Evidence map›Paper›PMID 42094595›Full record

ArticleTheranostics2026

CIAPIN1 functions as a redox-sensitive transcriptional repressor of

Seongpyo Lee, Joo-Hui Han

Abstract read
In one paragraph

Article in Theranostics, 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.

Seongpyo LeeCollege of Pharmacy, Woosuk University, Wanju 55338, Republic of Korea.
Joo-Hui HanCollege of Pharmacy, Woosuk University, Wanju 55338, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Phenotypic switching in vascular smooth muscle cells (VSMCs) is a major driver of pathological vascular remodeling, including atherosclerosis and restenosis. Although p53 is a key regulator of VSMC homeostasis, the precise molecular mechanisms responsible for suppressing p53 expression during growth factor-induced phenotypic transitions remain incompletely understood. The present study identifies cytokine-induced apoptosis inhibitor 1 (CIAPIN1) as a novel redox-sensitive regulator of the p53 signaling axis. Methods: Primary cultured VSMCs and a rat carotid balloon injury model were used to investigate the role of CIAPIN1 in VSMC dynamics. CIAPIN1 expression was modulated using both gain- and loss-of-function approaches. The interaction between CIAPIN1 and the Results: In human atherosclerotic lesions, CIAPIN1 expression was markedly upregulated, whereas Conclusions: CIAPIN1 functions as a redox-sensitive transcriptional repressor of

Indexed as

Intracellular Signaling Peptides and ProteinsTumor Suppressor Protein p53Vascular RemodelingAnimalsAtherosclerosisCarotid Artery InjuriesCell ProliferationCells, CulturedHumansMaleMuscle, Smooth, VascularMyocytes, Smooth MuscleNeointimaOxidation-ReductionPromoter Regions, GeneticRatsCIAPIN1 protein, humanIntracellular Signaling Peptides and ProteinsTumor Suppressor Protein p53CIAPIN1intimal hyperplasiap53PDGF-BBreactive oxygen species

Identifiers

PMID42094595
PMCPMC13142666

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.