Role of Endometrial Autophagy in Physiological and Pathophysiological Processes

As a fundamental activity of cells, autophagy is essential in biological process of endometrium in both physiology and pathology. In endometrium-related diseases, autophagy plays a multifunctional and complicated role as revealed by more and more evidence, which increased the difficulties for us to understand the effect of it in a certain situation. As a matter of fact, the function of autophagy in different endometrium-related diseased may be totally different. Here, we make a brief discussion of autophagy in endometrium-related diseases separately based on the researches till now, and more thorough studies are needed to help us understand the role of autophagy in endometrium.

Autophagy is a highly conserved biological behavior in eukaryotic cells to disassemble unnecessary or dysfunctional components of the cell under exquisite regulation mechanism which can be initiated under the conditions of hypoxia, starvation, lack of nutrition, or extreme pH values 1 - 3 . In macroautophagy (commonly referred to autophagy), substances such as proteins, organelles or cytoplasm are encapsulated in a double-membraned vesicle named as autophagosome, and degraded into small molecules for reuse by the fusion of autophagosome with lysosome 4 . Autophagy can also dispose the misfolded proteins, aging organelles, and other damaged cell components to maintain the homeostasis of the cells. Basic level of autophagy is essential for almost all of the eukaryotic cells and many cellular activities, and the absence or aberration of autophagy may lead to a series of pathological states. Recent studies revealed that autophagy also plays an indispensable role in the physiological and pathophysiological processes related to the endometria, including the cyclic menstruation, the decidualization or reconstitution during normal pregnancy, and the endometrium-related diseases such as endometriosis, endometrial carcinoma and infertility. As a basic biological activity, autophagy is closely related to the cell proliferation and apoptosis, which ubiquitously occur in the dynamic refreshment of endometrium. What's more, the autophagy level in endometrium cells reflects the condition of the disease or physiological process, and can influence the function of cells in some way. Therefore, autophagy in endometrium needs to be further studied and may be beneficial for the future treatment of endometrium-related diseases. And this article is to review the present studies about this topic.

Autophagy takes part in variety of biological activities, and the level of autophagy can influence the cellular metabolism, the proliferation and program cell death, and the drug resistance or sensibility of cancer cells. Thus, autophagy is precisely regulated in different condition. Factors such as hormones, cytokines, metabolic products and non-coding RNAs can regulate the autophagy level independently or interdependently. Hormones are the main factors that regulate the cyclic proliferation, secretion and shedding of endometrium. Considering that autophagy also changes during the menstrual cycle, it's not difficult to imagine that hormones play important roles in adjusting the level of autophagy in endometrium. Estrogen is the predominant hormone during the proliferative phase, and many researches have proved that it can inhibit the autophagy activity in endometrium 13 , 15 , 17 , 29 , 30 . Mei et al. found that estradiol (E 2 ) treatment induced a marked increase in CXCL12 secretion and CXCR4 expression together with decreases in autophagy grade, punctuate LC3B immunofluorescent staining and autophagy-associated protein levels, while the suppression of autophagy induced by E2 and recombinant human CXCL12 protein could be abrogated by an anti-CXCR4 neutralizing antibody, suggesting that estrogen could suppress the autophagy of ESCs by upregulating CXCL12 and CXCR4 expression 29 . Estrogen was also reported to induce the autophagy level in normal endometrial cancer cells and endometrial carcinoma stem cells by promoting the expression of estrogen induced gene 121(EIG121), which can induce cytoplasmic vacuolization, induce the formation of autophagosomes and enhance lysosomal degradation of long-lived proteins 31 . Knockdown of EIG121 compromises starvation-induced autophagy and sensitizes cells to cell death induced by nutrient deprivation and exposure to cytotoxic agents 28 , 31 . In a ovariectomized rats menopausal model, autophagy was observed to be increased in uterine endometrium when estrogen was deprived, and the estrogen depletion induced autophagy was possibly via endoplasmic reticulum (ER) stress-dependent arachidonic acid /prostaglandin E2 axis inhibition and Akt-mTOR signaling pathway suppressing in uterine epithelial cells 13 . Relationship between estrogen and progestogen can be both synergistic and antagonistic depending on the tissues or cells receiving the signals. As is the case, their role in regulating the activity of autophagy may be complicated. In the study of Mei et al., the estrogen induced autophagy in ESCs could be reversed by progestogen 15 , suggesting that progestogen plays an antagonistic role in controlling the autophagy in ESCs. Consistent with this, Choi et al. 32 found that dienogest, but not progestogen, can enhance autophagy induction in endometriotic cells by impairing activation of AKT, ERK1/2, and mTOR signal pathways. On the contrary, Choi et al. 14 found that progesterone and estrogen both reduced the autophagic response in the uteri in ovariectomized mice model. The differences may occur from the tested samples, actually, the mice uteri contain different kinds of cells, and the total mRNA or protein may not reflect the separate change of autophagy in ESCs, EECs, or other cells precisely. Other hormones are also involved in regulating the autophagy condition in endometrium. After menopause, the level of estrogen and progestogen goes down while follicle-stimulating hormone (FSH) commonly rises with the decline of ovary function. It was reported that high circulating levels of FSH in postmenopausal women activated the phosphorylation of Smad2/ Smad3 through transforming growth factor beta receptor II (TbRII). The complexes of phosphorylated Smad2/Smad3 subsequently transported into the nucleus and launched the expression and activation of several autophagy-related molecules such as ATG5, ATG12, ATG3, and ATG7. Persistent activation of cell autophagy may directly or indirectly induce cell apoptosis. Thus, FSH can promote the autophagy of endometrial adenocytes 33 . Autophagy may also be related with increased androgen availability in PCOS. It was found that autophagy related genes were significantly reduced in anovulatory PCOS compared to healthy endometrium, and was negatively correlated with free androgen index. Treatment of PCOS patients with metformin significantly increased the endometrial mRNA levels of autophagy-associated genes, suggesting that the increased androgen level in PCOS is associated with metformin-sensitive transcriptional downregulation of endometrial autophagy 34 . And dexamethasone, a widely used anti-inflammatory compound, was also observed to inhibit the autophagy of mice uteri at the first day of pregnancy, when the autophagy level should have been the highest 14 . This effect suggests that inflammatory response may be associated with increased autophagy in the day 1 pregnant uterus. Other hormones, such as luteinizing hormone (LH), anti mullerian hormone (AMH), prolactin (PRL), and Human Chorionic Gonadotropin (HCG), which also take vital part in the menstruation cycle or gestation of fertile women, still need to be investigated on their role of regulating the autophagy of endometrium. Autophagy can be influenced by many metabolites, and it can affect the metabolic condition of cells simultaneously. Rhee et al. found that a high level of palmitic acid, which is commonly observed in obese people as a result of imbalance of energy metabolism, can impaired the autophagy of human endometrial cells during decidualization 16 . This may be one of the mechanisms that lead to the poor reproductive outcome and early pregnancy loss in obese women. Folate acid, a widely applied supplement by women during pregnancy, was reported to induce the autophagy of endometrium, thus benefits the decidualization process 35 . In another experiment, researchers found that compared to the control group, caloric restriction can significantly increase the autophagy activity and inhibit the p-Akt and mTOR levels in endometriotic lesions of endometriosis mice model 36 . Apart from this, the amino acid metabolism can also regulate the autophagy condition in endometrium. It was detected that the level of phenylalanine, indoleacrylic acid (IAA), phosphocholine and lyso- platelet-activating factor-16 (lyso-PAF) in serum were higher in endometrial carcinoma patients than normal controls, and all of them played a role in regulating the autophagy tumor cells. PAF can induce tumor cell apoptosis and autophagy, while IAA triggered apoptosis and had a biphasic effect on autophagy: inhibiting autophagy with doses <1 mmol/L but inducing at 1 mmol/L. Interestingly, the alterations in apoptosis and autophagy caused by 1 mmol/L IAA coule be reversed by the concomitant treatment of tryptophan (100 