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白藜芦醇对人食管癌EC109细胞的生长抑制及诱导凋亡作用 被引量:4

Effects of Growth Inhibition and Apoptosis Induced by Resveratrol on Human Esophageal Carcinoma EC109 cells
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摘要 背景与目的:探讨白藜芦醇(resveratrol,Res)抑制人食管癌EC109细胞生长、诱导凋亡的作用机制。材料与方法:不同浓度Res作用EC109细胞后,采用MTT法检测Res对人食管癌EC109细胞生长的抑制作用;Hoechst33258荧光染色和倒置相差显微镜观察EC109细胞的形态学改变;流式细胞术分析细胞周期分布和细胞凋亡。结果:Res(15.62-500μmol/L)可以抑制人食管癌EC109细胞的生长,且具有时间和剂量依赖性(r=0.918、0.996,P〈0.05、0.01),500μmol/LRes作用72h后对细胞的生长抑制率可达87.43%。500μmol/LRes作用48h,荧光染色及相差显微镜下可见典型凋亡细胞形态学改变。细胞周期分析显示Res能诱导EC109细胞在S期停滞,抑制细胞DNA的合成并可明显诱导EC109细胞凋亡,凋亡率最高为62.3%。结论:Res可抑制人食管癌EC109细胞生长,引起细胞周期的S期阻滞,并诱导细胞凋亡。 BACKGROUND & AIM: To explore the effects of resveratrol in suppressing growth and inducing apoptosis in human esophageal carcinoma EC109 cells. MATERIALS AND METHODS: EC109 cells were treated with resveratrol at different concentrations,methyl thiazolyhetrazolium (MTT)assay was used to examine the effect of resveratrol on growth of EC109 cells. Hoechst 33258 staining and phase contrast microscope were used to examine the apoptosis status of EC109 cells. The cell cycle arrest and cell apeptosis were analyzed by flow cytometry. RESULTS: Resveratrol(15. 62 - 500 μmol/ L) could inhibit the growth of EC109 ceils in time-and dose-dependent manner. 500μmol/ L resveratrol had 87.43% inhibitory rate on the growth of EC109 cells at 72 h, 48 h after treatment with resveratrol, typical apeptosis was seen under phase contrast microscope and fluorescence microscope in 500 μmol/ L treatment groups. Resveratrol could arrest EC109 cells growth in S phase, inhibit DNA synthesis and induce cell apeptosis and the apeptotic ratio was 62.3%. CONCLUSION: Resveratrol could inhibit proliferation, cause S phase arrest and induce apoptosis of EC 109 cells.
出处 《癌变.畸变.突变》 CAS CSCD 2007年第4期272-275,共4页 Carcinogenesis,Teratogenesis & Mutagenesis
基金 汕头大学李嘉诚研究发展基金资助项目(2001022)
关键词 白藜芦醇 食管癌细胞 生长抑制 凋亡 resveratrol esophageal carcinoma ceils growth inhibition apoptosis
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参考文献10

  • 1Aggarwal BB,Bhardwaj A,Aggarwal RS,et al.Role of resveratrol in prevention and therapy of cancer:preclinical and clinical studies[J].Anticancer Res,2004,24(5A):2783-2840.
  • 2Kundu JK,Chun KS,Kim SO,et al.Resveratrol inhibits phorbol ester-induced cyelooxygenase-2 expression in mouse skin:MAPKs and Ap-1 as potential molecular targets[J].Biofactors,2004,21(1-4):33-39.
  • 3田雪梅,张展霞.白藜芦醇抗肿瘤作用的体外实验研究[J].中山大学学报(自然科学版),2000,39(6):64-67. 被引量:18
  • 4Pace-Asciak CR,Hahn S,Diamandis EP,et al.The red wine phenolics trans-resveratrol and quercetin block human platelet aggregation and eicosanoid synthesis:implications for protection against coronary heart disease[J].Clin Chim Acta,1995,235(5):207-219.
  • 5Aziz MH,Kumar R,Ahamd N.Cancer chemoprvention by resveratml in vitro and in vivo studies and the underlying mechanisms[J].Int Oncol,2003,23(1):17-28.
  • 6Estrov Z,Shishodia S,Faded S,et al.Resveratrol blocksinterleukin-1β-induced activation of the nuclear transcription factor NF-κB,inhibits proliferation,causes S-phase arrest,and induces apoptosis of acute myeloid leukemia cells[J].Blood,2003,102(8):987-995.
  • 7Kuwajerwala N,Cifuentes E,Gautam S,et al.Resveratrol induces prostate cancer cell entry into S phase and inhibits DNA synthesis[J].Cancer Research,2002,62(5):2488-2492.
  • 8Jiang H,Zhang LJ,Jarret K,et al.Resveratrol-induced apoptotic death in human U251 glioma cells[J].Mol Cancer Ther,2005,4(4):554-561.
  • 9Ahmad N,Adhami VM,Afaq F,et al.Resveratrol causes WAF21/p21-mediated G1-phase arrest of cell cycle and induction of apoptosis in human epidermoid carcinoma A431 cells[J].Clin Cancer Res,2001,7(5):1466-1473.
  • 10Liang YC,Tsai SH,chen L,et al.Resveratrol-induced G2 arrest through the inhibition of CDK7 and p34CDC2 kinases in colon carcinoma HT29 cells[J].Biochem Pharmacol,2003,65(7):1053-1060.

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