Abstract
Protein phosphorylation and post-phosphorylation events regulate many cellular signaling pathways. Peptidyl-prolyl isomerase (Pin1) is the only peptidyl-prolyl cis/trans isomerase that interacts with numerous oncogenic or tumor suppressive phosphorylated proteins, causes conformational changes in target proteins, and eventually regulates the activities of such proteins. These alterations in activity play a pivotal role in tumorigenesis. Since Pin1 is overexpressed and/or activated in various types of cancers, and the dysregulation of proline-directed phosphorylation contributes to tumorigenesis, Pin1 represents an attractive target for cancer therapy. This review will describe the role of Pin1 in cancer and the current status of Pin1 inhibitor development.
| Original language | English |
|---|---|
| Pages (from-to) | 1609-1620 |
| Number of pages | 12 |
| Journal | Archives of Pharmacal Research |
| Volume | 39 |
| Issue number | 12 |
| DOIs | |
| State | Published - 1 Dec 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cancer-driving pathways
- Pin1
- Pin1 inhibitor
- Proline-directed phosphorylation
- Prolyl isomerase
- Tumorigenesis
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