2003
DOI: 10.1016/s0041-008x(03)00254-0
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Evaluation of genotoxic risk and oxidative DNA damage in mammalian cells exposed to mycotoxins, patulin and citrinin

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Cited by 182 publications
(87 citation statements)
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“…Patulin is stable in an acidic environment and is not destroyed during thermal processing; therefore, it may exist in juices even after processing [5,6]. Patulin has been classified as a group 3 carcinogen, which means that there is no evidence of carcinogenicity in humans and that data in experimental animals on carcinogenesis is sparse [7], although a few studies have reported patulin to be both teratogenic and genotoxic [8,9]. Patulin toxicity is believed to be due to its reactions with sulphydryl groups, proteins and amino acids in the plasma membrane [10,11].…”
Section: Introductionmentioning
confidence: 99%
“…Patulin is stable in an acidic environment and is not destroyed during thermal processing; therefore, it may exist in juices even after processing [5,6]. Patulin has been classified as a group 3 carcinogen, which means that there is no evidence of carcinogenicity in humans and that data in experimental animals on carcinogenesis is sparse [7], although a few studies have reported patulin to be both teratogenic and genotoxic [8,9]. Patulin toxicity is believed to be due to its reactions with sulphydryl groups, proteins and amino acids in the plasma membrane [10,11].…”
Section: Introductionmentioning
confidence: 99%
“…There are dozens of reports showing that high doses of citrinin act as a cytotoxin and nephrotoxin (Ambrose and DeEds, 1946;Friis et al, 1969;Krogh et al, 1970;Scott et al, 1972;Nelson et al, 1985;Aleo et al, 1991;Chagas et al, 1992aChagas et al, , 1992bDa Lozzo et al, 1998;Abramson et al, 2001;Liu et al, 2003;Yu et al, 2006;Bouslimi et al, 2008). In contrast, our results indicate a new role/implication for low-dose citrinin in health and disease.…”
Section: Discussionmentioning
confidence: 41%
“…The toxic effects of citrinin observed in vitro were reported in HEK 293 cells (Liu et al, 2005), mouse embryonic stem cells (Chan, 2008), CHO-K1 cells (Liu et al, 2003), and V79 cells (Pfeiffer et al, 1998). These studies used 10-100 μM citrinin to assess the toxic effects, with lower concentrations having no signifi cant effect (Pfeiffer et al, 1998).…”
Section: Discussionmentioning
confidence: 99%
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“…CTN has yielded both negative and positive scores in Ames tests and in in vitro comet assays [108][109][110][111] as well as positive scores in in vitro and in vivo chromosomal aberration tests 108,[112][113][114] . When groups of five male F344 rats were orally administered 40 and 20 mg CTN /10 mL/kg/day by gavage for two days there were no significant differences in tail intensity and tail length in comet assays of the CTN-treated groups.…”
Section: Genotoxicity and Carcinogenicity Testsmentioning
confidence: 99%