Differential expression of Oct-4, CD44, and E-cadherin in eutopic and ectopic endometrium in ovarian endometriomas and their correlations with clinicopathological variables

Endometriosis is one of the most common chronic inflammatory diseases in reproductive–age women. Its prevalence is 5–10% and can cause chronic pelvic pain and infertility [1]. Ovarian endometrioma is the most prevalent subtype of endometriosis. Endometriosis is currently treated medically, surgically or with a combination of both medical and surgical techniques.

Although it is highly prevalent and decreases quality of life, the molecular and cellular mechanisms of endometriosis are still unknown. However, recent studies have shown that endometrial stem cells play a role in the etiopathogenesis of endometriosis [1‐4].

The human endometrium is a dynamic tissue with a high regenerative capacity [5]. Previous studies have suggested that this high regenerative capacity is mediated by endometrial stem cells [6]. Octamer-binding protein 4 (Oct-4) is a molecular marker for stem cells that plays an essential role in maintaining cell pluripotency and self–renewal processes in various types of benign and malignant tissues [2‐4].. Previous studies have demonstrated that Oct-4 is expressed in many types of pluripotent cells, such as embryonic stem cells, germ cells, and endometrial cells [1, 7, 8].

Endometriosis is known as a benign condition. However, it has demonstrated characteristics of malignant neoplasms, including neoangiogenesis, tissue invasion, and cell implantation to distant organs [9]. Retrograde menstruation is the most widely hypothesized cause for the implantation of endometrial tissue in the peritoneal cavity and the survival of endometrial cells [10]. Recent studies have suggested that the loss or reduced expression of adhesion proteins, including CD44 and E-cadherin, is associated with benign and/or malignant cell proliferation, cell migration, tumor invasion, and cancer metastasis in a wide array of cells and tissues [11, 12]. CD44 is an integrated membrane protein that acts as a multifunctional cell surface adhesion molecule and plays a role in cell–cell and cell–matrix interactions [13, 14]. Previous studies have shown thatin women with endometrioma, the expression of CD44 is lower in ectopic endometrial tissues than in eutopic endometrial tissues [12]. E-cadherin is an adhesion glycoprotein that is expressed by eutopic and ectopic endometrium [15]. It is an epithelial cell–cell adhesion molecule that modulates a wide variety of processes, including cell polarization, cell migration, and cancer metastasis [16, 17]. Decreased expression of E-cadherin, which could promote malignant transformation, tumor invasion, and metastasis, has been observed in various cancers [18].

Few studies have investigated adhesion molecule expression in eutopic and ectopic endometrial tissues and those that have produced varied results. Therefore, we investigated the expression patterns of Oct-4, CD44, and E-cadherin in eutopic and ectopic endometrial tissues from women with endometrioma, as well asthe detailed correlations of these patterns with clinicopathological findings.

In this cross-sectional study, histopathological specimens of eutopic and ectopic endometrial tissues from 32 women with endometrioma were evaluated and compared with control endometrial tissues from 30 women without endometrioma. The mean age of participants was 29.9 ± 3.6 years in the endometrioma group and 31.8 ± 4.7 years in the control group. There were no significant differences in age (p = 0.0841) or parity (p = 0.5140) between the two groups. Participants’ characteristics are summarized in Table 1.

In the immunohistochemical analysis of the eutopic and ectopic endometrial tissues, Oct-4 expression was predominantly localized in the nuclei of glandular and stromal cells (Fig. 1a and b). In contrast, CD44 expression was predominantly localized in the cytoplasm of glandular and stromal cells (Fig. 2a and b), and E-cadherin expression was predominantly localized in the cell membranes of glandular epithelial cells (Fig. 3a and b). The stromal cells of the eutopic and ectopic endometrial tissues were not stained for E-cadherin.

Notably, we found that women with endometrioma had significantly higher Oct-4 expression in their ectopic endometrial tissues than the control group (p = 0.0002). However, CD44 and E-cadherin expressions were significantly lower in the ectopic endometrial tissues of women with endometrioma than in the control group (p = 0.0137 and p = 0.0060, respectively). There were no statistically significant differences between the eutopic and control endometrial tissue samples. These results are shown in Table 2.

A correlation analysis of the Oct-4, CD44 and E-cadherin expressions and the participants’ clinicopathological variables revealed a significant correlation between Oct-4 expression and endometrioma cyst diameter (p = 0.0162), rASRM stage (p = 0.0343), and total rASRM score (p = 0.0223). Moreover, CD44 expression was negatively correlated with the presence of peritoneal endometriotic lesions (p = 0.0304), while E-cadherin expression was negatively correlated with the presence of deep infiltrating endometriosis (p = 0.0445;Table 3).

