2015
DOI: 10.1016/j.tiv.2015.09.029
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Antigenotoxic, anti-photogenotoxic and antioxidant activities of natural naphthoquinone shikonin and acetylshikonin and Arnebia euchroma callus extracts evaluated by the umu-test and EPR method

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Cited by 32 publications
(20 citation statements)
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“…Although EXTs revealed an antioxidative potential, the increase in the 4NQO-induced genotoxicity was observed. Previously, it was reported that antioxidants did not exhibit a protective effect against 4NQO [36] or an increase in the genotoxicity [37]. This could be explained by the fact that the oxidative stress is not the only possible mechanism of action of this mutagen.…”
Section: Discussionmentioning
confidence: 96%
“…Although EXTs revealed an antioxidative potential, the increase in the 4NQO-induced genotoxicity was observed. Previously, it was reported that antioxidants did not exhibit a protective effect against 4NQO [36] or an increase in the genotoxicity [37]. This could be explained by the fact that the oxidative stress is not the only possible mechanism of action of this mutagen.…”
Section: Discussionmentioning
confidence: 96%
“…Acetylshikonin, a major bioactive component of leaf extracts of L . erythrorhizon root (Gwon et al, 2012; Pietrosiuk et al, 2006; Zhao, Wu, Wu, Zhao, & Chen, 2016), exhibits various pharmacological activities including induction of autophagy, anti‐oxidative, anti‐inflammatory, anti‐proliferative, anti‐fertility, and anticancer effects (He, Li, Su, Huang, & Zhu, 2016; Pietrosiuk et al, 2006; Skrzypczak et al, 2015; Wu et al, 2011; Zeng, Zhu, & Su, 2018). Several studies have demonstrated that the compound inhibits growth of a variety of cancers, including colorectal, breast, liver, medullary thyroid carcinoma, pancreas, melanoma, and gastric cancers (Cho & Choi, 2015; Hasenoehrl et al, 2017; Kim, Lee, Park, & Choi, 2016; Kretschmer et al, 2012; Park et al, 2017; Vukic et al, 2017; Zeng, Liu, & Zhou, 2009).…”
Section: Discussionmentioning
confidence: 99%
“…Three different concentrations of extracts (25, 50 and 100 μg/mL, chosen starting dilutions from the highest concentration of the value 1/10 lower than the concentration used to evaluate the eventual genotoxic effect, 1000 μg/mL) were pre-incubated for 2 h at 37˚C with known genotoxins, 4-NQO and 2-AA in the absence and presence of metabolic PLOS ONE activation S9, respectively. The percentage of antimutagenicity was calculated [31]:…”
Section: Umu Testmentioning
confidence: 99%