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WAF1/CIP1基因产物p21在二乙基亚硝胺或苯巴比妥诱导的大鼠肝脏酶改变灶中的低表达。

Low expression of the WAF1/CIP1 gene product, p21, in enzyme-altered foci induced in rat liver by diethylnitrosamine or phenobarbital.

作者信息

Martens U, Lennartsson P, Högberg J, Stenius U

机构信息

Department of Toxicology, National Institute for Working Life, Solna, Sweden.

出版信息

Cancer Lett. 1996 Jun 24;104(1):21-6. doi: 10.1016/0304-3835(96)04218-8.

Abstract

The expression of the WAF1/CIP1 gene product, p21, in enzyme-altered foci (EAF) induced by diethylnitrosamine (DEN) and phenobarbital (PB) was examined. p21 expression in the nucleus of hepatocytes in EAF was decreased compared to surrounding tissue. Fifty-eight percent of all GST-P-positive EAF induced by DEN and 79% of the EAF induced by PB were p21-negative. The proportion of p21-negative EAF increased with the size of the foci and more than 90% of the largest EAF were p21-negative. p21 is a mediator of p53 signals leading to block of the cell cycle. In conjunction with previous data indicating that p53 is not induced in GST-P-positive hepatocytes isolated from EAF-bearing rats, the results of this study suggest a role for altered signaling in the G1-S check point in rat hepatocarcinogenesis.

摘要

研究了由二乙基亚硝胺(DEN)和苯巴比妥(PB)诱导的酶改变灶(EAF)中WAF1/CIP1基因产物p21的表达。与周围组织相比,EAF中肝细胞细胞核中的p21表达降低。由DEN诱导的所有GST-P阳性EAF中,58%为p21阴性;由PB诱导的EAF中,79%为p21阴性。p21阴性EAF的比例随病灶大小增加,最大的EAF中超过90%为p21阴性。p21是导致细胞周期阻滞的p53信号的介质。结合先前表明从携带EAF的大鼠中分离出的GST-P阳性肝细胞中未诱导p53的数据,本研究结果提示信号改变在大鼠肝癌发生的G1-S检查点中起作用。

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