mumol/L). Phosphocholine inhibited tumor cell invasion and migration, and promoted cell proliferation and autophagy, all in a dose-dependent manner 37 . Other substance, such as retinoic acid, was also reported to enhance the autophagy in ESCs 38 . According to this, we can learn that autophagy is widely regulated by many kinds of metabolic products, and closely related to various biological activities. What's more, the supply of oxygen plays a critical role in the process of cell growth. The lack of oxygen, namely hypoxia, can induce the autophagy of cultured human endometrial stromal cells (HESCs) in a time-dependent manner through hypoxia-inducible factor-1alpha (HIF-1α) 23 . LC3-II expression and the number of autophagosomes were gradually increased by hypoxia treatment 22 . This autophagy inducing effect of hypoxia was also reported in other cells and diseases, such as preeclampsia, non-alcoholic steatohepatitis, neurodegenerative diseases, and so on 39 , 40 . Oxidative stress is another good candidate responsible for autophagy induction in endometriotic cells. The persistent oxidative stress, by itself and/or a positive feedback with heme oxygenase-1(HO-1), reactive oxygen species (ROS), and other down-stream response, can stimulate the autophagic process 41 - 43 . Oxidative stress induces a rapid calcium release from intracellular stores, which play an important role in apoptosis and necrosis, senescence, as well as autophagy. With a sublethal H 2 O 2 treatment, an artificial environment of oxidative stress was formed. It was found that in H 2 O 2 -treated human endometrium-derived stem cells, intracellular calcium ([Ca2+]i) chelation by BAPTA-AM can effectively initiate an early onset of autophagy, as observed by both the phosphorylation status of AMPK/mTORC1 pathway and the dynamics of the LC3 lipidization. In other word, the calcium release under oxidative stress could inhibit the activation of autophagy, which may be related to the prevention of the premature senescence and DNA damage 26 . Different from the free state of calcium, iron is presented in cells as ferric ammonium citrate (FAC). Treatment with FAC can significantly increase the protein level of LC3-II and the number of autophagosomes in a dose dependent manner in immortalized endometriotic Cells, by the activation of AKT and MAPK pathway 41 . Serum and glucocorticoid-regulated kinase 1 (SGK1) is a serine/threonine protein kinase that shares structural and functional similarities with the AKT family of kinases 44 . It plays an important role in cellular stress response by activating certain potassium, sodium, and chloride channels, suggesting an involvement in the regulation of processes such as cell survival, neuronal excitability, and renal sodium excretion 45 - 47 . In endometrial carcinoma, the expression of SGK1 was upregulated in tumor tissues than normal control, and inhibiting SGK1 with SI113 can induce a reduction of endometrial cancer cells viability as well as a significant increase of autophagy, as revealed by the increase of the markers LC3B-II and beclin I, detected by both immunofluorescence and western blot analysis 48 . This effect may be associated to the induction of endoplasmic reticulum stress markers GRP78 and CHOP evaluated by both real-time PCR and western blot analysis. Inhibitors of the key enzymes can also influence the process of autophagy in endometrium. Liraglutide, which is an agonist of glucagon-like peptide-1 receptor (GLP-1R), can significantly induced autophagy of endometrial carcinoma cells and inhibited Ishikawa cell growth, as well as the elevated AMPK expression 49 . Bortezomib is an inhibitor of 26S proteasome, which has been reported to inhibit protein degradation in lysosomesmay by inducing ERK phosphorylation and suppress cathepsin B in endometrial carcinoma cells and enhance chemotherapy efficacy by abolishing chemotherapy-related autophagy 50 . A new synthetic histone deacetylase inhibitor, MHY2256, was found to induce apoptosis and autophagy cell death in endometrial cancer cells via p53 acetylation 51 . Similarly, as an inhibitor of mTOR, RAD001 significantly decreased phosphorylation of mTOR and inhibited proliferation of progestin- resistant cancer cells and induced a higher sensitivity to paclitaxel-induced apoptosis by promoting autophagy 52 , 53 . Rapamycin is another inhibitor of mTOR, which is the most commonly used as an inducer of autophagy, but we should notice that it can affect both mTORC1 and mTORC2. What's more, mTOR is a major regulatory protein that is part of several signaling pathways, including for example those that respond to INS/insulin, EGF/epidermal growth factor and amino acids, and