Literature DB >> 15377263

JNK: a key modulator of intracellular signaling.

S Vlahopoulos1, V C Zoumpourlis.   

Abstract

JNK is a family of stress activated protein kinase enzymes that is under intense study. JNK family members are involved in diverse phenomena, but the focus of research has been until now involvement of JNK in apoptosis. A great number of JNK substrates indeed play major roles in cell death. Conversely, accumulating data supports a key role of JNK substrates in cell survival and proliferation. Continuous progress is being made, while several important questions remain unanswered. Does JNK cause cancer or prevent it? This paper attempts to evaluate the role of JNK in cell physiology and describe the effects of intracellular signaling pathways that are mediated by JNK family members. Copyright 2004 MAIK

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Year:  2004        PMID: 15377263     DOI: 10.1023/b:biry.0000040215.02460.45

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  25 in total

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Journal:  Cytokine Growth Factor Rev       Date:  2015-06-20       Impact factor: 7.638

3.  JNK pathway inhibition enhances chemotherapeutic sensitivity to Adriamycin in nasopharyngeal carcinoma cells.

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Journal:  Oncol Lett       Date:  2017-06-08       Impact factor: 2.967

4.  Estrogen regulates JNK1 genomic localization to control gene expression and cell growth in breast cancer cells.

Authors:  Miao Sun; Gary D Isaacs; Nasun Hah; Nina Heldring; Elizabeth A Fogarty; W Lee Kraus
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5.  SIRT1 deficiency downregulates PTEN/JNK/FOXO1 pathway to block reactive oxygen species-induced apoptosis in mouse embryonic stem cells.

Authors:  Hee-Don Chae; Hal E Broxmeyer
Journal:  Stem Cells Dev       Date:  2011-01-03       Impact factor: 3.272

6.  An upregulation of SIAH1 after spinal cord injury in adult rats.

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7.  Serpin-derived peptides are antiangiogenic and suppress breast tumor xenograft growth.

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8.  Differential cleavage of Mst1 by caspase-7/-3 is responsible for TRAIL-induced activation of the MAPK superfamily.

Authors:  Jae J Song; Yong J Lee
Journal:  Cell Signal       Date:  2008-01-11       Impact factor: 4.315

9.  Synthesis, biological evaluation, and molecular modeling of 11H-indeno[1,2-b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime as c-Jun N-terminal kinase inhibitors.

Authors:  Igor A Schepetkin; Andrei I Khlebnikov; Andrei S Potapov; Anastasia R Kovrizhina; Vladislava V Matveevskaya; Maxim L Belyanin; Dmitriy N Atochin; Svitlana O Zanoza; Nadiya M Gaidarzhy; Sergiy A Lyakhov; Liliya N Kirpotina; Mark T Quinn
Journal:  Eur J Med Chem       Date:  2018-10-12       Impact factor: 6.514

10.  Identification of learning and memory genes in canine; promoter investigation and determining the selective pressure.

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Journal:  Mol Biol Rep       Date:  2014-09-06       Impact factor: 2.316

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