The Stem Cell Expression Profile of Odontogenic Tumors and Cysts: A Systematic Review and Meta-Analysis

Author:

Kalogirou Eleni-Marina1ORCID,Lekakis Georgios2,Petroulias Aristodimos2,Chavdoulas Konstantinos2,Zogopoulos Vasileios L.3ORCID,Michalopoulos Ioannis3ORCID,Tosios Konstantinos I.2ORCID

Affiliation:

1. Faculty of Health and Rehabilitation Sciences, Metropolitan College, 10672 Athens, Greece

2. School of Dentistry, National and Kapodistrian University of Athens, 11527 Athens, Greece

3. Centre of Systems Biology, Biomedical Research Foundation, Academy of Athens, 11527 Athens, Greece

Abstract

Background: Stem cells have been associated with self-renewing and plasticity and have been investigated in various odontogenic lesions in association with their pathogenesis and biological behavior. We aim to provide a systematic review of stem cell markers’ expression in odontogenic tumors and cysts. Methods: The literature was searched through the MEDLINE/PubMed, EMBASE via OVID, Web of Science, and CINHAL via EBSCO databases for original studies evaluating stem cell markers’ expression in different odontogenic tumors/cysts, or an odontogenic disease group and a control group. The studies’ risk of bias (RoB) was assessed via a Joanna Briggs Institute Critical Appraisal Tool. Meta-analysis was conducted for markers evaluated in the same pair of odontogenic tumors/cysts in at least two studies. Results: 29 studies reported the expression of stem cell markers, e.g., SOX2, OCT4, NANOG, CD44, ALDH1, BMI1, and CD105, in various odontogenic lesions, through immunohistochemistry/immunofluorescence, polymerase chain reaction, flow cytometry, microarrays, and RNA-sequencing. Low, moderate, and high RoBs were observed in seven, nine, and thirteen studies, respectively. Meta-analysis revealed a remarkable discriminative ability of SOX2 for ameloblastic carcinomas or odontogenic keratocysts over ameloblastomas. Conclusion: Stem cells might be linked to the pathogenesis and clinical behavior of odontogenic pathologies and represent a potential target for future individualized therapies.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference72 articles.

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