Assessment of the anti-genotoxic, anti-proliferative, and anti-metastatic potential of crude watercress extract in human colon cancer cells

被引:59
作者
Boyd, Lindsay A. [1 ]
McCann, Mark J.
Hashim, Yumi
Bennett, Richard N.
Gill, Chris I. R.
Rowland, Ian R.
机构
[1] Univ Ulster, Fac Life & Hlth Sci, No Ireland Ctr Food & Hlth, NICHE,CMB, Coleraine BT52 1SA, Londonderry, North Ireland
[2] Univ Tras Os Montes & Alto Douro, CECEA, Dept Fitotecnia & Engn Rural, P-5001801 Vila Real, Portugal
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 2006年 / 55卷 / 02期
关键词
D O I
10.1207/s15327914nc5502_15
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although it is known to be a rich source of the putative anti-cancer chemicals isothiocyanates, watercress has not been extensively studied for its cancer preventing properties. The aim of this study was to investigate the potential chemoprotective effects of crude watercress extract toward three important stages in the carcinogenic process, namely initiation, proliferation, and metastasis (invasion) using established in vitro models. HT29 cells were used to investigate the protective effects of the extract on DNA damage and the cell cycle. The extract was not genotoxic but inhibited DNA damage induced by two of the three genotoxins used, namely hydrogen peroxide and fecal water indicating the potential to inhibit initiation. It also caused an accumulation of cells in the S phase of the cell cycle indicating (possible) cell cycle delay at this stage. The extract was shown to significantly inhibit invasion of HT115 cells through matrigel. Component analysis was also carried out in an attempt to determine the major phytochemicals present in both watercress leaves and the crude extract. In conclusion, the watercress extract proved to be significantly protective against the three stages of the carcinogenesis process investigated.
引用
收藏
页码:232 / 241
页数:10
相关论文
共 50 条
[1]   Comparative effects of flavonoids on the growth, viability and metabolism of a colonic adenocarcinoma cell line (HT29 cells) [J].
Agullo, G ;
GametPayrastre, L ;
Fernandez, Y ;
Anciaux, N ;
Demigne, C ;
Remsey, C .
CANCER LETTERS, 1996, 105 (01) :61-70
[2]  
Bonnesen C, 2001, CANCER RES, V61, P6120
[3]   Effect of a propolis extract and caffeic acid phenethyl ester on formation of aberrant crypt foci and tumors in the rat colon [J].
Borrelli, F ;
Izzo, AA ;
Di Carlo, G ;
Maffia, P ;
Russo, A ;
Maiello, FM ;
Capasso, F ;
Mascolo, N .
FITOTERAPIA, 2002, 73 :S38-S43
[4]   Antigenotoxicity of probiotics and prebiotics on faecal water-induced DNA damage in human colon adenocarcinoma cells [J].
Burns, AJ ;
Rowland, IR .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2004, 551 (1-2) :233-243
[5]   Ingestion of an isothiocyanate metabolite from cruciferous vegetables inhibits growth of human prostate cancer cell xenografts by apoptosis and cell cycle arrest [J].
Chiao, JW ;
Wu, HY ;
Ramaswamy, G ;
Conaway, CC ;
Chung, FL ;
Wang, LG ;
Liu, DL .
CARCINOGENESIS, 2004, 25 (08) :1403-1408
[6]   2,3-EPOXY-4-HYDROXYNONANAL AS A POTENTIAL TUMOR-INITIATING AGENT OF LIPID-PEROXIDATION [J].
CHUNG, FL ;
CHEN, HJC ;
GUTTENPLAN, JB ;
NISHIKAWA, A ;
HARD, GC .
CARCINOGENESIS, 1993, 14 (10) :2073-2077
[7]   DIRECT ENZYMATIC DETECTION OF ENDOGENOUS OXIDATIVE BASE DAMAGE IN HUMAN LYMPHOCYTE DNA [J].
COLLINS, AR ;
DUTHIE, SJ ;
DOBSON, VL .
CARCINOGENESIS, 1993, 14 (09) :1733-1735
[8]   Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes [J].
Duthie, SJ ;
Collins, AR ;
Duthie, GG ;
Dodson, VL .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 393 (03) :223-231
[9]  
Ebert MN, 2001, NUTR CANCER, V41, P156, DOI 10.1207/S15327914NC41-1&amp
[10]  
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