High Maternal Serum Estradiol in First Trimester of Multiple Pregnancy Contributes to Small for Gestational Age via DNMT1-Mediated CDKN1C Upregulation

High maternal serum estradiol (E2) levels in the first trimester of pregnancy are associated with a high incidence of low birth weight (LBW) and small for gestational age (SGA). This study aimed to investigate the effect of first-trimester high maternal serum E2 levels on fetal growth and the underlying mechanisms in multiple pregnancies. Maternal serum E2 levels of women at 8 weeks of gestation were measured. The expression levels of imprinted genes and DNMT1 were determined by RT-qPCR, and KvDMR1 methylation in embryo tissue, placenta, and newborn cord blood samples was examined by bisulfite sequencing PCR. The effect of E2 on CDKN1C expression was investigated in HTR8 cells. The incidence of SGA was significantly higher in multiple pregnancies reduced to singleton than that in primary singleton pregnancies (11.4% vs. 2.9%) (P < 0.01) and multiple pregnancies reduced to twins than primary twins (38.5% vs. 27.3%) (P < 0.01). The maternal serum E2 level at 8 weeks of gestation increased with the number of fetuses and was negatively correlated with offspring birth weight. CDKN1C and DNMT1 expression was significantly upregulated in embryo tissue, placenta, and cord blood from multiple pregnancies. Furthermore, there was a positive correlation between CDKN1C mRNA expression and KvDMR1 methylation levels. In HTR8 cells, DNMT1 mediated the estrogen-induced upregulation of CDKN1C, which might contribute to SGA. To minimize the risks of LBW and SGA, our findings suggest that abnormally high maternal serum E2 levels should be avoided during the first trimester of multiple pregnancies from assisted reproductive technology (ART). Supplementary Information The online version contains supplementary material available at 10.1007/s43032-021-00735-8.


Background
Studies from diverse human cohorts and animal models have demonstrated that low birth weight (LBW) is a great risk for developing future adult chronic diseases [1,2]. Indeed, the maternal intrauterine environment plays a critical role in fetal development and growth. However, the mechanisms by which an adverse intrauterine environment affects fetal growth are still largely unknown.
A multiple gestation pregnancy is a common iatrogenic outcome of assisted reproductive technology (ART) mainly due to ovarian hyperstimulation. The frequency of multiple births with in vitro fertilization (IVF) ranges from 25 to 50% [3]. Multiple gestation pregnancies have an increased risk of LBW, especially when more than two fetuses are present [4][5][6]. It has been proposed that the reduced intrauterine growth of fetuses results from the constraints imposed by uterine size and a restricted ability of the placenta to support the nutrients required for fetuses during late gestation [5]. However, the procedure of fetal reduction in early gestation cannot eliminate all the detrimental effects of multiple gestations on the remaining fetuses. Our study showed that multiple pregnancies reduced to twins after ART treatment were still associated with a higher incidence of LBW and small for gestational age (SGA) than primary twin pregnancies. Moreover, the birth weights of singleton pregnancies from reduction were significantly lower than those of primary singleton pregnancies. Epidemiological studies of different cohorts showed that LBW was associated with adverse health outcomes, such as perinatal mortality and childhood neurologic diseases [7,8]. Furthermore, newborns of LBW have a higher incidence of hypertension, type 2 diabetes, stroke, and coronary artery disease in later adult life [7,9].
Although safety concerns in the first trimester of multiple pregnancies in ART are an issue, the mechanisms underlying LBW have not been well studied. The dramatic increase in estradiol (E 2 ) in pregnant women may influence placental function and fetal development and play an important role in the development of numerous human diseases [10,11].
A study in rats has demonstrated that estrogenic exposure during maternal pregnancy increases the risk of breast cancer in offspring of multiple generations [12]. Our previous study found that a high maternal E 2 environment in the first trimester was correlated with increased risks of LBW and SGA [13]. Thus, we propose that fetuses of the first trimester of multiple pregnancies exposed to an excessive E 2 intrauterine environment may have a higher risk of LBW and SGA.
The epigenome is most susceptible to perturbation in early development [14,15]. The adverse effects of abnormal intrauterine exposure on fetuses may lead to epigenetic dysregulation. DNA methylation is one of the best-characterized epigenetic modifications. Abnormal DNA methylation is associated with many diseases [12,16,17]. DNA methyltransferase 1 (DNMT1) is the major DNMT for the maintenance of methylation and catalyzes DNA methylation by transferring a methyl group from the donor S-adenosyl methionine to the fifth carbon of cytosine [16]. Ample evidence has revealed that DNMT1 overexpression contributes to hypermethylation associated with human disease [16,18,19]. In cancer cells, DNMT1 overexpression might cause abnormal hypermethylation [20].
Genomic imprinting is an epigenetic phenomenon that results in monoallelic expression of certain genes in a parent-of-origin-dependent manner. Imprinted genes play important roles in the control of fetal growth and development [21]. CDKN1C is one of the best-studied imprinted genes that encodes a cyclin-dependent kinase inhibitor known to negatively regulate cellular proliferation and differentiation [22]. KvDMR1 methylation on the maternal chromosome is proposed to activate CDKN1C, whereas demethylation of KvDMR1 may cause CDKN1C silencing [23][24][25]. CDKN1C overexpression is one of the causes of Silver-Russell syndrome (SRS), a heterogeneous disorder characterized by severe intrauterine and postnatal growth retardation [26]. In contrast, aberrant CDKN1C silencing is associated with Beckwith-Wiedemann syndrome (BWS), which exhibits a loss of methylation (LOM) at the maternal KvDMR1 imprinting control region [24,27].
In the present study, we examined the expression levels of imprinted genes in embryo tissue from multiple and singleton gestation. We further examined the expression of imprinted CDKN1C in neonatal umbilical cord blood (UCB) and placenta. We also investigated changes in CDKN1C expression in HTR8 cells treated with different E 2 concentrations and the underlying mechanisms by which the dramatic increase of E 2 levels in pregnant women adversely affects fetal development and growth during the first trimester of multiple pregnancies.

