Oxidative DNA damage and total antioxidant status in serum of patients with esophageal squamous cell carcinoma

被引:0
作者
Diakowska, Dorota
Lewandowski, Andrzej
Kopec, Waclaw
Diakowski, Witold
Chrzanowska, Teresa
机构
[1] Wroclaw Med Univ, Dept Gastrointestinal & Gen Surg, PL-50417 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Nephrol & Transplantat, Wroclaw, Poland
[3] Wroclaw Med Univ, Cent Lab Clin Hosp, Wroclaw, Poland
[4] Univ Wroclaw, Inst Biochem & Mol Biol, Dept Cytobiochem, PL-50138 Wroclaw, Poland
关键词
esophageal squamous cell cancer; oxidative stress; oxidative DNA damage; antioxidants;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Oxidative stress is connected with activation of somatic mutations and rates of cell proliferation existing in cancer tissue. High level of reactive oxygen species is a mutagenic factor for DNA damage. Antioxidants are the components of the cellular defense mechanism against reactive oxygen molecules. The aim of our study was to analyze DNA peroxidation products' concentration and total antioxidant level in serum of the patients with esophageal squamous cell carcinoma before and after esophagectomy. We examined these parameters as markers of cancer development. Methodology: We tested 18 patients (2 woman and 16 men, mean age 59.4 years) with esophageal squamous cell cancer before and after esophagectomy and 12 healthy people as a control group. Concentrations of 8-OHdG and enzymatic antioxidants level were analyzed in serum. Data were statistically analyzed by Mann-Whitney test. Results: We observed statistically significant higher concentrations of 8-OHdG and significant lower levels of enzymatic antioxidants in the patients with cancer in comparison to the control group. After esophagectomy we observed normalization of these parameters. In four patients the level of total antioxidants was low and 8-OHdG concentration was high during the whole time of treatment. These patients had disease progression. Conclusions: Estimation of serum 8-OHdG concentration and total antioxidant status may be helpful for monitoring cancer therapy in patients with esophageal squamous cell cancer.
引用
收藏
页码:1701 / 1704
页数:4
相关论文
共 33 条
[1]  
BARTOSZ G, 2001, DURGA TWARZ TLENU
[2]   REDOX REGULATION OF PROGRAMMED CELL-DEATH IN LYMPHOCYTES - INVITED COMMENTARY [J].
BUTTKE, TM ;
SANDSTROM, PA .
FREE RADICAL RESEARCH, 1995, 22 (05) :389-397
[3]   OXYRADICALS AND CANCER [J].
CERUTTI, PA .
LANCET, 1994, 344 (8926) :862-863
[4]   Esophageal adenocarcinoma: a review and perspectives on the mechanism of carcinogenesis and chemoprevention [J].
Chen, XX ;
Yang, CS .
CARCINOGENESIS, 2001, 22 (08) :1119-1129
[5]   Role of oxygen free radicals in cancer development [J].
Dreher, D ;
Junod, AF .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (01) :30-38
[6]   DNA degradation and protein peroxidation in cells exposed to hydroxyl free radicals [J].
Du, J ;
Gebicki, JM .
REDOX REPORT, 2002, 7 (05) :329-331
[7]   Oxidative DNA damage accumulation in gastric carcinogenesis [J].
Farinati, F ;
Cardin, R ;
Degan, P ;
Rugge, M ;
Di Mario, F ;
Bonvicini, P ;
Naccarato, R .
GUT, 1998, 42 (03) :351-356
[8]   GENERATION AND ELIMINATION OF 8-OXO-7,8-DIHYDRO-2'-DEOXYGUANOSINE 5'-TRIPHOSPHATE, A MUTAGENIC SUBSTRATE FOR DNA-SYNTHESIS, IN HUMAN-CELLS [J].
HAYAKAWA, H ;
TAKETOMI, A ;
SAKUMI, K ;
KUWANO, M ;
SEKIGUCHI, M .
BIOCHEMISTRY, 1995, 34 (01) :89-95
[9]   Novel mechanism of nitrosative stress from dietary nitrate with relevance to gastro-oesophageal junction cancers [J].
Iijima, K ;
Grant, J ;
McElroy, K ;
Fyfe, V ;
Preston, T ;
McColl, KEL .
CARCINOGENESIS, 2003, 24 (12) :1951-1960
[10]   Enhanced expression of manganese superoxide dismutase mRNA and increased TNF alpha mRNA expression by gastric mucosa in gastric cancer [J].
Izutani, R ;
Katoh, M ;
Asano, S ;
Ohyanagi, H ;
Hirose, K .
WORLD JOURNAL OF SURGERY, 1996, 20 (02) :228-233