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An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions

INTRODUCTION: Ki-67 is a nuclear protein. It is a proliferation marker that has an essential function in tumorigenesis due to its positive connection with tumor expansion. AIM: The aim of this study was to evaluate the articulation of Ki‑67 as prognostic marker in various grades of oral epithelial d...

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Autores principales: Dash, Kailash C, Mahapatra, Niva, Bhuyan, Lipsa, Panda, Abikshyeet, Behura, Shyam S, Mishra, Pallavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595483/
https://www.ncbi.nlm.nih.gov/pubmed/33149470
http://dx.doi.org/10.4103/jpbs.JPBS_83_20
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author Dash, Kailash C
Mahapatra, Niva
Bhuyan, Lipsa
Panda, Abikshyeet
Behura, Shyam S
Mishra, Pallavi
author_facet Dash, Kailash C
Mahapatra, Niva
Bhuyan, Lipsa
Panda, Abikshyeet
Behura, Shyam S
Mishra, Pallavi
author_sort Dash, Kailash C
collection PubMed
description INTRODUCTION: Ki-67 is a nuclear protein. It is a proliferation marker that has an essential function in tumorigenesis due to its positive connection with tumor expansion. AIM: The aim of this study was to evaluate the articulation of Ki‑67 as prognostic marker in various grades of oral epithelial dysplasia (OED) and in oral squamous cell carcinoma (OSCC). MATERIALS AND METHODS: A total of 100 histologically affirmed samples of normal oral mucosa (NOM), OED, and OSCC were divided into three groups—Group I (10 samples of normal oral mucosa), Group II (45 samples of OED), Group III (45 samples of OSCC). Routine hematoxylin and eosin and immunohistochemical staining with Ki-67 monoclonal antibody were carried out in all the samples. RESULTS: Within Group I, articulation of Ki-67 was constrained to the basal layers. In Group II, cells showing positive expression of Ki-67 were available in the basal, suprabasal, and spinous layers. Cells showing positive expression of Ki-67 among well-differentiated OSCC were presented mainly in the periphery of the tumor nests; in moderately differentiated OSCC, cells were located in both peripheral and part of a center of the tumor nests; and in most cases of poorly differentiated OSCC, cells were diffused. Statistically significant difference in positive expression of Ki-67 was appreciated between three groups. CONCLUSION: Ki-67 antigen may perhaps be used as a marker for the histological reviewing of OED and OSCC. With the increase in the severity of OED, cells showing positive expression of Ki-67 also increased.
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spelling pubmed-75954832020-11-03 An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions Dash, Kailash C Mahapatra, Niva Bhuyan, Lipsa Panda, Abikshyeet Behura, Shyam S Mishra, Pallavi J Pharm Bioallied Sci Original Article INTRODUCTION: Ki-67 is a nuclear protein. It is a proliferation marker that has an essential function in tumorigenesis due to its positive connection with tumor expansion. AIM: The aim of this study was to evaluate the articulation of Ki‑67 as prognostic marker in various grades of oral epithelial dysplasia (OED) and in oral squamous cell carcinoma (OSCC). MATERIALS AND METHODS: A total of 100 histologically affirmed samples of normal oral mucosa (NOM), OED, and OSCC were divided into three groups—Group I (10 samples of normal oral mucosa), Group II (45 samples of OED), Group III (45 samples of OSCC). Routine hematoxylin and eosin and immunohistochemical staining with Ki-67 monoclonal antibody were carried out in all the samples. RESULTS: Within Group I, articulation of Ki-67 was constrained to the basal layers. In Group II, cells showing positive expression of Ki-67 were available in the basal, suprabasal, and spinous layers. Cells showing positive expression of Ki-67 among well-differentiated OSCC were presented mainly in the periphery of the tumor nests; in moderately differentiated OSCC, cells were located in both peripheral and part of a center of the tumor nests; and in most cases of poorly differentiated OSCC, cells were diffused. Statistically significant difference in positive expression of Ki-67 was appreciated between three groups. CONCLUSION: Ki-67 antigen may perhaps be used as a marker for the histological reviewing of OED and OSCC. With the increase in the severity of OED, cells showing positive expression of Ki-67 also increased. Wolters Kluwer - Medknow 2020-08 2020-08-28 /pmc/articles/PMC7595483/ /pubmed/33149470 http://dx.doi.org/10.4103/jpbs.JPBS_83_20 Text en Copyright: © 2020 Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Dash, Kailash C
Mahapatra, Niva
Bhuyan, Lipsa
Panda, Abikshyeet
Behura, Shyam S
Mishra, Pallavi
An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title_full An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title_fullStr An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title_full_unstemmed An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title_short An Immunohistochemical Study Showing Ki-67 as an Analytical Marker in Oral Malignant and Premalignant Lesions
title_sort immunohistochemical study showing ki-67 as an analytical marker in oral malignant and premalignant lesions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595483/
https://www.ncbi.nlm.nih.gov/pubmed/33149470
http://dx.doi.org/10.4103/jpbs.JPBS_83_20
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