Evidence map›Paper›PMID 32041780›Full record

ArticleThe Journal of biological chemistry2020

Opposing effects of polysulfides and thioredoxin on apoptosis through caspase persulfidation.

Ilana Braunstein, Rotem Engelman, Ofer Yitzhaki, Tamar Ziv, Erwan Galardon, Moran Benhar

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. SQOR regulates HResearch square · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Fundamentals of redox regulation in biology.Nature reviews. Molecular cell biology · 2024
    Review
  7. Article
  8. Article
  9. Sulfide catabolism in hibernation and neuroprotection.Nitric oxide : biology and chemistry · 2024
    Review
  10. Impact of Reactive Sulfur Species onAntioxidants (Basel, Switzerland) · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors at 2 institutions in 2 countries.

Ilana BraunsteinDepartment of Biochemistry, Rappaport Institute for Research in the Medical Sciences, Faculty of Medicine, Technion Israel Institute of Technology, Haifa, 3200003 Israel.
Rotem EngelmanDepartment of Biochemistry, Rappaport Institute for Research in the Medical Sciences, Faculty of Medicine, Technion Israel Institute of Technology, Haifa, 3200003 Israel.
Ofer YitzhakiDepartment of Biochemistry, Rappaport Institute for Research in the Medical Sciences, Faculty of Medicine, Technion Israel Institute of Technology, Haifa, 3200003 Israel.
Tamar ZivSmoler Proteomics Center and Faculty of Biology, Technion Israel Institute of Technology, Haifa, 31096 Israel.
Erwan GalardonUMR 8601, CNRS, Université Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France.
Moran BenharDepartment of Biochemistry, Rappaport Institute for Research in the Medical Sciences, Faculty of Medicine, Technion Israel Institute of Technology, Haifa, 3200003 Israel. Electronic address: benhar@technion.ac.il.
Technion – Israel Institute of Technology · ILDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogen sulfide has been implicated in a large number of physiological processes including cell survival and death, encouraging research into its mechanisms of action and therapeutic potential. Results from recent studies suggest that the cellular effects of hydrogen sulfide are mediated in part by sulfane sulfur species, including persulfides and polysulfides. In the present study, we investigated the apoptosis-modulating effects of polysulfides, especially on the caspase cascade, which mediates the intrinsic apoptotic pathway. Biochemical analyses revealed that organic or synthetic polysulfides strongly and rapidly inhibit the enzymatic activity of caspase-3, a major effector protease in apoptosis. We attributed the caspase-3 inhibition to persulfidation of its catalytic cysteine. In apoptotically stimulated HeLa cells, short-term exposure to polysulfides triggered the persulfidation and deactivation of cleaved caspase-3. These effects were antagonized by the thioredoxin/thioredoxin reductase system (Trx/TrxR). Trx/TrxR restored the activity of polysulfide-inactivated caspase-3

Indexed as

ApoptosisCaspase 3Caspase 9Caspase InhibitorsCaspasesEnzyme ActivationHeLa CellsHumansSignal TransductionSulfidesThioredoxin-Disulfide ReductaseThioredoxinsCaspase 3Caspase 9Caspase InhibitorsCaspasespersulfidespolysulfideSulfidesThioredoxin-Disulfide ReductaseThioredoxinsapoptosiscancercaspasescell signalingdepersulfidationhydrogen sulfide (H2S)polysulfidesprotein persulfidationredox regulationsulfhydrationthioredoxin

Identifiers

PMID32041780
PMCPMC7076224
OpenAlexW3006028094

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.