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World Journal of Oncology

Original Article

Volume 6, Number 3, June 2015, pages 364-374

Correlation of NQO1 and Nrf2 in Female Genital Tract Cancer and Their Precancerous Lesions (Cervix, Endometrium and Ovary)

Cancers of the female reproductive system include cervical, endometrial and ovarian cancers, which are relatively common and cause significant morbidity and mortality worldwide, whereas vulvar, vaginal and fallopian tube cancers are very rare [1]. Cervical cancer is the third most common cancer in women worldwide and the seventh most common cancer overall. Its overall mortality incidence ratio is 52% [2]. Endometrial cancer is the sixth most common cancer in women worldwide. Its incidence and mortality rates are higher in more developed regions and lowest rates occurring in Asia and Africa. Overall, the mortality incidence ratio of endometrial cancer is 26% [3]. Cancers of the ovary constitutes the eighth most common cancers among women worldwide with mortality incidence ratio of 62% [2]. In Middle Egypt with regional registry in Minia, the incidence of cervical, endometrial and ovarian cancer is 1.06%, 0.67% and 3.75% respectively of cancer sites in females [4]. Understanding the mechanisms of carcinogenesis in female reproductive organs could contribute to early detection, and will be helpful in the prevention and treatment of these cancers.

NAD (P) H/quinone oxidoreductase-1 (NQO1), also known as DT-diaphorase, is a cytosolic enzyme that uses NADH or NADPH as substrates to catalyze the two-electron reduction of quinones and related compounds, and it is encoded by a gene located on chromosome 16q22 [5]. In normal cells, NQO1 protects cells against oxidative stress, as well as against carcinogenesis by stabilization of the p53 tumor suppressor [6]. However, studies on NQO1 expression in cancer have been contradictory. On the one hand, NQO1 is induced along with a battery of defensive genes that provide protection against different stresses to prevent organs from undergoing carcinogen-induced tumorigenesis. On the other hand, reductive activation of environmental carcinogens including heterocyclic amines by NQO1 could contribute to carcinogenesis. Also, the disruption of the NQO1 gene or genetic polymorphism increased the risk of chemical-induced toxicity and cancers [7]. Comparing normal and malignant tissue, NQO1 was reported to be up-regulated in malignant tissue of the pancreas, interlobular biliary epithelial cells, breast and lung [8-11] and down-regulated in tumors of the kidney and esophagus [12, 13]. In addition, the high level of NQO1 expression in various tumors in combination with its ability to reduce many quinine-containing antitumor drugs has drawn attention to NQO1 as a potential molecular target in cancer treatment [14]. The molecular mechanism of NQO1 responsible for tumors of the female reproductive system progression remains unclear, and additional studies are needed to understand its role in female tumorigenesis.

The transcription factor, nuclear factor erythroid 2-related factor 2 (Nrf2) is a nuclear transcription factor maintaining intracellular redox homeostasis that induces transcription of a variety of genes through binding to the antioxidant response element in target gene promoters [15, 16]. It is induced in response to various agents at the transcriptional level. In addition, more than 200 gene products including an antioxidative enzyme NQO1 are under the transcriptional control for Nrf2 [17]. Therefore, activation of Nrf2 confers protection against cancer [18]. Furthermore, the beneficial effects of many chemopreventive compounds rely on the activation of the Nrf2-mediated antioxidant response through inhibition of Nrf2 degradation [19]. Mutations and deregulation of Nrf2 expression levels have been identified in many cancers [18] and lead to chemoresistance to many chemotherapeutic drugs [20, 21].

To date, the association and correlation between NQO1 and Nrf2 expression in cancers of the female reproductive system have not been adequately studied. In this study, we aimed to analyze the expression and relationship between both markers in carcinomas of the cervix, endometrium, ovary and their precancerous lesions. Also, we studied their relation with clinicopathological parameters in carcinoma cases for better understanding their role in tumorigenesis.

