Evidence map›Paper›PMID 40362186›Full record

ReviewInternational journal of molecular sciences2025

Advancing Ischemic Stroke Prognosis: Key Role of MiR-155 Non-Coding RNA.

Catherine Hering, Gloria M Conover

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

2 authors.

Catherine HeringDepartment of Medical Education, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Gloria M ConoverDepartment of Medical Education, College of Medicine, Texas A&M University, Bryan, TX 77807, USA.

Funding

Texas A&M Presidential Transformational Teaching (TTLC) Grant NA
6 · The paper itself

Abstract

Ischemic stroke (IS) is the leading cause of long-term disability and the second leading cause of death worldwide. It remains a significant clinical problem because only supportive therapies exist, such as thrombolytic agents and surgical thrombectomy, which do not restore function. Understanding the molecular pathogenesis of IS, including dysfunction in oxidative homeostasis, apoptosis, neuroinflammation and neuroprotection, is crucial to developing therapies. Non-coding RNAs (ncRNAs) are master regulators, and one ncRNA that stands out is miR-155, a pro-inflammatory micro-RNA elevated in stroke. This review addresses the biological mechanisms reported in the literature that support using miR-155 as a biomarker and therapeutic agent to treat IS in patients.

Indexed as

Brain IschemiaIschemic StrokeMicroRNAsAnimalsBiomarkersHumansPrognosisBiomarkersMicroRNAsMIRN155 microRNA, humanapoptosisischemic strokemicroglia polarizationmicroRNAsmiR-155neuroinflammationneuroprotectionnon-coding RNAsoxidative stressSIRT1stroke therapeutics

Identifiers

PMID40362186
PMCPMC12071504

What OpenQuestion 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 OpenQuestion graph.