Disease Markers

Disease Markers / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 8012979 | 9 pages | https://doi.org/10.1155/2019/8012979

Associations between TAB2 Gene Polymorphisms and Epithelial Ovarian Cancer in a Chinese Population

Academic Editor: Giuseppe Biondi-Zoccai
Received28 Apr 2019
Revised03 Jul 2019
Accepted17 Jul 2019
Published14 Aug 2019


Background. Epithelial ovarian cancer (EOC) is highly lethal worldwide. Factors involved in the inflammation and hormone-associated signaling pathway play vital roles in EOC carcinogenesis. The transforming growth factor-β- (TGF-β-) activated kinase 1 (MAP3K7) binding protein 2 (TAB2), mediating convergence of inflammatory and estrogen, may be implicated in EOC. The present study is aimed at exploring the association between the TAB2 gene polymorphisms and EOC. Methods. Three single nucleotide polymorphisms (SNPs) (rs237028, rs521845, and rs652921) of TAB2 were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 221 patients and 252 healthy controls. Associations between SNPs and clinical characteristics were performed either with the test or with Fisher’s exact test. The Kaplan-Meier method and Cox proportional hazard models were used to detect associations between genotypes and overall survival. Results. The rs237028 polymorphism was significantly associated with an increased risk of EOC with an allelic genetic model (A vs. G; ; ; ), dominant genetic model (AA vs. AG-GG; ; CI 1.14–2.41; ), and overdominant genetic model (AA-GG vs. AG; ; CI 1.08–2.36; ). However, no significant association was observed between rs237028 polymorphism and overall survival. Conclusions. Our study indicated that the rs237028 polymorphism in the TAB2 gene was associated with EOC susceptibility and the TAB2 gene might contribute to the initiation of EOC.

1. Introduction

Ovarian cancer is the eighth most common malignancy in women. In 2018, there were an estimated 295,414 new cases and 184,799 deaths from ovarian cancer worldwide [1]. Of these, epithelial ovarian cancer (EOC) is the most common cancer, accounting for 90% of all cases [2]. Although ovarian cancer accounts for 3.4% of new cancer cases in females, it also accounts for 4.4% of cancer-related deaths owing to poor five-year survival rates [1]. Late diagnosis at advanced stages is the leading cause of death from ovarian cancer. Therefore, early screening methods are needed to reduce its mortality rates. However, the two most common screening methods, transvaginal ultrasound and measuring serum cancer antigen 125 (CA-125) levels, have failed to show a clinically significant mortality benefit [3, 4]. Hence, analyses of lifestyle-based and genetic risk cofactors are required to identify high-risk populations for appropriate screening. Many lifestyle-based risk factors have already been identified, including childbearing, tubal ligation, oral contraceptive use, and menopausal hormone therapy [58]. In addition, several common genetic variants have been found to be risk factors; a combination of polygenic risk scores and epidemiologic risk factors has been identified in genome-wide association studies (GWAS) [912]. However, these genetic variants typically rely on the most significant single variants, which account for only slight increases in the prediction of EOC risk, implying that many more potential risk loci need to be identified.

Evidence from various sources has suggested that inflammation contributes to EOC carcinogenesis, and several risk factors associated with inflammation have been found to play a role in the development of EOC [1315]. Furthermore, SNPs from genes controlling several inflammation-related pathways have been found to have an association with ovarian cancer risk, such as those in the nuclear factor-κB (NF-κB) signaling pathway [16].

Transforming growth factor-β- (TGF-β-) activated kinase 1 (MAP3K7) binding protein 2 (TAB2), a protein linking TGF-β-activated kinase 1 (TAK1) to tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6) in the TAK1 pathway, mediates the activation of NF-κB [17]. The TAB2 protein, which is encoded by the TAB2 gene and facilitates the activation of the NF-κB signaling pathway, may play important roles in the development of EOC. Moreover, TAB2, which is located on chromosome 6q25.1, has been recognized as a breast cancer risk locus mainly owing to its association with estrogen [18]. Additionally, EOC is a hormone-related tumor that shares many risk factors with breast cancer [19]. However, there are no previous studies investigating the genetic variants of TAB2 in EOC pathogenesis. Thus, the aim of this study was to assess the association of three SNPs in TAB2 with EOC susceptibility by genotyping TAB2 in EOC patients and healthy subjects.

