Progesterone Actions and Resistance in Gynecological Disorders

Estrogen and progesterone and their signaling mechanisms are tightly regulated to maintain a normal menstrual cycle and to support a successful pregnancy. The imbalance of estrogen and progesterone disrupts their complex regulatory mechanisms, leading to estrogen dominance and progesterone resistance. Gynecological diseases are heavily associated with dysregulated steroid hormones and can induce chronic pelvic pain, dysmenorrhea, dyspareunia, heavy bleeding, and infertility, which substantially impact the quality of women’s lives. Because the menstrual cycle repeatably occurs during reproductive ages with dynamic changes and remodeling of reproductive-related tissues, these alterations can accumulate and induce chronic and recurrent conditions. This review focuses on faulty progesterone signaling mechanisms and cellular responses to progesterone in endometriosis, adenomyosis, leiomyoma (uterine fibroids), polycystic ovary syndrome (PCOS), and endometrial hyperplasia. We also summarize the association with gene mutations and steroid hormone regulation in disease progression as well as current hormonal therapies and the clinical consequences of progesterone resistance.


Introduction
Progesterone is one of the key steroid hormones in the complex regulation of female reproductive functions, largely controlled in multiple organs such as the uterus, ovary, mammary gland, and brain (reviewed in [1]). High levels of progesterone are produced from the corpus luteum and placenta, which are necessary to maintain a successful pregnancy. Beyond pregnancy, the majority of female reproductive processes are also controlled by progesterone, including oocyte maturation, ovulation, menstruation, facilitation of implantation and decidualization, uterine growth, suppression of myometrial contraction, mammary gland development, regulation of milk production, and sexual behavior as summarized in [1]. Progesterone actions are mediated by progesterone receptors (PGR). Female mice with ablation of Pgr (PGRKO) clearly show complete sterility with multiple abnormalities in reproductive functions: ovulation failure, hyperplastic uterine response to estrogen and progesterone, decidualization failure, disruption of mammary gland development, and a lack of sexual behavior [2]. PGR consists primarily of two nuclear isoforms (PRA and PRB) which have distinct expression patterns and functional profiles [3]. A single gene with independently regulated promoters is responsible for encoding PRA and PRB, producing similar proteins with PRB having an extra 164 amino acids at the N-terminus [4]. Characterization of PRA or PRB mutations in female mice indicates that PRA mainly regulates uterine PGR functions, whereas PRB is important for mammary gland development [5,6]. While progesterone and its activation of downstream mechanisms are mediated by PGR, the actions of progesterone are tightly integrated with estrogen and its responsive signaling pathways [1,[7][8][9].
The endometrium, the lining of the uterus, is one of the most dynamic tissues in adults. The endometrium undergoes a persistent cycle of remodeling including shedding, proliferation to regenerate layers, and differentiation during menstruation. These processes are The goal of this review is to highlight the inroads by which faulty progesterone signaling mechanisms and cellular responses to progesterone lead to the initiation or progression of gynecological disorders, including endometriosis, adenomyosis, leiomyoma (uterine fibroids), polycystic ovary syndrome (PCOS), and endometrial hyperplasia. We focus on summarizing the established and putative gene mutations and misregulation of steroid hormone signaling in disease progression, as well as current hormonal therapies and the clinical consequences of progesterone resistance (Table 1).

Progesterone Resistance in the Endometrium
Progesterone resistance is widely recognized as endometrial progesterone unresponsiveness with subsequent dysregulation of epithelial and stromal gene networks in the endometrium [12][13][14][15]. The accumulation of impaired progesterone and persistent estrogen actions from one menstrual cycle to another induces abnormal pathophysiological changes in the endometrium. These could lead to the development of endometrial-related disorders such as endometriosis, adenomyosis, PCOS, endometrial hyperplasia, and implantation failure [12][13][14][15]20]. To date, large-scale gene expression studies in endometriosis [16,17] and PCOS [21] have revealed that progesterone-regulated genes are most likely altered in their endometrial expression during the early-and mid-secretory phases and these dysregulated genes are associated with loss of normal endometrial functions and disease establishment and progression (Figure 1). Aberrant induction of inflammatory and/or oncogenic related genes are also strongly correlated to the dysregulation of endometrial functions in these diseases [12,22,23]. Epigenetic alterations, including hypermethylation which reduces PGR expression [14,24] and the expression of other endometrial genes directly or indirectly linked to progesterone [25][26][27][28][29], can result in progesterone unresponsiveness. The recent advances in whole-exome or genome sequencing (WES or WGS) have allowed the identification of common somatic mutations in the endometrial epithelial cells that potentially lead to the development of endometriosis and/or adenomyosis [30][31][32][33][34]. Especially significant are KRAS mutations which are observed in adenomyosis co-occurring endometriosis with downregulated PGR expression [31]. Aberrancies of gene expression, epigenetic marks, and/or gene mutations likely influence progesterone signaling in the endometrium. Further details of the mechanisms in each disease are summarized in the sections below.

Disease Features in Endometriosis
Endometriosis is defined as the presence of endometrial-like tissues containing endometrial glands and stroma, often with hemosiderin outside of the uterus, mainly on pelvic organs and tissues [35][36][37][38]. Retrograde menstruation, which is the reflux of menstrual debris containing endometrial tissues through the fallopian tubes into the pelvic cavity [39], has been widely accepted as the origin of endometriotic tissues. However, as retrograde menstruation occurs in more than 90% of menstruating women [40], other factors must contribute to the establishment of endometriotic lesions [35,37,38]. The common types in endometriosis include superficial peritoneal lesions, deep-infiltrating endometriosis, and ovarian endometrioma, as well as extensive adhesion to the lesions with other pelvic organs which is also one of the common features of endometriosis [35][36][37][38]. The prevalence of endometriosis is estimated to affect approximately 10% of reproductive-age women, representing nearly 190 million women worldwide [37,41]. It is associated with debilitating chronic pelvic pain and infertility which substantially reduce the quality of life of women and their families [38,42]. Indeed, the health care costs for endometriosis in 2008 have been estimated at approximately $4000 per person in the United States (U.S.) [37,43].

