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Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour

OBJECTIVE: The aim of the study is to analyse the Immuno-histochemical expression of Ki-67 and P16(INK4a) in CIN and cervical cancer cases and their utility to determine the accuracy of histological diagnosis and prediction of biological behavior of cervical lesion. METHODOLOGY: A retrospective cros...

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Autores principales: Sarma, Usha, Das, Gokul Chandra, Sarmah, Bidula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607082/
https://www.ncbi.nlm.nih.gov/pubmed/34319047
http://dx.doi.org/10.31557/APJCP.2021.22.7.2237
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author Sarma, Usha
Das, Gokul Chandra
Sarmah, Bidula
author_facet Sarma, Usha
Das, Gokul Chandra
Sarmah, Bidula
author_sort Sarma, Usha
collection PubMed
description OBJECTIVE: The aim of the study is to analyse the Immuno-histochemical expression of Ki-67 and P16(INK4a) in CIN and cervical cancer cases and their utility to determine the accuracy of histological diagnosis and prediction of biological behavior of cervical lesion. METHODOLOGY: A retrospective cross-sectional study was carried in 110 numbers of cervical biopsy that included 25 CIN1, 21 CIN2, 12 CIN3, 26 SCC and 01 adenocarcinoma and 25 non neoplastic lesion. The tissue sections were stained with Ki-67 and P16(INK4a). RESULTS: Ki-67 expression was seen in 55.5% (61/110) cases of cervical lesion., out of which 3.6% (4/110; cervicitis -2/110 and metaplasia-2/110) cases were non dysplaia, 51.8% (57/110) cases were dysplasia /CIN of varying grade including invasive cancer. P16(INK4a) expression was noted 51.8% (57/110). There was an increasing trend of the intensity of Ki-67 and P16(INK4a) from focal positivity in low grade lesion to diffuse intensity in higher grade lesion and is statistically significant. There was strong association between the two variables Ki-67 and P16(INK4a) positive cases with their histologic grade. CONCLUSION: Though histopathology remains the ‘‘gold standard’’ for the diagnosis of CIN, both low and high-grade, biomarkers like Ki-67 and P16(INK4a )have emerged as helpful adjuncts. Their combined use may assist in the histopathologic classification of preinvasive lesions and facilitate the distinction from nondysplasia.
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spelling pubmed-86070822021-11-26 Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour Sarma, Usha Das, Gokul Chandra Sarmah, Bidula Asian Pac J Cancer Prev Research Article OBJECTIVE: The aim of the study is to analyse the Immuno-histochemical expression of Ki-67 and P16(INK4a) in CIN and cervical cancer cases and their utility to determine the accuracy of histological diagnosis and prediction of biological behavior of cervical lesion. METHODOLOGY: A retrospective cross-sectional study was carried in 110 numbers of cervical biopsy that included 25 CIN1, 21 CIN2, 12 CIN3, 26 SCC and 01 adenocarcinoma and 25 non neoplastic lesion. The tissue sections were stained with Ki-67 and P16(INK4a). RESULTS: Ki-67 expression was seen in 55.5% (61/110) cases of cervical lesion., out of which 3.6% (4/110; cervicitis -2/110 and metaplasia-2/110) cases were non dysplaia, 51.8% (57/110) cases were dysplasia /CIN of varying grade including invasive cancer. P16(INK4a) expression was noted 51.8% (57/110). There was an increasing trend of the intensity of Ki-67 and P16(INK4a) from focal positivity in low grade lesion to diffuse intensity in higher grade lesion and is statistically significant. There was strong association between the two variables Ki-67 and P16(INK4a) positive cases with their histologic grade. CONCLUSION: Though histopathology remains the ‘‘gold standard’’ for the diagnosis of CIN, both low and high-grade, biomarkers like Ki-67 and P16(INK4a )have emerged as helpful adjuncts. Their combined use may assist in the histopathologic classification of preinvasive lesions and facilitate the distinction from nondysplasia. West Asia Organization for Cancer Prevention 2021-07 /pmc/articles/PMC8607082/ /pubmed/34319047 http://dx.doi.org/10.31557/APJCP.2021.22.7.2237 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sarma, Usha
Das, Gokul Chandra
Sarmah, Bidula
Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title_full Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title_fullStr Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title_full_unstemmed Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title_short Predictive Value of Marker of Proliferation Ki-67 and Cell Cycle Dependent Protein kinase Inhibitor P16(INK4a) in Cervical Biopsy to Determine Its Biological Behaviour
title_sort predictive value of marker of proliferation ki-67 and cell cycle dependent protein kinase inhibitor p16(ink4a) in cervical biopsy to determine its biological behaviour
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607082/
https://www.ncbi.nlm.nih.gov/pubmed/34319047
http://dx.doi.org/10.31557/APJCP.2021.22.7.2237
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