Formalin-fixed and paraffin-embedded specimens were collected and prepared for this study from Minia University Hospital in collaboration with the cancer unit in the Obstetrics and Gynecology Department, Minia University between January 2008 and December 2014. The histology of all cases using hematoxylin-eosin (H&E) stained slides was reviewed. The histological grade was assessed according to the World Health Organization (WHO) classification standards [22]. Tumors were staged according to the pathologic tumor-node-metastasis (TNM) and FIGO classification according to the Union for International Cancer Control (UICC) criteria seventh Edition and WHO classification [23]. The clinicopathological data were obtained from the pathology reports of cases. The available data include patients’ age, tumor grade and stage.

Cervical specimens, include 10 non-neoplastic cervical tissues, 20 squamous intraepithelial lesion (SIL) (eight cases of low-grade squamous intraepithelial lesion (LSIL) and 12 cases of high-grade squamous intraepithelial lesion (HSIL)) and 50 squamous cell carcinomas (SCCs). All cervical tissue specimens were selected from punch biopsies, loop electrosurgical excisions, cone biopsies and hysterectomies.

Endometrial specimens included 10 cyclic endometrium (CE) (six cases were proliferative phase (PP) and four cases were secretory phase (SP)), 20 cases endometrial hyperplasia (EH) (eight cases without atypia, 12 cases atypical EH) and 50 were endometrial carcinoma (EC) specimens. CE and hyperplasia samples were obtained either by curettage or biopsy specimens. Hyperplasia specimens were evaluated according to WHO classification [22]. All EC patients had undergone total abdominal hysterectomy and bilateral salpingo-oophrectomy.

Ovarian specimens included 10 cases of normal ovarian tissues, 20 cases of benign ovarian tumors (12 cases serous and eight cases mucinous), 20 cases of borderline ovarian tumors (12 cases serous and eight cases mucinous) and 50 cases of ovarian carcinoma (35 cases serous and 15 cases mucinous carcinoma). Normal ovarian specimens from hysterectomy specimens resected for non-ovarian disease were used. The majority of patients with a diagnosis of primary ovarian cancer had undergone radical surgery (staging laparotomy) according to standard operating procedures with the primary objective of maximal tumor reduction.

Paraffin-embedded sections on coated slides were used for staining. Sections were cut at 4 μm thick. Immunohistochemistry was performed using the DAKO LSAB kit (DAKO A/S, Glostrup, Denmark) as follows: slides were deparaffinized in xylene and rehydrated in a graded alcohol series. Antigen retrieval was achieved by microwaving in sodium citrate buffer at pH 6 for 10 min at 95 °C. Endogenous peroxidase was blocked with 0.3% hydrogen peroxide in methanol for 30 min. The slides were incubated with the mouse monoclonal primary antibody for NQO1 (A180, ab28947, Abcam, 1:200), mouse monoclonal primary antibody for human Nrf2 (IgG2a, ab89443, Abcam, 1:100) overnight in a humidity chamber at 4 °C overnight. Then samples were washed with rinse puffer (PBS) and biotinylated secondary antibody for 30 min at room temperature. Streptavidin was applied for 30 min at room temperature. Visualization was performed using 3,3’-diaminobenzidine (DAB) chromogen, and Mayer’s hematoxylin was used for counterstaining for 10 min. A section of breast carcinoma and lung carcinoma were used as a positive control for NQO1 and Nrf2 proteins respectively. A negative control was carried out by replacing primary antibodies with rise buffer on a section.

Five random fields of vision in each section were selected and analyzed. The positive area, which was shown in percentage (ratio of positive area to the whole visual field) was calculated.

