Secreted and O-GlcNAcylated MIF binds to the human EGF receptor and inhibits its activation

被引:0
|
作者
Yanhua Zheng
Xinjian Li
Xu Qian
Yugang Wang
Jong-Ho Lee
Yan Xia
David H. Hawke
Gang Zhang
Jianxin Lyu
Zhimin Lu
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Neuro
[2] The University of Texas MD Anderson Cancer Center,Oncology
[3] Affiliated Hospital of Hebei University,Department of Systems Biology
[4] Key Laboratory of Laboratory Medicine,Department of Surgical Oncology
[5] Ministry of Education,Department of Molecular and Cellular Oncology
[6] Zhejiang Provincial Key Laboratory of Medical Genetics,undefined
[7] School of Laboratory Medicine and Life Sciences,undefined
[8] Wenzhou Medical University,undefined
[9] The University of Texas MD Anderson Cancer Center,undefined
[10] Cancer Biology Program,undefined
[11] The University of Texas Graduate School of Biomedical Sciences at Houston,undefined
来源
Nature Cell Biology | 2015年 / 17卷
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学科分类号
摘要
Lu and colleagues report that the O-GlcNAcylated MIF cytokine binds the extracellular domain of EGFR and prevents EGF-induced EGFR activation. Conversely, EGFR activation leads to MMP13-mediated MIF degradation and EGFR-induced tumorigenesis
引用
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页码:1348 / 1355
页数:7
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