- Open Access
A five-DNA methylation signature act as a novel prognostic biomarker in patients with ovarian serous cystadenocarcinoma
Clinical Epigeneticsvolume 10, Article number: 142 (2018)
Ovarian cancer is the most fatal tumor of the female reproductive system and the fifth leading cause of cancer death among women in the USA. The prognosis is poor due to the lack of biomarkers for treatment options.
The methylation array data of 551 patients with ovarian serous cystadenocarcinoma (OSC) in The Cancer Genome Atlas (TCGA) database were assessed in this study to explore the methylation biomarkers associated with prognosis and improve the prognosis of patients. These patients were divided into training (first two thirds) and validation datasets (remaining one third). A five-DNA methylation signature was found to be significantly associated with the overall survival of patients with OSC using the Cox regression analysis in the training dataset. The Kaplan–Meier analysis showed that the five-DNA methylation signature could significantly distinguish the high- and low-risk patients in both training and validation sets. The receiver operating characteristic (ROC) analysis further confirmed that the five-DNA methylation signature exhibited high sensitivity and specificity to predict the prognostic survival of patients. Also, the five-DNA methylation signature was not only applicable in patients of different ages, stages, histologic grade, and size of residual tumor after surgery but also more accurate in predicting OSC prognosis compared with known biomarkers.
This five-DNA methylation signature demonstrated the potential of being a novel independent prognostic indicator and served as an important tool for guiding the clinical treatment of OSC to improve outcome prediction and management for patients. Hence, the findings of this study might have potential clinical significance.
Ovarian cancer is the most lethal cancer of the female reproductive system and the fifth leading cause of cancer death among women in the USA with an estimated 22,240 new cases and 14,070 deaths expected to occur in 2018 [1, 2]. Ovarian serous cystadenocarcinoma (OSC), a common type of ovarian cancer, accounts for about 90% of all ovarian cancers . The standard treatment consists of cytoreductive surgery followed by a combination of platinum- and taxane-based chemotherapy . Although advances in treatment technology in the last few decades have substantially improved the average survival time, the cure rates remain relatively unchanged . The overall 5-year survival probability of women diagnosed with ovarian cancer is still less than 50% (47%) . Assessment of patients prior to therapy might enable a risk-adapted approach and hence offer an opportunity to provide improved personalized treatment. Physicians can direct low-risk patients to conventional treatments, while high-risk patients can be channeled to trials of novel therapies. This selection may enhance the ability of clinical trials to demonstrate clinical benefits. Therefore, determining high-risk patients with OSC and improving the clinical outcome are urgently needed for current clinical management. The identification of highly specific, sensitive, and independent predictive prognostic biomarkers that will allow the stratification of care is essential.
DNA methylation is well known to be associated with ovarian cancer and has great potential to serve as a biomarker in screening the disease, monitoring response to therapy, and predicting the prognosis [5, 6]. The methylation of particular subsets of CpG islands may have consequences for specific processes of tumorigenesis . Aberrant DNA methylation occurs commonly in tumors and is recognized as one of the earliest distinguishing molecular characteristic in carcinogenesis [8, 9]. A number of genes have been identified as being hypermethylated or silenced in ovarian cancer . Thus, cancer methylation studies hold great promise in revealing potential biomarkers for improving the survival rate. Using DNA methylation as a biomarker has several advantages over other molecular markers, including the relative stability of DNA methylation both in vivo and ex vivo ; need for a smaller amount of tissues to obtain adequate DNA for methylation analysis ; and relative accuracy thanks to quantitative assay because DNA methylation measurements can be compared with absolute reference points . An increasing number of reports are available about the potential of DNA methylation as a prognostic biomarker . For instance, patients with higher methylation levels of ABCA1 have shorter overall survival ; hypomethylation of CpG sites within the MSX1 gene is associated with resistant high-grade serous ovarian cancer ; and OPCML gene promoter methylation can serve as a useful biomarker for predicting the prognosis of patients with ovarian cancer . However, the use of genome-wide methylation analysis in clinical practice is limited by the large sets of DNA methylation identified and the difficulties in complex statistical analyses. Moreover, the reproducibility of prognostic methylation signature identified is limited by different specimens and the lack of adjustment for major confounding factors .
