Evidence map›Paper›PMID 39400728›Full record

ReviewArchives of dermatological research2024

Immunohistochemical examination of immunoreactivity of transient receptor potential melastatin 2, glutathione peroxidase 4 and spexin in lichen planus.

Mehmet Semih Celik, Demet Cicek, Betül Demir, Tuncay Kuloğlu, Gökhan Artaş, Serhat Hançer

Abstract readReview
PubMed Publisher
In one paragraph

Review in Archives of dermatological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Mehmet Semih CelikDepartment of Dermatology, Firat University Hospital, Elazig, Turkey. drmsemihcelik@gmail.com.ORCID http://orcid.org/0000-0002-3378-0619
Demet CicekDepartment of Dermatology, Firat University Hospital, Elazig, Turkey.ORCID http://orcid.org/0000-0001-8405-7730
Betül DemirDepartment of Dermatology, Firat University Hospital, Elazig, Turkey.ORCID http://orcid.org/0000-0002-6190-5124
Tuncay KuloğluDepartment of Histology and Embryology, Firat University Hospital, Elazig, Turkey.ORCID http://orcid.org/0000-0001-9874-3838
Gökhan ArtaşDepartment of Pathology, Firat University Hospital, Elazig, Turkey.ORCID http://orcid.org/0000-0001-5529-4155
Serhat HançerDepartment of Histology and Embryology, Firat University Hospital, Elazig, Turkey.ORCID http://orcid.org/0000-0003-3237-3672

Funding

Fırat University Scientific Research Projects TF.22.16
6 · The paper itself

Abstract

backroundIn this study, we aimed to investigate the potential contributions to the disease by examining the immunoreactivities of SPX in LP-affected skin tissue using immunohistochemical methods, in light of its recent prominence as a molecule related to diabetes mellitus, along with apoptosis and ferroptosis mediated by GPX4 and TRPM2 channels facilitating oxidative stress-induced cell death.

objectiveThis research explored the immunohistochemical expressions of TRPM2, GPX4, and SPX in Lichen Planus (LP) patients compared to healthy individuals. MATERIALS AND

methodsForty skin samples were collected, split equally between LP patients and healthy controls, excluding those with other conditions. Samples underwent immunohistochemical staining for TRPM2, SPX, and GPX4, using secondary antibodies and chromogens AEC or DAB. Histoscores were calculated based on staining diffusiveness and severity. Statistical analyses were performed with SPSS 22.0, using t-tests and ANOVA, with significance set at p < 0.05.

resultsThere were no demographic differences between groups (p > 0.05). LP patients showed significantly lower TRPM2 and GPX4 histoscores and higher SPX histoscores compared to controls (TRPM2 and GPX4: p < 0.001, SPX: p < 0.001). Gender and age did not affect histoscores significantly.

conclusionsFindings suggest TRPM2, GPX4, and SPX play roles in LP pathogenesis, indicating a need for further molecular studies to clarify their involvement. This contributes to understanding LP beyond the traditional apoptosis perspective.

Indexed as

ImmunohistochemistryLichen PlanusPhospholipid Hydroperoxide Glutathione PeroxidaseTRPM Cation ChannelsAdultAgedApoptosisCase-Control StudiesFemaleHumansMaleMiddle AgedOxidative StressSkinYoung AdultPhospholipid Hydroperoxide Glutathione PeroxidaseTRPM2 protein, humanTRPM Cation ChannelsGlutathione peroxidase-4Lichen planusSpexinTransient receptor potential melastatin-2

Identifiers

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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.