Current Treatments in Endometriosis
Because endometriosis is an estrogen-dependent disorder, current treatments focus on suppression and/or inhibition of local or systemic estrogen production and its actions. However, medical treatments such as hormonal therapies do not remove lesions and therefore cannot completely abrogate disease-associated symptoms [44,45]. The most common and long-term treatment is the use of oral contraceptive pills formulated with estrogen and progestin or progestin-only. These are effective at reducing chronic pelvic pain and/or dysmenorrhea [46,47]. The consensus from clinical reports in the literature has shown that contraceptive pills are beneficial in women with dysmenorrhea and endometriosisassociated pain [44,45]. The levonorgestrel intrauterine device (LNG-IUD) often results in amenorrhea, which is especially effective for dysmenorrhea [48]. However, the efficacy of progestin therapy is limited due to only minimally improving the symptoms in the short term, and symptoms frequently reappear after treatment discontinuation [44,49]. GnRH agonists are preferentially used for the second-line pharmacological treatment of endometriosis-associated pain and act to inhibit estrogen production by the ovary, limiting its cellular functions [35,50]. While GnRH agonists effectively reduce the deleterious effects of endometriosis and lesion development, they are not compatible with the restoration of fertility as folliculogenesis in the ovary is shut down. Laparoscopic surgery to remove lesions can provide some pain relief. However, hormonal treatments, as well as laparoscopic surgeries, are often of limited efficacy with high recurrence rates, frequent side effects, additional costs, and potential morbidity [51]. The recurrence rate of surgical excision of lesions is over 50% after five years [52,53]. GnRH agonist therapy induces temporary menopause with unwanted side effects and over 50% of women exhibit a recurrence of symptoms within two years [54,55]. Progesterone resistance is a major complication for progestin therapy, leading to the escalation of estrogen activity [8]. Thus, a critical need exists to develop more effective therapies for endometriosis that target the biologically important mechanisms that underpin the pathophysiology of this disease.

PGR Expression in Endometriosis
PGR mediates progesterone actions in the progesterone responsive tissues, including the endometrium. While PRA and PRB isoforms are detected in human eutopic endometrium with endometriosis during the menstrual cycle, both the expression of PRA and PRB are generally lower in any type of ectopic lesions [56]. In particular, deficient PRB expression has been reported from several groups [27,57,58]. The consensus abnormal regulatory mechanism stems from epigenetic alteration of the PGR promoter regions in the chronic high cytokine state induced by the presence of lesions. This results in differential expression at the PRB transcription start sites that are hypermethylated, but the regions associated with PRA transcription are not, leading to the disproportional expression of the two PGR isoforms [26,27,59]. However, the relative abundance of PGR isoforms in the cells cannot explain the progesterone actions due to the complex mechanisms of PGR signaling [12,60]. For instance, endometrial stromal cells become more sensitive to PGR signaling during the decidualization process when the cyclic AMP (cAMP) levels are elevated and then the protein kinase A (PKA) pathway is activated [12, 61,62]. Furthermore, some studies have reported no differences of PGR isoforms observed in the eutopic endometrium with/without endometriosis [63,64]. Ectopic rectosigmoid lesions do not show any different PGR expressions either [65]. Those results suggest that it would be hard to conclude that loss or altered PGR expression alone in the eutopic endometrium or the ectopic lesions directly leads to progesterone resistance in endometriosis.

Altered Gene Expression in Endometriosis
The pathogenesis of endometriosis is a complex process and still remains to be fully understood. Endometrial stem or progenitor cells have been proposed to contribute to the development of endometriosis [66]. Altered local immune dysfunction and inflammatory responses can be the consequence of endometriosis [67]. Elevated ESR2 activity in retrograded endometrial tissues interacts with the cytoplasmic inflammasome to increase IL-1β to enhance cellular adhesion and proliferation, as well as epithelial-mesenchymal transition (EMT), leading to an escape from immune surveillance and development of endometriotic lesions [68]. On the other hand, estrogen is a key promoter for endometriotic lesion growth and progression and establishment of the chronic endometriotic environment within the pelvic cavity, whereas progesterone is a master regulator tightly controlling estrogen actions. Endometriosis and its established inflammatory environment disrupt the balance of hormonal regulation and reduce coordinated progesterone responses or vice versa, resulting in the development of progesterone resistance [12][13][14]69].
Progesterone resistance includes the disruption of progesterone-dependent genes in the eutopic endometrium with endometriosis [16,17,70,71]. Burney et al. [16] have reported impaired gene expression in the eutopic endometrium with endometriosis throughout the cycle, whereas the most extensive changes are incomplete transitions of the endometrium occurring from the proliferative to early secretory phase, especially in the persistence of estrogen-regulated genes. The best characterized dysregulated genes identified in the secre-tory phase are progesterone targets such as FOXO1A, MIG6, and CYP26A1, indicating the attenuation of progesterone response [16]. Garcia-Alonso et al. have recently profiled singlecell (sc) and temporal/spatial transcriptome of human endometrium using 10× scRNA-seq and single-nucleus RNA-seq, as well as Genomics Visium platforms [72]. Spatiotemporal characterization during the proliferative and secretory phases of endometrium shows that SOX9+LGR5+ populations are present that are associated with proliferative and regenerative potential stem cell niche. When the authors explore the expression of specific epithelial genes from endometriosis public data sets, SOX9+LGR5+ subset populations show upregulated epithelial gene markers (WNT7A and KRT17) in the lesions which are similar to those expression levels in proliferative endometrium [72]. Furthermore, WNT and NOTCH signaling regulate ciliated and secretory epithelial cells with opposing roles to distinct epithelial lineages. Although it is not clear whether the expression levels are compared with eutopic endometrial tissues from endometriosis and control patients, the studies using these new techniques in endometriosis will improve further understanding of altered gene regulation in specific cellular populations of endometriosis. Currently, two preprint papers are available for single-cell transcriptomics in endometriosis lesions [73,74].

