2016
DOI: 10.1016/j.fct.2015.11.020
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New in vitro insights on a cell death pathway induced by magnolol and honokiol in aristolochic acid tubulotoxicity

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Cited by 24 publications
(15 citation statements)
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“…Since the recognition of the high nephrotoxicity and carcinogenicity of AAs, Aristolochia species have been classified as human carcinogens (International Agency for Research on Cancer, 2002); banned from many markets, they should no longer be used. Nevertheless, this potentiation warrants further studies as it could bring regulatory authorities to take into account indirect genotoxicities in their safety assessment schemes (Nachtergael et al, 2015;Bunel et al, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…Since the recognition of the high nephrotoxicity and carcinogenicity of AAs, Aristolochia species have been classified as human carcinogens (International Agency for Research on Cancer, 2002); banned from many markets, they should no longer be used. Nevertheless, this potentiation warrants further studies as it could bring regulatory authorities to take into account indirect genotoxicities in their safety assessment schemes (Nachtergael et al, 2015;Bunel et al, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…A few in vitro studies described that cells treated with AA led to generation of high amounts of reactive oxygen and nitrogen species (ROS/RNS) [122,123,124,125]. Oxidative stress therefore constitutes the primary triggering event of AA cytotoxicity and could be responsible for related DNA damage through activation of the MEK/ERK1/2 signaling pathway and depletion of intracellular glutathione (GSH) [122] resulting in cell cycle arrest in G2/M phase [123].…”
Section: Properties Of Aa and Mechanisms Of Nephrotoxicity And Carmentioning
confidence: 99%
“…HKL has various pharmacological effects, including an anti-inflammatory effect through regulation of the nuclear factor-κB (NF-κB) signaling pathway [6], an anti-tumor effect, and an anti-angiogenic effect [7], and acts as a scavenger of reactive oxygen species through NADPH oxidase (NOX)-mediated oxidative stress [8]. HKL also has a protective effect on renal diseases such as acute ischemia-reperfusion injury [9], toxic renal injury [10], and chronic tubulointerstitial fibrosis [11]. These findings suggest that HKL has cytoprotective properties against various noxious stimulations.…”
Section: Introductionmentioning
confidence: 99%