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Open AccessJournal ArticleDOI

Nuclear receptor coregulators and human disease.

David M. Lonard, +2 more
- 01 Mar 2008 - 
- Vol. 28, Iss: 5, pp 575-587
TLDR
It is substantiated that coregulators are broadly implicated in human pathological states and will be of growing future interest in clinical medicine.
Abstract
Nuclear receptor (NR) coregulators (coactivators and corepressors) are essential elements in regulating nuclear receptor-mediated transcription. In a little more than a decade since their discovery, these proteins have been studied mechanistically and reveal that the regulation of transcription is a highly controlled and complex process. Because of their central role in regulating NR-mediated transcription and in coordinating intercompartmental metabolic processes, disruptions in coregulator biology can lead to pathological states. To date, the extent to which they are involved in human disease has not been widely appreciated. In a complete literature survey, we have identified nearly 300 distinct coregulators, revealing that a great variety of enzymatic and regulatory capabilities exist for NRs to regulate transcription and other cellular events. Here, we substantiate that coregulators are broadly implicated in human pathological states and will be of growing future interest in clinical medicine.

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Novel mechanisms of glucocorticoid resistance in childhood acute lymphoblastic leukemia.

TL;DR: It is reported that PTEN activation contributes to trastuzumab's antitumor activity and PTEN deficiency is a powerful predictor for trastzumab resistance, suggesting that PI3K-targeting therapies could overcome this resistance.
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Transcriptional control of energy homeostasis by the estrogen-related receptors.

TL;DR: Recent and rapid advances in understanding the functions of the ERRs in regulating bioenergetic pathways are reviewed, with an emphasis on their roles in the specification of energetic properties required for cell- and tissue-specific functions.
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Deconstructing repression: evolving models of co-repressor action

TL;DR: Specific strategies that underlie repression events are considered — for example, those mediated by the nuclear receptor co-repressor (NCoR, also known as NCOR1) and silencing mediator of retinoic acid and thyroid hormone receptor (SMRT) co- repressor complexes — and emerging themes in gene repression are discussed.
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Nuclear Receptor Coregulators: Judges, Juries, and Executioners of Cellular Regulation

TL;DR: The implications of coregulators as versatile regulatory agents, influencing not only transcriptional initiation but also elongation, splicing, and translation are discussed, suggesting a sophisticated epigenetic regulatory scheme from which a complex and dynamic mammalian phenotype emanates.
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Structural Overview of the Nuclear Receptor Superfamily: Insights into Physiology and Therapeutics

TL;DR: The concepts and work to date underlying the development of steroidal and nonsteroidal receptor ligands are summarized, including the use of crystal structures, high-throughput screens, and rational design approaches for finding useful therapeutic molecules.
References
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Journal ArticleDOI

Molecular portraits of human breast tumours

TL;DR: Variation in gene expression patterns in a set of 65 surgical specimens of human breast tumours from 42 different individuals were characterized using complementary DNA microarrays representing 8,102 human genes, providing a distinctive molecular portrait of each tumour.
Journal ArticleDOI

A haplotype map of the human genome

John W. Belmont, +232 more
TL;DR: A public database of common variation in the human genome: more than one million single nucleotide polymorphisms for which accurate and complete genotypes have been obtained in 269 DNA samples from four populations, including ten 500-kilobase regions in which essentially all information about common DNA variation has been extracted.
Journal ArticleDOI

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

TL;DR: This study reports the first disease-causing mutations in RTT and points to abnormal epigenetic regulation as the mechanism underlying the pathogenesis of RTT.
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