- Research article
- Open Access
- Open Peer Review
Preoperative serum 8-hydroxydeoxyguanosine is associated with chemoresistance and is a powerful prognostic factor in endometrioid-type epithelial ovarian cancer
© Pylväs-Eerola et al. 2015
- Received: 18 February 2015
- Accepted: 19 June 2015
- Published: 2 July 2015
Oxidative stress is a widely seen phenomenon in several carcinomas. Increasing evidence also suggests that it has a significant role in the development of epithelial ovarian carcinoma (EOC). 8-Hydroxydeoxyguanosine (8-OHdG) is one of the main indicators of oxidative stress and increased expression of 8-OHdG has previously been seen in EOC. DJ-1 is an oncoprotein connected to oxidative stress regulation, but its role in ovarian cancer is not well known. We investigated redox status in different histotypes of EOC by measuring serum 8-OHdG and DJ-1 concentrations and their associations with known prognostic factors.
Serum samples from newly diagnosed EOC patients were collected in 1996–2009 and stored at the Department of Obstetrics and Gynecology, Oulu University Hospital. Serum 8-OHdG and DJ-1 levels were measured by using commercially available ELISA kits. Clinical data was gathered retrospectively from the patients` files. Results were analyzed by using SPSS software.
In total, 112 patient samples were analyzed (38 serous, 20 mucinous, 34 endometrioid and 20 clear-cell). High serum 8-OHdG levels were associated with poor overall survival (OS) (p = 0.019), poor disease-free survival (DFS) (p = 0.020), platinum resistance (p = 0.002), serous histology versus other (p = 0.033), stage III–IV versus I–II (p = 0.009) and suboptimal surgical outcome (p = 0.012). Regarding histotypes, in the endometrioid EOC group in particular, serum 8-OHdG levels were significantly associated with poor DFS (p = 0.005), suboptimal surgical outcome (p = 0.025), and platinum resistance (p = 0.007). The prognostic significance of 8-OHdG in patients with endometrioid cancer in terms of DFS was confirmed in Cox regression analysis. High DJ-1 levels were associated with high histological grade (p = 0.029) and nonsignificantly associated with serous histology vs. other histology (p = 0.089).
An elevated serum 8-OHdG level is a significant predictor of poor prognosis, especially in cases of the endometrioid subtype of ovarian carcinoma. High 8-OHdG levels are associated with all traditional factors of poor prognosis in ovarian cancer and they also predict earlier development of platinum resistance. These results could be valuable when deciding the primary treatment mode for EOC patients.
- Oxidative stress
- Epithelial ovarian cancer
- Endometrioid ovarian cancer
- Platinum resistance
Ovarian cancer is the seventh most common cancer worldwide and one of the main causes of cancer-related death. Usually it is diagnosed at an advanced stage when the prognosis is poor. In most cases relapse occurs within two years, the patient becomes chemoresistant and five-year survival is only 45 % at best. The known risk factors of ovarian cancer are infertility, family history, smoking and hormone replacement therapy, but the main reasons for the occurrence of ovarian cancer are still unclear. In recent years many studies have shown the role of oxidative stress in the development of ovarian and other cancers.
Evidence suggests that ovulation increases the levels of inflammatory agents, which can further lead to mutations in DNA [1–4]. Ovulation creates a void on the ovarian surface, which leads to the wound-healing process, with increased levels of inflammatory mediators and reactive oxygen species (ROS) [1–3]. It has been suggested that cancer cells from the fallopian tubes, the cervix or endometriotic lesions migrate to the ovaries and form tumors near the corpus luteum .
Reactive oxygen species are formed either from incomplete reduction of oxygen during cellular respiration, or following exposure to external agents such as ultraviolet light, ionizing radiation or redox-state-modifying drugs, which are factors known to be connected with carcinogenesis . Because of their unpaired electrons, ROS molecules are very unstable and react easily with other molecules. They can interact directly with DNA and they can oxidize lipids and proteins, generating intermediates that react with DNA, a cascade with the potential to cause DNA mutations when antioxidant defenses are overwhelmed . The hydroxyl radical (•OH) is extremely unstable and reacts rapidly with other molecules. When it attacks DNA, 8-hydroxydeoxyguanosine (8-OHdG) can be formed. Tissue expression of 8-OHdG and its serum concentrations are associated with the prognosis of several carcinomas, including ovarian cancer, breast cancer, colorectal cancer, cutaneous melanoma, non-small-cell lung cancer, diffuse large B-cell lymphoma and esophageal cancer [7–13]. In colorectal carcinomas, immunohistochemical expression levels of 8-OHdG and nitrotyrosine are significantly higher in malignant tissues compared with adenomas or non-tumorous tissues of the colon [14, 15].
