2012
DOI: 10.1016/j.taap.2012.07.022
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Quercetin 3-O-methyl ether protects FL83B cells from copper induced oxidative stress through the PI3K/Akt and MAPK/Erk pathway

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Cited by 47 publications
(25 citation statements)
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“…40) Quercetin, kaempferol, and myricetin, which act as ROS scavengers, suppressed the production of ROS in cancer cells and lowered PI3K/Akt and MAPK/Erk signals. 53) These changes are thought to result in the prevention of growth and metastasis of colon and prostate cancer cells. 53) Other studies also demonstrated that antioxidant activities reduced MMP expression and tumor invasion.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…40) Quercetin, kaempferol, and myricetin, which act as ROS scavengers, suppressed the production of ROS in cancer cells and lowered PI3K/Akt and MAPK/Erk signals. 53) These changes are thought to result in the prevention of growth and metastasis of colon and prostate cancer cells. 53) Other studies also demonstrated that antioxidant activities reduced MMP expression and tumor invasion.…”
Section: Discussionmentioning
confidence: 99%
“…53) These changes are thought to result in the prevention of growth and metastasis of colon and prostate cancer cells. 53) Other studies also demonstrated that antioxidant activities reduced MMP expression and tumor invasion. [54][55][56] Based on these reports, it is likely that antioxidants in UE could greatly suppress PI3K/Akt signaling and prevent prostate cancer cell metastasis.…”
Section: Discussionmentioning
confidence: 99%
“…2,7-Dichlorodihydrofluorescein diacetate (H 2 DCFDA; Molecular Probes, Eugene, OR) can be deacetylated inside the cells and then reacted quantitatively with intracellular radicals resulting in its conversion to 2,7-dichlorofluorescent (DCF) byproduct retained within the cells (Tseng et al, 2012). Production of ROS was analyzed by flow cytometry as described previously (Hour et al, 2000).…”
Section: Quantitative Analysis Of Intracellular Rosmentioning
confidence: 99%
“…In addition, quercetin has been shown to block JNK- and p38 MAPK-related signaling triggered by oxidation, and it may regulate the expression of apoptotic downstream genes, thereby preventing apoptosis and promoting cell survival [23]. Quercetin 3-O-methyl ether has been shown to protect FL83B liver cells from Cu (2+)-induced apoptosis and mitochondrial dysfunction, and PI3K, Akt and Erk have been shown to be critically involved in the survival of such quercetin ether-treated cells [24]. We hypothesize that the regulation of PI3K and Bax by the F1 fraction may be due to its quercetin derivatives.…”
Section: Discussionmentioning
confidence: 99%