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The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study

OBJECTIVE: To evaluate the effect of streptozotocin-induced experimental diabetes mellitus on p16, p53, Ki67, and Bcl2 expressions and histopathological changes in the tongue of the rats. MATERIAL AND METHODS: Twenty-two adult female Sprague-Dawley rats were used. The rats were randomly divided into...

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Autores principales: Altun, Eren, Yazici, Hasmet, Arslan, Erhan, Tulaci, Kamil Gokce, Erken, Haydar Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800967/
https://www.ncbi.nlm.nih.gov/pubmed/31687322
http://dx.doi.org/10.1155/2019/3563215
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author Altun, Eren
Yazici, Hasmet
Arslan, Erhan
Tulaci, Kamil Gokce
Erken, Haydar Ali
author_facet Altun, Eren
Yazici, Hasmet
Arslan, Erhan
Tulaci, Kamil Gokce
Erken, Haydar Ali
author_sort Altun, Eren
collection PubMed
description OBJECTIVE: To evaluate the effect of streptozotocin-induced experimental diabetes mellitus on p16, p53, Ki67, and Bcl2 expressions and histopathological changes in the tongue of the rats. MATERIAL AND METHODS: Twenty-two adult female Sprague-Dawley rats were used. The rats were randomly divided into 2 groups (n = 14) as control (C) (n = 8) and diabetic (DM) (n = 6). The rats in the DM group were given streptozotocin as a single intraperitoneal dose for induction of diabetes. Histopathological and immunohistochemical evaluations of formalin-fixed and paraffin-embedded tissue sections of the tongue were used. RESULTS: Significant differences were observed between the DM group and the control group in terms of epithelial thickness, length of filiform papillae, and width of filiform papillae (p = 0.005, p = 0.001, and p = 0.006, respectively). There was no significant difference between the groups in terms of mononuclear inflammatory cell infiltration, capillary proliferation, and dysplasia (p = 0.204, p = 0.244, and p = 0.204, respectively). As a result of immunohistochemical studies, no significant difference was found between the groups in terms of p53, Ki67, and Bcl-2 expressions (p = 0.588, p = 0.662, and p = 0.686, respectively). A significant difference was found between the groups when p16 expression was evaluated (p = 0.006). CONCLUSIONS: In our study, streptozotocin-induced experimental diabetes mellitus induced p16 expression but did not show any difference in p53, Bcl-2, and Ki67 levels. It should be considered in the studies that the pathological changes at the early stages of the relationship between DM and oral cancer may be related to p16 expression; however, it may also be linked with p16-related aging process.
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spelling pubmed-68009672019-11-04 The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study Altun, Eren Yazici, Hasmet Arslan, Erhan Tulaci, Kamil Gokce Erken, Haydar Ali Anal Cell Pathol (Amst) Research Article OBJECTIVE: To evaluate the effect of streptozotocin-induced experimental diabetes mellitus on p16, p53, Ki67, and Bcl2 expressions and histopathological changes in the tongue of the rats. MATERIAL AND METHODS: Twenty-two adult female Sprague-Dawley rats were used. The rats were randomly divided into 2 groups (n = 14) as control (C) (n = 8) and diabetic (DM) (n = 6). The rats in the DM group were given streptozotocin as a single intraperitoneal dose for induction of diabetes. Histopathological and immunohistochemical evaluations of formalin-fixed and paraffin-embedded tissue sections of the tongue were used. RESULTS: Significant differences were observed between the DM group and the control group in terms of epithelial thickness, length of filiform papillae, and width of filiform papillae (p = 0.005, p = 0.001, and p = 0.006, respectively). There was no significant difference between the groups in terms of mononuclear inflammatory cell infiltration, capillary proliferation, and dysplasia (p = 0.204, p = 0.244, and p = 0.204, respectively). As a result of immunohistochemical studies, no significant difference was found between the groups in terms of p53, Ki67, and Bcl-2 expressions (p = 0.588, p = 0.662, and p = 0.686, respectively). A significant difference was found between the groups when p16 expression was evaluated (p = 0.006). CONCLUSIONS: In our study, streptozotocin-induced experimental diabetes mellitus induced p16 expression but did not show any difference in p53, Bcl-2, and Ki67 levels. It should be considered in the studies that the pathological changes at the early stages of the relationship between DM and oral cancer may be related to p16 expression; however, it may also be linked with p16-related aging process. Hindawi 2019-10-08 /pmc/articles/PMC6800967/ /pubmed/31687322 http://dx.doi.org/10.1155/2019/3563215 Text en Copyright © 2019 Eren Altun et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Altun, Eren
Yazici, Hasmet
Arslan, Erhan
Tulaci, Kamil Gokce
Erken, Haydar Ali
The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title_full The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title_fullStr The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title_full_unstemmed The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title_short The Impact of Type II Diabetes on Tongue Dysplasia and p16-Related Aging Process: An Experimental Study
title_sort impact of type ii diabetes on tongue dysplasia and p16-related aging process: an experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800967/
https://www.ncbi.nlm.nih.gov/pubmed/31687322
http://dx.doi.org/10.1155/2019/3563215
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