The redox-regulated multifunctional protein DJ-1 is involved in diverse cell processes such as chemotaxis, cell migration, cell adhesion, angiogenesis, apoptosis, cell–extracellular matrix interactions and immune regulation . It protects cells from oxidative stress, detoxifies reactive oxygen species and is converted into a variant with a more acidic isoelectric point . Overexpression of DJ-1 increases the chemoresistance of neoplastic cells by inhibiting apoptotic pathways [16, 17]. It has been associated with early-onset parkinsonism , hence its other name PARK7, and it is overexpressed in several malignant tumors including breast, lung, glottic and esophageal carcinomas [19–22]. Increased serum DJ-1 levels have been reported in patients with metastatic uveal melanoma, pancreatic cancer and endometrioid-type endometrial cancers (EECs) [23–25].
We have previously reported that high serum and tumor tissue levels of 8-OHdG in epithelial ovarian carcinoma (EOC) patients are associated with traditional factors of poor prognosis and also with serous histology . In this previous study, 75 % of patients had serous histology and we were therefore unable to assess the prognostic value in different histological subtypes. We included 35 patients from the previous study to the current study (32 serous, 2 endometrioid and 1 clear cell histology) aiming to evaluate the roles of serum 8-OHdG and DJ-1 as prognostic factors in different histological types of epithelial ovarian cancer.
The study involved 112 epithelial ovarian cancer patients diagnosed and treated at Oulu University Hospital in 1996–2009. In most cases, the patients were operated upon at Oulu University Hospital. In some cases the primary operation was in the central hospital, as the tumor was assumed to be benign. In those cases, the staging operation was carried out at Oulu University Hospital. Operations were categorized as optimal if no macroscopic tumor remained and suboptimal if there was any residual tumor. After the operation, the patients underwent taxane- and platinum-based chemotherapy for a total of six treatments at three-week intervals. If the patients showed a complete response after chemotherapy, they were transferred to a routine follow-up program.
38 (33.9 %)
20 (17.9 %)
34 (30.4 %)
20 (17.9 %)
22–85 (mean 59)
50 (44.6 %)
60 (53.6 %)
2 (1.8 %)
22 (19.6 %)
17 (15.2 %)
71 (63.4 %)
2 (1.8 %)
55 (49.1 %)
21 (18.8 %)
35 (31.3 %)
1 (0.9 %)
43 (38.4 %)
48 (42.9 %)
2 (1.8 %)
19 (17.0 %)
58 (51.8 %)
51 (45.5 %)
3 (2.7 %)
Serum samples were collected from every patient the day before the operation or at the time of diagnosis and the samples were stored at −70 °C until use. Commercial ELISA kits for assay of 8-OHdG (JaICA, Japan) and DJ-1 (Nordic BioSite, Sweden) were used. The assays were carried out by following the manufacturers’ instructions, except that sample filtering was omitted.
The data was analyzed by using IBM SPSS Statistics for Windows 126.96.36.199 software. The significance of associations was assessed by using the Mann–Whitney U test and the Kruskal–Wallis test. In survival analysis, serum concentrations were re-formatted as two-class variables using the median level as a cut-off point. Survival was analyzed by using Kaplan–Meier curves and the log-rank test. Cox multivariate regression analysis was used for multivariate analysis. Probability values < 0.05 were considered significant.
This study was approved by the National Supervisory Authority for Welfare and Health (1339/05.01.00.06/2009) and The Regional Ethics Committee of the Northern Ostrobothnia Hospital District (53/2008).
Correlation with traditional EOC risk factors
Associations between prognostic factors and serum concentrations of 8-OHdG in the whole study population, in the endometrioid subgroup, and levels of DJ-1
High DJ-1 levels were significantly associated with a high histological grade (p = 0.029) and non-significantly associated with serous histology versus other histology (p = 0.089). No associations between levels of 8-OHdG and the stage of the disease, or 8-OHdG and DJ-1 levels were found.
In Cox regression analysis a high level of serum 8-OHdG in the patients with endometrioid histology was a more significant predictor of poor DFS (OR 1.387; 95 % CI 1.095–1.758; p = 0.007) than a suboptimal surgical result (OR 2.898; 95 % CI 0.925–9.076; p = 0.068), high stage (OR 1.221; 95 % CI 0.215–6.915, p = 0.822) or high histological grade (OR 1.566; 95 % CI 0.259–9.457, p = 0.625).