Subjects and Tissues
This study was a retrospective study on patients that underwent ART from January 2010 to June 2014 at the Assisted Reproductive Unit of the Women's Hospital, School of Medicine, Zhejiang University (Hangzhou, China). Written informed consent was obtained from all patients who provided samples, and the study protocol was approved by the Ethics Committee of the Women's Hospital, School of Medicine, Zhejiang University. The inclusion criteria consisted of the selective reduction of one or more gestational sacs or embryos to singletons or twins before the 12th week of gestation. Patients with obstetric complications (e.g., gestational diabetes mellitus, hypertension, and placenta previa) or parents who consumed alcohol or smoked during pregnancy were excluded from this study. The control group included assisted reproduction patients with primary singletons or twins during the same period. Primary singletons were matched by a stratified random selection. In particular, the primary singletons chosen for the control group shared a similar maternal age, sex ratio, and gestational age to the reduced singletons. Analyses were restricted to pregnancies in which the duration of gestation was 28 weeks or longer. All pregnancies were confirmed by transvaginal ultrasonography. SGA was defined as a birth weight below the 10th percentile for the gestational age at delivery.
Multifetal pregnancy reduction (MFPR) was performed as previously described [28]. MFPR was performed early in pregnancy (about 8 weeks). Under ultrasound guidance, a 17-gauge needle was inserted through the vaginal wall into the chosen sac. Suction was applied, and all the embryonic parts were aspirated. The same technique was used for additional embryos, as needed. Maternal peripheral blood samples were obtained before MFPR at 8 weeks of gestation. UCB and placenta tissues of newborns from twins were collected at birth.
In total, 195 maternal serum samples were collected, 77 aspirated embryo tissues were collected from MFPR, and 29 embryo tissues of singleton pregnancies were collected from elective terminations of unintended normal pregnancies as controls. Mononuclear cells from UCB (UCBMNC) were separated using density gradient centrifugation and stored at −80°C, as previously described [29]. All tissue samples were collected immediately after surgical removal and were snap-frozen in liquid nitrogen.

Measurement of Estradiol
Maternal serum E 2 levels were measured using electrochemiluminescence (Hoffman-La Roche, Mannheim, USA). The detection limit of for E 2 was 18.4 pmol/L, and the CV% was 2.4-4.6%.

Total RNA Extraction and Real-time Quantitative RT-PCR (qRT-PCR)
Total RNA was isolated from tissue samples or cells using Trizol reagent (Takara, Dalian, China). cDNA was synthesized using the PrimeScript™ RT reagent Kit (Takara). qRT-PCR was carried out with an ABI Prism 7900HT (Applied Biosystems, Foster City, CA, USA) using SYBR® Premix Ex Taq™ (Takara). The relative gene expression was normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH), as previously described [31]. The primers used in this study are listed in Supplemental Table 1.

