Literature DB >> 29194686

New insights into the role and mechanism of c-Jun-N-terminal kinase signaling in the pathobiology of liver diseases.

Sanda Win1, Tin Aung Than1, Jun Zhang1, Christina Oo1, Robert Win Maw Min1, Neil Kaplowitz1.   

Abstract

The c-Jun-N-terminal-kinase (JNK) family is highly conserved across species such as Drosophila, C. elegans, zebrafish and mammals, and plays a central role in hepatic physiologic and pathophysiologic responses. These responses range from cell death to cell proliferation and carcinogenesis, as well as metabolism and survival, depending on the specific context and duration of activation of the JNK signaling pathway. Recently, several investigators identified the key molecules in the JNK activation loop which include apoptosis signal-regulating kinase (ASK1) and SH3-domain binding protein 5 (Sab) and their involvement in acute or chronic liver disease models. Thus, regulating JNK activation through modulating the JNK activation loop may represent an important new strategy in the prevention and treatment of acute and chronic liver diseases. In this review, we will discuss the molecular pathophysiology of the JNK activation loop and its role in the pathogenesis of liver diseases. (Hepatology 2018;67:2013-2024).
© 2017 by the American Association for the Study of Liver Diseases.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29194686      PMCID: PMC5906137          DOI: 10.1002/hep.29689

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  62 in total

1.  c-Jun N-terminal kinase modulates oxidant stress and peroxynitrite formation independent of inducible nitric oxide synthase in acetaminophen hepatotoxicity.

Authors:  Chieko Saito; John J Lemasters; Hartmut Jaeschke
Journal:  Toxicol Appl Pharmacol       Date:  2010-04-25       Impact factor: 4.219

Review 2.  The MAPK cascades: signaling components, nuclear roles and mechanisms of nuclear translocation.

Authors:  Alexander Plotnikov; Eldar Zehorai; Shiri Procaccia; Rony Seger
Journal:  Biochim Biophys Acta       Date:  2010-12-16

3.  Hepatocyte-specific deletion of the keap1 gene activates Nrf2 and confers potent resistance against acute drug toxicity.

Authors:  Hiromi Okawa; Hozumi Motohashi; Akira Kobayashi; Hiroyuki Aburatani; Thomas W Kensler; Masayuki Yamamoto
Journal:  Biochem Biophys Res Commun       Date:  2005-11-08       Impact factor: 3.575

4.  Saturated fatty acids induce c-Src clustering within membrane subdomains, leading to JNK activation.

Authors:  Ryan G Holzer; Eek-Joong Park; Ning Li; Helen Tran; Monica Chen; Crystal Choi; Giovanni Solinas; Michael Karin
Journal:  Cell       Date:  2011-09-30       Impact factor: 41.582

Review 5.  JNK regulation of hepatic manifestations of the metabolic syndrome.

Authors:  Mark J Czaja
Journal:  Trends Endocrinol Metab       Date:  2010-10-01       Impact factor: 12.015

6.  Deletion of apoptosis signal-regulating kinase 1 attenuates acetaminophen-induced liver injury by inhibiting c-Jun N-terminal kinase activation.

Authors:  Hayato Nakagawa; Shin Maeda; Yohko Hikiba; Tomoya Ohmae; Wataru Shibata; Ayako Yanai; Kei Sakamoto; Keiji Ogura; Takuya Noguchi; Michael Karin; Hidenori Ichijo; Masao Omata
Journal:  Gastroenterology       Date:  2008-07-09       Impact factor: 22.682

7.  Blocking c-Jun N-terminal kinase (JNK) translocation to the mitochondria prevents 6-hydroxydopamine-induced toxicity in vitro and in vivo.

Authors:  Jeremy W Chambers; Shannon Howard; Philip V LoGrasso
Journal:  J Biol Chem       Date:  2012-11-26       Impact factor: 5.157

8.  The role of MAP2 kinases and p38 kinase in acute murine liver injury models.

Authors:  Jun Zhang; Robert W M Min; Khanh Le; Sheng Zhou; Mariam Aghajan; Tin A Than; Sanda Win; Neil Kaplowitz
Journal:  Cell Death Dis       Date:  2017-06-29       Impact factor: 8.469

9.  Combined Activities of JNK1 and JNK2 in Hepatocytes Protect Against Toxic Liver Injury.

Authors:  Francisco Javier Cubero; Miguel Eugenio Zoubek; Wei Hu; Jin Peng; Gang Zhao; Yulia A Nevzorova; Malika Al Masaoudi; Lars P Bechmann; Mark V Boekschoten; Michael Muller; Christian Preisinger; Nikolaus Gassler; Ali E Canbay; Tom Luedde; Roger J Davis; Christian Liedtke; Christian Trautwein
Journal:  Gastroenterology       Date:  2015-12-19       Impact factor: 22.682

