原癌基因酪氨酸蛋白激酶Src
血管生成
酪氨酸激酶
转移
癌症
癌症研究
生物
癌基因
受体酪氨酸激酶
信号转导
细胞生物学
遗传学
细胞周期
作者
Rumey C. Ishizawar,Sarah J. Parsons
出处
期刊:Cancer Cell
[Elsevier]
日期:2004-09-01
卷期号:6 (3): 209-214
被引量:587
标识
DOI:10.1016/j.ccr.2004.09.001
摘要
The proto-oncogene c-src is rarely mutated in human cancers, and when overexpressed in normal cells is non- or weakly oncogenic. These observations have raised doubts about the involvement of c-src in the etiology of human tumors. However, recent studies have shown that c-Src, a non-receptor tyrosine kinase, exhibits elevated protein levels and activity in numerous types of human cancers. Furthermore, it has been found to be a critical component of multiple signaling pathways that regulate proliferation, survival, metastasis, and angiogenesis. Because of its important role in these oncogenic processes, it represents a therapeutic target ripe for exploitation.
科研通智能强力驱动
Strongly Powered by AbleSci AI