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核激素受体共抑制因子

Nuclear hormone receptor co-repressors.

作者信息

Baniahmad Aria

机构信息

Institute of Human Genetics and Anthropology, Medical Department, Friedrich-Schiller-University, 07740 Jena, Germany.

出版信息

J Steroid Biochem Mol Biol. 2005 Feb;93(2-5):89-97. doi: 10.1016/j.jsbmb.2004.12.012. Epub 2005 Jan 24.

Abstract

Gene silencing is an essential transcriptional regulatory process. Co-repressors mediate gene repression through their recruitment by DNA bound transcriptional silencer proteins. Co-repressors repress gene expression through several mechanisms, mostly investigated on the level of chromatin. Lack or aberrant gene silencing is associated with many defects both on cellular and organismic level. Several human diseases are based on dysregulated co-repressor binding to transcriptional silencers indicating that co-repressor recruitment and the strength of gene silencing must be under strict control. In line with that gene silencing is important for animal development, cellular proliferation and transformation. Co-repressors play also a major role in the treatment of hormone-dependent growing cancers, such as for breast and prostate cancer therapy. The molecular basis of anti-hormone therapy lies in the recruitment of co-repressors to the estrogen or androgen receptors, respectively, which leads to their inactivation and to inhibition of cancer growth. The molecular mechanisms of selected topics are summarized here.

摘要

基因沉默是一种重要的转录调控过程。共抑制因子通过与结合在DNA上的转录沉默蛋白结合而介导基因抑制。共抑制因子通过多种机制抑制基因表达,其中大部分是在染色质水平上进行研究的。基因沉默的缺失或异常与细胞和机体水平上的许多缺陷相关。几种人类疾病是基于共抑制因子与转录沉默因子的结合失调,这表明共抑制因子的募集和基因沉默的强度必须受到严格控制。与此一致的是,基因沉默对动物发育、细胞增殖和转化很重要。共抑制因子在激素依赖性生长癌症的治疗中也起着重要作用,例如在乳腺癌和前列腺癌治疗中。抗激素治疗的分子基础在于分别将共抑制因子募集到雌激素或雄激素受体上,这会导致它们失活并抑制癌症生长。本文总结了所选主题的分子机制。

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