Altered PGR Signaling in the Eutopic Endometrium with Endometriosis
Endometriosis is known as an estrogen-dependent disease because alterations of progesterone-regulated genes and signaling cause persistent estrogen activation [12]. To modulate PGR downstream target genes, steroid receptor coactivators (SRC) are first recruited for the modification of chromatin structures to form complexes with PGR and other transcription factors [75,76]. Based on a series of studies from O'Malley's group [77][78][79][80][81][82], SRC-1 and SRC-2 are likely most relevant to regulating progesterone-dependent endometrial functions. On the other hand, SRC functions also contribute to PGR-dependent disease progression. Loss of Src-1 reduces endometriotic lesion progression using a mouse model of endometriosis [83]. A newly identified 70 kDa SRC-1 isoform is highly elevated in the ectopic lesions; this lesion-specific form is generated by abnormal TNFα-induced MMP9 activity and it prevents TNFα-mediated cell death induced by estrogen-dependent fulllength SRC-1 function. These studies suggest that the endometriosis-induced inflammatory environment alters the molecular properties of SRC-1, and the SRC-1 isoform promotes endometriosis progression via EMT and epithelial cell invasion [83].
Dysregulation of PGR signaling as a part of progesterone resistance has been reported in endometriosis [9,12-14]. IHH signaling is one of the major PGR-mediated pathways which inhibits the epithelial proliferation stimulated by estrogen that is required for successful implantation, followed by stimulation of COUP-TFII and BMP2 for successful decidualization [84][85][86][87]. Nuclear and cytoplasmic IHH in the endometrium generally increases from the late proliferative to secretory phases [88]. However, both nuclear and stromal IHH expression decreases in the secretory phase of eutopic endometrium with endometriosis [88]. The loss of IHH in the mouse uterus produces a similar phenotype to PGRKO mice with global ablation of PGR signaling, confirming the importance of IHH signaling in the endometrium [86]. The expression of COUP-TFII is also reduced in the eutopic endometrium with endometriosis and ectopic lesions [89]. Other critical PGR signaling mediators: WNT4 [90], HOXA10 [71], MIG6 [16,91,92], FOXO1 [16,93], and CRISPLD2 [94] decrease in the eutopic endometrium with endometriosis, especially during the secretory phase. WNT4 [95], HOXA10 [96,97], MIG6 [91,92], and FOXO1 [98,99] are PGR targets and/or mediators in the endometrium and critical for embryo implantation and decidualization. These results indicate that dysregulated and/or disrupted PGR targets in the eutopic endometrium can cause unresponsiveness of progesterone actions, probably further leading to disease progression.
NOTCH signaling modulates crucial mechanisms for endometrial decidualization and successful pregnancy [100,101]. NOTCH signaling receptors, ligands, and direct target genes are also decreased in the eutopic endometrium of women and baboons with endometriosis [93]. Knockdown of NOTCH1 disturbs decidualization with the downregu-lation of FOXO1 in vitro stromal cell culture [93]. On the other hand, NOTCH intracellular domain 1, NICD1, is increased and inversely associated with its expression with decreased PGR expression in the eutopic endometrium and ectopic lesions [102]. Furthermore, inhibition of NOTCH signaling activation restores progesterone responsiveness and PGR expression [102].
Progesterone resistance can be explained by the dysregulation of immunophilin FKBP52, a PGR chaperone protein that governs progesterone actions like implantation and decidualization in the uterus [103,104]. In endometriosis patients, FKBP52 is reduced in both the proliferative and secretory phases within eutopic endometrium and ectopic lesions [105,106]. Deletion of FKBP52 enhances endometriotic lesion growth and progression with increased inflammation, proliferation, and angiogenesis [105]. In vitro cell culture studies suggest that FKBP52 expression might be regulated by HOXA10 [106] or miR-29c [107]. Reduction of FKBP52 is also observed in a non-human primate model of endometriosis [108].
The presence of altered chronic inflammation is one of the well-known features of endometriosis [37,38]. Activated STAT3 and NFκB signaling by cytokines and chemokines associated with immune cells have been shown in endometriosis [109][110][111][112][113]. Aberrant p-STAT3, co-occurring with HIF1A, presents in the eutopic endometrium in humans and non-human primates with endometriosis [111]. Although STAT3 directly interacts with the PRA isoform and is required for normal endometrial functions such as decidualization [114], STAT3 constitutive stimulation is activated by inflammatory factors from tissue residential or peritoneal immune cells in endometriosis [112,113,115]. Yoo et al. [116] have reported that PIAS3, which is a negative regulator of STAT3 activity, is decreased in the eutopic endometrium with endometriosis in humans and non-human primates inversely associated with aberrant p-STAT3. In support of PIAS3 having an active role in preventing endometriosis, an in vitro study has shown that INFγ can reduce PIAS3 but increases p-STAT3, suggesting aberrant STAT3 activation by attenuation of PIAS3 [116]. On the other hand, overexpression of KRAS and the histone deacetylase SIRT1 has been observed in the eutopic endometrium with endometriosis [117]. In the mouse model, Kras activation increases SIRT1 and decreases PGR target genes, including the genes related to IHH signaling [117]. SIRT1 colocalizes with BCL6, a known target of STAT3 [118], in the nuclei of eutopic endometrium [117,119]. BCL6 binds the GLI1 promoter, a transcription factor mediating the Hedgehog pathway, to suppress GLI1 transcription, resulting in the disruption of progesterone-mediated IHH signaling [117]. The KRAS gene is often mutated to become constitutively activated in the endometrium [30,31,33,34,120]. The involvement of somatic mutations in endometriosis is summarized in Section 3.7. SOX17 has been identified as an essential uterine PGR-regulated gene [121] and regulates implantation and gland development, especially epithelial proliferation and differentiation through IHH signaling [122,123]. In endometriosis, SOX17 is decreased in the proliferative and secretory phases of eutopic endometrium compared with normal endometrium [124]. Reduced SOX17 is correlated with reduced IHH expression. Interestingly, transcriptome profiles with loss of Sox17 overlap with those from Arid1a ablation [124]. Reduction of ARID1A is observed in the Sox17-ablated uterus, but SOX17 exhibits normal expression in the Arid1a-ablated uterus, indicating that ARID1A is potentially regulated by SOX17. Because ablation of Arid1a disrupts PGR signaling and ARID1A can directly bind to PRA, ARID1A is essential for normal endometrial functions and reduced ARID1A expression can alter PGR signaling leading to progesterone resistance in the endometrium with endometriosis [125]. Kim et al. [126] have also recently demonstrated that one of the histone deacetylases, HDAC3, has an essential role in endometrial decidualization and loss of Hdac3 in the uterus disturbs PGR signaling. HDAC3 expression is decreased in the endometrium with endometriosis and might be involved in a part of progesterone resistance.

