Evidence map›Paper›PMID 40332009›Full record

ReviewInternational journal of molecular sciences2025

Extracellular Cold-Inducible RNA-Binding Protein: Progress from Discovery to Present.

Monowar Aziz, Irshad H Chaudry, Ping Wang

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

3 authors.

Monowar AzizCenter for Immunology and Inflammation, The Feinstein Institutes for Medical Research, Manhasset, NY 11030, USA.ORCID 0000-0002-8195-4505
Irshad H ChaudryDepartment of Surgery, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Ping WangCenter for Immunology and Inflammation, The Feinstein Institutes for Medical Research, Manhasset, NY 11030, USA.ORCID 0000-0002-1557-0394

Funding

Neutrophils in Sepsis: Role of CIRPR01GM129633 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI AZIZ, MONOWAR · 2018 to 2022
$1.6M
NIGMS NIH HHS R01 GM129633NIH HHS R01GM129633 (MA), U01AI170018 (MA), R35GM118337 (PW), R01HL076179 (PW), U01AI170018 (PW), R01AA028947 (PW), and U01AI186997 (PW)
6 · The paper itself

Abstract

Extracellular cold-inducible RNA-binding protein (eCIRP) is a critical damage-associated molecular pattern (DAMP) that drives inflammation and tissue injury in hemorrhagic and septic shock, and has emerged as a promising therapeutic target. Since then, extensive research using preclinical models of diseases and patient materials has explored eCIRP's role in driving inflammatory responses and its potential as a biomarker. The main objective of this comprehensive review is to provide a detailed overview of eCIRP, covering its discovery, role in disease pathophysiology, mechanisms of release and action, potential as a biomarker, and therapeutic strategies targeting eCIRP in preclinical models of inflammatory and ischemic diseases. We examine the molecular, cellular, and immunological mechanisms through which eCIRP contributes to disease progression, and explore both well-established and emerging areas of research. Furthermore, we discuss potential therapeutic strategies targeting eCIRP across a broad spectrum of inflammatory conditions, including shock, ischemia-reperfusion injury, neurodegenerative diseases, and radiation injury.

Indexed as

RNA-Binding ProteinsAnimalsBiomarkersHumansInflammationBiomarkersCIRBP protein, humanRNA-Binding ProteinsDAMPsdiseasesimmune cellsimmunityinflammation

Identifiers

PMID40332009
PMCPMC12026706

What Socratic holds

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LicenceCC BY
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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 Socratic graph.