Literature DB >> 17496914

Role of mitogen-activated protein kinase kinase 4 in cancer.

A J Whitmarsh1, R J Davis.   

Abstract

Mitogen-activated protein (MAP) kinase kinase 4 (MKK4) is a component of stress activated MAP kinase signaling modules. It directly phosphorylates and activates the c-Jun N-terminal kinase (JNK) and p38 families of MAP kinases in response to environmental stress, pro-inflammatory cytokines and developmental cues. MKK4 is ubiquitously expressed and the targeted deletion of the Mkk4 gene in mice results in early embryonic lethality. Further studies in mice have indicated a role for MKK4 in liver formation, the immune system and cardiac hypertrophy. In humans, it is reported that loss of function mutations in the MKK4 gene are found in approximately 5% of tumors from a variety of tissues, suggesting it may have a tumor suppression function. Furthermore, MKK4 has been identified as a suppressor of metastasis of prostate and ovarian cancers. However, the role of MKK4 in cancer development appears complex as other studies support a pro-oncogenic role for MKK4 and JNK. Here we review the biochemical and functional properties of MKK4 and discuss the likely mechanisms by which it may regulate the steps leading to the formation of cancers.

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Year:  2007        PMID: 17496914     DOI: 10.1038/sj.onc.1210410

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  63 in total

Review 1.  Role of C-Jun N-terminal Kinase in Hepatocellular Carcinoma Development.

Authors:  Juan Wang; Guixiang Tai
Journal:  Target Oncol       Date:  2016-12       Impact factor: 4.493

2.  Synthetic Lethality Induced by Loss of PKC δ and Mutated Ras.

Authors:  Tongbo Zhu; Lihua Chen; Wei Du; Takanori Tsuji; Changyan Chen
Journal:  Genes Cancer       Date:  2010-02

3.  Requirement of c-Jun NH(2)-terminal kinase for Ras-initiated tumor formation.

Authors:  Cristina Cellurale; Guadalupe Sabio; Norman J Kennedy; Madhumita Das; Marissa Barlow; Peter Sandy; Tyler Jacks; Roger J Davis
Journal:  Mol Cell Biol       Date:  2011-01-31       Impact factor: 4.272

4.  Loss of Wip1 sensitizes cells to stress- and DNA damage-induced apoptosis.

Authors:  Yun Xia; Pat Ongusaha; Sam W Lee; Yih-Cherng Liou
Journal:  J Biol Chem       Date:  2009-04-24       Impact factor: 5.157

5.  SAPK pathways and p53 cooperatively regulate PLK4 activity and centrosome integrity under stress.

Authors:  Takanori Nakamura; Haruo Saito; Mutsuhiro Takekawa
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

6.  Delphinidin suppresses ultraviolet B-induced cyclooxygenases-2 expression through inhibition of MAPKK4 and PI-3 kinase.

Authors:  Jung Yeon Kwon; Ki Won Lee; Jong-Eun Kim; Sung Keun Jung; Nam Joo Kang; Mun Kyung Hwang; Yong-Seok Heo; Ann M Bode; Zigang Dong; Hyong Joo Lee
Journal:  Carcinogenesis       Date:  2009-09-23       Impact factor: 4.944

7.  Induced overexpression of protein kinase D1 stimulates mitogenic signaling in human pancreatic carcinoma PANC-1 cells.

Authors:  Krisztina Kisfalvi; Cliff Hurd; Sushovan Guha; Enrique Rozengurt
Journal:  J Cell Physiol       Date:  2010-05       Impact factor: 6.384

8.  Synthesis and Biological Evaluation of 3-Arylindazoles as Selective MEK4 Inhibitors.

Authors:  Kristine K Deibler; Gary E Schiltz; Matthew R Clutter; Rama K Mishra; Purav P Vagadia; Matthew O'Connor; Mariam Donny George; Ryan Gordon; Graham Fowler; Raymond Bergan; Karl A Scheidt
Journal:  ChemMedChem       Date:  2019-02-19       Impact factor: 3.466

9.  Role of JNK in a Trp53-dependent mouse model of breast cancer.

Authors:  Cristina Cellurale; Claire R Weston; Judith Reilly; David S Garlick; D Joseph Jerry; Hayla K Sluss; Roger J Davis
Journal:  PLoS One       Date:  2010-08-30       Impact factor: 3.240

Review 10.  Signal integration by JNK and p38 MAPK pathways in cancer development.

Authors:  Erwin F Wagner; Angel R Nebreda
Journal:  Nat Rev Cancer       Date:  2009-08       Impact factor: 60.716

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