We report here that the preoperative serum concentration of 8-OHdG is a highly significant prognostic marker in cases of EOC, especially in endometrioid ovarian carcinomas. On the other hand, serum DJ-1 levels seem not to have prognostic significance in cases of EOC.
As one of the most studied oxidative stress markers, 8-OHdG has been investigated by way of immunohistochemistry in connection with various carcinomas, but via serum 8-OHdG levels in only a few cancer types. The main repair enzyme connected with 8-OHdG is (human) 8-oxoguanine DNA glycosylase 1 (hOGG1), which cleaves damaged guanosine from DNA and thereafter it is secreted to extracellular fluids . The existing data suggest that extracellular 8-OHdG levels are not affected by diet, cell death or artifact formation . High serum 8-OHdG levels have been recognized as a predictor of short-term survival in non-small-cell lung cancer patients , serous ovarian cancer patients [26, 30] and in children with acute leukemia . In one of our previous studies  we reported that high serum 8-OHdG levels as well as high 8-OHdG immunohistochemical expression were associated with poor clinical outcome in cases of serous ovarian cancer. However, that particular study was focused mainly on serous carcinomas, serum 8-OHdG associated to poor survival only in low grade disease, we were not able to assess progression-free survival and prognostic significance was not observed in multivariate analysis. On the basis of the results, we suggested that there could be variation in oxidative stress levels between different ovarian cancer histological subtypes, and 8-OHdG levels could possibly reflect chemoresistance – hence the current study was undertaken.
We have previously reported higher 8-OHdG tissue expression in borderline ovarian tumors than in benign ones, suggesting a role of 8-OHdG in early ovarian epithelial carcinogenesis . Epithelial ovarian cancers can be assigned to different groups not only by their different histological appearances but also by their obviously different carcinogenetic patterns. In this study serous carcinomas were associated with the highest serum 8-OHdG levels, but the endometrioid histotype was the one where the most significant association between serum 8-OHdG levels and the outcome of the disease was observed. Some endometrioid ovarian cancers are known to arise from atypical endometriosis. We have previously shown biochemical connections between endometriosis and endometriosis-associated endometrioid cancers. In those studies immunohistochemical 8-OHdG expression in endometrioid cancer tissue was significantly lower than in the related endometriosis tissue . This finding suggests that at a certain phase of cancer development, DNA guanine adducts are degraded at the tissue level and 8-OHdG is released to the serum. Thus, 8-OHdG might be a surrogate marker of induced cancer metabolism.
One of the main findings in this study was the association between preoperative serum 8-OHdG levels, not only with all studied traditional prognostic factors, but also with the earlier development of chemoresistance. One of the most important mechanisms of action of platinum regimens used in cases of ovarian carcinoma is based on ROS generation. Therefore, we cannot rule out the possibility that the association with chemoresistance could be explained by the induction of antioxidant enzymes in the most oxidatively stressed tumors. Our observation of a lack of association between serum concentrations of 8-OHdG and DJ-1 is not necessarily contradictory to this hypothesis, since there are also DJ-1-independent redox-regulating pathways such as Nrf2, which recently was connected to platinum resistance in cases of bladder cancer . On the other hand, elevated levels of ROS may simply generate mutations that are able to favor the survival of some cancer cell subpopulations.
High disease burden, poor differentiation and suboptimal surgical outcome are well characterized prognostic factors in all subtypes of ovarian cancer. However, an elevated serum 8-OHdG level was an even more powerful predictor of disease relapse, but only in connection with endometrioid histology. Although it did not significantly reflect OS in multivariate analysis, DFS is a valid endpoint from a clinical point of view. The median survival time of the patients with an endometrioid histotype and high 8-OHdG serum concentrations was 48 months, compared with 111 months in the endometrioid ovarian cancer patients with low 8-OHdG serum levels. In clear-cell and mucinous cancer types the serum 8-OHdG level was not of prognostic value in this patient cohort.