it thus controls process other than autophagy 54 - 57 . Therefore, rapamycin will ultimately affect many metabolic pathways and the pleiotropic effects need to be considered 58 . Many drugs, especially those used in the anti-tumor treatment, were discovered with the effect of adjusting the autophagy activation. Metformin, a commonly used medicine for treating type II diabetes, which has recently been reported to possess anti-proliferative properties in a variety of cancers, was reported to regulate the autophagy of tumor cells 59 , 60 .It was found that metformin could increase the apoptosis, inhibited the growth, and promote the autophagy of endometrial carcinoma cells with different concentrations in a dose- and time-dependent manner 59 - 62 . And the autophagy inducing effect was proved to be related with CEBPD or AMPKα 63 , 64 in several tumor cells. Sorafenib is another anti-tumor drug, or more precisely, a multi-target tyrosine and serine/threonine kinase inhibitor approved by FDA for the treatment of hepatocellular carcinoma, advanced renal carcinoma and radioactive iodine-resistant thyroid carcinoma 65 , 66 . Sorafenib could induce an unfolded protein response (UPR) in EC cells that connects with an autophagic output through a MAPK/JNK-dependent mechanism and this MAPK/JNK-dependent early protective autophagic response in endometrial carcinoma cells may count for the limited effect of sorafenib in a multi-institutional phase II trial in advanced uterine carcinoma patients 67 . Programmed cell death 4 (PDCD4), a newly identified tumor suppressor, was uncovered to effectively inhibit the proliferation and suppress the migration and invasion of endometrial cells by inhibiting cell autophagy, probably through NF-κB/MMP2/MMP9 signal pathway 68 . Cisplatin was also reported to upregulate cell autophagy in endometrial cancer cells via the PI3K/AKT/mTOR signaling pathway 69 . And interestingly, the combination of cisplatin and rapamycin showed a synergetic anti-endometrial cancer effect 58 . Also, other drugs 70 , including traditional Chinese medicine such as Isoliquiritigenin (ISL), Protopanaxadiol (PPD) showed a potential to regulate the autophagy in endometrium 30 , 71 , 72 . The role of autophagy in endometrial cancer is worthy investigating and is discussed in the next part. With the constant-depth study, non-coding RNA has been unveiled to participate in more and more biological activities. It was now clear that many micro RNA and long non-coding RNA (lncRNA) have a regulatory effect on the activation of autophagy in endometrium. For example, miR-101-3p was reported to upregulate the expression of autophagy-related proteins LC3-II and beclin-1 in EC cells in a time- and dose-dependent manner, by downregulating the expression of enhancer of zeste homolog 2 (EZH2) 73 . EZH2 is a critical component of the polycomb repressive complex 2 with intrinsic histone methyl transferase activity that mediates gene silencing by catalyzing trimethylation on lysine 27 of histone H3 74 . And it can epigenetically repress tuberous sclerosis 2 (TSC2), a negative regulator of the mTOR pathway. Downregulation of TSC2 by EZH2 elicited mTOR activation, which in turn induced the inhibition of autophagy 75 . MiR-210, a micro RNA which was significantly induced by hypoxic treatment, was found to promote autophagy partly by inhibiting the Bcl-2 expression 76 . MiR-218 can also inhibit the autophagy of endometrial cancer cells by directly bind to the 3'-UTR of HMGB1 gene, which is one of the most important regulators of cellular autophagy 77 . lncRNAs, specifically HOTAIR, can regulate the level of autophagy in human endometrial cancer cells by influencing Beclin-1, MDR, and P-gp expression. Interference of HOTAIR enhanced the autophagy activity of cisplatin-resistant Ishikawa cells and further reduced the proliferation of cisplatin- resistant Ishikawa cells 78 . lncRNA-MALAT1 also promoted hypoxia-induced autophagy in endometrial stromal cells and reduced their apoptosis, which facilitated the survival of ectopic endometrium 79 . DNA mismatch repair (MMR) can induce autophagy in human endometrial tumor cells via signal transferred by p53 after exposure to 6-thioguanine (6-TG), a chemotherapy drug which can be recognized by MMR. Autophagy induced by DNA mismatch repair inhibits apoptosis of endometrial carcinoma cells. An inhibition of autophagy by Atg5 knockdown will significantly promotes the apoptosis of cancer cells after DNA mismatch repair processing of 6-TG, suggesting that autophagy mediated the survival of cancer cells with MMR in the treatment of 6-TG 80 . A brief summary of regulators of autophagy in endometrium is shown in Table 2 .

