Evidence map›Paper›PMID 17145963›Full record

ArticleThe Journal of cell biology2006

Oxidation state governs structural transitions in peroxiredoxin II that correlate with cell cycle arrest and recovery.

Timothy J Phalen, Kelly Weirather, Paula B Deming, Vikas Anathy, Alan K Howe, Albert van der Vliet, Thomas J Jönsson, Leslie B Poole, Nicholas H Heintz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

72 citing papers in PubMed, 129 citations in OpenAlex.

  1. Trial
  2. Article
  3. Navigating the redox landscape: reactive oxygen species in regulation of cell cycle.Redox report : communications in free radical research · 2024
    Review
  4. Review
  5. Redox Signaling in Plant Heat Stress Response.Antioxidants (Basel, Switzerland) · 2023
    Review
  6. Glutathione-Related Enzymes and Proteins: A Review.Molecules (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Role of Cytosolic 2-Cys Prx1 and Prx2 in Redox Signaling.Antioxidants (Basel, Switzerland) · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

12 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

9 authors at 2 institutions in 1 country.

Timothy J PhalenDepartment of Pathology, University of Vermont College of Medicine, Burlington, VT 05405, USA.
Kelly Weirather
Paula B Deming
Vikas Anathy
Alan K Howe
Albert van der Vliet
Thomas J Jönsson
Leslie B Poole
Nicholas H Heintz
University of Vermont · USWake Forest University · US

Funding

SIGNALING IN EPITHELIAL INJURY, PROLIFERATION &FIBROSISP01HL067004 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI MOSSMAN, BROOKE TAYLOR · 2001 to 2005
$7.6M
Mechanistic Studies of Alkyl Hydroperoxide Reductase and Related Redox SystemsR01GM050389 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI POOLE, LESLIE B · 1994 to 2013
$4.8M
ENVIRONMENTAL PATHOLOGY TRAINING PROGRAMT32ES007122 · NIEHS · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI VAN DER VLIET, ALBERT · 1985 to 2012
$4.2M
Spatial regulation of Protein Kinase A in cell migrationR01GM074204 · NIGMS · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI HOWE, ALAN K · 2005 to 2010
$1.4M
NHLBI NIH HHS P01 HL067004NHLBI NIH HHS P01 HL67004NIEHS NIH HHS T32 ES007122NIGMS NIH HHS R01 GM050389NIGMS NIH HHS R01 GM074204NIGMS NIH HHS R01 GM74204
6 · The paper itself

Abstract

Inactivation of eukaryotic 2-Cys peroxiredoxins (Prxs) by hyperoxidation has been proposed to promote accumulation of hydrogen peroxide (H2O2) for redox-dependent signaling events. We examined the oxidation and oligomeric states of PrxI and -II in epithelial cells during mitogenic signaling and in response to fluxes of H2O2. During normal mitogenic signaling, hyperoxidation of PrxI and -II was not detected. In contrast, H2O2-dependent cell cycle arrest was correlated with hyperoxidation of PrxII, which resulted in quantitative recruitment of approximately 66- and approximately 140-kD PrxII complexes into large filamentous oligomers. Expression of cyclin D1 and cell proliferation did not resume until PrxII-SO2H was reduced and native PrxII complexes were regenerated. Ectopic expression of PrxI or -II increased Prx-SO2H levels in response to oxidant exposure and failed to protect cells from arrest. We propose a model in which Prxs function as peroxide dosimeters in subcellular processes that involve redox cycling, with hyperoxidation controlling structural transitions that alert cells of perturbations in peroxide homeostasis.

Indexed as

Cell CycleOxidation-ReductionAnimalsCell LineCell ProliferationHydrogen PeroxideMiceModels, BiologicalOxidative StressPeroxidasesPeroxidesPeroxiredoxinsSerumSignal TransductionHydrogen PeroxidePeroxidasesPeroxidesPeroxiredoxins

Identifiers

PMID17145963
PMCPMC2064677
OpenAlexW2110096570

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.