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类视黄醇作为化学预防剂。

Retinoids as chemopreventive agents.

作者信息

Ralhan R, Kaur J

机构信息

Department of Biochemistry, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

J Biol Regul Homeost Agents. 2003 Jan-Mar;17(1):66-91.

Abstract

Retinoids are promising agents for cancer chemoprevention. The myriad effects of retinoids on biological processes including development, differentiation, homeostasis, carcinogenesis and apoptosis are mediated through their molecular targets, the retinoid and rexinoid receptors. Tissue specific expression patterns, ligand specificities, receptor numbers, their distinct functions and functional redundancy make retinoid signaling highly complex. The cross-talks of these receptors with cell surface receptors signaling pathways, as well as their interactions with multiple co-activators and co-repressors further add to the complexity of the pleiotropic effects of retinoids. Elucidation of retinoid signaling pathways and indepth understanding of the mechanisms that underlie the anti-proliferative and apoptotic action of retinoids has paved the way for designing synthetic retinoids for effective chemoprevention and therapy of cancer. Development of receptor selective synthetic retinoids is a major focus of molecular retinoid development. Other new avenues encompass identification of novel retinoid regulated genes, orphan-receptor ligands/functions, novel retinoid mechanisms involving receptor-independent apoptosis inducing activity and synergistic combinations with other agents for cancer prevention and therapy. This review focuses on recent advances in the understanding of molecular mechanisms underlying the action of retinoids and retinoid molecular targeting studies designed primarily to develop retinoids with reduced toxicity, while maintaining or enhancing activity in context of chemoprevention. The clinical efficacy of retinoid based chemoprevention trials is discussed.

摘要

维甲酸是癌症化学预防的有前景的药物。维甲酸对包括发育、分化、内稳态、致癌作用和细胞凋亡在内的生物过程的多种影响是通过其分子靶点——维甲酸和视黄酸X受体介导的。组织特异性表达模式、配体特异性、受体数量、它们独特的功能和功能冗余使得维甲酸信号传导高度复杂。这些受体与细胞表面受体信号通路的相互作用,以及它们与多种共激活剂和共抑制剂的相互作用,进一步增加了维甲酸多效性作用的复杂性。维甲酸信号通路的阐明以及对维甲酸抗增殖和凋亡作用机制的深入理解为设计用于有效化学预防和癌症治疗的合成维甲酸铺平了道路。受体选择性合成维甲酸的开发是分子维甲酸开发的主要重点。其他新途径包括鉴定新的维甲酸调节基因、孤儿受体配体/功能、涉及受体非依赖性凋亡诱导活性的新维甲酸机制以及与其他癌症预防和治疗药物的协同组合。本综述重点关注维甲酸作用分子机制理解方面的最新进展以及主要为开发毒性降低同时在化学预防背景下保持或增强活性的维甲酸而设计的维甲酸分子靶向研究。还讨论了基于维甲酸的化学预防试验的临床疗效。

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