An appraisal of the therapeutic value of lycopene for the chemoprevention of prostate cancer: A nutrigenomic approach

被引:12
作者
Lee, L. K. [1 ]
Foo, K. Y. [2 ,3 ]
机构
[1] Univ Sains Malaysia, Sch Hlth Sci, Nutr Programme, Kubang Kerian 16150, Kelantan, Malaysia
[2] Univ Sains Malaysia, Sch Hlth Sci, Environm & Occupat Hlth Programme, Kubang Kerian 16150, Kelantan, Malaysia
[3] Univ Sains Malaysia, River Engn & Urban Drainage Res Ctr REDAC, Nibong Tebal 14300, Penang, Malaysia
关键词
Foodomic; Gene expressions; Lycopene; Nutrigenomic; Prostate cancer; Tomato; MANGANESE SUPEROXIDE-DISMUTASE; ACTIVATED RECEPTOR-GAMMA; POLY(ADP-RIBOSE) POLYMERASE; PLASMINOGEN-ACTIVATOR; GENETIC POLYMORPHISMS; PLASMA ANTIOXIDANTS; CHOLESTEROL EFFLUX; BINDING-PROTEINS; EPITHELIAL-CELLS; DNA METHYLATION;
D O I
10.1016/j.foodres.2013.03.027
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Lycopene is the predominant and bioactive carotenoid present in the tomato (Solarium lycopersicum), a widely appreciated healthful vegetable. In vivo, in vitro and clinical studies conducted in recent years have revealed an inverse association between the dietary intakes of lycopene with the risk of prostate cancer (PCa). Lycopene has been proposed to protect against PCa by the reduction of lipid oxidation, inhibition of cancer cell proliferation, and its antioxidative properties. Attention has been paid towards the interactive impact of lycopene and its genetic predisposition with the prostate carcinogenesis. In particular, lycopene is believed to play a key role in regulating the gene expressions and modulating the development of PCa. This paper presents a state of art review of the lycopene x gene interaction for the protective treatment of PCa. The key pathway for deoxyribonucleic acid (DNA) repair, insulin-like growth factor (IGF), cell cycle, androgen receptor, steroid signaling, inflammation and inflammatory cytokines, gap junction communications, carotenoid cleavage enzymes, and endogenous antioxidant enzymes are concisely elucidated. Furthermore, the evidence underlying its potent impacts on the integrin, nitric oxide synthase (NOS), prostate specific antigen (PSA) and urokinase plasminogen activator receptor (uPAR) expressions is outlined. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1217 / 1228
页数:12
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