2. Materials and Methods

2.1. Patients and Subjects

A total of 473 blood samples from 221 EOC patients who underwent surgical resection at the West China Second University Hospital of Sichuan University (China), as well as 252 matched healthy females, were collected between June 2008 and June 2013. The patients were histologically verified to have EOC using the resected specimens. Patients were excluded if they had any other malignancies. The control samples were collected from women aged 29–70 years (: ) who were admitted to the same hospital for routine scheduled physical exams; controls were confirmed to have no serious disease or a family history of major cancers. The study was performed with the approval of the ethics review board of the West China Second University Hospital of Sichuan University (approval no. 2012016), and all the participants gave written informed consent.

2.2. DNA Extraction and Genotyping Assays

DNA was isolated from the peripheral blood of patients using a whole blood DNA isolation kit (BioTeke, Beijing, China) and then stored at -20°C for PCR. The following primers were used: rs237028, forward 5-GCAGACTTGGAAAAGCAAACA-3 and reverse 5-CCAGCCTGAGCAACAAGAG-3; rs521845, forward 5-TAGGGCGGTTGAGAAGTGAA-3 and reverse 5-CCTGGGTGACTGAGCTCTTA-3; and rs652921, forward 5-GGCCATTTGGCTCAGAAAT-3 and reverse 5-GAGGGAGCTCAGTGGAATTG-3. PCR was performed at a final reaction volume of 10 μL containing 100 ng DNA, 0.15 μL forward and reverse primers, 1 μL 10x Taq Buffer, and 5 μL 2x Power Taq PCR Master Mix (BioTeke) under the following conditions: 95°C for 4 min, followed by 30 cycles at 94°C for 30 s, 60°C for 30 s, and 72°C for 30 s, with a final extension step at 72°C for 10 min. The genetic polymorphisms of TAB2 were genotyped using PCR-restriction fragment length polymorphism (PCR-RFLP). The PCR products of rs237028, rs521845, and rs652921 were digested using the restriction enzymes Hpy188I (2 h at 37°C), Psp1406I (16 h at 37°C), and BseDI (45 min at 37°C), respectively. Next, 5 μL digested PCR products were isolated on a 6% polyacrylamide gel and stained with silver nitrate. The genotypes of rs237028 were designated as follows: A/A, a single band consisting of 138 bp; A/G, three bands consisting of 138 bp, 106 bp, and 32 bp; and G/G, two bands consisting of 106 bp and 32 bp. Similarly, for rs521845, the 120 bp and 100 bp fragments were, respectively, designated as allele T and G; and for rs652921, the 120 bp and 100 bp fragments were, respectively, designated as allele C and T.

2.3. Clinical Information and Follow-Up

Patients were excluded from survival analysis if follow-up information was not available. Ultimately, 140 patients were eligible for survival analysis. The clinical information of the patients was obtained from medical records. The overall survival was defined as the time from diagnosis to the last follow-up date or the date of death. The clinical stage and grade of the tumors were determined based on the criteria of the International Federation of Obstetrics and Gynecology (FIGO) and WHO [20, 21].

2.4. Statistical Analyses

The Hardy-Weinberg equilibrium (HWE) and the association between TAB2 gene polymorphisms and EOC were calculated by SNPstats online software (http://www.snpstats.net/start.htm), which assessed the frequency distributions between patients and healthy controls in four genetic models: codominant, dominant, recessive, and overdominant [22]. The association between rs237028 and clinical characteristics was analyzed using either the test or Fisher’s exact test. Survival curves were analyzed by the Kaplan-Meier and log-rank test, and multivariable overall survival analysis was performed using Cox proportional hazard models. All data were analyzed using SPSS 22.0 (SPSS Inc., Chicago, IL, USA). Differences were considered statistically significant at a value of .

