatory drugs, antifibrinolytics, gonadotropin-releasing hormone agonists. Selective E2 or P4 receptor modulator progestins, danazol and aromatase inhibitors are in current clinical practice41.
SPRMs are small molecules binding with high affinity to the PR receptor binding pocket, modulating the activity of the receptor. SPRMs include a wide spectrum of substances ranging from highly potent receptor antagonists to compounds with a balanced mix of partial-agonistic and antagonistic effects such as UPA or vilaprisan and mesoprogestins like ASO. It is clear from our in silico molecular docking studies that EC313 exhibited higher binding energies towards PR when compared to ASO and UPA. In clinical trials, UPA as well as ASO showed significant decrease in uterine fibroid volumes after termination of treatment, collectively due to reduced cell proliferation, angiogenesis, extracellular matrix and enhanced apoptosis42,43,44,45,46. Previously we have demonstrated that EC313 induces proapoptotic genes and possesses antiproliferative effects in breast cancer cells47. Improved antiprogestational activity probably gives EC313 a higher rate of antiproliferative activity and proapoptotic effects. Previously documented studies show that antagonistic SPRMs including mifepristone, UPA and vilaprisan have progestagenic activity compared to mesoprogestins like ASO and EC313 and reduced PR agonism in animal models48. It is well accepted that uterine fibroid growth is dependent on E2 and P449. More recent studies suggest that progesterone and the PR shows additional significant role than E2 in PR synthesis27,46,50. However, latest scientific thoughts point to the fact that different progestins interacts with ER differently51. This study states that, PR associates with ERα and modulate ERα chromatin binding events51. In our studies we have seen a similar effect with EC313 where it modulates ER52 and partially downregulates ER when compared to full PR antagonist (unpublished data). Based on the current study we believe that molecules such as EC313 that preferentially binds to PR in an agonistic mode slightly different than ASO and UPA helps to attain a favorable drug like characteristics. EC313 may effectively handle issues with estrogen induced complications (occult breast tumors, reduced bone mineral density and irregular bleeding profiles) and potentially minimize the necessity of estrogen add-back therapy. The differential effects of progestins on its agonistic versus antagonistic profiles on PR binding is not completely resolved yet. In the current study we have made an attempt to systematically compare 2 different SPRMs UPA and ASO with EC313 on its receptor bound structures in the presence and absence co-regulators using in silico. Our data explain differential PR binding effects and perhaps tissue selectively of EC313 over UPA and ASO.
Summary
In summary, we have demonstrated that both E2 and P4 are essential for fibroid xenograft growth, and a novel mesoprogestin (EC313), exhibiting antiprogestational as well as mild PR agonistic activity. EC313 may be superior or comparable to current standard of care (SOC) such as UPA to abolish growth of uterine fibroids. As a novel SPRM of the mesoprogestin-type with tissue selectivity, EC313 has distinct pharmacologic advantageous of oral bioavailability and in vivo stability. Potentially based on the mix of PR agonistic and antagonistic activities, EC313 showed comparable efficacy to UPA in the UF mouse model. The partial PR agonistic activity and the lack of unopposed estrogenicity makes EC313 an interesting candidate for the continuing treatment for uterine fibroids. Even though the human patient derived xenograft (PDX) UF model recapitulates the disease morphologically and biochemically, further studies regarding the mutation status of recently noted genes inhuman uterine fibroids such as MED12 or HMGA2 is warranted. We are aware that this study is also limited due to the lack of components of the immune system and possible artefacts due to effects of the human-mouse microenvironment.
References
Archer, D. F. et al. Elagolix for the management of heavy menstrual bleeding associated with uterine fibroids: results from a phase 2a proof-of-concept study. Fertil Steril 108, 152–160 e154, https://doi.org/10.1016/j.fertnstert.2017.05.006 (2017).
Fritsch, M. et al. Application of a Patient Derived Xenograft Model for Predicative Study of Uterine Fibroid Disease. PLoS One 10, e0142429, https://doi.org/10.1371/journal.pone.0142429 (2015).
Gupta, S., Jose, J. & Manyonda, I. Clinical presentation of fibroids. Best Pract Res Clin Obstet Gynaecol 22, 615–626, https://doi.org/10.1016/j.bpobgyn.2008.01.008 (2008).
Schutt, B. et al. Effect of the Novel Selective Progesterone Receptor Modulator Vilaprisan on Ovarian Activity in Healthy Women. J Clin Pharmacol 58, 228–239, https://doi.org/10.1002/jcph.998 (2018).
