Cancer chemoprevention through dietary antioxidants: Progress and promise

被引:435
作者
Khan, Naghma [1 ]
Afaq, Farrukh [1 ]
Mukhtar, Hasan [1 ]
机构
[1] Univ Wisconsin, Med Sci Ctr, Dept Dermatol, Madison, WI 53706 USA
关键词
D O I
10.1089/ars.2007.1740
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
It is estimated that nearly one-third of all cancer deaths in the United States could be prevented through appropriate dietary modification. Various dietary antioxidants have shown considerable promise as effective agents for cancer prevention by reducing oxidative stress which has been implicated in the development of many diseases, including cancer. Therefore, for reducing the incidence of cancer, modifications in dietary habits, especially by increasing consumption of fruits and vegetables rich in antioxidants, are increasingly advocated. Accumulating research evidence suggests that many dietary factors may be used alone or in combination with traditional chemotherapeutic agents to prevent the occurrence of cancer, their metastatic spread, or even to treat cancer. The reduced cancer risk and lack of toxicity associated with high intake of fruits and vegetables suggest that specific concentrations of antioxidant agents from these dietary sources may produce cancer chemopreventive effects without causing significant levels of toxicity. This review presents an extensive analysis of the key findings from studies on the effects of dietary antioxidants such as tea polyphenols, curcumin, genistein, resveratrol, lycopene, pomegranate, and lupeol against cancers of the skin, prostate, breast, lung, and liver. This research is also leading to the identification of novel cancer drug targets.
引用
收藏
页码:475 / 510
页数:36
相关论文
共 329 条
[71]   Inhibition of hepatic glucose 6-phosphatase system by the green tea flavanol epigallocatechin gallate [J].
Csala, Miklos ;
Margittai, Eva ;
Senesi, Silvia ;
Gamberucci, Alessandra ;
Banhegyi, Gabor ;
Mandl, Jozsef ;
Benedetti, Angelo .
FEBS LETTERS, 2007, 581 (08) :1693-1698
[72]  
Dalu A, 1998, PROSTATE, V37, P36
[73]   The soy isoflavone genistein promotes apoptosis in mammary epithelial cells by inducing the tumor suppressor PTEN [J].
Dave, B ;
Eason, RR ;
Till, SR ;
Geng, Y ;
Velarde, MC ;
Badger, TM ;
Simmen, RCM .
CARCINOGENESIS, 2005, 26 (10) :1793-1803
[74]   Dietary genistein increased DMBA-induced mammary adenocarcinoma in wild-type, but not ERαKO, mice [J].
Day, JK ;
Besch-Williford, C ;
McMann, TR ;
Hufford, MG ;
Lubahn, DB ;
MacDonald, RS .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2001, 39 (02) :226-232
[75]   Curcumin [1,7-bis(4-hydroxy-3-methoxyphenyl)-1-6-heptadine-3,5-dione; C21H20O6] sensitizes human prostate cancer cells to tumor necrosis factor-related apoptosis-inducing ligand/Apo2L-induced apoptosis by suppressing nuclear factor-κB via inhibition of the prosurvival akt signaling pathway [J].
Deeb, Dorrah ;
Jiang, Hao ;
Gao, Xiaohua ;
Al-Holou, Shaza ;
Danyluk, Andrew L. ;
Dulchavsky, Scott A. ;
Gautam, Subhash C. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 321 (02) :616-625
[76]   p21 response to DNA damage induced by genistein and etoposide in human lung cancer cells [J].
Ding, H ;
Duan, WR ;
Zhu, WG ;
Ju, R ;
Srinivasan, K ;
Otterson, GA ;
Villalona-Calero, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 305 (04) :950-956
[77]   A physiological pharmacokinetic model describing the disposition of lycopene in healthy men [J].
Diwadkar-Navsariwala, V ;
Novotny, JA ;
Gustin, DM ;
Sosman, JA ;
Rodvold, KA ;
Crowell, JA ;
Stacewicz-Sapuntzakis, M ;
Bowen, PE .
JOURNAL OF LIPID RESEARCH, 2003, 44 (10) :1927-1939
[78]   Therapeutic potential of curcumin in human prostate cancer - I. curcumin induces apoptosis in both androgen-dependent and androgen-independent prostate cancer cells [J].
Dorai, T ;
Gehani, N ;
Katz, A .
PROSTATE CANCER AND PROSTATIC DISEASES, 2000, 3 (02) :84-93
[79]   Effect of the consumption of tomato paste on plasma prostate-specific antigen levels in patients with benign prostate hyperplasia [J].
Edinger, M. S. ;
Koff, W. J. .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2006, 39 (08) :1115-1119
[80]   Identification of both Myt-1 and Wee-1 as necessary mediators of the p21-independent inactivation of the Cdc-2/cyclin B1 complex and growth inhibition of TRAMP cancer cells by genistein [J].
El Touny, Lara H. ;
Banerjee, Partha P. .
PROSTATE, 2006, 66 (14) :1542-1555