DJ-1 is an oxidative response protein with oncogenic properties. It induces PI3K-AKT and ERK1/3 signaling, influences c-myc expression and provides protection from ROS-induced apoptosis in vitro [35–37]. Increased serum DJ-1 levels have been detected in endometrioid-type endometrial cancer (EEC) patients compared with healthy controls . In the same study, higher DJ-1 serum levels and immunohistochemical expression in the serous type of endometrial cancer (ESC) were observed when set against the levels in cases of EEC. In ovarian cancer, DJ-1 levels, measured by PCR from effusions, were more expressed at an advanced stage . In gastric carcinoma DJ-1 plays an important role in the development of peritoneal carcinomatosis in vitro  and in breast cancer low DJ-1 immunohistochemical and FISH (fluorescence in situ hybridization) expression seems to predict pathological complete remission after neoadjuvant chemotherapy . High DJ-1 immunohistochemical expression in pancreatic cancer is associated with chemoresistance . In prostate carcinoma tissue DJ-1 is overexpressed compared with that in benign hyperplasia , and in non-small-cell lung cancer overexpression has been described compared with that in normal lung tissue . In the current material elevated DJ-1 concentrations were observed in patients with high-grade EOC, but no associations with other traditional prognostic factors or survival were found.
The present results confirm the hypothesis that different epithelial ovarian cancer histotypes represent different carcinogenic backgrounds and clinical behavior and they should be categorized in more detail according to their biomolecular characteristics. Serum concentrations of 8-OHdG also predict the development of platinum resistance and could thus assist in the choice of chemotherapy. This is in line with the results of our previous clinical pilot study of biomarkers of the response to bevacizumab in serous ovarian cancer. In that study, immunohistochemical expression of 8-OHdG appeared to predict a longer-term response to bevacizumab treatment .
An elevated serum 8-OHdG level is a highly significant predictor of poor prognosis, especially in cases of the endometrioid subtype of epithelial ovarian cancer. In addition, high 8-OHdG levels predict earlier development of platinum resistance, which may have a significant clinical impact if confirmed in future studies. These results could be beneficial as regards chemotherapy and maintenance treatment in cases of ovarian cancer.
We thank Elina Huikari for skilful technical assistance in ELISAs.
- Murdoch WJ, Martinchick JF. Oxidative damage to DNA of ovarian surface epithelial cells affected by ovulation: carcinogenic implication and chemoprevention. Exp Biol Med. 2004;229:546–52.Google Scholar
- Murdoch WJ. Carcinogenic potential of ovulatory genotoxity. Biol Reprod. 2005;73:586–90.View ArticlePubMedGoogle Scholar
- Murdoch WJ, Van Kirk EA, Alexander BM. Damages in ovarian surface epithelial cells of ovulatory hens. Exp Biol Med. 2005;230:429–33.Google Scholar
- Ness RB, Cottreau C. Possible role of ovarian epithelial inflammation in ovarian cancer. J Natl Cancer Inst. 1999;91:1459–67.View ArticlePubMedGoogle Scholar
- Yang-Hartwich Y, Gurrea-Soteras M, Sumi N, Joo WD, Holmberg JC, Craveiro V, et al. Ovulation and extra-ovarian origin of ovarian cancer. Sci Rep. 2014; doi:10.1038/srep06116.Google Scholar
- Valko M, Izakovic M, Mazur M, Rhodes CJ, Telser J. Role of oxygen radicals in DNA damage and cancer incidence. Mol Cell Biochem. 2004;266:37–56.View ArticlePubMedGoogle Scholar
- Karihtala P, Soini Y, Vaskivuo L, Bloigu R, Puistola U. DNA adduct 8-hydroxydeoxyguanosine, a novel putative marker of prognostic significance in ovarian carcinoma. Int J Gynecol Cancer. 2009;19:1047–51.View ArticlePubMedGoogle Scholar