Tsikouras, P. et al. Ovarian reserve after fibroid embolization in premenopausal women. Minim Invasive Ther Allied Technol 26, 284–291, https://doi.org/10.1080/13645706.2017.1292919 (2017).
Reis, F. M., Bloise, E. & Ortiga-Carvalho, T. M. Hormones and pathogenesis of uterine fibroids. Best Pract Res Clin Obstet Gynaecol 34, 13–24, https://doi.org/10.1016/j.bpobgyn.2015.11.015 (2016).
Sozen, I. & Arici, A. Cellular biology of myomas: interaction of sex steroids with cytokines and growth factors. Obstet Gynecol Clin North Am 33, 41–58, https://doi.org/10.1016/j.ogc.2005.12.005 (2006).
Donnez, J., Arriagada, P., Donnez, O. & Dolmans, M. M. Emerging treatment options for uterine fibroids. Expert Opin Emerg Drugs 23, 17–23, https://doi.org/10.1080/14728214.2018.1446943 (2018).
Rabe, T. et al. Selective Progesterone Receptor Modulators for the Medical Treatment of Uterine Fibroids with a Focus on Ulipristal Acetate. Biomed Res Int 2018, 1374821, https://doi.org/10.1155/2018/1374821 (2018).
Kessel, B., Liu, J., Mortola, J., Berga, S. & Yen, S. S. Treatment of uterine fibroids with agonist analogs of gonadotropin-releasing hormone. Fertil Steril 49, 538–541 (1988).
Lethaby, A., Vollenhoven, B. & Sowter, M. Pre-operative GnRH analogue therapy before hysterectomy or myomectomy for uterine fibroids. Cochrane Database Syst Rev, CD000547, https://doi.org/10.1002/14651858.CD000547 (2001).
Lethaby, A., Puscasiu, L. & Vollenhoven, B. Preoperative medical therapy before surgery for uterine fibroids. Cochrane Database Syst Rev 11, CD000547, https://doi.org/10.1002/14651858.CD000547.pub2 (2017).
Minaguchi, H., Wong, J. M. & Snabes, M. C. Clinical use of nafarelin in the treatment of leiomyomas. A review of the literature. J Reprod Med 45, 481–489 (2000).
Bartels, C. B. et al. An Evidence-based Approach to the Medical Management of Fibroids: A Systematic Review. Clin Obstet Gynecol 59, 30–52, https://doi.org/10.1097/GRF.0000000000000171 (2016).
Farris, M., Bastianelli, C., Rosato, E., Brosens, I. & Benagiano, G. Uterine fibroids: an update on current and emerging medical treatment options. Ther Clin Risk Manag 15, 157–178, https://doi.org/10.2147/TCRM.S147318 (2019).
Leppert, P. C. et al. Comparative ultrastructure of collagen fibrils in uterine leiomyomas and normal myometrium. Fertil Steril 82(Suppl 3), 1182–1187, https://doi.org/10.1016/j.fertnstert.2004.04.030 (2004).
Jayes, F. L. et al. Loss of stiffness in collagen-rich uterine fibroids after digestion with purified collagenase Clostridium histolyticum. Am J Obstet Gynecol 215, 596 e591–596 e598, https://doi.org/10.1016/j.ajog.2016.05.006 (2016).
Holdsworth-Carson, S. J. et al. Differences in the cellular composition of small versus large uterine fibroids. Reproduction 152, 467–480, https://doi.org/10.1530/REP-16-0216 (2016).
Klein-Hitpass, L. et al. The progesterone receptor stimulates cell-free transcription by enhancing the formation of a stable preinitiation complex. Cell 60, 247–257, https://doi.org/10.1016/0092-8674(90)90740-6 (1990).
Tsai, M. J. & O’Malley, B. W. Molecular mechanisms of action of steroid/thyroid receptor superfamily members. Annu Rev Biochem 63, 451–486, https://doi.org/10.1146/annurev.bi.63.070194.002315 (1994).
Leonhardt, S. A. & Edwards, D. P. Mechanism of action of progesterone antagonists. Exp Biol Med (Maywood) 227, 969–980, https://doi.org/10.1177/153537020222701104 (2002).
McKenna, N. J., Lanz, R. B. & O’Malley, B. W. Nuclear receptor coregulators: cellular and molecular biology. Endocr Rev 20, 321–344, https://doi.org/10.1210/edrv.20.3.0366 (1999).
Spitz, I. M. & Chwalisz, K. Progesterone receptor modulators and progesterone antagonists in women’s health. Steroids 65, 807–815 (2000).