Methylation-Specific PCR (MSP)
Genomic DNA was extracted from tissue samples or cells using a standard phenol-chloroform extraction method and modified with sodium bisulfite using the EpiTect®Bisulfite Kit (Qiagen, USA). DNA from peripheral blood mononuclear cells treated with SssI methyltransferase (New England Biolabs, Beverly, MA, USA) was used as a positive control for methylated alleles. The methylation-specific primers for KvDMR1 are listed in Supplemental Table 2.

Bisulfite Sequencing PCR
Bisulfite sequencing was performed using specific tissue samples and cells. The primers used for bisulfite sequencing of the KvDMR1 fragment are listed in Supplemental Table 3. The amplified area contained 28 CpG sites. Amplified PCR products were purified using a gel extraction kit (Takara) and ligated into the pMD19-T plasmid using the TA-cloning system (Takara). The sequences were analyzed using 3730 DNA Analyzer polymers (Applied Biosystems, Carlsbad, CA).

E 2 and ICI182780 Treatment of HTR8 Cells
E 2 (Roche, Basel, Switzerland) and the estrogen receptor inhibitor ICI182780 (Sigma, St. Louis, MO, USA) were dissolved in dimethyl sulfoxide (DMSO, Sigma). HTR8 cells were seeded in 6-well plates in 2 mL of culture medium. Cells were treated with 0, 10 -9 , 10 -8 , or 10 -7 M E 2 for 24 h. To investigate the effects of estrogen, cells were pretreated with 10 -5 M ICI182780 for 4 h followed by stimulation with 10 -7 M E 2 for 24 h.

Gene Silencing with DNMT1 Small Interfering RNAs (siRNAs)
For DNMT1 gene silencing, HTR8 cells were transiently transfected with DNMT1-specific siRNAs (Sigma) using Lipofectamine TM 2000 (Invitrogen, Carlsbad, CA), according to the manufacturer's instructions. Scrambled siRNA was used as a control. The knockdown efficiency was confirmed by qRT-PCR and western blotting.

Western Blotting
Western blot analysis was performed as previously described [32]. Briefly, proteins were separated by SDS-PAGE, transferred to nitrocellulose membranes, and exposed to a rabbit anti-DNMT1 antibody (1:800; Santa Cruz Biotechnology, Santa Cruz, CA) for 2 h. The blots were incubated with a horseradish peroxidase-linked antirabbit IgG (1:5000; KPL, Maryland, USA) for 1 h at room temperature, and the specific protein band was visualized using the Licor Odyssey Infrared Imaging System (Licor, Lincoln, North Carolina, USA).

Plasmid Construction and Luciferase Reporter Assay
The human DNMT1 promoter region (−2493 to −1 bp) was inserted into the pGL3-basic plasmid (Promega, Madison, WI, USA), resulting in the DNMT1 promoter-firefly luciferase reporter plasmid DNMT1-luc. The construct was verified by sequencing. HTR8 cells were co-transfected with DNMT1-luc and the Renilla luciferase plasmid pRL-TK (Promega, Southampton, UK), which served as an internal transfection control. Transfection was performed using Fugene-HP (Roche, Basel, Switzerland), as per the manufacturer's instructions. The transfected cells were treated with 10 -7 M E 2 for 24 h, and luciferase activity was measured using the Dual-Luciferase Reporter Assay System (Promega). Firefly luciferase was normalized to Renilla luciferase activity.

Chromatin Immunoprecipitation (ChIP) Analysis
ChIP experiments were performed as previously described with minor modifications [33]. Briefly, cells were crosslinked with 1% formaldehyde for 10 min at 37°C, and the reaction stopped by the addition of glycine to a final concentration of 0.125 M. Lysates were sonicated on ice to shear the DNA to 200-800 bp fragments. ChIP was performed with a ChIP assay kit (Millipore, Billerica, MA, USA), according to the manufacturer's instructions. The estrogen receptor α (ERα) antibody was obtained from Upstate (Millipore). The DNMT1 primers used for PCR are listed in Supplemental Table 4.

Statistical Analysis
Data are presented as the mean ± standard error (SE). The two-tailed student's t-test or ANOVA was used to evaluate the statistical significance of continuous parametric data. The chi-square test was used to compare categorical data. All statistical analyses were performed using SPSS 23.0 software. Statistical significance was defined as P < 0.05.

