Corbiere Cecile, Liagre Bertrand, Bianchi Arnaud, Bordji Karim, Dauça Michel, Netter Patrick, Beneytout Jean-Louis
Laboratoire de Biochimie, UPRES EA 1085, Faculté de Pharmacie, 87025 Limoges Cedex, France.
Int J Oncol. 2003 Apr;22(4):899-905.
Regulation of growth arrest and apoptosis are, in part, controlled by the tumor suppressor p53 after its phosphorylation which causes a determinant role in its functional activation. Moreover, PPAR regulate many functions such as proliferation and apoptosis. We compared the biological activity of diosgenin with hecogenin and tigogenin, plant steroids structurally close to diosgenin, on proliferation rate, cell cycle distribution and apoptosis in human 1547 osteosarcoma cells. We found that all three molecules have an antiproliferative effect but gel shift analysis demonstrated that none of the plant steroids transactivated PPAR in human 1547 osteosarcoma cells whereas these molecules induced NF-kappaB binding to DNA. Although these plant steroids have a very close structure, only diosgenin caused a cell cycle arrest associated with strong apoptosis. This biological action seems correlated with a large increase of p53 protein expression. This fact was showed by immunofluorescence analysis which confirmed that diosgenin strongly enhanced the activation of p53 in contrast to hecogenin and tigogenin actions.
生长停滞和细胞凋亡的调节部分受肿瘤抑制因子p53磷酸化后的控制,这在其功能激活中起决定性作用。此外,过氧化物酶体增殖物激活受体(PPAR)调节许多功能,如增殖和细胞凋亡。我们比较了薯蓣皂苷元与海柯皂苷元和替告皂苷元(结构上与薯蓣皂苷元相近的植物甾体)对人1547骨肉瘤细胞增殖率、细胞周期分布和细胞凋亡的生物学活性。我们发现这三种分子都有抗增殖作用,但凝胶迁移分析表明,这些植物甾体在人1547骨肉瘤细胞中均未激活PPAR,而这些分子可诱导核因子κB(NF-κB)与DNA结合。尽管这些植物甾体结构非常相似,但只有薯蓣皂苷元导致细胞周期停滞并伴有强烈的细胞凋亡。这种生物学作用似乎与p53蛋白表达的大幅增加相关。免疫荧光分析证实了这一事实,与海柯皂苷元和替告皂苷元的作用相反,薯蓣皂苷元强烈增强了p53的激活。