Evidence map›Paper›PMID 42856670›Full record

ArticleFrontiers in cell and developmental biology2026

Integrated lipidomic and transcriptomic profiling of imiquimod-induced psoriasiform dermatitis.

Eva Wisniewski, Wenwen Du, Jenna A Himelstein, Gergő Szanda, Taylor J Woodward, Ken Mackie, Heather B Bradshaw

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

7 authors.

Eva WisniewskiGill Institute for Neuroscience, Indiana University, Bloomington, IN, United States.
Wenwen DuDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, United States.
Jenna A HimelsteinDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, IN, United States.
Gergő SzandaGill Institute for Neuroscience, Indiana University, Bloomington, IN, United States.
Taylor J WoodwardGill Institute for Neuroscience, Indiana University, Bloomington, IN, United States.
Ken MackieGill Institute for Neuroscience, Indiana University, Bloomington, IN, United States.
Heather B BradshawGill Institute for Neuroscience, Indiana University, Bloomington, IN, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic inflammatory skin disease characterized by keratinocyte hyperproliferation and immune dysregulation. Emerging clinical and experimental evidence suggests that endogenous lipid (endolipid) signaling systems, including the endocannabinoid system (ECS), represent a promising therapeutic target to treat psoriasis; however, comprehensive characterization of small-molecule endolipids and related proteins in psoriatic skin and their relationship to systemic changes remains limited. Here, we used the imiquimod (IMQ)-induced mouse model of psoriasis to perform combined lipidomic and transcriptional profiling of endolipid signaling in both skin and plasma. Targeted lipidomics revealed a striking divergence between tissues: most endolipids increased in inflamed skin but decreased in plasma, including the canonical ECS lipids anandamide and 2-arachidonoylglycerol. In contrast, selected lipid species, including taurine-conjugated metabolites (both

Indexed as

endocannabinoid systempsoriasiform dermatitisskin compartmentalizationtargeted lipidomicstranscriptomics

Identifiers

PMID42856670
PMCPMC13649676

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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.