Data were analyzed using the statistical package for the Social Sciences version 17.0 (SPSS 17.0). Raw data were used to determine means, standard deviations (SDs) and ranges. Kruskal-Wallis test was used to compare markers expression in different groups followed by Mann-Whitney test which was used to compare expression between two groups. Pearson correlation was used to determine whether there was a positive or negative correlation between each examined marker and each histopathological entity. Kruskal-Wallis test was used to examine the correlation of NQO1, Nrf2 staining scores in relation to tumor grade and stage. ANOVA test was used to examine the correlation of NQO1, Nrf2 staining scores in relation to age. Statistical significance was set at P ≤ of 0.05.

Positive expression rates, mean values and SDs for NQO1 and Nrf2 in different lesions for organs examined are listed in Tables 1, 2. NQO1 expression was detected in the cytoplasm of examined tissue as shown in Figure 1 while Nrf2 was nuclear and cytoplasmic marker in cervical and ovarian tissue while in the endometrium its expression was mainly cytoplasmic with little nuclear expression in CE and EH, and nuclear expression was more pronounced in EC as shown in Figure 2.

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Table 1. Positive Expression Rates, Mean Values and SDs for NQO1 in Different Lesions With Examined Sites

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Table 2. Positive Expression Rates, Mean Values and SDs for Nrf2 in Different Lesions With Examined Organs

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Figure 1. NQO1 protein expression in different lesions using IHC (× 400, DAB was used as the chromogen and hematoxylin as counterstain). (a) NQO1 protein was weak in normal cervical epithelium. (b) NQO1 protein staining was moderate positive in LSIL. (c) NQO1 protein showed diffuse and strong cytoplasmic-positive staining in HSIL. (d) NQO1 was strong positive in grade I cervical SCC. (e) NQO1 protein was weak in proliferative endometrium. (f) NQO1 was moderate positive in simple EH. (g) NQO1 was strong positive in atypical EH. (h) NQO1 was strong positive in EC. (i) NQO1 was negative in normal ovarian epithelium. (j) NQO1 was positive mucinous cystadenoma. (k) NQO1 was moderate positive in borderline serous tumor. (l) NQO1 was strong positive in ovarian carcinoma.

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Figure 2. Nrf2 protein expression in different lesions using IHC (× 400, DAB was used as the chromogen and hematoxylin as counterstain). (a) Nrf2 protein was weak in normal cervical epithelium. (b) Nrf2 protein staining was moderate positive in LSIL. (c) Nrf2 protein showed moderate nuclear-positive staining in HSIL, but weak positive in adjacent normal cervical glands. (d) Nrf2 was strong positive in grade II cervical SCC. (e) Nrf2 protein was positive in proliferative endometrium. (f) Nrf2 was moderate positive in simple EH. (g) Nrf2 was moderate positive in atypical EH. (h) Nrf2 was strong positive in EC. (i) Nrf2 was negative in normal ovarian epithelium. (j) Nrf2 was positive serous cystadenoma. (k) Nrf2 was moderate positive in borderline serous tumor. (l) Nrf2 was strong positive in ovarian carcinoma.

On studying the mean NQO1 expression in different lesions, we found increased expression in SIL (45%, mean ± SD: 18.35 ± 24.94) and cervical carcinoma (76%, mean ± SD: 44.34 ± 29.52) cases compared to normal tissue (20%, mean ± SD: 3.70 ± 5.01) and the difference between all examined groups was statistically significant (P < 0.001) as shown in Table 1, Figure 3a.

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Figure 3. NQO1 expression box plots (a) in different cervical lesions; (b) in different endometrial lesions; (c) in different ovarian lesions. Horizontal lines in the boxes represent the median value of each group. The top and bottom edges of the boxes indicate the score values from 75th percentile and the 25th percentile respectively. Whiskers represent the highest and lowest values. The range is shown as a vertical line.

As regard SIL, we found in LSIL, NQO1, mean ± SD: 21.37 ± 3.11, while in HLSIL, NQO1: 16.33 ± 2.11, that was lower than in LSIL, and this difference did not reach a significant level (P = 0.885).

