Evidence map›Paper›PMID 41614884›Full record

ArticleCurrent issues in molecular biology2025

Dermofunctional Vehicle Downregulates LL-37 and MMPs and Upregulates IGFBP-3.

Hudson Polonini, Fabiana Regina da Silva Olímpio, Carlos Rocha Oliveira

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2025. 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.

Hudson PoloniniFagron BV, Fascinatio Boulevard 350, 3065 WB Rotterdam, The Netherlands.ORCID 0000-0002-2119-3660
Fabiana Regina da Silva OlímpioGap Biotech, Biotechnology Laboratory, Sao Jose dos Campos 12243-020, Brazil.ORCID 0000-0002-7590-3904
Carlos Rocha OliveiraGap Biotech, Biotechnology Laboratory, Sao Jose dos Campos 12243-020, Brazil.ORCID 0000-0001-8634-2850

Funding

Fagron (Rotterdam, The Netherlands) Fagron
6 · The paper itself

Abstract

backgroundFunctional dermatological bases can contribute more than just delivery-they may actively modulate cutaneous homeostasis. Cleoderm™ is a dermofunctional base containing a patented

objectiveTo determine whether Cleoderm™ exhibits intrinsic immunomodulatory and matrix-protective effects in a physiologically relevant skin co-culture and to clarify the biomarkers most impacted, with translational relevance to acne and rosacea.

methodsHuman keratinocytes and fibroblasts were maintained in a transwell co-culture. Non-cytotoxic concentrations of Cleoderm™ (1.0% and 10.0%,

resultsCleoderm™ showed no cytotoxicity up to 10% (

conclusionIn a dermo-epidermally relevant in vitro model, Cleoderm™ functions as an active dermofunctional base, not merely a vehicle simultaneously tempering inflammatory signaling, preserving extracellular matrix integrity, and modulating mechanistic nodes (LL-37 and IGFBP-3) linked to rosacea and acne. These findings is consistent with the use of Cleoderm™ as a biologically supportive base for personalized compounding and justify controlled clinical evaluation.

Indexed as

acneCleoderm™dermocosmetic basefibroblastsIGFBP-3IL-10IL-6keratinocytesLL-37MMP-1MMP-13MMP-3rosaceaTGF-βTNF-α

Identifiers

PMID41614884
PMCPMC12840455

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Registered trials

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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.