Interaction with Suv39H1 is critical for Snail-mediated E-cadherin repression in breast cancer.

TitleInteraction with Suv39H1 is critical for Snail-mediated E-cadherin repression in breast cancer.
Publication TypeJournal Article
Year of Publication2013
JournalOncogene
Volume32
Issue11
Pagination1351-62
Date Published2013 Mar 14
ISSN0950-9232
AbstractExpression of E-cadherin, a hallmark of epithelial-mesenchymal transition (EMT), is often lost due to promoter DNA methylation in basal-like breast cancer (BLBC), which contributes to the metastatic advantage of this disease; however, the underlying mechanism remains unclear. Here, we identified that Snail interacted with Suv39H1 (suppressor of variegation 3-9 homolog 1), a major methyltransferase responsible for H3K9me3 that intimately links to DNA methylation. We demonstrated that the SNAG domain of Snail and the SET domain of Suv39H1 were required for their mutual interactions. We found that H3K9me3 and DNA methylation on the E-cadherin promoter were higher in BLBC cell lines. We showed that Snail interacted with Suv39H1 and recruited it to the E-cadherin promoter for transcriptional repression. Knockdown of Suv39H1 restored E-cadherin expression by blocking H3K9me3 and DNA methylation and resulted in the inhibition of cell migration, invasion and metastasis of BLBC. Our study not only reveals a critical mechanism underlying the epigenetic regulation of EMT, but also paves a way for the development of new treatment strategies against this disease.
URLhttp://dx.doi.org/10.1038/onc.2012.169
DOI10.1038/onc.2012.169
PubMed Linkhttp://www.ncbi.nlm.nih.gov/pubmed/22562246?dopt=Abstract
Short TitleOncogene