Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6420
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dc.contributor.authorXue, KSen_US
dc.contributor.authorQian, Gen_US
dc.contributor.authorLin, Sen_US
dc.contributor.authorSu, Jen_US
dc.contributor.authorTang, Len_US
dc.contributor.authorGelderblom, Wentzelen_US
dc.contributor.authorRiley, RTen_US
dc.contributor.authorPhillips, TDen_US
dc.contributor.authorWang, JSen_US
dc.date.accessioned2018-07-04T07:29:08Z-
dc.date.available2018-07-04T07:29:08Z-
dc.date.issued2018-
dc.identifier.citationXue, K.S., Qian, G., Lin, S., Su, J., Tang, L., Gelderblom, W.C., Riley, R.T., Phillips, T.D. and Wang, J.S. 2018. Modulation of pre-neoplastic biomarkers induced by sequential aflatoxin B1 and fumonisin B1 exposure in F344 rats treated with UPSN clay. Food and Chemical Toxicology, 114: 316-324.en_US
dc.identifier.issn0278-6915-
dc.identifier.urihttp://hdl.handle.net/11189/6420-
dc.description.abstractPopulations consuming aflatoxin (AF) and fumonisin (FN)-contaminated foods may be at increased risk for hepatocellular carcinoma (HCC) and developmental disorders; consequently, development of intervention strategies to reduce AF/FN-induced liver disease and adverse health effects in humans could be very useful. Calcium montmorillonite clay (NovaSil) has been shown to absorb AF in vitro, in multiple animal models, as well as in human studies. In the present study, we aimed to evaluate whether uniform particle size NovaSil (UPSN) possessed an ability to modulate the co-carcinogenic potentials of aflatoxin B1 (AFB1) and fumonisin B1 (FB1) in F344 rats. Sequential treatment of FB1 following AFB1 synergistically induces preneoplastic alterations as well as liver damage, indicating that AFB1 acts as an initiator while FB1 as a promoter in the carcinogenesis model, confirming findings from previous studies. The enterosorbent agent UPSN clay at dose of up to 0.5% in diet was shown to be effective in modulating the toxicity and carcinogenicity of co-exposure to AFB1 and FB1, as demonstrated by significant reduction in number and size of hepatic GST-P+ foci, in alterations indicative of liver toxicity, and in levels of AFB1 and FB1 biomarkers.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofFood and Chemical Toxicologyen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subjectAflatoxinen_US
dc.subjectCarcinogenesisen_US
dc.subjectFumonisinen_US
dc.subjectUniform particle size NovaSilen_US
dc.titleModulation of pre-neoplastic biomarkers induced by sequential aflatoxin B1 and fumonisin B1 exposure in F344 rats treated with UPSN clay.en_US
dc.type.patentArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.fct.2018.02.048-
Appears in Collections:Journal Articles (DHET Subsidised)
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