Evidence map›Paper›PMID 42499679›Full record

ArticleActa naturae

A Comparative Study of Genital Lichen Sclerosus Transcriptomes.

S D Margasyuk, A L Kuznetsova, D A Skvortsov, E M Alekberov, M M Iritsyan, S A Pulbere, S V Kotov, A A Sokolova, D D Pervouchine

Abstract read
In one paragraph

Article in Acta naturae. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

S D MargasyukCenter for Molecular and Cellular Biology, Moscow, 121205 Russia.
A L KuznetsovaCenter for Molecular and Cellular Biology, Moscow, 121205 Russia.
D A SkvortsovCenter for Molecular and Cellular Biology, Moscow, 121205 Russia.
E M AlekberovN.I. Pirogov Russian National Research Medical University, Moscow, 117513 Russia.
M M IritsyanN.I. Pirogov City Clinical Hospital No. 1 of the Moscow Department of Health, Moscow, 119049 Russia.
S A PulbereN.I. Pirogov Russian National Research Medical University, Moscow, 117513 Russia.
S V KotovN.I. Pirogov Russian National Research Medical University, Moscow, 117513 Russia.
A A SokolovaYevdokimov Moscow State University of Medicine and Dentistry, Moscow, 127473 Russia.
D D PervouchineCenter for Molecular and Cellular Biology, Moscow, 121205 Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genital lichen sclerosus (GLS) is a chronic inflammatory dermatosis that affects the genital skin. Despite different clinical manifestations, the pathogenesis of GLS in men and women is believed to be common and is attributed to a combination of autoimmune and genetic factors. In this study, we compared the transcriptomic profiles of penile (mGLS) and vulvar lichen sclerosus (VLS), aiming to identify commonly deregulated genes. We observed a substantial heterogeneity in the transcriptomic signatures in mGLS samples, which is driven by different compositions of immune infiltrates. In mGLS, gene expression signatures strongly indicate epidermis dysfunction and overexpression of the epithelial inflammation marker Keratin 6 (KRT6) and chitinase CHIT1. No significant changes in the expression levels of known GLS markers, such as VIM, CTNNB1, LGALS7 and ECM1, were detected. However, significant changes in the expression levels of the genes associated with autoimmune diseases and the genes upregulated in squamous cell carcinoma, including TNF, CCNB1 and RUNX3, were observed. There was no enrichment in the polyU/UC insertions that were reported previously. Instead, we have identified a long non-coding RNA DRAIC with a high coding potential that is commonly upregulated in mGLS and VLS. Taken together, our results provide a comprehensive picture of the shared transcriptomic signatures, including novel biomarkers and potential therapeutic targets.

Indexed as

Genital lichen sclerosusGLSinflammationinnate immunitylong non-coding RNAtranscriptomics

Identifiers

PMID42499679
PMCPMC13399664

What Socratic holds

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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 Socratic graph.