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Role of phosphatase and tensin homolog in pathogenesis of ameloblastoma: An immunohistochemical study.

Identifieur interne : 000002 ( Main/Exploration ); précédent : 000001; suivant : 000003

Role of phosphatase and tensin homolog in pathogenesis of ameloblastoma: An immunohistochemical study.

Auteurs : Bhaskar Narayan [Inde] ; Aadithya B. Urs [Inde] ; Jeyaseelan Augustine [Inde] ; Hanspal Singh [Inde]

Source :

RBID : pubmed:32719259

Descripteurs français

English descriptors

Abstract

Background

Altered molecular signaling pathways in ameloblastoma have been identified to play a pivotal role in the mechanism of oncogenesis, differentiation, and tumor progression. Phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin pathway is one of the signaling pathways that are associated with the pathogenesis of ameloblastoma. Phosphatase and tensin homolog (PTEN) controls cell migration and proliferation. It monitors the level of the Akt and maintains cellular integrity. The present study was aimed to study the immunoexpression of PTEN in ameloblastoma to understand its role in the pathogenesis of ameloblastoma.

Materials and Methods

Twenty cases of ameloblastoma and ten cases of normal tooth germ were subjected to immunohistochemical staining against PTEN.

Results

Strong PTEN immunopositivity was seen in the tooth germs, while weak positivity was seen in the ameloblastoma. The immunoscore for PTEN was calculated by adding the percentage score and the intensity score. Seventeen cases showed the reduced PTEN expression in the epithelial component of ameloblastoma. The unpaired t-test showed a statistically significant difference in the mean PTEN immunoscore in tooth germ and ameloblastoma.

Conclusion

The study showed reduced PTEN immunoreactivity, which plays a role in the pathogenesis of ameloblastoma, through Akt pathway.


DOI: 10.4103/jcrt.JCRT_528_18
PubMed: 32719259


Affiliations:


Links toward previous steps (curation, corpus...)


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<term>Adolescent (MeSH)</term>
<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Ameloblastoma (metabolism)</term>
<term>Ameloblastoma (pathology)</term>
<term>Biomarkers, Tumor (metabolism)</term>
<term>Case-Control Studies (MeSH)</term>
<term>Cell Differentiation (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Immunohistochemistry (MeSH)</term>
<term>Infant (MeSH)</term>
<term>Jaw Neoplasms (metabolism)</term>
<term>Jaw Neoplasms (pathology)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>PTEN Phosphohydrolase (metabolism)</term>
<term>Proto-Oncogene Proteins c-akt (metabolism)</term>
<term>Signal Transduction (MeSH)</term>
<term>Young Adult (MeSH)</term>
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<term>Adolescent (MeSH)</term>
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Améloblastome (anatomopathologie)</term>
<term>Améloblastome (métabolisme)</term>
<term>Différenciation cellulaire (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Immunohistochimie (MeSH)</term>
<term>Jeune adulte (MeSH)</term>
<term>Marqueurs biologiques tumoraux (métabolisme)</term>
<term>Mâle (MeSH)</term>
<term>Nourrisson (MeSH)</term>
<term>Phosphohydrolase PTEN (métabolisme)</term>
<term>Protéines proto-oncogènes c-akt (métabolisme)</term>
<term>Sujet âgé (MeSH)</term>
<term>Transduction du signal (MeSH)</term>
<term>Tumeurs de la mâchoire (anatomopathologie)</term>
<term>Tumeurs de la mâchoire (métabolisme)</term>
<term>Études cas-témoins (MeSH)</term>
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<term>Biomarkers, Tumor</term>
<term>PTEN Phosphohydrolase</term>
<term>Proto-Oncogene Proteins c-akt</term>
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<term>Améloblastome</term>
<term>Tumeurs de la mâchoire</term>
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<term>Ameloblastoma</term>
<term>Jaw Neoplasms</term>
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<term>Améloblastome</term>
<term>Marqueurs biologiques tumoraux</term>
<term>Phosphohydrolase PTEN</term>
<term>Protéines proto-oncogènes c-akt</term>
<term>Tumeurs de la mâchoire</term>
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<term>Ameloblastoma</term>
<term>Jaw Neoplasms</term>
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Case-Control Studies</term>
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<term>Immunohistochemistry</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Différenciation cellulaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Immunohistochimie</term>
<term>Jeune adulte</term>
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<div type="abstract" xml:lang="en">
<p>
<b>Background</b>
</p>
<p>Altered molecular signaling pathways in ameloblastoma have been identified to play a pivotal role in the mechanism of oncogenesis, differentiation, and tumor progression. Phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin pathway is one of the signaling pathways that are associated with the pathogenesis of ameloblastoma. Phosphatase and tensin homolog (PTEN) controls cell migration and proliferation. It monitors the level of the Akt and maintains cellular integrity. The present study was aimed to study the immunoexpression of PTEN in ameloblastoma to understand its role in the pathogenesis of ameloblastoma.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Materials and Methods</b>
</p>
<p>Twenty cases of ameloblastoma and ten cases of normal tooth germ were subjected to immunohistochemical staining against PTEN.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Results</b>
</p>
<p>Strong PTEN immunopositivity was seen in the tooth germs, while weak positivity was seen in the ameloblastoma. The immunoscore for PTEN was calculated by adding the percentage score and the intensity score. Seventeen cases showed the reduced PTEN expression in the epithelial component of ameloblastoma. The unpaired t-test showed a statistically significant difference in the mean PTEN immunoscore in tooth germ and ameloblastoma.</p>
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<p>
<b>Conclusion</b>
</p>
<p>The study showed reduced PTEN immunoreactivity, which plays a role in the pathogenesis of ameloblastoma, through Akt pathway.</p>
</div>
</front>
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<AbstractText Label="Background" NlmCategory="UNASSIGNED">Altered molecular signaling pathways in ameloblastoma have been identified to play a pivotal role in the mechanism of oncogenesis, differentiation, and tumor progression. Phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin pathway is one of the signaling pathways that are associated with the pathogenesis of ameloblastoma. Phosphatase and tensin homolog (PTEN) controls cell migration and proliferation. It monitors the level of the Akt and maintains cellular integrity. The present study was aimed to study the immunoexpression of PTEN in ameloblastoma to understand its role in the pathogenesis of ameloblastoma.</AbstractText>
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<Keyword MajorTopicYN="N">Ameloblastoma</Keyword>
<Keyword MajorTopicYN="N">immunohistochemistry</Keyword>
<Keyword MajorTopicYN="N">phosphatase and tensin homolog</Keyword>
<Keyword MajorTopicYN="N">tooth germs</Keyword>
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<CoiStatement>None</CoiStatement>
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<Month>7</Month>
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<Hour>6</Hour>
<Minute>0</Minute>
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