{"paper_id":"ddbeb169-be02-4c84-8e55-91ad4018139d","body_text":"Endometriosis is a benign gynecological estrogen-dependent inflammatory condition defined by the presence of endometrial-like tissue in extrauterine locations [ 1 ]. Endometriosis affects up to 10% of women of reproductive age and is responsible for infertility and pelvic pain [ 2 ]. Due to its complexity, endometriosis is usually referred to as exhibiting a polygenic and multifactorial basis [ 3 ]. Estrogen plays a significant role in the pathogenesis of the disease by promoting endometriotic tissue cell survival, maintenance, and differentiation [ 2 ,  3 ]. Estrogen activates a wide array of tissue- and organ-specific physiological responses by binding to its receptor ESR1, mostly located at the thecal layer, and modulating uterine events preparing the endometrium for embryo attachment and implantation [ 4 ].\nThough many studies suggest that genetic polymorphisms of estrogen receptor  α  gene ( ESR1 ) modify susceptibility to women's disorders including osteoporosis, preeclampsia, and breast cancer, limited studies have demonstrated associations of  ESR1  polymorphisms in women with endometriosis-related infertility [ 5 – 7 ]. Previous reports have shown associations of  ESR1  genetic variants with susceptibility to endometriosis and fertility status [ 6 ,  8 – 13 ], but many studies failed to achieve an association regarding  ESR1  variants and endometriosis-related infertility [ 9 ,  14 – 16 ]. Interestingly, Lamp et al. linked  ESR1  SNPs only to endometriosis without infertility [ 12 ], while Wang et al. associated  ESR1  rs3798573 with risk of both endometriosis and infertile endometriosis in Han Chinese women [ 13 ].  ESR1  rs2234693 ( PvuII)  polymorphism was significantly more prevalent in infertile women at premature ovarian aging [ 17 ] and was predictive of an improved controlled ovarian stimulation [ 18 ]. Both rs9340799 ( XbaI ) and  ESR1  rs2234693 ( PvuII ) polymorphisms are associated with differences in the response to ovarian stimulation bestowing an indirect role that might affect implantation rates [ 19 ].\nIn a recent investigation, gene-array analysis revealed more than 300 genes downregulated in patients with repeated  in vitro  fertilization (IVF) failure, with at least 8% of them being estrogen dependent [ 20 ]. Numerous factors as folliculogenesis, endometrial receptivity, and oocyte maturation have been associated with failure of  in vitro  fertilization (IVF) failure, but the lack of estrogen responsiveness might be a great challenge in these situations [ 20 ]. The embryonic implantation process requires a receptive endometrium and both estrogen and TP53 present essential roles during implantation through the regulation of leukemia inhibitory factor ( LIF ), a polyfunctional glycoprotein cytokine critical for blastocyst implantation [ 21 ]. LIF expression is continuous in the uterus; however, it shows a transient expression peak during pregnancy and this peak coincides with the onset of implantation at the 12th day after fertilization in humans [ 22 ].  LIF  has been described as an important gene in differentiation, proliferation, and cell survival pathways [ 23 ] and its expression is reduced in endometrium from women with unexplained infertility [ 24 ].\nTo our knowledge, no study has focused on  ESR1  polymorphisms and infertile women who were submitted to conventional  in vitro  fertilization (IVF) procedures with unsuccessful blastocyst implantations. Meanwhile estrogen functions are so important to blastocyst implantation and to the pathogenesis of endometriosis;  ESR1  gene variants might be one of the causative factors for these conditions in infertile women. We then hypothesized that genetic variants in  ESR1 ,  MDM2 ,  MDM4 ,  USP7 , and  LIF  genes may differ between fertile women and two groups of infertile women: first, women with endometriosis-related infertility and second, women with failure of  in vitro  fertilization procedures.