Consequently, the whole-genome methylation profiles of tumor tissues from patients with OSC in The Cancer Genome Atlas (TCGA) database were analyzed in this study to identify DNA methylation biomarkers so as to explore the utility of DNA methylation analysis for cancer prognosis. The potential clinical significance of methylation biomarkers serving as molecular prognostic markers was examined using Kaplan–Meier method and receiver operating characteristic (ROC) analysis. Furthermore, the independence and reproducibility of identified methylation biomarkers in different groups were also investigated.
Clinical characteristics of the patients
All 551 patients in this study were clinically and pathologically diagnosed with OSC. The median age and median survival of these patients were 60 years (range, 30–89 years) and 1227 days, respectively. The 3-year overall survival (OS) rate of all patients was 51.60%. The clinical stage was defined according to the Federation Internationale des Gynaecologistes et Obstetristes (FIGO) staging system. The tumor histologic grade was assigned according to the World Health Organization criteria. OSC was divided into stages I, II, III, and IV, and the neoplasm histologic grade included G2, G3, and G4. Anatomic neoplasm subdivisions were obtained from different positions, including left, right, and bilateral. Tumor residual diseases were dichotomized into no macroscopic disease, 1–10 mm, 11–20 mm, and > 20 mm. The clinicopathological characteristics of patients are summarized in Table 1.
Identification of DNA methylation markers associated with the OS of patients in the training dataset
The univariate Cox proportional hazard regression analysis (see the “Materials and methods” section) was performed using the methylation levels as variables in the training dataset to identify DNA methylation markers associated with the OS of patients with OSC. As a result, a total of 1630 DNA methylation sites were found to be significantly associated with the OS of patients (P < 0.05). Subsequently, multivariate Cox regression, stepwise regression, and screening were performed for these 1282 DNA methylation sites, and a hazard ratio model consisting of 5 methylation sites (cg05254747, cg13652336, cg25123470, cg06038133, and cg04907664) was identified as the optimum prognostic model for predicting the OS of patients. In this model, these 5 methylation sites were all significantly (P < 0.05) associated with the OS of patients. The risk scoring formula of these 5 methylation sites was obtained: Risk score = − 1.034 × β value of cg05254747 + 2.433 × β value of cg13652336 + 1.552 × β value of cg25123470 + 2.284 × β value of cg06038133–1.030 × β value of cg04907664. Obviously, the hypermethylation levels of cg13652336, cg25123470, and cg06038133 were associated with a higher risk, whereas the hypomethylation levels of cg05254747 and cg04907664 were associated with a higher risk. The corresponding gene symbol of these 5 sites was SLC39A14, PREX2, KCNIP2, CORO6, and EFNB1, respectively. The chromosomal locations of these 5 methylation sites and related log-rank test P values are shown in Additional file 1: Table S1.
Association between five-DNA methylation signature and patient OS in the training and validation datasets
Hazard ratios (HRs) from the Cox regression analysis indicated that the five-DNA methylation signature was significantly associated with the OS of patients (P < 0.001, HR 2.72, 95% CI 2.03–3.65). The Kaplan–Meier analysis was performed in the training and validation datasets to determine the potential predictive value of this five-DNA methylation signature in the prognosis. The five-DNA methylation signature was assigned to each patient in the high-risk (N = 174) or the low-risk (N = 174) group in the training dataset using the median of prognostic risk scores as the cutoff point. The mean OS in the high-risk and low-risk groups was 1080 days and 1499 days, respectively. The patients in the high-risk group had a significantly (P < 0.001) worse prognosis (Fig. 1a). A similar result was observed in the validation dataset (Fig. 1b). These results showed that the novel five-DNA methylation signature could distinguish high-risk patients from low-risk patients, implying its significance in the prognostic prediction of OSC. Meanwhile, the individual methylation levels of these five methylation sites in patients in the high- and low-risk groups were analyzed. As a result, high-risk patients exhibited significantly lower methylation levels for cg05254747 and cg04907664 and significantly higher methylation levels for the other three methylation sites in both training (Fig. 1c) and validation datasets (Additional file 1: Figure S1) (P < 0.01, Mann–Whitney U test), which were consistent with the previous results.
