Genistein Inhibits Cell Growth by Modulating Various Mitogen-Activated Protein Kinases and AKT in Cervical Cancer Cells

被引:56
作者
Kim, Su-Hyeon [2 ]
Kim, Su-Hyeong [2 ]
Kim, Yong-Beom [1 ,2 ]
Jeon, Yong-Tark [1 ,2 ]
Lee, Sang-Chul [3 ]
Song, Yong-Sang [1 ,2 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Obstet & Gynecol, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110744, South Korea
[3] Seoul Natl Univ, Coll Med, Inst Complementary & Integrat Med, Med Res Ctr, Seoul 110744, South Korea
[4] Seoul Natl Univ, World Class Univ, Seoul 110744, South Korea
来源
NATURAL COMPOUNDS AND THEIR ROLE IN APOPTOTIC CELL SIGNALING PATHWAYS | 2009年 / 1171卷
关键词
genistein; ERK1/2; p38; MAPK; JNK; AKT; INDUCED APOPTOSIS; PROSTATE-CANCER; KAPPA-B; PATHWAYS; SURVIVAL; P38; PHOSPHORYLATION; INDUCTION; PI3K/AKT;
D O I
10.1111/j.1749-6632.2009.04899.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genistein, a soy-derived isoflavone, inhibits growth of tumor cells from various malignancies. Here we investigated the effect of genistein on the growth of cervical cancer cells (HeLa and CaSki) and its possible mechanism. Genistein significantly suppressed cell growth of HeLa and CaSki cells at concentrations of 20 and 60 mu mol/L, respectively, for 24 h. Western blotting analysis showed that genistein reduced phosphorylation of AKT and extracellular signal-regulated kinase (ERK)-1/2 and induced phosphorylation of p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK). Moreover, inhibition of ERK1/2 activity enhanced cell growth inhibition by genistein, whereas inhibition of p38 MAPK activity rescued from genistein-mediated growth inhibition. Interestingly, inhibition of AKT activity recovered genistein-induced growth inhibition in CaSki cells but did not in HeLa cells. However, inhibition of JNK activity seemed to have little effect on cell growth inhibition by genistein. Taken together, these results suggest that genistein could inhibit cell growth by inhibiting ERK1/2 activity and activating p38 MAPK.
引用
收藏
页码:495 / 500
页数:6
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