\n\nPatients and subjects were invited to participate and signed a consent form at inclusion. The research project was approved by the Hospital de Clínicas de Porto Alegre (HCPA) Ethics Committee (GPPG 05-182; GPPG 09-430). Infertile patients with and without endometriosis and controls were divided into three study groups as previously described [ 25 ]. Infertility was defined as the inability of a couple to achieve pregnancy after 1 year of regular unprotected sexual intercourse [ 26 ]. The IVF Failure Group consisted of 115 infertile women with at least one IVF failure, submitted to conventional IVF with 35 years or less. Patients with endometriosis, previous thyroid disease, positive anti-lupus or anticardiolipin antibodies, and thrombophilias were excluded from our sample. Controlled ovarian hyperstimulation was performed with the use of recombinant human FSH and pituitary suppression with GnRh antagonist (fixed day-6 protocol). Ovulation was induced by 6500 IU recombinant hCG when at least three follicles had reached a diameter of 17 mm, and transvaginal follicle aspiration was performed 36 hours later under ultrasound guidance. Embryos were classified according to the cumulative embryo classification, taking into account cleavage speed, blastomere symmetry, extent of fragmentation, and the presence or absence of multinucleated blastomeres. The Endometriosis Group comprised 98 infertile women with minimal or mild endometriosis as diagnosed by laparoscopy according to the classification proposed by the American Society for Reproductive Medicine recruited at the Gynecology Service of HCPA, in Southern Brazil [ 26 ]. Other causes of infertility were excluded by hysterosalpingography, sperm evaluation, and hormonal measurements whenever necessary. The Fertile Group consisted of 134 women with no history of infertility, who already had two or more children without any difficulties or assisted reproduction and underwent laparoscopy for tubal ligation at HCPA.\nGenomic DNA was extracted from peripheral blood leukocytes using the Illustra blood genomic Prep Mini Spin Kit (GE Healthcare, Piscataway, NJ, USA) as described by the manufacturer. DNA concentration was measured with Nano-Drop 1000 (Thermo Scientific, Wilmington, USA) and diluted to a final concentration of 10 ng/ µ L.\nTaqMan allelic discrimination analyses were performed according to Applied Biosystems standard protocols (Applied Biosystems, Carlsbad, USA). The analyzed SNPs were as follows:  MDM4  rs1563828 (C_9493064_10),  USP7  rs1529916 (C_9688119_1),  LIF  rs929271 (C_7545901_10),  ESR1  rs9340799 (C_3163591_10),  ESR1  rs2234693 (C_3163590_10) (Applied Biosystems), and  MDM2  rs2279744 for which a custom-made TaqMan assay was made, using forward primer 5′-CGGGAGTTCAGGGTAAAGGT-3′, reverse primer 5′-ACAGGCACCTGCGATCATC-3′, VIC probe 5′-CTCCCGCGCCGAAG-3′ and FAM probe 5′-TCCCGCGCCGCAG-3′ (Applied Biosystems). PCR cycling reactions were performed on an ABI StepOne System (Applied Biosystems) and consisted of initial denaturation at 95°C for 15 min, 40 cycles with denaturation 95°C for 15 s, and then annealing and extension at 60°C for 1 min.\nClinical features of women in all study groups were compared by  t -test. Differences in genotype distribution were assessed by chi-square analysis, which was also used to test for Hardy-Weinberg equilibrium. Logistic regression analysis was carried out to estimate the odds ratios with 95% confidence intervals (CIs) in order to assess the influence of  ESR1  rs9340799 genotypes on endometriosis-related infertility and IVF failure. Statistical analyses were performed using the SPSS 20.0 statistical package. All reported  P  values are two-tailed and were considered statistically significant when equal to 0.05 or less.\n\nThe clinical and demographic characteristics of the women enrolled in the study are shown in  Table 1 . Mean age at recruitment was higher in the Fertile Group (42.6 ± 12.88 years) than in both the Endometriosis (32.87 ± 4.7 years) and IVF Failure (31.65 ± 3.24 years) groups since only women of 35 years or less were included in these two latter groups. The population-based fertile control women presented a mean of 3.62 ± 1.94 pregnancies reflecting the average number of pregnancies in the normal population from Southern Brazil. Both Endometriosis and IVF Failure groups presented low frequencies of pregnancy, abortion, and caesarean due to their infertility status. Patients and healthy study subjects did not differ significantly regarding self-attributed skin color as a self-denomination of “white” color predominated in all study groups as previously described in [ 25 ].