Evaluation of the predictive performance of the five-DNA methylation signature using ROC analysis
The sensitivity and specificity of the five-DNA methylation signature in predicting survival were evaluated using the ROC analysis to further assess the predictive accuracy of the five-DNA methylation signature in the validation dataset. The AUC of the five-DNA methylation signature was 0.715 (P < 0.001, 95% CI 0.62–0.81) (Fig. 2), indicating that the five-DNA methylation signature had high sensitivity and specificity. Therefore, it could be used to predict the prognostic survival of patients with OSC with high accuracy, and it might have potentially great significance in clinical application.
Predictive performance of the five-DNA methylation signature based on different regrouping methods
Furthermore, several factors were associated with prognostic survival, including age [1, 17], stage , histologic grade , and size of residual tumor after cytoreductive surgery , and the reproducibility was poor in the prognostic markers identified by different groups . Regrouping was carried out based on different clinicopathological characteristics so as to confirm that this five-DNA methylation signature was of high applicability and could precisely predict the OS of patients. Gillen et al. found that increasing age was correlated with shorter survival , and Chi et al. found that patient age might serve as a significant prognostic factor for ovarian carcinoma . Patients were divided into three cohorts based on their ages at initial diagnosis: ≤ 50 (N = 127, 23.05%), 51–60 (N = 178, 32.30%), and > 60 (N = 246, 44.65%), to analyze the clinical effect of the five-DNA methylation signature in patients with different ages. Kaplan–Meier curves showed that patients in the low-risk group had significantly (P < 0.01) longer OS, and the AUC value was 0.680, 0.774, and 0.720 respectively for the three age cohorts (Fig. 3), suggesting that the five-DNA methylation signature was independent of age. Patients in stages III and IV had significantly shorter OS compared with patients in stages I and II , and the 5-year survival of women diagnosed with distant-stage disease was only 29% . Despite the markedly different outcomes by the extent of disease, the OS was obviously different in high- and low-risk groups, and the AUC in stages I and II and stages III and IV cohorts was 0.778 and 0.735, respectively (Additional file 1: Figure S2). As for the histologic grade, considering the number of samples, we verified the predictive performance of the five-DNA methylation signature in G2 (N = 69) and G3 (N = 478). Irrespective of grades, the patients in the high-risk group had significantly (P < 0.05) shorter OS, and the AUC values were 0.696 and 0.740 (Additional file 1: Figure S3). The anatomic subdivisions from left alone and right alone were combined as unilateral cohorts for these analyses due to small numbers. The differences (P < 0.001) in the OS between the two groups were also observed, and the AUC values in all the subgroups were more than 0.72, in both unilateral (N = 140) and bilateral cohorts (N = 383) (Additional file 1: Figure S4). Recent investigations highlighted that the distribution of residual disease was an important predictor and a determinant of OS of patients . The present data showed that the five-DNA methylation signature could provide a fairly better reference for different residual disease cohorts owing to the effectiveness of risk stratification (Additional file 1: Figure S5). All these results indicated that the signature showed satisfactory applicability when patients were regrouped by different clinicopathological characteristics, suggesting that the signature was an independent applicable prognostic predictor of patient survival. The results are summarized in Table 2.
Comparison of the five-DNA methylation signature with other known prognostic biomarkers
In addition, several prognostic biomarkers were identified in previous studies. For instance, Luo et al. demonstrated that the expression of HER2 was a predictor of poor prognosis for ovarian cancer . The expression model of MANF combined with DOCK11 was associated with the prognostic outcomes of patients with OSC, and the model could potentially serve as a novel prognostic indicator . The methylation of the BRCA1 promoter was associated with a poor patient outcome . Expression of HOTAIR was an independent prognostic factor of OS, and its surrogate DNA methylation signature indicated carboplatin resistance in ovarian cancer [27, 28]. The sensitivity and specificity of known biomarkers from other studies were chosen to be evaluated in the validation dataset so as to verify whether the five-DNA methylation signature had the advantage of stable and reliable performance. The ROC analyses for other known biomarker is just as the analysis for our five-DNA methylation signature, and the results showed that the five-DNA methylation signature outperformed other known prognostic biomarkers, including the types of mRNA, lncRNA, and DNA methylation. And statistical comparison using Z test revealed that our signature had significantly higher (P < 0.05) predictive performance than most of the other known biomarker. The AUCs of these biomarkers are shown in Fig. 4 and Additional file 1: Table S2. All these results inspiringly revealed that the five-DNA methylation signature provided better stability and reliability in predicting the OS of patients with OSC and was a superior predictor. Additionally, the expression of the genes corresponding to the five DNA methylation sites and genes in the five-mRNA signature  whose accuracy is second only to the five-DNA methylation signature were also analyzed. And the results demonstrated that the latter genes had higher fold changes in the comparison of high- and low-risk patients, and no difference was noted in the expression of almost all the former five genes in this study (Additional file 1: Figure S6).
