Brizio Moreno-Jaime , José Esparza-López , Andrea Castro-Sánchez , Elizabeth Escobar-Arriaga , Heriberto Medina-Franco , Eucario León-Rodríguez , María de Jesús Ibarra-Sánchez
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引用次数: 1
Abstract
Background
Epithelial-mesenchymal transition (EMT) is a biological process where immobile and polarised epithelial cells acquire mesenchymal characteristics with high migration. This process produces changes in the cytoskeleton of the tumour cells, with the loss of E-cadherin and the acquisition of N-cadherin being the main biochemical changes of the EMT. This study investigates the role of epidermal growth factor (EGF) on the EMT induction in breast cancer cell lines and primary cultures.
Methods
MCF-7 cell line and the primary cultures MBCDF and MBCD25 were used in this study. EMT was induced by continuous EGF treatment. Mesenchymal EGF-induced phenotype was evaluated by Western blot of the following markers: pSTAT3, STAT3, repression of E-cadherin, and expression of Snail.
Results
Our results demonstrate that EGF treatment induced STAT3 phosphorylation without changes in STAT3 in MBCDF, MBCD25 and MCF-7. Additionally, EGF treatment induced EMT, as shown by the loss of E-cadherin and Snail expression after 5 days.
Conclusion
EGF was able to induce EMT in primary breast cancer cell cultures, MBCDF, MBCD25, as well as MCF-7 cell line. These results suggest that EGF produces a putative aggressive phenotype.