The Effect of First-Trimester Multiple Pregnancies on Birth Weight
Information for all patients who underwent reduction was available. There were 105 singleton deliveries with selective reduction (< 12 weeks), 217 twin deliveries after selective reduction, 210 primary singleton births, and 864 primary twins without spontaneous or selective reduction for analysis. The mean birth weight in patients whose fetuses were reduced to singletons or twins was significantly lower than that of their corresponding controls (3226.71 ± 513.96 g vs. 3378.19 ± 473.32 g (P < 0.01) and 2428.80 ± 485.64 g vs. 2495.31 ± 520.06 g (P < 0.05), respectively). Fetus birth weights could also be affected by the gestational age at delivery. To further elucidate this issue, we analyzed the proportion of SGA infants. The incidence of SGA in multiple pregnancies reduced to singletons (11.4%, 12/105) was significantly higher than that to primary singleton pregnancies (2.9%, 6/210) (P < 0.01). In addition, SGA in multiple pregnancies reduced to twins (38.5%, 167/434) was significantly higher than that with primary twin pregnancies (27.3%, 472/1728) (P < 0.01).

Maternal Serum E 2 Levels were Significantly Elevated with Increasing Number of Fetuses
We analyzed maternal serum E 2 levels at 8 weeks of gestation (n = 195), including 82 singleton conceptions, 45 twin conceptions, 58 triplet conceptions, and ten quadruplet conceptions. The results showed that maternal serum E 2 levels were significantly elevated with an increasing number of fetuses. The mean serum E 2 concentrations were 10,322.79 ± 701.32 pmol/L for twin conceptions, 18,883.01 ± 8321.94 pmol/L for triplet conceptions, and 31,794.10 ± 6413.26 pmol/L for quadruplet conceptions, which were all significantly higher than that of singleton pregnancies (7240.09 ± 465.48 pmol/L, P < 0.01). Furthermore, there were significant differences in E 2 levels among the four groups (P < 0.01) (Fig. 1A).

The Association between Maternal Serum E 2 Levels of Multiple Pregnancies at 8 Weeks Gestation and Offspring Birth Weight
We analyzed the correlation between maternal serum E 2 levels of multiple pregnancies at 8 weeks gestation and the birth weights of pregnancies reduced to twins. The analysis showed that maternal serum E 2 levels at 8 weeks gestation were negatively correlated with offspring birth weight (r = −0.32, P < 0.05, Fig. 1B), suggesting that offspring birth weight could be inversely affected by increasing maternal serum E 2 levels.

CDKN1C and DNMT1 Expression in Embryo Tissue, Newborn UCBMNC, and Placenta
qRT-PCR was performed on 77 early embryo tissues from selective MFPR and 29 embryo tissues from naturally conceived singleton pregnancies to investigate the mRNA levels of imprinted genes related to growth and development in multiple and singleton embryo tissue. The results showed that CDKN1C mRNA levels were significantly higher in early embryo tissue from triplet and quadruplet pregnancies than those in singleton pregnancies. The CDKN1C mRNA levels in embryo tissue from quadruplet pregnancies were also higher than those in triplet pregnancy embryo tissue; however, the difference was not significant. We further analyzed CDKN1C expression levels in newborn UCBMNC and placenta of 20 multiple pregnancies reduced to twins and matched primary twin pregnancies. Consistent with the results from the embryo tissue, CDKN1C expression levels in the UCBMNC and placenta from multiple pregnancies reduced to twins were significantly increased compared to those from the matched twin pregnancies ( Fig. 2A). Significantly higher DNMT1 expression levels were also observed in MFPR embryo tissue, UCBMNC, and placenta from multiple pregnancies reduced to twins compared to the controls (Fig. 2B).

E 2 Modulates the Expression of DNMT1 and CDKN1C mRNA Levels
We found that serum E 2 levels were significantly higher in multiple pregnancies than those in singleton pregnancies and were elevated with the increasing numbers of fetuses. To investigate whether E 2 could regulate CDKN1C and DNMT1 mRNA levels, HTR-8 cells were treated with E 2 and the ER inhibitor ICI182780. Treatment of estrogen-starved HTR8 cells with E 2 for 24 h increased CDKN1C and DNMT1 mRNA levels in a dose-dependent manner. However, incubation with ICI182780 significantly reduced the effects of E 2 on CDKN1C and DNMT1 mRNA expression ( Fig. 3A and  B). We next investigated the effect of DNMT1 on CDKN1C expression. As shown in Fig. 3C, DNMT1 siRNA effectively knocked down DNMT1 expression. Notably, DNMT1 knockdown reversed the E 2 -induced increase in CDKN1C mRNA levels, indicating that DNMT1 mediates E 2 -induced upregulation of CDKN1C (Fig. 3D).

