Evidence map›Paper›PMID 31783008›Full record

ReviewThe American journal of pathology2020

Necroptosis in the Pathophysiology of Disease.

Mitri K Khoury, Kartik Gupta, Sarah R Franco, Bo Liu

Abstract readReview
In one paragraph

Review in The American journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 193 papers.

0numbers the graph read from it
0cells of the map it votes in
193citing 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

193 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
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  6. Article
  7. Role of PANoptosis in intestinal diseases and its therapeutic implications.Journal of molecular medicine (Berlin, Germany) · 2026
    Review
  8. Review
  9. Article
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  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
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  18. Review
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  20. Review

133 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

4 authors.

Mitri K KhouryDivision of Vascular Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin.
Kartik GuptaDivision of Vascular Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin.
Sarah R FrancoDivision of Vascular Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin.
Bo LiuDivision of Vascular Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin. Electronic address: liub@surgery.wisc.edu.

Funding

Molecular Mechanisms in Abdominal Aortic AneuysmR01HL088447 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI LIU, BO · 2011 to 2020
$3.8M
Vascular Surgery Research Training ProgramT32HL110853 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MATSUMURA, JON STEVEN · 2012 to 2021
$2.6M
Vascular smooth muscle cell apoptosis in intimal hyperplasiaR01HL122562 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI LIU, BO · 2015 to 2018
$1.6M
NHLBI NIH HHS R01 HL088447NHLBI NIH HHS R01 HL122562NHLBI NIH HHS T32 HL110853
6 · The paper itself

Abstract

Over the past 15 years, elegant studies have demonstrated that in certain conditions, programed cell death resembles necrosis and depends on a unique molecular pathway with no overlap with apoptosis. This form of regulated necrosis is represented by necroptosis, in which the receptor-interacting protein kinase-3 and its substrate mixed-lineage kinase domain-like protein play a crucial role. With the development of knockout mouse models and molecular inhibitors unique to necroptotic proteins, this cell death has been found to occur in virtually all tissues and diseases evaluated. There are different immunologic consequences depending on whether cells die through apoptosis or necroptosis. Therefore, distinguishing between these two forms of cell death may be crucial during pathologic evaluations. In this review, we provide an understanding of necroptotic cell-death and highlight diseases in which necroptosis has been found to play a role. We also discuss the inhibitors of necroptosis and the ways these inhibitors have been used in preclinical models of diseases. These two discussions offer an understanding of the role of necroptosis in diseases and will foster efforts to pharmacologically target this unique yet pervasive form of programed cell death in the clinic.

Indexed as

NecroptosisAnimalsChronic DiseaseDiseaseHumansInflammation

Identifiers

PMID31783008
PMCPMC6983729

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.