Benagiano, G., Bastianelli, C. & Farris, M. Selective progesterone receptor modulators 3: use in oncology, endocrinology and psychiatry. Expert Opin Pharmacother 9, 2487–2496, https://doi.org/10.1517/14656566.9.14.2487 (2008).
Benagiano, G., Bastianelli, C. & Farris, M. Selective progesterone receptor modulators 2: use in reproductive medicine. Expert Opin Pharmacother 9, 2473–2485, https://doi.org/10.1517/14656566.9.14.2473 (2008).
Benagiano, G., Bastianelli, C. & Farris, M. Selective progesterone receptor modulators 1: use during pregnancy. Expert Opin Pharmacother 9, 2459–2472, https://doi.org/10.1517/14656566.9.14.2459 (2008).
Chwalisz, K. et al. Selective progesterone receptor modulator development and use in the treatment of leiomyomata and endometriosis. Endocr Rev 26, 423–438, https://doi.org/10.1210/er.2005-0001 (2005).
Chwalisz, K., Elger, W., Stickler, T., Mattia-Goldberg, C. & Larsen, L. The effects of 1-month administration of asoprisnil (J867), a selective progesterone receptor modulator, in healthy premenopausal women. Hum Reprod 20, 1090–1099, https://doi.org/10.1093/humrep/deh738 (2005).
Xu, E. H. & Lambert, M. H. Structural insights into regulation of nuclear receptors by ligands. Nucl Recept Signal 1, e004, https://doi.org/10.1621/nrs.01004 (2003).
Edwards, D. P. The role of coactivators and corepressors in the biology and mechanism of action of steroid hormone receptors. J Mammary Gland Biol Neoplasia 5, 307–324 (2000).
Tetel, M. J., Giangrande, P. H., Leonhardt, S. A., McDonnell, D. P. & Edwards, D. P. Hormone-dependent interaction between the amino- and carboxyl-terminal domains of progesterone receptor in vitro and in vivo. Mol Endocrinol 13, 910–924, https://doi.org/10.1210/mend.13.6.0300 (1999).
Kalkhoven, E., Wissink, S., van der Saag, P. T. & van der Burg, B. Negative interaction between the RelA(p65) subunit of NF-kappaB and the progesterone receptor. J Biol Chem 271, 6217–6224, https://doi.org/10.1074/jbc.271.11.6217 (1996).
Lusher, S. J. et al. Structural basis for agonism and antagonism for a set of chemically related progesterone receptor modulators. J Biol Chem 286, 35079–35086, https://doi.org/10.1074/jbc.M111.273029 (2011).
Shiau, A. K. et al. Structural characterization of a subtype-selective ligand reveals a novel mode of estrogen receptor antagonism. Nat Struct Biol 9, 359–364, https://doi.org/10.1038/nsb787 (2002).
Lusher, S. J. et al. X-ray structures of progesterone receptor ligand binding domain in its agonist state reveal differing mechanisms for mixed profiles of 11beta-substituted steroids. J Biol Chem 287, 20333–20343, https://doi.org/10.1074/jbc.M111.308403 (2012).
Madauss, K. P. et al. A structural and in vitro characterization of asoprisnil: a selective progesterone receptor modulator. Mol Endocrinol 21, 1066–1081, https://doi.org/10.1210/me.2006-0524 (2007).
Ritchie, D. W., Kozakov, D. & Vajda, S. Accelerating and focusing protein-protein docking correlations using multi-dimensional rotational FFT generating functions. Bioinformatics 24, 1865–1873, https://doi.org/10.1093/bioinformatics/btn334 (2008).
Ritchie, D. W. & Venkatraman, V. Ultra-fast FFT protein docking on graphics processors. Bioinformatics 26, 2398–2405, https://doi.org/10.1093/bioinformatics/btq444 (2010).
Silberzweig, J. E., Powell, D. K., Matsumoto, A. H. & Spies, J. B. Management of Uterine Fibroids: A Focus on Uterine-sparing Interventional Techniques. Radiology 280, 675–692, https://doi.org/10.1148/radiol.2016141693 (2016).
Soliman, A. M., Yang, H., Du, E. X., Kelkar, S. S. & Winkel, C. The direct and indirect costs of uterine fibroid tumors: a systematic review of the literature between 2000 and 2013. Am J Obstet Gynecol 213, 141–160, https://doi.org/10.1016/j.ajog.2015.03.019 (2015).
Bonafede, M. M. et al. Women with Newly Diagnosed Uterine Fibroids: Treatment Patterns and Cost Comparison for Select Treatment Options. Popul Health Manag 21, S13–S20, https://doi.org/10.1089/pop.2017.0151 (2018).