Regarding its mean expression in different lesions, statistically significant differences were seen between normal and carcinoma (P = 0.001) and between SIL and carcinoma (P = 0.004). In addition, no significant difference was noticed between NQO1 mean expression in normal and SIL (P = 0.091).

We found increased mean expression rate in EH and EC was 30%, 60% with mean ± SD: 10.15 ± 15.61 and 36.92 ± 31.94 respectively, while decrease in CE (10%, mean ± SD: 2.40 ± 3.30), and the difference was statistically significant (P = 0.001) (Table 1, Fig.3b).

For EH, we found in typical EH and atypical EH the mean ± SD was 3.00 ± 3.33, 14.91 ± 18.75 respectively, and there were no statistically significant differences between both (P = 0.118).

Regarding its mean expression in different lesions, statistically significant differences between EC and EH, CE (P = 0.003, P = 0.007 respectively) were noted. There were no statistically significant differences between EH and CE (P = 0.402).

On studying the NQO1 mean expression in different lesions, we found increased expression in carcinoma cases (56%, mean ± SD: 28.30 ± 27.29) than other lesions (20%, mean ± SD: 6.30 ± 9.88 in benign; and 25%, mean ± SD: 12.40 ± 21.08 in borderline tumors), and the difference was statistically significant (P < 0.001) as shown in Table 1, Figure 3c.

Regarding NQO1 mean expression in different lesions, statistically significant differences were seen between normal and each benign, borderline and malignant tumors (P = 0.005, P = 0.003 and P < 0.001 respectively). Statistically significant difference was seen between benign and carcinoma (P = 0.006). No statistically significant difference was seen between benign and borderline (P = 0.554), between borderline and carcinoma (P = 0.076).

Associations between clinicopathological data and NQO1 mean expression were summarized in Table 3.

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Table 3. Associations Between NQO1 and Nrf2 Expression Scores and Clinicopathological Data in Carcinoma Cases

As regarding cervical carcinoma, a significant association between increased NQO1 mean expression and tumor grade (P = 0.045) was detected. No significant associations were noticed between its expression and either age or stage.

In EC, a significant association was noticed between increased NQO1 mean expression and tumor grade (P = 0.011). No significant associations were noticed between its expression and either age or stage.

Regards ovarian carcinoma, no significant associations were noticed between NQO1 mean expression and any clinicopathological data.

As regard Nrf2 expression in different lesions, we found increased mean expression from normal tissue (10%, mean ± SD: 4.60 ± 5.42) to SIL (30%, mean ± SD: 14.50 ± 18.20) and to cervical carcinoma (62%, mean ± SD: 39.24 ± 29.25). The difference between all examined groups was statistically significant (P = 0.001) as shown in Table 2, Figure 4a.

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Figure 4. NrF2 expression box plots (a) in different cervical lesions; (b) in different endometrial lesions; (c) in different ovarian lesions. Horizontal lines in the boxes represent the median value of each group. The top and bottom edges of the boxes indicate the score values from 75th percentile and the 25th percentile respectively. Whiskers represent the highest and lowest values. The range is shown as a vertical line.

Regarding Nrf2 expression in SIL, we found that its expression in LSIL mean ± SD: 11.12 ± 14.21 and in HSIL 16.75 ± 20.37, and there was no statistically significant difference between both (P = 0.451).

Regarding its mean expression in different lesions, statistically significant differences between normal and carcinoma (P = 0.002) and between SIL and carcinoma (P = 0.005) were found. No significant difference was noticed between Nrf2 mean expression in normal and SIL (P = 0.155).

Nrf2 expression rate was increased in EH (35%, mean ± SD: 12.20 ± 16.91) and EC (64%, mean ± SD: 39.82 ± 32.65) than in CE (10%), and the difference was statistically significant (P = 0.001) as shown in Table 2, Figure 4b.

