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Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study

BACKGROUND/PURPOSE: There are few studies comparing the expression of enamel proteins, such as amelogenin, and cytokeratins in cyst and odontogenic tumors like in ameloblastoma and odontogenic keratocyst, indicating that amelogenin could be a potential biomarker for the aggressiveness in the odontog...

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Autores principales: Urzúa, Blanca, Ahumada-Ossandón, Richard, Casa-Weisser, Daniel, Franco-Martínez, María Eugenia, Ortega-Pinto, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association for Dental Sciences of the Republic of China 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770315/
https://www.ncbi.nlm.nih.gov/pubmed/33384773
http://dx.doi.org/10.1016/j.jds.2020.05.028
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author Urzúa, Blanca
Ahumada-Ossandón, Richard
Casa-Weisser, Daniel
Franco-Martínez, María Eugenia
Ortega-Pinto, Ana
author_facet Urzúa, Blanca
Ahumada-Ossandón, Richard
Casa-Weisser, Daniel
Franco-Martínez, María Eugenia
Ortega-Pinto, Ana
author_sort Urzúa, Blanca
collection PubMed
description BACKGROUND/PURPOSE: There are few studies comparing the expression of enamel proteins, such as amelogenin, and cytokeratins in cyst and odontogenic tumors like in ameloblastoma and odontogenic keratocyst, indicating that amelogenin could be a potential biomarker for the aggressiveness in the odontogenic tumors. The aim of this study was to evaluate if the expression of amelogenin, cytokeratin AE1/AE3 (CKAE1/AE3) and cytokeratin 14 (CK14) in cysts and odontogenic tumors with calcified matrices such as calcifying odontogenic cyst (COC), compound (CdO) and complex (CxO) odontomas, adenomatoid odontogenic tumor (AOT) and calcifying epithelial odontogenic tumor (CEOT) as an aggressiveness indicator. MATERIALS AND METHODS: Three COC, eight CxO, three CdO, twelve AOT, two CEOT and three dental germs were submitted to an immunohistochemistry panel of antibodies composed of amelogenin, CKAE1/AE3 and CK14. RESULTS: CKAE1/AE3 and CK14 was present in all odontogenic epithelia. The amelogenin protein was detected in prismatic and amorphous calcified matrices of epithelial origin belonging to CxO, CdO, AOT, COC and the tooth germs used as controls. On the other hand, the CEOT was the only tumor or cyst studied that did not present immunostaining for amelogenin in calcified matrices. CONCLUSION: Amelogenin was detected in pathologies with a low or absent recurrence rate and excellent prognosis. CEOT was the lesion of greater clinical aggressiveness which did not express amelogenin. The presence of amelogenin in calcified matrices of odontogenic arise could be an indicator of low aggressiveness.
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spelling pubmed-77703152020-12-30 Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study Urzúa, Blanca Ahumada-Ossandón, Richard Casa-Weisser, Daniel Franco-Martínez, María Eugenia Ortega-Pinto, Ana J Dent Sci Original Article BACKGROUND/PURPOSE: There are few studies comparing the expression of enamel proteins, such as amelogenin, and cytokeratins in cyst and odontogenic tumors like in ameloblastoma and odontogenic keratocyst, indicating that amelogenin could be a potential biomarker for the aggressiveness in the odontogenic tumors. The aim of this study was to evaluate if the expression of amelogenin, cytokeratin AE1/AE3 (CKAE1/AE3) and cytokeratin 14 (CK14) in cysts and odontogenic tumors with calcified matrices such as calcifying odontogenic cyst (COC), compound (CdO) and complex (CxO) odontomas, adenomatoid odontogenic tumor (AOT) and calcifying epithelial odontogenic tumor (CEOT) as an aggressiveness indicator. MATERIALS AND METHODS: Three COC, eight CxO, three CdO, twelve AOT, two CEOT and three dental germs were submitted to an immunohistochemistry panel of antibodies composed of amelogenin, CKAE1/AE3 and CK14. RESULTS: CKAE1/AE3 and CK14 was present in all odontogenic epithelia. The amelogenin protein was detected in prismatic and amorphous calcified matrices of epithelial origin belonging to CxO, CdO, AOT, COC and the tooth germs used as controls. On the other hand, the CEOT was the only tumor or cyst studied that did not present immunostaining for amelogenin in calcified matrices. CONCLUSION: Amelogenin was detected in pathologies with a low or absent recurrence rate and excellent prognosis. CEOT was the lesion of greater clinical aggressiveness which did not express amelogenin. The presence of amelogenin in calcified matrices of odontogenic arise could be an indicator of low aggressiveness. Association for Dental Sciences of the Republic of China 2021-01 2020-08-20 /pmc/articles/PMC7770315/ /pubmed/33384773 http://dx.doi.org/10.1016/j.jds.2020.05.028 Text en © 2020 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Urzúa, Blanca
Ahumada-Ossandón, Richard
Casa-Weisser, Daniel
Franco-Martínez, María Eugenia
Ortega-Pinto, Ana
Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title_full Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title_fullStr Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title_full_unstemmed Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title_short Amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: An immunohistochemical study
title_sort amelogenin in calcified matrices of odontogenic cysts and odontogenic tumors: an immunohistochemical study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770315/
https://www.ncbi.nlm.nih.gov/pubmed/33384773
http://dx.doi.org/10.1016/j.jds.2020.05.028
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