Molecular signatures have been proven to predict the clinical prognosis in different kinds of tumors [6, 10, 30, 31]. For instance, the methylation of PCDH19 predicted a poor prognosis of hepatocellular carcinoma ; the methylation of DFNA5 showed strong potential as a prognostic biomarker for breast cancer; and the signature of CXCL11 combined with HMGA2 could precisely predict the OS of patients with high-grade serous ovarian cancer . However, many of these studies were limited by either small sample size or lack of validation of the biomarker as an independent prognostic biomarker. Some studies showed that combinations of DNA methylation as biomarkers achieved higher sensitivity and specificity compared with individual DNA methylation . In the present study, a five-DNA methylation signature significantly associated with the OS of patients with OSC was predicted based on genome-wide DNA methylation analysis using the Cox regression and ROC analyses. The five-DNA methylation signature also performed well in differentiating low- and high-risk groups and in associated log-rank tests with significant P values, demonstrating that it was an independent predictor of patient survival when adjusted by age, FIGO stages, histologic grade, and residual disease after cytoreductive surgery. Furthermore, the results of the univariate Cox regression and Kaplan–Meier analyses for the five individual methylation sites were not as good as for the combination of these five-DNA methylation sites in both training and validation datasets, indicating that a combination of methylation sites might offer a better potential to fulfill much more sensitive and specific prognostic tests for patients with OSC.
Researchers have revealed that the aforementioned five methylation sites may be crucial in cancer development. SLC39A14 has been identified as an independent factor for predicting the biochemical recurrence-free survival of patients with prostate cancer, and the decreased expression of SLC39A14 is associated with the tumor aggressiveness of human prostate cancer . PREX2 (also known as P-Rex2) was highly expressed in the brain, heart, skeletal muscle, placenta, and lymph node and promoted cancer cell migration and/or invasion [33,34,35]. The CORO6 promoter was frequently methylated in renal cell cancer . The expression of EFNB1 was related to the metastasis of breast cancer, and its enhanced expression conferred a poor prognosis . The elevated co-expression of NGFR, EFNB1, and APP was associated with longer overall and metastasis-free survival of patients with breast cancer . In addition, SLC39A14 participates in manganese ion transmembrane transporter activity; KCNIP2 regulates calcium ion binding; PREX2 and EFNB1 are involved in the G-protein coupled receptor signaling pathway and ephrin receptor signaling pathway, respectively. Although the functional mechanism of these five genes still needs further study, their methylation has significant correlations with the prognosis of patients with OSC and may serve as a potential therapeutic target for OSC.
Meanwhile, a comparison of the five-DNA methylation signature with other known prognostic biomarkers showed that it had distinctly higher sensitivity and specificity in the outcome prediction of OSC. The five-mRNA signature identified in a previous study  also had high accuracy surpassed only by the five-DNA methylation signature. However, these five mRNAs were completely different from the genes that corresponded to the five DNA methylation sites in this study. The expression analysis of these ten genes between high- and low-risk patients indicated that one possible reason was that mRNAs acting as biomarkers had larger fold changes in the expression level to be captured by our statistical methods. Further, it is generally believed that DNA methylation has an effect on the gene regulation with several exceptions [6, 39]. The potential association between the methylation level and the gene expression levels of these five genes demonstrated that only the expression of SLC39A14 and CORO6 was significantly (P < 0.05) correlated with the methylation levels at cg05254747 and cg06038133 sites, respectively, and no statistically significant association was observed between the methylation level and the expression of the other three genes. Further studies should be performed to establish a better prognostic biomarker for the combination of mRNAs and DNA methylation signature.
