Pleiotropic Effects of Epithelial Mesenchymal Crosstalk on Head and Neck Cancer: EMT and beyond.
Steinbichler Teresa BernadetteD SavicD DejacoA RomaniB KoflerI I SkvortsovaH RiechelmannJ DudasPublished in: Cancer microenvironment : official journal of the International Cancer Microenvironment Society (2019)
Epithelial mesenchymal crosstalk (EMC) describes the interaction of the tumor stroma and associated fibroblasts with epithelial cancer cells. In this study we analysed the effects of EMC on head and neck cancer cells. In tumor cell lines EMC was induced using media conditioned from a mix-culture of cancer cells and fibroblasts. Cell proliferation and chemotherapy response were assessed using direct cell counting. Flow cytometry, immunohistochemistry of markers of epithelial-mesenchymal transition (EMT) and subsequent TissueFaxs™ acquisition and quantification and western blot analysis were performed. Holotomographic microscopy imaging was used to visualize the effects of EMC on Cisplatin response of SCC-25 cells. EMC induced a hybrid epithelial-mesenchymal phenotype in SCC-25 cells with co-expression of vimentin and cytokeratin. This hybrid phenotype was associated with chemotherapy resistance and increased proliferation of the cells. The EMC conditioned medium led to an activation of the IL-6/STAT3 pathway with subsequent phosphorylation of STAT3. EMC induced a hybrid epithelial-mesenchymal phenotype in HNSCC cells accompanied by increased therapy resistance and cell proliferation. The IL-6/STAT3 pathway might be one of the major pathways involved in these EMC-related effects.
Keyphrases
- cell proliferation
- induced apoptosis
- epithelial mesenchymal transition
- cell cycle arrest
- stem cells
- bone marrow
- signaling pathway
- high glucose
- flow cytometry
- oxidative stress
- squamous cell carcinoma
- high resolution
- diabetic rats
- pi k akt
- cell cycle
- cell death
- single cell
- endoplasmic reticulum stress
- drug induced
- endothelial cells
- radiation therapy
- mass spectrometry
- south africa
- long non coding rna
- extracellular matrix
- optical coherence tomography
- single molecule
- replacement therapy