癌变·畸变·突变 ›› 2006, Vol. 18 ›› Issue (6): 443-446.doi: 10.3969/j.issn.1004-616x.2006.06.008

• 论著 • 上一篇    下一篇

莱菔硫烷对人膀胱癌细胞周期的影响及机制研究

单毓娟;王舒然;赵秀娟;吴 坤   

  1. 哈尔滨医科大学公共卫生学院营养与食品卫生学教研室
  • 收稿日期:2005-10-31 修回日期:2006-02-16 出版日期:2006-11-30 发布日期:2006-11-30
  • 通讯作者: 吴 坤

Effects and Mechanisms of Sulforaphane on the Cell Cycle of Human Bladder Cancer Cell Lines

SHAN Yu-juan, WANG Shu-ran, ZHAO Xiu-juan,WU Kun   

  1. Department of Nutrition & Food Hygiene, Public Health College, Harbin Medical University
  • Received:2005-10-31 Revised:2006-02-16 Online:2006-11-30 Published:2006-11-30
  • Contact: WU Kun

摘要: 【摘要】 背景与目的: 探讨莱菔硫烷对人膀胱癌细胞(T24)细胞周期的影响及作用机制。材料与方法: 采用噻唑蓝(MTT)法研究不同浓度的莱菔硫烷对T24细胞生长的抑制作用并测定其半数抑制浓度(IC50);采用流式细胞仪检测莱菔硫烷对T24细胞周期的影响;采用western blot研究莱菔硫烷对T24细胞中细胞周期蛋白依赖激酶抑制剂P16和P27的表达情况。 结果: 在较低剂量范围内(≤40 μmol/L),随着作用剂量的增加,莱菔硫烷对T24细胞的生长的抑制作用也明显增强。10、20、40 μmol/L莱菔硫烷的抑制率分别为(12.5±3.95)%,(25.0±2.50)%、(50.0±5.33)%;在较高剂量(60 μmol/L~160 μmol/L)时,这种抑制作用不再呈剂量依赖性;莱菔硫烷作用72 h后的IC50值为(51.12±7.10)μmol/L;莱菔硫烷能使T24细胞周期阻滞于G0/G1期,20 μmol/L莱菔硫烷作用48 h后,在G0/G1峰之前出现凋亡峰;20 μmol/L莱菔硫烷作用于T24细胞8、12、24 h后能明显诱导P27蛋白的表达,作用早期(8 h)时能诱导P16蛋白的表达。 结论: 莱菔硫烷能抑制T24细胞生长并使该细胞周期阻断在G0/G1期,其作用机制主要是通过诱导P27蛋白及早期诱导P16蛋白来实现的。

关键词: 莱菔硫烷, 细胞周期, P16, P27

Abstract: 【ABSTRACT】 BACKGROUND &AIM: To study the effects and mechanisms of sulforaphane on T24 cell cycle. MATERIALS AND METHODS: The inhibitory effects of sulforaphane on the growth of T24 cells were investigated and its value of IC50 after 72 h incubation were measured by 3-(4,5-dimethyl-thiazolyl-2)-2,5-diphenyl tetrazolium bromide(MTT) method. The effect of sulforaphane on the T24 cell cycle was determined by flow cytometry; and expressions of P27 and P16 induced by sulforaphane were studied by western blotting analysis. RESULTS: Sulforaphane in low concentrations (≤40 μmol/L)could significantly suppress the growth of T24 cells in a dose-dependent way.The inhibitory rates for 10 μmol/L,20 μmol/L and 40 μmol/L were (12.5±3.95)%,(25.0±2.50)% and (50.0±5.33)%,respectively. High concentrations of sulforaphane(60 μmol/L-160 μmol/L), the inhibitory effects showed no obvious dose-dependency. The IC50 value of sulforaphane treatment for 72 h was (51.12±7.10)μmol/L. Sulforaphane could block T24 cell cycle at the G0/G1 phase as showed by flow cytometry. Moreover, the treatment of 20 μmol/L sulforaphane for 48 h caused the appearance of pre-G1 before G0/G1 phase. Treatments with 20 μmol/L sulforaphane for 8, 12, 24 h significantly induced the expression of P27 protein in a time-dependent manner. At early stage of sulforaphane treatment(8 h) ,the expression of P16 protein was also induced. CONCLUSION: Sulforaphane could inhibit the growth of T24 cells and block cell cycle at G0/G1 phase. The induction of P27 protein by sulforaphane mainly involved molecular mechanisms, may be including the early induction of P16 protein.

Key words: Sulforaphane, Cell cycle, P16, P27

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