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山东大学学报(医学版) ›› 2008, Vol. 46 ›› Issue (12): 1158-1161.

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丙戊酸长期给药对抑制PC3细胞系裸鼠移植瘤生长的影响

高德轩 夏庆华 吕家驹 张辉   

  1. 山东大学附属省立医院泌尿外科,  济南 250021
  • 收稿日期:2007-12-24 出版日期:2008-12-16 发布日期:2009-12-16
  • 通讯作者: 吕家驹(1964- ),男,博士,教授,主要从事泌尿系统肿瘤研究。
  • 作者简介:高德轩(1976- ),男,博士,主治医师,主要从事泌尿系统肿瘤研究。

Longterm use of Valproic acid inhibits the PC3 cell line growth in nude mice in vivo

 GAO De-Han, JIA Qing-Hua, LV Jia-Ju, ZHANG Hui   

  1. Department of Urology, Provincial Hospital Affiliated to Shandong University, Jinan 250021, China
  • Received:2007-12-24 Online:2008-12-16 Published:2009-12-16

摘要:

目的 探讨丙戊酸(VPA)长期给药抑制人雄激素非依赖性前列腺癌PC3细胞裸鼠移植瘤生长的效应。方法 建立PC3细胞裸鼠移植瘤模型,实验组给予含0.4%丙戊酸钠饮用水,对照组给予纯的饮用水,给药4周,每隔2d测量肿瘤体积1次。取裸鼠移植瘤组织,免疫组化检测p21WAF/CIP和Ki67,Western blot检测p21WAF/CIP和乙酰化H3(Ac-H3)蛋白的表达,Tunnel法检测肿瘤细胞的凋亡。结果 对照组肿瘤体积大于实验组,肿瘤生长抑制率为77.27%。实验组p21WAF/CIP表达强于对照组(P<0.01),而Ki67表达弱于对照组。实验组Ac-H3表达增加(P<0.01)。实验组平均每个视野中凋亡细胞数高于对照组(P<0.01)。结论 VPA长期给药对PC3细胞移植瘤生长抑制作用明显,该作用是通过抑制细胞增殖、诱导凋亡实现的。

关键词: 前列腺肿瘤;丙戊酸;增殖;细胞凋亡;小鼠,裸

Abstract:

Objective Valproic acid (VPA) is an established drug in the long-term therapy of seizure disorders. Recently, VPA has been associated with anticancer activity, an effect thought to be produced by inhibition of cellular histone deacetylase 1.  Methods  The PC3 cell line tumor xenografts was established. Animals in the experimental group were given 0.4% VPA in their drinking water until tumors reached 5 mm in the longest dimension. At the end of day 28, tumors were harvested, whole blood was collected and serum was analyzed for VPA, liver function tests (transaminases) and complete blood count. The DNA strand breaks were identified by the terminal deoxynucleotidyltransferasemediated UTP end labeling technique using the in situ Cell Death Detection Kit. Effects of VPA on histone acetylation and p21WAF/CIP gene expression were investigated by Western blot. Ki67 and p21WAF/CIP were detected by Immunohistochemistry in tissues of PC3 cell line tumor xenografts. ResultsChronic VPA treatment resulted in statistically significant reduction of tumor xenograft growth in vivo. Tumor volumes were measured and compared using the Wilcoxon ranksum test and 2way ANOVA with posthoc testing. Animals treated with VPA showed a statistically significant decrease in tumor volume compared with controls with 77.27% growth inhibition. Treatment of xenografts with VPA induced a significant increase in levels of acetylated histone H3 and p21WAF/CIP compared with the controls (P<0.01). In the VPA treated tumors, apoptotic cell death was markedly increased compared with the control tumors (P<0.01). Ki67 expression in the control group was stronger than in the experimental group (P<0.01). Conclusion  We conclude that chronic administration of VPA results in a significant reduction in PC3 cell line tumor xenograft volume in vivo. These data provide compelling evidence that additional studies are warranted in evaluating the potential use of chronic VPA as a means of altering androgen independent prostate cancer cell growth and progression.

Key words: Prostate tumor; Valproic acid; Proliferation; Apoptosis; Mice, nude

中图分类号: 

  • R737.25
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