\nHardy-Weinberg equilibrium was achieved for all SNPs in the three study groups (data not shown).   Table 2  presents genotype frequencies of the SNPs included in the study. No association was found between  LIF ,  MDM2 ,  MDM4 , and  USP7  SNPs and endometriosis-related infertility or  in vitro  fertilization failure. However, a strong association was found between the  ESR1  rs9340799 polymorphism and clinical phenotype in both case groups (Endometriosis,  P  < 0.001 and IVF Failure,  P  = 0.018) when compared with the Fertile Group. Interestingly, no association was found between  ESR1  rs2234693 and the outcomes.\nTo evaluate the effects of the  ESR1  rs9340799 polymorphism, we carried out a logistic regression analysis, controlled by age, with endometriosis-related infertility and IVF failure as outcomes. Results are summarized in  Table 3  and show a statistically significant effect of AG (OR 2.67, 95% CI 1.49–4.78,  P  = 0.001) and GG (OR 4.67, 95% CI 1.84–11.83,  P  = 0.001) genotypes with endometriosis-related infertility. Regarding the IVF Failure Group, genotype GG contributed significantly to the outcome as women with genotype GG had 3-fold-increased risk of IVF failure (OR 3.33, 95% CI 1.38–8.03,  P  = 0.007).\n\nIn the present study, we have analyzed common SNPs in  ESR1 ,  MDM2 ,  MDM4 ,  USP7 , and  LIF  genes in infertile women with endometriosis or failure of  in vitro  fertilization procedures. Our results demonstrate an association between  ESR1  rs9340799 polymorphism with infertile women with endometriosis and also with women who were submitted to IVF procedures and had no embryo implantation.\nTP53  regulates maternal reproduction through the expression of  LIF  [ 27 ]. At 12 days of pregnancy,  LIF  is expressed at high levels making the uterus receptive to the blastocyst [ 27 ]. Both  TP53  and estrogen are essential for  LIF  expression in the endometrial glands, and impaired function of these proteins are clearly associated with failure of blastocyst implantation [ 27 ]. Different studies have demonstrated that SNPs modulate the activity of  TP53 , and also in its regulators  MDM2 ,  MDM4 , and  USP7  are more frequent in IVF patients [ 25 ,  28 ]. We have previously shown that  TP53  polymorphisms are associated with both endometriosis-related infertility and IVF failure in patients from Southern Brazil [ 25 ]. Using the same cohort, we expanded the analysis to other  TP53  signaling network genes [ 29 ], and in contrast with previous findings, our results demonstrated no association of  MDM2 ,  MDM4 ,  USP7 , and  LIF  polymorphisms with endometriosis-related infertility or IVF failure patients.\nLIF  is regulated by both  TP53  and estrogen. Estrogen signaling is mediated through its nuclear receptor alpha. Studies have demonstrated an association between  ESR1  polymorphisms and endometriotic women with and without infertility [ 13 ,  17 ], but to our knowledge, no study has evaluated  ESR1  polymorphisms in IVF failure. Our results demonstrate an association between  ESR1  rs9340799 polymorphism (also known as  ER - αXbal ) and endometriosis-related infertility. In regard to the association found here, a previous meta-analysis performed to derive a more precise association between the  ESR1  polymorphisms and risk of endometriosis found no obvious associations [ 30 ]. However, it is important to note that even though the authors indicate that ethnicity (Caucasian or Asian), country (Japan, China, Korea, Germany, and Italy), and sample size could not explain heterogeneity across the fifteen studies included in the meta-analyses, only two studies included Caucasian populations (totalizing only 111 cases and 146 controls from a total of 1349 cases and 1411 controls). In addition, there was no uniformity in the classifications regarding “endometriosis” among the different studies. To minimize bias towards endometriosis classification, we only included in the present study infertile women with minimal or mild endometriosis as diagnosed by laparoscopy according to the classification proposed by the American Society for Reproductive Medicine [ 26 ]. The classification of endometriosis is changing from a local disorder to a complex disease as new molecular mechanisms are being discovered [ 2 ]. The endometriotic process is classified as an estrogen-dependent inflammatory disease similar to cancer due to its capability to invade surrounding tissues, to promote angiogenesis, inflammation, and apoptosis in favor of the new endometriotic tissue survival [ 31 – 36 ]. Estrogen production plays a central role in the pathology of endometriosis enhancing the survival of the endometriotic tissue, and together with prostaglandins and cytokines, mediating pelvic pain and infertility [ 37 ,  38 ]. The fact that estrogen inhibitors such as GnRh analogues, oral, and aromatase inhibitors are used to reduce pelvic disease and pain also corroborates conceptive to the fact that estrogen signaling is critical for endometriosis [ 39 ].\nEstrogen receptor polymorphisms have been associated with ovarian response to follicle stimulating hormone in IVF patients [ 40 ], with poor responders to IVF [ 41 ], with IVF parameters such as the number of follicles and collected oocytes, maturation, pregnancy rates, and embryo quality in women with unexplained infertility [ 42 ] and with the outcome of ovarian stimulation in IVF [ 43 ]. This is the first time that an association between  ESR1  rs9340799 and failure of IVF is demonstrated. Remarkably, we did not find any association between  ESR1  rs2234693 polymorphism (also known as  PvuII ) and endometriosis-related infertility or failure of IVF. Both rs9340799 (A-351G) and rs2234693 (C-397T) SNPs are localized in intron 1 of the  ESR1  gene in chromosome 6q25 and are in linkage disequilibrium [ 42 ]. Although both SNPs are present in intron 1 and do not lead to any amino acid change, it is plausible that they may directly influence  ESR1  gene expression or alternatively could be linked to some unidentified causative DNA sequence variants. Introns can significantly affect gene expression in a variety of ways, as they may contain enhancer elements or promoters that might control alternative splicing, as well as various  cis-  and  trans -regulatory elements that may lead to different proteins isoforms [ 44 – 46 ].\nAlthough, to our knowledge, this is the first study to report an association between  ESR1  genetic variants and failure of  in vitro  fertilization, our study had limitations. First, only two common  ESR1  polymorphisms were investigated, so haplotype analysis was not performed. Second, examination of endometrial tissue to evaluate the effect of the analyzed SNPs regarding  TP53  and  LIF  expression was not performed. Endometrial samples are being collected at this time, so analyses of protein response at the implantation stage are underway. Lastly, it is known that allele frequencies are greatly affected by racial and ethnic backgrounds. Although ancestral informative markers were not used to infer individual ancestry, we used self-reported skin color as a control for ethnic background, and no significant difference in the distribution of self-denominated skin color was observed among the study groups as the majority of individuals self-denominated them as “white.”\n\nOur results reveal a potential novel candidate biomarker for the diagnostic and prognostic assessment of endometriosis-related infertility and IVF failure. Our results demonstrate a 4-fold increased risk of endometriosis and a 3-fold increased risk of IVF failure in infertile women with  ESR1  rs9340799 GG genotype. Further studies exploring a haplotype analysis of the  ESR1  gene will help to clarify the role of  ESR1  genetic variants in infertile women. Along with that, functional studies are needed to elucidate the possible effect that  ESR1  rs9340799 might have on ESR1 and LIF expression.","source_license":"CC0","license_restricted":false}