We also evaluated the cycle fluctuation of adhesion molecules in eutopic and control endometrial tissue, and we found that the expressions of CD44 and E-cadherin were lower in the proliferative phase of the menstrual cycle than in the secretory phase (Figs. 4 and 5). Additionally, CD44 and E-cadherin expressions were lower in the eutopic endometrial tissues than in the control endometrial tissues, especially in the secretory phase of the menstrual cycle. However, there were no significant differences in CD44 and E-cadherin expressions between the eutopic and control endometrial tissues (p = 0.0607 and p = 0.3291, respectively).

In the present study, we investigated the expression patterns of Oct-4, CD44, and E-cadherin in the eutopic and ectopic endometrial tissues of women with and without endometrioma and determined the correlations of these patterns with clinicopathological findings. According to the our results, Oct-4 expression was significantly higher in the ectopic endometrial tissues than in the eutopic and control endometrial tissues. In contrast, CD44 and E-cadherin expressions were significantly lower in the ectopic endometrial tissues than in the eutopic and control endometrial tissues. A correlation analysis showed that Oct-4 expression was correlated with endometrioma cyst diameter, rASRM stage, and total rASRM score. Additionally, CD44 expression was negatively correlated with the presence of peritoneal endometriotic lesions, and E-cadherin expression was negatively correlated with the presence of deep infiltrating endometriosis.

The molecular and cellular basis of endometriosis has long been an area of active investigation [21]. The most common hypotheses in the literature, for the etiopathogenesis of endometriosis include retrograde menstruation [22], coelomic metaplasia [23], embryonic rest, and lymphovascular metastasis [22]. However, none of these theories can explain the survival of endometrial cells found outside of the uterine cavity across all cases of endometriosis. It is most likely that a combination of several aberrant molecular and cellular processes and genetic predispositions cause implantation of the endometrial cells, invasion into the extrauterine tissue, and proliferation and survival of endometriotic lesions outside the uterine cavity [24].

The human endometrium is a dynamic tissue with a high regenerative capacity [5]. Previous studies have suggested that endometrial regeneration is mediated by endometrial stem cells [6]. Recent studies have also shown that eutopic and ectopic endometrial cells express several non-specific embryonic stem cell markers, including Oct-4, (sex determining region Y-box 2 (SOX-2), and c-KIT (CD117) [6, 8, 21]. Oct-4 is a transcription factor in the regulation of genes containing self-renewal and pluripotency capacities in embryonic stem cells and primordial germ cells [4, 25]. Oct-4 is also a key factor in the reprogramming of somatic cells to a pluripotent state [26]. Previous studies have demonstrated that overexpression of Oct-4 reflects benign development or malignant degeneration capacity in many tissues, including the prostate [27], and the endometrium [28]. Further, a recent study revealed relatively high expression of Oct-4 in the ectopic endometrium [28]. In a recent study conducted by Chang et al., the transcription of the Oct-4 gene was significantly up-regulated in the human ectopic endometrium, and Oct-4 positive pluripotent cells contributed to the pathological growth of ectopic endometrial tissue by stimulating the migration activity of endometrial cells [5]. Pacchiarotti et al. demonstrated that increased expression of Oct-4 in ectopic endometrial tissues may foster self-renewal, increased cell survival, and epithelial–mesenchymal transition in endometriosis [29]. In the present study, we found that Oct-4 expression was significantly higher in ectopic endometrial tissue than in eutopic or control endometrium. Moreover, we found that Oct-4 expression was positively correlated with endometrioma cyst diameter and rASRM stage. In light of aforementioned studies, our findings may indicate that overexpression of Oct-4 and its correlation with clinicopathological findings in endometriotic tissues may reflect tissue growth and neighborhood tissue destruction.

