Axl as a mediator of cellular growth and survival

被引:144
作者
Axelrod, Haley [1 ,2 ]
Pienta, Kenneth J. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Sch Med, Cellular & Mol Med Program, Baltimore, MD 21287 USA
[2] Johns Hopkins Sch Med, Dept Urol, James Buchanan Brady Urol Inst, Baltimore, MD USA
[3] Johns Hopkins Sch Med, Dept Oncol, Baltimore, MD USA
[4] Johns Hopkins Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD USA
[5] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD USA
关键词
Axl; TAM receptors; Gas6; cancer; tyrosine kinase; proliferation; apoptosis; immune; migration; inhibitor; RECEPTOR TYROSINE KINASE; VASCULAR SMOOTH-MUSCLE; LUNG-CANCER CELLS; PHOSPHATE-INDUCED CALCIFICATION; TO-MESENCHYMAL TRANSITION; ARREST-SPECIFIC GENE-6; BREAST-CANCER; TAM RECEPTORS; HEPATOCELLULAR-CARCINOMA; THERAPEUTIC TARGET;
D O I
10.18632/oncotarget.2422
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The control of cellular growth and proliferation is key to the maintenance of homeostasis. Survival, proliferation, and arrest are regulated, in part, by Growth Arrest Specific 6 (Gas6) through binding to members of the TAM receptor tyrosine kinase family. Activation of the TAM receptors leads to downstream signaling through common kinases, but the exact mechanism within each cellular context varies and remains to be completely elucidated. Deregulation of the TAM family, due to its central role in mediating cellular proliferation, has been implicated in multiple diseases. Axl was cloned as the first TAM receptor in a search for genes involved in the progression of chronic to acute-phase leukemia, and has since been established as playing a critical role in the progression of cancer. The oncogenic nature of Axl is demonstrated through its activation of signaling pathways involved in proliferation, migration, inhibition of apoptosis, and therapeutic resistance. Despite its recent discovery, significant progress has been made in the development of effective clinical therapeutics targeting Axl. In order to accurately define the role of Axl in normal and diseased processes, it must be analyzed in a cell type-specific context.
引用
收藏
页码:1 / 35
页数:35
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