4.8 Article

The receptor tyrosine kinase Axl regulates cell-cell adhesion and stemness in cutaneous squamous cell carcinoma

Journal

ONCOGENE
Volume 33, Issue 32, Pages 4185-4192

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/onc.2013.388

Keywords

adhesion; Axl; cancer stem cell; chemotherapy resistance; epithelial-mesenchymal transition

Funding

  1. DAT PhD studentship from the Medical Research Council
  2. MRC Centenary award (MAC)
  3. DEBRA Ireland
  4. British Skin Foundation
  5. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) [NC/L00061X/1, G1000053/1] Funding Source: researchfish

Ask authors/readers for more resources

Axl is a receptor tyrosine kinase (RTK) upregulated in various tumors including cutaneous squamous cell carcinoma (SCC). Axl expression correlates with poor prognosis and induction of epithelial-mesenchymal transition (EMT), hence we hypothesized that Axl is involved in the disruption of cell-cell adhesion to allow invasion and chemotherapy resistance of the cancer stem cell population. Cutaneous SCC cell lines with stable knockdown of Axl were generated using retroviral vectors. Axl depletion altered expression of intercellular junction molecules increasing cell-cell adhesion with downregulation of Wnt and TGF beta R signaling. Furthermore, Axl expression correlated with the expression of putative cancer stem cell markers, CD44 and ALDH1, increased resistance to chemotherapy drugs, enhanced sphere formation ability and expression of EMT features by cancer stem cells. Axl depletion resulted in loss of tumor formation in an in vivo zebrafish xenograft model. In conclusion, these data suggest that abrogation of Axl results in loss of cancer stem cell properties indicating a role for Axl as a therapeutic target in chemotherapy-resistant cancer.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available