Evidence map›Paper›PMID 29971493›Full record

ArticleHistochemistry and cell biology2018

Oct-4 and CD44 in epithelial stem cells like of benign odontogenic lesions.

Eduardo Alonso Cruz Monroy, Pedro Paulo de Andrade Santos, Maria Luiza Diniz de Sousa Lopes, Adalberto Mosqueda-Taylor, Leão Pereira Pinto, Lélia Batista de Souza

Abstract read
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In one paragraph

Article in Histochemistry and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. The role of OCT4 and CD44 in lower lip carcinogenesis.Oral and maxillofacial surgery · 2025
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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

6 authors at 2 institutions in 2 countries.

Eduardo Alonso Cruz MonroyPost Graduate Program in Oral Pathology, Department of Dentistry, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
Pedro Paulo de Andrade SantosPost Graduate Program in Oral Pathology, Department of Morphology, Federal University of Rio Grande do Norte, Natal, RN, Brazil.ORCID http://orcid.org/0000-0002-5793-3886
Maria Luiza Diniz de Sousa LopesPost Graduate Program in Oral Pathology, Department of Dentistry, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
Adalberto Mosqueda-TaylorHealth Care Department, Universidad Autónoma Metropolitana, Xochimilco, Mexico.
Leão Pereira PintoPost Graduate Program in Oral Pathology, Department of Dentistry, Federal University of Rio Grande do Norte, Av. Senador Salgado Filho, 1787, Lagoa Nova, Natal, RN, CEP 59056-000, Brazil.
Lélia Batista de SouzaPost Graduate Program in Oral Pathology, Department of Dentistry, Federal University of Rio Grande do Norte, Av. Senador Salgado Filho, 1787, Lagoa Nova, Natal, RN, CEP 59056-000, Brazil. leliabsouza@gmail.com.
Universidade Federal do Rio Grande do Norte · BRUniversidad Autónoma Metropolitana · MX

Funding

This study was funded by National Council for Scientific and Technological Development (CNPq). Grant Nº. 307539/2010-5
6 · The paper itself

Abstract

Benign epithelial odontogenic lesions are great clinical importance entities that develop in the jaws from the tissues that form teeth. It has been shown that benign and malignant tumors are present in a large number of tumor stem cells, which has great implications in the development of these lesions. Oct-4 and CD44 have been demonstrated as important markers for tumoral stem cells. The aim of this study was investigate the presence of stem cell markers Oct-4 and CD44 in benign epithelial odontogenic lesions. Twenty odontogenic keratocysts (OKC), 20 ameloblastomas (AMB) of the solid/multicystic type and 20 adenomatoid odontogenic tumors (AOT) were retrospectively analyzed for immunohistochemical detection of Oct-4 and CD44 in their epithelial component. All cases were positive for the two markers, with the majority exhibiting a high expression. Analysis of the expression of Oct-4 revealed no statistically significant differences (p = 0.406) between the lesions studied. Regarding CD44, there was a significant difference between the cases of AMB and AOT in relation with OKC, with the latter presenting a greater labelling (p = 0.034). No statistically significant correlation between Oct-4 and CD44 was observed in the lesions. In our findings, the presence of stem cell-like phenotype at various sites of the epithelial component of the odontogenic lesions was identified, suggesting its possible participation in histogenesis and differentiation without, however, exerting influence on the aggressiveness of the lesions.

Indexed as

Dentigerous CystEpithelial CellsHumansHyaluronan ReceptorsJaw NeoplasmsOctamer Transcription Factor-3Retrospective StudiesCD44 protein, humanHyaluronan ReceptorsOctamer Transcription Factor-3ImmunohistochemistryOdontogenic cystsOdontogenic tumorsStem cells

Identifiers

PMID29971493
OpenAlexW2811027599

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.