DNA damage of tumor-associated lymphocytes and total antioxidant capacity in cancerous patients

被引:44
作者
Liu, XJ
Zhao, J
Zheng, RL [1 ]
机构
[1] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Peoples R China
[2] Lanzhou Med Coll, Affiliated Hosp 1, Lanzhou 730000, Peoples R China
[3] NW Minorities Univ, Coll Med, Lanzhou 730000, Peoples R China
关键词
malignant pleural effusion; tumor-associated lymphocytes; total antioxidant capacity; DNA damage; melatonin; repair;
D O I
10.1016/S1383-5718(03)00112-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The purpose of this study was to assess DNA damage of tumor-associated lymphocytes (TALs) in malignant pleural effusion (MPE), the total antioxidant capacity (TAC) of plasma and MPE from patients with carcinoma, and DNA repair effect of melatonin. TAC of plasma was measured in 28 cancer patients with MPE and in 33 healthy persons, and also TAC of MPE supernatant was measured in these patients. DNA damages of peripheral blood mononuclear cells (PBMCs) and of TALs were assessed using comet assay. The TAC of plasma was remarkably lower in cancer patients (8.41 +/- 1.78 U/ml) than that in healthy persons (10.52 +/- 1.64 U/ml, P < 0.001). The TAC of MPE supernatant (6.34 +/- 1.57 U/ml) was significantly lower than that of plasma in cancer patients (8.41 1.78 U/ml, P < 0.001). The comet percentage of PBMCs was higher in cancer patients (16.8 +/- 7.9) than that in healthy persons (10.4 +/- 4.9, P < 0.01). Within cancer patients, the comet percentage of TALs (41.9 +/- 11.7) was significantly higher than that of PBMCs (16.8 +/- 7.9, P < 0.001). A negative correlation was observed between the TAC of MPE supernatant and the comet percentage of TALs in patients (r = -0.538, P < 0.01). After treatment with melatonin, comet percentage of TALs declined significantly from 42.6 +/- 12.8 to 27.1 +/- 9.9 (P < 0.001). These data show that lower TAC of MPE supernatant may be related to higher degree of DNA damage of TALs and that melatonin may facilitate the repair of the damaged DNA. (C) 2003 Elsevier B.V. All rights reserved.
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页码:1 / 8
页数:8
相关论文
共 48 条
[1]   Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA [J].
Aas, PA ;
Otterlei, M ;
Falnes, PO ;
Vågbo, CB ;
Skorpen, F ;
Akbari, M ;
Sundheim, O ;
Bjorås, M ;
Slupphaug, G ;
Seeberg, E ;
Krokan, HE .
NATURE, 2003, 421 (6925) :859-863
[2]   O6-alkylguanine-DNA alkyltransferase:: influence on susceptibility to the genetic effects of alkylating agents [J].
Kyrtopoulos, SA .
TOXICOLOGY LETTERS, 1998, 103 :53-57
[3]   Melatonin protects against gastric ulceration and increases the efficacy of ranitidine and omeprazole in reducing gastric damage [J].
Bandyopadhyay, D ;
Bandyopadhyay, A ;
Das, PK ;
Reiter, RJ .
JOURNAL OF PINEAL RESEARCH, 2002, 33 (01) :1-7
[4]   The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay [J].
Benzie, IFF ;
Strain, JJ .
ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) :70-76
[5]   Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA [J].
Bruner, SD ;
Norman, DPG ;
Verdine, GL .
NATURE, 2000, 403 (6772) :859-866
[6]   Oxidative nucleobase modifications leading to strand scission [J].
Burrows, CJ ;
Muller, JG .
CHEMICAL REVIEWS, 1998, 98 (03) :1109-1151
[7]   Resveratrol, melatonin, vitamin E, and PBN protect against renal oxidative DNA damage induced by the kidney carcinogen KBrO3 [J].
Cadenas, S ;
Barja, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (11-12) :1531-1537
[8]  
Cadet J., 2000, FREE RADICAL CHEM BI, P45
[9]  
Cao GH, 1998, CLIN CHEM, V44, P1309
[10]   Cross regulation by IL-10 and 1L-2/IL-12 of the helper T cells and the cytolytic activity of lymphocytes from malignant effusions of lung cancer patients [J].
Chen, YM ;
Yang, WK ;
Ting, CC ;
Tsai, WY ;
Yang, DM ;
WhangPeng, J ;
Perng, RP .
CHEST, 1997, 112 (04) :960-966