For EH, we found, in typical EH and atypical EH the mean ± SD was 10.25 ± 12.72, 13.50 ± 19.66 respectively, and there were no statistically significant differences between both (P = 0.603).

As regard Nrf2 mean expression in different lesions, statistically significant differences between CE and EH, EC (P = 0.009, P = 0.005 respectively). There were no statistically significant differences between CE and EH (P = 0.350).

Nrf2 expression in different ovarian lesions, we noticed that increased mean expression in carcinoma (72%, mean ± SD: 32.70 ± 29.44) than other examined lesions (0% for normal; 25%, mean ± SD: 10.30 ± 14.50 for benign tumors; and 20%, mean ± SD: 14.60 ± 19.33 for borderline tumors), and the difference reached a significant statistical level (P = 0.004) (Table 2, Fig.4c).

Regarding its mean expression in different lesions, statistically significant differences were identified between normal and carcinoma (P < 0.001). Statistically significant differences were identified between benign and carcinoma (P = 0.005), and between borderline and carcinoma (P = 0.029). Similarly, statistically significant difference was seen between normal and benign and borderline (P = 0.015, P = 0.003 respectively). In addition, no statistically significant difference was seen between benign and borderline (P = 0.529).

Associations between clinicopathological data and Nrf2 mean expression were summarized in Table 3.

In cervical carcinoma, we found that a significant association between increased Nrf2 mean expression and high tumor grade (P = 0.016) was detected. No significant associations were noticed between its mean expression and age or stage.

For Nrf2 overexpression in EC, we found that a significant association between increased its mean expression and tumor grade and stage (P = 0.002, P = 0.025 respectively) was detected.

Regarding ovarian carcinoma, a significant association was noticed between increased Nrf2 mean expression and advanced tumor stage (P = 0.020). No significant associations were noticed between its expression and either age or grade.

Correlations between immunohistochemical markers expression in different cervical lesions were found. A significant positive correlation was noted between NQO1 and Nrf2 mean expression in all examined cases (r = 0.734, P < 0.001). A significant positive correlation was noted between NQO1/Nrf2 (r = 0.818, P < 0.001) in SIL. Similarly, a significant positive correlation was noted (r = 0.615, P < 0.001) in carcinoma. No significant correlations were noted between them in normal cervical tissue (r = 0.615, P = 0.051).

Correlations between immunohistochemical markers expression in different endometrial lesions were found. A significant positive correlation was noted between NQO1 and Nrf2 mean expression in all examined cases (r = 0.922, P < 0.001). A significant positive correlation was noted (r = 0.909, P < 0.001) in CE. Similarly, a significant positive correlation was noted (r = 0.637, P = 0.003) in EH. Also a significant correlation was in EC (r = 0. 925, P < 0.001).

Correlations between immunohistochemical markers expression in different ovarian lesions were found. A significant negative correlation was noted between NQO1 and Nrf2 (r = 0.741, P < 0.001) in all cases. Similarly, a significant positive correlation was noted in benign tumors (r = 0.623, P = 0.003) and in carcinoma (r = 0.740, P < 0.001). No significant correlations were noted in borderline tumors (r = 0.6432, P = 0.057).

NQO1 flavoprotein has been found to be expressed in many body tissues [9-11]. It is conceivable that NQO1 is primarily involved in protecting normal cells from oxidant stress. Such finding has led to the suggestion that NQO1 can be important in cancer chemoprevention. However, polymorphism in the NQO1 gene has been reported to be associated with an increased risk of various cancers such as breast [10], lung [11], gastric [24] and head and neck cancer [25].

