Digital scoring of EpCAM and slug expression as prognostic markers in head and neck squamous cell carcinomas.
Henrik SchinkeTheresa HeiderTimm HerkommerFlorian SimonAlexandra Blancke SoaresGisela KranzDaniel SamagaLaura DajkaAnnette FeuchtingerAxel WalchLaura ValeanuChristoph WalzThomas KirchnerMartin CanisPhilipp BaumeisterClaus BelkaCornelius MaihöferSebastian MarschnerUlrike PflugradtUte GanswindtJulia HessHorst ZitzelsbergerOlivier GiresPublished in: Molecular oncology (2020)
Head and neck squamous cell carcinomas (HNSCCs) have poor clinical outcome owing to therapy resistance and frequent recurrences that are among others attributable to tumor cells in partial epithelial-to-mesenchymal transition (pEMT). We compared side-by-side software-based and visual quantification of immunohistochemistry (IHC) staining of epithelial marker EpCAM and EMT regulator Slug in n = 102 primary HNSCC to assess optimal analysis protocols. IHC scores incorporated expression levels and percentages of positive cells. Digital and visual evaluation of membrane-associated EpCAM yielded correlating scorings, whereas visual evaluation of nuclear Slug resulted in significantly higher overall scores. Multivariable Cox proportional hazard analysis defined the median EpCAM expression levels resulting from visual quantification as an independent prognostic factor of overall survival. Slug expression levels resulting from digital quantification were an independent prognostic factor of recurrence-free survival, locoregional recurrence-free survival, and disease-specific survival. Hence, we propose to use visual assessment for the membrane-associated EpCAM protein, whereas nuclear protein Slug assessment was more accurate following digital measurement.
Keyphrases
- free survival
- epithelial mesenchymal transition
- prognostic factors
- poor prognosis
- squamous cell
- circulating tumor cells
- cell adhesion
- binding protein
- long non coding rna
- oxidative stress
- small molecule
- amino acid
- induced apoptosis
- high resolution
- bone marrow
- cell proliferation
- protein protein
- endoplasmic reticulum stress