Evidence map›Paper›PMID 41566787›Full record

ArticleACS biomaterials science & engineering2026

MiRNAs in Interstitial Skin Fluid Sampled with Swellable Hydrogel Microneedles Are Locally Deregulated Near Malignant Skin Lesions in Early Stages of Cutaneous Squamous Cell Carcinoma.

Ahmad Kenaan, Oliver Teenan, Connor Daniels, Christina Malaktou, Mo Akhavani, Nikolaos Sideris, Leandro Castellano, Jessica Strid, Claire A Higgins, Sylvain Ladame

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 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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0cells of the map it votes in
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

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

10 authors.

Ahmad KenaanDepartment of Bioengineering, Imperial College London, White City Campus, London W12 0BZ, U.K.
Oliver TeenanDepartment of Bioengineering, Imperial College London, White City Campus, London W12 0BZ, U.K.ORCID 0000-0003-4469-2574
Connor DanielsDepartment of Bioengineering, Imperial College London, White City Campus, London W12 0BZ, U.K.
Christina MalaktouDepartment of Immunology and Inflammation, Imperial College London, Hammersmith Campus, London W12 0NN, U.K.
Mo AkhavaniThe Plastic Surgery Group, 100 Harley Street, Marylebone, London W1G 7JA, U.K.
Nikolaos SiderisDepartment of Biochemistry, University of Sussex, Brighton CN1 9QJ, U.K.
Leandro CastellanoDepartment of Biochemistry, University of Sussex, Brighton CN1 9QJ, U.K.
Jessica StridDepartment of Immunology and Inflammation, Imperial College London, Hammersmith Campus, London W12 0NN, U.K.
Claire A HigginsDepartment of Bioengineering, Imperial College London, White City Campus, London W12 0BZ, U.K.ORCID 0000-0002-9742-5149
Sylvain LadameDepartment of Bioengineering, Imperial College London, White City Campus, London W12 0BZ, U.K.ORCID 0000-0002-3358-9638

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interrogating molecular biomarkers in bodily fluids has emerged as a clinically useful strategy for the early diagnosis of many cancer types. Interstitial skin fluid is currently being explored as a possible alternative to blood, containing the same types of biomarkers but lacking cells and debris that hold little or no clinical value. The discovery and validation of molecular biomarkers with diagnostic or prognostic value and the development of clinical tests based on their detection require minimally invasive technologies capable of sampling this fluid in a pain-free manner. Biomarkers must also be easily recoverable for follow-on analysis. Herein, we combine standard genomic approaches with innovative bioengineering technologies to demonstrate that short noncoding miRNAs are significantly deregulated in extracellular skin fluid surrounding malignant skin lesions, providing a yet largely unexplored window of opportunity for early diagnosis of skin cancers. Hydrogel-based microneedle patches offering clinically useful sampling capacity were developed that enable the rapid capture and recovery of endogenous miRNAs from human skin through deformation of the epidermal-dermal junction. Using mouse models of cutaneous squamous cell carcinoma, a significantly greater level of deregulation of selected miRNAs was observed in perilesional skin fluid compared to that in blood levels.

Indexed as

Carcinoma, Squamous CellExtracellular FluidHydrogelsMicroRNAsSkinSkin NeoplasmsAnimalsBiomarkers, TumorCutaneous Squamous Cell CarcinomaFemaleHumansMiceMicroneedle Drug DeliveryNeedlesBiomarkers, TumorHydrogelsMicroRNAsdiagnostic biomarkersinterstitial skin fluidmicroneedlesmicroRNAsskin cancerswellable hydrogels

Identifiers

PMID41566787
PMCPMC12892239

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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.