WNT11-FZD7-DAAM1 signalling supports tumour initiating abilities and melanoma amoeboid invasion.
Irene Rodriguez-HernandezOscar MaiquesLeonie KohlhammerGaia CantelliAnna Perdrix-RosellJoanne MongerBruce FanshaweVictoria L BridgemanSophia N KaragiannisRosa M PeninJoaquim MarcolvalRosa María MartíXavier M GuiuGilbert O FruhwirthJose L OrgazIlaria MalanchiVictoria Sanz-MorenoPublished in: Nature communications (2020)
Melanoma is a highly aggressive tumour that can metastasize very early in disease progression. Notably, melanoma can disseminate using amoeboid invasive strategies. We show here that high Myosin II activity, high levels of ki-67 and high tumour-initiating abilities are characteristic of invasive amoeboid melanoma cells. Mechanistically, we find that WNT11-FZD7-DAAM1 activates Rho-ROCK1/2-Myosin II and plays a crucial role in regulating tumour-initiating potential, local invasion and distant metastasis formation. Importantly, amoeboid melanoma cells express both proliferative and invasive gene signatures. As such, invasive fronts of human and mouse melanomas are enriched in amoeboid cells that are also ki-67 positive. This pattern is further enhanced in metastatic lesions. We propose eradication of amoeboid melanoma cells after surgical removal as a therapeutic strategy.
Keyphrases
- stem cells
- cell proliferation
- endothelial cells
- squamous cell carcinoma
- induced apoptosis
- cell migration
- genome wide
- small cell lung cancer
- binding protein
- lymph node
- oxidative stress
- risk assessment
- gene expression
- cell cycle arrest
- signaling pathway
- climate change
- cell death
- helicobacter pylori
- human health
- rectal cancer