Ohara, N. et al. Comparative effects of SPRM asoprisnil (J867) on proliferation, apoptosis, and the expression of growth factors in cultured uterine leiomyoma cells and normal myometrial cells. Reprod Sci 14, 20–27, https://doi.org/10.1177/1933719107311464 (2007).
Sasaki, H. et al. A novel selective progesterone receptor modulator asoprisnil activates tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated signaling pathway in cultured human uterine leiomyoma cells in the absence of comparable effects on myometrial cells. J Clin Endocrinol Metab 92, 616–623, https://doi.org/10.1210/jc.2006-0898 (2007).
Morikawa, A. et al. Selective progesterone receptor modulator asoprisnil down-regulates collagen synthesis in cultured human uterine leiomyoma cells through up-regulating extracellular matrix metalloproteinase inducer. Hum Reprod 23, 944–951, https://doi.org/10.1093/humrep/den025 (2008).
Wilkens, J. et al. Effects of the selective progesterone receptor modulator asoprisnil on uterine artery blood flow, ovarian activity, and clinical symptoms in patients with uterine leiomyomata scheduled for hysterectomy. J Clin Endocrinol Metab 93, 4664–4671, https://doi.org/10.1210/jc.2008-1104 (2008).
Stewart, E. A. et al. Safety and efficacy of the selective progesterone receptor modulator asoprisnil for heavy menstrual bleeding with uterine fibroids: pooled analysis of two 12-month, placebo-controlled, randomized trials. Hum Reprod 34, 623–634, https://doi.org/10.1093/humrep/dez007 (2019).
Nair, H. B., Santhamma, B., Krishnegowda, N. K., Dileep, K. V. & Nickisch, K. J. Effects of Combination of Estradiol with Selective Progesterone Receptor Modulators (SPRMs) on Human Breast Cancer Cells In Vitro and In Vivo. PLoS One 11, e0151182, https://doi.org/10.1371/journal.pone.0151182 (2016).
Elger, W. et al. Endocrine pharmacological characterization of progesterone antagonists and progesterone receptor modulators with respect to PR-agonistic and antagonistic activity. Steroids 65, 713–723 (2000).
Carr, B. R. et al. An evaluation of the effect of gonadotropin-releasing hormone analogs and medroxyprogesterone acetate on uterine leiomyomata volume by magnetic resonance imaging: a prospective, randomized, double blind, placebo-controlled, crossover trial. J Clin Endocrinol Metab 76, 1217–1223, https://doi.org/10.1210/jcem.76.5.8496313 (1993).
Stewart, E. A. Clinical practice. Uterine fibroids. N Engl J Med 372, 1646–1655, https://doi.org/10.1056/NEJMcp1411029 (2015).
Mohammed, H. et al. Progesterone receptor modulates ERalpha action in breast cancer. Nature 523, 313–317, https://doi.org/10.1038/nature14583 (2015).
Singhal, H. et al. Progesterone receptor isoforms, agonists and antagonists differentially reprogram estrogen signaling. Oncotarget 9, 4282–4300, https://doi.org/10.18632/oncotarget.21378 (2018).
Acknowledgements
K.V.D. acknowledges JSPS for the postdoctoral fellowship.
Author information
Authors and Affiliations
Contributions
H.B.N. conceptualized the study, implemented, conducted animal experiments, analyzed the data and wrote the manuscript. K.N. conceptualized and implemented the study. P.B. conducted the animal experiments. R.S. provided the clinical samples for the study and involved in scientific discussions for implementing the study. Edited the manuscript. B.S. synthesized the chemical compounds for the study. K.A. synthesized the chemical compounds for the study. K.V.D. conducted the in silico study and prepared the report and wrote molecular docking section of the manuscript. K.Y.J.Z. supervised the in silico study and prepared the report and wrote molecular docking section of the manuscript. All authors has read or corrected and approved the final manuscript.
Corresponding author
Ethics declarations
Competing interests
K.N. is a co-founder and shareholder of Evestra, Inc. H.B.N., B.S., and K.A. are salaried full time employees of Evestra, Inc. R.S., P.B., K.Y.J.Z. and K.V.D. declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
41598_2019_53467_MOESM1_ESM.docx
EC313-a tissue selective SPRM reduces the growth and proliferation of uterine fibroids in a human uterine fibroid tissue xenograft model
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Nair, H.B., Santhamma, B., Dileep, K.V. et al. EC313-a tissue selective SPRM reduces the growth and proliferation of uterine fibroids in a human uterine fibroid tissue xenograft model. Sci Rep 9, 17279 (2019). https://doi.org/10.1038/s41598-019-53467-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-019-53467-w
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.