首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Enhancement of transformed foci and induction of prostaglandins in Balb/c 3T3 cells by palytoxin: in vitro model reproduces carcinogenic responses in animal models regarding the inhibitory effect of indomethacin and reversal of indomethacin's effect
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Enhancement of transformed foci and induction of prostaglandins in Balb/c 3T3 cells by palytoxin: in vitro model reproduces carcinogenic responses in animal models regarding the inhibitory effect of indomethacin and reversal of indomethacin's effect

机译:通过palytoxin增强Balb / c 3T3细胞中转化灶的表达和前列腺素的诱导:体外模型在动物模型中重现有关吲哚美辛的抑制作用和吲哚美辛作用的逆转的致癌反应

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摘要

Cell transforming activity of palytoxin, a non-TPA type tumor-promoter, was investigated with the two-stage transformation assay using Balb/c 3T3 cells. Palytoxin showed potent promoting activity; treatment at 1.9 pM or more increased the number of transformed foci after initiation by 3-methylcholanthrene (MCA). Determination of prostaglandin (PG) E2 and PGF(2alpha) concentrations in the culture medium revealed that palytoxin (1.9-3.7 pM for 24 h) stimulated the production of PG in Balb/c 3T3 cells (the concentration reached 3-4 microM), and treatment with PGE2 or PGF(2alpha) itself increased the number of transformed foci of Balb/c 3T3 cells after initiation by MCA. Neither palytoxin nor PGs showed initiating activity. Indomethacin suppressed the promoting activity of palytoxin, but not that of PGE2 and PGF(2alpha). Interestingly, concomitant treatment with PGE2 or PGF(2alpha) in addition to indomethacin markedly reversed the suppressive effect of indomethacin. These findings indicated that the in vitro transformation model could reproduce experiments that have been performed in animal models regarding the inhibitory effect of indomethacin on carcinogenic responses and reversal of indomethacin's effect by exogenous prostaglandin and, therefore, may provide insight into molecular modes of action of palytoxin. In the present study, palytoxin also induced prostaglandin synthesis, and therefore, the Balb/c 3T3 cell model should provide insight into the molecular mechanism by which palytoxin regulates prostaglandin biosynthesis.
机译:使用Balb / c 3T3细胞通过两阶段转化试验研究了非TPA型肿瘤促进剂palytoxin的细胞转化活性。 Palytoxin显示出有效的促进活性; 1.9 pM或更高的浓度处理可以增加3-甲基胆甾烯(MCA)引发后转化灶的数量。测定培养基中前列腺素(PG)E2和PGF(2alpha)的浓度表明,草毒素(1.9-3.7 pM持续24 h)刺激了Balb / c 3T3细胞中PG的产生(浓度达到3-4 microM), PGE2或PGF(2alpha)本身的处理增加了MCA启动后Balb / c 3T3细胞转化灶的数量。谷胱甘肽毒素和PG均未显示出启动活性。消炎痛抑制Ply2,而不是PGE2和PGF(2alpha)的促进活性。有趣的是,除消炎痛外,同时用PGE2或PGF(2alpha)进行治疗显着逆转了消炎痛的抑制作用。这些发现表明,体外转化模型可以重现在动物模型中进行的有关吲哚美辛对外源性前列腺素的致癌反应和吲哚美辛作用的抑制作用的抑制作用的实验,因此,可以提供深入研究palytoxin作用的分子模式。在本研究中,palytoxin还诱导了前列腺素的合成,因此,Balb / c 3T3细胞模型应该提供深入了解palytoxin调节前列腺素生物合成的分子机制。

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