受体酪氨酸激酶
AXL受体酪氨酸激酶
蛋白激酶B
癌症研究
MAPK/ERK通路
酪氨酸激酶
PI3K/AKT/mTOR通路
ROR1型
癌细胞
生物
激酶
气体6
原癌基因酪氨酸蛋白激酶Src
化学
受体蛋白酪氨酸激酶
受体
癌症
酪氨酸激酶抑制剂
信号转导
血小板源性生长因子受体
梅尔特克
细胞生物学
蛋白质酪氨酸磷酸酶
表皮生长因子受体
生长因子受体
酪氨酸
JAK-STAT信号通路
遗传学
作者
Cristina Corno,Laura Gatti,Cinzia Lanzi,Nadia Zaffaroni,Diego Colombo,Paola Perego
标识
DOI:10.2174/0929867323666160405112954
摘要
Aberrant expression and activation of receptor tyrosine kinases (RTK) is a frequent feature of tumor cells that may underlie tumor aggressiveness. Among RTK, Axl, a member of the Tyro3-Axl-Mer family, represents a potential therapeutic target in different tumor types given its over-expression which leads to activation of oncogenic signaling promoting cell proliferation and survival, as well as migration and invasion. Axl can promote aggressiveness of various cell types through PI3K/Akt and/or MAPK/ERK, and its expression can be transcriptionally regulated by multiple factors. Deregulated Axl expression and activation have been shown to be implicated in reduced sensitivity of tumor cells to target-specific and conventional antitumor agents, but the precise mechanism underlying these phenomena are still poorly understood. Several small molecules acting as Axl inhibitors have been reported, and some of them are undergoing clinical investigation. In this review, we describe Axl biological functions, its expression in cancer and in drug-resistant tumor cells and the development of inhibitors tailored to this receptor tyrosine kinase. Keywords: Cancer, receptor tyrosine kinases, Axl, drug resistance, invasion, inhibitors.
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