Evidence map›Paper›PMID 42602525›Full record

ArticleiScience2026

Insights into the activity, production, and signaling circuits of homoserine lactones in mammalian cells.

Sepand Tehrani Fateh, Sahand Tehrani Fateh, Seyed Ali Ziai

Abstract read
In one paragraph

Article in iScience, 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

3 authors.

Sepand Tehrani FatehSchool of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sahand Tehrani FatehSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Seyed Ali ZiaiDepartment of Pharmacology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence suggests that acyl homoserine lactones (AHLs), bacterial signaling metabolites, also play signaling roles in eukaryotic organisms, including human cells. Through a meta-analysis of prior investigations, we mapped the effects of AHLs and their signaling roles. Given their evolutionary significance and potential physiological roles, we further asked whether human cells possess the machinery to perceive and produce AHLs or similar compounds. AHLs commonly regulate pathways involved in cell-fate decisions, with RXRs and peroxisome proliferator-activated receptors (PPARs) identified as potential upstream AHL receptors. Structural specificity was supported by the observation that both the γ-butyrolactone ring and the acyl tail contribute to receptor affinity. Furthermore, human glycine/glutamine acyltransferases showed structural and functional homology to bacterial AHL synthases using

Indexed as

acyl-transferasehomoserine lactonemetabolite signalingperoxisome proliferator-activated receptorretinoic X receptor

Identifiers

PMID42602525
PMCPMC13474087

What OpenQuestion holds

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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.