8-Hydroxy-2′-deoxyguanosine as a Discriminatory Biomarker for Early Detection of Breast Cancer

被引:27
作者
Eldin, Essam Eldin Mohamed Nour [1 ]
El-Readi, Mahmoud Zaki [1 ,2 ]
Eldein, Mohamed Mahmoud Nour [1 ,3 ]
Alfalki, Albagir Ali [4 ]
Althubiti, Mohammad Ahmad [1 ]
Kamel, Hala Fawzy Mohamed [1 ,3 ]
Eid, Safaa Yehia [1 ]
Al-Amodi, Hiba Saeed [1 ]
Mirza, Ahmad A. [5 ]
机构
[1] Umm Al Qura Univ, Fac Med, Dept Biochem, Mecca, Saudi Arabia
[2] Al Azhar Univ, Fac Pharm, Dept Biochem, Assiut, Egypt
[3] Ain Shams Univ, Fac Med, Dept Med Biochem, Cairo, Egypt
[4] Umm Al Qura Univ, Fac Med, Dept Surg, Mecca, Saudi Arabia
[5] King Abdulaziz Univ, Fac Med Rabigh, Dept Otolaryngol Head & Neck Surg, Jeddah, Saudi Arabia
关键词
Antioxidants; Diagnostic tools; DNA; Neoplasm; Oxidative damage; OXIDATIVE DNA-DAMAGE; CA; 15-3; 8-HYDROXY-2-DEOXYGUANOSINE DNA; TUMOR-MARKERS; SERUM-LEVELS; 8-OHDG; STRESS; LEVEL; RISK; CEA;
D O I
10.1016/j.clbc.2018.12.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For early detection of malignant tumors, serum levels of 8-hydroxy-2'-deoxyguanosine were determined in 50 women with benign breast tumors, 50 women with breast cancer (BC), and 50 healthy women as a control group. 8-hydroxy-2'-deoxyguanosine levels were significantly increased in the BC group compared with the benign tumor and the healthy control groups; thus it can be used as a potential noninvasive biomarker for early detection of BC. Background: Breast cancer (BC) is one of the most prevalent and reported cancers among Saudi women. Detection of BC in the early invasive stage (stages I, II) has an advantage in treating patients over detection in the late invasive stage (stages III, IV). Tumor markers are used to aid in diagnosis, treatment monitoring, and recurrence detection of malignant tumors. 8-hydroxy-2'-deoxyguanosine (8-OHdG) is a marker of nucleic damage owing to oxidative stress. Patients and Methods: We studied the blood levels of 8-OHdG in 50 women with benign breast tumors, 50 women with BC, and 50 healthy women as a control group. Results: The concentrations of 8-OHdG were significantly increased in the BC group (55.2 ng/dL) compared with the benign tumor group (30.2 ng/dL) and with the healthy control group (9.08 ng/dL). The same pattern was observed with other diagnostic markers, including carcinoembryonic antigen and cancer antigen 15-3. Significant positive correlations between 8-OHdG and both carcinoembryonic antigen (r = 0.63; P < .001) and cancer antigen 15-3 (r = 0.51; P < .001) were noticed. The levels of 8-OHdG were significantly higher in stage I (81 ng/dL) compared with stage II (51 ng/dL; P < .05), stage III (38 ng/dL; P < .01), and stage IV (19 ng/dL; P < .001). In addition, serum 8-OHdG had a high diagnostic performance in BC (area under the curve, 0.86; sensitivity = 82%; specificity = 80% at cutoff value 21.4 ng/mL). 8-OHdG is associated with BC risk according to logistic regression analysis. Conclusion: We concluded that the significant increase of serum levels of 8-OHdG in patients with BC can be used as a potential noninvasive biomarker for early detection of BC. However, large sample sizes from different stages and types of BC should be included in any future study to confirm the present findings before translating the findings into routine clinical application. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:E385 / E393
页数:9
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