3. Results

3.1. Subject Characteristics

A total of 221 EOC patients and 252 healthy female controls were investigated in this study. The clinical characteristics of the patients are shown in Table 1.


Sample size
, range (years), 15-71
FIGO stage, number (%)
 I31 (22.1)
 II11 (7.9)
 III90 (64.3)
 IV8 (5.7)
Tumor grade, number (%)
 G112 (8.6)
 G219 (13.6)
 G396 (68.6)
 Unknown13 (9.3)
Histology, number (%)
 Serous76 (54.3)
 Clear cell16 (11.4)
 Endometrioid8 (5.7)
 Mucinous9 (6.4)
 Mixed and other31 (22.1)

SD = standard deviation, FIGO = International Federation of Gynecology and Obstetrics. Clear cell carcinoma.
3.2. TAB2 SNPs in EOC

In this study, the genotypes of three SNPs (rs237028, rs521845, and rs652921) in the patients and controls followed the HWE. The distributions of the allelic and genotypic frequencies are shown in Table 2. For rs237028, the frequencies of the AA, AG, and GG genotypes, respectively, were 66.4%, 28.1%, and 5.5% in patients and 54.4%, 38.5%, and 7.1% in controls. The distribution of the SNPs between EOC patients and the control group was significantly different based on the codominant (AG vs. GG; ; 95% confidence interval (95% CI): 0.73–3.39; ), dominant (AA vs. AG-GG; ; 95% CI: 1.14–2.41; ), and overdominant genetic models (AA-GG vs. AG; ; 95% CI: 1.08–2.36; ), as well as in terms of allele frequencies (A vs. G; ; 95% CI: 1.07–1.96; ). No significant associations were observed for rs521845 or rs652921.

Genotype or alleleCase
OR (95% CI) value

Genetic model
 CodominantA/A144 (66.4)137 (54.4)1.000.03
A/G61 (28.1)97 (38.5)1.67 (1.12-2.49)
G/G12 (5.5)18 (7.1)1.58 (0.73-3.39)
 DominantA/A144 (66.4)137 (54.4)1.000.008
A/G-G/G73 (33.6)115 (45.6)1.66 (1.14-2.41)
 RecessiveA/A-A/G205 (94.5)234 (92.9)1.000.47
G/G12 (5.5)18 (7.1)1.31 (0.62-2.79)
 OverdominantA/A-G/G156 (71.9)155 (61.5)1.000.017
A/G61 (28.1)97 (38.5)1.60 (1.08-2.36)
AlleleA349 (80)371 (74)0.016
G85 (20)133 (26)1.45 (1.07-1.96)
Genetic model
 CodominantT/T85 (40.5)105 (41.7)1.000.97
T/G100 (47.6)118 (46.8)0.96 (0.65-1.41)
G/G25 (11.9)29 (11.5)0.94 (0.51-1.72)
 DominantT/T85 (40.5)105 (41.7)1.000.80
T/G-G/G125 (59.5)147 (58.3)0.95 (0.66-1.38)
 RecessiveT/T-T/G185 (88.1)223 (88.5)1.000.89
G/G25 (11.9)29 (11.5)0.96 (0.54-1.70)
 OverdominantT/T-G/G110 (52.4)134 (53.2)1.000.86
T/G100 (47.6)118 (46.8)0.97 (0.67-1.40)
AlleleT270 (64)328 (65)0.96 (0.73-1.27)0.8
G150 (36)176 (35)
Genetic model
 CodominantT/T66 (32.5)85 (33.7)1.000.53
T/C87 (42.9)116 (46)1.04 (0.68-1.58)
C/C50 (24.6)51 (20.2)0.79 (0.48-1.31)
 DominantT/T66 (32.5)85 (33.7)1.000.78
T/C-C/C137 (67.5)167 (66.3)0.95 (0.64-1.40)
 RecessiveT/T-T/C153 (75.4)201 (79.8)1.000.26
C/C50 (24.6)51 (20.2)0.78 (0.50-1.21)
 OverdominantT/T-C/C116 (57.1)136 (54)1.000.5
T/T87 (42.9)116 (46)1.14 (0.78-1.65)
AlleleT219 (54)286 (57)0.90 (0.70-1.16)0.42
C187 (46)218 (43)

