生物
癌症研究
AXL受体酪氨酸激酶
CD44细胞
癌症干细胞
受体酪氨酸激酶
Wnt信号通路
癌症
细胞粘附分子
干细胞
下调和上调
细胞粘附
细胞
细胞生物学
信号转导
基因
生物化学
JAK-STAT信号通路
遗传学
作者
Monika A. Cichoń,Zsófia Szentpétery,Matthew Caley,Emmanouil Papadakis,Ian C. Mackenzie,Caroline H. Brennan,Edel A. O’Toole
出处
期刊:Oncogene
[Springer Nature]
日期:2013-09-23
卷期号:33 (32): 4185-4192
被引量:61
摘要
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 TGFβR 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.
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