Reprint

Dual Specificity Phosphatases

From Molecular Mechanisms to Biological Function

Edited by
November 2019
240 pages
  • ISBN978-3-03921-688-8 (Paperback)
  • ISBN978-3-03921-689-5 (PDF)

This book is a reprint of the Special Issue Dual Specificity Phosphatases: From Molecular Mechanisms to Biological Function that was published in

Biology & Life Sciences
Chemistry & Materials Science
Medicine & Pharmacology
Summary

Dual specificity phosphatases (DUSPs) constitute a heterogeneous group of protein tyrosine phosphatases with the ability to dephosphorylate Ser/Thr and Tyr residues from proteins, as well as from other non-proteinaceous substrates including signaling lipids. DUSPs include, among others, MAP kinase (MAPK) phosphatases (MKPs) and small-size atypical DUSPs. MKPs are enzymes specialized in regulating the activity and subcellular location of MAPKs, whereas the function of small-size atypical DUSPs seems to be more diverse. DUSPs have emerged as key players in the regulation of cell growth, differentiation, stress response, and apoptosis. DUSPs regulate essential physiological processes, including immunity, neurobiology and metabolic homeostasis, and have been implicated in tumorigenesis, pathological inflammation and metabolic disorders. Accordingly, alterations in the expression or function of MKPs and small-size atypical DUSPs have consequences essential to human disease, making these enzymes potential biological markers and therapeutic targets. This Special Issue covers recent advances in the molecular mechanisms and biological functions of MKPs and small-size atypical DUSPs, and their relevance in human disease.

Format
  • Paperback
License
© 2020 by the authors; CC BY license
Keywords
E. coli infection; sepsis; liver steatosis; hypertriglyceridemia; Mkp-1; inflammation; asthma; COPD; MAPK; respiratory viruses; influenza; rhinovirus; RSV; neuroblastoma; neuronal differentiation; dual-specificity phosphatases; MAP kinases; MAP kinase phosphatases; atypical dual-specificity phosphatases; pseudophosphatase; MK-STYX (MAPK (mitogen-activated protein kinase) phosphoserine/threonine/tyrosine-binding protein); HDAC6 (histone deacetylase isoform 6); post-translational modification; microtubules; DUSP10; MAPK; inflammation; cancer; fungal MKPs; MAPKs; signaling; Msg5; Sdp1; Pmp1; Cpp1; dual-specificity phosphatases; MAP kinases; nucleotide receptors; P2X7; P2Y13; BDNF; cannabinoids; granule neurons; astrocytes; TLR signaling; hematopoietic cells; integrated omics analysis; dual-specificity phosphatase; mitogen-activated protein kinase; ubiquitination; protein stability; MAPK phosphatase; atypical DUSP; macrophage; T cell; cytokines; inflammation; circulating tumor cells (CTCs); DEPArray; dual-specificity phosphatase; HER2; brain metastasis; single cell analysis; triple-negative breast cancer (TNBC); MAP Kinase Phosphatase-2; DUSP-4; macrophages; proliferation; differentiation; n/a