CI = confidence interval, OR = odds ratio. .
3.3. Association between rs237028 and Clinical Characteristics

Stratification analyses were performed to evaluate the associations between each genetic polymorphism and clinical characteristics. As illustrated in Table 3, the A allele of rs237028 was associated with increased age (>50 years; ; 95% CI: 0.296–1.001; ) and higher tumor grade (G2 and G3; ; 95% CI: 1.143–6.211; ). There were no significant associations between rs237028 and other clinical characteristics, such as FIGO stage, histology type, tumor position, lymph node status, peritoneum invasion, or vascular invasion.

Clinical featuresGenotypeGenetic modelAllele
(A/A vs. A/G vs G/G)(A/A vs. A/G-G/G)(A/A-A/G vs. G/G)(A/A-G/G vs. A/G)
A/AA/GG/GOR (95% CI) valueOR (95% CI) valueOR (95% CI) valueOR (95% CI) valueAGOR (95% CI) value

 <5041206A/G: 0.658 (0.306-1.412)0.2810.565 (0.276-1.160)0.1180.290 (0.057-1.493)0.1150.726 (0.341-1.545)O.406102320.544 (0.296-1.001)0.049
 ≥5053172G/G: 0.258 (0.049-1.345)0.09012321
FIGO stage
 I-II3182A/G: 1.784 (0.730-4.357)0.2011.722 (0.756-3.926)0.1931.272 (0.246-6.579)0.5641.734 (0.715-4.204)0.22070121.543 (0.764-3.115)0.224
 III-IV63296G/G: 1.476 (0.282-7.741)0.48915541
 G1651A/G: 2.194 (0.623-7.729)0.1822.194 (0.662-7.273)0.1611.652 (0.182-14.994)0.5102.024 (0.597-6.860)0.20518102.664 (1.143-6.211)0.020
 G2-G379306G/G: 2.194 (0.226-21.324)0.43718739
 Serous49205A/G: 1.056 (0.492-2.286)0.8881.122 (0.549-2.295)0.7521.473 (0.338-6.423)0.4431.024 (0.481-2.180)0.951118301.183 (0.647-2.161)0.585
 Others44173G/G: 1.497 (0.338-6.628)0.43810723
Tumor position
 Unilateral2773A/G: 1.815 (0.693-4.753)0.2211.429 (0.603-3.387)0.2760.453 (0.087-2.362)0.2931.905 (0.735-4.939)0.18161131.117 (0.544-2.293)0.762
 Bilateral51243G/G: 0.529 (0.100-2.804)0.36512630
Lymph node status
 Negative36165A/G: 0.622 (0.228-1.696)0.3520.681 (0.266-1.743)0.4211.154 (0.209-6.377)0.6190.624 (0.235-1.662)0.34488260.802 (0.378-1.703)0.565
 Positive14102G/G: 0.972 (0.169-5.607)0.6433814
Peritoneum invasion
 Negative32133A/G: 0.905 (0.399-2.050)0.8110.907 (0.423-1.944)0.8030.947 (0.216-4.156)0.6270.912 (0.407-2.043)0.49577190.925 (0.490-1.747)0.811
 Positive49225G/G: 0.919 (0.205-4.114)0.61312032
Vascular invasion
 Negative72288A/G: 0.500 (0.170-1.472)0.1530.643 (0.221-1.866)0.4411.080 (1.024-1.139)0.3200.450 (0.153-1.322)0.121172440.914 (0.371-2.250)0.844
 Positive970G/G: 1.111 (1.033-1.195)0.410257

