New mechanisms for PRLr action in breast cancer

被引:82
作者
Clevenger, Charles V. [1 ,2 ]
Gadd, Samantha L. [3 ]
Zheng, Jiamao [1 ,2 ]
机构
[1] Northwestern Univ, Dept Pathol, Chicago, IL 60611 USA
[2] Northwestern Univ, H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[3] Childrens Mem Hosp, Chicago, IL 60611 USA
关键词
GROWTH-HORMONE RECEPTOR; RESONANCE ENERGY-TRANSFER; PROLACTIN-RECEPTOR; CYCLOPHILIN-A; BINDING PROTEIN; ACTIVATION; JAK2; DIMERIZATION; ASSOCIATION; EXPRESSION;
D O I
10.1016/j.tem.2009.03.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prolactin (PRL) is a pleiotrophic hormone that contributes to the growth of normal and malignant breast tissues. PRL signals through its receptor (PRLr), a transmembrane receptor that belongs to the cytokine receptor family. The mechanism of how the PRL:PRLr interaction triggers activation of signaling networks remains enigmatic. This review examines the effect of ligand binding on PRLr and the processes that initiate receptor-associated signaling. Evidence for PRLr predimerization in the absence of ligand and the actions of the prolyl isomerase cyclophilin A in ligand-induced activation of PRLr-associated Jak2 kinase are discussed. These studies reveal that ligand-induced conformational change of the PRLr complex is necessary for its function and open avenues for therapies to inhibit PRLr action in breast cancer.
引用
收藏
页码:223 / 229
页数:7
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