Abstract
Wild-type p53-induced phosphatase 1 (WIP1) belongs to the protein phosphatase 2C (PP2C) family and is a mammalian serine/threonine specific protein phosphatase to dephosphorylate numerous signaling molecules. Mammalian WIP1 regulates a wide array of targeting molecules and plays key regulatory roles in many cell processes such as DNA damage and repair, cell proliferation, differentiation, apoptosis, and senescence. WIP1 promotes the formation and development of tumors as an oncogene and a negative regulator of p53. It is also involved in the regulation of aging, neurological diseases and immune diseases. Recent studies demonstrated the critical roles of WIP1 in the differentiation and function of immune cells including T cells, neutrophils and macrophages. In the present manuscript, we briefly summarized the expression patterns, biological function and the target molecules and signal pathways of WIP1 and mainly discussed the latest advances on the regulatory effects of WIP1 in the immune system. WIP1 may be a potential target molecule to treat cancers and immune diseases such as allergic asthma.
Acknowledgments
The authors wish to thank Drs. Peng Wang and Zhanfeng Liang for their critical reading the manuscript.
Declaration of Interest
The authors declare no competing interests.
Authors’ contribution
Lu Shi drafted the manuscript. Qianchuan Tian made revision and gave suggestions during the preparation. Chang Feng, and Peng Zhang revised the manuscript. Yong Zhao gave supervision and made critical revisions. All authors read and approved the final manuscript.