CI = confidence interval, FIGO = International Federation of Gynecology and Obstetrics, OR = odds ratio. .
3.4. Survival Analysis

To evaluate the association of rs237028 and the prognosis of EOC patients, we conducted survival analysis for 140 patients. The Kaplan-Meier curves showed no significant associations between rs237028 and overall survival (AA vs. AG-GG; ). The prognostic factors in our study, including advanced stage (FIGO III–IV; ), peritoneum invasion (), and vascular invasion (), were significantly associated with a poor outcome; however, this association was not observed for age, grade histology, tumor position, or lymph node state. The Kaplan-Meier curves for overall survival in EOC patients are shown in Figure 1. According to multivariate Cox regression analysis, the prognostic value was only shown at advanced stages (FIGO III–IV; 95% CI: 1.015–64.914; ).

4. Discussion

In this study, we investigated the role of genetic variants of TAB2 in EOC. To our knowledge, the present study is the first to confirm that the rs237028 variant of TAB2 is associated with susceptibility to EOC; however, the other two genetic variants, rs521845 and rs652921, showed no associations with EOC. Additionally, patients with the rs237028 A allele tended to be older (>50 years) and had higher-grade tumors (G2 and G3) compared to patients with the G allele.

The rs237028 SNP is located in an intron of the TAB2 gene, which encodes the protein TAB2. TAB2 was originally recognized as an adaptor protein for TAK1 signaling; it acts by tethering TAK1 to the polyubiquitinated protein TRAF6, which in turn facilitates the activation of inhibitor of κB kinase (IKK) and NF-κB. Constitutive NF-κB signaling plays a vital role in tumorigenesis and metastasis in various types of cancers, including EOC [23]. Yung et al. recently reported that the TAK1/NF-κB expression and signaling were increased in ovarian metastatic cancer cells and that treatment targeting TAK1/NF-κB signaling significantly decreased the oncogenic and metastatic potential of the cancer cells [24]. Additionally, Chen et al. found that the transforming growth factor-β- (TGF-β-) activated kinase 1 (MAP3K7) binding protein 2 (TAB3), a homolog of TAB2 that is highly expressed in EOC cells and tissues, appears to play a role in accelerating EOC development [25]. Further evidence has suggested that SNPs related to NF-κB activation are associated with increased EOC risk [16]. The findings of the present study were consistent with this conclusion. In our study, we concluded that patients with the AA or AG genotypes of the rs237028 SNP had a higher risk of developing EOC than patients with the GG genotype. Notably, SNPs associated with disease risk are typically found in the non-protein-coding genome, and they function to influence gene expression by altering the non-protein-coding genome [26]. Thus, we proposed that the rs237028 risk allele, located in an intron of the TAB2 gene, may facilitate EOC development by dysregulating the function of the intron region to influence the TAK1/NF-κB signaling pathway.

In addition to its role as an important component in the inflammatory pathway, TAB2, which is located on chromosome 6q25.1 near the estrogen receptor 1 (ESR1) gene, is considered to be a risk factor for hormone-related cancers owing to its role in the regulation of the ESR1 expression. Li et al. found that ESR1 and TAB2 expression levels were decreased in hepatocellular carcinomas compared to those in adjacent normal tissues and that the ESR1 expression was significantly associated with the expression of TAB2 [27]. In a previous study, both TAB2 and ESR1 gene polymorphisms were found to be associated with breast cancer [18]. In addition, some researchers have suggested that TAB2, by interacting with the domain of estrogen receptor α (ERα), suppresses the transcriptional activity of nuclear receptor corepressor (NCoR), thus rescuing the repression of estrogen receptor (ER) signaling [28]. Notably, EOC, hepatocellular carcinoma, and breast cancer are collectively known as hormone-related cancers; several risk factors that are recognized to have exogenous or endogenous influences on estrogen exposure in breast cancer have also been shown to affect EOC [29]. In fact, GWAS have identified several risk loci demonstrating a shared association between breast and ovarian cancer risk [19]. Previous studies have also shown that ESR1 is involved in the development and progression of EOC [30], and genetic susceptibility studies have suggested that polymorphisms in the ER-α gene confer increased risk for EOC [31]. Thus, in line with the present study, it is possible that the association between rs237028 and EOC susceptibility be mediated through the ER signaling pathway. However, defining the underlying mechanism of the rs237028 SNP in the development of EOC required further detailed functional investigations.

