Phosphoprotein levels, MAPK activities and NFκB expression are affected by fisetin

被引:91
作者
De Sousa, Roberta R. Ruela
Souza Queiroz, Karla Cristiana
Santos Souza, Ana Carolina
Gurgueira, Sonia A.
Augusto, Amanda Cavallari
Miranda, Marcio Andre
Peppelenbosch, Maikel P.
Ferreira, Carmen Verissima
Aoyama, Hiroshi
机构
[1] Univ Estadual Campinas, Dept Biochem, Campinas, SP, Brazil
[2] Univ Sao Francisco, Braganca Paulista, SP, Brazil
[3] Univ Groningen, Med Ctr, Dept Cell Biol, NL-9713 AV Groningen, Netherlands
基金
巴西圣保罗研究基金会;
关键词
fisetin; flavonoids; HL60; NF kappa B; MAPK; phosphatases;
D O I
10.1080/14756360601162063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Flavonoids, polyphenolic phytochemicals, are ubiquitous in plants and are commonly present in the human diet. They may exert diverse beneficial effects, including antioxidant and anticarcinogenic activities. The present study was designed to evaluate three biomolecules that play important roles in the apoptotic process: mitogen-activated protein kinases, protein phosphatases and NFkB, using HL60 cells treated with fisetin as an experimental model. Our results demonstrated that cells treated with fisetin presented high expression of NFkB, activation of MAPK p38 and an increase of phosphoprotein levels; inhibition of enzymes involved in redox status maintenance were also observed. Our findings reinforce the hypothesis that fisetin is likely to exert beneficial and/or toxic actions on cells not through its potential as antioxidant but rather through its modulation of protein kinase and phosphatase signaling cascades. Additionally, our results also indicate that the cellular effects of fisetin will ultimately depend on the cell type and on the extent to which they associate with the cells, either by interactions at the membrane or by uptake into the cytosol.
引用
收藏
页码:439 / 444
页数:6
相关论文
共 49 条
[1]
Relationship between flavonoid structure and inhibition of phosphatidylinositol 3-kinase: A comparison with tyrosine kinase and protein kinase C inhibition [J].
Agullo, G ;
GametPayrastre, L ;
Manenti, S ;
Viala, C ;
Remesy, C ;
Chap, H ;
Payrastre, B .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (11) :1649-1657
[2]
ISOENZYMES OF SUPEROXIDE DISMUTASE FROM WHEAT-GERM [J].
BEAUCHAMP, CO ;
FRIDOVICH, I .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 317 (01) :50-64
[3]
Violacein cytotoxicity on human blood lymphocytes and effect on phosphatases [J].
Bromberg, N ;
Justo, GZ ;
Haun, M ;
Durán, N ;
Ferreira, CV .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2005, 20 (05) :449-454
[4]
Selective activation of NF-kappa B by nerve growth factor through the neurotrophin receptor p75 [J].
Carter, BD ;
Kaltschmidt, C ;
Kaltschmidt, B ;
Offenhauser, N ;
BohmMatthaei, R ;
Baeuerle, PA ;
Barde, YA .
SCIENCE, 1996, 272 (5261) :542-545
[5]
Wogonin and fisetin induction of apoptosis through activation of caspase 3 cascade and alternative expression of p21 protein in hepatocellular carcinoma cells SK-HEP-1 [J].
Chen, YC ;
Shen, SC ;
Lee, WR ;
Lin, HY ;
Ko, CH ;
Shih, CM ;
Yang, LL .
ARCHIVES OF TOXICOLOGY, 2002, 76 (5-6) :351-359
[6]
Signal transduction by the JNK group of MAP kinases [J].
Davis, RJ .
CELL, 2000, 103 (02) :239-252
[7]
Hydrogen peroxide-induced apoptosis is CD95-independent, requires the release of mitochondria-derived reactive oxygen species and the activation of NF-κB [J].
Dumont, A ;
Hehner, SP ;
Hofmann, TG ;
Ueffing, M ;
Dröge, W ;
Schmitz, ML .
ONCOGENE, 1999, 18 (03) :747-757
[8]
EFATIMA A, 2006, IN PRESS CURR MED CH
[9]
PROTEIN-KINASE C INHIBITION BY PLANT FLAVONOIDS - KINETIC MECHANISMS AND STRUCTURE-ACTIVITY-RELATIONSHIPS [J].
FERRIOLA, PC ;
CODY, V ;
MIDDLETON, E .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (10) :1617-1624
[10]
Fotsis T, 1997, CANCER RES, V57, P2916