Evidence map›Paper›PMID 27048812›Full record

ReviewCellular and molecular life sciences : CMLS2016

Generation of small molecules to interfere with regulated necrosis.

Alexei Degterev, Andreas Linkermann

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.4field-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

34 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. No Time to Die: How Kidney Cancer Evades Cell Death.International journal of molecular sciences · 2022
    Review
  7. Review
  8. Article
  9. Review
  10. The role of regulated necrosis in endocrine diseases.Nature reviews. Endocrinology · 2021
    Review
  11. Article
  12. Article
  13. Necroptosis in Hepatosteatotic Ischaemia-Reperfusion Injury.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Cell Death in the Kidney.International journal of molecular sciences · 2019
    Review
  18. Article
  19. Review
  20. 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

2 authors at 2 institutions in 2 countries.

Alexei DegterevDepartment of Developmental, Molecular & Chemical Biology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, MA, 02111, USA. alexei.degterev@tufts.edu.
Andreas LinkermannClinic for Nephrology and Hypertension, University-Hospital Schleswig-Holstein, Campus Kiel, Christian-Albrechts-University Kiel, Fleckenstr. 4, 24105, Kiel, Germany. andreas.linkermann@uksh.de.
Tufts University · USUniversity Hospital Schleswig-Holstein · DE

Funding

Molecular and functional analysis of necroptosis initiation complexR01GM080356 · NIGMS · TUFTS UNIVERSITY BOSTON · PI DEGTEREV, ALEXEI · 2008 to 2012
$1.9M
Mechanistic analysis of necrostatins: specific inhibitors of programmed necrosisR01GM084205 · NIGMS · TUFTS UNIVERSITY BOSTON · PI DEGTEREV, ALEXEI · 2009 to 2012
$1.8M
NIGMS NIH HHS R01 GM080356NIGMS NIH HHS R01 GM084205
6 · The paper itself

Abstract

Interference with regulated necrosis for clinical purposes carries broad therapeutic relevance and, if successfully achieved, has a potential to revolutionize everyday clinical routine. Necrosis was interpreted as something that no clinician might ever be able to prevent due to the unregulated nature of this form of cell death. However, given our growing understanding of the existence of regulated forms of necrosis and the roles of key enzymes of these pathways, e.g., kinases, peroxidases, etc., the possibility emerges to identify efficient and selective small molecule inhibitors of pathologic necrosis. Here, we review the published literature on small molecule inhibition of regulated necrosis and provide an outlook on how combination therapy may be most effective in treatment of necrosis-associated clinical situations like stroke, myocardial infarction, sepsis, cancer and solid organ transplantation.

Indexed as

AnimalsApoptosisCyclohexylaminesHeterocyclic Compounds, 4 or More RingsHumansImidazolesMiceNecrosisOrganic ChemicalsPhenylenediaminesProtein KinasesPyridazinesQuinoxalinesReceptor-Interacting Protein Serine-Threonine KinasesSpiro CompoundsSulfonesCyclohexylaminesferrostatin-1Heterocyclic Compounds, 4 or More RingsImidazolesliproxstatin-1MLKL protein, humanNecroX-5necrox-7Organic ChemicalsPhenylenediaminesponatinibProtein KinasesPyridazinesQuinoxalinesReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, humanRIPK3 protein, humanSpiro CompoundsSulfonesFerroptosisFerrostatinsNecroptosisNecrostatinsProgrammed cell deathRegulated necrosisTNF

Identifiers

PMID27048812
PMCPMC11108466
OpenAlexW2333116104

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.