Epigenetic Alterations in Endometriosis
Dysregulated PGR target genes can be explained as consequences of altered methylation status in the endometrium [14,24]. A well-known PGR target, HOXA10, reduces its expression in the eutopic endometrium with endometriosis [71]. Wu et al. have first reported that reduction of HOXA10 expression is due to hypermethylation of the putative promoter regions of HOXA10 in the eutopic endometrium with endometriosis [29]. Kim et al. [127] have demonstrated that a baboon model of endometriosis results in a gradually decreased HOXA10 in the eutopic endometrium after the lesion induction, owing to the increased DNA methylation of the proximal promoter of HOXA10. Hypermethylation of the HOXA10 promoter region is also observed in the mouse uterus with induced endometriosis [128]. Aberrant promoter methylation of SF1, PGRB, ESR2, which are important for the response of progesterone, has also been reported in the eutopic endometrium and ectopic lesions with resulting progesterone resistance [25-28]. On the other hand, the Giudice group [18] has reported the analysis of global DNA methylation in the eutopic endometrium with or without endometriosis during the proliferative, early-, and mid-secretory phases show no differential methylation of specific promoter regions of the above genes. However, their results show a significant number of loci with altered DNA methylation that are found in the mid-secretory phase of the endometrium with endometriosis. Furthermore, alterations of DNA methylation are associated with altered gene expression related to endometrial function, including cell proliferation, inflammation, angiogenesis, and steroid hormone response. Thus, epigenetic modification in the eutopic endometrium contributes to disrupted hormonal actions causing progesterone resistance in endometriosis [18]. It is known that steroid hormones (estrogen and progesterone) and chronic inflammation can alter the chromatin landscape in the endometrium [12,18]. The Giudice group [19] has further examined the effects of 17β-estradiol, progesterone, and their combination on the DNA methylome and transcriptome, comparing eutopic endometrial stromal fibroblasts isolated from normal (disease-free) and endometriosis patients from different disease stages. 17β-estradiol and progesterone individually and together promote unique profiles in DNA methylome. Overall, 17β-estradiol alone induces broad changes in the DNA methylome in normal endometrium, but progesterone alone has a lesser effect. The combination of 17β-estradiol and progesterone results in reduced numbers of differentially methylated loci compared to 17β-estradiol alone. Hormonal responses to the DNA methylome in the eutopic endometrial stromal fibroblast are aberrant in the early-and late-stage endometriosis, which is probably due to already existing DNA methylation marks prior to hormone treatments. Additionally, hormone-induced methylation alterations are largely enriched within enhancers and intergenic regions but are minimally involved in proximal promoters and CpG islands.
Dyson et al. [129] have reported that members of the GATA transcription factor family are differentially methylated in stromal cells from normal endometrium without endometriosis and ectopic stromal cells isolated from ovarian endometrioma. GATA2 regulates genes necessary for decidualization in the normal endometrium. GATA2 is hypermethylated in the ectopic stromal cells. In contrast, GATA6 is normally hypermethylated and its expression restricted, but in lesions, it becomes hypomethylated and replaces GATA2, which promotes endometriotic phenotypes. This study did not examine the methylation statuses of GATA2 or GATA6 in the eutopic endometrium with endometriosis, including different stages of the disease and different cyclic phases. This analysis would be of interest as it would conclusively determine whether this switch is causative of the disease or a result of tissue differences after the establishment of endometriosis.

Genomic Alterations and Somatic Mutations in Endometriosis
Endometriosis is a heterogeneous and complex disease. Currently, there are no wellcharacterized markers and no distinct causative evidence of endometriosis risk variants that are associated with putative genes of interest [38,130]. Genome-wide association studies (GWAS) have identified loci of interest with or without endometriosis, whereas it remains unclear how genome-wide significant loci contribute to the endometriosis pathogenesis [37]. However, analysis of genes located nearest to the risk loci indicates the impact of cell adhesion, migration, angiogenesis, inflammation, and hormone-related pathways, specifically WNT, MAPK, and STAT3 signaling under different conditions such as stages, fat distribution, pain scales, and cancers [37,38].
On the other hand, WES analyses show somatic epithelial mutations in ovarian endometrioma, deep-infiltrating endometriosis, and normal endometrium [30,32,34]. Suda et al. [34] have identified a number of somatic mutations that are associated with ovarian cancer in laser captured epithelial cells from ovarian endometrioma and normal endometrium. KRAS and PIK3CA are found especially as the most common mutations in both endometrioma and endometrium. Anglesio et al. [30] have reported that epithelium from deep-infiltrating endometriotic lesions carries known cancer driver mutations: KRAS, PPP2R1A, PIK3CA, and ARID1A from 5 of 24 patients (21%). A recent study [31] has indicated that KRAS mutations are more frequent in cases of adenomyosis with co-occurring endometriosis, leading to a reduced efficacy of progestin therapy by the silencing of PGR, and can be a driver for adenomyosis development as described in further detail in the adenomyosis section below.

Disease Features in Adenomyosis
Adenomyosis is characterized by the infiltration of endometrial-like tissues composed of glands and stroma into the myometrium [131]. It produces a diffusely enlarged uterus with ectopic adenomyosis lesions surrounded by the hypertrophic myometrium [132,133]. Adenomyosis has been considered to result in an invagination of the endometrium from the breakdown of the junctional zone between basalis endometrium and myometrium [134][135][136]. On the other hand, it has been suggested that de novo generation of endometrial tissues in ectopic locations such as embryonic Mullerian stem cells and adult stem and/or progenitor cells is an alternative theory [135,[137][138][139]. Although adenomyosis and endometriosis share several histological and molecular features [140], patients with adenomyosis often suffer menorrhagia and pregnancy loss, including recurrent implantation failures and miscarriages [141,142]. The prevalence of adenomyosis can be up to 20~35% based on data from patients who underwent hysterectomy [143][144][145] though there are large variations depending on the studies [146]. Because hysterectomy is the definitive cure for adenomyosis, a recent population-based study in the U.S. has reported that~82% of patients among women aged 16-60 years following incident adenomyosis undergo hysterectomy [147]. The highest incidence of adenomyosis is in women in their 40's, 41-45 years (27.3%), but 36-40 (20.7%) and 46-50 years (19.6%) also show higher prevalence [147], probably due to adenomyosis often being histologically diagnosed/confirmed after hysterectomy [148]. On the other hand, recent advanced imaging systems are able to detect the presence of smaller adenomyosis lesions. Indeed, transvaginal ultrasound (TVUS) or magnetic resonance imaging (MRI) have indicated >30% of women aged 18-30 years [149] or 60% of patients aged 18-42 years [150] might already have adenomyosis. Thus, initiation of adenomyosis, i.e., abnormal invagination of the endometrium into the myometrium, has occurred in younger reproductive-age women [148]. Therefore, the identification of marker genes or risk factors for early identification and treatment of adenomyosis needs to be developed.

Current Treatments in Adenomyosis
Adenomyosis is an estrogen-dependent gynecological disease like endometriosis. The progression of adenomyosis lesions with hypertrophic myometrium is enhanced by estrogen and abrogated by progesterone [136]. For those reasons, hormonal treatments such as GnRH agonists, progestins, and oral contraceptives have been used to suppress pain symptoms and abnormal heavy menorrhagia [132,151,152]. GnRH agonists are effective in causing systemic hypoestrogenism to reduce the size of adenomyosis and improve adenomyosis-associated symptoms [153][154][155], whereas the side effects of GnRH agonists (menopausal symptoms) limit their use. LNG-IUD has been considered most effective and successfully used to treat adenomyosis because it is efficient in suppressing menstrual bleeding [156][157][158][159][160]. The efficacy of LNG-IUD is generally higher than other progestin-based treatments [151,152]. This is because LNG-IUD consistently suppresses the menstrual cycle. Radzinsky et al. [161] have reported that LNG-IUD is also effective in reducing chronic pelvic pain. While LNG-IUD can be a cost-effective and reliable long-term treatment for adenomyosis patients, the efficacy of LNG-IUD significantly reduces in a large volume uterus [162].