- Sova H, Jukkola-Vuorinen A, Puistola U, Kauppila S, Karihtala P. 8-Hydroxydeoxyguanosine: a new potential independent prognostic factor in breast cancer. Br J Cancer. 2010;102:1018–23.View ArticlePubMedPubMed CentralGoogle Scholar
- Sheridan J, Wang LM, Tosetto M, Sheahan K, Hyland J, Fennelly D, et al. Nuclear oxidative damage correlates with poor survival in colorectal cancer. Br J Cancer. 2009;100:381–8.View ArticlePubMedGoogle Scholar
- Murtas D, Piras F, Minerba L, Ugalde J, Floris C, Maxia C, et al. Nuclear 8-hydroxy-2`-deoxyguanosine, a survival biomarker in patients with cutaneous melanoma. Oncol Rep. 2010;23:329–35.PubMedGoogle Scholar
- Shen J, Deiniger P, Hunt JD, Zhao H. 8-Hydroxy-2`-deoxyguanosine (8-OH-dG) as a potential survival biomarker in patients with non-small-cell lung cancer. Cancer. 2007;109:574–80.View ArticlePubMedGoogle Scholar
- Peroja P, Pasanen AK, Haapasaari KM, Jantunen E, Soini Y, Turpeenniemi-Hujanen T, et al. Oxidative stress and redox state-regulating enzymes have prognostic relevance in diffuse large B- cell lymphoma. Exp Hematol Oncol. 2012; doi:10.1186/2161-3619-1-2.Google Scholar
- He H, Zhao Y, Wang N, Zhang L, Wang C. 8-Hydroxy-2`-deoxyguanosine expression predicts outcome of esophageal cancer. Ann Diagn Pathol. 2014;18:326–38.View ArticlePubMedGoogle Scholar
- Kondo S, Toyokuni S, Iwasa Y. Persistent oxidative stress in human colorectal carcinoma, but not in adenoma. Free Radic Biol Med. 1999;27:401–10.View ArticlePubMedGoogle Scholar
- Murawaki Y, Tsuchiya H, Kanbe T, Harada K, Yashima K, Nozaka K, et al. Aberrant expression of selenoproteins in the progression of colorectal cancer. Cancer Lett. 2008;259:218–30.View ArticlePubMedGoogle Scholar
- Junn E, Taniguchi H, Jeong BS, Zhao X, Ichijo H, Mouradian MM. Interaction of DJ-1 with Daxx inhibits apoptosis signal-regulating kinase 1 activity and cell death. Proc Natl Acad Sci U S A. 2005;102:9691–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim RH, Peters M, Jang Y, Shi W, Pintilie M, Fletcher GC, et al. DJ-1, a novel regulator of the tumor suppressor PTEN. Cancer Cell. 2005;7:263–73.View ArticlePubMedGoogle Scholar
- Bonifati V, Rizzu P, Squitieri F, Krieger E, Vanacore N, van Swieten JC, et al. DJ-1 (PARK7), a novel gene for autosomal recessive, early onset parkinsonism. Neurol Sci. 2003;24:159–60.View ArticlePubMedGoogle Scholar
- Merikallio H, Pääkkö P, Kinnula VL, Harju T, Soini Y. Nuclear factor erythroid-derived 2-like 2 (Nrf2) and DJ1 are prognostic factors in lung cancer. Hum Pathol. 2012;43:577–84.View ArticlePubMedGoogle Scholar
- Le Naour F, Misek DE, Krause MC, Deneux L, Giordano TJ, Scholl S, et al. Proteomics-based identification of RS/DJ-1 as a novel circulating tumor antigen in breast cancer. Clin Cancer Res. 2001;7:3328–35.PubMedGoogle Scholar
- Zhu XL, Wang ZF, Lei WB, Zhuang HW, Jiang HY, Wen WP. DJ-1: a novel independent prognostic marker for survival in glottic squamous cell carcinoma. Cancer Sci. 2010;101:1320–5.View ArticlePubMedGoogle Scholar
- Yuen HF, Chan YP, Law S, Srivastava G, El-Tanani M, Mak TW, et al. DJ-1 could predict worse prognosis in esophageal squamous cell carcinoma. Cancer Epidemiol Biomarkers Prev. 2008;17:3593–602.View ArticlePubMedGoogle Scholar
- Chen LL, Tian JJ, Su L, Jing Y, Zhang SC, Zhang HX, et al. DJ-1: a promising marker in metastatic uveal melanoma. J Cancer Res Clin Oncol. 2015;141:315–21.View ArticlePubMedGoogle Scholar
- Tsiaousidou A, Lambropoulou M, Chatzitheoklitos E, Tripsiais G, Tsompanidou C, Simopoulos C, et al. B7H4, HSP27 and DJ-1 molecular markers as prognostic factors in pancreatic cancer. Pancreatology. 2013;13:564–9.View ArticlePubMedGoogle Scholar
- Morelli M, Scumaci D, Di Cello A, Venturella R, Donato G, Faniello MC, et al. DJ-1 in endometrial cancer: a possible biomarker to improve differential diagnosis between subtypes. Int J Gynecol Cancer. 2014;24:649–58.View ArticlePubMedGoogle Scholar
