Ingestion of selenium and other antioxidants during prostate cancer radiotherapy: A good thing?

被引:48
作者
Tabassum, A.
Bristow, R. G. [2 ,3 ,4 ]
Venkateswaran, V. [1 ]
机构
[1] Univ Toronto, Dept Surg, Div Urol, Sunnybrook Hlth Sci Ctr, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Radiat Oncol, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[4] Princess Margaret Hosp, Univ Hlth Network, Toronto, ON M5G 2M9, Canada
关键词
Selenium; Chemoprevention; Radiotherapy; Chemotherapy; Antioxidants; DNA repair; Cell cycle; Genetic stability; VITAMIN-E; CELL-CYCLE; PREVENTION; CHEMOPREVENTION; GROWTH; TRIAL; P53; SELENOMETHIONINE; SUPPLEMENTATION; CARCINOMA;
D O I
10.1016/j.ctrv.2009.12.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiation and many chemotherapy agents work to kill cells by inducing free radicals that damage DNA and proteins. Antioxidants such as vitamin E, beta carotene, lycopene, and selenium have been associated with a reduction in cancer risk when ingested by prostate cancer patients. Selenium is a promising agent currently being evaluated as a prostate cancer prevention agent. Selenium is an essential trace element and is involved in antioxidant protection and the redox-regulation in humans. Several adverse effects of radiotherapy and chemotherapy in cancer patients have been linked to oxidative cell processes in the human body. Selenium supplementation may protect healthy tissues and reduce the side effects of treatment. Despite two decades of research into this question, no clear answer has appeared. Therefore, understanding the mechanism(s) by which dietary nutrients exert their effects in prostate carcinogenesis, may lead to the exploitation of new chemoprevention agents. A large body of epidemiological evidence, including observational, trials, and randomized controlled clinical trials, support the proposition that selenium may prevent prostate cancer in humans. These clinical studies are supported by in vitro and in vivo data using prostate cancer models. This systematic review provides the first evidence that antioxidant supplementation during chemotherapy holds potential for reducing dose-limiting toxicities. The pre-clinical and clinical evidence as to whether ingestion of supplemental selenium, in addition to radiotherapy/chemotherapy is beneficial, detrimental or neutral towards patient outcome is also discussed. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:230 / 234
页数:5
相关论文
共 47 条
[1]   Chemoprevention of carcinoma prostate: A review [J].
Ansari M.S. ;
Gupta N.P. ;
Hemal A.K. .
International Urology and Nephrology, 2002, 34 (2) :207-214
[2]   Impact of antioxidant supplementation on chemotherapeutic toxicity: A systematic review of the evidence from randomized controlled trials [J].
Block, Keith I. ;
Koch, Amanda C. ;
Mead, Mark N. ;
Tothy, Peter K. ;
Newman, Robert A. ;
Gyllenhaal, Charlotte .
INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (06) :1227-1239
[3]   New molecular targets in radiotherapy: DNA damage signalling and repair in targeted and non-targeted cells [J].
Burdak-Rothkamm, Susanne ;
Prise, Kevin M. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 625 (1-3) :151-155
[4]   Role of diet in prostate cancer development and progression [J].
Chan, JM ;
Gann, PH ;
Giovannucci, EL .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (32) :8152-8160
[5]   Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin a randomized controlled trial - A randomized controlled trial [J].
Clark, LC ;
Combs, GF ;
Turnbull, BW ;
Slate, EH ;
Chalker, DK ;
Chow, J ;
Davis, LS ;
Glover, RA ;
Graham, GF ;
Gross, EG ;
Krongrad, A ;
Lesher, JL ;
Park, HK ;
Sanders, BB ;
Smith, CL ;
Taylor, JR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (24) :1957-1963
[6]   Randomized, controlled chemoprevention trials in populations at very high risk for prostate cancer: Elevated prostate-specific antigen and high-grade prostatic intraepithelial neoplasia [J].
Clark, LC ;
Marshall, JR .
UROLOGY, 2001, 57 (4A) :185-187
[7]   Inorganic selenium retards progression of experimental hormone refractory prostate cancer [J].
Corcoran, NM ;
Najdovska, M ;
Costello, AJ .
JOURNAL OF UROLOGY, 2004, 171 (02) :907-910
[8]   A randomized, controlled chemoprevention trial of selenium in familial prostate cancer: Rationale, recruitment, and design issues [J].
Costello, AJ .
UROLOGY, 2001, 57 (4A) :182-184
[9]   Selenium metabolism and bioavailability [J].
Daniels, LA .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1996, 54 (03) :185-199
[10]  
Dasgupta Anirban, 2006, J Cancer Res Ther, V2, P47