KRAS Mutations and Progesterone Treatment in Adenomyosis
Owing to PGR expression being less intense in adenomyosis lesions [136], progesterone resistance and hyperestrogenism are always a concern when using progestin-based therapies [136,163]. In support of this, the PRB isoform is also known to be downregulated in the eutopic and ectopic endometrium in adenomyosis, especially with severe cases [164,165]. However, the mechanisms of impaired progesterone signaling in the eutopic and ectopic endometrium, where adenomyosis is present, are not fully understood. A study published by Inoue et al.
[31] has indicated that KRAS mutations can be a driver of adenomyosis development and progression and linked to the PGR downregulation. This group performed the WES to understand the comprehensive genomic characterization of adenomyosis with co-occurring endometriosis and leiomyoma. Their WES detected 134 unique synonymous and non-synonymous single-nucleotide variations (SNV) in 31/51 (60.8%) adenomyosis cases, suggesting that adenomyosis is a clonal disorder with somatic mutations [31]. It was shown that a KRAS mutation at the location of G12, which is well-known as an oncogenic mutation, is the highest alteration (~37%) in adenomyosis. Additionally, isolation of epithelial cells by laser capture microdissection (LCM) reveals that the KRAS mutations have most likely occurred in the endometrial epithelial cells. Furthermore, the co-occurring gain of function mutations of KRAS with the PIK3CA p.H1047 is frequently observed in both adenomyosis and endometriosis. As an important finding, KRAS mutations are observed in not only adenomyosis lesions but also histologically normal endometrial tissues. The presence of KRAS and PIK3CA mutations in the normal endometrium is consistent with recent publications [33,34]. Thus, frequent KRAS mutations in the normal endometrium might initiate invasive and proliferative cellular functions to develop ectopic adenomyosis [31]. Importantly, KRAS mutations have been found to be significantly high in adenomyosis lesions from the patients who have been treated with dienogest (an oral progestin, 84%) but do not respond well and eventually underwent hysterectomy compared with the patients without dienogest (26%). The study further confirms less sensitivity to dienogest treatment in the KRAS mutated lesions, probably due to epigenetic silencing of PGR expression by KRAS mutations [31]. Therefore, the authors conclude that adenomyosis etiology is strongly associated with KRAS mutations in the endometrium, as well as the status of KRAS mutations is likely to be a critical factor in selecting effective medical treatments. Thus, the assessment of disease progression can be predicted by the frequency of KRAS mutations [31].

Disease Features in Leiomyoma
Leiomyomas are benign tumors of smooth muscle cells and fibroblasts developed in the myometrium [166,167]. The excessive accumulation of extracellular matrix (ECM) with collagens is one of the distinguishing characteristics of leiomyoma [168]. The prevalence of leiomyoma varies among the studies (4.5-68.6%) depending on study populations, races, ages, and diagnostic methods [169]. The estimated cumulative incidence of leiomyoma by the age of 50 is >80% for African-American women and~70% for Caucasians, suggesting that African-American women show a higher risk of developing uterine leiomyoma [170]. In addition, leiomyomas in African-American women generally develop tumors that are larger in size and cause more severe symptoms than those in women of other races [169,170]. Although the majority of women can remain asymptomatic, leiomyoma can cause severe and chronic symptoms; heavy, irregular, and prolonged menstrual bleeding with accompanying anemia, pelvic pain, and dysmenorrhea, as well as fertility issues and labor obstruction [167,171,172]. Treatment of leiomyoma depends on the severity of symptoms and whether patients desire to become pregnant and/or the sizes and locations of the leiomyoma. Although medical treatments are available to specifically control leiomyoma-associated symptoms, nearly 75% of leiomyoma patients end up having hysterectomy surgery in the U.S. [173], which represents the impetus for one-third to half of all hysterectomies [174][175][176]. Although leiomyoma is not a disease stemming from the endometrium, it is one of the gynecological diseases regulated by steroid hormones. The symptoms of diseases and treatment options are similar to other gynecological diseases.

Current Hormonal Treatments and Roles of Progesterone in Leiomyoma
The cause of leiomyoma-associated heavy bleeding has not been fully understood. Medical treatments primarily focus on reducing abnormal uterine bleeding. Because estrogen has been considered the primary driver to stimulate the progression of leiomyoma and accelerate abnormal uterine bleeding, GnRH agonists/antagonists, progestins, selective progesterone receptor modulators (SPRM), and aromatase inhibitors are available to inhibit estrogen actions and productions for leiomyoma-related symptoms [171,172]. LNG-IUD is the most common progestin treatment to induce amenorrhea and stop menorrhagia with anemia in up to 60% of premenopausal leiomyoma patients with minor side effects [177]. However, the efficacy of LNG-IUD significantly reduces in the patients with larger tumors (>3 cm) [177], which is similar to adenomyosis. Contraceptive pills combined with estrogen and progestin are commonly used for leiomyoma patients as well [171,172,178]. However, the efficacy of contraceptives for abnormal uterine and heavy bleeding is lower than that of LNG-IUD [177]. GnRH agonists are also effective in inducing amenorrhea and/or decreasing the size of leiomyoma [179,180]. However, the menopausal side effects induced by GnRH agonists are always a concern, therefore add-back hormonal therapies with GnRH agonists have been used for premenopausal women.
On the other hand, the effects of progesterone on leiomyoma can be different from other endometrial diseases. The reason is that progesterone/progestins stimulate cellular proliferation and the accumulation of ECM, which promote further development of uterine leiomyoma [8, 168,181,182]. Clinical evidence also supports the mitogenic functions of progestins in leiomyoma patients. For example, the proliferation of leiomyoma tumors is most active during the secretory phase where progesterone secretion is high [183,184]. The combinations of estrogen and progestin therapies for menopausal women considerably enhance the growth of leiomyoma tumors compared with estrogen treatment alone [184]. A high dose of medroxyprogesterone acetate (MPA), which is a hormonal medication of the progestin, unfortunately increases leiomyoma growth [185]. Furthermore, an add-back therapy of progestins with GnRH agonists reverses the efficacy of GnRH agonists [186,187]. A study employing a xenograft model by grafting human leiomyoma tissues to the kidney capsule [181] shows that the size of xenografts of human leiomyoma tissues increases cell proliferation and volumes of ECM in response to 17β-estradiol plus progesterone, but this is not induced by the xenografts in which normal myometrium is implanted. Interestingly, 17β-estradiol or progesterone alone is unable to stimulate the growth of leiomyoma. The authors further demonstrate that while 17β-estradiol alone does not stimulate proliferation, 17β-estradiol induces PGR expression and supports progesterone action on the leiomyoma xenografts. The results suggest that estrogen and progesterone can directly stimulate leiomyoma cell proliferation based on the expression of PGR and ESR1 in the proliferating cells [8,181]. Estrogen and progesterone have also been reported to enhance ECM proteins such as collagen types I and II [188,189], and also stimulate ECM accumulation to increase the size of leiomyoma [181]. Thus, progesterone with a permissive role of estrogen is critical for cell proliferation and ECM accumulation to increase the size of leiomyoma tumors [8,168].
Additional studies of ECM in leiomyoma regulated by growth factors [190,191], cytokines [192], and steroid hormones [181,182] have been reported. A number of in vitro studies support that progestins stimulate cellular mechanisms to increase the production of growth factors summarized in [168]. Qiang et al. [182] have reported that ECM accumulation in leiomyoma is regulated by steroid hormones via the downregulation of miR-29b. The authors demonstrate that the expression of miR-29b is lower in leiomyoma compared with myometrium. Restoring miR-29b inhibits ECM accumulation to develop solid tumors. Although increased collagen expression by miR-29b is not sufficient for the transformation from myometrial cells to leiomyoma cells, 17β-estradiol and progesterone decrease miR-29b and increase multiple collagen expressions. These results suggest that miR-29R is one of the critical factors to produce ECM accumulation regulated by steroid hormones in leiomyoma.

