Evidence map›Paper›PMID 18268023›Full record

ArticleRNA (New York, N.Y.)2008

Translational repression during chronic hypoxia is dependent on glucose levels.

Jeff D Thomas, Lizalynn M Dias, Gregg J Johannes

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. The hypoxia-induced changes in miRNA-mRNA in RNA-induced silencing complexes and HIF-2 induced miRNAs in human endothelial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
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  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Surviving hypoxia by modulation of mRNA translation rate.Journal of cellular and molecular medicine · 2009
    Review
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

3 authors at 1 institution in 1 country.

Jeff D ThomasDepartment of Pathology and Laboratory Medicine, Drexel University College of Medicine, Philadelphia, Pennsylvania 19102, USA.
Lizalynn M Dias
Gregg J Johannes
Drexel University · US

Funding

Translational Regulation During HypoxiaR01CA112086 · NCI · DREXEL UNIVERSITY · PI JOHANNES, GREGG J · 2004 to 2008
$1.2M
NCI NIH HHS CA112086NCI NIH HHS R01 CA112086
6 · The paper itself

Abstract

Translation is often repressed in cell lines that are exposed to hypoxic conditions (0.5% - 1.5% O2) but this repression requires prolonged exposure (> 16 h). We report here that prolonged exposure to hypoxia results in the depletion of glucose from the media and that the loss of glucose correlates with the shut down in translation. Furthermore, we show that the addition of glucose or reoxygenation restores translation in hypoxic PC3 cells. This indicates that both glucose depletion and hypoxia are required for translational repression. We also show that eIF2alpha phosphorylation is reversed by glucose addition. Moreover, we present data that strongly indicate that eIF2alpha phosphorylation as well as the translational inhibition that occurs when cells are grown under conditions of glucose depletion and hypoxia is pancreatic eIF2alpha kinase (PERK) independent. We believe this is the first report to show that glucose depletion is required for translational repression under hypoxic conditions and that this explains why prolonged exposure to hypoxia is required for this inhibition. Since the physiological conditions that lead to tumor hypoxia would also likely lead to reduced glucose levels, understanding the interplay of glucose and hypoxia in regulating tumor metabolism will provide important information on the growth and development of solid tumors.

Indexed as

Protein BiosynthesisCell HypoxiaCell Line, TumorCulture Media, ConditionedeIF-2 KinaseEukaryotic Initiation Factor-2GlucoseGlutamineHumansKineticsMaleMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesPhosphorylationProstatic NeoplasmsProteinsCulture Media, ConditionedeIF-2 KinaseEukaryotic Initiation Factor-2GlucoseGlutamineMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesProteinsRNA, MessengerRNA, NeoplasmRNA, Small InterferingTOR Serine-Threonine KinasesTranscription Factors

Identifiers

PMID18268023
PMCPMC2271361
OpenAlexW2121833747

What OpenQuestion holds

Textmetadata
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.