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一类具有选择性抑制AP-1作用的新型维甲酸可抑制细胞增殖。

A new class of retinoids with selective inhibition of AP-1 inhibits proliferation.

作者信息

Fanjul A, Dawson M I, Hobbs P D, Jong L, Cameron J F, Harlev E, Graupner G, Lu X P, Pfahl M

机构信息

Cancer Center, La Jolla Cancer Research Foundation, La Jolla, California 92037.

出版信息

Nature. 1994 Nov 3;372(6501):107-11. doi: 10.1038/372107a0.

Abstract

Retinoids regulate many biological processes, including differentiation, morphogenesis and cell proliferation. They are also important therapeutic agents, but their clinical usefulness is limited because of side effects. Retinoid activities are mediated by specific nuclear receptors, the RARs and RXRs, which can induce transcriptional activation through specific DNA sites or by inhibiting the transcription factor AP-1 (refs 12-15), which usually mediates cell proliferation signals. Because the two types of receptor actions are mechanistically distinct, we investigated whether conformationally restricted retinoids, selective for each type of receptor action, could be identified. Here we describe a new class of retinoids that selectively inhibits AP-1 activity but does not activate transcription. These retinoids do not induce differentiation in F9 cells but inhibit effectively the proliferation of several tumour cell lines, and could thus serve as candidates for new retinoid therapeutic agents with reduced side effects.

摘要

维甲酸可调节许多生物学过程,包括分化、形态发生和细胞增殖。它们也是重要的治疗药物,但其临床应用因副作用而受到限制。维甲酸的活性由特定的核受体RARs和RXRs介导,这些受体可通过特定的DNA位点诱导转录激活,或通过抑制通常介导细胞增殖信号的转录因子AP-1(参考文献12 - 15)来实现。由于这两种受体作用机制不同,我们研究了是否能够鉴定出对每种受体作用具有选择性的构象受限维甲酸。在此,我们描述了一类新型维甲酸,它们可选择性抑制AP-1活性,但不激活转录。这些维甲酸不会诱导F9细胞分化,但能有效抑制多种肿瘤细胞系的增殖,因此有望成为副作用更小的新型维甲酸治疗药物的候选物。

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