In conclusion, using genome-wide analysis of DNA methylation data of 551 patients with OSC, this study showed that a five-DNA methylation signature was significantly associated with the OS of patients, and its practical value in patients with different ages, FIGO stages, histologic grades, and some other clinical features was confirmed. Therefore, the five-DNA methylation signature may potentially be used as a novel independent prognostic biomarker to predict the OS of patients with OSC. Further clinical studies on the functional mechanism of the five-DNA methylation signature should be examined for the possibility of its participation in the carcinogenesis.
Materials and methods
DNA methylation data in OSC tissues from TCGA dataset
The DNA methylation data of patients with OSC were downloaded from TCGA database . TCGA level 3 methylation data and related clinical information for patients were obtained. TCGA DNA methylation data (level 3) were obtained using Infinium HumanMethylation27 BeadChip (Illumina Inc., CA, USA), and the genomic coordinates of the CpGs were based on GRCh38. All DNA methylation levels were expressed as β values, calculated as M/(M + U), where M is the signal from methylated beads, and U is the signal from unmethylated beads at the targeted CpG site. Only the data including patients with their clinical survival information were selected to analyze the correlation between DNA methylation levels and the corresponding survival in OSC. Considering that tumors in G1, GB, and GX may have a different biological behavior, they were excluded in this study. Ultimately, 551 samples containing information on 27,578 DNA methylation sites were included in this study, and the corresponding clinical information for each sample was also obtained from TCGA database. These 551 samples were separated into training dataset (first two thirds) and validation dataset (remaining one third) according to TCGA series number. The training dataset was applied for identifying and constructing prognostic biomarkers, and the validation dataset was used for verifying the accuracy of the biomarkers in predicting survival, thus determining the potential clinical predictive value.
All statistical analyses were conducted using the R statistical package (R version 3.4.4) unless otherwise stated. OS was defined as the interval from the date of patient’s first diagnosis to the date of last known contact or death. The univariate Cox proportional hazard analysis was first performed in the training dataset to identify methylation markers significantly (P value cutoff < 0.05) correlated with patient survival as candidate markers. Then, the multivariate Cox regression analysis was carried out to further screen the factors associated with patient survival. In brief, two, three, four, five, and six genes were selected from the candidate markers exhaustively as covariates to construct models. Subsequently, AUC was used to measure and compare the model performance; the model with a higher predictive performance was eventually selected out. The model could be used to construct a risk score formula that would be helpful to predict survival. The prognostic risk scores for each patient were calculated based on this formula. According to their prognostic risk scores, these patients were ranked and further separated into “low-risk” and “high-risk” groups using the median risk score as the cutoff point. Patients with risk score higher than the median risk score were assigned to the high-risk group, whereas patients with lower risk were assigned to the low-risk group. After that, the Kaplan–Meier estimator, a nonparametric statistic, with log-rank test (Mantel–Cox) was used to calculate the cumulative survival time and compare the differences in OS between the two groups. Kaplan–Meier curves were drawn using the “survival” package. Finally, the ROC analysis was conducted with the “pROC” package using a categorical variable for OS ≤ 3 years compared with methylation biomarkers. AUC was calculated along with 95% confidence interval (CI). The larger the AUC is, the better the model is for the risk prediction . And Z test was used to further compare the AUC of different biomarkers . Additionally, the potential association between methylation and gene expression level was evaluated using the Spearman’s rank correlation test.
Area under the ROC curve
Ovarian serous cystadenocarcinoma
Receiver operating characteristic
The Cancer Genome Atlas
Federation Internationale des Gynaecologistes et Obstetristes
Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68:7–30.
Cancer Genome Atlas Research N. Integrated genomic analyses of ovarian carcinoma. Nature. 2011;474:609–15.