- Pylväs M, Puistola U, Laatio L, Kauppila S, Karihtala P. Elevated serum 8-OHdG is associated with poor prognosis in epithelial ovarian cancer. Anticancer Res. 2011;21:1411–5.Google Scholar
- Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45:228–47.View ArticlePubMedGoogle Scholar
- Hirano T. Repair system of 7, 8-dihydro-8-oxoguanine as a defense line against carcinogenesis. J Radiat Res. 2008;49:329–40.View ArticlePubMedGoogle Scholar
- Cooke MS, Evans MD, Dove R, Rozalski R, Gackowski D, Siomek A, et al. DNA repair is responsible for the presence of oxidatively damaged DNA lesions in urine. Mutat Res. 2005;574:58–66.View ArticlePubMedGoogle Scholar
- Xu X, Wang Y, Guo W, Zhou Y, Lv C, Chen X, et al. The significance of the alteration of 8-OHdG in serous ovarian carcinoma. J Ovarian Res. 2013;doi:10.1186/1757-2215-6-74.Google Scholar
- Valavanidis A, Viachogianni T, Fiotakis C. 8-Hydroxy-2-deoxyguanisine (8-OHdG): A critical biomarker of oxidative stress and carcinogenesis. J Environ Sci Health C Environ Carcinog Exotoxicol Rev. 2009;27:120–39.View ArticleGoogle Scholar
- Pylväs M, Puistola U, Kauppila S, Karihtala P. Oxidative stress-induced antioxidant enzyme expression is an early phenomenon in ovarian carcinogenesis. Eur J Cancer. 2010;46:1661–7.View ArticlePubMedGoogle Scholar
- Sova H, Kangas J, Puistola U, Santala M, Liakka A, Karihtala P. Down-regulation of 8-hydroxyguanosine and peroxiredoxin II in the pathogenesis of endometriosis-associated ovarian cancer. Anticancer Res. 2012;32:3037–44.PubMedGoogle Scholar
- Hayden A, Douglas J, Sommerland M, Andrews L, Gould K, Hussain S, et al. The Nrf2 transcription factor contributes to resistance to cisplatin in bladder cancer. Urol Oncol. 2014;32:806–14.View ArticlePubMedGoogle Scholar
- Gu L, Cui T, Fan C, Zhao H, Zhao C, Lu L, et al. Involvement of ERK1/2 signaling pathway in DJ-1-induced neuroprotection against oxidative stress. Biochem Biophys Res Commun. 2009;383:469–74.View ArticlePubMedGoogle Scholar
- Ismail IA, Kang HS, Lee HJ, Kwon BM, Hong SH. 2'-Benzoyloxycinnamaldehyde-mediated DJ-1 upregulation protects MCF-7 cells from mitochondrial damage. Biol Pharm Bull. 2012;35:895–902.View ArticlePubMedGoogle Scholar
- Inberg A, Linial M. Protection of pancreatic beta-cells from various stress conditions is mediated by DJ-1. J Biol Chem. 2010;285:25686–98.View ArticlePubMedPubMed CentralGoogle Scholar
- Davidson B, Hadar R, Schlossberg A, Sternlicht T, Slipicevic A, Skrede M, et al. Expression and clinical role of DJ-1, a negative regulator of PTEN, in ovarian carcinoma. Hum Pathol. 2008;39:87–95.View ArticlePubMedGoogle Scholar
- Zhu ZM, Li ZR, Huang Y, Yu HH, Huang XS, Shao JH, et al. DJ-1 is involved in the peritoneal metastasis of gastric cancer through activation of the Akt signaling pathway. Oncol Rep. 2014;31:1489–97.PubMedGoogle Scholar
- Kawate T, Iwaya K, Kikuchi R, Kaise H, Oda M, Sato E, et al. DJ-1 protein expression as a predictor of pathological complete remission after neoadjuvant chemotherapy in breast cancer patients. Breast Cancer Res Treat. 2013;139:51–9.View ArticlePubMedGoogle Scholar
- Osman WM, Abd El Atti RM, Abou Gabal HH. DJ-1 and androgen receptor immunohistochemical expression in prostatic carcinoma: a possible role in carcinogenesis. J Egypt Natl Canc Inst. 2013;25:223–30.View ArticlePubMedGoogle Scholar
- Bai J, Guo C, Sun W, Li M, Meng X, Yu Y, et al. DJ-1 may contribute to metastasis of non-small cell lung cancer. Mol Biol Rep. 2012;39:2697–703.View ArticlePubMedGoogle Scholar
- Karihtala P, Mäenpää J, Turpeenniemi-Hujanen T, Puistola U. Front-line bevacizumab in serous epithelial ovarian cancer: biomarker analysis of the FINAVAST trial. Anticancer Res. 2010;30:1001–6.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.