KvDMR1 Hypermethylation Mediates E 2 -Induced CDKN1C Upregulation
We examined the methylation status of KvDMR1 in embryo tissue, UCBMNC, and placenta using MSP. We found that KvDMR1 was hypermethylated in MFPR embryo tissues, UCBMNC, and placenta for multiple pregnancies reduced to twins (Fig. 4A). These results were further confirmed using bisulfite DNA sequencing (Fig. 4B). Furthermore, treatment of HTR8 cells with E 2 led to KvDMR1 hypermethylation (Fig. 4C). Together, these results suggested that CDKN1C upregulation was associated with the increased methylation of KvDMR1.

DNMT1 Promoter Responses to E 2 and Its Receptors
E 2 is thought to exert its biological effects by binding to ERs [34]. To investigate if the regulation of DNMT1 expression by E 2 is at the promoter level, we determined the effect of E 2 stimulation on the activation of a luciferase reporter driven by the proximal 2.4-kb fragment of the DNMT1 promoter. As shown in Fig. 5, E 2 induced a DNMT1-luc activity fivefold compared to the control. Three putative estrogen response elements (EREs) were located in the DNMT1 promoter using the transcription factor binding sites and cis-regulatory search system (http:// rsat. ulb. ac. be/). Furthermore, CHIP demonstrated that ERα could bind to the DNMT1 promoter in HTR8 cells after treatment with E 2 (Fig. 5). In particular, ERα bound to the ERE-like site at −659 bp of the DNMT1 promoter. Collectively, these findings indicate that DNMT1 was the downstream target of E 2 .

