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乳腺癌中的BAF复合物与糖皮质激素受体

BAF Complexes and the Glucocorticoid Receptor in Breast Cancers.

作者信息

Dietrich Nicholas, Hoffman Jackson A, Archer Trevor K

机构信息

Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, North Carolina, United States.

出版信息

Curr Opin Endocr Metab Res. 2020 Dec;15:8-14. doi: 10.1016/j.coemr.2020.07.001. Epub 2020 Sep 6.

DOI:10.1016/j.coemr.2020.07.001
PMID:35128145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8813045/
Abstract

Breast cancers are a diverse group of diseases and are often characterized by their expression of receptors for hormones such as estrogen and progesterone. Recently another steroid hormone receptor, the glucocorticoid receptor (GR) has been shown to be a key player in breast cancer progression, metastasis, and treatment. These receptors bind to chromatin to elicit transcriptional changes within cells, which are often inhibited by the structure of chromatin itself. Chromatin remodeling proteins, such as Brahma-related gene 1 (BRG1), function to overcome this physical inhibition of transcription factor function and have been linked to many cancers including breast cancer. Recent efforts to understand the interactions of BRG1 and GR, including genomic and single cell analyses, within breast cancers may give insight into personalized medicine and other potential treatments.

摘要

乳腺癌是一组多样的疾病,通常以其对雌激素和孕激素等激素受体的表达为特征。最近,另一种类固醇激素受体,即糖皮质激素受体(GR),已被证明是乳腺癌进展、转移和治疗中的关键因素。这些受体与染色质结合,引发细胞内的转录变化,而这种变化常常受到染色质自身结构的抑制。染色质重塑蛋白,如与布拉马相关基因1(BRG1),其功能是克服转录因子功能的这种物理抑制,并且与包括乳腺癌在内的许多癌症有关。最近在乳腺癌中了解BRG1和GR相互作用的研究工作,包括基因组分析和单细胞分析,可能会为个性化医疗和其他潜在治疗方法提供见解。

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BAF Complexes and the Glucocorticoid Receptor in Breast Cancers.乳腺癌中的BAF复合物与糖皮质激素受体
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2
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USP22 overexpression fails to augment tumor formation in MMTV-ERBB2 mice but loss of function impacts MMTV promoter activity.USP22 过表达未能增强 MMTV-ERBB2 小鼠的肿瘤形成,但功能丧失会影响 MMTV 启动子活性。
PLoS One. 2024 Jan 18;19(1):e0290837. doi: 10.1371/journal.pone.0290837. eCollection 2024.
3
BRG1 HSA domain interactions with BCL7 proteins are critical for remodeling and gene expression.

本文引用的文献

1
Structure of SWI/SNF chromatin remodeller RSC bound to a nucleosome.SWI/SNF 染色质重塑酶 RSC 与核小体结合的结构。
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Tumor Functional Heterogeneity Unraveled by scRNA-seq Technologies.单细胞 RNA 测序技术揭示肿瘤功能异质性。
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Architecture of the chromatin remodeler RSC and insights into its nucleosome engagement.染色质重塑因子 RSC 的结构及其与核小体结合的机制。
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The Role of Glucocorticoids in Breast Cancer Therapy.糖皮质激素在乳腺癌治疗中的作用。
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Multimodal regulatory elements within a hormone-specific super enhancer control a heterogeneous transcriptional response.多种模态的调控元件位于一个激素特异性超级增强子内,控制着异质的转录反应。
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Thyroid hormone dependent transcriptional programming by TRβ requires SWI/SNF chromatin remodelers.甲状腺激素依赖的 TRβ 转录编程需要 SWI/SNF 染色质重塑酶。
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Simultaneous profiling of gene expression and chromatin accessibility in single cells.单细胞中基因表达与染色质可及性的同步分析。
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Structure of the RSC complex bound to the nucleosome.RSC 复合物与核小体结合的结构。
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6
PARP1 Co-Regulates EP300-BRG1-Dependent Transcription of Genes Involved in Breast Cancer Cell Proliferation and DNA Repair.PARP1共同调控参与乳腺癌细胞增殖和DNA修复的基因的EP300-BRG1依赖性转录。
Cancers (Basel). 2019 Oct 11;11(10):1539. doi: 10.3390/cancers11101539.
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Chromatin accessibility and the regulatory epigenome.染色质可及性和调控表观基因组。
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