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异黄酮对前列腺癌细胞及PTEN基因的影响 被引量:2

Study of isoflavones on inhibition of prostate cancer cells and effects on PTEN gene
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摘要 目的 通过大豆异黄酮抑制前列腺癌PC 3和LNCaP细胞生长和相关基因表达的影响 ,探讨大豆异黄酮类抑制前列腺癌的机制。方法 对染料木黄酮和大豆甙元作用后的雄激素非依赖型前列腺癌 (PC 3 )、雄激素依赖型前列腺癌LNCaP细胞的存活率、细胞毒作用、细胞周期和PTEN基因的mRNA表达等进行了研究。结果 染料木黄酮和大豆甙元对PC 3、LNCaP细胞抑制效应具有时间和剂量依赖性 ,具有诱导凋亡和引起坏死效应 ;染料木黄酮能诱导PC 3和LNCaP细胞的 (PTEN)表达 ,而大豆甙元只能诱导LNCaP细胞PTEN表达。结论 PTEN基因表达的变化可能在染料木黄酮和大豆甙元抑制PC 3和LNCaP细胞中具有重要的意义。染料木黄酮和大豆甙元抑制PC 3和LNCaP细胞可能存在多种作用途径。 Objective To explore the possible mechanisms in terms of the viability of prostate cancer cells and the changes of PTEN gene expression after incubation with genistein and daidzein.Methods In the present study,LNCaP cells and PC-3 cells were exposed to varying doses of genistein and daidzein to evaluate viability and cytotoxicity by use of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium (MTT) and lactate dehydrogenase (LDH).Flow cytometry (FCM) were used to assess the cycle in LNCaP and PC-3 cells by treatments with genistein and daidzein.Reverse transcription-polymerase chain reaction(RT-PCR) was conducted to examine the level of mRNA of the tumor suppressor gene (PTEN).Results The results showed:genistein and daidzein exerted a time and dose-dependent inhibitory effects on both prostate cancer cell lines;Genistein and daidzein manifested dual cell death pathways,apoptosis and necrosis,depending on doseage.Genistein induceed expression of PTEN in PC-3 and LNCaP,and daidzein induceed expression of PTEN in LNCaP but not in PC-3. Conclusion It is indicated that the expression of PTEN may play a critical role and there maybe several pathways in the process of growth inhibition caused by genistein and daidzein.
作者 曹锋 金泰廙
出处 《卫生毒理学杂志》 CSCD 北大核心 2004年第3期141-144,共4页 Journal of Health Toxicology
基金 国家科委课题 (2 0 0 2CB51 2 90 5)
关键词 异黄酮 前列腺癌 癌细胞 PTEN基因 性激素 Genistein Daidzein PC-3 LNCaP PTEN
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  • 1Parker SL, Tong T, Bolden S, et al. Cancer Statistics. CA Cancer J Clin, 1997, 47: 5-27.
  • 2Laura S, Ramon P. PTEN: Life as a Tumor Suppressor Experimental. Cell Res, 2001, 264: 29-41.
  • 3Grunwald V, DeGraffenried L, Russel D, et al. Inhibitors of mTOR Reverse Doxorubicin Resistance Conferred by PTEN Status in Prostate Cancer Cells. Cancer Res, 2002, 62:6141-6145.
  • 4Takashi K, Teruhiro N, Takejiro K. Effect of flavonoids on cell cycle progression in prostate cancer cells. Cancer Lett, 2002,176:17-23.
  • 5Kazuhiro S, Hidekazu K, Hiroshi M. Genistein, a soy isoflavone, induces glutathione peroxidase in the human prostate cancer cell lines LNCaP and PC-3. Int. J Cancer,2002, 99: 846-852.
  • 6Kazuko S. Synergistic effects of thearubigin and genistein on human prostate tumor cell (PC-3) growth via cell cycle arrest.Cancer Lett, 2000, 151: 103-109.
  • 7Davis JN, Singh B, Bhuiyan M, et al. Genistein-induced upregulation of p21WAF1, downregulation of cyclin B, and induction of apoptosis in prostate cancer cells. Nutr. Cancer,1998, 32:123-131.
  • 8Hedlund TE, Johannes WU, Miller GJ. Soy isoflavonoid equol modulates the growth of benign and malignant prostatic epithelial cells in vitro. Prostate, 2003, 54:68-78.
  • 9Rice L, Samedi V G, Medrano TA, et al. Mechanisms of the Growth Inhibitory Effects of the Isoflavonoid Biochanin A on LNCaP Cells and Xenografts. Prostate, 2002, 52: 201-212.
  • 10Kollara A, Diamandis EP, Brown TJ. Secretion of endogenous kallikreins 2 and 3 by androgen receptor-transfected PC-3prostate eaffcer cells. The Journal of Steroid Biochemistry and Mol Biol, 2003, 5:493-502.

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