首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Nuclear lesions during rat hepatocarcinogenesis. II. Measuring the micronuclei during initiation, promotion and progression of rat hepatocarcinogenesis induced with diethylnitrosamine.
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Nuclear lesions during rat hepatocarcinogenesis. II. Measuring the micronuclei during initiation, promotion and progression of rat hepatocarcinogenesis induced with diethylnitrosamine.

机译:大鼠肝癌发生过程中的核损害。二。在二乙基亚硝胺诱导的大鼠肝癌发生的起始,促进和进展过程中测量微核。

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We reported in our companion paper the strong correlation between elevated sister-chromatid exchange (SCE) frequencies and the initiation step of rat hepatocarcinogenesis. We have also shown that SCEs return to normal values during the promotion and the progression stages. In the present study, we evaluated the clastogenic activity of diethylnitrosamine (DEN) during initiation, promotion and progression of rat hepatocarcinogenesis. We measured, at various times after DEN administration, the number of micronuclei (MN) produced by the mitotic response to partial hepatectomy. The results established that the DEN treatment induces a great number of preclastogenic lesions. In subcarcinogenic conditions (initiation alone), the number of MN expressed after partial hepatectomy remains high regardless of the time interval between the end of the DEN treatment and the operation. In this condition, the preclastogenic lesions persist for up to 1 year after the DEN administration is discontinued. Conversely, in carcinogenic conditions (initiation + promotion + progression), the number of MN expressed after partial hepatectomy decreases during the promotion and progression stages. These observations indicate that promotion and progression but not initiation are associated with the expression of persistent preclastogenic lesions, resulting in the production of chromosomally abnormal hepatocytes.
机译:我们在同伴论文中报道了姊妹染色单体交换(SCE)频率升高与大鼠肝癌发生的起始步骤之间的强相关性。我们还表明,SCE在提升和进展阶段会恢复正常值。在本研究中,我们评估了大鼠肝癌发生过程中起始,促进和进展过程中二乙基亚硝胺(DEN)的裂解活性。我们在DEN给药后的不同时间测量了部分肝切除术的有丝分裂反应所产生的微核(MN)数量。结果证实,DEN治疗可诱发大量的前破伤性病变。在亚致癌条件下(仅启动),无论DEN治疗结束与手术之间的时间间隔如何,部分肝切除术后表达的MN数量仍然很高。在这种情况下,中止DEN给药后,致裂前病变持续长达1年。相反,在致癌条件下(起始+促进+进展),部分肝切除后所表达的MN数目在促进和进展阶段减少。这些观察结果表明促进和进展而不是启动与持续的前破伤性病变的表达有关,导致染色体异常的肝细胞的产生。

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