Literature DB >> 17439715

JNK pathway: diseases and therapeutic potential.

Jie Cui1, Ming Zhang, Yong-Qing Zhang, Zhi-Heng Xu.   

Abstract

c-Jun N-terminal protein kinases (JNK), also known as stress-activated protein kinases, were originally identified by their ability to phosphorylate the N-terminal of the transcription factor c-Jun and by their activation in response to a variety of stresses. JNK are multifunctional kinases involved in many physiological processes. The JNK pathway has been shown to play a major role in apoptosis in many cell death paradigms and its association with a variety of pathological processes is gradually been recognized. This review will concentrate on describing the involvement of the JNK pathway in the context of different diseases and the potential to adopt the JNK pathway components as therapeutic targets.

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Year:  2007        PMID: 17439715     DOI: 10.1111/j.1745-7254.2007.00579.x

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  61 in total

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2.  Increased JNK in males compared with females in a rodent model of abdominal aortic aneurysm.

Authors:  Paul D DiMusto; Guanyi Lu; Abhijit Ghosh; Karen J Roelofs; Omar Sadiq; Brendan McEvoy; Gang Su; Adriana Laser; Castigliano M Bhamidipati; Gorav Ailawadi; Peter K Henke; Jonathan L Eliason; Gilbert R Upchurch
Journal:  J Surg Res       Date:  2011-12-14       Impact factor: 2.192

3.  JNK signalling is necessary for a Wnt- and stem cell-dependent regeneration programme.

Authors:  Belen Tejada-Romero; Jean-Michel Carter; Yuliana Mihaylova; Bjoern Neumann; A Aziz Aboobaker
Journal:  Development       Date:  2015-06-10       Impact factor: 6.868

4.  Neuroprotective Effects of the Absence of JNK1 or JNK3 Isoforms on Kainic Acid-Induced Temporal Lobe Epilepsy-Like Symptoms.

Authors:  Luisa de Lemos; Felix Junyent; Antoni Camins; Rubén Darío Castro-Torres; Jaume Folch; Jordi Olloquequi; Carlos Beas-Zarate; Ester Verdaguer; Carme Auladell
Journal:  Mol Neurobiol       Date:  2017-06-29       Impact factor: 5.590

5.  MKK7 and ARF: new players in the DNA damage response scenery.

Authors:  Athanassios Kotsinas; Panagiota Papanagnou; Panagiotis Galanos; Daniel Schramek; Paul Townsend; Josef M Penninger; Jiri Bartek; Vassilis G Gorgoulis
Journal:  Cell Cycle       Date:  2014-03-26       Impact factor: 4.534

6.  Identification of an Adamantyl Azaquinolone JNK Selective Inhibitor.

Authors:  Nancy-Ellen Haynes; Nathan R Scott; Li C Chen; Cheryl A Janson; Jia Kui Li; Christine M Lukacs; Aruna Railkar; Effie Tozzo; Toni Whittard; Nicholas F Brown; Adrian Wai-Hing Cheung
Journal:  ACS Med Chem Lett       Date:  2012-08-08       Impact factor: 4.345

7.  Inhibition of c-Jun N-terminal kinase enhances temozolomide-induced cytotoxicity in human glioma cells.

Authors:  Shigeo Ohba; Yuichi Hirose; Takeshi Kawase; Hirotoshi Sano
Journal:  J Neurooncol       Date:  2009-06-11       Impact factor: 4.130

8.  Obesity and intestinal epithelial deletion of the insulin receptor, but not the IGF 1 receptor, affect radiation-induced apoptosis in colon.

Authors:  M Agostina Santoro; R Eric Blue; Sarah F Andres; Amanda T Mah; Laurianne Van Landeghem; P Kay Lund
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2015-08-06       Impact factor: 4.052

9.  Prunella vulgaris aqueous extract attenuates IL-1β-induced apoptosis and NF-κB activation in INS-1 cells.

Authors:  Huiping Wu; Ming Gao; Tuanzhu Ha; Jim Kelley; Ada Young; Kevin Breuel
Journal:  Exp Ther Med       Date:  2012-03-23       Impact factor: 2.447

10.  Modulation of c-Jun N-terminal kinase signaling and specific glucocorticoid receptor phosphorylation in the treatment of major depression.

Authors:  Milica J Jovicic; Iva Lukic; Marija Radojcic; Miroslav Adzic; Nadja P Maric
Journal:  Med Hypotheses       Date:  2015-06-02       Impact factor: 1.538

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