Literature DB >> 27259981

Mixed - Lineage Protein kinases (MLKs) in inflammation, metabolism, and other disease states.

Siobhan M Craige1, Michaella M Reif1, Shashi Kant2.   

Abstract

Mixed lineage kinases, or MLKs, are members of the MAP kinase kinase kinase (MAP3K) family, which were originally identified among the activators of the major stress-dependent mitogen activated protein kinases (MAPKs), JNK and p38. During stress, the activation of JNK and p38 kinases targets several essential downstream substrates that react in a specific manner to the unique stressor and thus determine the fate of the cell in response to a particular challenge. Recently, the MLK family was identified as a specific modulator of JNK and p38 signaling in metabolic syndrome. Moreover, the MLK family of kinases appears to be involved in a very wide spectrum of disorders. This review discusses the newly identified functions of MLKs in multiple diseases including metabolic disorders, inflammation, cancer, and neurological diseases.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Disease; Inflammation; Insulin resistance; Kinase; Metabolism; Mixed-lineage kinase; Signal transduction

Mesh:

Substances:

Year:  2016        PMID: 27259981     DOI: 10.1016/j.bbadis.2016.05.022

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  JNK is antagonized to ensure the correct number of interommatidial cells pattern the Drosophila retina.

Authors:  Henry L Bushnell; Christina E Feiler; Kwami F Ketosugbo; Mark B Hellerman; Valerie L Nazzaro; Ruth I Johnson
Journal:  Dev Biol       Date:  2017-11-11       Impact factor: 3.582

Review 2.  The Regulatory Roles of Mitogen-Activated Protein Kinase (MAPK) Pathways in Health and Diabetes: Lessons Learned from the Pancreatic β-Cell.

Authors:  Vaibhav Sidarala; Anjaneyulu Kowluru
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3.  A Protein Scaffold Coordinates SRC-Mediated JNK Activation in Response to Metabolic Stress.

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4.  TNFα-induced DLK activation contributes to apoptosis in the beta-cell line HIT.

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5.  Mixed Lineage Kinase 3 phosphorylates prolyl-isomerase PIN1 and potentiates GLI1 signaling in pancreatic cancer development.

Authors:  Navin Viswakarma; Gautam Sondarva; Daniel R Principe; Rakesh Sathish Nair; Sandeep Kumar; Sunil Kumar Singh; Subhasis Das; Subhash C Sinha; Paul J Grippo; Sam Grimaldo; Pier Cristoforo Giulianotti; Basabi Rana; Ajay Rana
Journal:  Cancer Lett       Date:  2021-05-27       Impact factor: 9.756

Review 6.  JNK and cardiometabolic dysfunction.

Authors:  Siobhan M Craige; Kai Chen; Robert M Blanton; John F Keaney; Shashi Kant
Journal:  Biosci Rep       Date:  2019-07-18       Impact factor: 3.840

7.  Neural JNK3 regulates blood flow recovery after hindlimb ischemia in mice via an Egr1/Creb1 axis.

Authors:  Shashi Kant; Siobhan M Craige; Kai Chen; Michaella M Reif; Heather Learnard; Mark Kelly; Amada D Caliz; Khanh-Van Tran; Kasmir Ramo; Owen M Peters; Marc Freeman; Roger J Davis; John F Keaney
Journal:  Nat Commun       Date:  2019-09-17       Impact factor: 14.919

Review 8.  Cdc42/Rac Interactive Binding Containing Effector Proteins in Unicellular Protozoans With Reference to Human Host: Locks of the Rho Signaling.

Authors:  Preeti Umarao; Pragyan Parimita Rath; Samudrala Gourinath
Journal:  Front Genet       Date:  2022-02-02       Impact factor: 4.599

9.  ZAK Gene Expression in Patients with Helicobacter pylori Infection.

Authors:  Delniya Khani; Manouchehr Ahmadi Hedayati; Sherko Nasseri; Farshad Sheikhesmaeili; Roghaie Ghadiany
Journal:  J Gastrointest Cancer       Date:  2021-02-23

10.  A screen for E3 ubiquitination ligases that genetically interact with the adaptor protein Cindr during Drosophila eye patterning.

Authors:  Kwami F Ketosugbo; Henry L Bushnell; Ruth I Johnson
Journal:  PLoS One       Date:  2017-11-08       Impact factor: 3.240

  10 in total

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