Dietary antioxidants during cancer chemotherapy: Impact on chemotherapeutic effectiveness and development of side effects

被引:344
作者
Conklin, KA [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Anesthesiol, Los Angeles, CA 90095 USA
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 2000年 / 37卷 / 01期
关键词
D O I
10.1207/S15327914NC3701_1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several studies suggest that dietary supplementation with antioxidants can influence the response to chemotherapy as well as the development of adverse side effects that results from treatment with antineoplastic agents. Administration of antineoplastic agents results in oxidative stress, i.e., the production of free radicals and other reactive oxygen species (ROS). Oxidative stress reduces the rate of cell proliferation, and that occurring during chemotherapy may interfere with the cytotoxic effects of antineoplastic drugs, which depend on rapid proliferation of cancer cells for optimal activity. Antioxidants detoxify ROS and may enhance the anticancer effects of chemotherapy. For some supplements, activities beyond their antioxidant properties, such as inhibition of topoisomerase II or protein tyrosine kinases, may also contribute. ROS cause or contribute to certain side effects that are common to many anticancer drugs, such as gastrointestinal toxicity and mutagenesis. ROS also contribute to side effects that occur only with individual agents, such as doxorubicin-induced cardiotoxicity, cisplatin-induced nephrotoxicity, and bleomycin-induced pulmonary fibrosis. Antioxidants can reduce or prevent many of these side effects, and for some supplements the protective effect results from activities other than their antioxidant properties. Certain side effects, however, such as alopecia and myelosuppression, are not prevented by antioxidants, and agents that interfere with these side effects may also interfere with the anticancer effects of chemotherapy.
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页码:1 / 18
页数:18
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共 217 条
[41]  
DIMITROV NV, 1987, AM J PATHOL, V126, P376
[42]   EFFICACY AND SAFETY OF HIGH-DOSE CISPLATIN AND CYCLOPHOSPHAMIDE WITH GLUTATHIONE PROTECTION IN THE TREATMENT OF BULKY ADVANCED EPITHELIAL OVARIAN-CANCER [J].
DIRE, F ;
BOHM, S ;
ORIANA, S ;
SPATTI, GB ;
ZUNINO, F .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1990, 25 (05) :355-360
[43]  
DOMAE N, 1981, CANCER TREAT REP, V65, P79
[44]   PREVENTION OF DOXORUBICIN CARDIAC TOXICITY IN THE MOUSE BY N-ACETYLCYSTEINE [J].
DOROSHOW, JH ;
LOCKER, GY ;
IFRIM, I ;
MYERS, CE .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (04) :1053-1064
[45]  
DURKEN M, 1995, BONE MARROW TRANSPL, V15, P757
[46]   Effects of anthracyclin-based chemotherapy on total plasma antioxidant capacity in small cell lung cancer patients [J].
Erhola, M ;
KellokumpuLehtinen, P ;
MetsaKetela, T ;
Alanko, K ;
Nieminen, MM .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (03) :383-390
[47]   LIPID-PEROXIDATION PRODUCTS, AND VITAMIN AND TRACE-ELEMENT STATUS IN PATIENTS WITH CANCER BEFORE AND AFTER CHEMOTHERAPY, INCLUDING ADRIAMYCIN - A PRELIMINARY-STUDY [J].
FABER, M ;
COUDRAY, C ;
HIDA, H ;
MOUSSEAU, M ;
FAVIER, A .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1995, 47 (1-3) :117-123
[48]   5-hydroxymethyluracil excretion, plasma Tbars and plasma antioxidant vitamins in adriamycin-treated patients [J].
Faure, H ;
Coudray, C ;
Mousseau, M ;
Ducros, V ;
Douki, T ;
Bianchini, F ;
Cadet, J ;
Favier, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (07) :979-983
[49]   ADRIAMYCIN - ENERGY METABOLISM AND MITOCHONDRIAL OXIDATIONS IN HEART OF TREATED RABBITS [J].
FERRERO, ME ;
FERRERO, E ;
GAJA, G ;
BERNELLIZAZZERA, A .
BIOCHEMICAL PHARMACOLOGY, 1976, 25 (02) :125-130
[50]  
FOLKERS K, 1985, DRUG EXP CLIN RES, V11, P539