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.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 217 条
[1]   SOME PROCEDURES TO REDUCE CIS-PLATINUM TOXICITY REDUCE ANTITUMOUR ACTIVITY [J].
AAMDAL, S ;
FODSTAD, O ;
PIHL, A .
CANCER TREATMENT REVIEWS, 1987, 14 (3-4) :389-395
[2]   Phyto-oestrogens and Western diseases [J].
Adlercreutz, H ;
Mazur, W .
ANNALS OF MEDICINE, 1997, 29 (02) :95-120
[3]  
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[4]  
ALBERTS DS, 1978, BIOMED EXPRESS, V29, P189
[5]   THE EFFECT OF ANTIOXIDANTS ON BLEOMYCIN TREATMENT IN IN-VITRO AND IN-VIVO GENOTOXICITY ASSAYS [J].
ANDERSON, D ;
BASARAN, N ;
BLOWERS, SD ;
EDWARDS, AJ .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 329 (01) :37-47
[6]   GLUTATHIONE MONOESTERS [J].
ANDERSON, ME ;
MEISTER, A .
ANALYTICAL BIOCHEMISTRY, 1989, 183 (01) :16-20
[7]   PROTECTION AGAINST CISPLATIN TOXICITY BY ADMINISTRATION OF GLUTATHIONE ESTER [J].
ANDERSON, ME ;
NAGANUMA, A ;
MEISTER, A .
FASEB JOURNAL, 1990, 4 (14) :3251-3255
[8]  
Anderson PM, 1998, CANCER, V83, P1433, DOI 10.1002/(SICI)1097-0142(19981001)83:7<1433::AID-CNCR22>3.0.CO
[9]  
2-4
[10]   BENEFICIAL EFFECT OF ACETYLCYSTEINE ON CISPLATIN NEPHROTOXICITY IN RATS [J].
APPENROTH, D ;
WINNEFELD, K ;
SCHROTER, H ;
ROST, M .
JOURNAL OF APPLIED TOXICOLOGY, 1993, 13 (03) :189-192