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Article Abstract

The receptor tyrosine kinase AXL is associated with epithelial plasticity in several solid tumors including breast cancer and AXL-targeting agents are currently in clinical trials. We hypothesized that AXL is a driver of stemness traits in cancer by co-option of a regulatory function normally reserved for stem cells. AXL-expressing cells in human mammary epithelial ducts co-expressed markers associated with multipotency, and AXL inhibition abolished colony formation and self-maintenance activities while promoting terminal differentiation . -null mice did not exhibit a strong developmental phenotype, but enrichment of cells was required for mouse mammary gland reconstitution upon transplantation, and null mice had reduced incidence of driven mammary tumors. An AXL-dependent gene signature is a feature of transcriptomes in basal breast cancers and reduced patient survival irrespective of subtype. Our interpretation is that AXL regulates access to epithelial plasticity programs in MaSCs and, when co-opted, maintains acquired stemness in breast cancer cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578759PMC
http://dx.doi.org/10.1016/j.isci.2020.101649DOI Listing

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