2008
DOI: 10.1016/j.mrgentox.2008.08.001
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Naturally occurring chlorophyll derivatives inhibit aflatoxin B1-DNA adduct formation in hepatoma cells

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Cited by 35 publications
(32 citation statements)
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“…Chlorophyllin is consumed by humans for a variety of health benefits including prevention of body odour, enhanced wound healing and as a chemopreventive drug in people who are at high risk of exposure to aflatoxin B1 [30][31][32]. It has also been shown to possess anti-oxidant, anti-apoptotic and immunostimulatory effects in experimental animal models [21,33].…”
Section: ϯϭmentioning
confidence: 99%
“…Chlorophyllin is consumed by humans for a variety of health benefits including prevention of body odour, enhanced wound healing and as a chemopreventive drug in people who are at high risk of exposure to aflatoxin B1 [30][31][32]. It has also been shown to possess anti-oxidant, anti-apoptotic and immunostimulatory effects in experimental animal models [21,33].…”
Section: ϯϭmentioning
confidence: 99%
“…Another plant-based chemoprotective strategy against aflatoxin-induced cancer using chlorophyll (chl) and derivatives, such as the natural metabolites chlorophyllides (chlide) and pheophorbides (pho) [230][231][232], and the semi-synthetic chlorophyllin (chln) is attracting increased commercial and scientific interest [230,233]. The antimutagenic and antigenotoxic activities of chl have long been known, and its anti-carcinogenicity has been extensively demonstrated in experimental animals or in vitro on cancer cell-lines [231,[233][234][235][236][237][238].…”
Section: Natural and Socioeconomic Challengesmentioning
confidence: 99%
“…Another plant-based chemoprotective strategy against aflatoxin-induced cancer using chlorophyll (chl) and derivatives, such as the natural metabolites chlorophyllides (chlide) and pheophorbides (pho) [192][193][194], and the semi-synthetic chlorophyllin (chln) is attracting increased commercial and scientific interest [192,195]. The antimutagenic and antigenotoxic activities of chl have long been known, and its anti-carcinogenicity has been extensively demonstrated in experimental animals or in vitro on cancer cell-lines [193,[195][196][197][198][199][200].…”
Section: Reducing the Risk By Interfering With The Toxicity Of Aflatomentioning
confidence: 99%