Autophagy is a conserved pathway in eukaryotic cells with the function to degrade misfolded proteins, aging organelles, and other damaged cell components, as well as participate in the regulation of biological activities such as proliferation, apoptosis, and immunoreaction. Endometrial cells undergo a dynamic autophagy in the periodic growth and shedding off during the menstrual cycle, and the autophagy level also changed in endometrium-related diseases, as well as the physiological processes including decidualization and atrophy. Although a lot has been done during the past years, much remains unknown related to the autophagy in endometrium. The researches about autophagy limit to the endometrium stromal cells and epithelial, while we believe that autophagy in endometrial immune cells was the same pivotal and even more important. What's more, autophagy influences different biological activities in the same disease or the same kind of cells, these effects may be mutually contradictory. The balance and relationship between these effects, or the synthetic role of autophagy at some certain conditions are still vague to our understanding. On the one side, autophagy could promote the drug resistance of tumor cells and the migration and invasion of ectopic endometrium; on the other side, autophagy may also induce the immune activation and cell apoptosis in the lesions area (Figure 1 ). There is no constant role of autophagy in different situation; at least the evidences were controversial related the function of autophagy even in the same diseases. For all this, there's no doubt that to determinate the law of autophagy is of great significance in improving the treatment and enhancing the medicine development in endometrium-related diseases.

Endometrial carcinoma is one of the most common malignant diseases in women all over the world. It was reported that autophagy has played important roles in the tumorigenesis, the proliferation, the drug resistance, and the immune regulation of endometrial carcinoma. To investigate the autophagy targeted treatment for endometrial carcinoma may be a potential way instead of the traditional method. Three autophagy related genes, RB1CC1, ULK4, and WDR45 were found to be significantly mutated in endometrial carcinoma patients compared with normal women, suggesting that aberrant activation or disruption of autophagy plays a role in the tumorigenesis of endometrial carcinoma 84 . LC3A reactivity was recognized in three basic patterns: diffuse cytoplasmic, cytoplasmic/juxta-nuclear, and the so-called “stone-like” structures (SLS). The latter has emerged as the hallmark of autophagic activity, being detected exclusively in endometrial carcinomas and mildly in the atypical hyperplasias, while other forms of hyperplasia without cytological atypia and normal endometrial tissues expressed only cytoplasmic staining patterns, suggesting that autophagy is more activated in endometrial carcinoma cells than normal or hyperplastic endometrial 85 . The highly activated autophagy may be related the proliferation, apoptosis and other biological activity of tumor cells, which contribute to the oncogenesis of endometrial carcinoma. Actually, it was reported that autophagy may promote cell survival under nutrient deprivation and other cellular stresses 31 . But in other cases, autophagy is more likely to associate with the cell apoptosis and cell death, which is negatively related to proliferation. Several anti-cancer drugs was found to induce the autophagy of cancer cells and inhibit the cell viability, suppress the cell proliferation and downregulate the cell growth 48 , 49 , 86 . Similarly, the lower level of autophagy in progestogen-resistant endometrial cancer cells was related to the increased proliferation 52 , and estrogen was also found to promote the cell proliferation and simultaneously inhibit the autophagy in endometrial cancer cells 30 . In conclusion, autophagy may play a beneficial role