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首页> 外文期刊>Journal of gastroenterology and hepatology >Echographic detection of diethylnitrosamine-induced liver tumors in rats and the effect of the intratumoral injection of an inhibitor of c-Jun N-terminal kinase.
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Echographic detection of diethylnitrosamine-induced liver tumors in rats and the effect of the intratumoral injection of an inhibitor of c-Jun N-terminal kinase.

机译:超声检测大鼠的二乙基亚硝胺诱导的肝肿瘤以及瘤内注射c-Jun N端激酶抑制剂的作用。

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摘要

BACKGROUND AND AIM: There have so far been few reports describing echographic studies of chemically-induced carcinogenesis in rodent livers. Using echography, we observed diethylnitrosamine-induced liver tumors in rats and examined the effect of an intratumoral injection of an inhibitor of c-Jun N-terminal kinase. METHODS: Male Wistar rats were given 100 ppm of diethylnitrosamine for 6 weeks and their liver nodules were examined by echography weekly. The size of the nodules was measured and they were examined histologically. The effect of SP600125, an inhibitor of c-Jun N-terminal kinase, on the growth of rat hepatoma cell line McA-RH7777 was tested in vitro. Thereafter, SP600125 was injected into the liver nodules under echographic guidance in vivo and the changes in the proliferating cell nuclear antigen expression and size of the nodules were examined. RESULTS: The four distinct lobes of rat livers were clearly observed by transabdominal echography. The nodules in the livers were first detected 6 weeks after the treatment began, when they were as small as 1.6 mm in diameter. The nodules thereafter became more malignant histologically as they grew larger than 4 mm. SP600125 decreased the expression of proliferating cell nuclear antigen and the growth of McA-RH7777 cells. After SP600125 was injected in vivo, the proliferating cell nuclear antigen level and the growth rate of the rat liver nodules all significantly decreased. CONCLUSIONS: Our results indicate that echography is quite useful for follow-up studies of liver carcinogenesis in rats, and c-Jun N-terminal kinase might be another therapeutic target in liver neoplasms.
机译:背景与目的:迄今为止,很少有报道描述在啮齿动物肝脏中化学诱导的致癌作用的超声检查研究。使用回波描记术,我们观察了大鼠中二乙基亚硝胺诱导的肝肿瘤,并检查了肿瘤内注射c-Jun N-末端激酶抑制剂的效果。方法:雄性Wistar大鼠给予100 ppm的二乙基亚硝胺6周,并每周通过超声检查检查其肝结节。测量结节的大小,并进行组织学检查。体外测试了c-Jun N端激酶抑制剂SP600125对大鼠肝癌细胞系McA-RH7777生长的影响。此后,在体内超声检查指导下将SP600125注入肝结节,并检查增殖细胞核抗原表达和结节大小的变化。结果:经腹部超声检查清楚地观察到大鼠肝脏的四个不同叶。开始治疗后6周,当直径小至1.6毫米时,首先发现了肝脏中的结节。此后,结节大于4 mm时在组织学上变得更加恶性。 SP600125降低了增殖细胞核抗原的表达和McA-RH7777细胞的生长。体内注射SP600125后,增殖细胞核抗原水平和大鼠肝结节的生长速度均明显降低。结论:我们的结果表明,回波描记术对于大鼠肝癌发生的后续研究非常有用,而c-Jun N端激酶可能是肝肿瘤的另一个治疗靶标。

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