Genetic Alterations and Steroid Hormones in Uterine Leiomyoma
Compared with other endometrial diseases, leiomyomas show a high incidence of somatic mutations. Makinen's group [193] has identified recurrent somatic mutations in MED12 that drive leiomyoma development. Strikingly, approximately 70% of leiomyoma patients possess MED12 mutations in leiomyoma tumors [193]. This finding has been further validated in multiple studies confirming the presence of MED12 mutations, but depending on the study, the incidence varies between 48 and 92% [194]. HMGA2 overexpression is the second major genetic alteration accounting for approximately 10% in uterine leiomyoma cases [194][195][196], but its expression is limited in the leiomyoma without underlying MED12 mutations [194,195,[197][198][199]. FH-deficient or COL4A5/6 deletions have also been identified as unique genetic alterations without co-occurring with other alternations [198,200]. While FH and COL4A5/6 mutations have been characterized, the majority of uterine leiomyoma (80-90%) harbor MED12 or HMGA2 alterations [194]. Kurita's group [201] has recently reported that subtypes of leiomyoma with either MED12 mutations or HMGA2 overexpression required progesterone and 17β-estradiol to stimulate tumor growth. Another important finding is that leiomyomas with HMGA2 overexpression mainly consist of smooth muscle cells. Tumors with MED12 mutations contain almost equal populations of smooth muscle cells and tumor-associated fibroblasts, although casual MED12 mutations are present only in the smooth muscle cells [201]. Thus, the growth of smooth muscle cells is important in HMGA2 overexpressing leiomyoma. On the other hand, paracrine interactions between smooth muscle cells and tumor-associated fibroblasts are crucial for the progression of the MED12 mutant leiomyoma, as tumor-associated fibroblasts do not carry MED12 mutations. Interestingly, the growth of smooth muscle cells is driven by progesterone in both MED12 mutant and HMGA2 overexpressing subtypes. In contrast, tumor-associated fibroblasts are stimulated by 17β-estradiol but not progesterone. Therefore, 17β-estradiol is likely to stimulate MED12-mutant smooth muscle cells to secrete paracrine factors that promote the growth of tumor-associated fibroblasts [201]. This study suggests that it is critical to consider the specific genetic alterations of leiomyoma subtypes when designing non-surgical therapeutic strategies and follow the tumor progression with different cell types due to the differential effects of steroid hormones on leiomyoma subtypes [201]. This group has also demonstrated that progesterone and 17β-estradiol activate MAPK and PI3K pathways with upregulation of IGF1 and IGF2 in the MED12-mutated leiomyoma [202].
RANKL has been identified as a progesterone responsive gene that is involved in the growth and progression of hormone-mediated leiomyoma [203,204]. Liu et al. [204] have shown that RANKL transcription is enhanced due to the hypomethylation of the regulatory element of PGR in leiomyoma stem cells, whereas higher DNA methylation at the PGR response element blocks PGR binding in the normal myometrium; leading to a decrease in RANKL expression. Furthermore, MED12 mutation, especially at G44D, further stabilizes PGR binding at the regulator element of RANKL, indicating that a complex network constituted by DNA methylation and MED12 mutations regulates the progesterone-mediated RANKL gene expression contributing to leiomyoma tumor development [204]. This group has further reported that the PGR gene locus and its genome-wide cistrome are hypermethylated in leiomyoma stem cells, repressing the expression of genes for progesterone-mediated leiomyoma stem cell differentiation [205].
WNT signaling has also been reported to mediate cellular processes in leiomyoma pathophysiology [197,[206][207][208]. Several WNT ligands and other mediators have been overexpressed in leiomyoma to activate the WNT/CTNNB1 pathway to enhance leiomyoma progression [206]. Ono et al. [207] have reported that estrogen and progesterone activate canonical WNT/CTNNB1 signaling to stimulate cellular proliferation in the leiomyoma side population of stem-like cells, but this is not seen in the myometrial cells. The group also shows that WNT4 is overexpressed in CD34 + /CD49b − leiomyoma cells and can stimulate leiomyoma cell proliferation via WNT/CTNNB1 signaling and AKT [209]. Additionally, MED12 mutations have been implicated in the misregulation of WNT/CTNNB1 signaling, providing additional linage between two common mechanisms of leiomyoma development [206,[210][211][212].

