2018
DOI: 10.1016/j.bioelechem.2018.07.010
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The effect of quercetin on the electrical properties of model lipid membranes and human glioblastoma cells

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Cited by 21 publications
(22 citation statements)
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“…It is noteworthy that theoretical and experimental results are in line with each other within the analyzed pH range (between pH 2 and pH 10). As such, below and above this range, cells might undergo cell death, which is typical for normal and cancer cells [ 16 , 56 ]. LN-229 cells treated with either CA or FA showed an increase in positive charge at low pH and a decrease in negative charge at high pH in comparison to untreated cells.…”
Section: Discussionmentioning
confidence: 99%
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“…It is noteworthy that theoretical and experimental results are in line with each other within the analyzed pH range (between pH 2 and pH 10). As such, below and above this range, cells might undergo cell death, which is typical for normal and cancer cells [ 16 , 56 ]. LN-229 cells treated with either CA or FA showed an increase in positive charge at low pH and a decrease in negative charge at high pH in comparison to untreated cells.…”
Section: Discussionmentioning
confidence: 99%
“…Briefly, cells were grown in DMEM containing 10% fetal bovine serum, 4.5 mg/cm 3 glucose, 100 μg/cm 3 streptomycin, 100 U/cm 3 penicillin, and 2 mmol/dm 3 L-glutamine and kept in an incubator (humidified atmosphere, 5% CO 2, 37 °C). Cells reaching confluence were seeded into 96-well plates (Nunclone) in a density of 1000 cells/well and growth medium was substituted with DMEM containing various concentrations of CA (0.25–8.00 mmol/dm 3 ) or FA (0.0625–8.00 mmol/dm 3 ) and further incubated for 24 h and 48 h. After incubation, cell viability was estimated using the metabolic activity-assessing tetrazolium test (MTT assay) performed according to the method of Carmichael et al [ 62 ] described in detail in our previous work [ 16 ].…”
Section: Methodsmentioning
confidence: 99%
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“…Briefly, cell lines were grown in DMEM containing 10% fetal bovine serum, 4.5 mg/cm 3 glucose, 100 μg/cm 3 streptomycin, 100 U/cm 3 penicillin, and 2 mmol/dm 3 L-glutamine, and kept in an incubator (humidified atmosphere, 5% CO 2, 37 °C). Confluent cells were supplemented with p-CoA (0–10 mmol/dm 3 ) and incubated for 24 and 48 h. Then, all cell lines were subjected to MTT analysis performed according to the method of [50], described in detail in our previous work [51]. Based on the MTT results, two concentrations of p-CoA (5 and 8 mmol/dm 3 ) were chosen to proceed for further Z-potential examinations.…”
Section: Methodsmentioning
confidence: 99%
“…In basal cell carcinomas, MTSS1 has also been identified as a sonic hedgehog responsive gene, potentiating Gli-dependent expression [128]. Additionally, MTSS1 regulates the EGFR signaling pathway [129]. MTSS1 DNA methylation and transcriptional silencing has been reported in bladder cancer cells, with detection of a promoter activity region 276 bp upstream of the metastasis suppressor protein 1 (MTSS1) gene within a CpG island [130].…”
Section: Epigenetics In Glioblastomamentioning
confidence: 99%