南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (04): 453-455.

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抑癌基因p53诱导Wnt通路抑制因子sFRP的表达

腊蕾1, 饶进军2, 吴曙光1   

  1. 1. 第一军医大学药物研究所, 广东, 广州, 510515;
    2. 第一军医大学分校药理教研室, 广东, 广州, 510315
  • 出版日期:2004-04-20 发布日期:2004-04-20
  • 基金资助:
    收稿日期:2003-9-18。
    作者简介:腊蕾(1972-),女,现读于第一军医大免疫药理学学博士,药师,电话:020-61648167,E-mail:LaLei88@163.com

Anti-oncogene p53-induced expression of secreted frizzled-related protein,a Wnt signaling inhibitor

LA Lei1, RAO Jin-jun2, WU Shu-guang1   

  1. 1. 第一军医大学药物研究所, 广东, 广州, 510515;
    2. 第一军医大学分校药理教研室, 广东, 广州, 510315
  • Online:2004-04-20 Published:2004-04-20

摘要: 目的 研究p53对Wnt通路抑制因子sFRP表达的调节作用。方法 将携带p53基因的复制缺陷型腺病毒载体(Adp53)导入到p53缺失的人肝癌细胞株Hep3B中,以流式细胞术检测Adp53转基因情况,以RT-PCR技术检测p53对sFRP表达的调节作用。结果 sFRP mRNA水平在转染p53 20 h后即有明显升高,其中以32 h达最高水平,随后逐渐降低。量效关系研究表明在转染剂量为0.05、0.5、5、50 pfu/cell的Adp53 sFRP mRNA表达均有显著增高,尤以5 pfu/cell时表达水平最高。结论 p53能明显诱导Wnt通路抑制剂sFRP的mRNA表达。

Abstract: Objective To investigate the effects of anti-oncogene p53 on the expression of secreted frizzled-related protein (sFRP), a Wnt pathway inhibitor. Methods Human hepatocarcinoma Hep3B cells were transfected with a replication-defective adenovirus encoding p53 (Adp53), and Adp53 transgene expression was measured by fluorescence-activated cell sorting (FACS) and sFRP mRNA expression detected by reverse transcriptional (RT)-PCR. Results sFRP mRNA expression in Hep3B cells was potentiated 20 h after the transfection with Adp53, reaching the peak level at 32 h. Dose-effect studies revealed that Adp53 at the doses of 0.5, 5 and 50 pfu/cell could promote the expression of sFRP mRNA, with the highest expression occurred with the dose of 5 pfu/cell. Conclusion Ectogenetic p53 promotes mRNA expression of Wnt signaling pathway inhibitor sFRP in Hep3B cells.

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