10.  FGF21 regulates metabolism and circadian behavior by acting on the nervous system.

Authors:  Angie L Bookout; Marleen H M de Groot; Bryn M Owen; Syann Lee; Laurent Gautron; Heather L Lawrence; Xunshan Ding; Joel K Elmquist; Joseph S Takahashi; David J Mangelsdorf; Steven A Kliewer
Journal:  Nat Med       Date:  2013-08-11       Impact factor: 53.440

View more
  36 in total

1.  Expression of mitochondrial membrane-linked SAB determines severity of sex-dependent acute liver injury.

Authors:  Sanda Win; Robert Wm Min; Christopher Q Chen; Jun Zhang; Yibu Chen; Meng Li; Ayako Suzuki; Manal F Abdelmalek; Ying Wang; Mariam Aghajan; Filbert Wm Aung; Anna Mae Diehl; Roger J Davis; Tin A Than; Neil Kaplowitz
Journal:  J Clin Invest       Date:  2019-12-02       Impact factor: 14.808

Review 2.  Fibroblast growth factors 19 and 21 in acute liver damage.

Authors:  Zhao Shan; Gloria Alvarez-Sola; Iker Uriarte; María Arechederra; Maite G Fernández-Barrena; Carmen Berasain; Cynthia Ju; Matías A Avila
Journal:  Ann Transl Med       Date:  2018-06

3.  The peptide hormone adropin regulates signal transduction pathways controlling hepatic glucose metabolism in a mouse model of diet-induced obesity.

Authors:  Su Gao; Sarbani Ghoshal; Liyan Zhang; Joseph R Stevens; Kyle S McCommis; Brian N Finck; Gary D Lopaschuk; Andrew A Butler
Journal:  J Biol Chem       Date:  2019-07-19       Impact factor: 5.157

4.  ASK1 inhibition reduces cell death and hepatic fibrosis in an Nlrp3 mutant liver injury model.

Authors:  Susanne Schuster-Gaul; Lukas Jonathan Geisler; Matthew D McGeough; Casey D Johnson; Anna Zagorska; Li Li; Alexander Wree; Vivian Barry; Igor Mikaelian; Lily J Jih; Bettina G Papouchado; Grant Budas; Hal M Hoffman; Ariel E Feldstein
Journal:  JCI Insight       Date:  2020-01-30

5.  Gastric Bypass Regulates Early Inflammatory Responses in High-Fat Diet-Induced Obese Mice.

Authors:  Rui Xu; Chenyu Zhu; Yuxin Li; Michael Andrade; Deng Ping Yin
Journal:  J Surg Res       Date:  2022-01-24       Impact factor: 2.192

6.  JNK activation and translocation to mitochondria mediates mitochondrial dysfunction and cell death induced by VDAC opening and sorafenib in hepatocarcinoma cells.

Authors:  K A Heslop; A Rovini; E G Hunt; D Fang; M E Morris; C F Christie; M B Gooz; D N DeHart; Y Dang; J J Lemasters; E N Maldonado
Journal:  Biochem Pharmacol       Date:  2019-11-21       Impact factor: 5.858

7.  SPHK1 deficiency protects mice from acetaminophen-induced ER stress and mitochondrial permeability transition.

Authors:  Longjun Li; Haitao Wang; Jun Zhang; Yeqin Sha; Fengjiao Wu; Shuang Wen; Lianping He; Liang Sheng; Qiang You; Meiqing Shi; Lixin Liu; Hong Zhou
Journal:  Cell Death Differ       Date:  2019-12-11       Impact factor: 15.828

Review 8.  From overnutrition to liver injury: AMP-activated protein kinase in nonalcoholic fatty liver diseases.

Authors:  Peng Zhao; Alan R Saltiel
Journal:  J Biol Chem       Date:  2020-07-10       Impact factor: 5.157

9.  Hepatic Mitochondrial SAB Deletion or Knockdown Alleviates Diet-Induced Metabolic Syndrome, Steatohepatitis, and Hepatic Fibrosis.

Authors:  Sanda Win; Robert W M Min; Jun Zhang; Gary Kanel; Brad Wanken; Yibu Chen; Meng Li; Ying Wang; Ayako Suzuki; Filbert W M Aung; Susan F Murray; Mariam Aghajan; Tin A Than; Neil Kaplowitz
Journal:  Hepatology       Date:  2021-10-10       Impact factor: 17.425

10.  Adipocyte Fatty Acid Binding Protein Promotes the Onset and Progression of Liver Fibrosis via Mediating the Crosstalk between Liver Sinusoidal Endothelial Cells and Hepatic Stellate Cells.

Authors:  Xiaoping Wu; Lingling Shu; Zixuan Zhang; Jingjing Li; Jiuyu Zong; Lai Yee Cheong; Dewei Ye; Karen S L Lam; Erfei Song; Cunchuan Wang; Aimin Xu; Ruby L C Hoo
Journal:  Adv Sci (Weinh)       Date:  2021-03-27       Impact factor: 16.806

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.