Induction of apoptosis in breast cancer cells MDA-MB-231 by genistein

被引:264
作者
Li, YW [1 ]
Upadhyay, S [1 ]
Bhuiyan, M [1 ]
Sarkar, FH [1 ]
机构
[1] Wayne State Univ, Dept Pathol, Sch Med, Karmanos Canc Inst, Detroit, MI 48201 USA
关键词
genistein; apoptosis; breast cancer cells;
D O I
10.1038/sj.onc.1202650
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer is the most common cancer among American women, whereas Asian women, who consume a traditional diet high in soy products, have a relatively low incidence, Genistein is a prominent isoflavonoid in soy products and has been proposed as the agent responsible for lowering the rate of breast cancer in Asian women. We investigated the effects of genistein on cell growth and apoptosis-related gene expression in breast cancer cells MDA-MB-231. We found upregulation of Bar and p21(WAF1) expressions and downregulation of Bcl-2 and p53 expression in genistein-treated cells. Furthermore, DNA ladder formation, CPP32 activation, and PARP cleavage were observed after treatment with genistein, indicating apoptotic cell deaths. Flow cytometry with 7-amino actinomycin D staining showed that the number of apoptotic cells increased with longer treatment of genistein. From these results, we conclude that genistein inhibits the growth of MDA-MB-231 breast cancer cells, regulates the expression of apoptosis-related genes, and induces apoptosis through a p53-independent pathway. The up-regulation of Bar and p21(WAF1) may be the molecular mechanisms by which genistein induces apoptosis, however, further definitive studies are needed. These results suggest that genistein may be a potentially effective chemopreventive or therapeutic agent against breast cancer.
引用
收藏
页码:3166 / 3172
页数:7
相关论文
共 47 条
  • [31] Salomons GS, 1997, INT J CANCER, V71, P959, DOI 10.1002/(SICI)1097-0215(19970611)71:6<959::AID-IJC9>3.0.CO
  • [32] 2-X
  • [33] SANO H, 1995, CANCER RES, V55, P3785
  • [34] SEDLAK ML, 1995, P NATL ACAD SCI USA, V92, P7934
  • [35] Shao ZM, 1998, J CELL BIOCHEM, V69, P44, DOI 10.1002/(SICI)1097-4644(19980401)69:1<44::AID-JCB5>3.3.CO
  • [36] 2-B
  • [37] THE NATURAL TYROSINE KINASE INHIBITOR GENISTEIN PRODUCES CELL-CYCLE ARREST AND APOPTOSIS IN JURKAT T-LEUKEMIA CELLS
    SPINOZZI, F
    PAGLIACCI, MC
    MIGLIORATI, G
    MORACA, R
    GRIGNANI, F
    RICCARDI, C
    NICOLETTI, I
    [J]. LEUKEMIA RESEARCH, 1994, 18 (06) : 431 - 439
  • [38] YAMA/CPP32-BETA, A MAMMALIAN HOMOLOG OF CED-3, IS A CRMA-INHIBITABLE PROTEASE THAT CLEAVES THE DEATH SUBSTRATE POLY(ADP-RIBOSE) POLYMERASE
    TEWARI, M
    QUAN, LT
    OROURKE, K
    DESNOYERS, S
    ZENG, Z
    BEIDLER, DR
    POIRIER, GG
    SALVESEN, GS
    DIXIT, VM
    [J]. CELL, 1995, 81 (05) : 801 - 809
  • [39] BIOTHERAPY OF B-CELL PRECURSOR LEUKEMIA BY TARGETING GENISTEIN TO CD19-ASSOCIATED TYROSINE KINASES
    UCKUN, FM
    EVANS, WE
    FORSYTH, CJ
    WADDICK, KG
    AHLGREN, LT
    CHELSTROM, LM
    BURKHARDT, A
    BOLEN, J
    MYERS, DE
    [J]. SCIENCE, 1995, 267 (5199) : 886 - 891
  • [40] SIGNAL TRANSDUCTION BY RECEPTORS WITH TYROSINE KINASE-ACTIVITY
    ULLRICH, A
    SCHLESSINGER, J
    [J]. CELL, 1990, 61 (02) : 203 - 212