Disease Features and Current Treatments in PCOS
PCOS is known as a complex endocrine disorder characterized by ovulatory dysfunction, polycystic-appearing ovary, oligomenorrhea, and hyperandrogenism. PCOS is one of the common causes of female infertility occurring in 6-12% of reproductive-aged women, representing as many as 5 million women in the U.S. [213][214][215]. Approximately 75% of women with PCOS experience anovulation-related infertility and >50% of them suffer miscarriages and recurrent pregnancy loss [216][217][218]. As additional clinical complications of this disease, women with PCOS further develop type 2 diabetes and insulin resistance as well as increased risk of both cardiovascular diseases and endometrial cancer [213,214,[219][220][221]. Although numerous factors impact the pathophysiology of PCOS, clinical, animal, and genetic studies support the involvement of abnormal neuroendocrine factors [222]. Dysregulation of hypothalamic GnRH and pituitary luteinizing hormone (LH) secretions [223,224], especially the high-frequency pulsatile release of GnRH following hypersecretion of LH, contribute to hyperandrogenisms [225]. In these women, the levels of the 17β-estradiol hormone are relatively normal, but their window of action can be prolonged [226,227]. Hypersecretion of LH and insulin with excess androgen arrests antral follicle growth and suppresses the follicle-stimulating hormone (FSH), leading to maturation inhibition in the follicles [228].
Currently, no universal treatments or drugs are available for the treatment of PCOS [229]. As risk factors for PCOS include being overweight, obesity, and type II diabetes with the consequences of insulin resistance, healthy lifestyle interventions are recommended to improve individual symptoms. On the other hand, anovulation and/or oligomenorrhea, a part of menstrual dysfunction, require hormonal therapies to have proper hormonal regulation not only in the ovary but also the uterus, which is also critical for the patients who seek fertility and successful pregnancy [229]. Oral contraceptive pills (combinations of estrogen and progesterone) and cyclic or continuous progesterone/progestin administration are often efficacious for patients with mild to moderate menstrual dysfunction [230]. On the other hand, it is known that chronic anovulation and oligomenorrhea elicit in women with PCOS when the endometrium is subject to prolonged estrogen exposure that is unopposed to subsequent progesterone signaling due to insufficient hormone production or PGR activation. This state results in endometrial hyperplasia, which can lead to endometrial cancer [221]. Indeed, PCOS patients have a significantly higher risk of developing endometrial cancer [221,[231][232][233]. For those reasons, progestin/progesterone (i.e., MPA, norethindrone acetate, and micronized progesterone) have also been used to manage prolonged estrogen actions preventing endometrial hyperplasia [221,234]. However, the endometrium of women with PCOS often exhibits progesterone resistance, altering progesterone-regulated genes in the endometrium [21]. In fact, approximately 30% of PCOS patients fail to respond to progesterone-based therapy [235]. Therefore, it is important to understand endometrial pathophysiology in PCOS patients to improve poor reproductive outcomes and to prevent endometrial hyperplasia and/or cancer.

Endometrial Progesterone Resistance in PCOS
Giudice and Lessey's groups [21] have performed microarray analysis to determine differential gene expressions in the mid-secretory phase of endometrium from (1) PCOS patients treated with clomiphene citrate, an estrogen modulator, (2) PCOS patients treated with progesterone, and (3) normal patients. Their results have indicated that progesteroneregulated genes, such as MIG6, LIF, GAB1, S100P, and CLDN4, are downregulated in the endometrium from PCOS patients [21]. Specifically, MIG6 and GAB1, related to the EGF signaling pathway that is important for implantation and decidualization, are significantly reduced in the mid-secretory phase of PCOS patients despite the presence of progesterone. On the other hand, the estrogen signaling pathway associated with cell proliferation is aberrant [21], supporting a higher risk of endometrial hyperplasia and cancer [221]. The study summarizes the findings with minimal or absent progesterone responsiveness or progesterone resistance and elevated estrogen activity in the PCOS endometrium [21]. Furthermore, stromal cells isolated from PCOS endometrium have an aberrant decidualization response associated with increased expression and secretion of pro-inflammatory cytokines, chemokines, and MMPs [236]. Additionally, altered gene expression profiles in epithelial cells, stromal fibroblasts, and mesenchymal stem cells have revealed that inflammatory and pro-oncogenic changes negatively impact endometrial functions in women with PCOS [22].
The absence of progesterone responsiveness and/or progesterone resistance could be explained by altered PGR expression. Quezada et al. [237] have reported that PGR is higher in the epithelium during the mid-secretory phase in PCOS patients. PRA expression is elevated in the proliferative endometrium in PCOS patients [238]. The altered PRA/PRB ratio has also been observed in the proliferative endometrium with PCOS [237,238]. However, it is still unclear whether direct correlations exist between loss of progesterone responsiveness and the altered expression of PGR and specific isoforms in the PCOS endometrium.

Metformin and Progesterone Resistance in PCOS
Metformin is an insulin sensitizer that has been widely used not only for type 2 diabetes but PCOS [239,240]. Treatment of PCOS patients with metformin improves menstrual irregularity and anovulation [239,240], resulting in inhibiting cytokine production, CYP19A1 (aromatase) activity, and endometrial cell proliferation [241]. Metformin can enhance PGR expression via inhibition of overactivated mTOR signaling [242]. Furthermore, the combination of metformin and oral contraceptives is effective in reducing progestin-resistant endometrial hyperplasia [243,244]. A few experimental studies and one clinical study support the use of metformin in endometriosis [245]. Further investigation is necessary to understand the molecular mechanisms to improve endometrial dysfunctions (endometrial hyperplasia and progesterone resistance) with insulin resistance and can provide the undiscovered impeccable pathophysiology of PCOS as well as other endometrial diseases.

