Evidence map›Paper›PMID 42719797›Full record

ArticleCureus2026

ALDH, SOX and CD147 Εxpression in Oral Lichen Planus Compared to Oral Squamous Cell Carcinoma Epithelium: An Immunohistochemical Study.

Vasileios Zisis, Petros Papadopoulos, Christina Charisi, Konstantinos Poulopoulos, Ioannis Fotopoulos, Theodoros Lillis, Nikolaos Dabarakis, Georgios Parlitsis, Nikolaos Shinas, Pavlos Theodosiadis and 3 more

Abstract read
In one paragraph

Article in Cureus, 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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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

13 authors.

Vasileios ZisisOral Medicine and Pathology, European University Cyprus, Nicosia, CYP.
Petros PapadopoulosOral Medicine and Pathology, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Christina CharisiOral Medicine and Pathology, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Konstantinos PoulopoulosDentoalveolar Surgery, Implantology and Oral Radiology, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Ioannis FotopoulosDentoalveolar Surgery, Implantology and Oral Radiology, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, GRC, Thessaloniki, GRC.
Theodoros LillisDentoalveolar Surgery, Implantology and Oral Radiology, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Nikolaos DabarakisDentoalveolar Surgery, Implantology and Oral Radiology, School of Dentistry, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Georgios ParlitsisMechanical Engineering, Eindhoven University of Technology, Eindhoven, NLD.
Nikolaos ShinasOral and Maxillofacial Radiology, Henry M. Goldman School of Dental Medicine, Boston University, Boston, USA.
Pavlos TheodosiadisOral Medicine and Pathology, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Konstantinos ParaskevopoulosOral and Maxillofacial Surgery, Papanikolaou Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Konstantinos VahtsevanosOral and Maxillofacial Surgery, Papanikolaou Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Athanasios PoulopoulosOral Medicine and Pathology, Aristotle University of Thessaloniki, Thessaloniki, GRC.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOral potential malignant diseases (OPMDs) are transformed into oral squamous cell carcinoma (OSCC) by cancer stem cells (CSCs), which also start the process of carcinogenesis de novo. Our study's objective was to examine the expression of ALDH, SOX, and CD147 in OSCCs and oral lichen planus (OLP).

methodsAn immunohistochemical detection was performed in 24 OLP samples (10 reticular OLPs (ROLPs) and 14 erosive OLPs (EOLPs)) and 21 OSCC samples of all differentiation levels to track the expression profile of ALDH1/2, SOX2, and CD147. Immunohistochemistry was applied in a semiquantative fashion to finish the aforementioned process. The paraffin-embedded tissue samples were taken from biopsies conducted in the Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki, Greece, between 2014 and 2019, as well as from the Oral and Maxillofacial Surgery Clinic of G. Papanikolaou General Hospital, Aristotle University, and the Oral and Maxillofacial Surgery Clinic of St Luke Hospital, Thessaloniki, Greece. A scale ranging from 0 to 2 was used to assess the expressions of ALDH1/2, SOX2, and CD147 based on the proportion of positive epithelial cells. Depending on the sample size, either Fischer's exact test or Pearson chi-square test was used for the statistical analysis, with a significance threshold of p≤0.05.

resultsALDH1/2 expression was statistically considerably greater in OSCC compared to EOLP (p=0.019) and ROLP (p<0.001), according to the statistical analysis. The statistical analysis of SOX2 staining revealed statistically significant greater expression in OSCC compared to ROLP (p=0.012) and EOLP compared to ROLP (p=0.024). The statistical analysis revealed that EOLP had statistically substantially higher expression of CD147 staining than ROLP (p=0.019). There were no statistically significant findings from the remaining comparisons. In conclusion, the distinctively increased expression of CD147 in EOLP as opposed to ROLP raises the possibility that erosive lichenoid lesions contain neoplastic cells with specific CSC traits. The distinctively increased expression of SOX2 in OSCC and EOLP as opposed to ROLP raises the possibility that erosive lichenoid lesions contain malignant cells with specific CSC traits. In any event, additional experimental testing in a greater number of samples is necessary for the clinical application of CSC biomarkers as prognostic variables.

Indexed as

aldhbiomarkerscancer stem cellscd147emmprinoral lichen planusoral squamous cell carcinomasox

Identifiers

PMID42719797
PMCPMC13556987

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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.