首页> 美国卫生研究院文献>World Journal of Gastroenterology >Effect of Qi-protecting powder (Huqi San) on expression of c-jun c-fos and c-myc in diethylnitrosamine-mediated hepatocarcinogenesis
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Effect of Qi-protecting powder (Huqi San) on expression of c-jun c-fos and c-myc in diethylnitrosamine-mediated hepatocarcinogenesis

机译:护气散对二乙基亚硝胺介导的肝癌发生过程中c-junc-fos和c-myc表达的影响

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摘要

AIM: To study the inhibitory effect of Huqi San (Qi-protecting powder) on rat prehepatocarcinoma induced by diethylinitrosamine (DEN) by analyzing the mutational activation of c-fos proto-oncogene and over-expression of c-jun and c-myc oncogenes.METHODS: A Solt-Farber two-step test model of prehepatocarcinoma was induced in rats by DEN and 2-acetylaminofluorene (AAF) to investigate the modifying effects of Huqi San on the expression of c-jun, c-fos and c-myc in DEN-mediated hepatocarcinogenesis. Huqi San was made of eight medicinal herbs containing glycoprival granules, in which each milliliter contains 0.38 g crude drugs. γ-glutamy-transpeptidase-isoenzyme (γ-GTase) was determined with histochemical methods. Level of 8-hydroxydeoxyguanosine (OHdG) formed in liver and c-jun, c-fos and c-myc proto-oncogenes were detected by immunohistochemical methods.RESULTS: The level of 8-OHdG, a mark of oxidative DNA damage, was significantly decreased in the liver of rats with prehepatocarcinoma induced by DEN who received 8 g/kg body weight or 4 g/kg body weight Huqi San before (1 wk) and after DEN exposure (4 wk). Huqi San-treated rats showed a significant decrease in number of γ-GT positive foci (P < 0.001, prevention group: 4.96 ± 0.72 vs 29.46 ± 2.17; large dose therapeutic group: 7.53 ± 0.88 vs 29.46 ± 2.17). On the other hand, significant changes in expression of c-jun, c-fos and c-myc were found in Huqi San-treated rats.CONCLUSION: Activation of c-jun, c-fos and c-myc plays a crucial role in the pathogenesis of liver cancer. Huqi San can inhibit the over-expression of c-jun, c-fos and c-myc oncogenes and liver preneolastic lesions induced by DEN.
机译:目的:通过分析c-fos原癌基因的突变激活以及c-jun和c-myc癌基因的过度表达,研究护气散对二乙基initrosamine(DEN)诱导的大鼠肝癌的抑制作用。方法:用DEN和2-乙酰氨基芴(AAF)诱导大鼠肝癌前期Solt-Farber两步试验模型,研究护芪散对c-jun,c-fos和c-myc表达的修饰作用。在DEN介导的肝癌发生中的作用。护肝散由八种含糖原颗粒的药材制成,每毫升中含0.38克粗药。用组织化学方法测定γ-谷氨酰胺转肽酶-同工酶(γ-GTase)。免疫组化方法检测肝脏和c-jun,c-fos和c-myc原癌基因中形成的8-羟基脱氧鸟苷(OHdG)水平。结果:氧化DNA损伤的标志物8-OHdG水平显着升高。在DEN暴露前(1 wk)和暴露后(4 wk)分别接受8 g / kg体重或4 g / kg体重虎起散的DEN所致的肝癌前期大鼠肝脏中的胆固醇水平降低。呼气散治疗的大鼠显示出γ-GT阳性灶的数量显着减少(P <0.001,预防组:4.96±0.72对29.46±2.17;大剂量治疗组:7.53±0.88对29.46±2.17)。另一方面,在虎气散治疗的大鼠中发现了c-jun,c-fos和c-myc表达的显着变化。结论:c-jun,c-fos和c-myc的激活在其中起着至关重要的作用。肝癌的发病机理。护气散可以抑制DEN诱导的c-jun,c-fos和c-myc癌基因及肝前弹性病变的过度表达。

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