Oxidative damage and antioxidant status in patients with cervical intraepithelial neoplasia and carcinoma of the cervix

被引:34
作者
Looi, Mee-Lee [1 ]
Dali, Ahmad Zailani Hatta Mohd [2 ]
Ali, Siti Aishah Md [3 ]
Ngah, Wan Zurinah Wan [1 ]
Yusof, Yasmin Anum Mohd [1 ]
机构
[1] Univ Kebangsaan Malaysia, Dept Biochem, Kuala Lumpur 50300, Malaysia
[2] Hosp Univ Kebangsaan Malaysia, Dept Obstet & Gynecol, Kuala Lumpur, Malaysia
[3] Hosp Univ Kebangsaan Malaysia, Dept Pathol, Kuala Lumpur, Malaysia
关键词
antioxidant enzymes; cervical carcinoma; cervical intraepithelial neoplasia; B-deoxyhydroxyguanosine; malondialdehyde;
D O I
10.1097/CEJ.0b013e328305a10b
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Free radicals that induced lipid peroxidation and DNA damage have been implicated in many diseases including cancer. Cellular antioxidant defense plays an important role in neoplastic disease to counteract oxidative damage. This study aims to investigate the status of oxidative damage by measuring plasma malondialdehyde (MDA) level and urinary 8-hydroxydeoxyguanosine (8-OHdG), and the level of antioxidant enzymes superoxide dismutase, glutathione peroxidase, and catalase in patients with cervical intraepithelial neoplasia (CIN) and squamous cell carcinoma (SCC) of the cervix. Urinary 8-OHdG was measured by an enzyme-linked immunosorbent assay kit. MDA and antioxidant enzyme activities were determined by high-performance liquid chromatography and spectrophotometry, respectively. Eighty patients with CIN and SCC of the cervix were recruited and compared with normal controls. Urinary 8-OHdG/creatinine ratio did not show any significant changes in any disease status studied as compared with controls (P=0.803). Plasma MDA was found to be increased in CIN and SCC patients when compared with controls (P=0.002). Glutathione peroxidase activity was increased (P=0.0001) whereas superoxide dismutase and catalase activity was decreased (P=0.019 and 0.0001, respectively) in both CIN and SCC patients when compared with controls. Urinary 8-OHdG may not be a good marker for enhanced oxidative stress in cervical cancer. Oxidative damage as demonstrated by the level of MDA is markedly increased in CIN and SCC patients with changes of enzymatic antioxidants observed. European Journal of Cancer Prevention 17:555-560 (C) 2008 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:555 / 560
页数:6
相关论文
共 36 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]  
[Anonymous], 2 REPORT NATL CANC R
[3]   Oxidative stress and lipid peroxidation-derived DNA-lesions in inflammation driven carcinogenesis [J].
Bartsch, H ;
Nair, J .
CANCER DETECTION AND PREVENTION, 2004, 28 (06) :385-391
[4]   ASSAYING FOR SUPEROXIDE-DISMUTASE ACTIVITY - SOME LARGE CONSEQUENCES OF MINOR CHANGES IN CONDITIONS [J].
BEYER, WF ;
FRIDOVICH, I .
ANALYTICAL BIOCHEMISTRY, 1987, 161 (02) :559-566
[5]   Role of oxygen free radicals in cancer development [J].
Dreher, D ;
Junod, AF .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (01) :30-38
[6]   Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[7]   The effect of prostate cancer and antianrogenic therapy on lipid peroxidation and antioxidant systems [J].
İynem Alkan Hacer ;
Alademir Ayşe Zeynep ;
Öbek Can ;
Kural Ali Riza ;
Konukoglu Dildar ;
Akçay Tülay .
International Urology and Nephrology, 2003, 36 (1) :57-62
[8]  
Halliwell B., 1991, AM J MED, V91, P14, DOI DOI 10.1016/0002-9343(91)90279-7
[9]   Urinary oxidative stress markers in young patients with type 1 diabetes [J].
Hata, I ;
Kaji, M ;
Hirano, S ;
Shigematsu, Y ;
Tsukahara, H ;
Mayumi, M .
PEDIATRICS INTERNATIONAL, 2006, 48 (01) :58-61
[10]  
Ho JCM, 2001, CANCER RES, V61, P8578