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PMID: 17721435 Published · ppublish English Review

Oestrogen-receptor-mediated transcription and the influence of co-factors and chromatin state.

Nature reviews. Cancer ·Vol. 7 ·No. 9 ·2007-00-00 ·Pages 713-22

Green KA, Carroll JS

Abstract

Oestrogen receptor-alpha (ERalpha)-regulated transcription in breast cancer cells involves protein co-factors that contribute to the regulation of chromatin structure. These include co-factors with the potential to regulate histone modifications such as acetylation or methylation, and therefore the transcriptional state of target genes. Although much of the information regarding the interaction of specific co-factors with ER has been generated by studying specific promoter regions, we now have an improved understanding of the nature of these interactions and are better placed to relate these with ER activity and potentially with the activity of breast cancer drugs, including tamoxifen.

MeSH Terms
Amino Acid Sequence Carrier Proteins/pharmacology Chromatin/metabolism Chromatin Immunoprecipitation Corticosterone Estrogen Receptor alpha/chemistry,physiology Humans Models, Biological Nuclear Proteins/pharmacology Nuclear Receptor Co-Repressor 1 Repressor Proteins/pharmacology Tamoxifen/pharmacology Transcription, Genetic Transcriptional Activation Trefoil Factor-1 Tumor Suppressor Proteins/pharmacology p300-CBP Transcription Factors/pharmacology
Chemicals
Carrier Proteins Chromatin Estrogen Receptor alpha NCOR1 protein, human Nuclear Proteins Nuclear Receptor Co-Repressor 1 Repressor Proteins TFF1 protein, human Trefoil Factor-1 Tumor Suppressor Proteins Tamoxifen p300-CBP Transcription Factors Corticosterone
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Green Kelly A
Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge, UK.
Carroll Jason S
Article Info
Journal
Nature reviews. Cancer
Abbr.
Nat Rev Cancer
ISSN
1474-175X
Published
2007-00-00
Pages
713-22
Language
English
Region
England
NLM ID
101124168
Subset
IM
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