Conclusion
Many studies have implicated tyrosine phosphatases in the down-regulation of growth factor signaling pathways. It is becoming evident that some of them, including SHP-1, SHP-2 and PTPη, have a role in SSTR signaling. However, there are many issues which remain to be clarified. These include the identification of SST-mediated pathways in which these PTPs participate, as well as their physiological substrates and binding partners and the precise molecular mechanisms, which permit their interaction with sst receptors and/or associated molecules. In addition, the respective role of these PTP for each receptor subtype pathway awaits further study. Genetic approaches including gene targeting, RNA interference (RNAi) and new technologies including proteomic analysis and cell imaging for the detection and analysis of signalling complexes, will provide powerful tools to elucidate these important questions.
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Lahlou, H. et al. (2004). Somatostatin Receptor Signaling via Protein Tyrosine Phosphatases. In: Srikant, C.B. (eds) Somatostatin. Endocrine Updates, vol 24. Springer, Boston, MA. https://doi.org/10.1007/1-4020-8033-6_10
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