Discussion
Many studies have shown that MFPR is associated with a reduced risk of preterm birth, LBW, and no increase in pregnancy loss compared to that in unreduced multiple pregnancies [28,[35][36][37]. The perinatal outcomes of twin pregnancies after early and late MFPR appear similar [38]. MFPR has been widely accepted as a legitimate treatment option for patients with triplets or higher-order pregnancies [36]. However, these previous studies all compared obstetric outcomes before and after MFPR. To date, only three studies have compared reduced and unreduced multiple pregnancies. Mheen et al. [39] reported that the median neonatal birth weight in multiple pregnancies reduced to singleton pregnancies was significantly lower than that in primary singleton pregnancies. Razaz et al. [37] found that the rate of very low birth weight was significantly higher among pregnancies reduced to twins than unreduced twin pregnancies. Zipori et al. [40] found that the incidence of SGA was not different between the MFPR and unreduced triplet groups. Our findings are consistent with these results. In the current study, we found an increased risk of LBW and SGA when maternal serum E 2 levels were high in the first trimester of multiple pregnancies. Although the results for pregnancies reduced to singletons were better than those reduced to twins, the mean birth weight of pregnancies reduced to singletons was still significantly lower than that of primary singletons. When we excluded the effects of the duration of gestation, there was a higher incidence rate of SGA in multiple pregnancies reduced to singletons and twins. These results indicate that some effects of the first trimester of multiple pregnancies persist and cannot be completely eliminated by fetal reduction.
Maternal serum E 2 levels in the first trimester of pregnancy were increased with the number of fetuses and negatively correlated with offspring birth weight. E 2 is the most bioactive estrogen. In mice, high E2 exposure during early pregnancy decreases offspring body weight [41]. Moreover, high E 2 doses cause embryonic mortality and fetal and placental growth retardation in rats [42]. However, the mechanisms by which the dramatic increase in E 2 levels in pregnant women adversely affects fetal development and Evidence from animals and humans has indicated that certain transient environmental influences can produce persistent changes in epigenetic marks that last throughout life [14]. Imprinted genes are implicated in the regulation of fetal growth and development and are especially sensitive to environment-mediated changes in DNA methylation [43]. Endocrine disruptors can alter DNA methylation patterns of key genes, resulting in transcriptional changes [44]. Cases of ART-conceived children afflicted with imprinting mutations have been reported [45]. CDKN1C is a maternally expressed imprinted gene with a major role in regulating embryonic growth. Previous studies demonstrated that excess CDKN1C could cause embryonic growth retardation in animals and humans [46,47]. In the present study, we found that the expression levels of CDKN1C and DNTM1 were significantly upregulated in embryo tissue from multiple pregnancies compared to singleton pregnancies.
The expression of imprinted genes is regulated by the methylation status of the CpGs in the differentially methylated regions (DMRs) of each gene [48]. DNMTs are responsible for DNA methylation, and high DNMT1 activity contributes to abnormal hypermethylation of certain genes [15]. These observations suggest that E 2 might interact with DNMT1 and positively regulate its enzymatic activity. DNMT1 overexpression leads to hypermethylation of KvDMR1. KvDMR1 is the predominant imprinting control region of CDKN1C on human chromosome 11p15. We found that the methylation levels of KvDMR1 and the DMR of CDKN1C are significantly increased in response to E 2 , resulting in the CDKN1C upregulation. This upregulation could contribute to the LBW and SGA of multiple pregnancies. Moreover, increased CDKN1C and DNMT1 expression levels were also associated with the hypermethylation of KvDMR1 in UCBMNC and placenta of multiple pregnancies reduced to twin pairs, indicating that transiently high serum E 2 levels might induce persistent changes in epigenetic marks during early gestation.
To confirm that CDKN1C expression was regulated by high E 2 levels, we further investigated the regulation of CDKN1C expression by E 2 . In the "classical" mechanism of estrogen action, the long-term effects of E 2 are generally ascribed to transcriptional modulation of target genes through the binding of estrogen receptors (ERs). These receptors modulate gene expression directly through EREs in the promoter regions of target genes or indirectly through interaction with transcription factors, co-activators, or transcription complexes [49,50]. Using a reporter gene assay, we demonstrated that ERα activated DNMT1 transcription through an ERE located at −659 bp upstream of the transcriptional starting site. The respectively. (C) MSP and bisulfite sequencing analysis of KvDMR1 methylation in HTR8 cells without or with 10 -7 M E 2 treatment. Ten independent clones of the indicated groups were sequenced. Black circles denote methylated cytosine in specific CpGs, and white circles denote nonmethylated cytosine in specific CpGs. U and M denote unmethylated DNA-specific and methylated DNA-specific amplification, respectively. P denotes the positive control palindromic sequence of the ERE in the DNMT1 promoter was similar to the canonical ERE [51]. The direct binding of ERα to the DNMT1 promoter was confirmed by ChIP. Collectively, our results clearly confirmed that CDKN1C acted as a key mediator of E 2 effects in HTR-8 cells.
To the best of our knowledge, this study is the first to demonstrate that high E 2 levels in the first trimester of multiple pregnancies are an independent risk factor for SGA. This conclusion was based on a single-center study with a relatively large sample size. However, we acknowledge that the study has some limitations. First, it was retrospective in design, and E 2 levels post-reduction could be evaluated in a prospective study. Second, multiple pregnancies were achieved through ART, which included controlled ovarian hyperstimulation and IVF. Therefore, it is hard to exclude the effects of infertility on our findings. Third, pregnancy reduction from twin to singleton is not as commonly accepted as reducing higher-order multiples. Thus, the DNMT1 and CDKN1C expression levels in singletons from reduced twins could not be obtained.

Conclusions
The present study demonstrated that high maternal E 2 levels might induce high CDKN1C expression, leading to LBW and SGA in the first trimester of multiple pregnancies. To minimize the risks of LBW and SGA, abnormally high maternal serum E 2 levels during early pregnancy in ART patients should be avoided.
Data Availability All raw data and material are available upon request.
Code Availability Not applicable.

Ethics Approval
The study was conducted with the approval of the Ethics Committee from the Women's Hospital, School of Medicine, Zhejiang University, No. 20130031, 27 June 2013.

Consent to Participate
All subjects consented to the sample retrieval as well as collection of clinical information as approved by the Ethics Committee in Women' Hospital, School of Medicine, Zhejiang University.

Consent for Publication
All the authors consent to the publication of this paper.

Conflict of Interest The authors declare no competing interests.
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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will promoter. ChIP analysis of the human DNMT1 promoter was performed after HTR8 cells were treated with E 2 for 24 h. ChIP assays were performed using IgG, anti-RNA polymerase, and anti-ERα antibodies as indicated. After cross-link reversal, the co-immunoprecipitated DNA was amplified by PCR using primers specific for the DNMT1 ERE containing region (− 659 to − 647) or a control region (− 2123 to − 2111 or − 728 to − 716). The PCR products were resolved using a 2% agarose gel. Representative data from three independent experiments are presented need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.