The present study also indicated that older patients (>50 years) were more likely to have the rs237028 A allele. Generally, older patients were also found to be undergoing menopause, and their estrogen levels were therefore considerably lower than those in premenopausal women. Accordingly, this result may indicate an underlying connection between TAB2 and the ER signaling pathway to stimulate the development of EOC. Moreover, the activation of the TAK1/NF-κB pathway affects the production of steroid hormones and may contribute to the pathogenesis of EOC. Collectively, our evidence suggests that TAB2 is a central factor with a role in several pathways involved in inflammation and estrogen production; it is therefore likely associated with EOC and may play a role in EOC initiation and progression. Although this study identified associations between the rs237028 SNP and susceptibility to EOC, no significant associations were observed between any polymorphisms of TAB2 and overall survival, as shown by univariate and multivariate overall survival analysis. The rs237028 SNP seems to act as a risk factor for the development of EOC but is not a predictive factor for cancer prognosis. Moreover, our analysis of the underlying factors affecting overall survival in EOC, including age, FIGO stage, grade, histology, tumor position, lymph node status, peritoneum invasion, and vascular invasion showed that only FIGO stage, peritoneum invasion, and vascular invasion had a significant association with EOC.

This study has several limitations. Firstly, the clinical information of some patients was missing, although this part of missing was randomized, and these patients were not included in survival analysis. But the limited sample size may have affected the veracity and objectivity of our results. Therefore, these findings need to be further corroborated in larger cohorts. Secondly, the functions of the three SNPs investigated in this research are unclear, and the underlying mechanisms of the rs237028 SNP in the development of EOC remain poorly understood. Further investigations are warranted.

5. Conclusions

Taken together, our study identified a potential EOC susceptibility locus, and through stratified analysis, the A allele of rs237028 was found to be significantly associated with increased age and higher tumor grade in EOC. The identification of multiple genetic polymorphisms with effects on susceptibility in many diseases, as well as the important roles of TAB2 in the pathogenesis of EOC based on previous research, led us to conclude that rs237028 in TAB2 potentially plays a major role in the development of EOC. Thus, with the exception of several lifestyle-based risk factors that have been recognized for several years, TAB2 may be used as a potential marker for screening high-risk populations for EOC.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


This work was funded by the National Natural Science Foundation of China (No. 81670346), the Applied Basic Research Programs of Science and Technology Commission Foundation of Sichuan Province (No. 2016SZ0013), the International Cooperation Project of Science and Technology Department of Sichuan Province (No. 2018HH0014), and Science and Technology Major Project of Sichuan Province (No. 2017SZDZX0013).


