| Literature DB >> 34050190 |
Tamar Zahavi1,2,3, Mali Salmon-Divon3, Roberto Salgado4,5, Michael Elkin6, Esther Hermano6, Ariel M Rubinstein7, Prudence A Francis8,9,10, Angelo Di Leo11, Giuseppe Viale12, Evandro de Azambuja13, Lieveke Ameye13, Christos Sotiriou13, Asher Salmon14, Nataly Kravchenko-Balasha7, Amir Sonnenblick15,16.
Abstract
Heparanase promotes tumor growth in breast tumors. We now evaluated heparanase protein and gene-expression status and investigated its impact on disease-free survival in order to gain better insight into the role of heparanase in ER-positive (ER+) breast cancer prognosis and to clarify its role in cell survival following chemotherapy. Using pooled analysis of gene-expression data, we found that heparanase was associated with a worse prognosis in estrogen receptor-positive (ER+) tumors (log-rank p < 10-10) and predictive to chemotherapy resistance (interaction p = 0.0001) but not hormonal therapy (Interaction p = 0.62). These results were confirmed by analysis of data from a phase III, prospective randomized trial which showed that heparanase protein expression is associated with increased risk of recurrence in ER+ breast tumors (log-rank p = 0.004). In vitro experiments showed that heparanase promoted tumor progression and increased cell viability via epithelial-mesenchymal transition, stemness, and anti-apoptosis pathways in luminal breast cancer. Taken together, our results demonstrated that heparanase is associated with worse outcomes and increased cell viability in ER+ BC.Entities:
Year: 2021 PMID: 34050190 DOI: 10.1038/s41523-021-00277-x
Source DB: PubMed Journal: NPJ Breast Cancer ISSN: 2374-4677