EVI1 Promotes the Proliferation and Invasive Properties of Human Head and Neck Squamous Cell Carcinoma Cells.
Alexander Michael GranditsSophie BrombergerGerwin HellerBarbara Andrea ReinoehlErwin TomasichKlaudia SchossleitnerAnna Sophie BerghoffThorsten FuerederRotraud WieserPublished in: International journal of molecular sciences (2022)
Head and neck squamous cell carcinoma (HNSCC) is a frequent malignancy with a poor prognosis. So far, the EGFR inhibitor cetuximab is the only approved targeted therapy. A deeper understanding of the molecular and genetic basis of HNSCC is needed to identify additional targets for rationally designed, personalized therapeutics. The transcription factor EVI1, the major product of the MECOM locus, is an oncoprotein with roles in both hematological and solid tumors. In HNSCC, high EVI1 expression was associated with an increased propensity to form lymph node metastases, but its effects in this tumor entity have not yet been determined experimentally. We therefore overexpressed or knocked down EVI1 in several HNSCC cell lines and determined the impact of these manipulations on parameters relevant to tumor growth and invasiveness, and on gene expression patterns. Our results revealed that EVI1 promoted the proliferation and migration of HNSCC cells. Furthermore, it augmented tumor spheroid formation and the ability of tumor spheroids to displace an endothelial cell layer. Finally, EVI1 altered the expression of numerous genes in HNSCC cells, which were enriched for Gene Ontology terms related to its cellular functions. In summary, EVI1 represents a novel oncogene in HNSCC that contributes to cellular proliferation and invasiveness.
Keyphrases
- poor prognosis
- gene expression
- long non coding rna
- induced apoptosis
- endothelial cells
- lymph node
- genome wide
- transcription factor
- cell cycle arrest
- signaling pathway
- squamous cell
- small cell lung cancer
- dna methylation
- small molecule
- epidermal growth factor receptor
- squamous cell carcinoma
- copy number
- tyrosine kinase
- genome wide identification
- cell death
- drug induced
- single molecule
- pluripotent stem cells
- pi k akt
- rectal cancer
- wild type
- genome wide analysis