In the present study, we found that staining of NQO1 is mainly localized in the cytoplasm and these observations were in agreement with previous studies [8-10, 26, 27]. NQO1 has positive cytoplasmic expression in 76%, 60% and 65% in cervical, endometrial and ovarian carcinoma respectively. Previous studies demonstrated that NQO1 immunopositivity rate ranged between 21% and 80% [10, 11, 28] in various tumors. We found increased NQO1 expression from normal tissue to SIL and cervical carcinoma and then from SIL to carcinoma. The difference between all examined groups was statistically significant. This finding was also observed in the endometrial and ovarian lesions. In a previous study, a strong positive rate of NQO1 protein expression in both SCCs (54.80%) and cervical intraepithelial neoplasia (CINs) (27.59% in CIN-1, 34.21% in CIN-2 and 40.74% in CIN-3) was significantly higher than in the normal cervix (4%). Interestingly, the strongly positive rate of NQO1 protein was slightly higher in well-differentiated SCC (43.75%) than in CIN3 (40.74%) [26]. In addition, previous results noted more NQO1 overexpression in carcinoma than in normal or precancerous lesions in breast [10], colon [27] and liver [28], and the difference reached a significant level. Our results with previous results indicate that NQO1 up-regulation may be an early event in cancer progression. These findings suggest that NQO1 protein level might be used as an early diagnostic indicator of this disease.

To further illustrate that NQO1 may be an effective predictor of poor prognosis, the correlation between NQO1 expression and clinicopathological features of cervical, endometrial and ovarian carcinomas was analyzed. We found that high-level expression of the NQO1 protein was significantly correlated with poor differentiation in cervical and EC and not associated with advanced stage. NQO1 overexpression was reported to be associated with high tumor grade in carcinoma of cervix and breast [10, 26], with advanced stage cervical [26], breast [10], colon [27] and liver [28] carcinomas and with nodal metastases [10]. NQO1 overexpression induced tumor cell proliferation via the up-regulation of cyclins [29] and was accompanied by an increase in other antioxidant enzymes, such as HMOX-1 and GST, providing tumors with increased protection against cytotoxic agents allowing for rapid cancer progression [30]. These results indicated that NQO1 played a predictive role in tumor progression and might be useful as a poor prognostic biomarker of cancer.

NQO1 overexpression in tumors but not normal tissue has made it an attractive target for treatment of lung cancer. It is the main activator of quinone-containing alkylating agents such as mitomycins [31]. So that, patients with KRAS mutations may utilize quinone-containing alkylating agents more efficiently due to increased NQO1 expression [11]. On the contrary, loss of NQO1 expression appeared to be candidates for adjuvant chemotherapy in patients with cholangiocarcinoma [32]. Therefore, the role of NQO1 and related inhibitors in chemotherapy appears questionable. A comprehensive similar analysis of the relationship between NQO1 enzyme activity and chemosensitivity in female tract cancer is essential.

In this study, we found that Nrf2 is nuclear, and cytoplasmic marker by immunohistochemistry in cervical and ovarian tissue, while in the endometrium its expression was mainly cytoplasmic with little nuclear expression and these observations were in agreement with previous studies [33-35]. Other reports detect Nrf2 expression mainly in the nucleus [27, 36, 37]. It is well established that oxidative stress is the primary signal that causes cytoplasmic Nrf2 to accumulate within the nucleus [34]. It has been documented that persistent nuclear expression of Nrf2 results in the production of antioxidants that protect cancer cells from reactive oxygen species. Higher concentration of Nrf2 in the nucleus may reflect upstaging of cancer, aggressive tumor behavior and poor clinical outcome [26, 33, 37]. Half of ovarian carcinomas with positive nuclear Nrf2 staining had either Keap1 mutations or absent Keap1 mRNA expression resulting in platinum resistance [38]. So, nuclear Nrf2 expression in cancer cells would have a higher malignant potential. Therefore, it is essential to evaluate nuclear expression of Nrf2.

We found Nrf2 expression was 62%, 64% and 72% in cervical, endometrial and ovarian carcinoma respectively. Previous studies demonstrated that Nrf2 immunoreactivity was frequently detected in various human malignancies, such as intrahepatic chorangiocellular [32], endometrial [33], breast [36], gastric [35, 37], ovarian [38], lung [39], pancreatic [40] and gallbladder [41] carcinomas, and its rate of immunopositivity ranged between 26% and 76% in these studies.