in the initiation of endometrial carcinoma and the survival of tumor cells under stress, but excessive autophagy may lead to the apoptosis and cell death, which is bad for the proliferation of endometrial carcinoma. Autophagy is also related to the drug resistance of endometrial carcinoma cells for some traditional anti-tumor medicines. For example, cisplatin was reported to upregulate cell autophagy in endometrial cancer cells via the PI3K/AKT/mTOR signalling pathway 69 . And by inhibiting the level of autophagy, chloroquine can effectively suppress the proliferation in endometrial cancer cell lines in a dose-dependent manner, the sensitivity of endometrial carcinoma cells to cisplatin was also improved by knocking down ATG5 or ATG7 87 . Autophagy has also been shown to be involved in cell resistance to paclitaxel. Paclitaxel-mediated cell death was further potentiated by pretreatment with autophagy inhibitor chloroquine or shRNA against the autophagic gene beclin 1, suggesting that paclitaxel- elicited autophagic response plays a protective role that impedes the eventual death of endometrial carcinoma cell, and autophagy-inhibitor therapy could be an effective and potent strategy to improve paclitaxel treatment outcomes in the treatment of endometrial carcinoma 88 . This kind of protective auphagic response was also observed in some new drugs, such as sorafenib. Sorafenib is currently used to treat hepatocellular carcinoma, advanced renal carcinoma and radioactive iodine-resistant thyroid carcinoma, but it has not showed much effect in a multi-institutional phase II trial in advanced uterine carcinoma patients. A recent study shows that targeting autophagy enhances sorafenib cytotoxicity and suppresses tumor growth and pulmonary metastasis progression, which can provide insights into the unopposed resistance of advanced endometrial carcinoma to sorafenib and highlight a new strategy for therapeutic intervention in recurrent endometrial carcinoma 67 . For those patients who are insensitive to chemotherapy, inhibiting the autophagy of tumor cells may be one of the new strategies for effective treatment. On the other hand, autophagy is necessary for the anti-tumor effect in some of the drugs, meaning that they can induce the cancer cell death at least partly by promoting the autophagy. More and more evidence showed that metformin has effects on suppressing the growth of different kinds of tumor cells. It was revealed that metformin can induce the autophagy of endometrial cancer cells, and inhibition of autophagy either by beclin1 knockdown or by 3-methyladenine-mediated inhibition of caspase-3/7 can significantly suppress the anti-proliferative effects of metformin on endometrial cancer cells, indicating that the anti-proliferative effects and apoptosis- inducing effect caused by metformin were partially or completely dependent on autophagy 62 . Autophagy was also involved in the cell death inducing effect of suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, which was a promising therapeutic agent for endometrial stromal sarcoma 89 . These results told us that autophagy may be a double-edged sword in the treatment of endometrial carcinoma. Just like the relationship of autophagy and proliferation, in a certain condition, autophagy may promote the drug resistance or the drug effect according to specific circumstances. Apart from this, autophagy is related to the immune regulation of the local tumor environment. Exposure with rapamycin results in a significantly increased autophagy in endometrial cancer cells, and it can further enhanced the cytotoxicity of NK cells by upregulating the expression of IL-27 in endometrial cancer cells and IL-27 receptors on NK cells, which can restricted the growth of tumor in Ishikawa- xenografted nude mice 58 . In contrast, high expression of Beclin-1 is related to high tumor grade, high myometrial invasion, and a poor 5-year survival in endometrioid adenocarcinoma 90 , 91 .

