2018
DOI: 10.1111/jfbc.12597
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Industrial furan and its biological effects on the body systems

Abstract: Furan as a product of thermal processing is found in many foods and beverages. In vitro and in vivo genotoxicity was positive for furan, also when metabolic preconditions for the formation of Z‐2‐butene‐1,4dialdehyde (BDA), the reactive compound, was met. However, in major studies, high doses represented the genotoxic effect. Moreover, data on toxicity in different cells and organs are inconsistent. For preparing remarkable risk assessments in human, providing bioassay data is necessary. We aimed to review ava… Show more

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Cited by 11 publications
(6 citation statements)
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“…In line with furan-induced free radical production [ 35 ] (here, we show that furan induces a marked dose-related DNA guanine oxidation (approximately a 6-fold increase over endogenous levels of DNA 8-oxodG) when mammalian cells are exposed in vitro. In our cells this phenomenon seems to be independent of conversion of furan to BDA as this last one is a poor inducer of oxidative DNA damage.…”
Section: Discussionsupporting
confidence: 86%
“…In line with furan-induced free radical production [ 35 ] (here, we show that furan induces a marked dose-related DNA guanine oxidation (approximately a 6-fold increase over endogenous levels of DNA 8-oxodG) when mammalian cells are exposed in vitro. In our cells this phenomenon seems to be independent of conversion of furan to BDA as this last one is a poor inducer of oxidative DNA damage.…”
Section: Discussionsupporting
confidence: 86%
“…In animal studies, HMF is potent to undergo biotransformation into the genotoxic and mutagenic metabolite, sulphoxymethylfurfural [ 65 , 66 ], while furfural may lead to hepatotoxicity [ 67 ]. It was already found before that furan is highly potent with regard to exerting carcinogenic and mutagenic effects in rats and mice, probably due to cis-butene-1,4-dial reactive metabolites, which originate from furan oxidation by cytochrome P450 and bind to proteins and nucleosides [ 68 , 69 , 70 ]. In 1995 the IARC classified furan, together with furfural in the Group 2B, as “possibly carcinogenic to humans” [ 71 ].…”
Section: Maillard Reaction As a Source Of Bread Processing Contaminantsmentioning
confidence: 99%
“…In manufacturing industry, furan is used in the production of organic-based compounds as lacquers, resins, insecticides, stabilizers, and some pharmaceuticals [6]. In addition, furan and its derivatives are used as flavoring agents in some foods and in tobacco products [7]. Human exposure to furan is unavoidable because of its widespread persistent and extensive commercial use.…”
Section: Introductionmentioning
confidence: 99%