We found increased expression from normal tissue to SIL and cervical carcinoma and then from SIL to carcinoma. The difference between all examined groups was statistically significant. In the endometrium, we found Nrf2 expression was increased from CE to EH to EC, and the difference was statistically significant. Similar results were reported in the endometrium with lower expression of Nrf2 in atypical EH and higher in endometrial cancer [33, 42-44]. Finally in ovarian tissue we found the same results as Nrf2 expression was increased from normal to benign tumors and from benign to borderline tumors and from borderline tumors to carcinomas with a significant difference between the examined groups. This elevated Nrf2 expression may be induced by gonadotropins and sex-steroid hormones, which suggest that these hormones are involved in ovarian cancer development via modulation of Nrf2 signaling. Therefore, its inhibition may represent an effective therapeutic strategy for treatment [45].

Previous studies in different organs reported that Nrf2 expression was more overexpressed in carcinoma than normal and precancerous lesions in pancreatic [34, 40], gastric [35] and breast [36] carcinomas. Nrf2 expression may represent one of the early molecular events in the neoplastic transformation of several tumors.

Regarding association of Nrf2 overexpression and clinicopathological data, we found that its expression was significantly associated with high tumor grade in cervical and EC and with advanced tumor stage in endometrial and ovarian carcinoma and no significant association with the age. Our findings are in accordance with those reported by [27, 35-37, 41]. No differences were noted in age, grade and stage in ovarian carcinoma [38, 45]. Overexpression of Nrf2 in gallbladder adenocarcinoma was correlated with tumor differentiation, staging, metastasis and shorter overall survival [41].

Furthermore, overexpression of Nrf2, a regulator of an intracellular antioxidant response and is negatively regulated by Keap1, may be partially responsible to the aggressive biological behavior and poor clinical outcome due to its known effect of increased resistance to chemotherapeutic drugs as cisplatin in both endometrial and ovarian cancer cells [18, 20, 21]. These findings may also provide an opportunity for therapeutic intervention against chemoresistance via applications of either Nrf2 inhibitors or gene knockdown approaches [33]. Therefore, a new chemotherapeutic protocol that includes antioxidant therapy may be a useful method for solving chemoresistance [37].

Regarding correlation between NQO1 and Nrf2 mean expression in different lesions, we found positive correlations between the two proteins especially in carcinomas. Similar correlations were reported [27]. This Nrf2-NQO1/MRP1 signal pathway may be attributed to the stress response and self-protective effort of the cells during malignant transformation. Considering the role of Nrf2 in regulating genes as NQO1 and MRP1, which act to detoxify drugs or attenuate drug-induced oxidative stress, it is possible that highly expressed nuclear Nrf2 plays a role in increasing treatment resistance and results in short survival [27]. To the best of our knowledge, this was the first study examining NQO1 and Nrf2 in cervical, endometrial and ovarian tissue and the change of their expression in different lesions in each tissue type.

NQO1 and Nrf2 play a key role in the progression of female tract tumors, and high level of both proteins were strongly associated with high grade and advanced stage. The high proportion of NQO1 expression suggests that NQO1 may be a significant biomarker and a potential therapeutic target for carcinoma patients. Nrf2 expression in cancer may be useful for evaluation of biological malignant potential. Overall, our present work implies that NQO1 and Nrf2 might be new biomarkers for early diagnosis and tumorigenesis in patients with tumors of female genital tract.

Competing Interests

The authors declare that they have no competing interests.

Author Contributions

N. A. Osman performed project development, data collection, immunostaining, data analysis and manuscript writing. N. M. Abd El-Maqsoud performed project development, data collection, immunostaining, data analysis and manuscript writing. S. A. El Gelany performed data collection and manuscript writing. All authors read and approved the final manuscript.

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