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Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers

BACKGROUND: Although various improvements have been made in the reporting of the Papanicolaou (PAP) test in recent years, there remain several challenges that have yet to be addressed in terms of determining a standardized methodology for categorizing atypical squamous cells of undetermined signific...

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Autores principales: Singh, Palak, Kitkumthorn, Nakarin, Yanatatsaneejit, Pattamawadee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924328/
https://www.ncbi.nlm.nih.gov/pubmed/36308381
http://dx.doi.org/10.31557/APJCP.2022.23.10.3541
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author Singh, Palak
Kitkumthorn, Nakarin
Yanatatsaneejit, Pattamawadee
author_facet Singh, Palak
Kitkumthorn, Nakarin
Yanatatsaneejit, Pattamawadee
author_sort Singh, Palak
collection PubMed
description BACKGROUND: Although various improvements have been made in the reporting of the Papanicolaou (PAP) test in recent years, there remain several challenges that have yet to be addressed in terms of determining a standardized methodology for categorizing atypical squamous cells of undetermined significance (ASC US). METHODS: The present study focuses on evaluating the performance of the methylation status of two genes (CGB3 and NOP56) using a total of 200 PAP samples, which were divided into the “determined” group, with 78 samples based on cytology, and the “undetermined” group (ASC US), with 122 samples. The promoter methylation status of the CGB3 and NOP56 genes was detected for the 200 PAP samples using methylation specific PCR (MSP). The diagnostic abilities of the CGB3 and NOP56 genes in PAP samples were measured, and receiver operating characteristic (ROC) curves were generated using Python programming language. RESULTS: Based on the validation of CGB3 and NOP56 methylation in the 200 PAP samples, both genes exhibited higher methylation percentages in abnormal samples compared with normal samples. In addition, on the basis of diagnostic performance analysis, the CGB3 gene exhibited the highest sensitivity and specificity in both histology based ASC US and cytology based ‘determined’ PAP samples, with significant diagnostic abilities [area under the curve (AUC) values of 0.83 and 0.74, respectively, where AUC ≥0.5 was determined to be significant] to distinguish between the “normal” and “abnormal” samples. CONCLUSION: The findings of the present study will contribute toward identifying a DNA methylation marker for the early detection of abnormal samples before they reach the initial stages of cervical cancer, and should prove to be helpful for clinicians in terms of diagnosing patients whose cells are ASC US.
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spelling pubmed-99243282023-02-16 Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers Singh, Palak Kitkumthorn, Nakarin Yanatatsaneejit, Pattamawadee Asian Pac J Cancer Prev Research Article BACKGROUND: Although various improvements have been made in the reporting of the Papanicolaou (PAP) test in recent years, there remain several challenges that have yet to be addressed in terms of determining a standardized methodology for categorizing atypical squamous cells of undetermined significance (ASC US). METHODS: The present study focuses on evaluating the performance of the methylation status of two genes (CGB3 and NOP56) using a total of 200 PAP samples, which were divided into the “determined” group, with 78 samples based on cytology, and the “undetermined” group (ASC US), with 122 samples. The promoter methylation status of the CGB3 and NOP56 genes was detected for the 200 PAP samples using methylation specific PCR (MSP). The diagnostic abilities of the CGB3 and NOP56 genes in PAP samples were measured, and receiver operating characteristic (ROC) curves were generated using Python programming language. RESULTS: Based on the validation of CGB3 and NOP56 methylation in the 200 PAP samples, both genes exhibited higher methylation percentages in abnormal samples compared with normal samples. In addition, on the basis of diagnostic performance analysis, the CGB3 gene exhibited the highest sensitivity and specificity in both histology based ASC US and cytology based ‘determined’ PAP samples, with significant diagnostic abilities [area under the curve (AUC) values of 0.83 and 0.74, respectively, where AUC ≥0.5 was determined to be significant] to distinguish between the “normal” and “abnormal” samples. CONCLUSION: The findings of the present study will contribute toward identifying a DNA methylation marker for the early detection of abnormal samples before they reach the initial stages of cervical cancer, and should prove to be helpful for clinicians in terms of diagnosing patients whose cells are ASC US. West Asia Organization for Cancer Prevention 2022-10 /pmc/articles/PMC9924328/ /pubmed/36308381 http://dx.doi.org/10.31557/APJCP.2022.23.10.3541 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. https://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Research Article
Singh, Palak
Kitkumthorn, Nakarin
Yanatatsaneejit, Pattamawadee
Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title_full Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title_fullStr Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title_full_unstemmed Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title_short Identification of Malignancy in PAP Smear Samples Using the CGB3 and NOP56 Genes as Methylation Markers
title_sort identification of malignancy in pap smear samples using the cgb3 and nop56 genes as methylation markers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924328/
https://www.ncbi.nlm.nih.gov/pubmed/36308381
http://dx.doi.org/10.31557/APJCP.2022.23.10.3541
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