Cargando…

A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia

CONTEXT: Oral cancer is the third most prevalent malignancy in India. Leukoplakia is its most common precursor lesion. AIMS: This study aimed at evaluation of the Ki-67 expression and thereby detection of the dysplastic potential in histopathologically nondysplastic oral leukoplakia (OL). Secondaril...

Descripción completa

Detalles Bibliográficos
Autores principales: Mondal, Krishnendu, Mandal, Rupali, Sarkar, Badal Chandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141664/
https://www.ncbi.nlm.nih.gov/pubmed/27994417
http://dx.doi.org/10.4103/0976-237X.194106
_version_ 1782472657052106752
author Mondal, Krishnendu
Mandal, Rupali
Sarkar, Badal Chandra
author_facet Mondal, Krishnendu
Mandal, Rupali
Sarkar, Badal Chandra
author_sort Mondal, Krishnendu
collection PubMed
description CONTEXT: Oral cancer is the third most prevalent malignancy in India. Leukoplakia is its most common precursor lesion. AIMS: This study aimed at evaluation of the Ki-67 expression and thereby detection of the dysplastic potential in histopathologically nondysplastic oral leukoplakia (OL). Secondarily, another purpose was to correlate various clinicopathological factors with the labeling indices (LIs) of Ki-67 in those cases as well. SETTINGS AND DESIGN: In total, 97 OL cases were examined. Relevant clinical and demographic information was retrieved from the pro forma, prefilled by the patients themselves during their first visit. SUBJECTS AND METHODS: Ki-67 immunohistochemical staining was performed on paraffin-embedded tissue samples. Its LIs were calculated and correlated with different clinicopathological parameters using statistical software SPSS version 16.0. RESULTS: 58.8% (57 cases) lesions exhibited a Ki-67 positivity of ≤5%, and 25.8% (25 cases) lesions exhibited it in the range of 6%–25%. Only 15 (15.4%) patches were stained positively between 26% and 60%. Patients’ age beyond 50 years, nonhomogeneous leukoplakia, and tobacco addiction were the significant risk factors for high Ki-67 scores (P < 0.05). CONCLUSIONS: Ki-67 is an essential immunohistochemical marker for epithelial dysplasia in OL, especially when the conventional histopathology fails to appreciate the same. In this purpose, Ki-67 labeling on a routine basis delivers the most convenient results for patients aged above 50 years, and/or addicted to tobacco products, and/or suffering from nonhomogeneous patches.
format Online
Article
Text
id pubmed-5141664
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-51416642016-12-19 A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia Mondal, Krishnendu Mandal, Rupali Sarkar, Badal Chandra Contemp Clin Dent Original Article CONTEXT: Oral cancer is the third most prevalent malignancy in India. Leukoplakia is its most common precursor lesion. AIMS: This study aimed at evaluation of the Ki-67 expression and thereby detection of the dysplastic potential in histopathologically nondysplastic oral leukoplakia (OL). Secondarily, another purpose was to correlate various clinicopathological factors with the labeling indices (LIs) of Ki-67 in those cases as well. SETTINGS AND DESIGN: In total, 97 OL cases were examined. Relevant clinical and demographic information was retrieved from the pro forma, prefilled by the patients themselves during their first visit. SUBJECTS AND METHODS: Ki-67 immunohistochemical staining was performed on paraffin-embedded tissue samples. Its LIs were calculated and correlated with different clinicopathological parameters using statistical software SPSS version 16.0. RESULTS: 58.8% (57 cases) lesions exhibited a Ki-67 positivity of ≤5%, and 25.8% (25 cases) lesions exhibited it in the range of 6%–25%. Only 15 (15.4%) patches were stained positively between 26% and 60%. Patients’ age beyond 50 years, nonhomogeneous leukoplakia, and tobacco addiction were the significant risk factors for high Ki-67 scores (P < 0.05). CONCLUSIONS: Ki-67 is an essential immunohistochemical marker for epithelial dysplasia in OL, especially when the conventional histopathology fails to appreciate the same. In this purpose, Ki-67 labeling on a routine basis delivers the most convenient results for patients aged above 50 years, and/or addicted to tobacco products, and/or suffering from nonhomogeneous patches. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5141664/ /pubmed/27994417 http://dx.doi.org/10.4103/0976-237X.194106 Text en Copyright: © 2016 Contemporary Clinical Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mondal, Krishnendu
Mandal, Rupali
Sarkar, Badal Chandra
A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title_full A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title_fullStr A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title_full_unstemmed A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title_short A study of Ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
title_sort study of ki-67 expression and its clinicopathological determinants in nondysplastic oral leukoplakia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141664/
https://www.ncbi.nlm.nih.gov/pubmed/27994417
http://dx.doi.org/10.4103/0976-237X.194106
work_keys_str_mv AT mondalkrishnendu astudyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia
AT mandalrupali astudyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia
AT sarkarbadalchandra astudyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia
AT mondalkrishnendu studyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia
AT mandalrupali studyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia
AT sarkarbadalchandra studyofki67expressionanditsclinicopathologicaldeterminantsinnondysplasticoralleukoplakia