  1. F. Bray, J. Ferlay, I. Soerjomataram, R. L. Siegel, L. A. Torre, and A. Jemal, “Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries,” CA: a Cancer Journal for Clinicians, vol. 68, no. 6, pp. 394–424, 2018. View at: Publisher Site | Google Scholar
  2. L. A. Torre, B. Trabert, C. E. DeSantis et al., “Ovarian cancer statistics, 2018,” CA: a Cancer Journal for Clinicians, vol. 68, no. 4, pp. 284–296, 2018. View at: Publisher Site | Google Scholar
  3. S. S. Buys, E. Partridge, A. Black et al., “Effect of screening on ovarian cancer mortality: the prostate, lung, colorectal and ovarian (PLCO) cancer screening randomized controlled trial,” JAMA, vol. 305, no. 22, pp. 2295–2303, 2011. View at: Publisher Site | Google Scholar
  4. I. J. Jacobs, U. Menon, A. Ryan et al., “Ovarian cancer screening and mortality in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS): a randomised controlled trial,” The Lancet, vol. 387, no. 10022, pp. 945–956, 2016. View at: Publisher Site | Google Scholar
  5. L. Titus-Ernstoff, K. Perez, D. W. Cramer, B. L. Harlow, J. A. Baron, and E. R. Greenberg, “Menstrual and reproductive factors in relation to ovarian cancer risk,” British Journal of Cancer, vol. 84, no. 5, pp. 714–721, 2001. View at: Publisher Site | Google Scholar
  6. S. A. Narod, P. Sun, P. Ghadirian et al., “Tubal ligation and risk of ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study,” The Lancet, vol. 357, no. 9267, pp. 1467–1470, 2001. View at: Publisher Site | Google Scholar
  7. “Ovarian cancer and oral contraceptives: collaborative reanalysis of data from 45 epidemiological studies including 23 257 women with ovarian cancer and 87 303 controls,” The Lancet, vol. 371, no. 9609, pp. 303–314, 2008. View at: Publisher Site | Google Scholar
  8. “Menopausal hormone use and ovarian cancer risk: individual participant meta-analysis of 52 epidemiological studies,” The Lancet, vol. 385, no. 9980, pp. 1835–1842, 2015. View at: Publisher Site | Google Scholar
  9. P. D. P. Pharoah, Y.-Y. Tsai, S. J. Ramus et al., “GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer,” Nature Genetics, vol. 45, no. 4, pp. 362–370, 2013. View at: Publisher Site | Google Scholar
  10. J. Permuth-Wey, K. Lawrenson, H. C. Shen et al., “Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31,” Nature Communications, vol. 4, no. 1, article 1627, 2013. View at: Publisher Site | Google Scholar
  11. S. Jervis, H. Song, A. Lee et al., “Ovarian cancer familial relative risks by tumour subtypes and by known ovarian cancer genetic susceptibility variants,” Journal of Medical Genetics, vol. 51, no. 2, pp. 108–113, 2014. View at: Publisher Site | Google Scholar
  12. K. B. Kuchenbaecker, S. J. Ramus, J. Tyrer et al., “Identification of six new susceptibility loci for invasive epithelial ovarian cancer,” Nature Genetics, vol. 47, no. 2, pp. 164–171, 2015. View at: Publisher Site | Google Scholar
  13. D. M. Purdie, C. J. Bain, V. Siskind, P. M. Webb, and A. C. Green, “Ovulation and risk of epithelial ovarian cancer,” International Journal of Cancer, vol. 104, no. 2, pp. 228–232, 2003. View at: Publisher Site | Google Scholar
  14. H.-W. Lin, Y. Y. Tu, S. Y. Lin et al., “Risk of ovarian cancer in women with pelvic inflammatory disease: a population-based study,” The Lancet Oncology, vol. 12, no. 9, pp. 900–904, 2011. View at: Publisher Site | Google Scholar
  15. C. L. Pearce, C. Templeman, M. A. Rossing et al., “Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case–control studies,” The Lancet Oncology, vol. 13, no. 4, pp. 385–394, 2012. View at: Publisher Site | Google Scholar
  16. B. Charbonneau, M. S. Block, W. R. Bamlet et al., “Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10,” Cancer Research, vol. 74, no. 3, pp. 852–861, 2014. View at: Publisher Site | Google Scholar
