Suppr超能文献

DNA甲基化作为药物设计的靶点。

DNA methylation as a target for drug design.

作者信息

Bender C M, Zingg J M, Jones P A

机构信息

Urologic Cancer Research Laboratory, USC/Norris Comprehensive Cancer Center, University of Southern California School of Medicine, Los Angeles 90033, USA.

出版信息

Pharm Res. 1998 Feb;15(2):175-87. doi: 10.1023/a:1011946030404.

Abstract

DNA methylation is essential for normal embryonic development. Distinctive genomic methylation patterns must be formed and maintained with high fidelity to ensure the inactivities of specific promoters during development. The mutagenic and epigenetic aspects of DNA methylation are especially interesting because they may lead to the inactivation of genes which are involved in human carcinogenesis. The mutagenicity of 5-Methylcytosine (5mC) and the role of promoter hypermethylation in gene silencing, particularly in cancer, suggest a clinical significance for the design of novel DNA methylation inhibitors which may be utilized to reverse the effects of DNA methylation.

摘要

DNA甲基化对于正常胚胎发育至关重要。必须以高保真度形成并维持独特的基因组甲基化模式,以确保发育过程中特定启动子的无活性。DNA甲基化的诱变和表观遗传方面尤其有趣,因为它们可能导致参与人类致癌作用的基因失活。5-甲基胞嘧啶(5mC)的诱变性以及启动子高甲基化在基因沉默中的作用,特别是在癌症中的作用,表明设计新型DNA甲基化抑制剂具有临床意义,这些抑制剂可用于逆转DNA甲基化的影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验