Back to Search
Start Over
A CD44high/EGFRlow subpopulation within head and neck cancer cell lines shows an epithelial-mesenchymal transition phenotype and resistance to treatment.
- Source :
-
PloS one [PLoS One] 2012; Vol. 7 (9), pp. e44071. Date of Electronic Publication: 2012 Sep 25. - Publication Year :
- 2012
-
Abstract
- Mortality in head and neck squamous cell carcinoma (HNSCC) is high due to emergence of therapy resistance which results in local and regional recurrences that may have their origin in resistant cancer stem cells (CSCs) or cells with an epithelial-mesenchymal transition (EMT) phenotype. In the present study, we investigate the possibility of using the cell surface expression of CD44 and epidermal growth factor receptor (EGFR), both of which have been used as stem cell markers, to identify subpopulations within HNSCC cell lines that differ with respect to phenotype and treatment sensitivity. Three subpopulations, consisting of CD44(high)/EGFR(low), CD44(high)/EGFR(high) and CD44(low) cells, respectively, were collected by fluorescence-activated cell sorting. The CD44(high)/EGFR(low) population showed a spindle-shaped EMT-like morphology, while the CD44(low) population was dominated by cobblestone-shaped cells. The CD44(high)/EGFR(low) population was enriched with cells in G0/G1 and showed a relatively low proliferation rate and a high plating efficiency. Using a real time PCR array, 27 genes, of which 14 were related to an EMT phenotype and two with stemness, were found to be differentially expressed in CD44(high)/EGFR(low) cells in comparison to CD44(low) cells. Moreover, CD44(high)/EGFR(low) cells showed a low sensitivity to radiation, cisplatin, cetuximab and gefitinib, and a high sensitivity to dasatinib relative to its CD44(high)/EGFR(high) and CD44(low) counterparts. In conclusion, our results show that the combination of CD44 (high) and EGFR (low) cell surface expression can be used to identify a treatment resistant subpopulation with an EMT phenotype in HNSCC cell lines.
- Subjects :
- Antibodies, Monoclonal pharmacology
Antibodies, Monoclonal, Humanized
Antineoplastic Agents pharmacology
Carcinoma, Squamous Cell drug therapy
Carcinoma, Squamous Cell genetics
Carcinoma, Squamous Cell metabolism
Carcinoma, Squamous Cell radiotherapy
Cell Cycle drug effects
Cell Cycle radiation effects
Cell Line, Tumor
Cell Lineage drug effects
Cell Lineage radiation effects
Cell Proliferation drug effects
Cell Proliferation radiation effects
Cell Shape drug effects
Cell Shape radiation effects
Cetuximab
Cisplatin pharmacology
Drug Resistance, Neoplasm drug effects
Drug Resistance, Neoplasm radiation effects
Epithelial-Mesenchymal Transition immunology
ErbB Receptors immunology
Flow Cytometry
Gamma Rays
Gefitinib
Gene Expression drug effects
Gene Expression radiation effects
Head and Neck Neoplasms drug therapy
Head and Neck Neoplasms genetics
Head and Neck Neoplasms metabolism
Head and Neck Neoplasms radiotherapy
Humans
Hyaluronan Receptors immunology
Neoplastic Stem Cells drug effects
Neoplastic Stem Cells radiation effects
Oligonucleotide Array Sequence Analysis
Organ Specificity
Quinazolines pharmacology
Cell Lineage genetics
Epithelial-Mesenchymal Transition genetics
ErbB Receptors genetics
Hyaluronan Receptors genetics
Neoplastic Stem Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 7
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 23049743
- Full Text :
- https://doi.org/10.1371/journal.pone.0044071