Evidence map›Paper›PMID 38195700›Full record

ReviewEMBO molecular medicine2024

Mediators of necroptosis: from cell death to metabolic regulation.

Xiaoqin Wu, Laura E Nagy, Jérémie Gautheron

Erratum issuedAbstract readReview
In one paragraph

Review in EMBO molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Xiaoqin WuNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, USA.
Laura E NagyNorthern Ohio Alcohol Center, Department of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, USA.ORCID 0000-0002-0580-2809
Jérémie GautheronSorbonne Université, Inserm UMRS_938, Centre de Recherche Saint-Antoine (CRSA), Paris, 75012, France. jeremie.gautheron@inserm.fr.ORCID 0000-0002-7727-9893

Funding

Project Two - Exercise Training Decreases Alcohol Drinking by an FGF21-Dependent MechanismP50AA024333 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAURA E. NAGY · 2016 to 2026
$19.6M
Transcriptional and non-transcriptional functions of IRF3 in ALDR01AA027456 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAURA E. NAGY · 2019 to 2026
$3.5M
IRAKM and MINCLE in ALDR01AA030699 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI LAURA E. NAGY · 2023 to 2026
$2.4M
Microbial metabolites and Innate Immunity in AH: Biomarkers of injury and repairU01AA026938 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2018 to 2023
$1.4M
Role of MLKL in Alcohol-associated Liver DiseaseR00AA029146 · NIAAA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, XIAOQIN · 2023 to 2025
$747k
Role of MLKL in Alcohol-associated Liver DiseaseK99AA029146 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI WU, XIAOQIN · 2021 to 2022
$341k
NIAAA NIH HHS K99 AA029146NIAAA NIH HHS P50 AA024333NIAAA NIH HHS R00 AA029146NIAAA NIH HHS R01 AA027456NIAAA NIH HHS R01 AA030699NIAAA NIH HHS U01 AA026938
6 · The paper itself

Abstract

Necroptosis, a programmed cell death mechanism distinct from apoptosis, has garnered attention for its role in various pathological conditions. While initially recognized for its involvement in cell death, recent research has revealed that key necroptotic mediators, including receptor-interacting protein kinases (RIPKs) and mixed lineage kinase domain-like protein (MLKL), possess additional functions that go beyond inducing cell demise. These functions encompass influencing critical aspects of metabolic regulation, such as energy metabolism, glucose homeostasis, and lipid metabolism. Dysregulated necroptosis has been implicated in metabolic diseases, including obesity, diabetes, metabolic dysfunction-associated steatotic liver disease (MASLD) and alcohol-associated liver disease (ALD), contributing to chronic inflammation and tissue damage. This review provides insight into the multifaceted role of necroptosis, encompassing both cell death and these extra-necroptotic functions, in the context of metabolic diseases. Understanding this intricate interplay is crucial for developing targeted therapeutic strategies in diseases that currently lack effective treatments.

Indexed as

Liver DiseasesMetabolic DiseasesApoptosisCell DeathHumansNecroptosisNecrosisProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesProtein KinasesReceptor-Interacting Protein Serine-Threonine KinasesRIP1 Kinase; RIP3 Kinase; MLKL; Cell Death; Metabolism

Identifiers

PMID38195700
PMCPMC10897313

What OpenQuestion holds

Textmetadata
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.