BMB Rep. 2016; 49(10): 578-583  
Epigenetic regulation of long noncoding RNA UCA1 by SATB1 in breast cancer
Jong-Joo Lee1,2, Mikyoung Kim1 & Hyoung-Pyo Kim1,2,*
1Department of Environmental Medical Biology, Institute of Tropical Medicine, Yonsei University College of Medicine, 2Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 03722, Korea
Correspondence to: Tel: +82-2-2228-1842; Fax: +82-2-363-8676; E-mail: kimhp@yuhs.ac
Received: September 12, 2016; Revised: September 20, 2016; Accepted: September 22, 2016; Published online: October 31, 2016.
© Korean Society for Biochemistry and Molecular Biology. All rights reserved.

Abstract
Special AT-rich sequence binding protein 1 (SATB1) is a nuclear matrix-associated DNA-binding protein that functions as a chromatin organizer. SATB1 is highly expressed in aggressive breast cancer cells and promotes growth and metastasis by reprograming gene expression. Through genomewide cross-examination of gene expression and histone methylation, we identified SATB1 target genes for which expression is associated with altered epigenetic marks. Among the identified genes, long noncoding RNA urothelial carcinoma-associated 1 (UCA1) was upregulated by SATB1 depletion. Upregulation of UCA1 coincided with increased H3K4 trimethylation (H3K4me3) levels and decreased H3K27 trimethylation (H3K27me3) levels. Our study showed that SATB1 binds to the upstream region of UCA1 in vivo, and that its promoter activity increases with SATB1 depletion. Furthermore, simultaneous depletion of SATB1 and UCA1 potentiated suppression of tumor growth and cell survival. Thus, SATB1 repressed the expression of oncogenic UCA1, suppressing growth and survival of breast cancer cells.
Keywords: Breast cancer, Epigenetic regulation, Histone methylation, SATB1, UCA1


This Article

e-submission

Archives