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综述:在大鼠肝癌发生模型中探索抗癌剂——关注硒和他汀类药物。

Review: Exploring anticarcinogenic agents in a rat hepatocarcinogenesis model--focus on selenium and statins.

机构信息

Division of Clinical Pharmacology C1-68, Department of Laboratory Medicine, Karolinska University Hospital, Huddinge, Karolinska Institute, 141 86, Stockholm, Sweden.

出版信息

In Vivo. 2012 Jul-Aug;26(4):527-35.

Abstract

In this review, we describe a rat model for chemically induced hepatocarcinogenesis that can be used for studying the anticarcinogenic effects of different agents. In this model the process of carcinogenesis can be followed through the different stages of initiation, promotion and progression. Mechanistic studies of anticarcinogenic agents can be carried out and two examples are given by studies on selenium and statins as anticarcinogenic agents. These compounds suppress cancer via different mechanisms. In the case of selenium the induction of glutathione peroxidase 4 and inhibition of lipid peroxidation might be a part of the anticarcinogenic effect. In the case of statins, the inhibition of ubiquinone synthesis, as well as of the selenium-containing enzyme thioredoxin reductase 1 (TrxR1) might explain their anticarcinogenic properties. Interestingly, also in the case of selenium the inhibited carcinogenesis was associated with reduced TrxR activity, indicating an important role for this enzyme in carcinogenesis.

摘要

在这篇综述中,我们描述了一种化学诱导肝癌发生的大鼠模型,可用于研究不同药物的抗癌作用。在该模型中,致癌过程可以通过起始、促进和进展的不同阶段进行跟踪。可以对抗癌药物的机制进行研究,并通过对硒和他汀类药物作为抗癌药物的研究给出两个例子。这些化合物通过不同的机制抑制癌症。在硒的情况下,诱导谷胱甘肽过氧化物酶 4 和抑制脂质过氧化可能是抗癌作用的一部分。在他汀类药物的情况下,抑制泛醌合成以及含硒酶硫氧还蛋白还原酶 1 (TrxR1)的抑制可能解释了它们的抗癌特性。有趣的是,即使在硒的情况下,被抑制的致癌作用也与 TrxR 活性的降低有关,这表明该酶在致癌作用中起着重要作用。

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