Evidence map›Paper›PMID 24657741›Full record

ArticleFree radical biology & medicine2014

Endosomal H2O2 production leads to localized cysteine sulfenic acid formation on proteins during lysophosphatidic acid-mediated cell signaling.

Chananat Klomsiri, LeAnn C Rogers, Laura Soito, Anita K McCauley, S Bruce King, Kimberly J Nelson, Leslie B Poole, Larry W Daniel

Open access · greenAbstract read
In one paragraph

Article in Free radical biology & medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. HIV-1 gp120-induced lysosomal stress responses are controlled by TRPML1 redox sensors.Redox report : communications in free radical research · 2026
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  11. Insights into the Role of Oxidative Stress in Ovarian Cancer.Oxidative medicine and cellular longevity · 2021
    Review
  12. Article
  13. Regulation of the Proteolytic Activity of Cysteine Cathepsins by Oxidants.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. ROLE OF THIOLS IN OXIDATIVE STRESS.Current opinion in toxicology · 2018
    Article
  19. Article
  20. Article
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

8 authors at 1 institution in 1 country.

Chananat KlomsiriDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: cklomsir@wakehealth.edu.
LeAnn C RogersDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: rlrogers@wakehealth.edu.
Laura SoitoDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: lsoito@lib.ucdavis.edu.
Anita K McCauleyDepartment of Biology, Wake Forest University, Winston-Salem, NC 27109, USA. Electronic address: mccaulak@wfu.edu.
S Bruce KingDepartment of Chemistry, Wake Forest University, Winston-Salem, NC 27109, USA. Electronic address: kingsb@wfu.edu.
Kimberly J NelsonDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: kinelson@wakehealth.edu.
Leslie B PooleDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: lbpoole@wakehealth.edu.
Larry W DanielDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA. Electronic address: ldaniel@wakehealth.edu.
Wake Forest University · US

Funding

The Wake Forest Center for Botanical Lipids and Inflammatory Disease PreventionP50AT002782 · NCCIH · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHILTON, FLOYD H · 2005 to 2014
$15.3M
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
Role of redox state in ovarian cancer response to cisplatinR01CA142838 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DANIEL, LARRY W · 2010 to 2014
$1.4M
New Reagents for Tracking Protein Oxidation in Cells by MS and Imaging MethodsR33CA177461 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2013 to 2015
$1.0M
Proteomic Profiling of Cancer-Related Redox Signaling PathwaysR33CA126659 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI POOLE, LESLIE B · 2008 to 2010
$948k
NCCIH NIH HHS P50 AT002782NCCIH NIH HHS P50AT002782NCI NIH HHS R01 CA142838NCI NIH HHS R01CA142838NCI NIH HHS R33 CA126659NCI NIH HHS R33 CA177461NCI NIH HHS R33CA177461NIGMS NIH HHS R01 GM050389NIGMS NIH HHS R01GM050389
6 · The paper itself

Abstract

Lysophosphatidic acid (LPA) is a growth factor for many cells including prostate and ovarian cancer-derived cell lines. LPA stimulates H2O2 production which is required for growth. However, there are significant gaps in our understanding of the spatial and temporal regulation of H2O2-dependent signaling and the way in which signals are transmitted following receptor activation. Herein, we describe the use of two reagents, DCP-Bio1 and DCP-Rho1, to evaluate the localization of active protein oxidation after LPA stimulation by detection of nascent protein sulfenic acids. We found that LPA stimulation causes internalization of LPA receptors into early endosomes that contain NADPH oxidase components and are sites of H2O2 generation. DCP-Rho1 allowed visualization of sulfenic acid formation, indicative of active protein oxidation, which was stimulated by LPA and decreased by an LPA receptor antagonist. Protein oxidation sites colocalized with LPAR1 and the endosomal marker EEA1. Concurrent with the generation of these redox signaling-active endosomes (redoxosomes) is the H2O2- and NADPH oxidase-dependent oxidation of Akt2 and PTP1B detected using DCP-Bio1. These new approaches therefore enable detection of active, H2O2-dependent protein oxidation linked to cell signaling processes. DCP-Rho1 may be a particularly useful protein oxidation imaging agent enabling spatial resolution due to the transient nature of the sulfenic acid intermediate it detects.

Indexed as

Gene Expression RegulationBenzamidesCell Line, TumorCysteineEndosomesFemaleHumansHydrogen PeroxideLysophospholipidsMaleNADPH OxidasesOxidation-ReductionPhenylpropionatesProtein TransportProtein Tyrosine Phosphatase, Non-Receptor Type 1Proto-Oncogene Proteins c-akt3-(2,6-dimethyl-4-carbamoylphenyl)propanoic acidAKT2 protein, humanBenzamidesCysteinecysteinesulfenic acidearly endosome antigen 1Hydrogen Peroxidelysophosphatidic acidLysophospholipidsNADPH OxidasesPhenylpropionatesProtein Tyrosine Phosphatase, Non-Receptor Type 1Proto-Oncogene Proteins c-aktPTPN1 protein, humanReceptors, Lysophosphatidic AcidSulfenic AcidsVesicular Transport ProteinsCysteine modificationsLipid mediatorsLPA signalingProliferative signalingProtein oxidation

Identifiers

PMID24657741
PMCPMC4064372
OpenAlexW1979189930

What OpenQuestion holds

Textmetadata
LicenceTDM
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.