Evidence map›Paper›PMID 39303918›Full record

ArticleThe Journal of biological chemistry2024

Protein phosphatase PP2Cα S-glutathionylation regulates cell migration.

Dhanushika S K Kukulage, Kusal T G Samarasinghe, Nadee N J Matarage Don, Madhu C Shivamadhu, Kyosuke Shishikura, William Schiff, Faezeh Mashhadi Ramezani, Rayavarapu Padmavathi, Megan L Matthews, Young-Hoon Ahn

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Redox Regulation of Cell Migration via Nischarin S-glutathionylation.bioRxiv : the preprint server for biology · 2025
    Article
  5. 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

10 authors.

Dhanushika S K KukulageDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Kusal T G SamarasingheAmgen Inc., Thousand Oaks, California, USA.
Nadee N J Matarage DonDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Madhu C ShivamadhuDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Kyosuke ShishikuraDepartment of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
William SchiffDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Faezeh Mashhadi RamezaniDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Rayavarapu PadmavathiDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA.
Megan L MatthewsDepartment of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Young-Hoon AhnDepartment of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA. Electronic address: ya426@drexel.edu.

Funding

Chemical Methods for Dissecting Protein Glutathionylation in SarcomereR01HL131740 · NHLBI · WAYNE STATE UNIVERSITY · PI AHN, YOUNG-HOON, BHAGWAT, ASHOK S · 2017 to 2021
$1.8M
Chemical Proteomic Strategy to Investigate Cysteine GlutathionylationR01GM143214 · NIGMS · WAYNE STATE UNIVERSITY · PI AHN, YOUNG-HOON · 2021 to 2024
$1.1M
NHLBI NIH HHS R01 HL131740NIGMS NIH HHS R01 GM143214
6 · The paper itself

Abstract

Redox signaling is a fundamental mechanism that controls all major biological processes partly via protein cysteine oxidations, including S-glutathionylation. Despite over 2000 cysteines identified to form S-glutathionylation in databases, the identification of redox cysteines functionally linked to a biological process of interest remains challenging. Here, we demonstrate a strategy combining glutathionylation proteomic database, bioinformatics, and biological screening, which resulted in the identification of S-glutathionylated proteins, including PP2Cα, as redox players of cell migration. We showed that PP2Cα, a prototypical magnesium-dependent serine/threonine phosphatase, is susceptible to S-glutathionylation selectively at nonconserved C314. PP2Cα glutathionylation causes increased migration and invasion of breast cancer cell lines in oxidative stress or upon hydrogen peroxide production. Mechanistically, PP2Cα glutathionylation modulates its protein-protein interactions, activating c-Jun N-terminal kinase and extracellular signal-regulated kinase pathways to elevate migration and invasion. In addition, PP2Cα glutathionylation occurs in response to epidermal growth factor, supporting a serine/threonine phosphatase PP2Cα as a new redox player in growth factor signal transduction.

Indexed as

Cell MovementGlutathioneProtein Phosphatase 2CCell Line, TumorHumansOxidation-ReductionOxidative StressGlutathionePPM1A protein, humanProtein Phosphatase 2Ccell migrationepidermal growth factorglutathionylationPP2Cα phosphatasereactive oxygen speciesredox signaling

Identifiers

PMID39303918
PMCPMC11530597

What OpenQuestion holds

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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.