Literature DB >> 8305679

The receptor-like protein tyrosine phosphatase alpha: a role in cell proliferation and oncogenesis.

C J Pallen1.   

Abstract

The transmembrane nature of the receptor-like protein tyrosine phosphatases (PTPases) suggests that they transduce as yet unidentified extracellular signals to intracellular events via a phosphotyrosyl-protein dephosphorylation step, although little is known of their regulation and cellular activities. Structure/function studies of PTP alpha demonstrate that both catalytic domains are required for full enzymatic efficiency and that interdomain interactions may modulate PTP alpha activity and specificity. Overexpression of PTP alpha results in cell transformation and tumorigenesis, likely as a consequence of the ability of PTP alpha to dephosphorylate and activate the c-src tyrosine kinase. This suggests a role for PTP alpha in normal cell proliferation. PTP alpha is so far unique among the PTPases in terms of its oncogenic potential, and overexpression or deregulation of PTP alpha may be involved in the genesis, progression or maintenance of certain tumor states.

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Year:  1993        PMID: 8305679     DOI: 10.1006/scel.1993.1048

Source DB:  PubMed          Journal:  Semin Cell Biol        ISSN: 1043-4682


  3 in total

1.  Investigational Strategies for Detection and Intervention in Early-Stage Pancreatic Cancer. April 24-27, Annapolis, Maryland. Abstracts.

Authors: 
Journal:  Int J Pancreatol       Date:  1994 Oct-Dec

2.  Modulation of protein tyrosine phosphorylation in gastric mucosa during re-epithelization processes.

Authors:  Olena V Bogdanova; Larysa I Kot; Kateryna V Lavrova; Volodymyr B Bogdanov; Erica K Sloan; Tetyana V Beregova; Ludmyla I Ostapchenko
Journal:  World J Biol Chem       Date:  2010-11-26

3.  Phosphonate inhibitors of protein-tyrosine and serine/threonine phosphatases.

Authors:  H K Kole; M S Smyth; P L Russ; T R Burke
Journal:  Biochem J       Date:  1995-11-01       Impact factor: 3.857

  3 in total

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