Ross-Innes, CS and Stark, R and Teschendorff, AE and Holmes, KA and Ali, HR and Dunning, MJ and Brown, GD and Gojis, O and Ellis, IO and Green, AR and Ali, S and Chin, SF and Palmieri, C and Caldas, C and Carroll, JS (2012) Differential oestrogen receptor binding is associated with clinical outcome in breast cancer. Nature , 481 (7381) 389 - 393. 10.1038/nature10730.
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Oestrogen receptor-α (ER) is the defining and driving transcription factor in the majority of breast cancers and its target genes dictate cell growth and endocrine response, yet genomic understanding of ER function has been restricted to model systems. Here we map genome-wide ER-binding events, by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq), in primary breast cancers from patients with different clinical outcomes and in distant ER-positive metastases. We find that drug-resistant cancers still recruit ER to the chromatin, but that ER binding is a dynamic process, with the acquisition of unique ER-binding regions in tumours from patients that are likely to relapse. The acquired ER regulatory regions associated with poor clinical outcome observed in primary tumours reveal gene signatures that predict clinical outcome in ER-positive disease exclusively. We find that the differential ER-binding programme observed in tumours from patients with poor outcome is not due to the selection of a rare subpopulation of cells, but is due to the FOXA1-mediated reprogramming of ER binding on a rapid timescale. The parallel redistribution of ER and FOXA1 binding events in drug-resistant cellular contexts is supported by histological co-expression of ER and FOXA1 in metastatic samples. By establishing transcription-factor mapping in primary tumour material, we show that there is plasticity in ER-binding capacity, with distinct combinations of cis-regulatory elements linked with the different clinical outcomes.
|Title:||Differential oestrogen receptor binding is associated with clinical outcome in breast cancer.|
|Additional information:||PMCID: PMC3272464|
|Keywords:||Base Sequence, Breast Neoplasms, Cell Line, Tumor, Drug Resistance, Neoplasm, Female, Gene Expression Regulation, Neoplastic, Hepatocyte Nuclear Factor 3-alpha, Humans, Neoplasm Metastasis, Prognosis, Protein Binding, Receptors, Estrogen, Regulatory Sequences, Nucleic Acid, Survival Analysis, Tamoxifen, Treatment Outcome|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Wolfson Institute and Cancer Institute Administration > Cancer Institute > Research Department of Cancer Biology|
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