Anticarcinogenic actions of melatonin which involve antioxidative processes: comparison with other antioxidants

被引:135
作者
Karbownik, M
Lewinski, A
Reiter, RJ
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[2] Med Univ Lodz, Inst Endocrinol, Dept Thyroidol, PL-91425 Lodz, Poland
关键词
melatonin; antioxidants; oxidative damage; carcinogens; cancer;
D O I
10.1016/S1357-2725(01)00059-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The complex processes of carcinogenesis often involve oxidative stress. Numerous indicators of oxidative damage are enhanced as the result of the action of carcinogens. Several antioxidants, with different efficacies, protect against oxidative abuse caused by carcinogens. Recently, melatonin (N-acetyl-5-mothoxytryptamine) and related indoleamines have attracted attention because of their high antioxidant and anticarcinogenic activity. Some antioxidants, e.g. ascorbic acid, play an ambivalent role in antioxidative defense, since, under specific conditions, they are strongly prooxidant. Among known antioxidants, melatonin has been an often investigated experimental agent in reducing cancer initiation and inhibiting the growth of established tumors. The indoleamine has been shown to protect macromolecules from oxidative mutilation induced by carcinogens. In these studies, a variety of in vitro and in vivo models were used and numerous indices of oxidative damage were evaluated. The protective effects of melatonin and several other indoleamine antioxidants against cellular damage caused by carcinogens make them potential supplements in the treatment or co-treatment at several stages of cancer. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:735 / 753
页数:19
相关论文
共 169 条
[91]  
LISSONI P, 1995, ONCOLOGY-BASEL, V52, P163
[92]   Decreased toxicity and increased efficacy of cancer chemotherapy using the pineal hormone melatonin in metastatic solid tumour patients with poor clinical status [J].
Lissoni, P ;
Barni, S ;
Mandalà, M ;
Ardizzoia, A ;
Paolorossi, F ;
Vaghi, M ;
Longarini, R ;
Malugani, F ;
Tancini, G .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (12) :1688-1692
[93]  
Lissoni P, 1996, ONCOLOGY, V53, P43
[94]   Ototoxicity caused by cisplatin is ameliorated by melatonin and other antioxidants [J].
Lopez-Ganzalez, MA ;
Guerrero, JM ;
Rojas, F ;
Delgado, F .
JOURNAL OF PINEAL RESEARCH, 2000, 28 (02) :73-80
[95]   Antioxidant properties of melatonin: A pulse radiolysis study [J].
Mahal, HS ;
Sharma, HS ;
Mukherjee, T .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (5-6) :557-565
[96]   Oxyradicals and DNA damage [J].
Marnett, LJ .
CARCINOGENESIS, 2000, 21 (03) :361-370
[97]  
Martín M, 2000, FASEB J, V14, P1677
[98]   Melatonin-induced increased activity of the respiratory chain complexes I and IV can prevent mitochondrial damage induced by ruthenium red in vivo [J].
Martín, M ;
Macías, M ;
Escames, G ;
Reiter, RJ ;
Agapito, MT ;
Ortiz, GG ;
Acuña-Castroviejo, D .
JOURNAL OF PINEAL RESEARCH, 2000, 28 (04) :242-248
[99]   OXYGEN-FREE RADICALS AND HUMAN-DISEASE [J].
MARTINEZCAYUELA, M .
BIOCHIMIE, 1995, 77 (03) :147-161
[100]   Role of reactive oxygen species in apoptosis:: implications for cancer therapy [J].
Matés, JM ;
Sánchez-Jiménez, FM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (02) :157-170