A Whole-Transcriptomic Analysis of Canine Oral Melanoma: A Chance to Disclose the Radiotherapy Effect and Outcome-Associated Gene Signature.
Greta MucignatLudovica MontanucciRamy ElgendyMery GiantinPaola LagangaMarianna PaulettoClaudio PorriniMarta VascellariVito Ferdinando LeoneMauro DacastoAnna GranatoPublished in: Genes (2024)
Oral melanoma (OM) is the most common malignant oral tumour among dogs and shares similarities with human mucosal melanoma (HMM), validating the role of canine species as an immunocompetent model for cancer research. In both humans and dogs, the prognosis is poor and radiotherapy (RT) represents a cornerstone in the management of this tumour, either as an adjuvant or a palliative treatment. In this study, by means of RNA-seq, the effect of RT weekly fractionated in 9 Gray (Gy), up to a total dose of 36 Gy (4 weeks), was evaluated in eight dogs affected by OM. Furthermore, possible transcriptomic differences in blood and biopsies that might be associated with a longer overall survival (OS) were investigated. The immune response, glycosylation, cell adhesion, and cell cycle were the most affected pathways by RT, while tumour microenvironment (TME) composition and canonical and non-canonical WNT pathways appeared to be modulated in association with OS. Taking these results as a whole, this study improved our understanding of the local and systemic effect of RT, reinforcing the pivotal role of anti-tumour immunity in the control of canine oral melanoma (COM).
Keyphrases
- rna seq
- cell cycle
- early stage
- single cell
- immune response
- cell proliferation
- stem cells
- skin cancer
- cell adhesion
- endothelial cells
- radiation therapy
- papillary thyroid
- radiation induced
- mass spectrometry
- locally advanced
- copy number
- combination therapy
- inflammatory response
- atomic force microscopy
- single molecule
- high speed
- ulcerative colitis