Evidence map›Paper›PMID 28757353›Full record

ArticleCellular signalling2017

Osmotic and heat stress-dependent regulation of MLK4β and MLK3 by the CHIP E3 ligase in ovarian cancer cells.

Natalya A Blessing, Srimathi Kasturirangan, Evan M Zink, April L Schroyer, Deborah N Chadee

Abstract read
In one paragraph

Article in Cellular signalling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Natalya A BlessingDepartment of Biological Sciences, The University of Toledo, Toledo, OH 43606, USA.
Srimathi KasturiranganDepartment of Biological Sciences, The University of Toledo, Toledo, OH 43606, USA.
Evan M ZinkDepartment of Biological Sciences, The University of Toledo, Toledo, OH 43606, USA.
April L SchroyerDepartment of Biological Sciences, The University of Toledo, Toledo, OH 43606, USA.
Deborah N ChadeeDepartment of Biological Sciences, The University of Toledo, Toledo, OH 43606, USA. Electronic address: deborah.chadee@utoledo.edu.
University of Toledo · US

Funding

Regulation of MLK3 by oxidative stress in colon cancer cellsR15CA199164 · NCI · UNIVERSITY OF TOLEDO · PI CHADEE, DEBORAH N · 2016 to 2016
$443k
MLK4 regulation of MAPK signalingR15GM102831 · NIGMS · UNIVERSITY OF TOLEDO · PI CHADEE, DEBORAH N · 2012 to 2012
$349k
NCI NIH HHS R15 CA199164NIGMS NIH HHS R15 GM102831
6 · The paper itself

Abstract

Mixed Lineage Kinase 3 (MLK3), a member of the MLK subfamily of protein kinases, is a mitogen-activated protein (MAP) kinase kinase kinase (MAP3K) that activates MAPK signalling pathways and regulates cellular responses such as proliferation, invasion and apoptosis. MLK4β, another member of the MLK subfamily, is less extensively studied, and the regulation of MLK4β by stress stimuli is not known. In this study, the regulation of MLK4β and MLK3 by osmotic stress, thermostress and heat shock protein 90 (Hsp90) inhibition was investigated in ovarian cancer cells. MLK3 and MLK4β protein levels declined under conditions of prolonged osmotic stress, heat stress or exposure to the Hsp90 inhibitor geldanamycin (GA); and MLK3 protein declined faster than MLK4β. Similar to MLK3, the reduction in MLK4β protein in cells exposed to heat or osmotic stresses occurred via a mechanism that involves the E3 ligase, carboxy-terminus of Hsc70-interacting protein (CHIP). Both heat shock protein 70 (Hsp70) and CHIP overexpression led to polyubiquitination and a decrease in endogenous MLK4β protein, and MLK4β was ubiquitinated by CHIP in vitro. In untreated cells and cells exposed to osmotic and heat stresses for short time periods, small interfering RNA (siRNA) knockdown of MLK4β elevated the levels of activated MLK3, c-Jun N-terminal kinase (JNK) and p38 MAPKs. Furthermore, MLK3 binds to MLK4β, and this association is regulated by osmotic stress. These results suggest that in the early response to stressful stimuli, MLK4β-MLK3 binding is important for regulating MLK3 activity and MAPK signalling, and after prolonged periods of stress exposure, MLK4β and MLK3 proteins decline via CHIP-dependent degradation. These findings provide insight into how heat and osmotic stresses regulate MLK4β and MLK3, and reveal an important function for MLK4β in modulating MLK3 activity in stress responses.

Indexed as

Heat-Shock ResponseOsmotic PressureBenzoquinonesCell Line, TumorFemaleHEK293 CellsHSC70 Heat-Shock ProteinsHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11Ovarian NeoplasmsProtein BindingRNA, Small InterferingUbiquitinationBenzoquinonesgeldanamycinHSC70 Heat-Shock ProteinsHSP90 Heat-Shock ProteinsHSPA8 protein, humanLactams, MacrocyclicMAP3K21 protein, humanMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11RNA, Small InterferingSTUB1 protein, humanUbiquitin-Protein LigasesCarboxyl-terminus of Hsc70-interacting protein (CHIP)Mitogen activated protein kinase (MAPK)Mixed Lineage Kinase 3 (MLK3)Mixed Lineage Kinase 4 (MLK4)Stress signallingUbiquitination

Identifiers

PMID28757353
PMCPMC5592140
OpenAlexW2740682444

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.