| Literature DB >> 26305708 |
Luke F Vistain1, Natsuho Yamamoto1, Richa Rathore1, Peter Cha1, Thomas J Meade2.
Abstract
The transition from a non-invasive to an invasive phenotype is an essential step in tumor metastasis. The Snail family of transcription factors (TFs) is known to play a significant role in this transition. These TFs are zinc fingers that bind to the CAGGTG Ebox consensus sequence. Co(III) -Ebox is a cobalt(III) complex attached to an Ebox oligonucleotide that confers specificity towards Snail TFs. Co(III) -Ebox has been shown to inhibit Snail-mediated embryonic neural crest development in Xenopus laevis, but its efficacy in inhibiting Snail-induced cancer cell invasiveness has not been explored. Here, we describe the efficacy of Co(III) -Ebox in inhibiting the invasive aspects of heregulin-β1(HRG)-treated breast cancer cells. Co(III) -Ebox was found to inhibit the capacity of Snail to repress target genes after HRG induction. Snail inhibition by Co(III) -Ebox reduced the invasive propensity of cells in 2D and 3D, thereby demonstrating promise in inhibiting metastasis.Entities:
Keywords: Snail; cancer; cobalt; metastasis; transcription factor
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Year: 2015 PMID: 26305708 PMCID: PMC4638217 DOI: 10.1002/cbic.201500289
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164