CD44 and E-cadherin are known adhesion molecules. Many previous reports have clearly demonstrated that reduced expression of these molecules is associated with benign and/or malignant cell proliferation, cell migration, tumor invasion, cancer metastasis, and chemotherapy resistance in a wide array of cells and tissues [11, 12, 14]. Previous studies have shown that alteration of adhesion molecule expressions in endometrial tissues may play a role in the etiopathogenesis of benign and malignant conditions such as embryo implantation, spontaneous abortion, and endometrial cancer progression. Leblanc et al. reported that E-cadherin and N-cadherin expressions were significantly lower and CD44v3 expression was significantly higher in the endometrial tissue samples of women with endometrial cancer than in those of controls [30]. Additionally, Poncelet et al. reported that infertile women with hydrosalpinges had decreased expressions of E-cadherin and N-cadherin in their endometrial tissue samples in comparison with fertile control subjects [31], whereas CD44 expression was similar between these groups. Sahin et al. demonstrated that placental tissue expression of P-cadherin was lower in the trophoblast cells of women who had experienced spontaneous abortions than in those of ectopic pregnancy and control subjects [32].

On the other hand, only a few studies have examined adhesion molecule expression in the eutopic and ectopic endometrial tissues of women with endometriosis, and the studies that have examined this subject yielded controversial results. Some of these studies demonstrated that both CD44 and E-cadherin expressions were higher in the eutopic and/or ectopic endometrial tissues of women with endometriosis than in control endometrial tissues [33‐35]. Contrary to these reports, Poncelet et al. found that the expression of CD44 and E-cadherin in epithelial cells was lower in cases of peritoneal endometriosis than in normal endometrium [36]. In the present study, we found that both CD44 and E-cadherin expressions were significantly lower in ectopic endometrial tissues than in control endometrial tissues. These conflicting results between studies may have been due to differences in the demographic features of the studied populations or in the investigated subtypes of endometriosis. To reduce the probability of error, we conducted the study in a homogeneous group with a single subtype of endometriosis. Moreover, we also found that CD44 expression was negatively correlated with the presence of peritoneal endometriotic lesions, whileE-cadherine expression was negatively correlated with the presence of deep infiltrating endometriosis. These correlations indicated that different expressions of adhesion molecules may contribute to the generation of the different subtype of the endometriosis.

Nuclear factor-kappa B (NF-kB) has been shown to critically increases the ability of endometriotic cells to invade and adhere to the peritoneal surface by early regulation of the inflammatory response in endometriotic tissues [37]. Activation of the NF-kB pathway mediates cell proliferation and angiogenesis. Moreover, previous cancer cell line studies have demonstrated that NF-kB stimulates the self-renewal mechanisms of cancer stem cells, which helping to maintain cancer stem sell (CSC)’ populations in tumors [38]. Similarly, a recent study clearly demonstrated that inhibition of NF-kB reduces the expression of stem cell transcription factors SOX-2, NANOG, and Oct-4 in CSCs that present overexpression in several cancers, including breast, prostate, and oral squamous cell carcinoma [39]. NF-kB activation has also been associated with the invasive and metastatic capabilities of cancer, mainly by modulating the epithelial to mesenchymal transition, which reduces the epithelial marker E-cadherin [40]. The overexpression of endometrial stem cell marker Oct-4, the decreased expression of adhesion molecules (especially E-Cadherin), and the correlation of these expressions with the clinicopathological findings of he present study demonstrated that these molecular markers may contribute to the generation and progression of endometriosis.

Regarding the cyclic fluctuation of CD44 and E-cadherin expressions in endometrial tissue, previous studies have shown that these expressions were lowest during the proliferative phase of menstruation and highest during the late secretory phase of menstruation [34, 36]. Similarly, our cyclic fashion analysis demonstrated that the expression of CD44 and E-cadherin in the endometrial tissue tended to be lower in the proliferation phase of the menstrual cycle and higher in the secretory phase. We also found that during the secretory phase of the menstrual cycle, the expression of adhesion molecules was lower in the eutopic endometrial tissues of women with endometriosis than in the control group. However, there were no significant differences between the different phases of menstruation and the expressions of these adhesion molecules in the eutopic and control endometrial tissues. Previous studies have indicated that these adhesion molecules might be involved in the implantation of fertilized ovum in the endometrium [41]. In light of these studies, decreased expression of adhesion molecules in the secretory phase of the menstrual cycle may contribute to the development of infertility in women with endometriosis.

The main limitation of the present study was the relatively small number of participants. However, this is the first study to investigate the stem cells and adhesion molecules expressions in the eutopic and ectopic endometrial tissue samples of patients with a single subtype of endometriosis.

The combination of an increased endometrial stem cell population and altered adhesion molecule expression in endometriotic tissue appears to contribute to the development and progression of endometriosis. To fully investigate the etiology of and therapeutic approaches to endometriosis, further animal model studies are recommended to test the inhibition of endometrial stem cells self-renewal and related pathways associated with adhesion molecule expression.