Coccolini F, Campanati L, Catena F, Ceni V, Ceresoli M, Jimenez Cruz J, Lotti M, Magnone S, Napoli J, Rossetti D, De Iaco P, Frigerio L, Pinna A, Runnebaum I, Ansaloni L. Hyperthermic intraperitoneal chemotherapy with cisplatin and paclitaxel in advanced ovarian cancer: a multicenter prospective observational study. J Gynecol Oncol. 2015;26:54–61.
Coleman RL, Monk BJ, Sood AK, Herzog TJ. Latest research and treatment of advanced-stage epithelial ovarian cancer. Nat Rev Clin Oncol. 2013;10:211–24.
Zhou F, Tao G, Chen X, Xie W, Liu M, Cao X. Methylation of OPCML promoter in ovarian cancer tissues predicts poor patient survival. Clin Chem Lab Med. 2014;52:735–42.
Croes L, Beyens M, Fransen E, Ibrahim J, Vanden Berghe W, Suls A, Peeters M, Pauwels P, Van Camp G, Op de Beeck K. Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancer. Clin Epigenetics. 2018;10:51.
Costello JF, Fruhwald MC, Smiraglia DJ, Rush LJ, Robertson GP, Gao X, Wright FA, Feramisco JD, Peltomaki P, Lang JC, Schuller DE, Yu L, Bloomfield CD, Caligiuri MA, Yates A, Nishikawa R, Su Huang H, Petrelli NJ, Zhang X, O’Dorisio MS, Held WA, Cavenee WK, Plass C. Aberrant CpG-island methylation has non-random and tumour-type-specific patterns. Nat Genet. 2000;24:132–8.
Ahluwalia A, Yan P, Hurteau JA, Bigsby RM, Jung SH, Huang TH, Nephew KP. DNA methylation and ovarian cancer. I. Analysis of CpG island hypermethylation in human ovarian cancer using differential methylation hybridization. Gynecol Oncol. 2001;82:261–8.
Wei SH, Balch C, Paik HH, Kim YS, Baldwin RL, Liyanarachchi S, Li L, Wang Z, Wan JC, Davuluri RV, Karlan BY, Gifford G, Brown R, Kim S, Huang TH, Nephew KP. Prognostic DNA methylation biomarkers in ovarian cancer. Clinical cancer research : an official journal of the American Association for Cancer Research. 2006;12:2788–94.
Chou JL, Huang RL, Shay J, Chen LY, Lin SJ, Yan PS, Chao WT, Lai YH, Lai YL, Chao TK, Lee CI, Tai CK, Wu SF, Nephew KP, Huang TH, Lai HC, Chan MW. Hypermethylation of the TGF-beta target, ABCA1 is associated with poor prognosis in ovarian cancer patients. Clin Epigenetics. 2015;7:1.
Keeley B, Stark A, Pisanic TR 2nd, Kwak R, Zhang Y, Wrangle J, Baylin S, Herman J, Ahuja N, Brock MV, Wang TH. Extraction and processing of circulating DNA from large sample volumes using methylation on beads for the detection of rare epigenetic events. Clinica Chimica Acta; International Journal of Clinical Chemistry. 2013;425:169–75.
Dai W, Teodoridis JM, Zeller C, Graham J, Hersey J, Flanagan JM, Stronach E, Millan DW, Siddiqui N, Paul J, Brown R. Systematic CpG islands methylation profiling of genes in the wnt pathway in epithelial ovarian cancer identifies biomarkers of progression-free survival. Clinical cancer research: an official journal of the American Association for Cancer Research. 2011;17:4052–62.
How Kit A, Nielsen HM, Tost J. DNA methylation based biomarkers: practical considerations and applications. Biochimie. 2012;94:2314–37.
Brown R, Curry E, Magnani L, Wilhelm-Benartzi CS, Borley J. Poised epigenetic states and acquired drug resistance in cancer. Nat Rev Cancer. 2014;14:747–53.
Bonito NA, Borley J, Wilhelm-Benartzi CS, Ghaem-Maghami S, Brown R. Epigenetic regulation of the Homeobox gene MSX1 associates with platinum-resistant disease in high-grade serous epithelial ovarian Cancer. Clinical cancer research: an official journal of the American Association for Cancer Research. 2016;22:3097–104.
