Evidence map›Paper›PMID 38846701›Full record

ArticleSkin health and disease2024

MicroRNA expression profiling of cutaneous squamous cell carcinomas and precursor lesions.

Akbor Hossain, Lisa N Tom, Ala Melati-Rad, Miko Yamada, Sabrina Hammerlindl, Kasturee Jagirdar, Tarl W Prow, H Peter Soyer, Mitchell S Stark

Abstract read
In one paragraph

Article in Skin health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

9 authors.

Akbor HossainFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.
Lisa N TomFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.ORCID https://orcid.org/0000-0002-9068-1107
Ala Melati-RadFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.ORCID https://orcid.org/0000-0003-1719-2523
Miko YamadaSkin Research Centre York Biomedical Research Institute Hull York Medical School University of York York UK.ORCID https://orcid.org/0000-0001-8795-4461
Sabrina HammerlindlFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.
Kasturee JagirdarFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.ORCID https://orcid.org/0000-0001-8761-132X
Tarl W ProwSkin Research Centre York Biomedical Research Institute Hull York Medical School University of York York UK.ORCID https://orcid.org/0000-0003-2892-6238
H Peter SoyerFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.ORCID https://orcid.org/0000-0002-4770-561X
Mitchell S StarkFrazer Institute The University of Queensland Dermatology Research Centre Brisbane Queensland Australia.ORCID https://orcid.org/0000-0002-4510-2161

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Actinic keratoses (AK) are pre-malignant skin lesions caused by chronic sun exposure. Progression from an AK to intraepidermal carcinoma (IEC) and a cutaneous squamous cell carcinoma (SCC) is well known but the rate of transformation to an invasive SCC is highly variable. Since no definitive biomarkers are available, treatment decisions are made ad hoc. Objectives: To fully characterise our AK to SCC progression series, we performed microRNA (miRNA) microarray expression profiling of normal and photodamaged skin, as well as AKs, IEC, and invasive SCCs. Methods: The study recruited 27 patients who donated fresh biopsies of normal skin, photodamaged skin, AK, IEC, and SCC ( Results: There were 234 robustly expressed miRNAs across the tissue collection, which resulted in 20 miRNA that were differentially expressed ((cor) Conclusions: This study confirmed the continuum of AK with IEC and SCC highlighting that miRNA expression plays a role in keratinocyte transformation. Development of our putative miRNA biomarker candidates is warranted to aid in clinical management of patients experiencing high AK load to determine the most appropriate treatment.

Identifiers

PMID38846701
PMCPMC11150735

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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.