Evidence map›Paper›PMID 29610153›Full record

ReviewMolecular and cellular biology2018

Signaling Pathways Involved in the Regulation of mRNA Translation.

Philippe P Roux, Ivan Topisirovic

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular and cellular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

197 citing papers in PubMed, 320 citations in OpenAlex.

  1. Trial
  2. Review
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  11. TAK1 Regulates Skeletal Muscle Mass, Hypertrophic Signaling, and Metabolic Homeostasis in Male and Female Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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  17. Review
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  19. Review
  20. Effects ofBiology · 2025
    Article

137 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Philippe P RouxInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Québec, Canada philippe.roux@umontreal.ca ivan.topisirovic@mcgill.ca.
Ivan TopisirovicLady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada philippe.roux@umontreal.ca ivan.topisirovic@mcgill.ca.
Institute for Research in Immunology and Cancer · CAMcGill University · CA

Funding

Control of Protein Synthesis by the UPS Under StressR01CA202021 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI RONAI, ZEEV A. · 2016 to 2020
$2.3M
NCI NIH HHS R01 CA202021
6 · The paper itself

Abstract

Translation is a key step in the regulation of gene expression and one of the most energy-consuming processes in the cell. In response to various stimuli, multiple signaling pathways converge on the translational machinery to regulate its function. To date, the roles of phosphoinositide 3-kinase (PI3K)/AKT and the mitogen-activated protein kinase (MAPK) pathways in the regulation of translation are among the best understood. Both pathways engage the mechanistic target of rapamycin (mTOR) to regulate a variety of components of the translational machinery. While these pathways regulate protein synthesis in homeostasis, their dysregulation results in aberrant translation leading to human diseases, including diabetes, neurological disorders, and cancer. Here we review the roles of the PI3K/AKT and MAPK pathways in the regulation of mRNA translation. We also highlight additional signaling mechanisms that have recently emerged as regulators of the translational apparatus.

Indexed as

AnimalsEukaryotic Initiation Factor-2Gene Expression RegulationHumansMechanistic Target of Rapamycin Complex 1Mitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesProtein BiosynthesisProto-Oncogene Proteins c-aktRNA, MessengerSignal TransductionTOR Serine-Threonine KinasesEukaryotic Initiation Factor-2Mechanistic Target of Rapamycin Complex 1Mitogen-Activated Protein KinasesMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, MessengerTOR Serine-Threonine KinaseseIF4EMAPKmitogen-activated protein kinasesMNKmRNAmRNA translationmTORprotein phosphorylationRSKsignal transductiontranslational control

Identifiers

PMID29610153
PMCPMC5974435
OpenAlexW2796317691

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.