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FYN promotes breast cancer progression through epithelial-mesenchymal transition.
- Source :
-
Oncology reports [Oncol Rep] 2016 Aug; Vol. 36 (2), pp. 1000-6. Date of Electronic Publication: 2016 Jun 22. - Publication Year :
- 2016
-
Abstract
- FYN, one of the members of the Src family of kinases (SFKs), has been reported to be overexpressed in various types of cancers and correlated with cell motility and proliferation. However, the mechanism is still unclear. In the present study, we found that FYN was overexpressed in breast cancer and overexpression of FYN promoted cell proliferation, migration and invasion in the MCF10A cells, whereas depletion of FYN suppressed cell proliferation, migration and invasion in the MDA-MB-231 cells. Moreover, FYN upregulated the expression of mesenchymal markers and epithelial-mesenchymal transition (EMT)-related transcription factors, and downregulated the expression of epithelial markers, suggesting that FYN induces EMT in breast cancer cells. Furthermore, FYN was transcriptionally regulated by FOXO1 and mediated FGF2-induced EMT through both the PI3K/AKT and ERK/MAPK pathways.
- Subjects :
- Breast pathology
Cell Line, Tumor
Cell Movement genetics
Cell Proliferation genetics
Disease Progression
Down-Regulation genetics
Female
Fibroblast Growth Factor 2 genetics
Forkhead Box Protein O1 genetics
Humans
MCF-7 Cells
Mitogen-Activated Protein Kinase Kinases genetics
Neoplasm Invasiveness genetics
Neoplasm Invasiveness pathology
Phosphatidylinositol 3-Kinases genetics
Proto-Oncogene Proteins c-akt genetics
Signal Transduction genetics
Transcription Factors genetics
Up-Regulation genetics
Breast Neoplasms genetics
Breast Neoplasms pathology
Epithelial-Mesenchymal Transition genetics
Proto-Oncogene Proteins c-fyn genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1791-2431
- Volume :
- 36
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Oncology reports
- Publication Type :
- Academic Journal
- Accession number :
- 27349276
- Full Text :
- https://doi.org/10.3892/or.2016.4894