PRL-3 Phosphatase and Cancer Metastasis

被引:124
|
作者
Al-Aidaroos, Abdul Qader O. [1 ,2 ]
Zeng, Qi [1 ,2 ,3 ]
机构
[1] ASTAR, Inst Mol & Cell Biol, Singapore 138648, Singapore
[2] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore 117456, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 119260, Singapore
关键词
PRL-3; PHOSPHATASE; CANCER METASTASIS; CANCER CELL SIGNALING; PROTEIN-TYROSINE-PHOSPHATASE; EPITHELIAL-MESENCHYMAL TRANSITION; REGENERATING LIVER; CELL-GROWTH; GENE-EXPRESSION; MONOCLONAL-ANTIBODIES; COLORECTAL-CANCER; TUMOR-METASTASIS; DOWN-REGULATION; LUNG-CANCER;
D O I
10.1002/jcb.22913
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The deregulated expression of members of the phosphatase of regenerating liver (PRL) family has been implicated in the metastatic progression of multiple human cancers. Importantly, PRL-1 and PRL-3 both possess the capacity to drive key steps in metastatic progression. Yet, little is known about the regulation and oncogenic mechanisms of this emerging class of dual-specificity phosphatases. This prospect article details the involvement of PRLs in the metastatic cascade, the regulatory mechanisms controlling PRL expression, and recent efforts in the characterization of PRL-modulated pathways and substrates using biochemical and high-throughput approaches. Current advances and future prospects in anti-cancer therapy targeting this family are also discussed. J. Cell. Biochem. 111: 1087-1098, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1087 / 1098
页数:12
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