Autophagy may be related to the endometrial hyperplasia induced by tamoxifen 99 . As a first generation of selective estrogen receptor modulators, tamoxifen is usually recommended for the hormone receptor positive breast cancer patients, but one of the side effects of tamoxifen is endometrial hyperplasia even endometrial cancer. Feng et al. found that tamoxifen could significantly induce the mRNA and protein expression of autophagy adaptor P62 in endometrial cells but not breast cancer cells, and inhibiting the expression of P62 retarded tamoxifen- promoted growth of endometrial cancer cells 99 , indicating that the selectively promotion of autophagy in endometrial and breast cancer cells may be the reason for tamoxifen-induced hyperplasia. Actually, we may hypothesize that autophagy was associated with hyperplasia of endometrium, not only in the tamoxifen-induced cases. Studies are needed to prove whether this was true in the spontaneous hyperplasia or hormone-related hyperplasia since the evidence was rare.

Endometriosis is a chronic, estrogen-dependent disease and characterized by the implantation of endometrial glands and stroma deep and haphazardly into the outside the uterine cavity 92 . Autophagy in endometriosis-derived tissues is reduced compared with normal endometriosis tissues, especially in ectopic endometrium and during the secretory phase 93 . The impaired autophagy plays critical roles in the process of cell apoptosis and proliferation, invasion and migration, cell immunity, and is associated to the stage and prognosis of endometriosis 93 , 94 . As a benign disease characterized by the presence, transfer, invasion, and cultivation of growing endometrial tissue, endometriosis is now found to be more and more closely related to the immune microenvironment at local peritoneal cavity. The impaired autophagy in ectopic ESCs results in the downregulation of hematopoietic cellular kinase (HCK) by inactivating signal transducer and activator of transcription 3 (STAT3), as well as the increased secretion of the downstream molecules CXCL8/IL-8 and IL23-A by ESCs, and this increase induced the upregulation of CD16- NK cells and decline of cytotoxic activity in ectopic lesion microenvironment 17 . Similarly, we also found that rapamycin decrease the level of IL-15 receptors in ESCs, which may downregulate the effect of IL-15 on stimulating the growth and invasion of ESCs and helping the immune escape of ESCs by suppressing the cytotoxic activity of NK cells in the ectopic milieu 95 . What's more, we proved that autophagy in ectopic ESCs enhances the cytotoxic activity of NK cells and suppresses the growth of ectopic lesions in a mouse EMS model. By increasing the autophagy of ectopic ESCs, protopanaxadiol significantly increased the expression of activating natural cytotoxicity receptors (NKp30 and NKp46) and cytokine IFN-γ, and decreased IL-10 expression in NK cells, and protopanaxadiol can also decreased the number and weight of mouse ectopic lesions 29 . Autophagy in ESCs can also influence the function of macrophage around the ectopic lesion. Ruiz et al. noted that autophagic flux inhibitor hydroxychloroquine (HCQ) increase the levels of peritoneal macrophages and the IP-10 (10 kDa interferon-γ-induced protein) chemokine in a mouse model of endometriosis 11 , whereas the role of macrophage in the development of endometriosis needs to be deep investigated. Autophagy is also reported to be related to the proliferation and apoptosis of eutopic or ectopic endometrial tissues from endometriosis patients. By inhibiting the activity of autophagy in endometriotic stromal cells, MK2206 (an AKT inhibitor) and chloroquine markedly reduced cell growth and regrowth after discontinuation of treatment, and reduced the size of endometriotic implants, indicating that autophagy played a cytoprotective role in endometriosis 96 . Autophagy was also reported to inhibit the proliferation and colony formation, and the growth of filopodia of the endometriotic cell line CRL-7566 through fascin-1 20 . A newly identified tumor suppressor, PDCD4, can effectively inhibit the proliferation and colony-forming ability and suppress the migration and invasion ability of endometrial cells probably by inhibiting cell autophagy 68 . Xu et al. also showed that autophagy in ovarian endometriotic cell line CRL-7566 may contribute to pathological development of endometriosis through enhancing cell survival 76 . However, some researcher deemed that autophagy may promote the apoptosis of endometriotic cells. Dienogest treatment of endometriotic cells was found to suppress AKT and ERK1/2 activity, thereby in turn inhibiting mTOR, inducing autophagy and promoting apoptosis 32 . Choi et al. also identified that rapamycin treatment induced autophagy and led to apoptosis promotion, which was reversed by the addition of 3-MA, suggesting that mTOR inhibition promotes endometriotic cell apoptosis via autophagy induction 12 . And rapamycin was observed to inhibit the proliferation and colony formation and inhibit the growth of filopodia of the endometriotic cell line CRL-7566, which can be reversed by 3-MA 20 . Collectively, autophagy may be essential for the proliferation and cell growth of endometriotic cells, but under some certain circumstances, the increased activity of autophagy could lead to their apoptosis. Migration and invasion are two typical characteristics of endometriotic cells contributing to the development of endometriosis, which are also uncovered to be regulated by the level of autophagy. Human endometrial epithelial cells treated by hypoxia displayed a higher level of autophagy and higher ability of migration and invasion compared to the control cells; however, when co-treated with autophagy inhibitors 3-MA and CQ, the migratory and invasive potential were dramatically decreased. These observations indicated that autophagy facilitates the hypoxia triggered migration and invasion 22 . Similar effects were also observed by inhibiting autophagy with specific inhibitors and Beclin1 siRNA in human endometrial stromal cells, the decreased autophagy activity attenuated their hypoxia triggered migration and invasion 23 . PDCD4 effectively suppressed the migration and invasion ability of endometrial cells, and the mechanism was also found out to be related to its function of inhibiting the autophagy of endometrial cells 68 . Based on the researches, we may conclude that autophagy play an important role in the migration and invasion of endometrial cells. CA125 is a critical index which can reflect the active inflammatory responses and the development or stage, as well as predict the recurrence of endometriosis 97 . As is shown in the study of Ren et al. 98 , Beclin 1 protein expression in eutopic endometrial tissues was negatively correlated with serum CA125 (r = -0.307, P = 0.015), and pelvic pain (r = -0.542, P = 0.000). Lu et al. 38 also found that Beclin1 expression showed a negative correlation with the clinical stage of endometriosis, demonstrated that autophagy is lower in the advanced stage of endometriosis. However, our previous work showed that there was no significant difference in autophagy grade between stage I-II and stage III-IV endometriosis-derived ectopic ESCs 15 . Zheng et al. 24 clarified that there was a significant positive correlation between serum CA125 level and LC3-II protein level and/or LC3-II/LC3-I ratio in endometrial tissues, whereas the correlation index was separately 0.307 and 0.405, and the CA125 level was negatively related to the mRNA expression of LC3B and Beclin and protein level of Beclin, while the correlation index was quite small and with no significance 24 . Since the relationship between autophagy and stage of endometriosis as well as the serum CA125 level remains to be controversial, more samples should be included in the research to figure out the fact, which may help to comprehend the role of autophagy and direct the future treatment of endometriosis with autophagy-related drugs.

Although many factors contribute to infertility and early pregnancy loss, decidualization defects was regarded as an important factor contributing to compromised endometrial receptivity and poor implantation. As is discussed above, autophagy is beneficial to the process of decidualization, and impaired autophagy in endometrial cells may be related to infertility. In obese women, the increased level of palmitic acid may decrease the autophagy in endometrial cells as well as the process of decidualization, and further cause the implantation failure 16 . And autophagy in polycystic ovary syndrome patients was reported to be negative associated to the androgen level, indicating that the inspired autophagy may be related to the increased level of androgen, which inhibits the growth of follicle and is detrimental to the endometrial receptivity 34 . Much remains unknown in the field of infertility. Apart from the quality of zygote, the endometrium related process, including the decidualization, the implantation, the remodeling of uterus spiral artery and the endometrial receptivity, are all closely linked to a successful pregnancy. There's no doubt that the condition and function of endometrial or decidual stromal cells play a vital role, and autophagy activity of endometrial or decidual cells deserves more attention and may draw a new light on the way exploring the mechanisms of infertility.