原癌基因酪氨酸蛋白激酶Src
酪氨酸磷酸化
SH2域
车站3
磷酸化
斯达
酪氨酸激酶
生物
细胞生物学
状态4
分子生物学
酪氨酸
癌症研究
信号转导
生物化学
作者
Chao‐Lan Yu,Debra J. Meyer,George S. Campbell,Andrew C. Larner,Christin Carter‐Su,Jessica Schwartz,Richard Jove
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1995-07-07
卷期号:269 (5220): 81-83
被引量:948
标识
DOI:10.1126/science.7541555
摘要
Cytokines and growth factors induce tyrosine phosphorylation of signal transducers and activators of transcription (STATs) that directly activate gene expression. Cells stably transformed by the Src oncogene tyrosine kinase were examined for STAT protein activation. Assays of electrophoretic mobility, DNA-binding specificity, and antigenicity indicated that Stat3 or a closely related STAT family member was constitutively activated by the Src oncoprotein. Induction of this DNA-binding activity was accompanied by tyrosine phosphorylation of Stat3 and correlated with Src transformation. These findings demonstrate that Src can activate STAT signaling pathways and raise the possibility that Stat3 contributes to oncogenesis by Src.
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