Co-amplification of CBX3 with EGFR or RAC1 in human cancers corroborated by a conserved genetic interaction among the genes.
Giuseppe BossoFrancesca CipressaLiliana TulloGiovanni CenciPublished in: Cell death discovery (2023)
Chromobox Protein 3 (CBX3) overexpression is a common event occurring in cancer, promotes cancer cell proliferation and represents a poor prognosis marker in a plethora of human cancers. Here we describe that a wide spectrum of human cancers harbors a co-amplification of CBX3 gene with either EGFR or RAC1, which yields a statistically significant increase of both mRNA and protein levels of CBX3, EGFR and RAC1. We also reveal that the simultaneous overexpression of CBX3, RAC1 and EGFR gene products correlates with a worse prognosis compared to the condition when CBX3, RAC1 and EGFR are singularly upregulated. Furthermore, we also show that a co-occurrence of low-grade amplification, in addition to high-grade amplification, between CBX3 and EGFR or RAC1 is associated with a reduced patient lifespan. Finally, we find that CBX3 and RAC1/EGFR genetically interact in the model organism Drosophila melanogaster, suggesting that the simultaneous overexpression as well as well the co-occurrence of high- or low-grade copy number alterations in these genes is not accidental and could reflect evolutionarily conserved functional relationships.
Keyphrases
- low grade
- small cell lung cancer
- high grade
- epidermal growth factor receptor
- copy number
- genome wide
- tyrosine kinase
- cell proliferation
- poor prognosis
- endothelial cells
- cell migration
- transcription factor
- mitochondrial dna
- nucleic acid
- dna methylation
- induced pluripotent stem cells
- genome wide identification
- papillary thyroid
- drosophila melanogaster
- long non coding rna
- pluripotent stem cells
- gene expression
- small molecule
- genome wide analysis
- protein protein
- label free