| Literature DB >> 31075076 |
Suhaib K Abdeen1, Rami I Aqeilan1,2.
Abstract
Basal-like breast cancer (BLBC) and triple-negative breast cancer (TNBC) are aggressive forms of human breast cancer with poor prognosis and limited treatment response. Molecular understanding of BLBC and TNBC biology is instrumental to improve detection and management of these deadly diseases. Tumor suppressors WW domain-containing oxidoreductase (WWOX) and TP53 are altered in BLBC and in TNBC. Nevertheless, the functional interplay between WWOX and p53 is poorly understood. In a recent study by Abdeen and colleagues, it has been demonstrated that WWOX loss drives BLBC formation via deregulating p53 functions. In this review, we highlight important signaling pathways regulated by WWOX and p53 that are related to estrogen receptor signaling, epithelial-to-mesenchymal transition, and genomic instability and how they impact BLBC and TNBC development.Entities:
Keywords: BLBC; ER; TNBC; breast cancer; fragile site; genomic instability
Mesh:
Substances:
Year: 2019 PMID: 31075076 PMCID: PMC6592247 DOI: 10.1080/15384101.2019.1616998
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534