  17. S. Aashaq, A. Batool, and K. I. Andrabi, “TAK1 mediates convergence of cellular signals for death and survival,” Apoptosis, vol. 24, no. 1-2, pp. 3–20, 2019. View at: Publisher Site | Google Scholar
  18. J. S. Brand, J. Li, K. Humphreys et al., “Identification of two novel mammographic density loci at 6Q25.1,” Breast Cancer Research, vol. 17, no. 1, p. 75, 2015. View at: Publisher Site | Google Scholar
  19. S. P. Kar, J. Beesley, A. Amin al Olama et al., “Genome-wide meta-analyses of breast, ovarian, and prostate cancer association studies identify multiple new susceptibility loci shared by at least two cancer types,” Cancer Discovery, vol. 6, no. 9, pp. 1052–1067, 2016. View at: Publisher Site | Google Scholar
  20. J. Prat and FIGO Committee on Gynecologic Oncology, “Staging classification for cancer of the ovary, fallopian tube, and peritoneum,” International Journal of Gynecology & Obstetrics, vol. 124, no. 1, pp. 1–5, 2014. View at: Publisher Site | Google Scholar
  21. I. Meinhold-Heerlein, C. Fotopoulou, P. Harter et al., “The new WHO classification of ovarian, fallopian tube, and primary peritoneal cancer and its clinical implications,” Archives of Gynecology and Obstetrics, vol. 293, no. 4, pp. 695–700, 2016. View at: Publisher Site | Google Scholar
  22. C. Liu, Y. Wang, H. Song et al., “Genetic association of interleukin-31 gene polymorphisms with epithelial ovarian cancer in Chinese population,” Disease Markers, vol. 2018, Article ID 3503858, 7 pages, 2018. View at: Publisher Site | Google Scholar
  23. K. P. Zeligs, M. K. Neuman, and C. M. Annunziata, “Molecular pathways: the balance between cancer and the immune system challenges the therapeutic specificity of targeting nuclear factor-κB signaling for cancer treatment,” Clinical Cancer Research, vol. 22, no. 17, pp. 4302–4308, 2016. View at: Publisher Site | Google Scholar
  24. M. M. H. Yung, H. W. M. Tang, P. C. H. Cai et al., “GRO-α and IL-8 enhance ovarian cancer metastatic potential via the CXCR2-mediated TAK1/NFκB signaling cascade,” Theranostics, vol. 8, no. 5, pp. 1270–1285, 2018. View at: Publisher Site | Google Scholar
  25. Y. Chen, X. Wang, C. Duan et al., “Loss of TAB3 expression by shRNA exhibits suppressive bioactivity and increased chemical sensitivity of ovarian cancer cell lines via the NF-κB pathway,” Cell Proliferation, vol. 49, no. 6, pp. 657–668, 2016. View at: Publisher Site | Google Scholar
  26. A. Gusev, K. Lawrenson, X. Lin et al., “A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants,” Nature Genetics, vol. 51, no. 5, pp. 815–823, 2019. View at: Publisher Site | Google Scholar
  27. J. Li, Y. Wang, Y. Zhu et al., “Breast cancer risk-associated variants at 6q25.1 influence risk of hepatocellular carcinoma in a Chinese population,” Carcinogenesis, vol. 38, no. 4, pp. 447–454, 2017. View at: Publisher Site | Google Scholar
  28. S. Reineri, S. Agati, V. Miano et al., “A novel functional domain of Tab2 involved in the interaction with estrogen receptor alpha in breast cancer cells,” PLoS One, vol. 11, no. 12, article e0168639, 2016. View at: Publisher Site | Google Scholar
  29. J. Long, Q. Cai, H. Sung et al., “Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer,” PLoS Genetics, vol. 8, no. 2, article e1002532, 2012. View at: Publisher Site | Google Scholar
  30. S. Benhadjeba, L. Edjekouane, K. Sauvé, E. Carmona, and A. Tremblay, “Feedback control of the CXCR7/CXCL11 chemokine axis by estrogen receptor α in ovarian cancer,” Molecular Oncology, vol. 12, no. 10, pp. 1689–1705, 2018. View at: Publisher Site | Google Scholar
  31. S. Pemmaraju, L. Amidyala, R. Vottery, P. Nallari, J. Akka, and V. Ananthapur, “Association of ER-α gene PvuII polymorphism with ovarian cancer,” Cancer Treatment and Research Communications, vol. 14, pp. 13–16, 2018. View at: Publisher Site | Google Scholar

Copyright © 2019 Xingming Huang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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