Evidence map›Paper›PMID 36745209›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2023

HMGB1/TLR4 signaling pathway enhances abdominal aortic aneurysm progression in mice by upregulating necroptosis.

Shuai Bian, Le Yang, Dongfang Zhao, Lizhi Lv, Tiezheng Wang, Hai Yuan

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. HMGB1: a multifaceted mediator of cell death pathways in cardiovascular diseases.Apoptosis : an international journal on programmed cell death · 2025
    Review
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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 3 institutions in 1 country.

Shuai Bian *Department of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Le Yang *Department of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Dongfang ZhaoBinzhou Medical University, Binzhou, China.
Lizhi LvDepartment of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Tiezheng WangDepartment of Medical Ultrasound, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Hai YuanDepartment of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. yhdoctor@163.com.
Shandong First Medical University · CNBinzhou University · CNShandong Provincial Hospital · CN

Funding

Natural Science Fund for Distinguished Young Scholars of Shandong Province ZR2021QH220
6 · The paper itself

Abstract

OBJECTIVE AND

designThe age-associated increases in aseptic inflammation and necroptosis are closely related to the emergence of various age-associated diseases.

methodsIn this study, the role of HMGB1/TLR4-induced necroptosis in abdominal aortic aneurysm (AAA) formation was investigated. First, the levels of sterile inflammatory mediators (HMGB1, TLR4) and necroptosis markers were measured in the abdominal aortas of young and old C57BL/6JNifdc mice. We observed that sterile inflammatory mediators and necroptosis markers were greatly increased in the abdominal aortas of old mice. Then, angiotensin II (Ang II)-induced AAA model in APOE

resultsWe found that HMGB1, TLR4, and necroptosis markers were elevated in old mice compared with those in young mice. Same elevation was also found in the development of AAA in APOE

conclusionsOur results indicated that HMGB1/TLR4-mediated necroptosis enhances AAA development in the Ang II-induced AAA model in APOE

Indexed as

Aortic Aneurysm, AbdominalHMGB1 ProteinAngiotensin IIAnimalsAorta, AbdominalApolipoproteins EDisease Models, AnimalInflammation MediatorsMiceMice, Inbred C57BLMice, KnockoutNecroptosisSignal TransductionSulfonamidesToll-Like Receptor 4Angiotensin IIApolipoproteins Eethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylateHMGB1 ProteinInflammation MediatorsSulfonamidesTlr4 protein, mouseToll-Like Receptor 4Abdominal aortic aneurysmAngiotensin IIHMGB1NecroptosisToll-like receptor 4

Identifiers

PMID36745209
OpenAlexW4319294521

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.