Characterization of Endometrial Hyperplasia
Endometrial hyperplasia is the condition of excessive proliferation of epithelial cells and thickening of the endometrium, usually resulting from chronic unopposed estrogen exposure associated with deficiency of progesterone [246][247][248]. Hyperplastic endometrium is induced by hormone imbalance, however, it might further develop into atypical hyperplasia (AH)/endometrioid intraepithelial neoplasia (EIN) [249]. AH has been histologically defined by complex hyperplastic glands composed of enlarged and irregular-shaped nuclei, displaying stratification and loss of polarity, and resembling the morphological feature in endometrial cancer [250,251]. Endometrial hyperplasia with or without cytologic atypia has been classified in the 2014 World Health Organization (WHO) classification for the purpose of clinical practice and the choice of treatment [250]. AH raises a significant risk of developing endometrial cancer [252][253][254]. Kurman et al. [255] has reported that 1.6% of patients with endometrial hyperplasia progress to carcinomas compared with 23% of patients with AH [255]. The study from Lacey et al. shows that AH/EIN has a nearly 40% probability of developing endometrial cancer [256]. Several case studies also report 14% up to 43% concurrent associations with endometrial carcinomas and AH [257][258][259]. These studies support that AH/EIN are considered precursor or premalignant tumors specifically for endometrioid endometrial carcinomas (EEC) [250,254,260]. EEC accounts for >80% of all endometrial carcinomas and usually develop in premenopausal and peri-menopausal women, whereas serous uterine carcinomas account for <10% and are highly aggressive, estrogen-independent, and diagnosed mainly in postmenopausal women [249,[261][262][263][264][265]. EEC are well known to be correlated with genetic alterations in PTEN, KRAS, CTNNB1, ARID1A, and PIK3CA [120,266]. Although multiple combinations of mutations have been observed in EEC, approximately 65% of EEC harbor PTEN mutations [266], which are the most frequent somatic mutation in EEC [249,267,268]. Somatic PTEN mutations have been observed not only in EEC but also in hyperplastic glands and AH/EIN [249,269]. A recent genome-wide mutation analysis from Li et al. [251] has reported that the common mutations between AH and EEC vary from 0.1% to 82%. Microsatellite stable AH have fewer cancer-driving mutations than EEC, and 79% of microsatellite stable EEC gain cancer driver mutations related to PTEN, CTNNB1, ARID1A, CHD4, and PIK3CA, indicating that some AH lesions are immediate precursors of EEC, and their progression depends on the acquisition of additional cancer driver mutations. In the genetically engineered mouse models of endometrial cancer, conditional ablation of PTEN in epithelial cells and/or endometrial cells induces AH/EIN and/or carcinomas [8, [270][271][272]. Thus, PTEN mutations in the endometrium can be a major driver of AH and appear to initiate the precursor of EEC, whereas a single mutation of Pik3ca E545K [270] or Arid1a [273,274] is insufficient to induce endometrial hyperplasia, AH/EIN, or cancerous lesions. On the other hand, PTEN mutations alone are considered to be insufficient to initiate malignant tumorigenesis unless other molecular alterations are acquired [249]. Genetically engineered mouse models have shown that the combinations with Pten ablation with mutations of Pik3ca [270], Arid1a [273], or Kras G12D [272] promote and aggressively develop invasive endometrial carcinomas, whereas solely PTEN loss does not or takes a long time to induce malignant tumors. Thus, PTEN ablation is likely an early event to induce endometrial hyperplasia and/or AH/EIN, but PTEN mutations can further accelerate the progression to endometrial carcinoma with other mutations. Interestingly, PTEN mutations with estrogen exposure result in an increased incidence of endometrial carcinomas [275]. However, Pten +/− mice with oophorectomies often develop hyperplastic lesions, and Pten +/− Esr −/− mice also exhibit atypical hyperplasia and endometrial tumorigenesis, indicating that AH/EIN induced by PTEN mutations is independent of estrogen and estrogen signaling [275].

Hormonal Therapy and Clinical Perspectives for Endometrial Hyperplasia, AH/EIN, and Endometrial Cancer
Because most of the patients with endometrial hyperplasia, AH/EIN, and/or carcinomas present with abnormal uterine bleeding, endometrial cancer is generally diagnosed at the early stages [248,254]. However, abnormal bleeding can be induced by many different causes. After ruling out other sources and causes of abnormal bleeding by physical and histological examinations and tests, removing the uterus (hysterectomy) and ovaries and fallopian tubes (bilateral salpingo-oophorectomy) is a primary option and the current standard for the treatment of endometrial cancer [248,254]. Of course, cytoreductive surgery, including hysterectomy and oophorectomy, is not the option for patients who wish to preserve fertility. It has been reported that hormonal therapy, mainly progestins, shows successful efficacy in resolving premalignant endometrial hyperplasia and/or early stages of EEC [276]. Long-term treatment with MPA and megestrol acerate resolve approximately 75% of endometrial hyperplasia [277][278][279][280][281]. LNG-IUD is effective in regressing endometrial hyperplasia after 2 years of LNG-IUD insertion [282]. Favorable responses to endometrial cancer depend on ESR and PGR expression, low-grade EEC, and low disease burden [263,283]. Hormonal therapy is often considered for women with AH. However, the efficacy of progestin therapy is limited for many AH patients [248,254]. The variability in response to progestins is due to the heterogeneity of AH lesions with different genetic mutation statuses as described above. If gene mutation(s) initiates AH and/or endometrial hyperplasia without dysregulation of steroid hormones, hormonal therapy is less likely to be effective. It will be crucial to understand the pathophysiology of endometrial hyperplasia and AH/EIC, as well as the cause and mechanism of transformation from endometrial hyperplasia to AH/EIC. Nevertheless, untreated premalignant lesions of the endometrium are highly likely to progress to endometrial cancer [254]. As it is estimated that there is an interval range of 4-7 years from the diagnosis from AH to EEC [256,284], preventing the progression from AH to EEC by hormonal therapy (progestin treatment) might be an option for patients who wish to preserve fertility using indicators of ESR1 and PGR expression.  [181,182,184,185,[201][202][203][204][205][206][207] MED12 HMGA2 overexpression [193][194][195][196][197][198][199] [248,254,[276][277][278][279][280][281][282]

Conclusions
While each gynecological disease described above may have different origins, mechanisms, and etiology, there are some similarities, chiefly dysregulated steroid hormone signaling. This may stem from a disruption of hormone production, progesterone resistance, altered hormone-dependent gene expression, common somatic gene mutations, and/or side effects of current hormonal treatments and approaches for one disease that establish or worsen another. Sadly, most of these patients have been battling disease-associated chronic pelvic pain, dysmenorrhea, menorrhagia, and/or fertility issues, reducing their quality of life, with few perfect therapy strategies to abrogate their disorders. The dynamic changes of endometrial tissues in the menstrual cycle regulated by responses of steroid hormones are complex mechanisms. Because menstrual cycles repeatably occur and alter the local endometrial environment, the local hormonal environment cannot be precisely defined in each cycle. Endometrial proliferation, differentiation, shedding, and regeneration are associated with massive inflammation which further affects endometrial hormonal responsiveness, including epigenomic and transcriptomic interplay. While numerous studies reveal the mechanisms of hormone unresponsiveness and progesterone resistance, we still do not know the initiation and establishment of each gynecological disorder and how they can be therapeutically treated. The studies from Fazleabas' group have indicated that the development of progesterone resistance is a gradual process and becomes evident at least 6 months after disease induction in the baboon model of endometriosis [285]. Thus, the establishment of disease (endometriotic lesions) can further affect the eutopic endometrial environment. Recent studies also indicate that somatic gene mutations can be drivers to promote disease establishment; leiomyoma and uterine hyperplasia with AH/EIC are especially likely initiated by gene mutations. Somatic mutations have been observed in the endometrium with endometriosis and adenomyosis and are also related to potentially transforming into malignant tumors. In this context, it would be important to understand the further mechanisms of disease pathophysiology and develop personalized medicine depending on the alterations of complex mechanisms, symptoms, and future goals for patients who desire fertility.