Two recent reports identify ZNF703 as an oncogene driving selection of frequent chromosome 8p12 amplifications in luminal B breast tumors. The estrogen-responsive ZNF703 gene encodes a transcriptional cofactor that, when overexpressed, induces cell proliferation and interferes with transforming growth factor beta signaling. In MCF7 cells, increased ZNF703 expression results in activation of genes involved in stem cell self-renewal - while in primary human mammary epithelial cells, ZNF703 increases the ratio of luminal to basal progenitors. Expression of the murine homolog of ZNF703 reduces cell adhesion and promotes metastasis. ZNF703 overexpression thus alters regulation of proliferation and differentiation in luminal B tumors.
Who is in the driver's seat in 8p12 amplifications? ZNF703 in luminal B breast tumors
Published 2011 in Breast Cancer Research
ABSTRACT
PUBLICATION RECORD
- Publication year
2011
- Venue
Breast Cancer Research
- Publication date
2011-05-25
- Fields of study
Biology, Medicine
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- External record
- Source metadata
Semantic Scholar, PubMed
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