Evidence map›Paper›PMID 39327577›Full record

ArticleBMC oral health2024

Comparative immunohistochemical expression of Beta catenin and CD163 between dysplastic / non-dysplastic oral lichen planus and lichenoid lesions (EX-VIVO STUDY).

Heba Ahmed Saleh, Ghada Nabil, Sarah Ahmed Mohammed Mahmoud Badawy

Abstract readComparative Study
In one paragraph

Article in BMC oral health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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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.

Heba Ahmed SalehOral & Maxillofacial Pathology, Faculty of Dentistry, Cairo University, Cairo, Egypt. heba_saleh@dentistry.cu.edu.eg.ORCID http://orcid.org/0000-0002-8794-6266
Ghada NabilOral Medicine, Faculty of Dentistry, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0003-1773-2227
Sarah Ahmed Mohammed Mahmoud BadawyOral & Maxillofacial Pathology, Faculty of Dentistry, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0002-6614-6796

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOral lichen planus is a well-known chronic inflammatory mucocutaneous disorder, which has clinical and histological presentation that mimics oral lichenoid reaction. According to the fifth edition of WHO, both conditions are considered as oral potentially malignant disorders. Recent studies on oral potential disorders documented deregulation of some signaling molecules related to the Wnt/β-catenin pathway. Therefore this study aimed to compare the immune expression of β-catenin & CD163 in dysplastic /non-dysplastic cases of Oral lichen planus & oral lichenoid lesion. In addition, a statistical correlation between both immune markers was done regardless of the type of the study group.

methodsFour study groups were designated as 2 groups of Oral lichen planus (one dysplastic & one non -dysplastic) and the other 2 groups were oral lichenoid lesions (one dysplastic & one non -dysplastic). Ten cases in each group were collected and investigated by immunohistochemistry. The area percent of beta catenin and also counting of m2 macrophages expressing + CD163 marker was calculated in the study groups.

resultsThe Statistical analysis highlighted a statistically significant difference between the studied groups. Moreover, Pearson correlation test reported a significant moderate positive correlation between beta catenin & CD163 expression in the studied cases.

conclusionOur findings supported new perceptions of the mechanism by which tumor associated macrophage specific β-catenin signaling promotes the aggressive behavior of oral potential malignant disorders. CLINICAL RELEVANCE: Evidence of the relationship between beta catenin and M2 macrophages (+ CD163) may enhance the development of macrophage-based strategies for treatment and improve the prognosis of such cases.

Indexed as

Antigens, CDAntigens, Differentiation, Myelomonocyticbeta CateninImmunohistochemistryLichen Planus, OralReceptors, Cell SurfaceCD163 AntigenFemaleHumansLichenoid EruptionsMacrophagesMaleMiddle AgedAntigens, CDAntigens, Differentiation, Myelomonocyticbeta CateninCD163 AntigenReceptors, Cell SurfaceCD163DysplasticM2 macrophagesNon-dysplastic OLLNon-dysplastic OLPOMPDTAMTAM-specific β-catenin signalingΒ-catenin

Identifiers

PMID39327577
PMCPMC11430547

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