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大鼠肝癌发生过程中的核病变。II. 测量二乙基亚硝胺诱导的大鼠肝癌发生起始、促进和进展过程中的微核。

Nuclear lesions during rat hepatocarcinogenesis. II. Measuring the micronuclei during initiation, promotion and progression of rat hepatocarcinogenesis induced with diethylnitrosamine.

作者信息

Herens C, Massart S, Bouzahzah B, Koulischer L, Barbason H

机构信息

Department of Genetics, University of Liège, CHU, Belgium.

出版信息

Mutat Res. 1995 Jul;329(2):161-71. doi: 10.1016/0027-5107(95)00025-e.

Abstract

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.

摘要

我们在姊妹篇论文中报道了姐妹染色单体交换(SCE)频率升高与大鼠肝癌发生起始步骤之间的强相关性。我们还表明,SCE在促进和进展阶段恢复到正常水平。在本研究中,我们评估了二乙基亚硝胺(DEN)在大鼠肝癌发生起始、促进和进展过程中的致断裂活性。在给予DEN后的不同时间,我们测量了部分肝切除术后有丝分裂反应产生的微核(MN)数量。结果表明,DEN处理诱导了大量前致断裂性损伤。在亚致癌条件下(仅起始阶段),无论DEN处理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,前致断裂性损伤在停止给予DEN后持续长达1年。相反,在致癌条件下(起始+促进+进展),部分肝切除术后表达的MN数量在促进和进展阶段减少。这些观察结果表明,促进和进展而非起始与持续性前致断裂性损伤的表达相关,导致染色体异常肝细胞的产生。

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