Evidence map›Paper›PMID 19906009›Full record

ReviewInflammation & allergy drug targets2010

High mobility group box 1 protein as a potential drug target for infection- and injury-elicited inflammation.

Shu Zhu, Wei Li, Mary F Ward, Andrew E Sama, Haichao Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Inflammation & allergy drug targets, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Tezepelumab: patient selection and place in therapy in severe asthma.The Journal of international medical research · 2024
    Review
  3. Article
  4. Decreasing mRNA HMGB1 expression inAnnals of medicine and surgery (2012) · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. HMGB1 as a potential new marker of disease activity in patients with multiple sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Thrombomodulin, alarmin signaling, and copeptin: cross-talk between obesity and acute ischemic stroke initiation and severity in Egyptians.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2018
    Article
  15. Emerging role of HMGB1 in lung diseases: friend or foe.Journal of cellular and molecular medicine · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. D-K6L 9 peptide combination with IL-12 inhibits the recurrence of tumors in mice.Archivum immunologiae et therapiae experimentalis · 2014
    Article
  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

5 authors at 4 institutions in 1 country.

Shu ZhuThe Feinstein Institute for Medical Research, North Shore-LIJ Health System, Manhasset, NY 11030, USA.
Wei Li
Mary F Ward
Andrew E Sama
Haichao Wang
North Shore University Hospital · USFeinstein Institute for Medical Research · USNational University of Health Sciences · USNorthwell Health · US

Funding

Regulation of HMGB1 Release in Endotoxemia.R01GM063075 · NIGMS · NORTH SHORE UNIVERSITY HOSPITAL · PI WANG, HAICHAO · 2002 to 2020
$4.2M
Neuroprotective Role of Fetuin in Cerebral IschemiaR01GM070817 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI WANG, HAICHAO · 2005 to 2008
$1.3M
NIGMS NIH HHS R01 GM063075NIGMS NIH HHS R01GM063075NIGMS NIH HHS R01 GM070817NIGMS NIH HHS R01GM070817
6 · The paper itself

Abstract

In response to infection or injury, a ubiquitous nucleosomal protein, HMGB1 is secreted actively by innate immune cells, and / or released passively by injured/damaged cells. Subsequently, extracellular HMGB1 alerts, recruits, and activates various innate immune cells to sustain a rigorous inflammatory response. A growing number of HMGB1 inhibitors ranging from neutralizing antibodies, endogenous hormones, to medicinal herb-derived small molecule HMGB1 inhibitors (such as nicotine, glycyrrhizin, tanshinones, and EGCG) are proven protective against lethal infection and ischemic injury. Here we review emerging evidence that support extracellular HMGB1 as a proinflammatory alarmin(g) danger signal, and discuss a wide array of HMGB1 inhibitors as potential therapeutic agents for sepsis and ischemic injury.

Indexed as

Amino Acid SequenceAnimalsFemaleHMGB1 ProteinHumansInfectionsInflammationIschemiaMiceMolecular Sequence DataWounds and InjuriesHMGB1 Protein

Identifiers

PMID19906009
PMCPMC2866444
OpenAlexW2087701622

What OpenQuestion holds

Textmetadata
LicenceTDM
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.