Hypotheses on the Potential of Rice Bran Intake to Prevent Gastrointestinal Cancer through the Modulation of Oxidative Stress

被引:19
作者
Law, Bernard M. H. [1 ]
Waye, Mary M. Y. [1 ]
So, Winnie K. W. [1 ]
Chair, Sek Ying [1 ]
机构
[1] Chinese Univ Hong Kong, Nethersole Sch Nursing, Shatin, Hong Kong, Peoples R China
关键词
rice bran; oxidative stress; gastrointestinal cancer; cancer prevention; antioxidants; NF-KAPPA-B; P-METHOXYCINNAMIC ACID; FERMENTED BROWN RICE; COLON-CANCER; COLORECTAL-CANCER; GAMMA-TOCOTRIENOL; LIPID-PEROXIDATION; PHYTIC ACID; ENTEROCOCCUS-FAECALIS; HELICOBACTER-PYLORI;
D O I
10.3390/ijms18071352
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
Previous studies have suggested the potential involvement of oxidative stress in gastrointestinal cancers. In light of this, research efforts have been focused on the potential of dietary antioxidant intake to prevent gastrointestinal cancer through the modulation of oxidative stress. Rice bran, a by-product of rice milling, has been shown to contain an abundance of phytochemicals, which are dietary antioxidants. To date, a number of studies have shown the antioxidative effect of rice bran intake, and some demonstrated that such an effect may contribute to gastrointestinal cancer prevention, largely through the antioxidative properties of rice bran phytochemicals. In addition, these phytochemicals were shown to provide protection against cancer through mechanisms linked to oxidative stress, including beta-catenin-mediated cell proliferation and inflammation. The present article provides an overview of current evidence for the antioxidative properties of rice bran and its phytochemicals, and for the potential of such properties in cancer prevention through the oxidative-stress-linked mechanisms mentioned above. The article also highlights the need for an evaluation of the effectiveness of rice bran dietary interventions among cancer survivors in ameliorating oxidative stress and reducing the level of gastrointestinal cancer biomarkers, thereby establishing the potential of such interventions among these individuals in the prevention of cancer recurrence.
引用
收藏
页数:20
相关论文
共 107 条
[1]   γ-Tocotrienol reversal of epithelial-to-mesenchymal transition in human breast cancer cells is associated with inhibition of canonical Wnt signalling [J].
Ahmed, R. A. ;
Alawin, O. A. ;
Sylvester, P. W. .
CELL PROLIFERATION, 2016, 49 (04) :460-470
[2]   Differential modulation of cyclooxygenase-mediated prostaglandin production by the putative cancer chemopreventive flavonoids tricin, apigenin and quercetin [J].
Al-Fayez, Mohammad ;
Cai, Hong ;
Tunstall, Richard ;
Steward, William P. ;
Gescher, Andreas J. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 58 (06) :816-825
[3]  
[Anonymous], 2012, Estimated Cancer Incidence, Mortality and Prevalence Worldwide in 2012
[4]   Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer [J].
Balamurugan, Ramadass ;
Rajendiran, Ethendhar ;
George, Sarah ;
Samuel, G. Vijay ;
Ramakrishna, Balakrishnan S. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 (08) :1298-1303
[5]   OXIDATIVE STRESS: AN ESSENTIAL FACTOR IN THE PATHOGENESIS OF GASTROINTESTINAL MUCOSAL DISEASES [J].
Bhattacharyya, Asima ;
Chattopadhyay, Ranajoy ;
Mitra, Sankar ;
Crowe, Sheila E. .
PHYSIOLOGICAL REVIEWS, 2014, 94 (02) :329-354
[6]   The Role of Inflammation in Liver Cancer [J].
Bishayee, Anupam .
INFLAMMATION AND CANCER, 2014, 816 :401-435
[7]  
Boateng J., 2009, International Journal of Cancer Research (USA), V5, P153, DOI 10.3923/ijcr.2009.153.166
[8]   The rice bran constituent tricin potently inhibits cyclooxygenase enzymes and interferes with intestinal carcinogenesis in ApcMin mice [J].
Cai, H ;
Al-Fayez, M ;
Tunstall, RG ;
Platton, S ;
Greaves, P ;
Steward, WP ;
Gescher, AJ .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (09) :1287-1292
[9]   Evaluation of oxidative stress in colorectal cancer patients [J].
Chang, Dong ;
Wang, Fan ;
Zhao, Ya-Shuang ;
Pan, Hong-Zhi .
BIOMEDICAL AND ENVIRONMENTAL SCIENCES, 2008, 21 (04) :286-289
[10]  
Cholewa K, 2008, ACTA POL PHARM, V65, P75