Cancer and Metastasis Reviews

, Volume 27, Issue 2, pp 263–272

Targeting PTPs with small molecule inhibitors in cancer treatment


DOI: 10.1007/s10555-008-9113-3

Cite this article as:
Jiang, ZX. & Zhang, ZY. Cancer Metastasis Rev (2008) 27: 263. doi:10.1007/s10555-008-9113-3


Protein tyrosine phosphorylation plays a major role in cellular signaling. The level of tyrosine phosphorylation is controlled by protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs). Disturbance of the normal balance between PTK and PTP activity results in aberrant tyrosine phosphorylation, which has been linked to the etiology of several human diseases, including cancer. A number of PTPs have been implicated in oncogenesis and tumor progression and therefore are potential drug targets for cancer chemotherapy. These include PTP1B, which may augment signaling downstream of HER2/Neu; SHP2, which is the first oncogene in the PTP superfamily and is essential for growth factor-mediated signaling; the Cdc25 phosphatases, which are positive regulators of cell cycle progression; and the phosphatase of regenerating liver (PRL) phosphatases, which promote tumor metastases. As PTPs have emerged as drug targets for cancer, a number of strategies are currently been explored for the identification of various classes of PTP inhibitors. These efforts have resulted many potent, and in some cases selective, inhibitors for PTP1B, SHP2, Cdc25 and PRL phosphatases. Structural information derived from these compounds serves as a solid foundation upon which novel anti-cancer agents targeted to these PTPs can be developed.


Protein tyrosine phosphatase (PTP)PTP1BSHP2Cdc25PRL phosphatasesSmall molecule inhibitor designPTP inhibitor



protein tyrosine kinase


protein tyrosine phosphatase


Src homology-2


phosphatase of regenerating liver

Copyright information

© Springer Science+Business Media, LLC 2008

Authors and Affiliations

  1. 1.Department of Biochemistry and Molecular BiologyIndiana University School of MedicineIndianapolisUSA