Borley J, Wilhelm-Benartzi C, Brown R, Ghaem-Maghami S. Does tumour biology determine surgical success in the treatment of epithelial ovarian cancer? A systematic literature review British journal of cancer. 2012;107:1069–74.
Gillen J, Gunderson C, Greenwade M, Rowland M, Ruskin R, Ding K, Crim A, Walter A, White E, Moore K. Contribution of age to clinical trial enrollment and tolerance with ovarian cancer. Gynecol Oncol. 2017;145:32–6.
Engel J, Eckel R, Schubert-Fritschle G, Kerr J, Kuhn W, Diebold J, Kimmig R, Rehbock J, Holzel D. Moderate progress for ovarian cancer in the last 20 years: prolongation of survival, but no improvement in the cure rate. Eur J Cancer. 2002;38:2435–45.
Peres LC, Cushing-Haugen KL, Kobel M, Harris HR, Berchuck A, Rossing MA, Schildkraut JM, Doherty JA. Invasive epithelial ovarian cancer survival by histotype and disease stage. J Natl Cancer Inst. 2018.
Chi DS, Eisenhauer EL, Zivanovic O, Sonoda Y, Abu-Rustum NR, Levine DA, Guile MW, Bristow RE, Aghajanian C, Barakat RR. Improved progression-free and overall survival in advanced ovarian cancer as a result of a change in surgical paradigm. Gynecol Oncol. 2009;114:26–31.
Chi DS, Liao JB, Leon LF, Venkatraman ES, Hensley ML, Bhaskaran D, Hoskins WJ. Identification of prognostic factors in advanced epithelial ovarian carcinoma. Gynecol Oncol. 2001;82:532–7.
Montavon C, Gloss BS, Warton K, Barton CA, Statham AL, Scurry JP, Tabor B, Nguyen TV, Qu W, Samimi G, Hacker NF, Sutherland RL, Clark SJ, O’Brien PM. Prognostic and diagnostic significance of DNA methylation patterns in high grade serous ovarian cancer. Gynecol Oncol. 2012;124:582–8.
Hamilton CA, Miller A, Miller C, Krivak TC, Farley JH, Chernofsky MR, Stany MP, Rose GS, Markman M, Ozols RF, Armstrong DK, Maxwell GL. The impact of disease distribution on survival in patients with stage III epithelial ovarian cancer cytoreduced to microscopic residual: a gynecologic oncology group study. Gynecol Oncol. 2011;122:521–6.
Luo H, Xu X, Ye M, Sheng B, Zhu X. The prognostic value of HER2 in ovarian cancer: a meta-analysis of observational studies. PLoS One. 2018;13:e0191972.
Zhang J, Xu M, Gao H, Guo JC, Guo YL, Zou M, Wu XF. Two protein-coding genes act as a novel clinical signature to predict prognosis in patients with ovarian serous cystadenocarcinoma. Oncol Lett. 2018;15:3669–75.
Chiang JW, Karlan BY, Cass L, Baldwin RL. BRCA1 promoter methylation predicts adverse ovarian cancer prognosis. Gynecol Oncol. 2006;101:403–10.
Qiu JJ, Lin YY, Ye LC, Ding JX, Feng WW, Jin HY, Zhang Y, Li Q, Hua KQ. Overexpression of long non-coding RNA HOTAIR predicts poor patient prognosis and promotes tumor metastasis in epithelial ovarian cancer. Gynecol Oncol. 2014;134:121–8.
Teschendorff AE, Lee SH, Jones A, Fiegl H, Kalwa M, Wagner W, Chindera K, Evans I, Dubeau L, Orjalo A, Horlings HM, Niederreiter L, Kaser A, Yang W, Goode EL, Fridley BL, Jenner RG, Berns EM, Wik E, Salvesen HB, Wisman GB, van der Zee AG, Davidson B, Trope CG, Lambrechts S, Vergote I, Calvert H, Jacobs IJ, Widschwendter M. HOTAIR and its surrogate DNA methylation signature indicate carboplatin resistance in ovarian cancer. Genome medicine. 2015;7:108.
Liu LW, Zhang Q, Guo W, Qian K, Wang Q, Five-Gene Expression A. Signature predicts clinical outcome of ovarian serous cystadenocarcinoma. Biomed Res Int. 2016;2016:6945304.
