Comparison of Xiphophorus and human melanoma transcriptomes reveals conserved pathway interactions.
Yuan LuMikki BoswellWilliam BoswellSusanne KneitzMichael HausmannBarbara KlotzJanine RegneriMarkita SavageAngel AmoresJohn PostlethwaitWesley WarrenManfred SchartlRonald WalterPublished in: Pigment cell & melanoma research (2018)
Comparative analysis of human and animal model melanomas can uncover conserved pathways and genetic changes that are relevant for the biology of cancer cells. Spontaneous melanoma in Xiphophorus interspecies backcross hybrid progeny may be informative in identifying genes and functional pathways that are similarly related to melanoma development in all vertebrates, including humans. To assess functional pathways involved in the Xiphophorus melanoma, we performed gene expression profiling of the melanomas produced in interspecies BC1 and successive backcross generations (i.e., BC5 ) of the cross: X. hellerii × [X. maculatus Jp 163 A × X. hellerii]. Using RNA-Seq, we identified genes that are transcriptionally co-expressed with the driver oncogene, xmrk. We determined functional pathways in the fish melanoma that are also present in human melanoma cohorts that may be related to dedifferentiation based on the expression levels of pigmentation genes. Shared pathways between human and Xiphophorus melanomas are related to inflammation, cell migration, cell proliferation, pigmentation, cancer development, and metastasis. Our results suggest xmrk co-expressed genes are associated with dedifferentiation and highlight these signaling pathways as playing important roles in melanomagenesis.
Keyphrases
- genome wide
- endothelial cells
- rna seq
- genome wide identification
- cell proliferation
- induced pluripotent stem cells
- single cell
- pluripotent stem cells
- skin cancer
- transcription factor
- dna methylation
- poor prognosis
- squamous cell carcinoma
- epithelial mesenchymal transition
- cell cycle
- papillary thyroid
- endoplasmic reticulum stress