2011
DOI: 10.1016/j.phrs.2010.11.005
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Allyl-, butyl- and phenylethyl-isothiocyanate activate Nrf2 in cultured fibroblasts

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Cited by 83 publications
(61 citation statements)
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“…For example, SF, PEITC, BITC, and AITC were generally shown to increase transcript and protein abundance of γ-GCS, HO-1, and NQO1 when applied to NIH3T3 fibroblast cells at the lowest dose tested (5 µM) [74]. A similar study using the same four ITCs and mouse skin papilloma cells found analogous results, with significant increases in NQO1 and GST activity.…”
Section: In Vitro Evidence Of Are-dependent Gene Induction By Itcsmentioning
confidence: 90%
“…For example, SF, PEITC, BITC, and AITC were generally shown to increase transcript and protein abundance of γ-GCS, HO-1, and NQO1 when applied to NIH3T3 fibroblast cells at the lowest dose tested (5 µM) [74]. A similar study using the same four ITCs and mouse skin papilloma cells found analogous results, with significant increases in NQO1 and GST activity.…”
Section: In Vitro Evidence Of Are-dependent Gene Induction By Itcsmentioning
confidence: 90%
“…Although NIH 3T3 cells do not fully reflect the cellular metabolism of cardiomyocytes, they comprise a valuable experimental tool to screen for Nrf2-inducing activity of plant bioactives. 55 All cell culture plasticware was purchased from Sarstedt (Nuembrecht, Germany) unless otherwise stated. For cell culture experiments, the olive oil phenolics were dissolved in dimethylsulfoxide (DMSO; Carl Roth, Karlsruhe, Germany), and stock solutions were stored at -80°C until usage.…”
Section: Rna Isolation and Real-time Quantitative Rt-pcrmentioning
confidence: 99%
“…4). It has been stated in the literature that kinases, including ERK1/2 and JNK, activate the transcription factor Nrf2 via phosphorylation, resulting in the stabilization of Nrf2 and, consequently, in its dissociation from its inhibitor protein Keap1 [30,34,42,43]. By applying the small-molecule inhibitors of the abovementioned kinases to our GER+MYR-treated HT-29 cells, we also detected changes in HO-1 gene expression (Fig.…”
Section: Discussionmentioning
confidence: 56%
“…The nuclear cell extracts, for Nrf2 detection, and the whole cell extracts, for HO-1 and ERK1/2/p-ERK1/2, JNK/p-JNK and p38/p-p38 detection, were prepared as described previously [30,31]. For the nuclear extracts, the cells were treated for 6 h with 25 μmol/L GER, 25 μmol/L GER plus 1.6 μl of MYR, 25 μmol/L SIN, 25 μmol/L SIN plus 1.6 μl of MYR, 25 μmol/L GRA, 25 μmol/L GRA plus 1.6 μl of MYR, 25 μmol/L GST and 25 μmol/L GST plus 1.6 μl of MYR or SFN (as a positive control).…”
Section: Western Blottingmentioning
confidence: 99%