Jin C, Xue Y, Li Y, Bu H, Yu H, Zhang T, Zhang Z, Yan S, Lu N, Kong B. A 2-protein signature predicting clinical outcome in high-grade serous ovarian cancer. International journal of gynecological cancer: official Journal of the International Gynecological Cancer Society. 2018;28:51–8.
Zhang T, Guan G, Chen T, Jin J, Zhang L, Yao M, Qi X, Zou J, Chen J, Lu F, Chen X. Methylation of PCDH19 predicts poor prognosis of hepatocellular carcinoma. Asia-Pacific journal of clinical oncology. 2018.
Xu XM, Wang CG, Zhu YD, Chen WH, Shao SL, Jiang FN, Liao QD. Decreased expression of SLC 39A14 is associated with tumor aggressiveness and biochemical recurrence of human prostate cancer. OncoTargets and therapy. 2016;9:4197–205.
Fine B, Hodakoski C, Koujak S, Su T, Saal LH, Maurer M, Hopkins B, Keniry M, Sulis ML, Mense S, Hibshoosh H, Parsons R. Activation of the PI3K pathway in cancer through inhibition of PTEN by exchange factor P-REX2a. Science. 2009;325:1261–5.
Mense SM, Barrows D, Hodakoski C, Steinbach N, Schoenfeld D, Su W, Hopkins BD, Su T, Fine B, Hibshoosh H, Parsons R, PTEN inhibits PREX2-catalyzed activation of RAC1 to restrain tumor cell invasion. Sci Signal 2015;8: ra32.
Srijakotre N, Man J, Ooms LM, Lucato CM, Ellisdon AM, Mitchell CA. P-Rex1 and P-Rex2 RacGEFs and cancer. Biochem Soc Trans. 2017;45:963–77.
Morris MR, Ricketts CJ, Gentle D, McRonald F, Carli N, Khalili H, Brown M, Kishida T, Yao M, Banks RE, Clarke N, Latif F, Maher ER. Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma. Oncogene. 2011;30:1390–401.
Yin H, Lu C, Tang Y, Wang H, Wang H, Wang J. Enhanced expression of EphrinB1 is associated with lymph node metastasis and poor prognosis in breast cancer. Cancer biomarkers: section A of Disease markers. 2013;13:261–7.
Fernandez-Nogueira P, Bragado P, Almendro V, Ametller E, Rios J, Choudhury S, Mancino M, Gascon P. Differential expression of neurogenes among breast cancer subtypes identifies high risk patients. Oncotarget. 2016;7:5313–26.
Phelps DL, Borley JV, Flower KJ, Dina R, Darb-Esfahani S, Braicu I, Sehouli J, Fotopoulou C, Wilhelm-Benartzi CS, Gabra H, Yazbek J, Chatterjee J, Ip J, Khan H, Likos-Corbett MT, Brown R, Ghaem-Maghami S. Methylation of MYLK3 gene promoter region: a biomarker to stratify surgical care in ovarian cancer in a multicentre study. Br J Cancer. 2017;116:1287–93.
International Cancer Genome C, Hudson TJ, Anderson W, Artez A, Barker AD, Bell C, et al. International network of cancer genome projects. Nature. 2010;464:993–8.
Mehdi T, Bashardoost N, Ahmadi M. Kernel smoothing for ROC curve and estimation for thyroid stimulating hormone. Inter J Env Res Pub Heal. 2011:239–42.
Pandis N. Comparison of 2 means (independent z test or independent t test). American journal of orthodontics and dentofacial orthopedics, Official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics. 2015;148:350–1.
The results shown in this manuscript are based upon the data generated by TCGA Research Network: http://cancergenome.nih.gov/.
This work was supported by grants from the National Natural Science Foundation of China (Grant No. 31501045, 31471200 and 31741073). This work was also supported by the Graduate Research and Innovation Fund of Nanjing University (No. 2017CL06).
Ethics approval and consent to participate
Ethical approval has been obtained by The Cancer Genome Atlas (TCGA).
Consent for publication
All authors declare that they have no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplemental Table S1-S2 and supplemental Figure S1-S6. (PDF 1215 kb)