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维甲酸通过抑制原癌基因c-fos的转录来抑制多瘤病毒转化。

Retinoic acid suppresses polyoma virus transformation by inhibiting transcription of the c-fos proto-oncogene.

作者信息

Talmage D A, Listerud M

机构信息

Institute of Human Nutrition, Columbia University, New York, NY 10032.

出版信息

Oncogene. 1994 Dec;9(12):3557-63.

PMID:7970716
Abstract

In a previous paper, we predicted that retinoic acid suppressed polyoma virus transformation of rat F111 fibroblasts by affecting the expression of one or more genes that are involved in signalling pathways normally activated by the viral mT oncogene (Talmage & Lackey, Oncogene 7, 1837-1845, 1992). We had identified the cellular c-fos proto-oncogene as a possible candidate target for both polyoma virus mT and retinoic acid regulated expression. In this report we present the results of experiments that demonstrate that retinoic acid does indeed inhibit transcriptional transactivation of the c-fos promoter by polyoma virus, as well as by calf serum and purified serum growth factors. Further experiments demonstrate that inhibition of c-fos expression with antisense fos RNA also prevents polyoma virus induced transformation. Restoration of c-fos expression, even in the presence of retinoic acid, restored transformation, indicating that retinoic acid inhibition of c-fos expression is sufficient to explain the retinoid suppression of transformation. These results identify the c-fos proto-oncogene as a key nuclear target for mT-dependent transformation and show that the anticarcinogenic properties of retinoic acid can be brought about by inhibiting c-fos expression.

摘要

在之前的一篇论文中,我们预测视黄酸通过影响一个或多个参与通常由病毒mT癌基因激活的信号通路的基因的表达,来抑制大鼠F111成纤维细胞的多瘤病毒转化(塔尔梅奇和拉克基,《癌基因》7卷,第1837 - 1845页,1992年)。我们已确定细胞原癌基因c - fos是多瘤病毒mT和视黄酸调控表达的一个可能候选靶点。在本报告中,我们展示了实验结果,这些结果表明视黄酸确实抑制多瘤病毒以及小牛血清和纯化血清生长因子对c - fos启动子的转录反式激活。进一步的实验表明,用反义fos RNA抑制c - fos表达也能阻止多瘤病毒诱导的转化。即使在存在视黄酸的情况下,恢复c - fos表达也能恢复转化,这表明视黄酸对c - fos表达的抑制足以解释类维生素A对转化的抑制作用。这些结果确定原癌基因c - fos是mT依赖型转化的关键核靶点,并表明视黄酸的抗癌特性可通过抑制c - fos表达来实现。

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