Evidence map›Paper›PMID 41017683›Full record

ArticleNeural regeneration research2026

Long non-coding RNAs: Emerging regulators of diverse programmed cell death pathways in neurons.

Noah C Mathew, Kevin K Park

Abstract read
In one paragraph

Article in Neural regeneration research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Noah C MathewDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Kevin K ParkDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-4796-3894

Funding

Stem Cell, Organoid and Cell Phenotyping ModuleP30EY030413 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI W MATTHEW PETROLL · 2019 to 2026
$5.9M
3D visualization and Investigation of Retinal Axon RegenerationR01EY032542 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI PARK, KEVIN KYUNG · 2021 to 2024
$1.5M
The role of novel lincRNAs in regulating RGC survival after injuryR01EY034531 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI KEVIN Kyung PARK · 2024 to 2026
$1.2M
NEI NIH HHS P30 EY030413NEI NIH HHS R01 EY032542NEI NIH HHS R01 EY034531
6 · The paper itself

Abstract

Long non-coding RNAs have emerged as pivotal regulators of diverse biological processes, particularly in the modulation of regulated neuronal cell death pathways. This review highlights the roles of long non-coding RNAs in programmed neuronal cell death, focusing on apoptosis, necroptosis, ferroptosis, and pyroptosis. Dysregulation of these processes contributes to neurodegenerative disorders and neurological injuries, emphasizing the importance of understanding how long non-coding RNAs influence these pathways. Apoptosis, essential for neuronal development, can lead to pathology when misregulated. Necroptosis, a caspase-independent inflammatory process, involves the modulation of necrosome components. Pyroptosis, mediated by inflammasomes, affects inflammasome assembly and cytokine release. Ferroptosis, driven by iron accumulation and lipid peroxidation, is influenced by changes in antioxidant defenses. By detailing the roles of long non-coding RNAs in these mechanisms, this review underscores their therapeutic potential for mitigating neuronal loss.

Indexed as

apoptosislncRNAnecroptosisneuronal deathnon-coding RNA

Identifiers

PMID41017683
PMCPMC13557654

What Socratic 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 Socratic graph.